Widening the Scientific Excellence for Studies on Women’s and Fetal Health and Wellbeing

CORDIS fournit des liens vers les livrables publics et les publications des projets HORIZON.

Les liens vers les livrables et les publications des projets du 7e PC, ainsi que les liens vers certains types de résultats spécifiques tels que les jeux de données et les logiciels, sont récupérés dynamiquement sur OpenAIRE .

Livrables

First workshop held on “female reproduction: ovulatory disorders”

Deliverable generated as a result of Task 4.1.

Report on utilizing the UTARTU’s endometrial biopsies for practical training (1)

The deliverable will be generated as a result of Task 1.4.

Co-authored article on female metabolic health as a predictor of fertility as a result of a PhD student’s short-term stay in UOXF (1)

Deliverable generated as a result of Task 2.1.

Report on off-site virtual trainings and consultations performed to apply the NIPT methods within clinical use at UTARTU (1)

Deliverable generated as a result of Task 1.6.

Report on on-site and off-site trainings performed between UTARTU and UOXF to transfer knowledge for analysing female reproductive ageing

Deliverable is generated as a result of Task 2.2.

Joint article written on fetal non-invasive genetic testing

Deliverable generated as a result of Task 4.2.

Workshop held on single cell genomics

Deliverable generated as a result of Task 4.1.

Report on off-site virtual trainings and consultations performed to apply the NIPT methods within clinical use at UTARTU (3)

Deliverable generated as a result of Task 1.6.

Biobank samples shared for learning purposes (1)

The deliverable is generated as part of Task 1.2.

Biobank samples shared for learning purposes (3)

The deliverable is generated as a result of Task 1.2.

Summer school held in Tartu, Estonia

Deliverable generated as a result of Task 4.1.

Co-authored article on female reproductive ageing as a result of a PhD students’ short-term stay in UOXF (2)

Deliverable generated as a result of Task 2.2.

Co-authored article on human preimplantation embryos as a result of PhD students’ short-term stay in KU LEUVEN (1)

Deliverable generated as a result of Task 2.4.

Report on cross-applying opportunities for EGCUT and WTCCC datasets

The deliverable will be generated as a result of Task 1.3.

Report on utilizing the UTARTU’s endometrial biopsies for practical training (2)

The deliverable will be generated as a result of Task 1.4.

Report 2 on dissemination performed as part of local events for the scientific and local communities

Deliverable generated as a result of Task 4.5.

Co-authored article on analysing and implementing fetal non-invasive genetic testing as a result of a PhD student’s short-term stay in KU LEUVEN

Deliverable generated as a result of Task 2.5.

Co-authored article on female metabolic health as a predictor of fertility as a result of a post-doc’s short-term stay in UOXF (2)

Deliverable generated as a result of Task 2.1.

Joint article written on human preimplantation embryos

Deliverable generated as a result of Task 4.2.

Report 1 on dissemination performed as part of international conferences

Deliverable generated as a result of Task 4.3.

Second workshop held on “female reproduction: ovulatory disorders”

Deliverable generated as a result of Task 4.1.

Senior staff exchanges completed between UTARTU and KU LEUVEN to transfer knowledge for isolating and amplifying DNA and RNA from single blastomere cells and to deploy time-lapse and NIPT methods

Deliverable generated as a result of Task 1.5 and Task 1.6.

Joint article written on female metabolic health as a predictor of fertility

Deliverable generated as a result of Task 4.2.

Report 3 on dissemination performed as part of international conferences

Deliverable generated as a result of Task 4.3.

Joint article written on female reproductive ageing

Deliverable generated as a result of Task 4.2.

Co-authored article on female reproductive ageing as a result of a PhD students’ short-term stay in UOXF (1)

Deliverable generated as a result of Task 2.2.

Joint article written on endometrial receptivity, implantation and endometriosis

Deliverable generated as a result of Task 4.2.

Report on on-site and off-site trainings performed between UTARTU and UOXF to transfer knowledge on female metabolic health as a predictor of fertility

Report generated as a result of Task 2.1.

Co-authored article on human preimplantation embryos as a result of PhD students’ short-term stay in KU LEUVEN (2)

Deliverable generated as a result of Task 2.4.

Report 3 on dissemination performed as part of local events for the scientific and local communities

Deliverable generated as a result of Task 4.4 and Task 4.5.

Report 2 on dissemination performed as part of international conferences

Deliverable generated as a result of Task 4.3.

Co-authored article on analysing and implementing fetal non-invasive genetic testing as a result of a post-doc’s short-term stay in KU LEUVEN

Deliverable generated as a result of Task 2.5.

Biobank samples shared for learning purposes (5)

The deliverable is generated as a result of Task 1.2.

Biobank samples shared for learning purposes (4)

The deliverable is generated as a result of Task 1.2.

Report 1 on dissemination performed as part of local events for the scientific and local communities

Deliverable generated as a result of Task 4.5.

Co-authored article on endometrial receptivity, implantation and endometriosis as a result of a PhD student’s short-term stay in UOXF

Deliverable generated as a result of Task 2.3.

Report on off-site virtual trainings and consultations performed to apply the NIPT methods within clinical use at UTARTU (2)

Deliverable generated as a result of Task 1.6.

Biobank samples shared for learning purposes (2)

The deliverable is generated as a result of Task 1.2.

Co-authored article on female reproductive ageing as a result of a post-doc’s short-term stay in UOXF

Report generated as a result of Task 2.2.

Test for non-invasive identification of endometriosis, which has been validated in partner organisations

Deliverable is generated as a result of Tasks 3.1 - 3.3.

Clinical use of NIPT technology

Deliverable generated as a result of Tasks 3.1 - 3.3.

NIPT technology adopted in an initial format by UTARTU’s scientists

Deliverable generated as a result of Tasks 3.1 - 3.3.

Clinical use of PGS in Tartu University Hospital

Deliverable generated as a result of Tasks 3.1 - 3.3.

Publications

Two familial microduplications of 15q26.3 causing overgrowth and variable intellectual disability with normal copy number of IGF1R

Auteurs: Melanie Leffler, Sanna Puusepp, Olga Žilina, Ying Zhu, Kati Kuuse, Nicole Bain, Trent Burgess, Katrin Õunap, Michael Field
Publié dans: European Journal of Medical Genetics, 2015, ISSN 1769-7212
Éditeur: Elsevier BV
DOI: 10.1016/j.ejmg.2015.12.002

Folic acid supplementation and methylenetetrahydrofolate reductase (MTHFR) gene variations in relation to in vitro fertilization pregnancy outcome

Auteurs: Tiina Murto, Theodora K. Kallak, Annica Hoas, Signe Altmäe, Andres Salumets, Torbjörn K. Nilsson, Agneta Skoog Svanberg, Kjell Wånggren, Agneta Yngve, Anneli Stavreus-Evers
Publié dans: Acta Obstetricia et Gynecologica Scandinavica, Numéro 94/1, 2015, Page(s) 65-71, ISSN 0001-6349
Éditeur: Wiley-Blackwell
DOI: 10.1111/aogs.12522

Intimate partner violence and sexual health outcomes: a population-based study among 16-44-year-old women in Estonia

Auteurs: M. Laanpere, I. Ringmets, K. Part, H. Karro
Publié dans: The European Journal of Public Health, Numéro 23/4, 2013, Page(s) 688-693, ISSN 1101-1262
Éditeur: Oxford University Press
DOI: 10.1093/eurpub/cks144

Patient with Dup(5)(q35.2-q35.3) reciprocal to the common Sotos syndrome deletion and review of the literature

Auteurs: Olga Žilina, Tiia Reimand, Pille Tammur, Vallo Tillmann, Ants Kurg, Katrin Õunap
Publié dans: European Journal of Medical Genetics, Numéro 56/4, 2013, Page(s) 202-206, ISSN 1769-7212
Éditeur: Elsevier BV
DOI: 10.1016/j.ejmg.2013.01.008

A History of Abuse and Operative Delivery – Results from a European Multi-Country Cohort Study

Auteurs: Berit Schei, Mirjam Lukasse, Elsa Lena Ryding, Jacquelyn Campbell, Helle Karro, Hildur Kristjansdottir, Made Laanpere, Anne-Mette Schroll, Ann Tabor, Marleen Temmerman, An-Sofie Van Parys, Anne-Marie Wangel, Thora Steingrimsdottir
Publié dans: PLoS ONE, Numéro 9/1, 2014, Page(s) e87579, ISSN 1932-6203
Éditeur: Public Library of Science
DOI: 10.1371/journal.pone.0087579

Pregnancy Rate in Endometriosis Patients according to the Severity of the Disease after Using a Combined Approach of Laparoscopy, GnRH Agonist Treatment and in vitro Fertilization

Auteurs: Deniss Sõritsa, Merli Saare, Triin Laisk-Podar, Maire Peters, Andrei Sõritsa, Kadri Matt, Helle Karro, Andres Salumets
Publié dans: Gynecologic and Obstetric Investigation, Numéro 79/1, 2015, Page(s) 34-39, ISSN 0378-7346
Éditeur: S. Karger AG
DOI: 10.1159/000365329

Syndromic intellectual disability: A new phenotype caused by an aromatic amino acid decarboxylase gene (DDC) variant

Auteurs: Claudio Graziano, Anita Wischmeijer, Tommaso Pippucci, Carlo Fusco, Chiara Diquigiovanni, Margit Nõukas, Martin Sauk, Ants Kurg, Francesca Rivieri, Nenad Blau, Georg F. Hoffmann, Alka Chaubey, Charles E. Schwartz, Giovanni Romeo, Elena Bonora, Livia Garavelli, Marco Seri
Publié dans: Gene, Numéro 559/2, 2015, Page(s) 144-148, ISSN 0378-1119
Éditeur: Elsevier BV
DOI: 10.1016/j.gene.2015.01.026

Mosaicism for maternal uniparental disomy 15 in a boy with some clinical features of Prader–Willi syndrome

Auteurs: Olga Žilina, Tiina Kahre, Inga Talvik, Eve Õiglane-Shlik, Vallo Tillmann, Katrin Õunap
Publié dans: European Journal of Medical Genetics, Numéro 57/6, 2014, Page(s) 279-283, ISSN 1769-7212
Éditeur: Elsevier BV
DOI: 10.1016/j.ejmg.2014.03.007

Monozygotic Twins with 17q21.31 Microdeletion Syndrome

Auteurs: Marketa Vlckova, Miroslava Hancarova, Jana Drabova, Zuzana Slamova, Monika Koudova, Renata Alanova, Katrin Mannik, Ants Kurg, Zdenek Sedlacek
Publié dans: Twin Research and Human Genetics, Numéro 17/05, 2014, Page(s) 405-410, ISSN 1832-4274
Éditeur: Australian Academic Press Pty Ltd.
DOI: 10.1017/thg.2014.29

Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta

Auteurs: Tauno Metsalu, Triin Viltrop, Airi Tiirats, Balaji Rajashekar, Ene Reimann, Sulev Kõks, Kristiina Rull, Lili Milani, Ganesh Acharya, Purusotam Basnet, Jaak Vilo, Reedik Mägi, Andres Metspalu, Maire Peters, Kadri Haller-Kikkatalo, Andres Salumets
Publié dans: Epigenetics, Numéro 9/10, 2014, Page(s) 1397-1409, ISSN 1559-2294
Éditeur: Landes Bioscience
DOI: 10.4161/15592294.2014.970052

Expression of B7 and CD28 family genes in newly diagnosed type 1 diabetes

Auteurs: Katrin Pruul, Kalle Kisand, Kristi Alnek, Kaja Metsküla, Kaire Heilman, Aleksandr Peet, Karin Varik, Raivo Uibo
Publié dans: Human Immunology, Numéro 74/10, 2013, Page(s) 1251-1257, ISSN 0198-8859
Éditeur: Elsevier BV
DOI: 10.1016/j.humimm.2013.07.007

Complementary seminovaginal microbiome in couples

Auteurs: Reet Mändar, Margus Punab, Natalja Borovkova, Eleri Lapp, Riinu Kiiker, Paul Korrovits, Andres Metspalu, Kaarel Krjutškov, Hiie Nõlvak, Jens-Konrad Preem, Kristjan Oopkaup, Andres Salumets, Jaak Truu
Publié dans: Research in Microbiology, Numéro 166/5, 2015, Page(s) 440-447, ISSN 0923-2508
Éditeur: Elsevier BV
DOI: 10.1016/j.resmic.2015.03.009

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

Auteurs: Alberto Magi, Lorenzo Tattini, Ingrid Cifola, Romina D’Aurizio, Matteo Benelli, Eleonora Mangano, Cristina Battaglia, Elena Bonora, Ants Kurg, Marco Seri, Pamela Magini, Betti Giusti, Giovanni Romeo, Tommaso Pippucci, Gianluca De Bellis, Rosanna Abbate, Gian Franco Gensini
Publié dans: Genome Biology, Numéro 14/10, 2013, Page(s) R120, ISSN 1465-6906
Éditeur: BioMed Central
DOI: 10.1186/gb-2013-14-10-r120

A genome-wide association study of early menopause and the combined impact of identified variants

Auteurs: J. R. B. Perry, T. Corre, T. Esko, D. I. Chasman, K. Fischer, N. Franceschini, C. He, Z. Kutalik, M. Mangino, L. M. Rose, A. Vernon Smith, L. Stolk, P. Sulem, M. N. Weedon, W. V. Zhuang, A. Arnold, A. Ashworth, S. Bergmann, J. E. Buring, A. Burri, C. Chen, M. C. Cornelis, D. J. Couper, M. O. Goodarzi, V. Gudnason, T. Harris, A. Hofman, M. Jones, P. Kraft, L. Launer, J. S. E. Laven, G. Li, B. McKnight, C. Masciullo, L. Milani, N. Orr, B. M. Psaty, P. M. Ridker, F. Rivadeneira, C. Sala, A. Salumets, M. Schoemaker, M. Traglia, G. Waeber, S. J. Chanock, E. W. Demerath, M. Garcia, S. E. Hankinson, F. B. Hu, D. J. Hunter, K. L. Lunetta, A. Metspalu, G. W. Montgomery, J. M. Murabito, A. B. Newman, K. K. Ong, T. D. Spector, K. Stefansson, A. J. Swerdlow, U. Thorsteinsdottir, R. M. Van Dam, A. G. Uitterlinden, J. A. Visser, P. Vollenweider, D. Toniolo, A. Murray
Publié dans: Human Molecular Genetics, Numéro 22/7, 2013, Page(s) 1465-1472, ISSN 0964-6906
Éditeur: Oxford University Press
DOI: 10.1093/hmg/dds551

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

Auteurs: Anubha Mahajan, Min Jin Go, Weihua Zhang, Jennifer E Below, Kyle J Gaulton, Teresa Ferreira, Momoko Horikoshi, Andrew D Johnson, Maggie C Y Ng, Inga Prokopenko, Danish Saleheen, Xu Wang, Eleftheria Zeggini, Goncalo R Abecasis, Linda S Adair, Peter Almgren, Mustafa Atalay, Tin Aung, Damiano Baldassarre, Beverley Balkau, Yuqian Bao, Anthony H Barnett, Ines Barroso, Abdul Basit, Latonya F Been, John Beilby, Graeme I Bell, Rafn Benediktsson, Richard N Bergman, Bernhard O Boehm, Eric Boerwinkle, Lori L Bonnycastle, Noël Burtt, Qiuyin Cai, Harry Campbell, Jason Carey, Stephane Cauchi, Mark Caulfield, Juliana C N Chan, Li-Ching Chang, Tien-Jyun Chang, Yi-Cheng Chang, Guillaume Charpentier, Chien-Hsiun Chen, Han Chen, Yuan-Tsong Chen, Kee-Seng Chia, Manickam Chidambaram, Peter S Chines, Nam H Cho, Young Min Cho, Lee-Ming Chuang, Francis S Collins, Marilyn C Cornelis, David J Couper, Andrew T Crenshaw, Rob M van Dam, John Danesh, Debashish Das, Ulf de Faire, George Dedoussis, Panos Deloukas, Antigone S Dimas, Christian Dina, Alex S F Doney, Peter J Donnelly, Mozhgan Dorkhan, Cornelia van Duijn, Josée Dupuis, Sarah Edkins, Paul Elliott, Valur Emilsson, Raimund Erbel, Johan G Eriksson, Jorge Escobedo, Tonu Esko, Elodie Eury, Jose C Florez, Pierre Fontanillas, Nita G Forouhi, Tom Forsen, Caroline Fox, Ross M Fraser, Timothy M Frayling, Philippe Froguel, Philippe Frossard, Yutang Gao, Karl Gertow, Christian Gieger, Bruna Gigante, Harald Grallert, George B Grant, Leif C Groop, Christopher J Groves, Elin Grundberg, Candace Guiducci, Anders Hamsten, Bok-Ghee Han, Kazuo Hara, Neelam Hassanali, Andrew T Hattersley, Caroline Hayward, Asa K Hedman, Christian Herder, Albert Hofman, Oddgeir L Holmen, Kees Hovingh, Astradur B Hreidarsson, Cheng Hu, Frank B Hu, Jennie Hui, Steve E Humphries, Sarah E Hunt, David J Hunter, Kristian Hveem, Zafar I Hydrie, Hiroshi Ikegami, Thomas Illig, Erik Ingelsson, Muhammed Islam, Bo Isomaa, Anne U Jackson, Tazeen Jafar, Alan James, Weiping Jia, Karl-Heinz Jöckel, Anna Jonsson, Jeremy B M Jowett, Takashi Kadowaki, Hyun Min Kang, Stavroula Kanoni, Wen Hong L Kao, Sekar Kathiresan, Norihiro Kato, Prasad Katulanda, Sirkka M Keinanen-Kiukaanniemi, Ann M Kelly, Hassan Khan, Kay-Tee Khaw, Chiea-Chuen Khor, Hyung-Lae Kim, Sangsoo Kim, Young Jin Kim, Leena Kinnunen, Norman Klopp, Augustine Kong, Eeva Korpi-Hyövälti, Sudhir Kowlessur, Peter Kraft, Jasmina Kravic, Malene M Kristensen, S Krithika, Ashish Kumar, Jesus Kumate, Johanna Kuusisto, Soo Heon Kwak, Markku Laakso, Vasiliki Lagou, Timo A Lakka, Claudia Langenberg, Cordelia Langford, Robert Lawrence, Karin Leander, Jen-Mai Lee, Nanette R Lee, Man Li, Xinzhong Li, Yun Li, Junbin Liang, Samuel Liju, Wei-Yen Lim, Lars Lind, Cecilia M Lindgren, Eero Lindholm, Ching-Ti Liu, Jian Jun Liu, Stéphane Lobbens, Jirong Long, Ruth J F Loos, Wei Lu, Jian'an Luan, Valeriya Lyssenko, Ronald C W Ma, Shiro Maeda, Reedik Mägi, Satu Männistö, David R Matthews, James B Meigs, Olle Melander, Andres Metspalu, Julia Meyer, Ghazala Mirza, Evelin Mihailov, Susanne Moebus, Viswanathan Mohan, Karen L Mohlke, Andrew D Morris, Thomas W Mühleisen, Martina Müller-Nurasyid, Bill Musk, Jiro Nakamura, Eitaro Nakashima, Pau Navarro, Peng-Keat Ng, Alexandra C Nica, Peter M Nilsson, Inger Njølstad, Markus M Nöthen, Keizo Ohnaka, Twee Hee Ong, Katharine R Owen, Colin N A Palmer, James S Pankow, Kyong Soo Park, Melissa Parkin, Sonali Pechlivanis, Nancy L Pedersen, Leena Peltonen, John R B Perry, Annette Peters, Janani M Pinidiyapathirage, Carl G P Platou, Simon Potter, Jackie F Price, Lu Qi, Venkatesan Radha, Loukianos Rallidis, Asif Rasheed, Wolfgang Rathmann, Rainer Rauramaa, Soumya Raychaudhuri, N William Rayner, Simon D Rees, Emil Rehnberg, Samuli Ripatti, Neil Robertson, Michael Roden, Elizabeth J Rossin, Igor Rudan, Denis Rybin, Timo E Saaristo, Veikko Salomaa, Juha Saltevo, Maria Samuel, Dharambir K Sanghera, Jouko Saramies, James Scott, Laura J Scott, Robert A Scott, Ayellet V Segrè, Joban
Publié dans: Nature Genetics, Numéro 46/3, 2014, Page(s) 234-244, ISSN 1061-4036
Éditeur: Nature Publishing Group
DOI: 10.1038/ng.2897

DNA mismatch repair gene MSH6 implicated in determining age at natural menopause

Auteurs: J. R. B. Perry, Y.-H. Hsu, D. I. Chasman, A. D. Johnson, C. Elks, E. Albrecht, I. L. Andrulis, J. Beesley, G. S. Berenson, S. Bergmann, S. E. Bojesen, M. K. Bolla, J. Brown, J. E. Buring, H. Campbell, J. Chang-Claude, G. Chenevix-Trench, T. Corre, F. J. Couch, A. Cox, K. Czene, A. P. D'adamo, G. Davies, I. J. Deary, J. Dennis, D. F. Easton, E. G. Engelhardt, J. G. Eriksson, T. Esko, P. A. Fasching, J. D. Figueroa, H. Flyger, A. Fraser, M. Garcia-Closas, P. Gasparini, C. Gieger, G. Giles, P. Guenel, S. Hagg, P. Hall, C. Hayward, J. Hopper, E. Ingelsson, S. L. R. Kardia, K. Kasiman, J. A. Knight, J. Lahti, D. A. Lawlor, P. K. E. Magnusson, S. Margolin, J. A. Marsh, A. Metspalu, J. E. Olson, C. E. Pennell, O. Polasek, I. Rahman, P. M. Ridker, A. Robino, I. Rudan, A. Rudolph, A. Salumets, M. K. Schmidt, M. J. Schoemaker, E. N. Smith, J. A. Smith, M. Southey, D. Stockl, A. J. Swerdlow, D. J. Thompson, T. Truong, S. Ulivi, M. Waldenberger, Q. Wang, S. Wild, J. F. Wilson, A. F. Wright, L. Zgaga, K. K. Ong, J. M. Murabito, D. Karasik, A. Murray
Publié dans: Human Molecular Genetics, Numéro 23/9, 2014, Page(s) 2490-2497, ISSN 0964-6906
Éditeur: Oxford University Press
DOI: 10.1093/hmg/ddt620

Prevalence of experienced abuse in healthcare and associated obstetric characteristics in six European countries

Auteurs: Mirjam Lukasse, Anne-Mette Schroll, Helle Karro, Berit Schei, Thora Steingrimsdottir, An-Sofie Van Parys, Elsa Lena Ryding, Ann Tabor
Publié dans: Acta Obstetricia et Gynecologica Scandinavica, Numéro 94/5, 2015, Page(s) 508-517, ISSN 0001-6349
Éditeur: Wiley-Blackwell
DOI: 10.1111/aogs.12593

High-Throughput Sequencing Approach Uncovers the miRNome of Peritoneal Endometriotic Lesions and Adjacent Healthy Tissues

Auteurs: Merli Saare, Kadri Rekker, Triin Laisk-Podar, Deniss Sõritsa, Anne Mari Roost, Jaak Simm, Agne Velthut-Meikas, Külli Samuel, Tauno Metsalu, Helle Karro, Andrei Sõritsa, Andres Salumets, Maire Peters
Publié dans: PLoS ONE, Numéro 9/11, 2014, Page(s) e112630, ISSN 1932-6203
Éditeur: Public Library of Science
DOI: 10.1371/journal.pone.0112630

Using Genetic Variants to Assess the Relationship Between Circulating Lipids and Type 2 Diabetes

Auteurs: Tove Fall, Weijia Xie, Wenny Poon, Hanieh Yaghootkar, Reedik Mägi, Joshua W. Knowles, Valeriya Lyssenko, Michael Weedon, Timothy M. Frayling, Erik Ingelsson
Publié dans: Diabetes, Numéro 64/7, 2015, Page(s) 2676-2684, ISSN 0012-1797
Éditeur: American Diabetes Association
DOI: 10.2337/db14-1710

Tissue-specific mitochondrial heteroplasmy at position 16,093 within the same individual

Auteurs: Kaarel Krjutškov, Marina Koltšina, Kelli Grand, Urmo Võsa, Martin Sauk, Neeme Tõnisson, Andres Salumets
Publié dans: Current Genetics, Numéro 60/1, 2014, Page(s) 11-16, ISSN 0172-8083
Éditeur: Springer Verlag
DOI: 10.1007/s00294-013-0398-6

Familial 1.3-Mb 11p15.5p15.4 Duplication in Three Generations Causing Silver-Russell and Beckwith-Wiedemann Syndromes

Auteurs: Mari-Anne Vals, Tiina Kahre, Pille Mee, Kai Muru, Eha Kallas, Olga �ilina, Vallo Tillmann, Katrin �unap
Publié dans: Molecular Syndromology, Numéro 6/3, 2015, Page(s) 147-151, ISSN 1661-8769
Éditeur: S. Karger AG
DOI: 10.1159/000437061

Characterization of the Vaginal Micro- and Mycobiome in Asymptomatic Reproductive-Age Estonian Women

Auteurs: Tiina Drell, Triin Lillsaar, Lea Tummeleht, Jaak Simm, Anu Aaspõllu, Edda Väin, Ivo Saarma, Andres Salumets, Gilbert G. G. Donders, Madis Metsis
Publié dans: PLoS ONE, Numéro 8/1, 2013, Page(s) e54379, ISSN 1932-6203
Éditeur: Public Library of Science
DOI: 10.1371/journal.pone.0054379

Expression Pattern and Localization Dynamics of Guanine Nucleotide Exchange Factor RIC8 during Mouse Oogenesis

Auteurs: Merly Saare, Sirje Lulla, Tambet Tõnissoo, Riho Meier, Keiu Kask, Katrin Ruisu, Alar Karis, Andres Salumets, Margus Pooga
Publié dans: PLOS ONE, Numéro 10/6, 2015, Page(s) e0129131, ISSN 1932-6203
Éditeur: Public Library of Science
DOI: 10.1371/journal.pone.0129131

Physical activity, fatness, educational level and snuff consumption as determinants of semen quality: findings of the ActiART study

Auteurs: Triin Pärn, Raúl Grau Ruiz, Theodora Kunovac Kallak, Jonatan R. Ruiz, Eva Davey, Julius Hreinsson, Kjell Wånggren, Andres Salumets, Michael Sjöström, Anneli Stavreus-Evers, Francisco B. Ortega, Signe Altmäe
Publié dans: Reproductive BioMedicine Online, Numéro 31/1, 2015, Page(s) 108-119, ISSN 1472-6483
Éditeur: Reproductive Healthcare Ltd
DOI: 10.1016/j.rbmo.2015.03.004

Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu

Auteurs: Liis Leitsalu, Toomas Haller, Tõnu Esko, Mari-Liis Tammesoo, Helene Alavere, Harold Snieder, Markus Perola, Pauline C Ng, Reedik Mägi, Lili Milani, Krista Fischer, Andres Metspalu
Publié dans: International Journal of Epidemiology, Numéro 44/4, 2015, Page(s) 1137-1147, ISSN 0300-5771
Éditeur: Oxford University Press
DOI: 10.1093/ije/dyt268

The prevalence and phenotypic characteristics of spontaneous premature ovarian failure: a general population registry-based study

Auteurs: K. Haller-Kikkatalo, R. Uibo, A. Kurg, A. Salumets
Publié dans: Human Reproduction, Numéro 30/5, 2015, Page(s) 1229-1238, ISSN 0268-1161
Éditeur: Oxford University Press
DOI: 10.1093/humrep/dev021

Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity

Auteurs: A. S. Dimas, V. Lagou, A. Barker, J. W. Knowles, R. Magi, M.-F. Hivert, A. Benazzo, D. Rybin, A. U. Jackson, H. M. Stringham, C. Song, A. Fischer-Rosinsky, T. W. Boesgaard, N. Grarup, F. A. Abbasi, T. L. Assimes, K. Hao, X. Yang, C. Lecoeur, I. Barroso, L. L. Bonnycastle, Y. Bottcher, S. Bumpstead, P. S. Chines, M. R. Erdos, J. Graessler, P. Kovacs, M. A. Morken, N. Narisu, F. Payne, A. Stancakova, A. J. Swift, A. Tonjes, S. R. Bornstein, S. Cauchi, P. Froguel, D. Meyre, P. E. H. Schwarz, H.-U. Haring, U. Smith, M. Boehnke, R. N. Bergman, F. S. Collins, K. L. Mohlke, J. Tuomilehto, T. Quertemous, L. Lind, T. Hansen, O. Pedersen, M. Walker, A. F. H. Pfeiffer, J. Spranger, M. Stumvoll, J. B. Meigs, N. J. Wareham, J. Kuusisto, M. Laakso, C. Langenberg, J. Dupuis, R. M. Watanabe, J. C. Florez, E. Ingelsson, M. I. McCarthy, I. Prokopenko
Publié dans: Diabetes, Numéro 63/6, 2014, Page(s) 2158-2171, ISSN 0012-1797
Éditeur: American Diabetes Association
DOI: 10.2337/db13-0949

Elevated blood plasma antioxidant status is favourable for achieving IVF/ICSI pregnancy

Auteurs: Agne Velthut, Mihkel Zilmer, Kersti Zilmer, Tanel Kaart, Helle Karro, Andres Salumets
Publié dans: Reproductive BioMedicine Online, Numéro 26/4, 2013, Page(s) 345-352, ISSN 1472-6483
Éditeur: Reproductive Healthcare Ltd
DOI: 10.1016/j.rbmo.2012.12.012

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

Auteurs: John R. B. Perry, Felix Day, Cathy E. Elks, Patrick Sulem, Deborah J. Thompson, Teresa Ferreira, Chunyan He, Daniel I. Chasman, Tõnu Esko, Gudmar Thorleifsson, Eva Albrecht, Wei Q. Ang, Tanguy Corre, Diana L. Cousminer, Bjarke Feenstra, Nora Franceschini, Andrea Ganna, Andrew D. Johnson, Sanela Kjellqvist, Kathryn L. Lunetta, George McMahon, Ilja M. Nolte, Lavinia Paternoster, Eleonora Porcu, Albert V. Smith, Lisette Stolk, Alexander Teumer, Natalia Tšernikova, Emmi Tikkanen, Sheila Ulivi, Erin K. Wagner, Najaf Amin, Laura J. Bierut, Enda M. Byrne, Jouke-Jan Hottenga, Daniel L. Koller, Massimo Mangino, Tune H. Pers, Laura M. Yerges-Armstrong, Jing Hua Zhao, Irene L. Andrulis, Hoda Anton-Culver, Femke Atsma, Stefania Bandinelli, Matthias W. Beckmann, Javier Benitez, Carl Blomqvist, Stig E. Bojesen, Manjeet K. Bolla, Bernardo Bonanni, Hiltrud Brauch, Hermann Brenner, Julie E. Buring, Jenny Chang-Claude, Stephen Chanock, Jinhui Chen, Georgia Chenevix-Trench, J. Margriet Collée, Fergus J. Couch, David Couper, Andrea D. Coviello, Angela Cox, Kamila Czene, Adamo Pio D’adamo, George Davey Smith, Immaculata De Vivo, Ellen W. Demerath, Joe Dennis, Peter Devilee, Aida K. Dieffenbach, Alison M. Dunning, Gudny Eiriksdottir, Johan G. Eriksson, Peter A. Fasching, Luigi Ferrucci, Dieter Flesch-Janys, Henrik Flyger, Tatiana Foroud, Lude Franke, Melissa E. Garcia, Montserrat García-Closas, Frank Geller, Eco E. J. de Geus, Graham G. Giles, Daniel F. Gudbjartsson, Vilmundur Gudnason, Pascal Guénel, Suiqun Guo, Per Hall, Ute Hamann, Robin Haring, Catharina A. Hartman, Andrew C. Heath, Albert Hofman, Maartje J. Hooning, John L. Hopper, Frank B. Hu, David J. Hunter, David Karasik, Douglas P. Kiel, Julia A. Knight, Veli-Matti Kosma, Zoltan Kutalik, Sandra Lai, Diether Lambrechts, Annika Lindblom, Reedik Mägi, Patrik K. Magnusson, Arto Mannermaa, Nicholas G. Martin, Gisli Masson, Patrick F. McArdle, Wendy L. McArdle, Mads Melbye, Kyriaki Michailidou, Evelin Mihailov, Lili Milani, Roger L. Milne, Heli Nevanlinna, Patrick Neven, Ellen A. Nohr, Albertine J. Oldehinkel, Ben A. Oostra, Aarno Palotie, Munro Peacock, Nancy L. Pedersen, Paolo Peterlongo, Julian Peto, Paul D. P. Pharoah, Dirkje S. Postma, Anneli Pouta, Katri Pylkäs, Paolo Radice, Susan Ring, Fernando Rivadeneira, Antonietta Robino, Lynda M. Rose, Anja Rudolph, Veikko Salomaa, Serena Sanna, David Schlessinger, Marjanka K. Schmidt, Mellissa C. Southey, Ulla Sovio, Meir J. Stampfer, Doris Stöckl, Anna M. Storniolo, Nicholas J. Timpson, Jonathan Tyrer, Jenny A. Visser, Peter Vollenweider, Henry Völzke, Gerard Waeber, Melanie Waldenberger, Henri Wallaschofski, Qin Wang, Gonneke Willemsen, Robert Winqvist, Bruce H. R. Wolffenbuttel, Margaret J. Wright, Dorret I. Boomsma, Michael J. Econs, Kay-Tee Khaw, Ruth J. F. Loos, Mark I. McCarthy, Grant W. Montgomery, John P. Rice, Elizabeth A. Streeten, Unnur Thorsteinsdottir, Cornelia M. van Duijn, Behrooz Z. Alizadeh, Sven Bergmann, Eric Boerwinkle, Heather A. Boyd, Laura Crisponi, Paolo Gasparini, Christian Gieger, Tamara B. Harris, Erik Ingelsson, Marjo-Riitta Järvelin, Peter Kraft, Debbie Lawlor, Andres Metspalu, Craig E. Pennell, Paul M. Ridker, Harold Snieder, Thorkild I. A. Sørensen, Tim D. Spector, David P. Strachan, André G. Uitterlinden, Nicholas J. Wareham, Elisabeth Widen, Marek Zygmunt, Anna Murray, Douglas F. Easton, Kari Stefansson, Joanne M. Murabito, Ken K. Ong
Publié dans: Nature, Numéro 514/7520, 2014, Page(s) 92-97, ISSN 0028-0836
Éditeur: Nature Publishing Group
DOI: 10.1038/nature13545

Comparison of serum exosome isolation methods for microRNA profiling

Auteurs: Kadri Rekker, Merli Saare, Anne Mari Roost, Anna-Liisa Kubo, Natasa Zarovni, Antonio Chiesi, Andres Salumets, Maire Peters
Publié dans: Clinical Biochemistry, Numéro 47/1-2, 2014, Page(s) 135-138, ISSN 0009-9120
Éditeur: Elsevier BV
DOI: 10.1016/j.clinbiochem.2013.10.020

The Diagnostic Utility of Single Long Contiguous Stretches of Homozygosity in Patients without Parental Consanguinity

Auteurs: Sander Pajusalu, Olga �ilina, Maria Yakoreva, Pille Tammur, Kati Kuuse, Triin M�lter-V��r, Margit N�ukas, Tiia Reimand, Katrin �unap
Publié dans: Molecular Syndromology, Numéro 6/3, 2015, Page(s) 135-140, ISSN 1661-8769
Éditeur: S. Karger AG
DOI: 10.1159/000438776

De novo deletion of HOXB gene cluster in a patient with failure to thrive, developmental delay, gastroesophageal reflux and bronchiectasis

Auteurs: Sander Pajusalu, Tiia Reimand, Oivi Uibo, Maire Vasar, Inga Talvik, Olga Zilina, Pille Tammur, Katrin Õunap
Publié dans: European Journal of Medical Genetics, Numéro 58/6-7, 2015, Page(s) 336-340, ISSN 1769-7212
Éditeur: Elsevier BV
DOI: 10.1016/j.ejmg.2015.04.002

Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genome

Auteurs: Olga Žilina, Marina Koltšina, Raivo Raid, Ants Kurg, Neeme Tõnisson, Andres Salumets
Publié dans: BMC Genomics, Numéro 16/1, 2015, ISSN 1471-2164
Éditeur: BioMed Central
DOI: 10.1186/s12864-015-1916-3

Autoimmune Activation toward Embryo Implantation is Rare in Immune-Privileged Human Endometrium

Auteurs: Kadri Haller-Kikkatalo, Aili Tagoma, Raivo Uibo, Andres Salumets, Signe Altmäe
Publié dans: Seminars in Reproductive Medicine, Numéro 32/05, 2014, Page(s) 376-384, ISSN 1526-8004
Éditeur: Thieme Medical Publishers
DOI: 10.1055/s-0034-1376356

Fear of Childbirth and Risk of Cesarean Delivery: A Cohort Study in Six European Countries

Auteurs: Elsa Lena Ryding, Mirjam Lukasse, An-Sophie Van Parys, Anne-Marie Wangel, Helle Karro, Hildur Kristjansdottir, Anne-Mette Schroll, Berit Schei
Publié dans: Birth, Numéro 42/1, 2015, Page(s) 48-55, ISSN 0730-7659
Éditeur: Blackwell Publishing Inc.
DOI: 10.1111/birt.12147

New genetic loci link adipose and insulin biology to body fat distribution

Auteurs: Dmitry Shungin, Thomas W. Winkler, Damien C. Croteau-Chonka, Teresa Ferreira, Adam E. Locke, Reedik Mägi, Rona J. Strawbridge, Tune H. Pers, Krista Fischer, Anne E. Justice, Tsegaselassie Workalemahu, Joseph M. W. Wu, Martin L. Buchkovich, Nancy L. Heard-Costa, Tamara S. Roman, Alexander W. Drong, Ci Song, Stefan Gustafsson, Felix R. Day, Tonu Esko, Tove Fall, Zoltán Kutalik, Jian’an Luan, Joshua C. Randall, André Scherag, Sailaja Vedantam, Andrew R. Wood, Jin Chen, Rudolf Fehrmann, Juha Karjalainen, Bratati Kahali, Ching-Ti Liu, Ellen M. Schmidt, Devin Absher, Najaf Amin, Denise Anderson, Marian Beekman, Jennifer L. Bragg-Gresham, Steven Buyske, Ayse Demirkan, Georg B. Ehret, Mary F. Feitosa, Anuj Goel, Anne U. Jackson, Toby Johnson, Marcus E. Kleber, Kati Kristiansson, Massimo Mangino, Irene Mateo Leach, Carolina Medina-Gomez, Cameron D. Palmer, Dorota Pasko, Sonali Pechlivanis, Marjolein J. Peters, Inga Prokopenko, Alena Stančáková, Yun Ju Sung, Toshiko Tanaka, Alexander Teumer, Jana V. Van Vliet-Ostaptchouk, Loïc Yengo, Weihua Zhang, Eva Albrecht, Johan Ärnlöv, Gillian M. Arscott, Stefania Bandinelli, Amy Barrett, Claire Bellis, Amanda J. Bennett, Christian Berne, Matthias Blüher, Stefan Böhringer, Fabrice Bonnet, Yvonne Böttcher, Marcel Bruinenberg, Delia B. Carba, Ida H. Caspersen, Robert Clarke, E. Warwick Daw, Joris Deelen, Ewa Deelman, Graciela Delgado, Alex S. F. Doney, Niina Eklund, Michael R. Erdos, Karol Estrada, Elodie Eury, Nele Friedrich, Melissa E. Garcia, Vilmantas Giedraitis, Bruna Gigante, Alan S. Go, Alain Golay, Harald Grallert, Tanja B. Grammer, Jürgen Gräßler, Jagvir Grewal, Christopher J. Groves, Toomas Haller, Goran Hallmans, Catharina A. Hartman, Maija Hassinen, Caroline Hayward, Kauko Heikkilä, Karl-Heinz Herzig, Quinta Helmer, Hans L. Hillege, Oddgeir Holmen, Steven C. Hunt, Aaron Isaacs, Till Ittermann, Alan L. James, Ingegerd Johansson, Thorhildur Juliusdottir, Ioanna-Panagiota Kalafati, Leena Kinnunen, Wolfgang Koenig, Ishminder K. Kooner, Wolfgang Kratzer, Claudia Lamina, Karin Leander, Nanette R. Lee, Peter Lichtner, Lars Lind, Jaana Lindström, Stéphane Lobbens, Mattias Lorentzon, François Mach, Patrik K. E. Magnusson, Anubha Mahajan, Wendy L. McArdle, Cristina Menni, Sigrun Merger, Evelin Mihailov, Lili Milani, Rebecca Mills, Alireza Moayyeri, Keri L. Monda, Simon P. Mooijaart, Thomas W. Mühleisen, Antonella Mulas, Gabriele Müller, Martina Müller-Nurasyid, Ramaiah Nagaraja, Michael A. Nalls, Narisu Narisu, Nicola Glorioso, Ilja M. Nolte, Matthias Olden, Nigel W. Rayner, Frida Renstrom, Janina S. Ried, Neil R. Robertson, Lynda M. Rose, Serena Sanna, Hubert Scharnagl, Salome Scholtens, Bengt Sennblad, Thomas Seufferlein, Colleen M. Sitlani, Albert Vernon Smith, Kathleen Stirrups, Heather M. Stringham, Johan Sundström, Morris A. Swertz, Amy J. Swift, Ann-Christine Syvänen, Bamidele O. Tayo, Barbara Thorand, Gudmar Thorleifsson, Andreas Tomaschitz, Chiara Troffa, Floor V. A. van Oort, Niek Verweij, Judith M. Vonk, Lindsay L. Waite, Roman Wennauer, Tom Wilsgaard, Mary K. Wojczynski, Andrew Wong, Qunyuan Zhang, Jing Hua Zhao, Eoin P. Brennan, Murim Choi, Per Eriksson, Lasse Folkersen, Anders Franco-Cereceda, Ali G. Gharavi, Åsa K. Hedman, Marie-France Hivert, Jinyan Huang, Stavroula Kanoni, Fredrik Karpe, Sarah Keildson, Krzysztof Kiryluk, Liming Liang, Richard P. Lifton, Baoshan Ma, Amy J. McKnight, Ruth McPherson, Andres Metspalu, Josine L. Min, Miriam F. Moffatt, Grant W. Montgomery, Joanne M. Murabito, George Nicholson, Dale R. Nyholt, Christian Olsson, John R. B. Perry, Eva Reinmaa, Rany M. Salem, Niina Sandholm, Eric E. Schadt, Robert A. Scott, Lisette Stolk, Edgar E. Vallejo, Harm-Jan Westra, Krina T. Zondervan, Philippe Amouyel, Dominique Arveiler, Stephan J. L. Bakker, John Beilby, Richard N. Bergman, John Blangero, Morris J. Brown, Michel Burnier, Harry Campbell, Aravinda Chakravarti, Peter S. Chines, Simone Claudi-Boehm, Francis S. Collins, Dana C. Crawford, Jo
Publié dans: Nature, Numéro 518/7538, 2015, Page(s) 187-196, ISSN 0028-0836
Éditeur: Nature Publishing Group
DOI: 10.1038/nature14132

The Human WBSCR22 Protein Is Involved in the Biogenesis of the 40S Ribosomal Subunits in Mammalian Cells

Auteurs: Kadri Õunap, Ly Käsper, Ants Kurg, Reet Kurg
Publié dans: PLoS ONE, Numéro 8/9, 2013, Page(s) e75686, ISSN 1932-6203
Éditeur: Public Library of Science
DOI: 10.1371/journal.pone.0075686

Pregnancy intendedness and the association with physical, sexual and emotional abuse – a European multi-country cross-sectional study

Auteurs: Mirjam Lukasse, Made Laanpere, Helle Karro, Hildur Kristjansdottir, Anne-Mette Schroll, An-Sofie Van Parys, Anne-Marie Wangel, Berit Schei
Publié dans: BMC Pregnancy & Childbirth, Numéro 15/1, 2015, ISSN 1471-2393
Éditeur: BioMed Central
DOI: 10.1186/s12884-015-0558-4

rs10732516 polymorphism at the IGF2/H19 locus associates with genotype-specific effects on placental DNA methylation and birth weight of newborns conceived by assisted reproductive technology

Auteurs: Heidi Marjonen, Pauliina Auvinen, Hanna Kahila, Olga Tšuiko, Sulev Kõks, Airi Tiirats, Triin Viltrop, Timo Tuuri, Viveca Söderström-Anttila, Anne-Maria Suikkari, Andres Salumets, Aila Tiitinen, Nina Kaminen-Ahola
Publié dans: Clinical Epigenetics, Numéro 10/1, 2018, ISSN 1868-7075
Éditeur: Springer Verlag
DOI: 10.1186/s13148-018-0511-2

NIPTmer: rapid k-mer-based software package for detection of fetal aneuploidies

Auteurs: Martin Sauk, Olga Žilina, Ants Kurg, Eva-Liina Ustav, Maire Peters, Priit Paluoja, Anne Mari Roost, Hindrek Teder, Priit Palta, Nathalie Brison, Joris R. Vermeesch, Kaarel Krjutškov, Andres Salumets, Lauris Kaplinski
Publié dans: Scientific Reports, Numéro 8/1, 2018, ISSN 2045-2322
Éditeur: Nature Publishing Group
DOI: 10.1038/s41598-018-23589-8

Variability of genome-wide DNA methylation and mRNA expression profiles in reproductive and endocrine disease related tissues

Auteurs: Nilufer Rahmioglu, Alexander W Drong, Helen Lockstone, Thomas Tapmeier, Karin Hellner, Merli Saare, Triin Laisk-Podar, Christine Dew, Emily Tough, George Nicholson, Maire Peters, Andrew P Morris, Cecilia M Lindgren, Christian M Becker, Krina T Zondervan
Publié dans: Epigenetics, Numéro 12/10, 2017, Page(s) 897-908, ISSN 1559-2294
Éditeur: Landes Bioscience
DOI: 10.1080/15592294.2017.1367475

DNA methylation changes in endometrium and correlation with gene expression during the transition from pre-receptive to receptive phase

Auteurs: Viktorija Kukushkina, Vijayachitra Modhukur, Marina Suhorutšenko, Maire Peters, Reedik Mägi, Nilufer Rahmioglu, Agne Velthut-Meikas, Signe Altmäe, Francisco J. Esteban, Jaak Vilo, Krina Zondervan, Andres Salumets, Triin Laisk-Podar
Publié dans: Scientific Reports, Numéro 7/1, 2017, ISSN 2045-2322
Éditeur: Nature Publishing Group
DOI: 10.1038/s41598-017-03682-0

The management of menopause in women with a history of endometriosis: a systematic review

Auteurs: L.C. Gemmell, K.E. Webster, S. Kirtley, K. Vincent, K.T. Zondervan, C.M. Becker
Publié dans: Human Reproduction Update, Numéro 23/4, 2017, Page(s) 481-500, ISSN 1355-4786
Éditeur: Oxford University Press
DOI: 10.1093/humupd/dmx011

The Influence of Different Maternal Microbial Communities on the Development of Infant Gut and Oral Microbiota

Auteurs: Tiina Drell, Jelena Štšepetova, Jaak Simm, Kristiina Rull, Aira Aleksejeva, Anne Antson, Vallo Tillmann, Madis Metsis, Epp Sepp, Andres Salumets, Reet Mändar
Publié dans: Scientific Reports, Numéro 7/1, 2017, ISSN 2045-2322
Éditeur: Nature Publishing Group
DOI: 10.1038/s41598-017-09278-y

Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions

Auteurs: Dmitry Shungin, Wei Q. Deng, Tibor V. Varga, Jian'an Luan, Evelin Mihailov, Andres Metspalu, Andrew P. Morris, Nita G. Forouhi, Cecilia Lindgren, Patrik K. E. Magnusson, Nancy L. Pedersen, Göran Hallmans, Audrey Y. Chu, Anne E. Justice, Mariaelisa Graff, Thomas W. Winkler, Lynda M. Rose, Claudia Langenberg, L. Adrienne Cupples, Paul M. Ridker, Nicholas J. Wareham, Ken K. Ong, Ruth J. F. Loos, Dan
Publié dans: PLOS Genetics, Numéro 13/6, 2017, Page(s) e1006812, ISSN 1553-7404
Éditeur: PLOS Genetics
DOI: 10.1371/journal.pgen.1006812

A Two-Cohort RNA-seq Study Reveals Changes in Endometrial and Blood miRNome in Fertile and Infertile Women

Auteurs: Kadri Rekker, Signe Altmäe, Marina Suhorutshenko, Maire Peters, Juan F. Martinez-Blanch, Francisco M. Codoñer, Felipe Vilella, Carlos Simón, Andres Salumets, Agne Velthut-Meikas
Publié dans: Genes, Numéro 9/12, 2018, Page(s) 574, ISSN 2073-4425
Éditeur: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/genes9120574

Differentially-Expressed miRNAs in Ectopic Stromal Cells Contribute to Endometriosis Development: The Plausible Role of miR-139-5p and miR-375

Auteurs: Kadri Rekker, Tõnis Tasa, Merli Saare, Külli Samuel, Ülle Kadastik, Helle Karro, Martin Götte, Andres Salumets, Maire Peters
Publié dans: International Journal of Molecular Sciences, Numéro 19/12, 2018, Page(s) 3789, ISSN 1422-0067
Éditeur: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/ijms19123789

Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria

Auteurs: Felix Day, Tugce Karaderi, Michelle R. Jones, Cindy Meun, Chunyan He, Alex Drong, Peter Kraft, Nan Lin, Hongyan Huang, Linda Broer, Reedik Magi, Richa Saxena, Triin Laisk, Margrit Urbanek, M. Geoffrey Hayes, Gudmar Thorleifsson, Juan Fernandez-Tajes, Anubha Mahajan, Benjamin H. Mullin, Bronwyn G. A. Stuckey, Timothy D. Spector, Scott G. Wilson, Mark O. Goodarzi, Lea Davis, Barbara Obermayer-Pietsc
Publié dans: PLOS Genetics, Numéro 14/12, 2018, Page(s) e1007813, ISSN 1553-7404
Éditeur: PLOS Genetics
DOI: 10.1371/journal.pgen.1007813

Large-scale meta-analysis highlights the hypothalamic–pituitary–gonadal axis in the genetic regulation of menstrual cycle length

Auteurs: Triin Laisk, Viktorija Kukuškina, Duncan Palmer, Samantha Laber, Chia-Yen Chen, Teresa Ferreira, Nilufer Rahmioglu, Krina Zondervan, Christian Becker, Jordan W Smoller, Margaret Lippincott, Andres Salumets, Ingrid Granne, Stephanie Seminara, Benjamin Neale, Reedik Mägi, Cecilia M Lindgren
Publié dans: Human Molecular Genetics, 2018, ISSN 0964-6906
Éditeur: Oxford University Press
DOI: 10.1093/hmg/ddy317

GWAS Identifies Risk Locus for Erectile Dysfunction and Implicates Hypothalamic Neurobiology and Diabetes in Etiology

Auteurs: Jonas Bovijn, Leigh Jackson, Jenny Censin, Chia-Yen Chen, Triin Laisk, Samantha Laber, Teresa Ferreira, Sara L. Pulit, Craig A. Glastonbury, Jordan W. Smoller, Jamie W. Harrison, Katherine S. Ruth, Robin N. Beaumont, Samuel E. Jones, Jessica Tyrrell, Andrew R. Wood, Michael N. Weedon, Reedik Mägi, Benjamin Neale, Cecilia M. Lindgren, Anna Murray, Michael V. Holmes
Publié dans: The American Journal of Human Genetics, Numéro 104/1, 2019, Page(s) 157-163, ISSN 0002-9297
Éditeur: University of Chicago Press
DOI: 10.1016/j.ajhg.2018.11.004

Genome-wide haplotyping embryos developing from 0PN and 1PN zygotes increases transferrable embryos in PGT-M

Auteurs: Aspasia Destouni, Eftychia Dimitriadou, Heleen Masset, Sophie Debrock, Cindy Melotte, Kris Van Den Bogaert, Masoud Zamani Esteki, Jia Ding, Thiery Voet, Ellen Denayer, Thomy de Ravel, Eric Legius, Christel Meuleman, Karen Peeraer, Joris R Vermeesch
Publié dans: Human Reproduction, 2018, ISSN 0268-1161
Éditeur: Oxford University Press
DOI: 10.1093/humrep/dey325

Endometrial receptivity revisited: endometrial transcriptome adjusted for tissue cellular heterogeneity

Auteurs: Marina Suhorutshenko, Viktorija Kukushkina, Agne Velthut-Meikas, Signe Altmäe, Maire Peters, Reedik Mägi, Kaarel Krjutškov, Mariann Koel, Francisco M Codoñer, Juan Fco Martinez-Blanch, Felipe Vilella, Carlos Simón, Andres Salumets, Triin Laisk
Publié dans: Human Reproduction, Numéro 33/11, 2018, Page(s) 2074-2086, ISSN 0268-1161
Éditeur: Oxford University Press
DOI: 10.1093/humrep/dey301

Karyotype of the blastocoel fluid demonstrates low concordance with both trophectoderm and inner cell mass

Auteurs: Olga Tšuiko, Daria I. Zhigalina, Tatjana Jatsenko, Nikolay A. Skryabin, Olga R. Kanbekova, Victoria G. Artyukhova, Anatoly V. Svetlakov, Katre Teearu, Aleksander Trošin, Andres Salumets, Ants Kurg, Igor N. Lebedev
Publié dans: Fertility and Sterility, Numéro 109/6, 2018, Page(s) 1127-1134.e1, ISSN 0015-0282
Éditeur: Elsevier BV
DOI: 10.1016/j.fertnstert.2018.02.008

Aberrant expression of genes associated with stemness and cancer in endometria and endometrioma in a subset of women with endometriosis

Auteurs: Sakthivignesh Ponandai-Srinivasan, Karin L Andersson, Monica Nister, Merli Saare, Halima A Hassan, Suby J Varghese, Maire Peters, Andres Salumets, Kristina Gemzell-Danielsson, Parameswaran Grace Luther Lalitkumar
Publié dans: Human Reproduction, Numéro 33/10, 2018, Page(s) 1924-1938, ISSN 0268-1161
Éditeur: Oxford University Press
DOI: 10.1093/humrep/dey241

Thinning and drilling laser-assisted hatching in thawed embryo transfer: A randomized controlled trial

Auteurs: Minh Tam Le, Thi Tam An Nguyen, Thi Thai Thanh Nguyen, Van Trung Nguyen, Dinh Duong Le, Vu Quoc Huy Nguyen, Ngoc Thanh Cao, Alar Aints, Andres Salumets
Publié dans: Clinical and Experimental Reproductive Medicine, Numéro 45/3, 2018, Page(s) 129, ISSN 2233-8233
Éditeur: Korean Society for Reproductive Medicine
DOI: 10.5653/cerm.2018.45.3.129

DNA methylation alterations—potential cause of endometriosis pathogenesis or a reflection of tissue heterogeneity?†

Auteurs: Merli Saare, Kertu Liis Krigul, Triin Laisk-Podar, Sakthivignesh Ponandai-Srinivasan, Nilufer Rahmioglu, Parameswaran Grace Lalit Kumar, Krina Zondervan, Andres Salumets, Maire Peters
Publié dans: Biology of Reproduction, Numéro 99/2, 2018, Page(s) 273-282, ISSN 0006-3363
Éditeur: Society for the Study of Reproduction
DOI: 10.1093/biolre/ioy067

A speculative outlook on embryonic aneuploidy: Can molecular pathways be involved?

Auteurs: Olga Tšuiko, Tatjana Jatsenko, Lalit Kumar Parameswaran Grace, Ants Kurg, Joris Robert Vermeesch, Fredrik Lanner, Signe Altmäe, Andres Salumets
Publié dans: Developmental Biology, 2018, ISSN 0012-1606
Éditeur: Academic Press
DOI: 10.1016/j.ydbio.2018.01.014

Principles guiding embryo selection following genome-wide haplotyping of preimplantation embryos

Auteurs: Eftychia Dimitriadou, Cindy Melotte, Sophie Debrock, Masoud Zamani Esteki, Kris Dierickx, Thierry Voet, Koen Devriendt, Thomy de Ravel, Eric Legius, Karen Peeraer, Christel Meuleman, Joris Robert Vermeesch
Publié dans: Human Reproduction, Numéro 32/3, 2017, Page(s) 687-697, ISSN 0268-1161
Éditeur: Oxford University Press
DOI: 10.1093/humrep/dex011

Genome stability of bovine in vivo-conceived cleavage-stage embryos is higher compared to in vitro-produced embryos

Auteurs: Olga Tšuiko, Maaike Catteeuw, Masoud Zamani Esteki, Aspasia Destouni, Osvaldo Bogado Pascottini, Urban Besenfelder, Vitezslav Havlicek, Katrien Smits, Ants Kurg, Andres Salumets, Thomas D’Hooghe, Thierry Voet, Ann Van Soom, Joris Robert Vermeesch
Publié dans: Human Reproduction, Numéro 32/11, 2017, Page(s) 2348-2357, ISSN 0268-1161
Éditeur: Oxford University Press
DOI: 10.1093/humrep/dex286

Challenges in endometriosis miRNA studies — From tissue heterogeneity to disease specific miRNAs

Auteurs: Merli Saare, Kadri Rekker, Triin Laisk-Podar, Nilufer Rahmioglu, Krina Zondervan, Andres Salumets, Martin Götte, Maire Peters
Publié dans: Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, Numéro 1863/9, 2017, Page(s) 2282-2292, ISSN 0925-4439
Éditeur: Elsevier BV
DOI: 10.1016/j.bbadis.2017.06.018

High-throughput mRNA sequencing of stromal cells from endometriomas and endometrium

Auteurs: Kadri Rekker, Merli Saare, Elo Eriste, Tõnis Tasa, Viktorija Kukuškina, Anne Mari Roost, Kristi Anderson, Külli Samuel, Helle Karro, Andres Salumets, Maire Peters
Publié dans: Reproduction, Numéro 154/1, 2017, Page(s) 93-100, ISSN 1470-1626
Éditeur: Society for Reproduction and Fertility
DOI: 10.1530/rep-17-0092

TAC-seq: targeted DNA and RNA sequencing for precise biomarker molecule counting

Auteurs: Hindrek Teder, Mariann Koel, Priit Paluoja, Tatjana Jatsenko, Kadri Rekker, Triin Laisk-Podar, Viktorija Kukuškina, Agne Velthut-Meikas, Olga Fjodorova, Maire Peters, Juha Kere, Andres Salumets, Priit Palta, Kaarel Krjutškov
Publié dans: npj Genomic Medicine, Numéro 3/1, 2018, ISSN 2056-7944
Éditeur: Springer Nature Limited
DOI: 10.1038/s41525-018-0072-5

Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases

Auteurs: O. Tšuiko, M. Nõukas, O. Žilina, K. Hensen, J.S. Tapanainen, R. Mägi, M. Kals, P.A. Kivistik, K. Haller-Kikkatalo, A. Salumets, A. Kurg
Publié dans: Human Reproduction, Numéro 31/8, 2016, Page(s) 1913-1925, ISSN 0268-1161
Éditeur: Oxford University Press
DOI: 10.1093/humrep/dew142

Ovarian Physiology and GWAS: Biobanks, Biology, and Beyond

Auteurs: Triin Laisk-Podar, Cecilia M. Lindgren, Maire Peters, Juha S. Tapanainen, Cornelis B. Lambalk, Andres Salumets, Reedik Mägi
Publié dans: Trends in Endocrinology & Metabolism, Numéro 27/7, 2016, Page(s) 516-528, ISSN 1043-2760
Éditeur: Elsevier BV
DOI: 10.1016/j.tem.2016.04.011

Imprinted genes and imprinting control regions show predominant intermediate methylation in adult somatic tissues

Auteurs: Natalia Pervjakova, Silva Kasela, Andrew P Morris, Mart Kals, Andres Metspalu, Cecilia M Lindgren, Andres Salumets, Reedik Mägi
Publié dans: Epigenomics, Numéro 8/6, 2016, Page(s) 789-799, ISSN 1750-1911
Éditeur: Future Medicine Ltd.
DOI: 10.2217/epi.16.8

The influence of menstrual cycle and endometriosis on endometrial methylome

Auteurs: Merli Saare, Vijayachitra Modhukur, Marina Suhorutshenko, Balaji Rajashekar, Kadri Rekker, Deniss Sõritsa, Helle Karro, Pille Soplepmann, Andrei Sõritsa, Cecilia M. Lindgren, Nilufer Rahmioglu, Alexander Drong, Christian M. Becker, Krina T. Zondervan, Andres Salumets, Maire Peters
Publié dans: Clinical Epigenetics, Numéro 8/1, 2016, ISSN 1868-7075
Éditeur: Springer Verlag
DOI: 10.1186/s13148-015-0168-z

C14orf132 gene is possibly related to extremely low birth weight

Auteurs: Airi Tiirats, Triin Viltrop, Margit Nõukas, Ene Reimann, Andres Salumets, Sulev Kõks
Publié dans: BMC Genetics, Numéro 17/1, 2016, ISSN 1471-2156
Éditeur: BioMed Central
DOI: 10.1186/s12863-016-0439-5

Compartmentalized gene expression profiling of receptive endometrium reveals progesterone regulated ENPP3 is differentially expressed and secreted in glycosylated form

Auteurs: Nageswara Rao Boggavarapu, Sujata Lalitkumar, Vijay Joshua, Sergo Kasvandik, Andres Salumets, Parameswaran Grace Lalitkumar, Kristina Gemzell-Danielsson
Publié dans: Scientific Reports, Numéro 6/1, 2016, ISSN 2045-2322
Éditeur: Nature Publishing Group
DOI: 10.1038/srep33811

Globin mRNA reduction for whole-blood transcriptome sequencing

Auteurs: Kaarel Krjutškov, Mariann Koel, Anne Mari Roost, Shintaro Katayama, Elisabet Einarsdottir, Eeva-Mari Jouhilahti, Cilla Söderhäll, Ülle Jaakma, Mario Plaas, Liselotte Vesterlund, Hannes Lohi, Andres Salumets, Juha Kere
Publié dans: Scientific Reports, Numéro 6/1, 2016, ISSN 2045-2322
Éditeur: Nature Publishing Group
DOI: 10.1038/srep31584

Stanniocalcin-1 expression in normal human endometrium and dysregulation in endometriosis

Auteurs: Lusine Aghajanova, Signe Altmäe, Sergo Kasvandik, Andres Salumets, Anneli Stavreus-Evers, Linda C. Giudice
Publié dans: Fertility and Sterility, Numéro 106/3, 2016, Page(s) 681-691.e1, ISSN 0015-0282
Éditeur: Elsevier BV
DOI: 10.1016/j.fertnstert.2016.05.023

A novel hypothesis for histone-to-protamine transition in Bos taurus spermatozoa

Auteurs: Gerly Sillaste, Lauris Kaplinski, Riho Meier, Ülle Jaakma, Elo Eriste, Andres Salumets
Publié dans: Reproduction, Numéro 153/3, 2016, Page(s) 241-251, ISSN 1470-1626
Éditeur: Society for Reproduction and Fertility
DOI: 10.1530/REP-16-0441

Determination of biological activity of gonadotropins hCG and FSH by Förster resonance energy transfer based biosensors

Auteurs: Olga Mazina, Anni Allikalt, Juha S. Tapanainen, Andres Salumets, Ago Rinken
Publié dans: Scientific Reports, Numéro 7, 2017, Page(s) 42219, ISSN 2045-2322
Éditeur: Nature Publishing Group
DOI: 10.1038/srep42219

Demographic associations for autoantibodies in disease-free individuals of a European population

Auteurs: Kadri Haller-Kikkatalo, Kristi Alnek, Andres Metspalu, Evelin Mihailov, Kaja Metsküla, Kalle Kisand, Heti Pisarev, Andres Salumets, Raivo Uibo
Publié dans: Scientific Reports, Numéro 7, 2017, Page(s) 44846, ISSN 2045-2322
Éditeur: Nature Publishing Group
DOI: 10.1038/srep44846

Syndromic intellectual disability: A new phenotype caused by an aromatic amino acid decarboxylase gene (DDC) variant

Auteurs: Claudio Graziano, Anita Wischmeijer, Tommaso Pippucci, Carlo Fusco, Chiara Diquigiovanni, Margit Nõukas, Martin Sauk, Ants Kurg, Francesca Rivieri, Nenad Blau, Georg F. Hoffmann, Alka Chaubey, Charles E. Schwartz, Giovanni Romeo, Elena Bonora, Livia Garavelli, Marco Seri
Publié dans: Gene, Numéro 03781119, 2015, Page(s) 144-148, ISSN 0378-1119
Éditeur: Elsevier BV
DOI: 10.1016/j.gene.2015.01.026

The Human WBSCR22 Protein Is Involved in the Biogenesis of the 40S Ribosomal Subunits in Mammalian Cells

Auteurs: Kadri Õunap, Ly Käsper, Ants Kurg, Reet Kurg
Publié dans: PLoS ONE, Numéro 19326203, 2013, Page(s) e75686, ISSN 1932-6203
Éditeur: Public Library of Science
DOI: 10.1371/journal.pone.0075686

Monozygotic Twins with 17q21.31 Microdeletion Syndrome

Auteurs: Marketa Vlckova, Miroslava Hancarova, Jana Drabova, Zuzana Slamova, Monika Koudova, Renata Alanova, Katrin Mannik, Ants Kurg, Zdenek Sedlacek
Publié dans: Twin Research and Human Genetics, Numéro 18324274, 2014, Page(s) 405-410, ISSN 1832-4274
Éditeur: Australian Academic Press Pty Ltd.
DOI: 10.1017/thg.2014.29

The prevalence and phenotypic characteristics of spontaneous premature ovarian failure: a general population registry-based study

Auteurs: K. Haller-Kikkatalo, R. Uibo, A. Kurg, A. Salumets
Publié dans: Human Reproduction, Numéro 02681161, 2015, Page(s) 1229-1238, ISSN 0268-1161
Éditeur: Oxford University Press
DOI: 10.1093/humrep/dev021

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

Auteurs: Alberto Magi, Lorenzo Tattini, Ingrid Cifola, Romina D’Aurizio, Matteo Benelli, Eleonora Mangano, Cristina Battaglia, Elena Bonora, Ants Kurg, Marco Seri, Pamela Magini, Betti Giusti, Giovanni Romeo, Tommaso Pippucci, Gianluca De Bellis, Rosanna Abbate, Gian Franco Gensini
Publié dans: Genome Biology, Numéro 14656906, 2013, Page(s) R120, ISSN 1465-6906
Éditeur: BioMed Central
DOI: 10.1186/gb-2013-14-10-r120

Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genome

Auteurs: Olga Žilina, Marina Koltšina, Raivo Raid, Ants Kurg, Neeme Tõnisson, Andres Salumets
Publié dans: BMC Genomics, Numéro 14712164, 2015, ISSN 1471-2164
Éditeur: BioMed Central
DOI: 10.1186/s12864-015-1916-3

Chromosomal microarray analysis as a first-tier clinical diagnostic test: Estonian experience

Auteurs: Olga Žilina, Rita Teek, Pille Tammur, Kati Kuuse, Maria Yakoreva, Eve Vaidla, Triin Mölter-Väär, Tiia Reimand, Ants Kurg, Katrin Õunap
Publié dans: Molecular Genetics & Genomic Medicine, Numéro 23249269, 2014, Page(s) 166-175, ISSN 2324-9269
Éditeur: Blackwell Publishing
DOI: 10.1002/mgg3.57

A patient with de novo 0.45 Mb deletion of 2p16.1: The role of BCL11A , PAPOLG , REL , and FLJ16341 in the 2p15-p16.1 microdeletion syndrome

Auteurs: Miroslava Hancarova, Martina Simandlova, Jana Drabova, Katrin Mannik, Ants Kurg, Zdenek Sedlacek
Publié dans: American Journal of Medical Genetics Part A, Numéro 15524825, 2013, Page(s) 865-870, ISSN 1552-4825
Éditeur: Wiley-Liss Inc
DOI: 10.1002/ajmg.a.35783

Patient with Dup(5)(q35.2-q35.3) reciprocal to the common Sotos syndrome deletion and review of the literature

Auteurs: Olga Žilina, Tiia Reimand, Pille Tammur, Vallo Tillmann, Ants Kurg, Katrin Õunap
Publié dans: European Journal of Medical Genetics, Numéro 17697212, 2013, Page(s) 202-206, ISSN 1769-7212
Éditeur: Elsevier BV
DOI: 10.1016/j.ejmg.2013.01.008

Circulating miR-200–family micro-RNAs have altered plasma levels in patients with endometriosis and vary with blood collection time

Auteurs: Kadri Rekker, Merli Saare, Anne Mari Roost, Tanel Kaart, Deniss Sõritsa, Helle Karro, Andrei Sõritsa, Carlos Simón, Andres Salumets, Maire Peters
Publié dans: Fertility and Sterility, Numéro 00150282, 2015, Page(s) 938-946.e2, ISSN 0015-0282
Éditeur: Elsevier BV
DOI: 10.1016/j.fertnstert.2015.06.029

Genetic variants associated with female reproductive ageing – potential markers for assessing ovarian function and ovarian stimulation outcome

Auteurs: Triin Laisk-Podar, Tanel Kaart, Maire Peters, Andres Salumets
Publié dans: Reproductive BioMedicine Online, Numéro 14726483, 2015, Page(s) 199-209, ISSN 1472-6483
Éditeur: Reproductive Healthcare Ltd
DOI: 10.1016/j.rbmo.2015.05.001

Expression Pattern and Localization Dynamics of Guanine Nucleotide Exchange Factor RIC8 during Mouse Oogenesis

Auteurs: Merly Saare, Sirje Lulla, Tambet Tõnissoo, Riho Meier, Keiu Kask, Katrin Ruisu, Alar Karis, Andres Salumets, Margus Pooga
Publié dans: PLOS ONE, Numéro 19326203, 2015, Page(s) e0129131, ISSN 1932-6203
Éditeur: Public Library of Science
DOI: 10.1371/journal.pone.0129131

Physical activity, fatness, educational level and snuff consumption as determinants of semen quality: findings of the ActiART study

Auteurs: Triin Pärn, Raúl Grau Ruiz, Theodora Kunovac Kallak, Jonatan R. Ruiz, Eva Davey, Julius Hreinsson, Kjell Wånggren, Andres Salumets, Michael Sjöström, Anneli Stavreus-Evers, Francisco B. Ortega, Signe Altmäe
Publié dans: Reproductive BioMedicine Online, Numéro 14726483, 2015, Page(s) 108-119, ISSN 1472-6483
Éditeur: Reproductive Healthcare Ltd
DOI: 10.1016/j.rbmo.2015.03.004

Complementary seminovaginal microbiome in couples

Auteurs: Reet Mändar, Margus Punab, Natalja Borovkova, Eleri Lapp, Riinu Kiiker, Paul Korrovits, Andres Metspalu, Kaarel Krjutškov, Hiie Nõlvak, Jens-Konrad Preem, Kristjan Oopkaup, Andres Salumets, Jaak Truu
Publié dans: Research in Microbiology, Numéro 09232508, 2015, Page(s) 440-447, ISSN 0923-2508
Éditeur: Elsevier BV
DOI: 10.1016/j.resmic.2015.03.009

Systemic oxidative stress could predict assisted reproductive technique outcome

Auteurs: A. Ahelik, R. Mändar, P. Korrovits, P. Karits, E. Talving, K. Rosenstein, M. Jaagura, A. Salumets, T. Kullisaar
Publié dans: Journal of Assisted Reproduction and Genetics, Numéro 10580468, 2015, Page(s) 699-704, ISSN 1058-0468
Éditeur: Kluwer Academic/Plenum Publishers
DOI: 10.1007/s10815-015-0466-6

Genetic studies of body mass index yield new insights for obesity biology

Auteurs: Adam E. Locke, Bratati Kahali, Sonja I. Berndt, Anne E. Justice, Tune H. Pers, Felix R. Day, Corey Powell, Sailaja Vedantam, Martin L. Buchkovich, Jian Yang, Damien C. Croteau-Chonka, Tonu Esko, Tove Fall, Teresa Ferreira, Stefan Gustafsson, Zoltán Kutalik, Jian’an Luan, Reedik Mägi, Joshua C. Randall, Thomas W. Winkler, Andrew R. Wood, Tsegaselassie Workalemahu, Jessica D. Faul, Jennifer A. Smith, Jing Hua Zhao, Wei Zhao, Jin Chen, Rudolf Fehrmann, Åsa K. Hedman, Juha Karjalainen, Ellen M. Schmidt, Devin Absher, Najaf Amin, Denise Anderson, Marian Beekman, Jennifer L. Bolton, Jennifer L. Bragg-Gresham, Steven Buyske, Ayse Demirkan, Guohong Deng, Georg B. Ehret, Bjarke Feenstra, Mary F. Feitosa, Krista Fischer, Anuj Goel, Jian Gong, Anne U. Jackson, Stavroula Kanoni, Marcus E. Kleber, Kati Kristiansson, Unhee Lim, Vaneet Lotay, Massimo Mangino, Irene Mateo Leach, Carolina Medina-Gomez, Sarah E. Medland, Michael A. Nalls, Cameron D. Palmer, Dorota Pasko, Sonali Pechlivanis, Marjolein J. Peters, Inga Prokopenko, Dmitry Shungin, Alena Stančáková, Rona J. Strawbridge, Yun Ju Sung, Toshiko Tanaka, Alexander Teumer, Stella Trompet, Sander W. van der Laan, Jessica van Setten, Jana V. Van Vliet-Ostaptchouk, Zhaoming Wang, Loïc Yengo, Weihua Zhang, Aaron Isaacs, Eva Albrecht, Johan Ärnlöv, Gillian M. Arscott, Antony P. Attwood, Stefania Bandinelli, Amy Barrett, Isabelita N. Bas, Claire Bellis, Amanda J. Bennett, Christian Berne, Roza Blagieva, Matthias Blüher, Stefan Böhringer, Lori L. Bonnycastle, Yvonne Böttcher, Heather A. Boyd, Marcel Bruinenberg, Ida H. Caspersen, Yii-Der Ida Chen, Robert Clarke, E. Warwick Daw, Anton J. M. de Craen, Graciela Delgado, Maria Dimitriou, Alex S. F. Doney, Niina Eklund, Karol Estrada, Elodie Eury, Lasse Folkersen, Ross M. Fraser, Melissa E. Garcia, Frank Geller, Vilmantas Giedraitis, Bruna Gigante, Alan S. Go, Alain Golay, Alison H. Goodall, Scott D. Gordon, Mathias Gorski, Hans-Jörgen Grabe, Harald Grallert, Tanja B. Grammer, Jürgen Gräßler, Henrik Grönberg, Christopher J. Groves, Gaëlle Gusto, Jeffrey Haessler, Per Hall, Toomas Haller, Goran Hallmans, Catharina A. Hartman, Maija Hassinen, Caroline Hayward, Nancy L. Heard-Costa, Quinta Helmer, Christian Hengstenberg, Oddgeir Holmen, Jouke-Jan Hottenga, Alan L. James, Janina M. Jeff, Åsa Johansson, Jennifer Jolley, Thorhildur Juliusdottir, Leena Kinnunen, Wolfgang Koenig, Markku Koskenvuo, Wolfgang Kratzer, Jaana Laitinen, Claudia Lamina, Karin Leander, Nanette R. Lee, Peter Lichtner, Lars Lind, Jaana Lindström, Ken Sin Lo, Stéphane Lobbens, Roberto Lorbeer, Yingchang Lu, François Mach, Patrik K. E. Magnusson, Anubha Mahajan, Wendy L. McArdle, Stela McLachlan, Cristina Menni, Sigrun Merger, Evelin Mihailov, Lili Milani, Alireza Moayyeri, Keri L. Monda, Mario A. Morken, Antonella Mulas, Gabriele Müller, Martina Müller-Nurasyid, Arthur W. Musk, Ramaiah Nagaraja, Markus M. Nöthen, Ilja M. Nolte, Stefan Pilz, Nigel W. Rayner, Frida Renstrom, Rainer Rettig, Janina S. Ried, Stephan Ripke, Neil R. Robertson, Lynda M. Rose, Serena Sanna, Hubert Scharnagl, Salome Scholtens, Fredrick R. Schumacher, William R. Scott, Thomas Seufferlein, Jianxin Shi, Albert Vernon Smith, Joanna Smolonska, Alice V. Stanton, Valgerdur Steinthorsdottir, Kathleen Stirrups, Heather M. Stringham, Johan Sundström, Morris A. Swertz, Amy J. Swift, Ann-Christine Syvänen, Sian-Tsung Tan, Bamidele O. Tayo, Barbara Thorand, Gudmar Thorleifsson, Jonathan P. Tyrer, Hae-Won Uh, Liesbeth Vandenput, Frank C. Verhulst, Sita H. Vermeulen, Niek Verweij, Judith M. Vonk, Lindsay L. Waite, Helen R. Warren, Dawn Waterworth, Michael N. Weedon, Lynne R. Wilkens, Christina Willenborg, Tom Wilsgaard, Mary K. Wojczynski, Andrew Wong, Alan F. Wright, Qunyuan Zhang, Eoin P. Brennan, Murim Choi, Zari Dastani, Alexander W. Drong, Per Eriksson, Anders Franco-Cereceda, Jesper R. Gådin, Ali G. Gharavi, Michael E. Goddard, Robert E. Handsaker, Jinyan Huang, Fredrik Karpe, Sekar Kathiresa
Publié dans: Nature, Numéro 00280836, 2015, Page(s) 197-206, ISSN 0028-0836
Éditeur: Nature Publishing Group
DOI: 10.1038/nature14177

New genetic loci link adipose and insulin biology to body fat distribution

Auteurs: Dmitry Shungin, Thomas W. Winkler, Damien C. Croteau-Chonka, Teresa Ferreira, Adam E. Locke, Reedik Mägi, Rona J. Strawbridge, Tune H. Pers, Krista Fischer, Anne E. Justice, Tsegaselassie Workalemahu, Joseph M. W. Wu, Martin L. Buchkovich, Nancy L. Heard-Costa, Tamara S. Roman, Alexander W. Drong, Ci Song, Stefan Gustafsson, Felix R. Day, Tonu Esko, Tove Fall, Zoltán Kutalik, Jian’an Luan, Joshua C. Randall, André Scherag, Sailaja Vedantam, Andrew R. Wood, Jin Chen, Rudolf Fehrmann, Juha Karjalainen, Bratati Kahali, Ching-Ti Liu, Ellen M. Schmidt, Devin Absher, Najaf Amin, Denise Anderson, Marian Beekman, Jennifer L. Bragg-Gresham, Steven Buyske, Ayse Demirkan, Georg B. Ehret, Mary F. Feitosa, Anuj Goel, Anne U. Jackson, Toby Johnson, Marcus E. Kleber, Kati Kristiansson, Massimo Mangino, Irene Mateo Leach, Carolina Medina-Gomez, Cameron D. Palmer, Dorota Pasko, Sonali Pechlivanis, Marjolein J. Peters, Inga Prokopenko, Alena Stančáková, Yun Ju Sung, Toshiko Tanaka, Alexander Teumer, Jana V. Van Vliet-Ostaptchouk, Loïc Yengo, Weihua Zhang, Eva Albrecht, Johan Ärnlöv, Gillian M. Arscott, Stefania Bandinelli, Amy Barrett, Claire Bellis, Amanda J. Bennett, Christian Berne, Matthias Blüher, Stefan Böhringer, Fabrice Bonnet, Yvonne Böttcher, Marcel Bruinenberg, Delia B. Carba, Ida H. Caspersen, Robert Clarke, E. Warwick Daw, Joris Deelen, Ewa Deelman, Graciela Delgado, Alex S. F. Doney, Niina Eklund, Michael R. Erdos, Karol Estrada, Elodie Eury, Nele Friedrich, Melissa E. Garcia, Vilmantas Giedraitis, Bruna Gigante, Alan S. Go, Alain Golay, Harald Grallert, Tanja B. Grammer, Jürgen Gräßler, Jagvir Grewal, Christopher J. Groves, Toomas Haller, Goran Hallmans, Catharina A. Hartman, Maija Hassinen, Caroline Hayward, Kauko Heikkilä, Karl-Heinz Herzig, Quinta Helmer, Hans L. Hillege, Oddgeir Holmen, Steven C. Hunt, Aaron Isaacs, Till Ittermann, Alan L. James, Ingegerd Johansson, Thorhildur Juliusdottir, Ioanna-Panagiota Kalafati, Leena Kinnunen, Wolfgang Koenig, Ishminder K. Kooner, Wolfgang Kratzer, Claudia Lamina, Karin Leander, Nanette R. Lee, Peter Lichtner, Lars Lind, Jaana Lindström, Stéphane Lobbens, Mattias Lorentzon, François Mach, Patrik K. E. Magnusson, Anubha Mahajan, Wendy L. McArdle, Cristina Menni, Sigrun Merger, Evelin Mihailov, Lili Milani, Rebecca Mills, Alireza Moayyeri, Keri L. Monda, Simon P. Mooijaart, Thomas W. Mühleisen, Antonella Mulas, Gabriele Müller, Martina Müller-Nurasyid, Ramaiah Nagaraja, Michael A. Nalls, Narisu Narisu, Nicola Glorioso, Ilja M. Nolte, Matthias Olden, Nigel W. Rayner, Frida Renstrom, Janina S. Ried, Neil R. Robertson, Lynda M. Rose, Serena Sanna, Hubert Scharnagl, Salome Scholtens, Bengt Sennblad, Thomas Seufferlein, Colleen M. Sitlani, Albert Vernon Smith, Kathleen Stirrups, Heather M. Stringham, Johan Sundström, Morris A. Swertz, Amy J. Swift, Ann-Christine Syvänen, Bamidele O. Tayo, Barbara Thorand, Gudmar Thorleifsson, Andreas Tomaschitz, Chiara Troffa, Floor V. A. van Oort, Niek Verweij, Judith M. Vonk, Lindsay L. Waite, Roman Wennauer, Tom Wilsgaard, Mary K. Wojczynski, Andrew Wong, Qunyuan Zhang, Jing Hua Zhao, Eoin P. Brennan, Murim Choi, Per Eriksson, Lasse Folkersen, Anders Franco-Cereceda, Ali G. Gharavi, Åsa K. Hedman, Marie-France Hivert, Jinyan Huang, Stavroula Kanoni, Fredrik Karpe, Sarah Keildson, Krzysztof Kiryluk, Liming Liang, Richard P. Lifton, Baoshan Ma, Amy J. McKnight, Ruth McPherson, Andres Metspalu, Josine L. Min, Miriam F. Moffatt, Grant W. Montgomery, Joanne M. Murabito, George Nicholson, Dale R. Nyholt, Christian Olsson, John R. B. Perry, Eva Reinmaa, Rany M. Salem, Niina Sandholm, Eric E. Schadt, Robert A. Scott, Lisette Stolk, Edgar E. Vallejo, Harm-Jan Westra, Krina T. Zondervan, Philippe Amouyel, Dominique Arveiler, Stephan J. L. Bakker, John Beilby, Richard N. Bergman, John Blangero, Morris J. Brown, Michel Burnier, Harry Campbell, Aravinda Chakravarti, Peter S. Chines, Simone Claudi-Boehm, Francis S. Collins, Dana C. Crawford, Jo
Publié dans: Nature, Numéro 00280836, 2015, Page(s) 187-196, ISSN 0028-0836
Éditeur: Nature Publishing Group
DOI: 10.1038/nature14132

Bovine sperm plasma membrane proteomics through biotinylation and subcellular enrichment

Auteurs: Sergo Kasvandik, Gerly Sillaste, Agne Velthut-Meikas, Aavo-Valdur Mikelsaar, Triin Hallap, Peeter Padrik, Tanel Tenson, Ülle Jaakma, Sulev Kõks, Andres Salumets
Publié dans: PROTEOMICS, Numéro 16159853, 2015, Page(s) 1906-1920, ISSN 1615-9853
Éditeur: John Wiley & Sons Ltd.
DOI: 10.1002/pmic.201400297

Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta

Auteurs: Tauno Metsalu, Triin Viltrop, Airi Tiirats, Balaji Rajashekar, Ene Reimann, Sulev Kõks, Kristiina Rull, Lili Milani, Ganesh Acharya, Purusotam Basnet, Jaak Vilo, Reedik Mägi, Andres Metspalu, Maire Peters, Kadri Haller-Kikkatalo, Andres Salumets
Publié dans: Epigenetics, Numéro 15592294, 2014, Page(s) 1397-1409, ISSN 1559-2294
Éditeur: Landes Bioscience
DOI: 10.4161/15592294.2014.970052

High-Throughput Sequencing Approach Uncovers the miRNome of Peritoneal Endometriotic Lesions and Adjacent Healthy Tissues

Auteurs: Merli Saare, Kadri Rekker, Triin Laisk-Podar, Deniss Sõritsa, Anne Mari Roost, Jaak Simm, Agne Velthut-Meikas, Külli Samuel, Tauno Metsalu, Helle Karro, Andrei Sõritsa, Andres Salumets, Maire Peters
Publié dans: PLoS ONE, Numéro 19326203, 2014, Page(s) e112630, ISSN 1932-6203
Éditeur: Public Library of Science
DOI: 10.1371/journal.pone.0112630

Pregnancy Rate in Endometriosis Patients according to the Severity of the Disease after Using a Combined Approach of Laparoscopy, GnRH Agonist Treatment and in vitro Fertilization

Auteurs: Deniss Sõritsa, Merli Saare, Triin Laisk-Podar, Maire Peters, Andrei Sõritsa, Kadri Matt, Helle Karro, Andres Salumets
Publié dans: Gynecologic and Obstetric Investigation, Numéro 03787346, 2015, Page(s) 34-39, ISSN 0378-7346
Éditeur: S. Karger AG
DOI: 10.1159/000365329

Folic acid supplementation and methylenetetrahydrofolate reductase (MTHFR) gene variations in relation to in vitro fertilization pregnancy outcome

Auteurs: Tiina Murto, Theodora K. Kallak, Annica Hoas, Signe Altmäe, Andres Salumets, Torbjörn K. Nilsson, Agneta Skoog Svanberg, Kjell Wånggren, Agneta Yngve, Anneli Stavreus-Evers
Publié dans: Acta Obstetricia et Gynecologica Scandinavica, Numéro 00016349, 2015, Page(s) 65-71, ISSN 0001-6349
Éditeur: Wiley-Blackwell
DOI: 10.1111/aogs.12522

Autoimmune Activation toward Embryo Implantation is Rare in Immune-Privileged Human Endometrium

Auteurs: Kadri Haller-Kikkatalo, Aili Tagoma, Raivo Uibo, Andres Salumets, Signe Altmäe
Publié dans: Seminars in Reproductive Medicine, Numéro 15268004, 2014, Page(s) 376-384, ISSN 1526-8004
Éditeur: Thieme Medical Publishers
DOI: 10.1055/s-0034-1376356

Sequencing and annotated analysis of full genome of Holstein breed bull

Auteurs: Sulev Kõks, Ene Reimann, Rutt Lilleoja, Freddy Lättekivi, Andres Salumets, Paula Reemann, Ülle Jaakma
Publié dans: Mammalian Genome, Numéro 09388990, 2014, Page(s) 363-373, ISSN 0938-8990
Éditeur: Springer Verlag
DOI: 10.1007/s00335-014-9511-5

Folic acid supplementation and IVF pregnancy outcome in women with unexplained infertility

Auteurs: T. Murto, A. Skoog Svanberg, A. Yngve, T.K. Nilsson, S. Altmäe, K. Wånggren, A. Salumets, A. Stavreus-Evers
Publié dans: Reproductive BioMedicine Online, Numéro 14726483, 2014, Page(s) 766-772, ISSN 1472-6483
Éditeur: Reproductive Healthcare Ltd
DOI: 10.1016/j.rbmo.2014.01.017

DNA mismatch repair gene MSH6 implicated in determining age at natural menopause

Auteurs: J. R. B. Perry, Y.-H. Hsu, D. I. Chasman, A. D. Johnson, C. Elks, E. Albrecht, I. L. Andrulis, J. Beesley, G. S. Berenson, S. Bergmann, S. E. Bojesen, M. K. Bolla, J. Brown, J. E. Buring, H. Campbell, J. Chang-Claude, G. Chenevix-Trench, T. Corre, F. J. Couch, A. Cox, K. Czene, A. P. D'adamo, G. Davies, I. J. Deary, J. Dennis, D. F. Easton, E. G. Engelhardt, J. G. Eriksson, T. Esko, P. A. Fasching, J. D. Figueroa, H. Flyger, A. Fraser, M. Garcia-Closas, P. Gasparini, C. Gieger, G. Giles, P. Guenel, S. Hagg, P. Hall, C. Hayward, J. Hopper, E. Ingelsson, S. L. R. Kardia, K. Kasiman, J. A. Knight, J. Lahti, D. A. Lawlor, P. K. E. Magnusson, S. Margolin, J. A. Marsh, A. Metspalu, J. E. Olson, C. E. Pennell, O. Polasek, I. Rahman, P. M. Ridker, A. Robino, I. Rudan, A. Rudolph, A. Salumets, M. K. Schmidt, M. J. Schoemaker, E. N. Smith, J. A. Smith, M. Southey, D. Stockl, A. J. Swerdlow, D. J. Thompson, T. Truong, S. Ulivi, M. Waldenberger, Q. Wang, S. Wild, J. F. Wilson, A. F. Wright, L. Zgaga, K. K. Ong, J. M. Murabito, D. Karasik, A. Murray
Publié dans: Human Molecular Genetics, Numéro 09646906, 2014, Page(s) 2490-2497, ISSN 0964-6906
Éditeur: Oxford University Press
DOI: 10.1093/hmg/ddt620

Circulating microRNA Profile throughout the Menstrual Cycle

Auteurs: Kadri Rekker, Merli Saare, Anne Mari Roost, Andres Salumets, Maire Peters
Publié dans: PLoS ONE, Numéro 19326203, 2013, Page(s) e81166, ISSN 1932-6203
Éditeur: Public Library of Science
DOI: 10.1371/journal.pone.0081166

Comparison of serum exosome isolation methods for microRNA profiling

Auteurs: Kadri Rekker, Merli Saare, Anne Mari Roost, Anna-Liisa Kubo, Natasa Zarovni, Antonio Chiesi, Andres Salumets, Maire Peters
Publié dans: Clinical Biochemistry, Numéro 00099120, 2014, Page(s) 135-138, ISSN 0009-9120
Éditeur: Elsevier BV
DOI: 10.1016/j.clinbiochem.2013.10.020

Guidelines for the design, analysis and interpretation of 'omics' data: focus on human endometrium

Auteurs: S. Altmae, F. J. Esteban, A. Stavreus-Evers, C. Simon, L. Giudice, B. A. Lessey, J. A. Horcajadas, N. S. Macklon, T. D'Hooghe, C. Campoy, B. C. Fauser, L. A. Salamonsen, A. Salumets
Publié dans: Human Reproduction Update, Numéro 13554786, 2013, Page(s) 12-28, ISSN 1355-4786
Éditeur: Oxford University Press
DOI: 10.1093/humupd/dmt048

Sequencing and annotated analysis of the Holstein cow genome

Auteurs: Sulev Kõks, Rutt Lilleoja, Ene Reimann, Andres Salumets, Paula Reemann, Ülle Jaakma
Publié dans: Mammalian Genome, Numéro 09388990, 2013, Page(s) 309-321, ISSN 0938-8990
Éditeur: Springer Verlag
DOI: 10.1007/s00335-013-9464-0

Changes in the Transcriptome of the Human Endometrial Ishikawa Cancer Cell Line Induced by Estrogen, Progesterone, Tamoxifen, and Mifepristone (RU486) as Detected by RNA-Sequencing

Auteurs: Karin Tamm-Rosenstein, Jaak Simm, Marina Suhorutshenko, Andres Salumets, Madis Metsis
Publié dans: PLoS ONE, Numéro 19326203, 2013, Page(s) e68907, ISSN 1932-6203
Éditeur: Public Library of Science
DOI: 10.1371/journal.pone.0068907

Tissue-specific mitochondrial heteroplasmy at position 16,093 within the same individual

Auteurs: Kaarel Krjutškov, Marina Koltšina, Kelli Grand, Urmo Võsa, Martin Sauk, Neeme Tõnisson, Andres Salumets
Publié dans: Current Genetics, Numéro 01728083, 2014, Page(s) 11-16, ISSN 0172-8083
Éditeur: Springer Verlag
DOI: 10.1007/s00294-013-0398-6

Research Resource: Small RNA-seq of Human Granulosa Cells Reveals miRNAs in FSHR and Aromatase Genes

Auteurs: Agne Velthut-Meikas, Jaak Simm, Timo Tuuri, Juha S. Tapanainen, Madis Metsis, Andres Salumets
Publié dans: Molecular Endocrinology, Numéro 08888809, 2013, Page(s) 1128-1141, ISSN 0888-8809
Éditeur: The Endocrine Society
DOI: 10.1210/me.2013-1058

Elevated blood plasma antioxidant status is favourable for achieving IVF/ICSI pregnancy

Auteurs: Agne Velthut, Mihkel Zilmer, Kersti Zilmer, Tanel Kaart, Helle Karro, Andres Salumets
Publié dans: Reproductive BioMedicine Online, Numéro 14726483, 2013, Page(s) 345-352, ISSN 1472-6483
Éditeur: Reproductive Healthcare Ltd
DOI: 10.1016/j.rbmo.2012.12.012

Characterization of the Vaginal Micro- and Mycobiome in Asymptomatic Reproductive-Age Estonian Women

Auteurs: Tiina Drell, Triin Lillsaar, Lea Tummeleht, Jaak Simm, Anu Aaspõllu, Edda Väin, Ivo Saarma, Andres Salumets, Gilbert G. G. Donders, Madis Metsis
Publié dans: PLoS ONE, Numéro 19326203, 2013, Page(s) e54379, ISSN 1932-6203
Éditeur: Public Library of Science
DOI: 10.1371/journal.pone.0054379

A genome-wide association study of early menopause and the combined impact of identified variants

Auteurs: J. R. B. Perry, T. Corre, T. Esko, D. I. Chasman, K. Fischer, N. Franceschini, C. He, Z. Kutalik, M. Mangino, L. M. Rose, A. Vernon Smith, L. Stolk, P. Sulem, M. N. Weedon, W. V. Zhuang, A. Arnold, A. Ashworth, S. Bergmann, J. E. Buring, A. Burri, C. Chen, M. C. Cornelis, D. J. Couper, M. O. Goodarzi, V. Gudnason, T. Harris, A. Hofman, M. Jones, P. Kraft, L. Launer, J. S. E. Laven, G. Li, B. McKnight, C. Masciullo, L. Milani, N. Orr, B. M. Psaty, P. M. Ridker, F. Rivadeneira, C. Sala, A. Salumets, M. Schoemaker, M. Traglia, G. Waeber, S. J. Chanock, E. W. Demerath, M. Garcia, S. E. Hankinson, F. B. Hu, D. J. Hunter, K. L. Lunetta, A. Metspalu, G. W. Montgomery, J. M. Murabito, A. B. Newman, K. K. Ong, T. D. Spector, K. Stefansson, A. J. Swerdlow, U. Thorsteinsdottir, R. M. Van Dam, A. G. Uitterlinden, J. A. Visser, P. Vollenweider, D. Toniolo, A. Murray
Publié dans: Human Molecular Genetics, Numéro 09646906, 2013, Page(s) 1465-1472, ISSN 0964-6906
Éditeur: Oxford University Press
DOI: 10.1093/hmg/dds551

MicroRNAs miR-30b, miR-30d, and miR-494 Regulate Human Endometrial Receptivity

Auteurs: S. Altmae, J. A. Martinez-Conejero, F. J. Esteban, M. Ruiz-Alonso, A. Stavreus-Evers, J. A. Horcajadas, A. Salumets
Publié dans: Reproductive Sciences, Numéro 19337191, 2013, Page(s) 308-317, ISSN 1933-7191
Éditeur: SAGE Publications
DOI: 10.1177/1933719112453507

Corrigendum: Rare coding variants and X-linked loci associated with age at menarche

Auteurs: Kathryn L. Lunetta, Felix R. Day, Patrick Sulem, Katherine S. Ruth, Joyce Y. Tung, David A. Hinds, Tõnu Esko, Cathy E. Elks, Elisabeth Altmaier, Chunyan He, Jennifer E. Huffman, Evelin Mihailov, Eleonora Porcu, Antonietta Robino, Lynda M. Rose, Ursula M. Schick, Lisette Stolk, Alexander Teumer, Deborah J. Thompson, Michela Traglia, Carol A. Wang, Laura M. Yerges-Armstrong, Antonis C. Antoniou, Caterina Barbieri, Andrea D. Coviello, Francesco Cucca, Ellen W. Demerath, Alison M. Dunning, Ilaria Gandin, Megan L. Grove, Daniel F. Gudbjartsson, Lynne J. Hocking, Albert Hofman, Jinyan Huang, Rebecca D. Jackson, David Karasik, Jennifer Kriebel, Ethan M. Lange, Leslie A. Lange, Claudia Langenberg, Xin Li, Jian'an Luan, Reedik Mägi, Alanna C. Morrison, Sandosh Padmanabhan, Ailith Pirie, Ozren Polasek, David Porteous, Alex P. Reiner, Fernando Rivadeneira, Igor Rudan, Cinzia F. Sala, David Schlessinger, Robert A. Scott, Doris Stöckl, Jenny A. Visser, Uwe Völker, Diego Vozzi, James G. Wilson, Marek Zygmunt, Eric Boerwinkle, Julie E. Buring, Laura Crisponi, Douglas F. Easton, Caroline Hayward, Frank B. Hu, Simin Liu, Andres Metspalu, Craig E. Pennell, Paul M. Ridker, Konstantin Strauch, Elizabeth A. Streeten, Daniela Toniolo, André G. Uitterlinden, Sheila Ulivi, Henry Völzke, Nicholas J. Wareham, Melissa Wellons, Nora Franceschini, Daniel I. Chasman, Unnur Thorsteinsdottir, Anna Murray, Kari Stefansson, Joanne M. Murabito, Ken K. Ong, John R. B. Perry
Publié dans: Nature Communications, Numéro 20411723, 2015, Page(s) 10257, ISSN 2041-1723
Éditeur: Nature Publishing Group
DOI: 10.1038/ncomms10257

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

Auteurs: Kyle J Gaulton, Teresa Ferreira, Yeji Lee, Anne Raimondo, Reedik Mägi, Michael E Reschen, Anubha Mahajan, Adam Locke, N William Rayner, Neil Robertson, Robert A Scott, Inga Prokopenko, Laura J Scott, Todd Green, Thomas Sparso, Dorothee Thuillier, Loic Yengo, Harald Grallert, Simone Wahl, Mattias Frånberg, Rona J Strawbridge, Hans Kestler, Himanshu Chheda, Lewin Eisele, Stefan Gustafsson, Valgerdur Steinthorsdottir, Gudmar Thorleifsson, Lu Qi, Lennart C Karssen, Elisabeth M van Leeuwen, Sara M Willems, Man Li, Han Chen, Christian Fuchsberger, Phoenix Kwan, Clement Ma, Michael Linderman, Yingchang Lu, Soren K Thomsen, Jana K Rundle, Nicola L Beer, Martijn van de Bunt, Anil Chalisey, Hyun Min Kang, Benjamin F Voight, Gonçalo R Abecasis, Peter Almgren, Damiano Baldassarre, Beverley Balkau, Rafn Benediktsson, Matthias Blüher, Heiner Boeing, Lori L Bonnycastle, Erwin P Bottinger, Noël P Burtt, Jason Carey, Guillaume Charpentier, Peter S Chines, Marilyn C Cornelis, David J Couper, Andrew T Crenshaw, Rob M van Dam, Alex S F Doney, Mozhgan Dorkhan, Sarah Edkins, Johan G Eriksson, Tonu Esko, Elodie Eury, João Fadista, Jason Flannick, Pierre Fontanillas, Caroline Fox, Paul W Franks, Karl Gertow, Christian Gieger, Bruna Gigante, Omri Gottesman, George B Grant, Niels Grarup, Christopher J Groves, Maija Hassinen, Christian T Have, Christian Herder, Oddgeir L Holmen, Astradur B Hreidarsson, Steve E Humphries, David J Hunter, Anne U Jackson, Anna Jonsson, Marit E Jørgensen, Torben Jørgensen, Wen-Hong L Kao, Nicola D Kerrison, Leena Kinnunen, Norman Klopp, Augustine Kong, Peter Kovacs, Peter Kraft, Jasmina Kravic, Cordelia Langford, Karin Leander, Liming Liang, Peter Lichtner, Cecilia M Lindgren, Eero Lindholm, Allan Linneberg, Ching-Ti Liu, Stéphane Lobbens, Jian'an Luan, Valeriya Lyssenko, Satu Männistö, Olga McLeod, Julia Meyer, Evelin Mihailov, Ghazala Mirza, Thomas W Mühleisen, Martina Müller-Nurasyid, Carmen Navarro, Markus M Nöthen, Nikolay N Oskolkov, Katharine R Owen, Domenico Palli, Sonali Pechlivanis, Leena Peltonen, John R B Perry, Carl G P Platou, Michael Roden, Douglas Ruderfer, Denis Rybin, Yvonne T van der Schouw, Bengt Sennblad, Gunnar Sigurðsson, Alena Stančáková, Gerald Steinbach, Petter Storm, Konstantin Strauch, Heather M Stringham, Qi Sun, Barbara Thorand, Emmi Tikkanen, Anke Tonjes, Joseph Trakalo, Elena Tremoli, Tiinamaija Tuomi, Roman Wennauer, Steven Wiltshire, Andrew R Wood, Eleftheria Zeggini, Ian Dunham, Ewan Birney, Lorenzo Pasquali, Jorge Ferrer, Ruth J F Loos, Josée Dupuis, Jose C Florez, Eric Boerwinkle, James S Pankow, Cornelia van Duijn, Eric Sijbrands, James B Meigs, Frank B Hu, Unnur Thorsteinsdottir, Kari Stefansson, Timo A Lakka, Rainer Rauramaa, Michael Stumvoll, Nancy L Pedersen, Lars Lind, Sirkka M Keinanen-Kiukaanniemi, Eeva Korpi-Hyövälti, Timo E Saaristo, Juha Saltevo, Johanna Kuusisto, Markku Laakso, Andres Metspalu, Raimund Erbel, Karl-Heinz Jöcke, Susanne Moebus, Samuli Ripatti, Veikko Salomaa, Erik Ingelsson, Bernhard O Boehm, Richard N Bergman, Francis S Collins, Karen L Mohlke, Heikki Koistinen, Jaakko Tuomilehto, Kristian Hveem, Inger Njølstad, Panagiotis Deloukas, Peter J Donnelly, Timothy M Frayling, Andrew T Hattersley, Ulf de Faire, Anders Hamsten, Thomas Illig, Annette Peters, Stephane Cauchi, Rob Sladek, Philippe Froguel, Torben Hansen, Oluf Pedersen, Andrew D Morris, Collin N A Palmer, Sekar Kathiresan, Olle Melander, Peter M Nilsson, Leif C Groop, Inês Barroso, Claudia Langenberg, Nicholas J Wareham, Christopher A O'Callaghan, Anna L Gloyn, David Altshuler, Michael Boehnke, Tanya M Teslovich, Mark I McCarthy, Andrew P Morris
Publié dans: Nature Genetics, Numéro 10614036, 2015, Page(s) 1415-1425, ISSN 1061-4036
Éditeur: Nature Publishing Group
DOI: 10.1038/ng.3437

Rare coding variants and X-linked loci associated with age at menarche

Auteurs: Kathryn L. Lunetta, Felix R. Day, Patrick Sulem, Katherine S. Ruth, Joyce Y. Tung, David A. Hinds, Tõnu Esko, Cathy E. Elks, Elisabeth Altmaier, Chunyan He, Jennifer E. Huffman, Evelin Mihailov, Eleonora Porcu, Antonietta Robino, Lynda M. Rose, Ursula M. Schick, Lisette Stolk, Alexander Teumer, Deborah J. Thompson, Michela Traglia, Carol A. Wang, Laura M. Yerges-Armstrong, Antonis C. Antoniou, Caterina Barbieri, Andrea D. Coviello, Francesco Cucca, Ellen W. Demerath, Alison M. Dunning, Ilaria Gandin, Megan L. Grove, Daniel F. Gudbjartsson, Lynne J. Hocking, Albert Hofman, Jinyan Huang, Rebecca D. Jackson, David Karasik, Jennifer Kriebel, Ethan M. Lange, Leslie A. Lange, Claudia Langenberg, Xin Li, Jian'an Luan, Reedik Mägi, Alanna C. Morrison, Sandosh Padmanabhan, Ailith Pirie, Ozren Polasek, David Porteous, Alex P. Reiner, Fernando Rivadeneira, Igor Rudan, Cinzia F. Sala, David Schlessinger, Robert A. Scott, Doris Stöckl, Jenny A. Visser, Uwe Völker, Diego Vozzi, James G. Wilson, Marek Zygmunt, Nita G. Forouhi, Nicola D. Kerrison, Stephen J. Sharp, Matt Sims, Inês Barroso, Panos Deloukas, Mark I. McCarthy, Larraitz Arriola, Beverley Balkau, Aurelio Barricarte, Heiner Boeing, Paul W. Franks, Carlos Gonzalez, Sara Grioni, Rudolf Kaaks, Timothy J. Key, Carmen Navarro, Peter M. Nilsson, Kim Overvad, Domenico Palli, Salvatore Panico, J Ramón Quirós, Olov Rolandsson, Carlotta Sacerdote, María‐José Sánchez, Nadia Slimani, Anne Tjonneland, Rosario Tumino, Daphne L. van der A, Yvonne T. van der Schouw, Elio Riboli, Blair H. Smith, Archie Campbell, Ian J. Deary, Andrew M. McIntosh, Eric Boerwinkle, Julie E. Buring, Laura Crisponi, Douglas F. Easton, Caroline Hayward, Frank B. Hu, Simin Liu, Andres Metspalu, Craig E. Pennell, Paul M. Ridker, Konstantin Strauch, Elizabeth A. Streeten, Daniela Toniolo, André G. Uitterlinden, Sheila Ulivi, Henry Völzke, Nicholas J. Wareham, Melissa Wellons, Nora Franceschini, Daniel I. Chasman, Unnur Thorsteinsdottir, Anna Murray, Kari Stefansson, Joanne M. Murabito, Ken K. Ong, John R. B. Perry
Publié dans: Nature Communications, Numéro 20411723, 2015, Page(s) 7756, ISSN 2041-1723
Éditeur: Nature Publishing Group
DOI: 10.1038/ncomms8756

Using Genetic Variants to Assess the Relationship Between Circulating Lipids and Type 2 Diabetes

Auteurs: Tove Fall, Weijia Xie, Wenny Poon, Hanieh Yaghootkar, Reedik Mägi, Joshua W. Knowles, Valeriya Lyssenko, Michael Weedon, Timothy M. Frayling, Erik Ingelsson
Publié dans: Diabetes, Numéro 00121797, 2015, Page(s) 2676-2684, ISSN 0012-1797
Éditeur: American Diabetes Association
DOI: 10.2337/db14-1710

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

Auteurs: John R. B. Perry, Felix Day, Cathy E. Elks, Patrick Sulem, Deborah J. Thompson, Teresa Ferreira, Chunyan He, Daniel I. Chasman, Tõnu Esko, Gudmar Thorleifsson, Eva Albrecht, Wei Q. Ang, Tanguy Corre, Diana L. Cousminer, Bjarke Feenstra, Nora Franceschini, Andrea Ganna, Andrew D. Johnson, Sanela Kjellqvist, Kathryn L. Lunetta, George McMahon, Ilja M. Nolte, Lavinia Paternoster, Eleonora Porcu, Albert V. Smith, Lisette Stolk, Alexander Teumer, Natalia Tšernikova, Emmi Tikkanen, Sheila Ulivi, Erin K. Wagner, Najaf Amin, Laura J. Bierut, Enda M. Byrne, Jouke-Jan Hottenga, Daniel L. Koller, Massimo Mangino, Tune H. Pers, Laura M. Yerges-Armstrong, Jing Hua Zhao, Irene L. Andrulis, Hoda Anton-Culver, Femke Atsma, Stefania Bandinelli, Matthias W. Beckmann, Javier Benitez, Carl Blomqvist, Stig E. Bojesen, Manjeet K. Bolla, Bernardo Bonanni, Hiltrud Brauch, Hermann Brenner, Julie E. Buring, Jenny Chang-Claude, Stephen Chanock, Jinhui Chen, Georgia Chenevix-Trench, J. Margriet Collée, Fergus J. Couch, David Couper, Andrea D. Coviello, Angela Cox, Kamila Czene, Adamo Pio D’adamo, George Davey Smith, Immaculata De Vivo, Ellen W. Demerath, Joe Dennis, Peter Devilee, Aida K. Dieffenbach, Alison M. Dunning, Gudny Eiriksdottir, Johan G. Eriksson, Peter A. Fasching, Luigi Ferrucci, Dieter Flesch-Janys, Henrik Flyger, Tatiana Foroud, Lude Franke, Melissa E. Garcia, Montserrat García-Closas, Frank Geller, Eco E. J. de Geus, Graham G. Giles, Daniel F. Gudbjartsson, Vilmundur Gudnason, Pascal Guénel, Suiqun Guo, Per Hall, Ute Hamann, Robin Haring, Catharina A. Hartman, Andrew C. Heath, Albert Hofman, Maartje J. Hooning, John L. Hopper, Frank B. Hu, David J. Hunter, David Karasik, Douglas P. Kiel, Julia A. Knight, Veli-Matti Kosma, Zoltan Kutalik, Sandra Lai, Diether Lambrechts, Annika Lindblom, Reedik Mägi, Patrik K. Magnusson, Arto Mannermaa, Nicholas G. Martin, Gisli Masson, Patrick F. McArdle, Wendy L. McArdle, Mads Melbye, Kyriaki Michailidou, Evelin Mihailov, Lili Milani, Roger L. Milne, Heli Nevanlinna, Patrick Neven, Ellen A. Nohr, Albertine J. Oldehinkel, Ben A. Oostra, Aarno Palotie, Munro Peacock, Nancy L. Pedersen, Paolo Peterlongo, Julian Peto, Paul D. P. Pharoah, Dirkje S. Postma, Anneli Pouta, Katri Pylkäs, Paolo Radice, Susan Ring, Fernando Rivadeneira, Antonietta Robino, Lynda M. Rose, Anja Rudolph, Veikko Salomaa, Serena Sanna, David Schlessinger, Marjanka K. Schmidt, Mellissa C. Southey, Ulla Sovio, Meir J. Stampfer, Doris Stöckl, Anna M. Storniolo, Nicholas J. Timpson, Jonathan Tyrer, Jenny A. Visser, Peter Vollenweider, Henry Völzke, Gerard Waeber, Melanie Waldenberger, Henri Wallaschofski, Qin Wang, Gonneke Willemsen, Robert Winqvist, Bruce H. R. Wolffenbuttel, Margaret J. Wright, Dorret I. Boomsma, Michael J. Econs, Kay-Tee Khaw, Ruth J. F. Loos, Mark I. McCarthy, Grant W. Montgomery, John P. Rice, Elizabeth A. Streeten, Unnur Thorsteinsdottir, Cornelia M. van Duijn, Behrooz Z. Alizadeh, Sven Bergmann, Eric Boerwinkle, Heather A. Boyd, Laura Crisponi, Paolo Gasparini, Christian Gieger, Tamara B. Harris, Erik Ingelsson, Marjo-Riitta Järvelin, Peter Kraft, Debbie Lawlor, Andres Metspalu, Craig E. Pennell, Paul M. Ridker, Harold Snieder, Thorkild I. A. Sørensen, Tim D. Spector, David P. Strachan, André G. Uitterlinden, Nicholas J. Wareham, Elisabeth Widen, Marek Zygmunt, Anna Murray, Douglas F. Easton, Kari Stefansson, Joanne M. Murabito, Ken K. Ong
Publié dans: Nature, Numéro 00280836, 2014, Page(s) 92-97, ISSN 0028-0836
Éditeur: Nature Publishing Group
DOI: 10.1038/nature13545

Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu

Auteurs: Liis Leitsalu, Toomas Haller, Tõnu Esko, Mari-Liis Tammesoo, Helene Alavere, Harold Snieder, Markus Perola, Pauline C Ng, Reedik Mägi, Lili Milani, Krista Fischer, Andres Metspalu
Publié dans: International Journal of Epidemiology, Numéro 03005771, 2015, Page(s) 1137-1147, ISSN 0300-5771
Éditeur: Oxford University Press
DOI: 10.1093/ije/dyt268

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

Auteurs: Anubha Mahajan, Min Jin Go, Weihua Zhang, Jennifer E Below, Kyle J Gaulton, Teresa Ferreira, Momoko Horikoshi, Andrew D Johnson, Maggie C Y Ng, Inga Prokopenko, Danish Saleheen, Xu Wang, Eleftheria Zeggini, Goncalo R Abecasis, Linda S Adair, Peter Almgren, Mustafa Atalay, Tin Aung, Damiano Baldassarre, Beverley Balkau, Yuqian Bao, Anthony H Barnett, Ines Barroso, Abdul Basit, Latonya F Been, John Beilby, Graeme I Bell, Rafn Benediktsson, Richard N Bergman, Bernhard O Boehm, Eric Boerwinkle, Lori L Bonnycastle, Noël Burtt, Qiuyin Cai, Harry Campbell, Jason Carey, Stephane Cauchi, Mark Caulfield, Juliana C N Chan, Li-Ching Chang, Tien-Jyun Chang, Yi-Cheng Chang, Guillaume Charpentier, Chien-Hsiun Chen, Han Chen, Yuan-Tsong Chen, Kee-Seng Chia, Manickam Chidambaram, Peter S Chines, Nam H Cho, Young Min Cho, Lee-Ming Chuang, Francis S Collins, Marilyn C Cornelis, David J Couper, Andrew T Crenshaw, Rob M van Dam, John Danesh, Debashish Das, Ulf de Faire, George Dedoussis, Panos Deloukas, Antigone S Dimas, Christian Dina, Alex S F Doney, Peter J Donnelly, Mozhgan Dorkhan, Cornelia van Duijn, Josée Dupuis, Sarah Edkins, Paul Elliott, Valur Emilsson, Raimund Erbel, Johan G Eriksson, Jorge Escobedo, Tonu Esko, Elodie Eury, Jose C Florez, Pierre Fontanillas, Nita G Forouhi, Tom Forsen, Caroline Fox, Ross M Fraser, Timothy M Frayling, Philippe Froguel, Philippe Frossard, Yutang Gao, Karl Gertow, Christian Gieger, Bruna Gigante, Harald Grallert, George B Grant, Leif C Groop, Christopher J Groves, Elin Grundberg, Candace Guiducci, Anders Hamsten, Bok-Ghee Han, Kazuo Hara, Neelam Hassanali, Andrew T Hattersley, Caroline Hayward, Asa K Hedman, Christian Herder, Albert Hofman, Oddgeir L Holmen, Kees Hovingh, Astradur B Hreidarsson, Cheng Hu, Frank B Hu, Jennie Hui, Steve E Humphries, Sarah E Hunt, David J Hunter, Kristian Hveem, Zafar I Hydrie, Hiroshi Ikegami, Thomas Illig, Erik Ingelsson, Muhammed Islam, Bo Isomaa, Anne U Jackson, Tazeen Jafar, Alan James, Weiping Jia, Karl-Heinz Jöckel, Anna Jonsson, Jeremy B M Jowett, Takashi Kadowaki, Hyun Min Kang, Stavroula Kanoni, Wen Hong L Kao, Sekar Kathiresan, Norihiro Kato, Prasad Katulanda, Sirkka M Keinanen-Kiukaanniemi, Ann M Kelly, Hassan Khan, Kay-Tee Khaw, Chiea-Chuen Khor, Hyung-Lae Kim, Sangsoo Kim, Young Jin Kim, Leena Kinnunen, Norman Klopp, Augustine Kong, Eeva Korpi-Hyövälti, Sudhir Kowlessur, Peter Kraft, Jasmina Kravic, Malene M Kristensen, S Krithika, Ashish Kumar, Jesus Kumate, Johanna Kuusisto, Soo Heon Kwak, Markku Laakso, Vasiliki Lagou, Timo A Lakka, Claudia Langenberg, Cordelia Langford, Robert Lawrence, Karin Leander, Jen-Mai Lee, Nanette R Lee, Man Li, Xinzhong Li, Yun Li, Junbin Liang, Samuel Liju, Wei-Yen Lim, Lars Lind, Cecilia M Lindgren, Eero Lindholm, Ching-Ti Liu, Jian Jun Liu, Stéphane Lobbens, Jirong Long, Ruth J F Loos, Wei Lu, Jian'an Luan, Valeriya Lyssenko, Ronald C W Ma, Shiro Maeda, Reedik Mägi, Satu Männistö, David R Matthews, James B Meigs, Olle Melander, Andres Metspalu, Julia Meyer, Ghazala Mirza, Evelin Mihailov, Susanne Moebus, Viswanathan Mohan, Karen L Mohlke, Andrew D Morris, Thomas W Mühleisen, Martina Müller-Nurasyid, Bill Musk, Jiro Nakamura, Eitaro Nakashima, Pau Navarro, Peng-Keat Ng, Alexandra C Nica, Peter M Nilsson, Inger Njølstad, Markus M Nöthen, Keizo Ohnaka, Twee Hee Ong, Katharine R Owen, Colin N A Palmer, James S Pankow, Kyong Soo Park, Melissa Parkin, Sonali Pechlivanis, Nancy L Pedersen, Leena Peltonen, John R B Perry, Annette Peters, Janani M Pinidiyapathirage, Carl G P Platou, Simon Potter, Jackie F Price, Lu Qi, Venkatesan Radha, Loukianos Rallidis, Asif Rasheed, Wolfgang Rathmann, Rainer Rauramaa, Soumya Raychaudhuri, N William Rayner, Simon D Rees, Emil Rehnberg, Samuli Ripatti, Neil Robertson, Michael Roden, Elizabeth J Rossin, Igor Rudan, Denis Rybin, Timo E Saaristo, Veikko Salomaa, Juha Saltevo, Maria Samuel, Dharambir K Sanghera, Jouko Saramies, James Scott, Laura J Scott, Robert A Scott, Ayellet V Segrè, Joban
Publié dans: Nature Genetics, Numéro 10614036, 2014, Page(s) 234-244, ISSN 1061-4036
Éditeur: Nature Publishing Group
DOI: 10.1038/ng.2897

Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity

Auteurs: A. S. Dimas, V. Lagou, A. Barker, J. W. Knowles, R. Magi, M.-F. Hivert, A. Benazzo, D. Rybin, A. U. Jackson, H. M. Stringham, C. Song, A. Fischer-Rosinsky, T. W. Boesgaard, N. Grarup, F. A. Abbasi, T. L. Assimes, K. Hao, X. Yang, C. Lecoeur, I. Barroso, L. L. Bonnycastle, Y. Bottcher, S. Bumpstead, P. S. Chines, M. R. Erdos, J. Graessler, P. Kovacs, M. A. Morken, N. Narisu, F. Payne, A. Stancakova, A. J. Swift, A. Tonjes, S. R. Bornstein, S. Cauchi, P. Froguel, D. Meyre, P. E. H. Schwarz, H.-U. Haring, U. Smith, M. Boehnke, R. N. Bergman, F. S. Collins, K. L. Mohlke, J. Tuomilehto, T. Quertemous, L. Lind, T. Hansen, O. Pedersen, M. Walker, A. F. H. Pfeiffer, J. Spranger, M. Stumvoll, J. B. Meigs, N. J. Wareham, J. Kuusisto, M. Laakso, C. Langenberg, J. Dupuis, R. M. Watanabe, J. C. Florez, E. Ingelsson, M. I. McCarthy, I. Prokopenko
Publié dans: Diabetes, Numéro 00121797, 2014, Page(s) 2158-2171, ISSN 0012-1797
Éditeur: American Diabetes Association
DOI: 10.2337/db13-0949

GADA and anti-ZnT8 complicate the outcome of phenotypic type 2 diabetes of adults

Auteurs: Kadri Haller-Kikkatalo, Katrin Pruul, Kalle Kisand, Virge Nemvalts, Koit Reimand, Raivo Uibo
Publié dans: European Journal of Clinical Investigation, Numéro 00142972, 2015, Page(s) 255-262, ISSN 0014-2972
Éditeur: Blackwell Publishing Inc.
DOI: 10.1111/eci.12404

The Diagnostic Utility of Single Long Contiguous Stretches of Homozygosity in Patients without Parental Consanguinity

Auteurs: Sander Pajusalu, Olga �ilina, Maria Yakoreva, Pille Tammur, Kati Kuuse, Triin M�lter-V��r, Margit N�ukas, Tiia Reimand, Katrin �unap
Publié dans: Molecular Syndromology, Numéro 16618769, 2015, Page(s) 135-140, ISSN 1661-8769
Éditeur: S. Karger AG
DOI: 10.1159/000438776

Familial 1.3-Mb 11p15.5p15.4 Duplication in Three Generations Causing Silver-Russell and Beckwith-Wiedemann Syndromes

Auteurs: Mari-Anne Vals, Tiina Kahre, Pille Mee, Kai Muru, Eha Kallas, Olga �ilina, Vallo Tillmann, Katrin �unap
Publié dans: Molecular Syndromology, Numéro 16618769, 2015, Page(s) 147-151, ISSN 1661-8769
Éditeur: S. Karger AG
DOI: 10.1159/000437061

Two familial microduplications of 15q26.3 causing overgrowth and variable intellectual disability with normal copy number of IGF1R

Auteurs: Melanie Leffler, Sanna Puusepp, Olga Žilina, Ying Zhu, Kati Kuuse, Nicole Bain, Trent Burgess, Katrin Õunap, Michael Field
Publié dans: European Journal of Medical Genetics, Numéro 17697212, 2015, ISSN 1769-7212
Éditeur: Elsevier BV
DOI: 10.1016/j.ejmg.2015.12.002

De novo deletion of HOXB gene cluster in a patient with failure to thrive, developmental delay, gastroesophageal reflux and bronchiectasis

Auteurs: Sander Pajusalu, Tiia Reimand, Oivi Uibo, Maire Vasar, Inga Talvik, Olga Zilina, Pille Tammur, Katrin Õunap
Publié dans: European Journal of Medical Genetics, Numéro 17697212, 2015, Page(s) 336-340, ISSN 1769-7212
Éditeur: Elsevier BV
DOI: 10.1016/j.ejmg.2015.04.002

Mosaicism for maternal uniparental disomy 15 in a boy with some clinical features of Prader–Willi syndrome

Auteurs: Olga Žilina, Tiina Kahre, Inga Talvik, Eve Õiglane-Shlik, Vallo Tillmann, Katrin Õunap
Publié dans: European Journal of Medical Genetics, Numéro 17697212, 2014, Page(s) 279-283, ISSN 1769-7212
Éditeur: Elsevier BV
DOI: 10.1016/j.ejmg.2014.03.007

Monosomy 1p36 – A multifaceted and still enigmatic syndrome: Four clinically diverse cases with shared white matter abnormalities

Auteurs: Eve Õiglane-Shlik, Sanna Puusepp, Inga Talvik, Ulvi Vaher, Reet Rein, Pille Tammur, Tiia Reimand, Rita Teek, Olga Žilina, Tiiu Tomberg, Katrin Õunap
Publié dans: European Journal of Paediatric Neurology, Numéro 10903798, 2014, Page(s) 338-346, ISSN 1090-3798
Éditeur: W. B. Saunders Co., Ltd.
DOI: 10.1016/j.ejpn.2014.01.008

Increased Blood Levels of Growth Factors, Proinflammatory Cytokines, and Th17 Cytokines in Patients with Newly Diagnosed Type 1 Diabetes

Auteurs: Kristi Alnek, Kalle Kisand, Kaire Heilman, Aleksandr Peet, Karin Varik, Raivo Uibo
Publié dans: PLOS ONE, Numéro 19326203, 2015, Page(s) e0142976, ISSN 1932-6203
Éditeur: Public Library of Science
DOI: 10.1371/journal.pone.0142976

Differences in B7 and CD28 family gene expression in the peripheral blood between newly diagnosed young-onset and adult-onset type 1 diabetes patients

Auteurs: K. Pruul, K. Kisand, K. Alnek, K. Metsküla, K. Reimand, K. Heilman, A. Peet, K. Varik, M. Peetsalu, Ü. Einberg, V. Tillmann, R. Uibo
Publié dans: Molecular and Cellular Endocrinology, Numéro 03037207, 2015, Page(s) 265-271, ISSN 0303-7207
Éditeur: Elsevier BV
DOI: 10.1016/j.mce.2015.05.012

Interferon and Interferon-Inducible Gene Activation in Patients with Type 1 Diabetes

Auteurs: M. Panarina, K. Kisand, K. Alnek, K. Heilman, A. Peet, R. Uibo
Publié dans: Scandinavian Journal of Immunology, Numéro 03009475, 2014, Page(s) 283-292, ISSN 0300-9475
Éditeur: Blackwell Publishing Inc.
DOI: 10.1111/sji.12204

Expression of B7 and CD28 family genes in newly diagnosed type 1 diabetes

Auteurs: Katrin Pruul, Kalle Kisand, Kristi Alnek, Kaja Metsküla, Kaire Heilman, Aleksandr Peet, Karin Varik, Raivo Uibo
Publié dans: Human Immunology, Numéro 01988859, 2013, Page(s) 1251-1257, ISSN 0198-8859
Éditeur: Elsevier BV
DOI: 10.1016/j.humimm.2013.07.007

Pregnancy intendedness and the association with physical, sexual and emotional abuse – a European multi-country cross-sectional study

Auteurs: Mirjam Lukasse, Made Laanpere, Helle Karro, Hildur Kristjansdottir, Anne-Mette Schroll, An-Sofie Van Parys, Anne-Marie Wangel, Berit Schei
Publié dans: BMC Pregnancy & Childbirth, Numéro 14712393, 2015, ISSN 1471-2393
Éditeur: BioMed Central
DOI: 10.1186/s12884-015-0558-4

Fear of Childbirth and Risk of Cesarean Delivery: A Cohort Study in Six European Countries

Auteurs: Elsa Lena Ryding, Mirjam Lukasse, An-Sophie Van Parys, Anne-Marie Wangel, Helle Karro, Hildur Kristjansdottir, Anne-Mette Schroll, Berit Schei
Publié dans: Birth, Numéro 07307659, 2015, Page(s) 48-55, ISSN 0730-7659
Éditeur: Blackwell Publishing Inc.
DOI: 10.1111/birt.12147

Prevalence of experienced abuse in healthcare and associated obstetric characteristics in six European countries

Auteurs: Mirjam Lukasse, Anne-Mette Schroll, Helle Karro, Berit Schei, Thora Steingrimsdottir, An-Sofie Van Parys, Elsa Lena Ryding, Ann Tabor
Publié dans: Acta Obstetricia et Gynecologica Scandinavica, Numéro 00016349, 2015, Page(s) 508-517, ISSN 0001-6349
Éditeur: Wiley-Blackwell
DOI: 10.1111/aogs.12593

Abortion trends from 1996 to 2011 in Estonia: special emphasis on repeat abortion

Auteurs: Made Laanpere, Inge Ringmets, Kai Part, Kärt Allvee, Piret Veerus, Helle Karro
Publié dans: BMC Women's Health, Numéro 14726874, 2014, Page(s) 81, ISSN 1472-6874
Éditeur: BioMed Central
DOI: 10.1186/1472-6874-14-81

Prevalence of emotional, physical and sexual abuse among pregnant women in six European countries

Auteurs: Mirjam Lukasse, Anne-Mette Schroll, Elsa Lena Ryding, Jacquelyn Campbell, Helle Karro, Hildur Kristjansdottir, Made Laanpere, Thora Steingrimsdottir, Ann Tabor, Marleen Temmerman, An-Sofie Van Parys, Anne-Marie Wangel, Berit Schei
Publié dans: Acta Obstetricia et Gynecologica Scandinavica, Numéro 00016349, 2014, Page(s) 669-677, ISSN 0001-6349
Éditeur: Wiley-Blackwell
DOI: 10.1111/aogs.12392

A History of Abuse and Operative Delivery – Results from a European Multi-Country Cohort Study

Auteurs: Berit Schei, Mirjam Lukasse, Elsa Lena Ryding, Jacquelyn Campbell, Helle Karro, Hildur Kristjansdottir, Made Laanpere, Anne-Mette Schroll, Ann Tabor, Marleen Temmerman, An-Sofie Van Parys, Anne-Marie Wangel, Thora Steingrimsdottir
Publié dans: PLoS ONE, Numéro 19326203, 2014, Page(s) e87579, ISSN 1932-6203
Éditeur: Public Library of Science
DOI: 10.1371/journal.pone.0087579

Teenage pregnancies in the European Union in the context of legislation and youth sexual and reproductive health services

Auteurs: Kai Part, Caroline Moreau, Serena Donati, Mika Gissler, Inês Fronteira, Helle Karro
Publié dans: Acta Obstetricia et Gynecologica Scandinavica, Numéro 00016349, 2013, Page(s) 1395-1406, ISSN 0001-6349
Éditeur: Wiley-Blackwell
DOI: 10.1111/aogs.12253

Intimate partner violence and sexual health outcomes: a population-based study among 16-44-year-old women in Estonia

Auteurs: M. Laanpere, I. Ringmets, K. Part, H. Karro
Publié dans: The European Journal of Public Health, Numéro 11011262, 2013, Page(s) 688-693, ISSN 1101-1262
Éditeur: Oxford University Press
DOI: 10.1093/eurpub/cks144

Circulating miR-200–family micro-RNAs have altered plasma levels in patients with endometriosis and vary with blood collection time

Auteurs: Kadri Rekker, Merli Saare, Anne Mari Roost, Tanel Kaart, Deniss Sõritsa, Helle Karro, Andrei Sõritsa, Carlos Simón, Andres Salumets, Maire Peters
Publié dans: Fertility and Sterility, Numéro 104/4, 2015, Page(s) 938-946.e2, ISSN 0015-0282
Éditeur: Elsevier BV
DOI: 10.1016/j.fertnstert.2015.06.029

Genetic studies of body mass index yield new insights for obesity biology

Auteurs: Adam E. Locke, Bratati Kahali, Sonja I. Berndt, Anne E. Justice, Tune H. Pers, Felix R. Day, Corey Powell, Sailaja Vedantam, Martin L. Buchkovich, Jian Yang, Damien C. Croteau-Chonka, Tonu Esko, Tove Fall, Teresa Ferreira, Stefan Gustafsson, Zoltán Kutalik, Jian’an Luan, Reedik Mägi, Joshua C. Randall, Thomas W. Winkler, Andrew R. Wood, Tsegaselassie Workalemahu, Jessica D. Faul, Jennifer A. Smith, Jing Hua Zhao, Wei Zhao, Jin Chen, Rudolf Fehrmann, Åsa K. Hedman, Juha Karjalainen, Ellen M. Schmidt, Devin Absher, Najaf Amin, Denise Anderson, Marian Beekman, Jennifer L. Bolton, Jennifer L. Bragg-Gresham, Steven Buyske, Ayse Demirkan, Guohong Deng, Georg B. Ehret, Bjarke Feenstra, Mary F. Feitosa, Krista Fischer, Anuj Goel, Jian Gong, Anne U. Jackson, Stavroula Kanoni, Marcus E. Kleber, Kati Kristiansson, Unhee Lim, Vaneet Lotay, Massimo Mangino, Irene Mateo Leach, Carolina Medina-Gomez, Sarah E. Medland, Michael A. Nalls, Cameron D. Palmer, Dorota Pasko, Sonali Pechlivanis, Marjolein J. Peters, Inga Prokopenko, Dmitry Shungin, Alena Stančáková, Rona J. Strawbridge, Yun Ju Sung, Toshiko Tanaka, Alexander Teumer, Stella Trompet, Sander W. van der Laan, Jessica van Setten, Jana V. Van Vliet-Ostaptchouk, Zhaoming Wang, Loïc Yengo, Weihua Zhang, Aaron Isaacs, Eva Albrecht, Johan Ärnlöv, Gillian M. Arscott, Antony P. Attwood, Stefania Bandinelli, Amy Barrett, Isabelita N. Bas, Claire Bellis, Amanda J. Bennett, Christian Berne, Roza Blagieva, Matthias Blüher, Stefan Böhringer, Lori L. Bonnycastle, Yvonne Böttcher, Heather A. Boyd, Marcel Bruinenberg, Ida H. Caspersen, Yii-Der Ida Chen, Robert Clarke, E. Warwick Daw, Anton J. M. de Craen, Graciela Delgado, Maria Dimitriou, Alex S. F. Doney, Niina Eklund, Karol Estrada, Elodie Eury, Lasse Folkersen, Ross M. Fraser, Melissa E. Garcia, Frank Geller, Vilmantas Giedraitis, Bruna Gigante, Alan S. Go, Alain Golay, Alison H. Goodall, Scott D. Gordon, Mathias Gorski, Hans-Jörgen Grabe, Harald Grallert, Tanja B. Grammer, Jürgen Gräßler, Henrik Grönberg, Christopher J. Groves, Gaëlle Gusto, Jeffrey Haessler, Per Hall, Toomas Haller, Goran Hallmans, Catharina A. Hartman, Maija Hassinen, Caroline Hayward, Nancy L. Heard-Costa, Quinta Helmer, Christian Hengstenberg, Oddgeir Holmen, Jouke-Jan Hottenga, Alan L. James, Janina M. Jeff, Åsa Johansson, Jennifer Jolley, Thorhildur Juliusdottir, Leena Kinnunen, Wolfgang Koenig, Markku Koskenvuo, Wolfgang Kratzer, Jaana Laitinen, Claudia Lamina, Karin Leander, Nanette R. Lee, Peter Lichtner, Lars Lind, Jaana Lindström, Ken Sin Lo, Stéphane Lobbens, Roberto Lorbeer, Yingchang Lu, François Mach, Patrik K. E. Magnusson, Anubha Mahajan, Wendy L. McArdle, Stela McLachlan, Cristina Menni, Sigrun Merger, Evelin Mihailov, Lili Milani, Alireza Moayyeri, Keri L. Monda, Mario A. Morken, Antonella Mulas, Gabriele Müller, Martina Müller-Nurasyid, Arthur W. Musk, Ramaiah Nagaraja, Markus M. Nöthen, Ilja M. Nolte, Stefan Pilz, Nigel W. Rayner, Frida Renstrom, Rainer Rettig, Janina S. Ried, Stephan Ripke, Neil R. Robertson, Lynda M. Rose, Serena Sanna, Hubert Scharnagl, Salome Scholtens, Fredrick R. Schumacher, William R. Scott, Thomas Seufferlein, Jianxin Shi, Albert Vernon Smith, Joanna Smolonska, Alice V. Stanton, Valgerdur Steinthorsdottir, Kathleen Stirrups, Heather M. Stringham, Johan Sundström, Morris A. Swertz, Amy J. Swift, Ann-Christine Syvänen, Sian-Tsung Tan, Bamidele O. Tayo, Barbara Thorand, Gudmar Thorleifsson, Jonathan P. Tyrer, Hae-Won Uh, Liesbeth Vandenput, Frank C. Verhulst, Sita H. Vermeulen, Niek Verweij, Judith M. Vonk, Lindsay L. Waite, Helen R. Warren, Dawn Waterworth, Michael N. Weedon, Lynne R. Wilkens, Christina Willenborg, Tom Wilsgaard, Mary K. Wojczynski, Andrew Wong, Alan F. Wright, Qunyuan Zhang, Eoin P. Brennan, Murim Choi, Zari Dastani, Alexander W. Drong, Per Eriksson, Anders Franco-Cereceda, Jesper R. Gådin, Ali G. Gharavi, Michael E. Goddard, Robert E. Handsaker, Jinyan Huang, Fredrik Karpe, Sekar Kathiresa
Publié dans: Nature, Numéro 518/7538, 2015, Page(s) 197-206, ISSN 0028-0836
Éditeur: Nature Publishing Group
DOI: 10.1038/nature14177

Differences in B7 and CD28 family gene expression in the peripheral blood between newly diagnosed young-onset and adult-onset type 1 diabetes patients

Auteurs: K. Pruul, K. Kisand, K. Alnek, K. Metsküla, K. Reimand, K. Heilman, A. Peet, K. Varik, M. Peetsalu, Ü. Einberg, V. Tillmann, R. Uibo
Publié dans: Molecular and Cellular Endocrinology, Numéro 412, 2015, Page(s) 265-271, ISSN 0303-7207
Éditeur: Elsevier BV
DOI: 10.1016/j.mce.2015.05.012

Teenage pregnancies in the European Union in the context of legislation and youth sexual and reproductive health services

Auteurs: Kai Part, Caroline Moreau, Serena Donati, Mika Gissler, Inês Fronteira, Helle Karro
Publié dans: Acta Obstetricia et Gynecologica Scandinavica, Numéro 92/12, 2013, Page(s) 1395-1406, ISSN 0001-6349
Éditeur: Wiley-Blackwell
DOI: 10.1111/aogs.12253

Genetic variants associated with female reproductive ageing – potential markers for assessing ovarian function and ovarian stimulation outcome

Auteurs: Triin Laisk-Podar, Tanel Kaart, Maire Peters, Andres Salumets
Publié dans: Reproductive BioMedicine Online, Numéro 31/2, 2015, Page(s) 199-209, ISSN 1472-6483
Éditeur: Reproductive Healthcare Ltd
DOI: 10.1016/j.rbmo.2015.05.001

Rare coding variants and X-linked loci associated with age at menarche

Auteurs: Kathryn L. Lunetta, Felix R. Day, Patrick Sulem, Katherine S. Ruth, Joyce Y. Tung, David A. Hinds, Tõnu Esko, Cathy E. Elks, Elisabeth Altmaier, Chunyan He, Jennifer E. Huffman, Evelin Mihailov, Eleonora Porcu, Antonietta Robino, Lynda M. Rose, Ursula M. Schick, Lisette Stolk, Alexander Teumer, Deborah J. Thompson, Michela Traglia, Carol A. Wang, Laura M. Yerges-Armstrong, Antonis C. Antoniou, Caterina Barbieri, Andrea D. Coviello, Francesco Cucca, Ellen W. Demerath, Alison M. Dunning, Ilaria Gandin, Megan L. Grove, Daniel F. Gudbjartsson, Lynne J. Hocking, Albert Hofman, Jinyan Huang, Rebecca D. Jackson, David Karasik, Jennifer Kriebel, Ethan M. Lange, Leslie A. Lange, Claudia Langenberg, Xin Li, Jian'an Luan, Reedik Mägi, Alanna C. Morrison, Sandosh Padmanabhan, Ailith Pirie, Ozren Polasek, David Porteous, Alex P. Reiner, Fernando Rivadeneira, Igor Rudan, Cinzia F. Sala, David Schlessinger, Robert A. Scott, Doris Stöckl, Jenny A. Visser, Uwe Völker, Diego Vozzi, James G. Wilson, Marek Zygmunt, Nita G. Forouhi, Nicola D. Kerrison, Stephen J. Sharp, Matt Sims, Inês Barroso, Panos Deloukas, Mark I. McCarthy, Larraitz Arriola, Beverley Balkau, Aurelio Barricarte, Heiner Boeing, Paul W. Franks, Carlos Gonzalez, Sara Grioni, Rudolf Kaaks, Timothy J. Key, Carmen Navarro, Peter M. Nilsson, Kim Overvad, Domenico Palli, Salvatore Panico, J Ramón Quirós, Olov Rolandsson, Carlotta Sacerdote, María‐José Sánchez, Nadia Slimani, Anne Tjonneland, Rosario Tumino, Daphne L. van der A, Yvonne T. van der Schouw, Elio Riboli, Blair H. Smith, Archie Campbell, Ian J. Deary, Andrew M. McIntosh, Eric Boerwinkle, Julie E. Buring, Laura Crisponi, Douglas F. Easton, Caroline Hayward, Frank B. Hu, Simin Liu, Andres Metspalu, Craig E. Pennell, Paul M. Ridker, Konstantin Strauch, Elizabeth A. Streeten, Daniela Toniolo, André G. Uitterlinden, Sheila Ulivi, Henry Völzke, Nicholas J. Wareham, Melissa Wellons, Nora Franceschini, Daniel I. Chasman, Unnur Thorsteinsdottir, Anna Murray, Kari Stefansson, Joanne M. Murabito, Ken K. Ong, John R. B. Perry
Publié dans: Nature Communications, Numéro 6, 2015, Page(s) 7756, ISSN 2041-1723
Éditeur: Nature Publishing Group
DOI: 10.1038/ncomms8756

Interferon and Interferon-Inducible Gene Activation in Patients with Type 1 Diabetes

Auteurs: M. Panarina, K. Kisand, K. Alnek, K. Heilman, A. Peet, R. Uibo
Publié dans: Scandinavian Journal of Immunology, Numéro 80/4, 2014, Page(s) 283-292, ISSN 0300-9475
Éditeur: Blackwell Publishing Inc.
DOI: 10.1111/sji.12204

Research Resource: Small RNA-seq of Human Granulosa Cells Reveals miRNAs in FSHR and Aromatase Genes

Auteurs: Agne Velthut-Meikas, Jaak Simm, Timo Tuuri, Juha S. Tapanainen, Madis Metsis, Andres Salumets
Publié dans: Molecular Endocrinology, Numéro 27/7, 2013, Page(s) 1128-1141, ISSN 0888-8809
Éditeur: The Endocrine Society
DOI: 10.1210/me.2013-1058

Guidelines for the design, analysis and interpretation of 'omics' data: focus on human endometrium

Auteurs: S. Altmae, F. J. Esteban, A. Stavreus-Evers, C. Simon, L. Giudice, B. A. Lessey, J. A. Horcajadas, N. S. Macklon, T. D'Hooghe, C. Campoy, B. C. Fauser, L. A. Salamonsen, A. Salumets
Publié dans: Human Reproduction Update, Numéro 20/1, 2013, Page(s) 12-28, ISSN 1355-4786
Éditeur: Oxford University Press
DOI: 10.1093/humupd/dmt048

Monosomy 1p36 – A multifaceted and still enigmatic syndrome: Four clinically diverse cases with shared white matter abnormalities

Auteurs: Eve Õiglane-Shlik, Sanna Puusepp, Inga Talvik, Ulvi Vaher, Reet Rein, Pille Tammur, Tiia Reimand, Rita Teek, Olga Žilina, Tiiu Tomberg, Katrin Õunap
Publié dans: European Journal of Paediatric Neurology, Numéro 18/3, 2014, Page(s) 338-346, ISSN 1090-3798
Éditeur: W. B. Saunders Co., Ltd.
DOI: 10.1016/j.ejpn.2014.01.008

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

Auteurs: Kyle J Gaulton, Teresa Ferreira, Yeji Lee, Anne Raimondo, Reedik Mägi, Michael E Reschen, Anubha Mahajan, Adam Locke, N William Rayner, Neil Robertson, Robert A Scott, Inga Prokopenko, Laura J Scott, Todd Green, Thomas Sparso, Dorothee Thuillier, Loic Yengo, Harald Grallert, Simone Wahl, Mattias Frånberg, Rona J Strawbridge, Hans Kestler, Himanshu Chheda, Lewin Eisele, Stefan Gustafsson, Valgerdur Steinthorsdottir, Gudmar Thorleifsson, Lu Qi, Lennart C Karssen, Elisabeth M van Leeuwen, Sara M Willems, Man Li, Han Chen, Christian Fuchsberger, Phoenix Kwan, Clement Ma, Michael Linderman, Yingchang Lu, Soren K Thomsen, Jana K Rundle, Nicola L Beer, Martijn van de Bunt, Anil Chalisey, Hyun Min Kang, Benjamin F Voight, Gonçalo R Abecasis, Peter Almgren, Damiano Baldassarre, Beverley Balkau, Rafn Benediktsson, Matthias Blüher, Heiner Boeing, Lori L Bonnycastle, Erwin P Bottinger, Noël P Burtt, Jason Carey, Guillaume Charpentier, Peter S Chines, Marilyn C Cornelis, David J Couper, Andrew T Crenshaw, Rob M van Dam, Alex S F Doney, Mozhgan Dorkhan, Sarah Edkins, Johan G Eriksson, Tonu Esko, Elodie Eury, João Fadista, Jason Flannick, Pierre Fontanillas, Caroline Fox, Paul W Franks, Karl Gertow, Christian Gieger, Bruna Gigante, Omri Gottesman, George B Grant, Niels Grarup, Christopher J Groves, Maija Hassinen, Christian T Have, Christian Herder, Oddgeir L Holmen, Astradur B Hreidarsson, Steve E Humphries, David J Hunter, Anne U Jackson, Anna Jonsson, Marit E Jørgensen, Torben Jørgensen, Wen-Hong L Kao, Nicola D Kerrison, Leena Kinnunen, Norman Klopp, Augustine Kong, Peter Kovacs, Peter Kraft, Jasmina Kravic, Cordelia Langford, Karin Leander, Liming Liang, Peter Lichtner, Cecilia M Lindgren, Eero Lindholm, Allan Linneberg, Ching-Ti Liu, Stéphane Lobbens, Jian'an Luan, Valeriya Lyssenko, Satu Männistö, Olga McLeod, Julia Meyer, Evelin Mihailov, Ghazala Mirza, Thomas W Mühleisen, Martina Müller-Nurasyid, Carmen Navarro, Markus M Nöthen, Nikolay N Oskolkov, Katharine R Owen, Domenico Palli, Sonali Pechlivanis, Leena Peltonen, John R B Perry, Carl G P Platou, Michael Roden, Douglas Ruderfer, Denis Rybin, Yvonne T van der Schouw, Bengt Sennblad, Gunnar Sigurðsson, Alena Stančáková, Gerald Steinbach, Petter Storm, Konstantin Strauch, Heather M Stringham, Qi Sun, Barbara Thorand, Emmi Tikkanen, Anke Tonjes, Joseph Trakalo, Elena Tremoli, Tiinamaija Tuomi, Roman Wennauer, Steven Wiltshire, Andrew R Wood, Eleftheria Zeggini, Ian Dunham, Ewan Birney, Lorenzo Pasquali, Jorge Ferrer, Ruth J F Loos, Josée Dupuis, Jose C Florez, Eric Boerwinkle, James S Pankow, Cornelia van Duijn, Eric Sijbrands, James B Meigs, Frank B Hu, Unnur Thorsteinsdottir, Kari Stefansson, Timo A Lakka, Rainer Rauramaa, Michael Stumvoll, Nancy L Pedersen, Lars Lind, Sirkka M Keinanen-Kiukaanniemi, Eeva Korpi-Hyövälti, Timo E Saaristo, Juha Saltevo, Johanna Kuusisto, Markku Laakso, Andres Metspalu, Raimund Erbel, Karl-Heinz Jöcke, Susanne Moebus, Samuli Ripatti, Veikko Salomaa, Erik Ingelsson, Bernhard O Boehm, Richard N Bergman, Francis S Collins, Karen L Mohlke, Heikki Koistinen, Jaakko Tuomilehto, Kristian Hveem, Inger Njølstad, Panagiotis Deloukas, Peter J Donnelly, Timothy M Frayling, Andrew T Hattersley, Ulf de Faire, Anders Hamsten, Thomas Illig, Annette Peters, Stephane Cauchi, Rob Sladek, Philippe Froguel, Torben Hansen, Oluf Pedersen, Andrew D Morris, Collin N A Palmer, Sekar Kathiresan, Olle Melander, Peter M Nilsson, Leif C Groop, Inês Barroso, Claudia Langenberg, Nicholas J Wareham, Christopher A O'Callaghan, Anna L Gloyn, David Altshuler, Michael Boehnke, Tanya M Teslovich, Mark I McCarthy, Andrew P Morris
Publié dans: Nature Genetics, Numéro 47/12, 2015, Page(s) 1415-1425, ISSN 1061-4036
Éditeur: Nature Publishing Group
DOI: 10.1038/ng.3437

Corrigendum: Rare coding variants and X-linked loci associated with age at menarche

Auteurs: Kathryn L. Lunetta, Felix R. Day, Patrick Sulem, Katherine S. Ruth, Joyce Y. Tung, David A. Hinds, Tõnu Esko, Cathy E. Elks, Elisabeth Altmaier, Chunyan He, Jennifer E. Huffman, Evelin Mihailov, Eleonora Porcu, Antonietta Robino, Lynda M. Rose, Ursula M. Schick, Lisette Stolk, Alexander Teumer, Deborah J. Thompson, Michela Traglia, Carol A. Wang, Laura M. Yerges-Armstrong, Antonis C. Antoniou, Caterina Barbieri, Andrea D. Coviello, Francesco Cucca, Ellen W. Demerath, Alison M. Dunning, Ilaria Gandin, Megan L. Grove, Daniel F. Gudbjartsson, Lynne J. Hocking, Albert Hofman, Jinyan Huang, Rebecca D. Jackson, David Karasik, Jennifer Kriebel, Ethan M. Lange, Leslie A. Lange, Claudia Langenberg, Xin Li, Jian'an Luan, Reedik Mägi, Alanna C. Morrison, Sandosh Padmanabhan, Ailith Pirie, Ozren Polasek, David Porteous, Alex P. Reiner, Fernando Rivadeneira, Igor Rudan, Cinzia F. Sala, David Schlessinger, Robert A. Scott, Doris Stöckl, Jenny A. Visser, Uwe Völker, Diego Vozzi, James G. Wilson, Marek Zygmunt, Eric Boerwinkle, Julie E. Buring, Laura Crisponi, Douglas F. Easton, Caroline Hayward, Frank B. Hu, Simin Liu, Andres Metspalu, Craig E. Pennell, Paul M. Ridker, Konstantin Strauch, Elizabeth A. Streeten, Daniela Toniolo, André G. Uitterlinden, Sheila Ulivi, Henry Völzke, Nicholas J. Wareham, Melissa Wellons, Nora Franceschini, Daniel I. Chasman, Unnur Thorsteinsdottir, Anna Murray, Kari Stefansson, Joanne M. Murabito, Ken K. Ong, John R. B. Perry
Publié dans: Nature Communications, Numéro 6, 2015, Page(s) 10257, ISSN 2041-1723
Éditeur: Nature Publishing Group
DOI: 10.1038/ncomms10257

Sequencing and annotated analysis of the Holstein cow genome

Auteurs: Sulev Kõks, Rutt Lilleoja, Ene Reimann, Andres Salumets, Paula Reemann, Ülle Jaakma
Publié dans: Mammalian Genome, Numéro 24/7-8, 2013, Page(s) 309-321, ISSN 0938-8990
Éditeur: Springer Verlag
DOI: 10.1007/s00335-013-9464-0

Sequencing and annotated analysis of full genome of Holstein breed bull

Auteurs: Sulev Kõks, Ene Reimann, Rutt Lilleoja, Freddy Lättekivi, Andres Salumets, Paula Reemann, Ülle Jaakma
Publié dans: Mammalian Genome, Numéro 25/7-8, 2014, Page(s) 363-373, ISSN 0938-8990
Éditeur: Springer Verlag
DOI: 10.1007/s00335-014-9511-5

Increased Blood Levels of Growth Factors, Proinflammatory Cytokines, and Th17 Cytokines in Patients with Newly Diagnosed Type 1 Diabetes

Auteurs: Kristi Alnek, Kalle Kisand, Kaire Heilman, Aleksandr Peet, Karin Varik, Raivo Uibo
Publié dans: PLOS ONE, Numéro 10/12, 2015, Page(s) e0142976, ISSN 1932-6203
Éditeur: Public Library of Science
DOI: 10.1371/journal.pone.0142976

MicroRNAs miR-30b, miR-30d, and miR-494 Regulate Human Endometrial Receptivity

Auteurs: S. Altmae, J. A. Martinez-Conejero, F. J. Esteban, M. Ruiz-Alonso, A. Stavreus-Evers, J. A. Horcajadas, A. Salumets
Publié dans: Reproductive Sciences, Numéro 20/3, 2013, Page(s) 308-317, ISSN 1933-7191
Éditeur: SAGE Publications
DOI: 10.1177/1933719112453507

Circulating microRNA Profile throughout the Menstrual Cycle

Auteurs: Kadri Rekker, Merli Saare, Anne Mari Roost, Andres Salumets, Maire Peters
Publié dans: PLoS ONE, Numéro 8/11, 2013, Page(s) e81166, ISSN 1932-6203
Éditeur: Public Library of Science
DOI: 10.1371/journal.pone.0081166

Chromosomal microarray analysis as a first-tier clinical diagnostic test: Estonian experience

Auteurs: Olga Žilina, Rita Teek, Pille Tammur, Kati Kuuse, Maria Yakoreva, Eve Vaidla, Triin Mölter-Väär, Tiia Reimand, Ants Kurg, Katrin Õunap
Publié dans: Molecular Genetics & Genomic Medicine, Numéro 2/2, 2014, Page(s) 166-175, ISSN 2324-9269
Éditeur: Blackwell Publishing
DOI: 10.1002/mgg3.57

Changes in the Transcriptome of the Human Endometrial Ishikawa Cancer Cell Line Induced by Estrogen, Progesterone, Tamoxifen, and Mifepristone (RU486) as Detected by RNA-Sequencing

Auteurs: Karin Tamm-Rosenstein, Jaak Simm, Marina Suhorutshenko, Andres Salumets, Madis Metsis
Publié dans: PLoS ONE, Numéro 8/7, 2013, Page(s) e68907, ISSN 1932-6203
Éditeur: Public Library of Science
DOI: 10.1371/journal.pone.0068907

Systemic oxidative stress could predict assisted reproductive technique outcome

Auteurs: A. Ahelik, R. Mändar, P. Korrovits, P. Karits, E. Talving, K. Rosenstein, M. Jaagura, A. Salumets, T. Kullisaar
Publié dans: Journal of Assisted Reproduction and Genetics, Numéro 32/5, 2015, Page(s) 699-704, ISSN 1058-0468
Éditeur: Kluwer Academic/Plenum Publishers
DOI: 10.1007/s10815-015-0466-6

A patient with de novo 0.45 Mb deletion of 2p16.1: The role of BCL11A , PAPOLG , REL , and FLJ16341 in the 2p15-p16.1 microdeletion syndrome

Auteurs: Miroslava Hancarova, Martina Simandlova, Jana Drabova, Katrin Mannik, Ants Kurg, Zdenek Sedlacek
Publié dans: American Journal of Medical Genetics Part A, Numéro 161/4, 2013, Page(s) 865-870, ISSN 1552-4825
Éditeur: Wiley-Liss Inc
DOI: 10.1002/ajmg.a.35783

Bovine sperm plasma membrane proteomics through biotinylation and subcellular enrichment

Auteurs: Sergo Kasvandik, Gerly Sillaste, Agne Velthut-Meikas, Aavo-Valdur Mikelsaar, Triin Hallap, Peeter Padrik, Tanel Tenson, Ülle Jaakma, Sulev Kõks, Andres Salumets
Publié dans: PROTEOMICS, Numéro 15/11, 2015, Page(s) 1906-1920, ISSN 1615-9853
Éditeur: John Wiley & Sons Ltd.
DOI: 10.1002/pmic.201400297

GADA and anti-ZnT8 complicate the outcome of phenotypic type 2 diabetes of adults

Auteurs: Kadri Haller-Kikkatalo, Katrin Pruul, Kalle Kisand, Virge Nemvalts, Koit Reimand, Raivo Uibo
Publié dans: European Journal of Clinical Investigation, Numéro 45/3, 2015, Page(s) 255-262, ISSN 0014-2972
Éditeur: Blackwell Publishing Inc.
DOI: 10.1111/eci.12404

Abortion trends from 1996 to 2011 in Estonia: special emphasis on repeat abortion

Auteurs: Made Laanpere, Inge Ringmets, Kai Part, Kärt Allvee, Piret Veerus, Helle Karro
Publié dans: BMC Women's Health, Numéro 14/1, 2014, Page(s) 81, ISSN 1472-6874
Éditeur: BioMed Central
DOI: 10.1186/1472-6874-14-81

Folic acid supplementation and IVF pregnancy outcome in women with unexplained infertility

Auteurs: T. Murto, A. Skoog Svanberg, A. Yngve, T.K. Nilsson, S. Altmäe, K. Wånggren, A. Salumets, A. Stavreus-Evers
Publié dans: Reproductive BioMedicine Online, Numéro 28/6, 2014, Page(s) 766-772, ISSN 1472-6483
Éditeur: Reproductive Healthcare Ltd
DOI: 10.1016/j.rbmo.2014.01.017

Prevalence of emotional, physical and sexual abuse among pregnant women in six European countries

Auteurs: Mirjam Lukasse, Anne-Mette Schroll, Elsa Lena Ryding, Jacquelyn Campbell, Helle Karro, Hildur Kristjansdottir, Made Laanpere, Thora Steingrimsdottir, Ann Tabor, Marleen Temmerman, An-Sofie Van Parys, Anne-Marie Wangel, Berit Schei
Publié dans: Acta Obstetricia et Gynecologica Scandinavica, Numéro 93/7, 2014, Page(s) 669-677, ISSN 0001-6349
Éditeur: Wiley-Blackwell
DOI: 10.1111/aogs.12392

Genomic imprinting in complex traits

Auteurs: Pervjakova, Natalja
Publié dans: 2018, ISBN 978-9949-77-735-8
Éditeur: University of Tartu Press

Unravelling chromosomal instability in mammalian preimplantation embryos using single-cell genomics

Auteurs: Tšuiko, Olga
Publié dans: 2018, ISBN 978-9949-77-862-1
Éditeur: University of Tartu Press

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