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

CORDIS oferuje możliwość skorzystania z odnośników do publicznie dostępnych publikacji i rezultatów projektów realizowanych w ramach programów ramowych HORYZONT.

Odnośniki do rezultatów i publikacji związanych z poszczególnymi projektami 7PR, a także odnośniki do niektórych konkretnych kategorii wyników, takich jak zbiory danych i oprogramowanie, są dynamicznie pobierane z systemu OpenAIRE .

Rezultaty

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.

Publikacje

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

Autorzy: Melanie Leffler, Sanna Puusepp, Olga Žilina, Ying Zhu, Kati Kuuse, Nicole Bain, Trent Burgess, Katrin Õunap, Michael Field
Opublikowane w: European Journal of Medical Genetics, 2015, ISSN 1769-7212
Wydawca: 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

Autorzy: Tiina Murto, Theodora K. Kallak, Annica Hoas, Signe Altmäe, Andres Salumets, Torbjörn K. Nilsson, Agneta Skoog Svanberg, Kjell Wånggren, Agneta Yngve, Anneli Stavreus-Evers
Opublikowane w: Acta Obstetricia et Gynecologica Scandinavica, Numer 94/1, 2015, Strona(/y) 65-71, ISSN 0001-6349
Wydawca: 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

Autorzy: M. Laanpere, I. Ringmets, K. Part, H. Karro
Opublikowane w: The European Journal of Public Health, Numer 23/4, 2013, Strona(/y) 688-693, ISSN 1101-1262
Wydawca: 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

Autorzy: Olga Žilina, Tiia Reimand, Pille Tammur, Vallo Tillmann, Ants Kurg, Katrin Õunap
Opublikowane w: European Journal of Medical Genetics, Numer 56/4, 2013, Strona(/y) 202-206, ISSN 1769-7212
Wydawca: 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

Autorzy: 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
Opublikowane w: PLoS ONE, Numer 9/1, 2014, Strona(/y) e87579, ISSN 1932-6203
Wydawca: 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

Autorzy: Deniss Sõritsa, Merli Saare, Triin Laisk-Podar, Maire Peters, Andrei Sõritsa, Kadri Matt, Helle Karro, Andres Salumets
Opublikowane w: Gynecologic and Obstetric Investigation, Numer 79/1, 2015, Strona(/y) 34-39, ISSN 0378-7346
Wydawca: S. Karger AG
DOI: 10.1159/000365329

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

Autorzy: 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
Opublikowane w: Gene, Numer 559/2, 2015, Strona(/y) 144-148, ISSN 0378-1119
Wydawca: 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

Autorzy: Olga Žilina, Tiina Kahre, Inga Talvik, Eve Õiglane-Shlik, Vallo Tillmann, Katrin Õunap
Opublikowane w: European Journal of Medical Genetics, Numer 57/6, 2014, Strona(/y) 279-283, ISSN 1769-7212
Wydawca: Elsevier BV
DOI: 10.1016/j.ejmg.2014.03.007

Monozygotic Twins with 17q21.31 Microdeletion Syndrome

Autorzy: Marketa Vlckova, Miroslava Hancarova, Jana Drabova, Zuzana Slamova, Monika Koudova, Renata Alanova, Katrin Mannik, Ants Kurg, Zdenek Sedlacek
Opublikowane w: Twin Research and Human Genetics, Numer 17/05, 2014, Strona(/y) 405-410, ISSN 1832-4274
Wydawca: 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

Autorzy: 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
Opublikowane w: Epigenetics, Numer 9/10, 2014, Strona(/y) 1397-1409, ISSN 1559-2294
Wydawca: Landes Bioscience
DOI: 10.4161/15592294.2014.970052

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

Autorzy: Katrin Pruul, Kalle Kisand, Kristi Alnek, Kaja Metsküla, Kaire Heilman, Aleksandr Peet, Karin Varik, Raivo Uibo
Opublikowane w: Human Immunology, Numer 74/10, 2013, Strona(/y) 1251-1257, ISSN 0198-8859
Wydawca: Elsevier BV
DOI: 10.1016/j.humimm.2013.07.007

Complementary seminovaginal microbiome in couples

Autorzy: 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
Opublikowane w: Research in Microbiology, Numer 166/5, 2015, Strona(/y) 440-447, ISSN 0923-2508
Wydawca: Elsevier BV
DOI: 10.1016/j.resmic.2015.03.009

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

Autorzy: 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
Opublikowane w: Genome Biology, Numer 14/10, 2013, Strona(/y) R120, ISSN 1465-6906
Wydawca: 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

Autorzy: 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
Opublikowane w: Human Molecular Genetics, Numer 22/7, 2013, Strona(/y) 1465-1472, ISSN 0964-6906
Wydawca: 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

Autorzy: 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
Opublikowane w: Nature Genetics, Numer 46/3, 2014, Strona(/y) 234-244, ISSN 1061-4036
Wydawca: Nature Publishing Group
DOI: 10.1038/ng.2897

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

Autorzy: 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
Opublikowane w: Human Molecular Genetics, Numer 23/9, 2014, Strona(/y) 2490-2497, ISSN 0964-6906
Wydawca: Oxford University Press
DOI: 10.1093/hmg/ddt620

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

Autorzy: Mirjam Lukasse, Anne-Mette Schroll, Helle Karro, Berit Schei, Thora Steingrimsdottir, An-Sofie Van Parys, Elsa Lena Ryding, Ann Tabor
Opublikowane w: Acta Obstetricia et Gynecologica Scandinavica, Numer 94/5, 2015, Strona(/y) 508-517, ISSN 0001-6349
Wydawca: Wiley-Blackwell
DOI: 10.1111/aogs.12593

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

Autorzy: 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
Opublikowane w: PLoS ONE, Numer 9/11, 2014, Strona(/y) e112630, ISSN 1932-6203
Wydawca: Public Library of Science
DOI: 10.1371/journal.pone.0112630

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

Autorzy: Tove Fall, Weijia Xie, Wenny Poon, Hanieh Yaghootkar, Reedik Mägi, Joshua W. Knowles, Valeriya Lyssenko, Michael Weedon, Timothy M. Frayling, Erik Ingelsson
Opublikowane w: Diabetes, Numer 64/7, 2015, Strona(/y) 2676-2684, ISSN 0012-1797
Wydawca: American Diabetes Association
DOI: 10.2337/db14-1710

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

Autorzy: Kaarel Krjutškov, Marina Koltšina, Kelli Grand, Urmo Võsa, Martin Sauk, Neeme Tõnisson, Andres Salumets
Opublikowane w: Current Genetics, Numer 60/1, 2014, Strona(/y) 11-16, ISSN 0172-8083
Wydawca: 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

Autorzy: Mari-Anne Vals, Tiina Kahre, Pille Mee, Kai Muru, Eha Kallas, Olga �ilina, Vallo Tillmann, Katrin �unap
Opublikowane w: Molecular Syndromology, Numer 6/3, 2015, Strona(/y) 147-151, ISSN 1661-8769
Wydawca: S. Karger AG
DOI: 10.1159/000437061

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

Autorzy: Tiina Drell, Triin Lillsaar, Lea Tummeleht, Jaak Simm, Anu Aaspõllu, Edda Väin, Ivo Saarma, Andres Salumets, Gilbert G. G. Donders, Madis Metsis
Opublikowane w: PLoS ONE, Numer 8/1, 2013, Strona(/y) e54379, ISSN 1932-6203
Wydawca: Public Library of Science
DOI: 10.1371/journal.pone.0054379

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

Autorzy: Merly Saare, Sirje Lulla, Tambet Tõnissoo, Riho Meier, Keiu Kask, Katrin Ruisu, Alar Karis, Andres Salumets, Margus Pooga
Opublikowane w: PLOS ONE, Numer 10/6, 2015, Strona(/y) e0129131, ISSN 1932-6203
Wydawca: 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

Autorzy: 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
Opublikowane w: Reproductive BioMedicine Online, Numer 31/1, 2015, Strona(/y) 108-119, ISSN 1472-6483
Wydawca: Reproductive Healthcare Ltd
DOI: 10.1016/j.rbmo.2015.03.004

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

Autorzy: 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
Opublikowane w: International Journal of Epidemiology, Numer 44/4, 2015, Strona(/y) 1137-1147, ISSN 0300-5771
Wydawca: Oxford University Press
DOI: 10.1093/ije/dyt268

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

Autorzy: K. Haller-Kikkatalo, R. Uibo, A. Kurg, A. Salumets
Opublikowane w: Human Reproduction, Numer 30/5, 2015, Strona(/y) 1229-1238, ISSN 0268-1161
Wydawca: Oxford University Press
DOI: 10.1093/humrep/dev021

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

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

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Comparison of serum exosome isolation methods for microRNA profiling

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

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

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

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

Autorzy: Kadri Haller-Kikkatalo, Aili Tagoma, Raivo Uibo, Andres Salumets, Signe Altmäe
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Fear of Childbirth and Risk of Cesarean Delivery: A Cohort Study in Six European Countries

Autorzy: Elsa Lena Ryding, Mirjam Lukasse, An-Sophie Van Parys, Anne-Marie Wangel, Helle Karro, Hildur Kristjansdottir, Anne-Mette Schroll, Berit Schei
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New genetic loci link adipose and insulin biology to body fat distribution

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

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

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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

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

Autorzy: 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
Opublikowane w: Scientific Reports, Numer 8/1, 2018, ISSN 2045-2322
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Variability of genome-wide DNA methylation and mRNA expression profiles in reproductive and endocrine disease related tissues

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

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

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

Autorzy: Tiina Drell, Jelena Štšepetova, Jaak Simm, Kristiina Rull, Aira Aleksejeva, Anne Antson, Vallo Tillmann, Madis Metsis, Epp Sepp, Andres Salumets, Reet Mändar
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Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions

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

Autorzy: Kadri Rekker, Signe Altmäe, Marina Suhorutshenko, Maire Peters, Juan F. Martinez-Blanch, Francisco M. Codoñer, Felipe Vilella, Carlos Simón, Andres Salumets, Agne Velthut-Meikas
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Differentially-Expressed miRNAs in Ectopic Stromal Cells Contribute to Endometriosis Development: The Plausible Role of miR-139-5p and miR-375

Autorzy: Kadri Rekker, Tõnis Tasa, Merli Saare, Külli Samuel, Ülle Kadastik, Helle Karro, Martin Götte, Andres Salumets, Maire Peters
Opublikowane w: International Journal of Molecular Sciences, Numer 19/12, 2018, Strona(/y) 3789, ISSN 1422-0067
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Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria

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

Autorzy: 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
Opublikowane w: Human Molecular Genetics, 2018, ISSN 0964-6906
Wydawca: Oxford University Press
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GWAS Identifies Risk Locus for Erectile Dysfunction and Implicates Hypothalamic Neurobiology and Diabetes in Etiology

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

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Endometrial receptivity revisited: endometrial transcriptome adjusted for tissue cellular heterogeneity

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

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Opublikowane w: Fertility and Sterility, Numer 109/6, 2018, Strona(/y) 1127-1134.e1, ISSN 0015-0282
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Aberrant expression of genes associated with stemness and cancer in endometria and endometrioma in a subset of women with endometriosis

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

Autorzy: 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
Opublikowane w: Clinical and Experimental Reproductive Medicine, Numer 45/3, 2018, Strona(/y) 129, ISSN 2233-8233
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DNA methylation alterations—potential cause of endometriosis pathogenesis or a reflection of tissue heterogeneity?†

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

Autorzy: Olga Tšuiko, Tatjana Jatsenko, Lalit Kumar Parameswaran Grace, Ants Kurg, Joris Robert Vermeesch, Fredrik Lanner, Signe Altmäe, Andres Salumets
Opublikowane w: Developmental Biology, 2018, ISSN 0012-1606
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Principles guiding embryo selection following genome-wide haplotyping of preimplantation embryos

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

Autorzy: 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
Opublikowane w: Human Reproduction, Numer 32/11, 2017, Strona(/y) 2348-2357, ISSN 0268-1161
Wydawca: Oxford University Press
DOI: 10.1093/humrep/dex286

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

Autorzy: Merli Saare, Kadri Rekker, Triin Laisk-Podar, Nilufer Rahmioglu, Krina Zondervan, Andres Salumets, Martin Götte, Maire Peters
Opublikowane w: Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, Numer 1863/9, 2017, Strona(/y) 2282-2292, ISSN 0925-4439
Wydawca: Elsevier BV
DOI: 10.1016/j.bbadis.2017.06.018

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

Autorzy: Kadri Rekker, Merli Saare, Elo Eriste, Tõnis Tasa, Viktorija Kukuškina, Anne Mari Roost, Kristi Anderson, Külli Samuel, Helle Karro, Andres Salumets, Maire Peters
Opublikowane w: Reproduction, Numer 154/1, 2017, Strona(/y) 93-100, ISSN 1470-1626
Wydawca: Society for Reproduction and Fertility
DOI: 10.1530/rep-17-0092

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

Autorzy: 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
Opublikowane w: npj Genomic Medicine, Numer 3/1, 2018, ISSN 2056-7944
Wydawca: 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

Autorzy: 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
Opublikowane w: Human Reproduction, Numer 31/8, 2016, Strona(/y) 1913-1925, ISSN 0268-1161
Wydawca: Oxford University Press
DOI: 10.1093/humrep/dew142

Ovarian Physiology and GWAS: Biobanks, Biology, and Beyond

Autorzy: Triin Laisk-Podar, Cecilia M. Lindgren, Maire Peters, Juha S. Tapanainen, Cornelis B. Lambalk, Andres Salumets, Reedik Mägi
Opublikowane w: Trends in Endocrinology & Metabolism, Numer 27/7, 2016, Strona(/y) 516-528, ISSN 1043-2760
Wydawca: Elsevier BV
DOI: 10.1016/j.tem.2016.04.011

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

Autorzy: Natalia Pervjakova, Silva Kasela, Andrew P Morris, Mart Kals, Andres Metspalu, Cecilia M Lindgren, Andres Salumets, Reedik Mägi
Opublikowane w: Epigenomics, Numer 8/6, 2016, Strona(/y) 789-799, ISSN 1750-1911
Wydawca: Future Medicine Ltd.
DOI: 10.2217/epi.16.8

The influence of menstrual cycle and endometriosis on endometrial methylome

Autorzy: 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
Opublikowane w: Clinical Epigenetics, Numer 8/1, 2016, ISSN 1868-7075
Wydawca: Springer Verlag
DOI: 10.1186/s13148-015-0168-z

C14orf132 gene is possibly related to extremely low birth weight

Autorzy: Airi Tiirats, Triin Viltrop, Margit Nõukas, Ene Reimann, Andres Salumets, Sulev Kõks
Opublikowane w: BMC Genetics, Numer 17/1, 2016, ISSN 1471-2156
Wydawca: 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

Autorzy: Nageswara Rao Boggavarapu, Sujata Lalitkumar, Vijay Joshua, Sergo Kasvandik, Andres Salumets, Parameswaran Grace Lalitkumar, Kristina Gemzell-Danielsson
Opublikowane w: Scientific Reports, Numer 6/1, 2016, ISSN 2045-2322
Wydawca: Nature Publishing Group
DOI: 10.1038/srep33811

Globin mRNA reduction for whole-blood transcriptome sequencing

Autorzy: 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
Opublikowane w: Scientific Reports, Numer 6/1, 2016, ISSN 2045-2322
Wydawca: Nature Publishing Group
DOI: 10.1038/srep31584

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

Autorzy: Lusine Aghajanova, Signe Altmäe, Sergo Kasvandik, Andres Salumets, Anneli Stavreus-Evers, Linda C. Giudice
Opublikowane w: Fertility and Sterility, Numer 106/3, 2016, Strona(/y) 681-691.e1, ISSN 0015-0282
Wydawca: Elsevier BV
DOI: 10.1016/j.fertnstert.2016.05.023

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

Autorzy: Gerly Sillaste, Lauris Kaplinski, Riho Meier, Ülle Jaakma, Elo Eriste, Andres Salumets
Opublikowane w: Reproduction, Numer 153/3, 2016, Strona(/y) 241-251, ISSN 1470-1626
Wydawca: 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

Autorzy: Olga Mazina, Anni Allikalt, Juha S. Tapanainen, Andres Salumets, Ago Rinken
Opublikowane w: Scientific Reports, Numer 7, 2017, Strona(/y) 42219, ISSN 2045-2322
Wydawca: Nature Publishing Group
DOI: 10.1038/srep42219

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

Autorzy: Kadri Haller-Kikkatalo, Kristi Alnek, Andres Metspalu, Evelin Mihailov, Kaja Metsküla, Kalle Kisand, Heti Pisarev, Andres Salumets, Raivo Uibo
Opublikowane w: Scientific Reports, Numer 7, 2017, Strona(/y) 44846, ISSN 2045-2322
Wydawca: Nature Publishing Group
DOI: 10.1038/srep44846

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

Autorzy: 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
Opublikowane w: Gene, Numer 03781119, 2015, Strona(/y) 144-148, ISSN 0378-1119
Wydawca: 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

Autorzy: Kadri Õunap, Ly Käsper, Ants Kurg, Reet Kurg
Opublikowane w: PLoS ONE, Numer 19326203, 2013, Strona(/y) e75686, ISSN 1932-6203
Wydawca: Public Library of Science
DOI: 10.1371/journal.pone.0075686

Monozygotic Twins with 17q21.31 Microdeletion Syndrome

Autorzy: Marketa Vlckova, Miroslava Hancarova, Jana Drabova, Zuzana Slamova, Monika Koudova, Renata Alanova, Katrin Mannik, Ants Kurg, Zdenek Sedlacek
Opublikowane w: Twin Research and Human Genetics, Numer 18324274, 2014, Strona(/y) 405-410, ISSN 1832-4274
Wydawca: 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

Autorzy: K. Haller-Kikkatalo, R. Uibo, A. Kurg, A. Salumets
Opublikowane w: Human Reproduction, Numer 02681161, 2015, Strona(/y) 1229-1238, ISSN 0268-1161
Wydawca: Oxford University Press
DOI: 10.1093/humrep/dev021

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

Autorzy: 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
Opublikowane w: Genome Biology, Numer 14656906, 2013, Strona(/y) R120, ISSN 1465-6906
Wydawca: 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

Autorzy: Olga Žilina, Marina Koltšina, Raivo Raid, Ants Kurg, Neeme Tõnisson, Andres Salumets
Opublikowane w: BMC Genomics, Numer 14712164, 2015, ISSN 1471-2164
Wydawca: BioMed Central
DOI: 10.1186/s12864-015-1916-3

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

Autorzy: Olga Žilina, Rita Teek, Pille Tammur, Kati Kuuse, Maria Yakoreva, Eve Vaidla, Triin Mölter-Väär, Tiia Reimand, Ants Kurg, Katrin Õunap
Opublikowane w: Molecular Genetics & Genomic Medicine, Numer 23249269, 2014, Strona(/y) 166-175, ISSN 2324-9269
Wydawca: 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

Autorzy: Miroslava Hancarova, Martina Simandlova, Jana Drabova, Katrin Mannik, Ants Kurg, Zdenek Sedlacek
Opublikowane w: American Journal of Medical Genetics Part A, Numer 15524825, 2013, Strona(/y) 865-870, ISSN 1552-4825
Wydawca: 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

Autorzy: Olga Žilina, Tiia Reimand, Pille Tammur, Vallo Tillmann, Ants Kurg, Katrin Õunap
Opublikowane w: European Journal of Medical Genetics, Numer 17697212, 2013, Strona(/y) 202-206, ISSN 1769-7212
Wydawca: 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

Autorzy: Kadri Rekker, Merli Saare, Anne Mari Roost, Tanel Kaart, Deniss Sõritsa, Helle Karro, Andrei Sõritsa, Carlos Simón, Andres Salumets, Maire Peters
Opublikowane w: Fertility and Sterility, Numer 00150282, 2015, Strona(/y) 938-946.e2, ISSN 0015-0282
Wydawca: 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

Autorzy: Triin Laisk-Podar, Tanel Kaart, Maire Peters, Andres Salumets
Opublikowane w: Reproductive BioMedicine Online, Numer 14726483, 2015, Strona(/y) 199-209, ISSN 1472-6483
Wydawca: 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

Autorzy: Merly Saare, Sirje Lulla, Tambet Tõnissoo, Riho Meier, Keiu Kask, Katrin Ruisu, Alar Karis, Andres Salumets, Margus Pooga
Opublikowane w: PLOS ONE, Numer 19326203, 2015, Strona(/y) e0129131, ISSN 1932-6203
Wydawca: 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

Autorzy: 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
Opublikowane w: Reproductive BioMedicine Online, Numer 14726483, 2015, Strona(/y) 108-119, ISSN 1472-6483
Wydawca: Reproductive Healthcare Ltd
DOI: 10.1016/j.rbmo.2015.03.004

Complementary seminovaginal microbiome in couples

Autorzy: 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
Opublikowane w: Research in Microbiology, Numer 09232508, 2015, Strona(/y) 440-447, ISSN 0923-2508
Wydawca: Elsevier BV
DOI: 10.1016/j.resmic.2015.03.009

Systemic oxidative stress could predict assisted reproductive technique outcome

Autorzy: A. Ahelik, R. Mändar, P. Korrovits, P. Karits, E. Talving, K. Rosenstein, M. Jaagura, A. Salumets, T. Kullisaar
Opublikowane w: Journal of Assisted Reproduction and Genetics, Numer 10580468, 2015, Strona(/y) 699-704, ISSN 1058-0468
Wydawca: Kluwer Academic/Plenum Publishers
DOI: 10.1007/s10815-015-0466-6

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

Autorzy: 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
Opublikowane w: Nature, Numer 00280836, 2015, Strona(/y) 197-206, ISSN 0028-0836
Wydawca: Nature Publishing Group
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New genetic loci link adipose and insulin biology to body fat distribution

Autorzy: 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
Opublikowane w: Nature, Numer 00280836, 2015, Strona(/y) 187-196, ISSN 0028-0836
Wydawca: Nature Publishing Group
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Bovine sperm plasma membrane proteomics through biotinylation and subcellular enrichment

Autorzy: Sergo Kasvandik, Gerly Sillaste, Agne Velthut-Meikas, Aavo-Valdur Mikelsaar, Triin Hallap, Peeter Padrik, Tanel Tenson, Ülle Jaakma, Sulev Kõks, Andres Salumets
Opublikowane w: PROTEOMICS, Numer 16159853, 2015, Strona(/y) 1906-1920, ISSN 1615-9853
Wydawca: John Wiley & Sons Ltd.
DOI: 10.1002/pmic.201400297

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

Autorzy: 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
Opublikowane w: Epigenetics, Numer 15592294, 2014, Strona(/y) 1397-1409, ISSN 1559-2294
Wydawca: Landes Bioscience
DOI: 10.4161/15592294.2014.970052

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

Autorzy: 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
Opublikowane w: PLoS ONE, Numer 19326203, 2014, Strona(/y) e112630, ISSN 1932-6203
Wydawca: 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

Autorzy: Deniss Sõritsa, Merli Saare, Triin Laisk-Podar, Maire Peters, Andrei Sõritsa, Kadri Matt, Helle Karro, Andres Salumets
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Wydawca: S. Karger AG
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Folic acid supplementation and methylenetetrahydrofolate reductase (MTHFR) gene variations in relation to in vitro fertilization pregnancy outcome

Autorzy: Tiina Murto, Theodora K. Kallak, Annica Hoas, Signe Altmäe, Andres Salumets, Torbjörn K. Nilsson, Agneta Skoog Svanberg, Kjell Wånggren, Agneta Yngve, Anneli Stavreus-Evers
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Wydawca: Wiley-Blackwell
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Autoimmune Activation toward Embryo Implantation is Rare in Immune-Privileged Human Endometrium

Autorzy: Kadri Haller-Kikkatalo, Aili Tagoma, Raivo Uibo, Andres Salumets, Signe Altmäe
Opublikowane w: Seminars in Reproductive Medicine, Numer 15268004, 2014, Strona(/y) 376-384, ISSN 1526-8004
Wydawca: Thieme Medical Publishers
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Sequencing and annotated analysis of full genome of Holstein breed bull

Autorzy: Sulev Kõks, Ene Reimann, Rutt Lilleoja, Freddy Lättekivi, Andres Salumets, Paula Reemann, Ülle Jaakma
Opublikowane w: Mammalian Genome, Numer 09388990, 2014, Strona(/y) 363-373, ISSN 0938-8990
Wydawca: Springer Verlag
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Folic acid supplementation and IVF pregnancy outcome in women with unexplained infertility

Autorzy: T. Murto, A. Skoog Svanberg, A. Yngve, T.K. Nilsson, S. Altmäe, K. Wånggren, A. Salumets, A. Stavreus-Evers
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Wydawca: Reproductive Healthcare Ltd
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DNA mismatch repair gene MSH6 implicated in determining age at natural menopause

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Circulating microRNA Profile throughout the Menstrual Cycle

Autorzy: Kadri Rekker, Merli Saare, Anne Mari Roost, Andres Salumets, Maire Peters
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Comparison of serum exosome isolation methods for microRNA profiling

Autorzy: Kadri Rekker, Merli Saare, Anne Mari Roost, Anna-Liisa Kubo, Natasa Zarovni, Antonio Chiesi, Andres Salumets, Maire Peters
Opublikowane w: Clinical Biochemistry, Numer 00099120, 2014, Strona(/y) 135-138, ISSN 0009-9120
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Guidelines for the design, analysis and interpretation of 'omics' data: focus on human endometrium

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Wydawca: Oxford University Press
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Sequencing and annotated analysis of the Holstein cow genome

Autorzy: Sulev Kõks, Rutt Lilleoja, Ene Reimann, Andres Salumets, Paula Reemann, Ülle Jaakma
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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

Autorzy: Karin Tamm-Rosenstein, Jaak Simm, Marina Suhorutshenko, Andres Salumets, Madis Metsis
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Wydawca: Public Library of Science
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Tissue-specific mitochondrial heteroplasmy at position 16,093 within the same individual

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

Autorzy: Agne Velthut-Meikas, Jaak Simm, Timo Tuuri, Juha S. Tapanainen, Madis Metsis, Andres Salumets
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Wydawca: The Endocrine Society
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Elevated blood plasma antioxidant status is favourable for achieving IVF/ICSI pregnancy

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Wydawca: Reproductive Healthcare Ltd
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Characterization of the Vaginal Micro- and Mycobiome in Asymptomatic Reproductive-Age Estonian Women

Autorzy: Tiina Drell, Triin Lillsaar, Lea Tummeleht, Jaak Simm, Anu Aaspõllu, Edda Väin, Ivo Saarma, Andres Salumets, Gilbert G. G. Donders, Madis Metsis
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Wydawca: Public Library of Science
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A genome-wide association study of early menopause and the combined impact of identified variants

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

Autorzy: S. Altmae, J. A. Martinez-Conejero, F. J. Esteban, M. Ruiz-Alonso, A. Stavreus-Evers, J. A. Horcajadas, A. Salumets
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Corrigendum: Rare coding variants and X-linked loci associated with age at menarche

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

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

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

Autorzy: Tove Fall, Weijia Xie, Wenny Poon, Hanieh Yaghootkar, Reedik Mägi, Joshua W. Knowles, Valeriya Lyssenko, Michael Weedon, Timothy M. Frayling, Erik Ingelsson
Opublikowane w: Diabetes, Numer 00121797, 2015, Strona(/y) 2676-2684, ISSN 0012-1797
Wydawca: American Diabetes Association
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Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

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

Autorzy: 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
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Wydawca: Oxford University Press
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Autorzy: Eve Õiglane-Shlik, Sanna Puusepp, Inga Talvik, Ulvi Vaher, Reet Rein, Pille Tammur, Tiia Reimand, Rita Teek, Olga Žilina, Tiiu Tomberg, Katrin Õunap
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Wydawca: W. B. Saunders Co., Ltd.
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Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

Autorzy: 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
Opublikowane w: Nature Genetics, Numer 47/12, 2015, Strona(/y) 1415-1425, ISSN 1061-4036
Wydawca: Nature Publishing Group
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Corrigendum: Rare coding variants and X-linked loci associated with age at menarche

Autorzy: 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
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Wydawca: Nature Publishing Group
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Sequencing and annotated analysis of the Holstein cow genome

Autorzy: Sulev Kõks, Rutt Lilleoja, Ene Reimann, Andres Salumets, Paula Reemann, Ülle Jaakma
Opublikowane w: Mammalian Genome, Numer 24/7-8, 2013, Strona(/y) 309-321, ISSN 0938-8990
Wydawca: Springer Verlag
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Sequencing and annotated analysis of full genome of Holstein breed bull

Autorzy: Sulev Kõks, Ene Reimann, Rutt Lilleoja, Freddy Lättekivi, Andres Salumets, Paula Reemann, Ülle Jaakma
Opublikowane w: Mammalian Genome, Numer 25/7-8, 2014, Strona(/y) 363-373, ISSN 0938-8990
Wydawca: Springer Verlag
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Increased Blood Levels of Growth Factors, Proinflammatory Cytokines, and Th17 Cytokines in Patients with Newly Diagnosed Type 1 Diabetes

Autorzy: Kristi Alnek, Kalle Kisand, Kaire Heilman, Aleksandr Peet, Karin Varik, Raivo Uibo
Opublikowane w: PLOS ONE, Numer 10/12, 2015, Strona(/y) e0142976, ISSN 1932-6203
Wydawca: Public Library of Science
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MicroRNAs miR-30b, miR-30d, and miR-494 Regulate Human Endometrial Receptivity

Autorzy: S. Altmae, J. A. Martinez-Conejero, F. J. Esteban, M. Ruiz-Alonso, A. Stavreus-Evers, J. A. Horcajadas, A. Salumets
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Wydawca: SAGE Publications
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Circulating microRNA Profile throughout the Menstrual Cycle

Autorzy: Kadri Rekker, Merli Saare, Anne Mari Roost, Andres Salumets, Maire Peters
Opublikowane w: PLoS ONE, Numer 8/11, 2013, Strona(/y) e81166, ISSN 1932-6203
Wydawca: Public Library of Science
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Chromosomal microarray analysis as a first-tier clinical diagnostic test: Estonian experience

Autorzy: Olga Žilina, Rita Teek, Pille Tammur, Kati Kuuse, Maria Yakoreva, Eve Vaidla, Triin Mölter-Väär, Tiia Reimand, Ants Kurg, Katrin Õunap
Opublikowane w: Molecular Genetics & Genomic Medicine, Numer 2/2, 2014, Strona(/y) 166-175, ISSN 2324-9269
Wydawca: Blackwell Publishing
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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

Autorzy: Karin Tamm-Rosenstein, Jaak Simm, Marina Suhorutshenko, Andres Salumets, Madis Metsis
Opublikowane w: PLoS ONE, Numer 8/7, 2013, Strona(/y) e68907, ISSN 1932-6203
Wydawca: Public Library of Science
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Systemic oxidative stress could predict assisted reproductive technique outcome

Autorzy: A. Ahelik, R. Mändar, P. Korrovits, P. Karits, E. Talving, K. Rosenstein, M. Jaagura, A. Salumets, T. Kullisaar
Opublikowane w: Journal of Assisted Reproduction and Genetics, Numer 32/5, 2015, Strona(/y) 699-704, ISSN 1058-0468
Wydawca: Kluwer Academic/Plenum Publishers
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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

Autorzy: Miroslava Hancarova, Martina Simandlova, Jana Drabova, Katrin Mannik, Ants Kurg, Zdenek Sedlacek
Opublikowane w: American Journal of Medical Genetics Part A, Numer 161/4, 2013, Strona(/y) 865-870, ISSN 1552-4825
Wydawca: Wiley-Liss Inc
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Bovine sperm plasma membrane proteomics through biotinylation and subcellular enrichment

Autorzy: Sergo Kasvandik, Gerly Sillaste, Agne Velthut-Meikas, Aavo-Valdur Mikelsaar, Triin Hallap, Peeter Padrik, Tanel Tenson, Ülle Jaakma, Sulev Kõks, Andres Salumets
Opublikowane w: PROTEOMICS, Numer 15/11, 2015, Strona(/y) 1906-1920, ISSN 1615-9853
Wydawca: John Wiley & Sons Ltd.
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GADA and anti-ZnT8 complicate the outcome of phenotypic type 2 diabetes of adults

Autorzy: Kadri Haller-Kikkatalo, Katrin Pruul, Kalle Kisand, Virge Nemvalts, Koit Reimand, Raivo Uibo
Opublikowane w: European Journal of Clinical Investigation, Numer 45/3, 2015, Strona(/y) 255-262, ISSN 0014-2972
Wydawca: Blackwell Publishing Inc.
DOI: 10.1111/eci.12404

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

Autorzy: Made Laanpere, Inge Ringmets, Kai Part, Kärt Allvee, Piret Veerus, Helle Karro
Opublikowane w: BMC Women's Health, Numer 14/1, 2014, Strona(/y) 81, ISSN 1472-6874
Wydawca: BioMed Central
DOI: 10.1186/1472-6874-14-81

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

Autorzy: T. Murto, A. Skoog Svanberg, A. Yngve, T.K. Nilsson, S. Altmäe, K. Wånggren, A. Salumets, A. Stavreus-Evers
Opublikowane w: Reproductive BioMedicine Online, Numer 28/6, 2014, Strona(/y) 766-772, ISSN 1472-6483
Wydawca: Reproductive Healthcare Ltd
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Prevalence of emotional, physical and sexual abuse among pregnant women in six European countries

Autorzy: 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
Opublikowane w: Acta Obstetricia et Gynecologica Scandinavica, Numer 93/7, 2014, Strona(/y) 669-677, ISSN 0001-6349
Wydawca: Wiley-Blackwell
DOI: 10.1111/aogs.12392

Genomic imprinting in complex traits

Autorzy: Pervjakova, Natalja
Opublikowane w: 2018, ISBN 978-9949-77-735-8
Wydawca: University of Tartu Press

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

Autorzy: Tšuiko, Olga
Opublikowane w: 2018, ISBN 978-9949-77-862-1
Wydawca: University of Tartu Press

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