European Joint Programme on Rare Diseases

CORDIS fornisce collegamenti ai risultati finali pubblici e alle pubblicazioni dei progetti ORIZZONTE.

I link ai risultati e alle pubblicazioni dei progetti del 7° PQ, così come i link ad alcuni tipi di risultati specifici come dataset e software, sono recuperati dinamicamente da .OpenAIRE .

Risultati finali

Fourth Public Call documents JTC2019-2022: call text, guidelines for applicants, proposal templates

Other lead beneficiaries ANR 11 FFRD 12 and ISCIII 44Public Call documents JTC20192022 call text guidelines for applicants proposal templates due at month 35

First Report on processed genome-phenome datasets and multi-omics use cases analysed, including description of new cloud and online analysis functionalities and tools

Other lead beneficiary UMCG (35) First Report on processed genome-phenome datasets and multi-omics use cases analysed, including description of new cloud and online analysis functionalities and tools due at month 12

Third Report on processed genome-phenome datasets and multi-omics use cases analysed, including description of new cloud and online analysis functionalities and tools

Other lead beneficiary UMCG 35Third Report on processed genomephenome datasets and multiomics use cases analysed including description of new cloud and online analysis functionalities and tools due at month 36

First Report on course on interpretation of genetic variants and quality standards

First Report on course on interpretation of genetic variants and quality standards due at month 12

Fourth Analysis of national state of play and alignment process with EJP RD

Other lead beneficiary MUW 38Analysis of national state of play and alignment process with EJP RD due at month 55

Second Public Call documents JTC2019-2022: call text, guidelines for applicants, proposal templates

Other lead beneficiaries: ANR (11), FFRD (12) and ISCIII (44) Public Call documents JTC2019-2022: call text, guidelines for applicants, proposal templates due at month 11

First Report on ExPRESS

First Report on ExPRESS EURORDIS Summer School due at month 12

Fifth report from the face-to-face ExCom and Policy Board meeting

Report from the facetoface ExCom and Policy Board meeting due at month 55

Fifth Report on processed genome-phenome datasets and multi-omics use cases analysed, including description of new cloud and online analysis functionalities and tools

Other lead beneficiary: UMCG (35)Fifth Report on processed genome-phenome datasets and multi-omics use cases analysed, including description of new cloud and online analysis functionalities and tools due at month 60

Fifth List of research and innovation needs requiring medium- or long-term approach and related Task Forces

List of research and innovation needs requiring medium- or long-term approach and related Task Forces due at month 54

Public Call document for Networking scheme

Other lead beneficiary: CSO/MOH (78) Public Call document for Networking scheme

First Report on International course on undiagnosed diseases

First Report on International course on undiagnosed diseases due at month 24

Final list of prioritization criteria

Other lead beneficiary FTELE 25Final list of prioritization criteria

Second List of research and innovation needs requiring medium- or long-term approach and related Task Forces

List of research and innovation needs requiring medium- or long-term approach and related Task Forces due at month 18

Second Report on processed genome-phenome datasets and multi-omics use cases analysed, including description of new cloud and online analysis functionalities and tools

Other lead beneficiary UMCG (35) Second Report on processed genome-phenome datasets and multi-omics use cases analysed, including description of new cloud and online analysis functionalities and tools due at month 24

Third report from the face-to-face ExCom and Policy Board meeting

Report from the face-to-face ExCom and Policy Board meeting due at Month 31

Second List of funded networks in Networking scheme

List of funded networks in Networking scheme due at month 54

Final report on evaluation and adaptation of training programmes according to EJP RD progress of work, specific needs of EU13 countries and ERN developing needs

Other lead beneficiaries: EURORDIS (77), IPCZD (40) and EKUT (58)Final report on evaluation and adaptation of training programmes according to EJP RD progress of work, specific needs of EU13 countries and ERN developing needs

Fourth Annual strategic report and Action plan for Pillar 2, including: Systematic surveys reports, QMS of Pillar 2 description, GDPR compliance report and sustainability planning reporting

Annual strategic report and Action plan for Pillar 2 including Systematic surveys reports QMS of Pillar 2 description GDPR compliance report and sustainability planning reporting update at month 45

Second Report on training of patient representatives on scientific innovation and translational research in RD

Second Report on training of patient representatives on scientific innovation and translational research in RD due at month 60

Second Report on ExPRESS

Second Report on ExPRESS EURORDIS Summer School due at month 60

Collection of 20 curated (sub)Portal on WikiPathways

Collection of 20 curated subPortal on WikiPathways

Third List of research and innovation needs requiring medium- or long-term approach and related Task Forces

List of research and innovation needs requiring medium or longterm approach and related Task Forces due at month 30

Report on core set of unified FAIR data standards
Report from the Kick-off meeting
Dynamic catalogue of EJP-RD sustainable resources including Service Roadmap Database

Dynamic catalogue of EJPRD sustainable resources including Service Roadmap Database Lead beneficiary INSERM RADICO

First RE(ACT) Congress report

First RE(ACT) Congress report due at M16

Second Annual reports on implementation of training programs

Second Annual reports on implementation of training programs due at month 60

Second Report on International course on undiagnosed diseases

Second Report on International course on undiagnosed diseases due at month 60

List of first phase projects financed
First List of research and innovation needs requiring medium- or long-term approach and related Task Forces

List of research and innovation needs requiring medium or longterm approach and related Task Forces due at month 6

Fourth Scoping paper

Other lead beneficiaries ISCIII 44 and INSERM 1Scoping paper due at month 43

Draft content of the online academic course
Set of template agreements for EJP RD website
Second Report on EURORDIS' Leadership Programme

Second Report on EURORDIS’ Leadership Programme due at month 48

Final Report of funded new methodology projects

Other lead beneficiaries: AP-HP (54), CCRI (10) and UUH (89)Final Report of funded new methodology projects

Third Analysis of national state of play and alignment process with EJP RD

Other lead beneficiary MUW 38Analysis of national state of play and alignment process with EJP RD due at month 32

Third Public Call documents JTC2019-2022: call text, guidelines for applicants, proposal templates

Other lead beneficiaries: ANR (11), FFRD (12) and ISCIII (44) Public Call documents JTC2019-2022: call text, guidelines for applicants, proposal templates due at mont 23

Training plan for paediatric patients' in the EJP

Other beneficiary FSJDTraining plan for paediatric patients in the EJP

First Report on sample data management training workshops

First Report on sample data management training workshops due at month 12

EJP RD ERN training programmes
First Public Call documents JTC2019-2022: call text, guidelines for applicants, proposal templates

Other lead beneficiaries: ANR (11), FFRD (12) and ISCIII (44) Public Call documents JTC2019-2022: call text, guidelines for applicants, proposal templates due at month 1

Call documents for validation
Second Analysis of national state of play and alignment process with EJP RD

Other lead beneficiary MUW (38) Analysis of national state of play and alignment process with EJP RD due at month 21

First Scoping paper

Other lead beneficiaries: ISCIII (44) and INSERM (1) Scoping paper due at Month 7

Fourth Report on processed genome-phenome datasets and multi-omics use cases analysed, including description of new cloud and online analysis functionalities and tools

Other lead beneficiary UMCG 35Fourth Report on processed genomephenome datasets and multiomics use cases analysed including description of new cloud and online analysis functionalities and tools due at month 48

Second Annual strategic report and Action plan for Pillar 2, including: Systematic surveys reports, QMS of Pillar 2 description, GDPR compliance report and sustainability planning reporting

Annual strategic report and Action plan for Pillar 2, including: Systematic surveys reports, QMS of Pillar 2 description, GDPR compliance report and sustainability planning reporting update at month 21

Completed pathway analysis workflow (data analysis including both types of genetic variant linking and network creation)

Completed pathway analysis workflow data analysis including both types of genetic variant linking and network creation

Fourth report from the face-to-face ExCom and Policy Board meeting

Report from the facetoface ExCom and Policy Board meeting due at Month 43

Results of survey on preferences, needs and resources from the ERNs ecosystem
Report on paediatric patients' experts training courses

Other beneficiary: FSJDReport on paediatric patients’ experts training courses

First Report on core set of FAIR software tools and on extended set of unified FAIR data standards, applied in EJP RD

First Report on core set of FAIR software tools and on extended set of unified FAIR data standards applied in EJP RD due at month 30

Second Report on sample data management training workshops

Second Report on sample data management training workshops due at month 60

First Report of Orphanet nomenclature training for trainers and national trainings

First Report of Orphanet nomenclature training for trainers and national trainings due at month 14

Summary Report of Task Force Group

Other lead beneficiary: AP-HP (54)Summary Report of the Task Force Group

First Report from strategic workshop with national policy makers

Other lead beneficiary MUW 38Report from strategic workshop with national policy makers due at month 34

Third Annual strategic report and Action plan for Pillar 2, including: Systematic surveys reports, QMS of Pillar 2 description, GDPR compliance report and sustainability planning reporting

Annual strategic report and Action plan for Pillar 2 including Systematic surveys reports QMS of Pillar 2 description GDPR compliance report and sustainability planning reporting update at month 33

Prioritization scheme including decision-making process

Other lead beneficiary FTELE 25Prioritization scheme including decisionmaking process

Second RE(ACT) Congress report

Second REACT Congress report due at Month 30

Report on the State of the Art of existing resources
First List of funded networks in Networking scheme

List of funded networks in Networking scheme due at month 21

First Analysis of national state of play and alignment process with EJP RD

Other lead beneficiary MUW (38) Analysis of national state of play and alignment process with EJP RD due at Month 9

First Report on International course on Rare Disease Registries and FAIRification of data at source

First Report on International course on Rare Disease Registries and FAIRification of data at source due at month 12

Second Report of Orphanet nomenclature training for trainers and national trainings

Second Report of Orphanet nomenclature training for trainers and national trainings due at month 60

Fifth Scoping paper

Other lead beneficiaries ISCIII (44) and INSERM (1)Scoping paper due at month 55

Second Scoping paper

Other lead beneficiaries ISCIII (44) and INSERM (1) Scoping paper due at month 19

Second Report on course on interpretation of genetic variants and quality standards

Second Report on course on interpretation of genetic variants and quality standards due at month 60

Second Report on International course on Rare Disease Registries and FAIRification of data at source

Second Report on International course on Rare Disease Registries and FAIRification of data at source due at month 60

First Annual strategic report and Action plan for Pillar 2, including: Systematic surveys reports, QMS of Pillar 2 description, GDPR compliance report and sustainability planning reporting

Annual strategic report and Action plan for Pillar 2, including: Systematic surveys reports, QMS of Pillar 2 description, GDPR compliance report and sustainability planning reporting due at M9

First Annual report on implementation of training programs

First Annual reports on implementation of training programs due at month 13

Second Report from strategic workshop with national policy makers

Other lead beneficiary MUW 38Report from strategic workshop with national policy makers due at month 58

Second Report on core set of FAIR software tools and on extended set of unified FAIR data standards, applied in EJP RD

Second Report on core set of FAIR software tools and on extended set of unified FAIR data standards applied in EJP RD due at month 48

Third Scoping paper

Other lead beneficiaries ISCIII (44) and INSERM (1) Scoping paper due at month 31

Completed network analysis workflow (active node detection, lifestyle factor network evaluation and extended network analysis for drugs and toxic compounds)

Completed network analysis workflow active node detection lifestyle factor network evaluation and extended network analysis for drugs and toxic compounds

Fourth List of research and innovation needs requiring medium- or long-term approach and related Task Forces

List of research and innovation needs requiring medium or longterm approach and related Task Forces due at month 42

First report from the face-to-face ExCom and Policy Board meeting

Report from the face-to-face ExCom and Policy Board meeting due at M7

First Report on EURORDIS’ Leadership Programme

First Report on EURORDIS’ Leadership Programme due at month 12

Final Report of funded demonstration projects

Other lead beneficiaries: AP-HP (54), IOR (61) and ERN EpiCAREFinal Report of funded demonstration projects

First Report on training of patient representatives on scientific innovation and translational research in RD

First Report on training of patient representatives on scientific innovation and translational research in RD due at month 24

Report on extended set of FAIR software tools, applied in EJP,including overview of FAIRification guidelines for RD data managers

Other lead beneficiary: LUMC (64)Report on extended set of FAIR software tools, applied in EJP,including overview of FAIRification guidelines for RD data managers

Second report from the face-to-face ExCom and Policy Board meeting

Report from the face-to-face ExCom and Policy Board meeting due at M19

Third update Virtual platform of RD resources annotated with EJP ontological model

Third update of the Virtual platform of RD resources annotated with EJP ontological model due at month 48

Second update Virtual platform of RD resources annotated with EJP ontological model

Second update of the Virtual platform of RD resources annotated with EJP ontological model due at month 36

EJP RD website
EJP RD Newsletter
Virtual platform of RD resources annotated with EJP ontological model

First version of the Virtual platform of RD resources annotated with EJP ontological model due at month 12

Fourth update Virtual platform of RD resources annotated with EJP ontological model

Fourth update of the Virtual platform of RD resources annotated with EJP ontological model due at month 60

First update Virtual platform of RD resources annotated with EJP ontological model

First update of the Virtual platform of RD resources annotated with EJP ontological model due at month 24

Fourth version Additional facilities integrated to resources regarding data deposition and access, including user guidelines and documentation

Other lead beneficiary: ELIXIR (76)Fourth version of the Additional facilities integrated to resources regarding data deposition and access, including user guidelines and documentation due at month 48

First Ontological model of resources metadata

First Ontological model of resources metadata due at mont 12

First version of Additional facilities integrated to resources regarding data deposition and access, including user guidelines and documentation

Other lead beneficiary ELIXIR (76) First version of Additional facilities integrated to resources regarding data deposition and access, including user guidelines and documentation due at month 12

Fifth version Additional facilities integrated to resources regarding data deposition and access, including user guidelines and documentation

Other lead beneficiary: ELIXIR (76)Fifth version of the Additional facilities integrated to resources regarding data deposition and access, including user guidelines and documentation due at month 60

Third version Additional facilities integrated to resources regarding data deposition and access, including user guidelines and documentation

Other lead beneficiary ELIXIR 76Third version of Additional facilities integrated to resources regarding data deposition and access including user guidelines and documentation due at month 36

Content of the first 5 online modules
Content of the full online course
Fifth Ontological model of resources metadata

Fifth Ontological model of resources metadata due at month 60

Second version Additional facilities integrated to resources regarding data deposition and access, including user guidelines and documentation

Other lead beneficiary: ELIXIR (76) Second version of Additional facilities integrated to resources regarding data deposition and access, including user guidelines and documentation due at month 24

Fourth Ontological model of resources metadata

Fourth Ontological model of resources metadata due at month 48

Second Ontological model of resources metadata

Second Ontological model of resources metadata due at month 24

Third Ontological model of resources metadata

Third Ontological model of resources metadata due at month 36

Pubblicazioni

CHARON: An Imaging-Based Diagnostic Algorithm to Navigate Through the Sea of Hereditary Degenerative Ataxias

Autori: Alessandra Scaravilli, Mario Tranfa, Giuseppe Pontillo, Bernard Brais, Giovanna De Michele, Roberta La Piana, Francesco Saccà, Filippo Maria Santorelli, Matthis Synofzik, Arturo Brunetti, Sirio Cocozza
Pubblicato in: The Cerebellum, 2024, ISSN 1473-4230
Editore: Springer Nature
DOI: 10.1007/s12311-024-01677-y

Common conditions of use elements. Atomic concepts for consistent and effective information governance

Autori: Maria del Carmen Sanchez Gonzalez, Pim Kamerling, Mariapia Iermito, Sara Casati, Umar Riaz, Colin D. Veal, Monika Maini, Francis Jeanson, Oussama Mohammed Benhamed, Esther van Enckevort, Annalisa Landi, Yanis Mimouni, Clèmence Le Cornec, Domenico A. Coviello, Tiziana Franchin, Francesca Fusco, Jose Antonio Ramírez García, Loes F. M. van der Zanden, Alexander Bernier, Mark D. Wilkinson, Heimo Mu
Pubblicato in: Scientific Data, Numero 11, 2024, ISSN 2052-4463
Editore: Springer Nature
DOI: 10.1038/s41597-024-03279-z

A FAIR catalog of ontology-driven conceptual models

Autori: Tiago Prince Sales, Pedro Paulo F. Barcelos, Claudenir M. Fonseca, Isadora Valle Souza, Elena Romanenko, César Henrique Bernabé, Luiz Olavo Bonino da Silva Santos, Mattia Fumagalli, Joshua Kritz, João Paulo A. Almeida, Giancarlo Guizzardi
Pubblicato in: Data & Knowledge Engineering, Numero 147, 2023, Pagina/e 102210, ISSN 0169-023X
Editore: Elsevier BV
DOI: 10.1016/j.datak.2023.102210

Phenotypic features of RETREG1‐related hereditary sensory autonomic neuropathy

Autori: Arman Çakar; Gulandam Bagırova; Hacer Durmuş; Oya Uyguner; Yeşim Parman
Pubblicato in: Journal of the peripheral nervous system., 2023, ISSN 1529-8027
Editore: -
DOI: 10.1111/jns.12581

Variant recurrence confirms the existence of a FBXO31 ‐related spastic‐dystonic cerebral palsy syndrome

Autori: Ivana Dzinovic, Matej Škorvánek, Petra Pavelekova, Chen Zhao, Boris Keren, Sandra Whalen, Somayeh Bakhtiari, Sheng Chih Jin, Michael C. Kruer, Robert Jech, Juliane Winkelmann, Michael Zech
Pubblicato in: Annals of Clinical and Translational Neurology, 2021, ISSN 2328-9503
Editore: Wiley
DOI: 10.1002/acn3.51335

Consensus recommendations on mental health issues in Phelan-McDermid syndrome

Autori: Ingrid D.C. van Balkom, Monica Burdeus-Olavarrieta, Jennifer Cooke, A. Graciela de Cuba, Alison Turner, Annick Vogels, Anna Maruani
Pubblicato in: European Journal of Medical Genetics, Numero 66, 2024, Pagina/e 104770, ISSN 1769-7212
Editore: Elsevier BV
DOI: 10.1016/j.ejmg.2023.104770

Innovative methodologies for rare diseases clinical trials

Autori: Rima Nabbout, Ralf-Dieter Hilgers
Pubblicato in: Orphanet Journal of Rare Diseases, Numero 19, 2024, ISSN 1750-1172
Editore: BioMed Central
DOI: 10.1186/s13023-024-03189-8

Generation of an induced pluripotent stem cell line carrying biallelic deletions (SCTCi019-B) in ALDH7A1 using CRISPR/Cas9

Autori: Imke M.E. Schuurmans, Ka M. Wu, Clara D.M. van Karnebeek, Nael Nadif Kasri, Alejandro Garanto
Pubblicato in: Stem Cell Research, Numero 71, 2024, Pagina/e 103173, ISSN 1873-5061
Editore: Elsevier
DOI: 10.1016/j.scr.2023.103173

Lissencephaly: Update on diagnostics and clinical management

Autori: Matti Koenig, William B. Dobyns, Nataliya Di Donato
Pubblicato in: European Journal of Paediatric Neurology, Numero 35, 2022, Pagina/e 147-152, ISSN 1090-3798
Editore: W. B. Saunders Co., Ltd.
DOI: 10.1016/j.ejpn.2021.09.013

Extending inherited metabolic disorder diagnostics with biomarker interaction visualizations

Autori: Denise N. Slenter, Irene M. G. M. Hemel, Chris T. Evelo, Jörgen Bierau, Egon L. Willighagen, Laura K. M. Steinbusch
Pubblicato in: Orphanet Journal of Rare Diseases, Numero 18, 2023, ISSN 1750-1172
Editore: BioMed Central
DOI: 10.1186/s13023-023-02683-9

Ensembl 2024

Autori: Peter W Harrison, M Ridwan Amode, Olanrewaju Austine-Orimoloye, Andrey G Azov, Matthieu Barba, If Barnes, Arne Becker, Ruth Bennett, Andrew Berry, Jyothish Bhai, Simarpreet Kaur Bhurji, Sanjay Boddu, Paulo R Branco Lins, Lucy Brooks, Shashank Budhanuru Ramaraju, Lahcen I Campbell, Manuel Carbajo Martinez, Mehrnaz Charkhchi, Kapeel Chougule, Alexander Cockburn, Claire Davidson, Nishadi H De S
Pubblicato in: Nucleic Acids Research, Numero 52, 2024, Pagina/e D891-D899, ISSN 0305-1048
Editore: Oxford University Press
DOI: 10.1093/nar/gkad1049

Remote visualization of large-scale genomic alignments for collaborative clinical research and diagnosis of rare diseases

Autori: Alberto Corvò, Leslie Matalonga, Dylan Spalding, Alexander Senf, Steven Laurie, Daniel Picó-Amador, Marcos Fernandez-Callejo, Ida Paramonov, Anna Foix Romero, Emilio Garcia-Rios, Jorge Izquierdo Ciges, Anand Mohan, Coline Thomas, Andres Felipe Silva Valencia, Csaba Halmagyi, Mallory Ann Freeberg, Ana Töpf, Rita Horvath, Gary Saunders, Ivo Gut, Thomas Keane, Davide Piscia, Sergi Beltran
Pubblicato in: Cell Genomics, Numero 3, 2023, Pagina/e 100246, ISSN 2666-979X
Editore: Elsevier Inc.
DOI: 10.1016/j.xgen.2022.100246

Genome Aggregation Database Version 4—New Challenges of Variant Analysis in Movement Disorders

Autori: Elisabetta Indelicato, Luigi Michele Romito, Philip Harrer, Nico Golfrè Andreasi, Isabel Colangelo, Robert Kopajtich, Juliane Winkelmann, Holger Prokisch, Barbara Garavaglia, Michael Zech
Pubblicato in: Movement Disorders, Numero 39, 2024, Pagina/e 1237-1238, ISSN 0885-3185
Editore: John Wiley & Sons Inc.
DOI: 10.1002/mds.29797

The phenotypic and genetic spectrum of patients with heterozygous mutations in cyclin M2 (CNNM2)

Autori: Gijs A. C. Franken, Dominik Müller, Cyril Mignot, Boris Keren, Jonathan Lévy, Anne‐Claude Tabet, David Germanaud, María‐Isabel Tejada, Hester Y. Kroes, Rutger A. J. Nievelstein, Elise Brimble, Maria Ruzhnikov, Felix Claverie‐Martin, Maria Szczepańska, Martin Ćuk, Femke Latta, Martin Konrad, Luis A. Martínez‐Cruz, René J. M. Bindels, Joost G. J. Hoenderop, Karl‐Peter Schlingmann, J
Pubblicato in: Human Mutation, 2021, ISSN 1059-7794
Editore: John Wiley & Sons Inc.
DOI: 10.1002/humu.24182

Definition and clinical variability of SHANK3-related Phelan-McDermid syndrome

Autori: Michael Schön, Pablo Lapunzina, Julián Nevado, Teresa Mattina, Cecilia Gunnarsson, Kinga Hadzsiev, Chiara Verpelli, Thomas Bourgeron, Sarah Jesse, Conny M.A. van Ravenswaaij-Arts, Raoul C. Hennekam
Pubblicato in: European Journal of Medical Genetics, Numero 66, 2023, Pagina/e 104754, ISSN 1769-7212
Editore: Elsevier BV
DOI: 10.1016/j.ejmg.2023.104754

Evaluating FAIR maturity through a scalable, automated, community-governed framework

Autori: Mark D. Wilkinson, Michel Dumontier, Susanna-Assunta Sansone, Luiz Olavo Bonino da Silva Santos, Mario Prieto, Dominique Batista, Peter McQuilton, Tobias Kuhn, Philippe Rocca-Serra, Mercѐ Crosas, Erik Schultes
Pubblicato in: Scientific Data, Numero 6/1, 2019, ISSN 2052-4463
Editore: Nature
DOI: 10.1038/s41597-019-0184-5

Combined Single Gene Testing and Genome Sequencing as an Effective Diagnostic Approach for Anophthalmia and Microphthalmia Patients

Autori: Rabia Basharat, Kim Rodenburg, María Rodríguez-Hidalgo, Afeefa Jarral, Ehsan Ullah, Jordi Corominas, Christian Gilissen, Syeda Tatheer Zehra, Usman Hameed, Muhammad Ansar, Suzanne E. de Bruijn
Pubblicato in: Genes, Numero 14, 2023, Pagina/e 1573, ISSN 2073-4425
Editore: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/genes14081573

Ensembl 2021

Autori: Kevin L Howe, Premanand Achuthan, James Allen, Jamie Allen, Jorge Alvarez-Jarreta, M Ridwan Amode, Irina M Armean, Andrey G Azov, Ruth Bennett, Jyothish Bhai, Konstantinos Billis, Sanjay Boddu, Mehrnaz Charkhchi, Carla Cummins, Luca Da Rin Fioretto, Claire Davidson, Kamalkumar Dodiya, Bilal El Houdaigui, Reham Fatima, Astrid Gall, Carlos Garcia Giron, Tiago Grego, Cristina Guijarro-Clarke, Lea
Pubblicato in: Nucleic Acids Research, Numero 49/D1, 2020, Pagina/e D884-D891, ISSN 0305-1048
Editore: Oxford University Press
DOI: 10.1093/nar/gkaa942

Ensembl 2022

Autori: Fiona Cunningham, James E Allen, Jamie Allen, Jorge Alvarez-Jarreta, M Ridwan Amode, Irina M Armean, Olanrewaju Austine-Orimoloye, Andrey G Azov, If Barnes, Ruth Bennett, Andrew Berry, Jyothish Bhai, Alexandra Bignell, Konstantinos Billis, Sanjay Boddu, Lucy Brooks, Mehrnaz Charkhchi, Carla Cummins, Luca Da Rin Fioretto, Claire Davidson, Kamalkumar Dodiya, Sarah Donaldson, Bilal El Houdaigui
Pubblicato in: Nucleic Acids Research, Numero 50, 2023, Pagina/e D988-D995, ISSN 0305-1048
Editore: Oxford University Press
DOI: 10.1093/nar/gkab1049

A neutral comparison of statistical methods for analyzing longitudinally measured ordinal outcomes in rare diseases

Autori: Martin Geroldinger, Johan Verbeeck, Konstantin E. Thiel, Geert Molenberghs, Arne C. Bathke, Martin Laimer, Georg Zimmermann
Pubblicato in: Biometrical Journal, Numero 66, 2024, ISSN 0323-3847
Editore: John Wiley & Sons Ltd.
DOI: 10.1002/bimj.202200236

Sustainable approaches for drug repurposing in rare diseases: recommendations from the IRDiRC Task Force

Autori: Galliano Zanello, Diego Ardigò, Florence Guillot, Anneliene H. Jonker, Oxana Iliach, Hervé Nabarette, Daniel O’Connor, Virginie Hivert
Pubblicato in: Rare Disease and Orphan Drugs Journal, Numero 2, 2024, Pagina/e 9, ISSN 2771-2893
Editore: OAE Publishing Inc.
DOI: 10.20517/rdodj.2023.04

Exploring the Therapeutic Potential of Ectoine in Duchenne Muscular Dystrophy: Comparison with Taurine, a Supplement with Known Beneficial Effects in the mdx Mouse

Autori: Caroline Merckx, Jana Zschüntzsch, Stefanie Meyer, Robrecht Raedt, Hanne Verschuere, Jens Schmidt, Boel De Paepe, Jan L. De Bleecker
Pubblicato in: International Journal of Molecular Sciences, Numero 23, 2024, Pagina/e 9567, ISSN 1422-0067
Editore: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/ijms23179567

Levels of Neurofilament Light at the Preataxic and Ataxic Stages of Spinocerebellar Ataxia Type 1

Autori: Carlo Wilke, David Mengel, Ludger Schöls, Holger Hengel, Maria Rakowicz, Thomas Klockgether, Alexandra Durr, Alessandro Filla, Bela Melegh, Rebecca Schüle, Kathrin Reetz, Heike Jacobi, Matthis Synofzik
Pubblicato in: Neurology, Numero 98, 2024, ISSN 0028-3878
Editore: Lippincott Williams & Wilkins Ltd.
DOI: 10.1212/wnl.0000000000200257

Additional file 2 of Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence

Autori: Hassanin, Emadeldin; Spier, Isabel; Bobbili, Dheeraj R.; Aldisi, Rana; Klinkhammer, Hannah; David, Friederike; Dueñas, Nuria; Hüneburg, Robert; Perne, Claudia; Brunet, Joan; Capella, Gabriel; Nöthen, Markus M.; Forstner, Andreas J.; Mayr, Andreas; Krawitz, Peter; May, Patrick; Aretz, Stefan; Maj, Carlo
Pubblicato in: BMC Medical Genomics, Numero 1, 2023, ISSN 1755-8794
Editore: BioMed Central
DOI: 10.6084/m9.figshare.22620470.v1

Additional file 1 of The de novo FAIRification process of a registry for vascular anomalies

Autori: Groenen, Karlijn H. J.; Jacobsen, Annika; Kersloot, Martijn G.; dos Santos Vieira, Bruna; van Enckevort, Esther; Kaliyaperumal, Rajaram; Arts, Derk L.; ‘t Hoen, Peter A. C.; Cornet, Ronald; Roos, Marco; Kool, Leo Schultze
Pubblicato in: Orphanet Journal of Rare Diseases, Numero 1, 2021, ISSN 1750-1172
Editore: BioMed Central
DOI: 10.6084/m9.figshare.16570885

Biallelic variants in the SORD gene are one of the most common causes of hereditary neuropathy among Czech patients

Autori: P. Laššuthová, R. Mazanec, D. Staněk, L. Sedláčková, B. Plevová, J. Haberlová, P. Seeman
Pubblicato in: Scientific Reports, Numero 11, 2022, ISSN 2045-2322
Editore: Nature Publishing Group
DOI: 10.1038/s41598-021-86857-0

Detection of Telomeric DNA:RNA Hybrids Using TeloDRIP-qPCR

Autori: Ilaria Rosso, Fabrizio d’Adda di Fagagna
Pubblicato in: International Journal of Molecular Sciences, Numero 21/24, 2020, Pagina/e 9774, ISSN 1422-0067
Editore: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/ijms21249774

Integrative analysis of multi-omics data reveals importance of collagen and the PI3K AKT signalling pathway in CAKUT

Autori: Jumamurat R. Bayjanov, Cenna Doornbos, Ozan Ozisik, Woosub Shin, Núria Queralt-Rosinach, Daphne Wijnbergen, Jean-Sébastien Saulnier-Blache, Joost P. Schanstra, Bénédicte Buffin-Meyer, Julie Klein, José M. Fernández, Rajaram Kaliyaperumal, Anaïs Baudot, Peter A. C. ’t Hoen, Friederike Ehrhart
Pubblicato in: Scientific Reports, Numero 14, 2024, ISSN 2045-2322
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orsum: A Python package for filtering and comparing enrichment analyses using comprehensible rules

Autori: Ozan Ozisik, Morgane Térézol, Anaı̈s Baudot
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Editore: BioMed Central
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Towards FAIRification of sensitive and fragmented rare disease patient data: challenges and solutions in European reference network registries.

Autori: Bruna dos Santos Vieira, César H. Bernabé, Shuxin Zhang, Haitham Abaza, Nirupama Benis, Alberto Cámara, Ronald Cornet, Clémence M. A. Le Cornec, Peter A. C. ’t Hoen, Franz Schaefer, K. Joeri van der Velde, Morris A. Swertz, Mark D. Wilkinson, Annika Jacobsen & Marco Roos
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Assessing resolvability, parsability, and consistency of RDF resources: a use case in rare diseases

Autori: Shuxin Zhang, Nirupama Benis, Ronald Cornet
Pubblicato in: Journal of Biomedical Semantics, Numero 14, 2023, ISSN 2041-1480
Editore: BioMed Central
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Building Expertise on FAIR Through Evolving Bring Your Own Data (BYOD) Workshops: Describing the Data, Software, and Management-focused Approaches and Their Evolution

Autori: César H. Bernabé, Lieze Thielemans, Rajaram Kaliyaperumal, Claudio Carta, Shuxin Zhang, Celia W.G. van Gelder, Nirupama Benis, Luiz Olavo Bonino da Silva Santos, Ronald Cornet, Bruna dos Santos Vieira, Nawel Lalout, Ines Henriques, Alberto Cámara Ballesteros, Kees Burger, Martijn G. Kersloot, Friederike Ehrhart, Esther van Enckevort, Chris T. Evelo, Alasdair J. G. Gray, Marc Hanauer, Kristina H
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The case for open science: rare diseases

Autori: Yaffa R Rubinstein, Peter N Robinson, William A Gahl, Paul Avillach, Gareth Baynam, Helene Cederroth, Rebecca M Goodwin, Stephen C Groft, Mats G Hansson, Nomi L Harris, Vojtech Huser, Deborah Mascalzoni, Julie A McMurry, Matthew Might, Christoffer Nellaker, Barend Mons, Dina N Paltoo, Jonathan Pevsner, Manuel Posada, Alison P Rockett-Frase, Marco Roos, Tamar B Rubinstein, Domenica Taruscio, Esther
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Dystonia in <scp>ATP</scp> Synthase Defects: Reconnecting Mitochondria and Dopamine

Autori: Elisabetta Indelicato, Sylvia Boesch, Niccolo' E. Mencacci, Daniele Ghezzi, Holger Prokisch, Juliane Winkelmann, Michael Zech
Pubblicato in: Movement Disorders, Numero 39, 2024, Pagina/e 29-35, ISSN 0885-3185
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Ten quick tips for building FAIR workflows

Autori: Casper de Visser, Lennart F. Johansson, Purva Kulkarni, Hailiang Mei, Pieter Neerincx, K. Joeri van der Velde, Péter Horvatovich, Alain J. van Gool, Morris A. Swertz, Peter A. C. ‘t Hoen, Anna Niehues
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Editore: San Francisco, CA Public Library of Science
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Heterogeneous Phenotypic Evolution in <scp>ANO3</scp>‐Related Dystonia Due to the Recurrent <scp>p.Glu510Lys</scp> Variant

Autori: Elisabetta Indelicato, Sylvia Boesch, Michael Zech
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Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias

Autori: Paulina Cunha, Emilien Petit, Marie Coutelier, Giulia Coarelli, Caterina Mariotti, Jennifer Faber, Judith Van Gaalen, Joana Damasio, Zofia Fleszar, Michele Tosi, Clarissa Rocca, Giovanna De Michele, Martina Minnerop, Claire Ewenczyk, Filippo M. Santorelli, Anna Heinzmann, Thomas Bird, Matthias Amprosi, Elisabetta Indelicato, Alberto Benussi, Perrine Charles, Claudia Stendel, Silvia Romano, Marina
Pubblicato in: The American Journal of Human Genetics, Numero 110, 2024, Pagina/e 1098-1109, ISSN 0002-9297
Editore: University of Chicago Press
DOI: 10.1016/j.ajhg.2023.05.009

Ensembl 2023.

Autori: Martin FJ et al
Pubblicato in: Nucleic Acids Research, 2022, ISSN 0305-1048
Editore: Oxford University Press
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Diagnostic yield from cardiac gene testing for inherited cardiac conditions and re-evaluation of pre-ACMG variants of uncertain significance

Autori: Jane Murphy, Claire W. Kirk, Deborah M. Lambert, Catherine McGorrian, Roddy Walsh, Terri P. McVeigh, Terence Prendiville, Deirdre Ward, Joseph Galvin, Sally Ann Lynch
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Drug repurposing in Rett and Rett-like syndromes: a promising yet underrated opportunity?

Autori: Claudia Fuchs, Peter A. C. ‘t Hoen, Annelieke R. Müller, Friederike Ehrhart, Clara D. M. Van Karnebeek
Pubblicato in: Frontiers in Medicine, Numero 11, 2024, ISSN 2296-858X
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Recommendations from the IRDiRC Working Group on methodologies to assess the impact of diagnoses and therapies on rare disease patients

Autori: Galliano Zanello; Chun-Hung Chan; David A. Pearce; IRDiRC Working Group
Pubblicato in: Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-10 (2022), Numero 1, 2022, ISSN 1750-1172
Editore: BioMed Central
DOI: 10.1186/s13023-022-02337-2

Towards the international interoperability of clinical research networks for rare diseases: recommendations from the IRDiRC Task Force

Autori: Rima Nabbout, Galliano Zanello, Dixie Baker, Lora Black, Isabella Brambilla, Orion J. Buske, Laurie S. Conklin, Elin Haf Davies, Daria Julkowska, Yeonju Kim, Thomas Klopstock, Harumasa Nakamura, Kim G. Nielsen, Anne R. Pariser, Jose Carlos Pastor, Maurizio Scarpa, Maureen Smith, Domenica Taruscio, Stephen Groft
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Editore: BioMed Central
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Consensus recommendations on counselling in Phelan-McDermid syndrome, with special attention to recurrence risk and to ring chromosome 22

Autori: Sylvia A. Koza, Anne C. Tabet, Maria C. Bonaglia, Stephanie Andres, Britt-Marie. Anderlid, Emmelien Aten, Dominique Stiefsohn, D. Gareth Evans, Conny M.A. van Ravenswaaij-Arts, Sarina G. Kant
Pubblicato in: European Journal of Medical Genetics, Numero 66, 2023, Pagina/e 104773, ISSN 1769-7212
Editore: Elsevier BV
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Age-dependent neurodegeneration and neuroinflammation in a genetic A30P/A53T double-mutated α-synuclein mouse model of Parkinson's disease

Autori: Lisa Rauschenberger, Jennifer Behnke, Alexander Grotemeyer, Susanne Knorr, Jens Volkmann, Chi Wang Ip
Pubblicato in: Neurobiology of Disease, Numero 171, 2024, Pagina/e 105798, ISSN 0969-9961
Editore: Academic Press
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Synthetic datasets for open software development in rare disease research

Autori: Ibraheem Al-Dhamari, Hammam Abu Attieh, Fabian Prasser
Pubblicato in: Orphanet Journal of Rare Diseases, Numero 19, 2024, ISSN 1750-1172
Editore: BioMed Central
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The European joint programme on rare diseases: building the rare diseases research ecosystem

Autori: Yanis Mimouni, Juliane Halftermeyer, Yanna Petton, Pauline Adam, Clément Moreau, Ana Rath, Roseline Favresse, Birute Tumiene, Daria Julkowska
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Head movement dynamics in dystonia: a multi-centre retrospective study using visual perceptive deep learning

Autori: Robert Peach, Maximilian Friedrich, Lara Fronemann, Muthuraman Muthuraman, Sebastian R. Schreglmann, Daniel Zeller, Christoph Schrader, Joachim K. Krauss, Alfons Schnitzler, Matthias Wittstock, Ann-Kristin Helmers, Steffen Paschen, Andrea Kühn, Inger Marie Skogseid, Wilhelm Eisner, Joerg Mueller, Cordula Matthies, Martin Reich, Jens Volkmann, Chi Wang Ip
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Editore: Springer Nature
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The use of foundational ontologies in biomedical research

Autori: César H. Bernabé; Núria Queralt-Rosinach; Vítor E. Silva Souza; Luiz Olavo Bonino da Silva Santos; Barend Mons; Annika Jacobsen; Marco Roos
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Editore: Biomed Central
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Artificial intelligence-enhanced electrocardiography derived body mass index as a predictor of future cardiometabolic disease

Autori: Libor Pastika, Arunashis Sau, Konstantinos Patlatzoglou, Ewa Sieliwonczyk, Antônio H. Ribeiro, Kathryn A. McGurk, Sadia Khan, Danilo Mandic, William R. Scott, James S. Ware, Nicholas S. Peters, Antonio Luiz P. Ribeiro, Daniel B. Kramer, Jonathan W. Waks, Fu Siong Ng
Pubblicato in: npj Digital Medicine, Numero 7, 2024, ISSN 2398-6352
Editore: Nature
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The FAIR Data Point: Interfaces and Tooling

Autori: Ousamma Mohammed Benhamed1, Kees Burger2, Rajaram Kaliyaperumal2, Luiz Olavo Bonino da Silva Santos2,3, Marek Suchánek4, Jan Slifka4, Mark D Wilkinson1*
Pubblicato in: Data Intelligence, 2022, ISSN 2641-435X
Editore: MIT Press
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De novo variants in neurodevelopmental disorders—experiences from a tertiary care center

Autori: Theresa Brunet, Robert Jech, Melanie Brugger, Reka Kovacs, Bader Alhaddad, Gloria Leszinski, Korbinian M. Riedhammer, Dominik S. Westphal, Isabella Mahle, Katharina Mayerhanser, Matej Skorvanek, Sandrina Weber, Elisabeth Graf, Riccardo Berutti, Ján Necpál, Petra Havránková, Petra Pavelekova, Maja Hempel, Urania Kotzaeridou, Georg F. Hoffmann, Steffen Leiz, Christine Makowski, Timo Roser, Sebas
Pubblicato in: Clinical Genetics, 2021, ISSN 0009-9163
Editore: Blackwell Publishing Inc.
DOI: 10.1111/cge.13946

Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence

Autori: Emadeldin Hassanin; Isabel Spier; Dheeraj R. Bobbili; Rana Aldisi; Hannah Klinkhammer; Friederike David; Nuria Dueñas; Robert Hüneburg; Claudia Perne; Joan Brunet; Gabriel Capella; Markus M. Nöthen; Andreas J. Forstner; Andreas Mayr; Peter Krawitz; Patrick May; Stefan Aretz; Carlo Maj
Pubblicato in: BMC Medical Genomics, 2023, ISSN 1755-8794
Editore: BioMed Central
DOI: 10.1101/2022.01.20.22269585

WikiPathways: connecting communities

Autori: Marvin Martens, Ammar Ammar, Anders Riutta, Andra Waagmeester, Denise N Slenter, Kristina Hanspers, Ryan A. Miller, Daniela Digles, Elisson N Lopes, Friederike Ehrhart, Lauren J Dupuis, Laurent A Winckers, Susan L Coort, Egon L Willighagen, Chris T Evelo, Alexander R Pico, Martina Kutmon
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Editore: Oxford University Press
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Exploring pathway interactions to detect molecular mechanisms of disease: 22q11.2 deletion syndrome

Autori: Woosub Shin, Martina Kutmon, Eleni Mina, Therese van Amelsvoort, Chris T Evelo, Friederike Ehrhart
Pubblicato in: Orphanet Journal of Rare Diseases, Numero 18, 2023, ISSN 1750-1172
Editore: BioMed Central
DOI: 10.1186/s13023-023-02953-6

Peripheral temperature dysregulation associated with functionally altered NaV1.8 channels

Autori: Simon Loose, Annette Lischka, Samuel Kuehs, Carla Nau, Stefan H. Heinemann, Ingo Kurth, Enrico Leipold
Pubblicato in: Pflügers Archiv - European Journal of Physiology, Numero 475, 2023, Pagina/e 1343-1355, ISSN 0031-6768
Editore: Springer Verlag
DOI: 10.1007/s00424-023-02856-2

Description of Osmolyte Pathways in Maturing Mdx Mice Reveals Altered Levels of Taurine and Sodium/Myo-Inositol Co-Transporters

Autori: Caroline Merckx, Gwenny Cosemans, Jana Zschüntzsch, Robrecht Raedt, Jens Schmidt, Boel De Paepe, Jan L. De Bleecker
Pubblicato in: International Journal of Molecular Sciences, Numero 23, 2024, Pagina/e 3251, ISSN 1422-0067
Editore: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/ijms23063251

SUsPECT: a pipeline for variant effect prediction based on custom long-read transcriptomes for improved clinical variant annotation

Autori: Renee Salz, Nuno Saraiva-Agostinho, Emil Vorsteveld, Caspar I. van der Made, Simone Kersten, Merel Stemerdink, Jamie Allen, Pieter-Jan Volders, Sarah E. Hunt, Alexander Hoischen, Peter A.C. ’t Hoen
Pubblicato in: BMC Genomics, Numero 24, 2023, ISSN 1471-2164
Editore: BioMed Central
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Overlap of vitamin A and vitamin D target genes with CAKUT-related processes [version 2; peer review: 2 approved, 2 approved with reservations]

Autori: Chris T. Evelo; Alberto Mantovani; Anaı̈s Baudot; Friederike Ehrhart; Ozan Ozisik
Pubblicato in: F1000Research, Vol 10 (2022), Numero 1, 2021, ISSN 2046-1402
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ABCA4 Variant c.5714+5G&gt;A in Trans With Null Alleles Results in Primary RPE Damage

Autori: Jana Sajovic, Andrej Meglič, Zelia Corradi, Mubeen Khan, Aleš Maver, Martina Jarc Vidmar, Marko Hawlina, Frans P. M. Cremers, Ana Fakin
Pubblicato in: Investigative Opthalmology & Visual Science, Numero 64, 2023, Pagina/e 33, ISSN 1552-5783
Editore: ARVO Journals
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FAIR Data Point: A FAIR-Oriented Approach for Metadata Publication

Autori: Luiz Olavo Bonino da Silva Santos, Kees Burger, Rajaram Kaliyaperumal, Mark D. Wilkinson
Pubblicato in: Data Intelligence, 2022, ISSN 2641-435X
Editore: MIT Press
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Use Cases Requiring Privacy-Preserving Record Linkage in Paediatric Oncology

Autori: Dieter Hayn, Karl Kreiner, Emanuel Sandner, Martin Baumgartner, Bernhard Jammerbund, Markus Falgenhauer, Vanessa Düster, Priyanka Devi-Marulkar, Gudrun Schleiermacher, Ruth Ladenstein, Guenter Schreier
Pubblicato in: Cancers, Numero 16, 2024, Pagina/e 2696, ISSN 2072-6694
Editore: Multidisciplinary Digital Publishing Institute (MDPI)
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Establishing the first pan-European Registry for rare bone and mineral disorders: EuRR-Bone

Autori: Corinna Grasemann, Marina Mordenti, Inês Alves, Rebecca Skarberg, Ondrej Soucek, Marco Roos, M. Kassim Javaid, S. Faisal Ahmed, Agnès Lignart, Klaus Mohnike, Wolfgang Högler, Luca Sangiorgi, Natasha M. Appelman-Dijkstra
Pubblicato in: Bone Reports, Numero 13, 2020, Pagina/e 100318, ISSN 2352-1872
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The RD-Connect Genome-Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases

Autori: Steven Laurie, Davide Piscia, Leslie Matalonga, Alberto Corvó, Marcos Fernández-Callejo, Carles Garcia-Linares, Carles Hernandez-Ferrer, Cristina Luengo, Inés Martínez, Anastasios Papakonstantinou, Daniel Picó-Amador, Joan Protasio, Rachel Thompson, Raul Tonda, Mònica Bayés, Gemma Bullich, Jordi Camps-Puchadas, Ida Paramonov, Jean-Rémi Trotta, Angel Alonso, Marcella Attimonelli, Christophe
Pubblicato in: Human Mutation, Numero Volume 43, Numero 6, 2022, Pagina/e Pages 717-733, ISSN 1098-1004
Editore: Hindawi
DOI: 10.1002/humu.24353

Getting your DUCs in a row - standardising the representation of Digital Use Conditions

Autori: Francis Jeanson, Spencer J. Gibson, Pinar Alper, Alexander Bernier, J. Patrick Woolley, Daniel Mietchen, Andrzej Strug, Regina Becker, Pim Kamerling, Maria del Carmen Sanchez Gonzalez, Nancy Mah, Ann Novakowski, Mark D. Wilkinson, Oussama Mohammed Benhamed, Annalisa Landi, Georg Philip Krog, Heimo Müller, Umar Riaz, Colin Veal, Petr Holub, Esther van Enckevort, Anthony J. Brookes
Pubblicato in: Scientific Data, Numero 11, 2024, ISSN 2052-4463
Editore: Springer Nature
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A catalogue of 863 Rett-syndrome-causing MECP2 mutations and lessons learned from data integration

Autori: Friederike Ehrhart, Annika Jacobsen, Maria Rigau, Mattia Bosio, Rajaram Kaliyaperumal, Jeroen F. J. Laros, Egon L. Willighagen, Alfonso Valencia, Marco Roos, Salvador Capella-Gutierrez, Leopold M. G. Curfs, Chris T. Evelo
Pubblicato in: Scientific Data, Numero 8/1, 2021, Pagina/e 10, ISSN 2052-4463
Editore: Nature
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Targeting shared molecular etiologies to accelerate drug development for rare diseases

Autori: Galliano Zanello; Macarena Garrido‐Estepa; Ana Crespo; Daniel O'Connor; Rima Nabbout; Christina Waters; Anthony Hall; Maurizio Taglialatela; Chun‐Hung Chan; David A Pearce; Marc Dooms; Philip John Brooks
Pubblicato in: EMBO Molecular Medicine, Vol 15, Iss 7, Pp n/a-n/a (2023), Numero 6, 2023, ISSN 1757-4684
Editore: Wiley Europe
DOI: 10.15252/emmm.202217159

A Resource for Guiding Data Stewards to Make European Rare Disease Patient Registries FAIR

Autori: Philip van Damme; Pablo Alarcón Moreno; César H. Bernabé; Alberto Cámara Ballesteros; Clémence M. A. Le Cornec; Bruna Dos Santos Vieira; K. Joeri van der Velde; Shuxin Zhang; Claudio Carta; Ronald Cornet; Peter A.C. ’t Hoen; Annika Jacobsen; Morris A. Swertz; Marco Roos; Nirupama Benis
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Editore: Committee on Data for Science and Technology (CODATA) International Council for Science (ICSU)
DOI: 10.5334/dsj-2023-012

Consensus recommendations on chewing, swallowing and gastrointestinal problems in Phelan-McDermid syndrome

Autori: Ausra Matuleviciene; Kamile Siauryte; Els Kuiper; Andreas M. Grabrucker
Pubblicato in: European Journal of Medical Genetics, Numero 8, 2023, ISSN 1769-7212
Editore: Elsevier BV
DOI: 10.1016/j.ejmg.2023.104763

A Generic Workflow for the Data FAIRification Process

Autori: Annika Jacobsen, Rajaram Kaliyaperumal, Luiz Olavo Bonino da Silva Santos, Barend Mons, Erik Schultes, Marco Roos, Mark Thompson
Pubblicato in: Data Intelligence, Numero 2/1-2, 2020, Pagina/e 56-65, ISSN 2641-435X
Editore: The MIT PressJournals
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FAIR Principles: Interpretations and Implementation Considerations

Autori: Annika Jacobsen, Ricardo de Miranda Azevedo, Nick Juty, Dominique Batista, Simon Coles, Ronald Cornet, Mélanie Courtot, Mercè Crosas, Michel Dumontier, Chris T. Evelo, Carole Goble, Giancarlo Guizzardi, Karsten Kryger Hansen, Ali Hasnain, Kristina Hettne, Jaap Heringa, Rob W.W. Hooft, Melanie Imming, Keith G. Jeffery, Rajaram Kaliyaperumal, Martijn G. Kersloot, Christine R. Kirkpatrick, Tobias K
Pubblicato in: Data Intelligence, Numero 2/1-2, 2020, Pagina/e 10-29, ISSN 2641-435X
Editore: The MIT PressJournals
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A pipeline‐friendly software tool for genome diagnostics to prioritize genes by matching patient symptoms to literature

Autori: K. Joeri Velde, Sander Hoek, Freerk Dijk, Dennis Hendriksen, Cleo C. Diemen, Lennart F. Johansson, Kristin M. Abbott, Patrick Deelen, Birgit Sikkema‐Raddatz, Morris A. Swertz
Pubblicato in: Advanced Genetics, Numero 1/1, 2020, Pagina/e e10023, ISSN 2641-6573
Editore: Wiley
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System-level analysis of genes mutated in muscular dystrophies reveals a functional pattern associated with muscle weakness distribution

Autori: Ozan Ozisik, Svetlana Gorokhova, Mathieu Cerino, Marc Bartoli, Anaïs Baudot
Pubblicato in: Scientific Reports, Numero 14, 2024, ISSN 2045-2322
Editore: Nature Publishing Group
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Leveraging Biolink as a “Rosetta Stone” Between C-Path and EJP-RD Semantic Models Provides Emergent Interoperability

Autori: Pablo Alarcon, Ian Braun, Emily Hartley, Daniel Olson, Nirupama Benis, Ronald Cornet, Mark Wilkinson, Ramona L. Walls
Pubblicato in: Journal of the Society for Clinical Data Management, Numero 2, 2023, ISSN 2694-1473
Editore: McLean VA
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IgLON5 deficiency produces behavioral alterations in a knockout mouse model

Autori: Jon Landa, Ana Beatriz Serafim, Mercedes Alba, Estibaliz Maudes, Laura Molina-Porcel, Anna Garcia-Serra, Francesco Mannara, Josep Dalmau, Francesc Graus, Lidia Sabater
Pubblicato in: Frontiers in Immunology, Numero 15, 2024, ISSN 1664-3224
Editore: Frontiers Media SA
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Scale for the Assessment and Rating of Ataxia (SARA): Development of a Training Tool and Certification Program

Autori: Marcus Grobe-Einsler, Arian Taheri Amin, Jennifer Faber, Hartmut Völkel, Matthis Synofzik, Thomas Klockgether
Pubblicato in: The Cerebellum, Numero 23, 2024, Pagina/e 877-880, ISSN 1473-4230
Editore: Springer Nature
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Composite endpoints, including patient reported outcomes, in rare diseases

Autori: Johan Verbeeck; Maya Dirani; Johann W. Bauer; Ralf-Dieter Hilgers; Geert Molenberghs; Rima Nabbout
Pubblicato in: Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-11 (2023), Numero 8, 2023, ISSN 1750-1172
Editore: BioMed Central
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Genetics meets function in sodium channel-related pain disorders

Autori: Jannis Körner, Natja Haag, Ingo Kurth, Angelika Lampert
Pubblicato in: Neuroforum, Numero 28, 2023, Pagina/e 67-75, ISSN 0947-0875
Editore: Spektrum Akademischer Verlag GmbH
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Additional file 1 of Towards the international interoperability of clinical research networks for rare diseases: recommendations from the IRDiRC Task Force

Autori: Nabbout, Rima; Zanello, Galliano; Baker, Dixie; Black, Lora; Brambilla, Isabella; Buske, Orion J.; Conklin, Laurie S.; Davies, Elin Haf; Julkowska, Daria; Kim, Yeonju; Klopstock, Thomas; Nakamura, Harumasa; Nielsen, Kim G.; Pariser, Anne R.; Pastor, Jose Carlos; Scarpa, Maurizio; Smith, Maureen; Taruscio, Domenica; Groft, Stephen
Pubblicato in: Orphanet Journal of Rare Diseases, Numero 1, 2023, ISSN 1750-1172
Editore: BioMed Central
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Autori: Ugo Sorrentino, Sylvia Boesch, Diane Doummar, Claudia Ravelli, Tereza Serranova, Elisabetta Indelicato, Juliane Winkelmann, Lydie Burglen, Robert Jech, Michael Zech
Pubblicato in: Journal of Neurology, Numero 271, 2024, Pagina/e 2859-2865, ISSN 0340-5354
Editore: Dr. Dietrich Steinkopff Verlag
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Genetic and drug-induced hypomagnesemia: different cause, same mechanism

Autori: Willem Bosman, Joost G. J. Hoenderop, Jeroen H. F. de Baaij
Pubblicato in: Proceedings of the Nutrition Society, Numero 80, 2023, Pagina/e 327-338, ISSN 0029-6651
Editore: CABI Publishing
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Incidence and Prevalence of Fibrous Dysplasia/McCune-Albright Syndrome: A Nationwide Registry-Based Study in Denmark

Autori: Maartje E Meier, Emese Vágó, Bo Abrahamsen, Olaf M Dekkers, Erzsébet Horváth-Puhó, Lars Rejnmark, Natasha M Appelman-Dijkstra
Pubblicato in: The Journal of Clinical Endocrinology & Metabolism, Numero 109, 2024, Pagina/e 1423-1432, ISSN 0021-972X
Editore: The Endocrine Society
DOI: 10.1210/clinem/dgad744

Unraveling dystonia circuitry in rodent models using novel neuromodulation techniques

Autori: Lisa Rauschenberger, Chi Wang Ip
Pubblicato in: Dystonia, Numero 3, 2024, ISSN 2813-2106
Editore: Frontiers Media SA
DOI: 10.3389/dyst.2024.11793

Consensus recommendations on altered sensory functioning in Phelan-McDermid syndrome

Autori: Margreet Walinga, Sarah Jesse, Norma Alhambra, Griet Van Buggenhout
Pubblicato in: European Journal of Medical Genetics, Numero 66, 2023, Pagina/e 104726, ISSN 1769-7212
Editore: Elsevier BV
DOI: 10.1016/j.ejmg.2023.104726

A Simple Standard for Sharing Ontological Mappings (SSSOM)

Autori: Nicolas Matentzoglu, James P Balhoff, Susan M Bello, Chris Bizon, Matthew Brush, Tiffany J Callahan, Christopher G Chute, William D Duncan, Chris T Evelo, Davera Gabriel, John Graybeal, Alasdair Gray, Benjamin M Gyori, Melissa Haendel, Henriette Harmse, Nomi L Harris, Ian Harrow, Harshad B Hegde, Amelia L Hoyt, Charles T Hoyt, Dazhi Jiao, Ernesto Jiménez-Ruiz, Simon Jupp, Hyeongsik Kim, Sebastian
Pubblicato in: Database, Numero 2022, 2022, ISSN 1758-0463
Editore: Oxford University Press
DOI: 10.1093/database/baac035

Multifactorial Assessment of Motor Behavior in Rats after Unilateral Sciatic Nerve Crush Injury

Autori: Susanne Knorr, Lisa Rauschenberger, Tami Lang, Jens Volkmann, Chi Wang Ip
Pubblicato in: Journal of Visualized Experiments, 2024, ISSN 1940-087X
Editore: MYJoVE Corporation
DOI: 10.3791/62606-v

Corrigendum: Reactive astrogliosis in the era of single-cell transcriptomics

Autori: Zuzana Matusova; Zuzana Matusova; Elly M. Hol; Milos Pekny; Milos Pekny; Milos Pekny; Mikael Kubista; Mikael Kubista; Lukas Valihrach; Lukas Valihrach
Pubblicato in: Frontiers in Cellular Neuroscience, Vol 17 (2023), Numero 2, 2023, ISSN 1662-5102
Editore: Frontiers Research Foundation
DOI: 10.3389/fncel.2023.1212975

Consensus recommendations on organization of care for individuals with Phelan-McDermid syndrome

Autori: A.M. van Eeghen, D. Stemkens, José Ramón Fernández-Fructuoso, A. Maruani, K. Hadzsiev, I.D.C. van Balkom, C.M.W. Gaasterland, M.J. Klein Haneveld, Klea Vyshka, A. Hugon, A.M. van Eeghen, Norma Alhambra, Britt-Marie Anderlid, Stephanie Andres, Emmelien Aten, Rui Barbosa Guedes, Maria C. Bonaglia, Thomas Bourgeron, Monica Burdeus-Olavarrieta, Maya J. Carbin, Jennifer Cooke, Robert J. Damstra, Ire
Pubblicato in: European Journal of Medical Genetics, Numero 66, 2023, Pagina/e 104747, ISSN 1769-7212
Editore: Elsevier BV
DOI: 10.1016/j.ejmg.2023.104747

Automated approach for quality assessment of RDF resources

Autori: Shuxin Zhang, Nirupama Benis, Ronald Cornet
Pubblicato in: BMC Medical Informatics and Decision Making, Numero 23, 2024, ISSN 1472-6947
Editore: BioMed Central
DOI: 10.1186/s12911-023-02182-8

Machine learning in Huntington’s disease: exploring the Enroll-HD dataset for prognosis and driving capability prediction

Autori: Jasper Ouwerkerk, Stephanie Feleus, Kasper F. van der Zwaan, Yunlei Li, Marco Roos, Willeke M. C. van Roon-Mom, Susanne T. de Bot, Katherine J. Wolstencroft, Eleni Mina
Pubblicato in: Orphanet Journal of Rare Diseases, Numero 18, 2023, ISSN 1750-1172
Editore: BioMed Central
DOI: 10.1186/s13023-023-02785-4

Interactive neuroinflammation pathways and transcriptomics-based identification of drugs and chemical compounds for schizophrenia

Autori: Lisa Koole, Pilar Martinez-Martinez, Therese van Amelsvoort, Chris T. Evelo, Friederike Ehrhart
Pubblicato in: The World Journal of Biological Psychiatry, Numero 25, 2024, Pagina/e 116-129, ISSN 1562-2975
Editore: WFSBP
DOI: 10.1080/15622975.2023.2281514

Improved Diagnosis of Rare Disease Patients through Systematic Detection of Runs of Homozygosity

Autori: Leslie Matalonga, Steven Laurie, Anastasios Papakonstantinou, Davide Piscia, Elisabetta Mereu, Gemma Bullich, Rachel Thompson, Rita Horvath, Luis Pérez-Jurado, Olaf Riess, Ivo Gut, Gert-Jan van Ommen, Hanns Lochmüller, Sergi Beltran, Alessandra Renieri, Ali Dursun, Antoni Matilla-Duenas, Bru Cormand, Carlo Rivolta, Carmen Ayuso, Carmen Espinós, Christian Scerri, Dilek Yalnizoglu, Doriette Soler
Pubblicato in: The Journal of Molecular Diagnostics, Numero 22/9, 2020, Pagina/e 1205-1215, ISSN 1525-1578
Editore: American Society for Investigative Pathology
DOI: 10.1016/j.jmoldx.2020.06.008

ABCA4 c.6480-35A>G, a novel branchpoint variant associated with Stargardt disease

Autori: María Rodríguez-Hidalgo, Suzanne E. de Bruijn, Zelia Corradi, Kim Rodenburg, Araceli Lara-López, Alicia Valverde-Megías, Almudena Ávila-Fernández, Lidia Fernandez-Caballero, Marta Del Pozo-Valero, Jordi Corominas, Christian Gilissen, Cristina Irigoyen, Frans P. M. Cremers, Carmen Ayuso, Javier Ruiz-Ederra, Susanne Roosing
Pubblicato in: Frontiers in Genetics, Numero 14, 2023, ISSN 1664-8021
Editore: Frontiers Media
DOI: 10.3389/fgene.2023.1234032

Appraising the Role of Astrocytes as Suppliers of Neuronal Glutathione Precursors

Autori: Dolores Pérez-Sala, María A. Pajares
Pubblicato in: International Journal of Molecular Sciences, Numero 24, 2023, Pagina/e 8059, ISSN 1422-0067
Editore: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/ijms24098059

Gene-environment interaction elicits dystonia-like features and impaired translational regulation in a DYT-TOR1A mouse model

Autori: Colette Reinhold, Susanne Knorr, Rhonda L. McFleder, Lisa Rauschenberger, Muthuraman Muthuraman, Panagiota Arampatzi, Tom Gräfenhan, Andreas Schlosser, Michael Sendtner, Jens Volkmann, Chi Wang Ip
Pubblicato in: Neurobiology of Disease, Numero 193, 2024, Pagina/e 106453, ISSN 0969-9961
Editore: Academic Press
DOI: 10.1016/j.nbd.2024.106453

Optimizing designs in clinical trials with an application in treatment of Epidermolysis bullosa simplex, a rare genetic skin disease

Autori: Joakim Nyberg, Andrew C. Hooker, Georg Zimmermann, Johan Verbeeck, Martin Geroldinger, Konstantin Emil Thiel, Geert Molenberghs, Martin Laimer, Verena Wally
Pubblicato in: Computational Statistics & Data Analysis, Numero 199, 2024, Pagina/e 108015, ISSN 0167-9473
Editore: Elsevier BV
DOI: 10.1016/j.csda.2024.108015

Beyond Pathway Analysis: Identification of Active Subnetworks in Rett Syndrome

Autori: Ryan A. Miller, Friederike Ehrhart, Lars M. T. Eijssen, Denise N. Slenter, Leopold M. G. Curfs, Chris T. Evelo, Egon L. Willighagen, Martina Kutmon
Pubblicato in: Frontiers in Genetics, Numero 10, 2019, ISSN 1664-8021
Editore: Frontiers Media
DOI: 10.3389/fgene.2019.00059

Statistical recommendations for count, binary, and ordinal data in rare disease cross-over trials

Autori: Martin Geroldinger; Johan Verbeeck; Andrew C. Hooker; Konstantin E. Thiel; Geert Molenberghs; Joakim Nyberg; Johann Bauer; Martin Laimer; Verena Wally; Arne C. Bathke; Georg Zimmermann
Pubblicato in: Orphanet J Rare Dis, Numero 18(1):391, 2023, ISSN 1750-1172
Editore: BioMed Central
DOI: 10.1186/s13023-023-02990-1

Semantic modelling of Common Data Elements for Rare Disease registries, and a prototype workflow for their deployment over registry data

Autori: Rajaram Kaliyaperumal; Mark D Wilkinson; Pablo Alarcón Moreno; Nirupama Benis; Ronald Cornet; Bruna dos Santos Vieira; Michel Dumontier; César Henrique Bernabé; Annika Jacobsen; Clémence M. A. Le Cornec; Mario Prieto Godoy; Núria Queralt-Rosinach; Leo J Schultze Kool; Morris A Swertz; Philip van Damme; Joeri K van der Velde; Nawel van Lin; Shuxin Zhang; Marco Roos
Pubblicato in: Journal of Biomedical Semantics, 2022, ISSN 2041-1480
Editore: BioMed Central
DOI: 10.1186/s13326-022-00264-6

Protein domains provide a new layer of information for classifying human variations in rare diseases

Autori: Mélanie Corcuff; Marc Garibal; Jean-Pierre Desvignes; Céline Guien; Coralie Grattepanche; Gwenaëlle Collod-Béroud; Estelle Ménoret; David Salgado; Christophe Béroud; Christophe Béroud
Pubblicato in: Front Bioinform, 2023, ISSN 2673-7647
Editore: Frontiers Media S.A
DOI: 10.3389/fbinf.2023.1127341

Copy number variant risk loci for schizophrenia converge on the BDNF pathway

Autori: Friederike Ehrhart, Ana Silva, Therese van Amelsvoort, Emma von Scheibler, Chris Evelo, David E.J Linden
Pubblicato in: The World Journal of Biological Psychiatry, Numero 25, 2024, Pagina/e 222-232, ISSN 1562-2975
Editore: WFSBP
DOI: 10.1080/15622975.2024.2327027

SUsPECT: A pipeline for variant effect prediction based on custom long-read transcriptomes for improved clinical variant

Autori: Renee Salz, Nuno Saraiva-Agostinho, Emil Vorsteveld, Caspar I. van der Made, Simone Kersten, Merel Stemerdink, Jamie Allen, Pieter-Jan Volders, Sarah E. Hunt, Alexander Hoischen, Peter A.C. ’t Hoen
Pubblicato in: BARI RD conference, 2022
Editore: CSHL
DOI: 10.1101/2022.10.23.513417

A Systems Biology Workflow to Support the Diagnosis of Inherited Metabolic Disorders: a study on Pyrimidine and Urea Cycle disorders

Autori: Denise N. Slenter, Irene M.G.M. Hemel, Chris T. Evelo, Jörgen Bierau, Egon L. Willighagen, Laura K.M. Steinbusch
Pubblicato in: medRxiv, 2022
Editore: Cold Spring Harbour Laboratory
DOI: 10.1101/2022.01.31.21265847

Lightweight Distributed Provenance Model for Complex Real–world Environments

Autori: Rudolf Wittner; Cecilia Mascia; Matej Gallo; Francesca Frexia; Heimo Müller; Markus Plass; Jörg Geiger; Petr Holub
Pubblicato in: Crossref, Numero 1, 2022
Editore: Sci Data
DOI: 10.1038/s41597-022-01537-6

A polymorphic AT-repeat causes frequent allele dropout for an MME mutational hotspot exon

Autori: Helle Høyer; Hilde T Hilmarsen; Raute Sunder-Plassmann; Geir J Braathen; Peter M Andersen; Christian Beetz; Sandra Hacker; Øystein L Holla; Ingo Kurth; Wolfgang N Löscher; Simone B C F Reiter; Sabine Rudnik-Schöneborn; Linda Strand; Reinhard Windhager; Martina Witsch-Baumgartner; Jan Senderek; Michaela Auer-Grumbach
Pubblicato in: Crossref, Numero Oct;59(10):1024-1026, 2022
Editore: J Med Genet
DOI: 10.1136/jmedgenet-2021-108281

Alpha‐Synuclein is Involved in <scp>DYT1</scp> Dystonia Striatal Synaptic Dysfunction

Autori: Giulia Ponterio; Gaia Faustini; Ilham El Atiallah; Giuseppe Sciamanna; Maria Meringolo; Annalisa Tassone; Paola Imbriani; Silvia Cerri; Giuseppina Martella; Paola Bonsi; Arianna Bellucci; Antonio Pisani
Pubblicato in: Crossref, Numero 37(5):949-961, 2022
Editore: Mov Disord
DOI: 10.1002/mds.29024

The European Genome-phenome Archive in 2021.

Autori: Mallory A. Freeberg; Lauren A Fromont; Teresa D’Altri; Anna Foix Romero; Jorge Izquierdo Ciges; Aina Jene; Giselle Kerry; Mauricio Moldes; Roberto Ariosa; Silvia Bahena; Daniel Barrowdale; Marcos Casado Barbero; Dietmar Fernandez-Orth; Carles Garcia-Linares; Emilio Garcia-Rios; Frédéric Haziza; Bela Juhasz; Oscar Martinez Llobet; Gemma Milla; Anand Mohan; Manuel Rueda; Aravind Sankar; Dona Sha
Pubblicato in: Nucleic Acids Research, Numero Volume 50, Numero D1, 7 January 2022, 2021, Pagina/e Pages D980–D987
Editore: Oxford Academic
DOI: 10.1093/nar/gkab1059

A mosaic PIK3CA variant in a young adult with diffuse gastric cancer: case report.

Autori: te Paske, Iris B. A. W.; Garcia-Pelaez, José; Sommer, Anna K.; Matalonga, Leslie; Starzynska, Teresa; Jakubowska, Anna; Valle, Laura; Capella, Gabriel; Aretz, Stefan; Holinski-Feder, Elke; Steinke-Lange, Verena; Laner, Andreas; Schröck, Evelin; Rump, Andreas; Ligtenberg, Marjolijn; Hoischen, Alexander; Geverink, Nicoline; Evans, D. Gareth; Tischkowitz, Marc; Laurie, Steven; van der Post, Rachel
Pubblicato in: European Journal of Human Genetics ,, Numero vol. 29 , no. 9, 2021, Pagina/e pp. 1354-1358
Editore: European Journal of Genetics
DOI: 10.1038/s41431-021-00853-6

Isolation and transfection of myenteric neurons from mice for patch-clamp applications

Autori: Samuel Kuehs; Laura Teege; Ann-Katrin Hellberg; Christina Stanke; Natja Haag; Ingo Kurth; Robert Blum; Carla Nau; Enrico Leipold
Pubblicato in: Crossref, Numero 1, 2022
Editore: Front. Mol. Neurosci
DOI: 10.3389/fnmol.2022.1076187

De-novo FAIRification via an Electronic Data Capture system by automated transformation of filled electronic Case Report Forms into machine-readable data.

Autori: Martijn G. Kersloot; Annika Jacobsen; Karlijn H. J. Groenen; Bruna dos Santos Vieira; Rajaram Kaliyaperumal; Ameen Abu-Hanna; Ronald Cornet; Peter A C 't Hoen; Marco Roos; Leo J. Schultze Kool; Derk L. Arts
Pubblicato in: VOLUME=122;TITLE=Journal of Biomedical Informatics, Numero 1, 2021
Editore: Science direct
DOI: 10.1016/j.jbi.2021.103897

Variant recurrence confirms the existence of a FBXO31 ‐related spastic‐dystonic cerebral palsy syndrome

Autori: Dzinovic, I.; Škorvánek, M.; Pavelekova, P.; Zhao, C.; Keren, B.; Whalen, S.; Bakhtiari, S.; Chih Jin, S.; Kruer, M.C.; Jech, R.; Winkelmann, J.; Zech, M.
Pubblicato in: Annals of Clinical and Translational Neurology, Vol 8, Iss 4, Pp 951-955 (2021), Numero 1, 2021
Editore: Ann Clin Transl Neurol

Vesicular Acetylcholine Transporter Alters Cholinergic Tone and Synaptic Plasticity in DYT1 Dystonia.

Autori: Annalisa Tassone; Giuseppina Martella; Maria Meringolo; Valentina Vanni; Giuseppe Sciamanna; Giulia Ponterio; Paola Imbriani; Paola Bonsi; Antonio Pisani
Pubblicato in: Movement disorders, Numero 1, 2021
Editore: Movement disorders
DOI: 10.1002/mds.28698

FAIR Genomes metadata schema promoting Next Generation Sequencing data reuse in Dutch healthcare and research

Autori: K. Joeri van der Velde; Gurnoor Singh; Rajaram Kaliyaperumal; XiaoFeng Liao; Sander de Ridder; Susanne Rebers; Hindrik H. D. Kerstens; Fernanda de Andrade; Jeroen van Reeuwijk; Fini E. De Gruyter; Saskia Hiltemann; Maarten Ligtvoet; Marjan M. Weiss; Hanneke W. M. van Deutekom; Anne M. L. Jansen; Andrew P. Stubbs; Lisenka E. L. M. Vissers; Jeroen F. J. Laros; Esther van Enckevort; Daphne Stemkens;
Pubblicato in: van der Velde , K J , Singh , G , Kaliyaperumal , R , Liao , X , de Ridder , S , Rebers , S , Kerstens , H H D , de Andrade , F , van Reeuwijk , J , de Gruyter , F E , Hiltemann , S , Ligtvoet , M , Weiss , M M , van Deutekom , H W M , Jansen , A M L , Stubbs , A P , Vissers , L E L M , Laros , J F J , van Enckevort , E , Stemkens , D , ‘t Hoen , P A C , Beliën , J A M , van Gijn , M E & Swertz, Numero 1, 2022
Editore: Scientific data
DOI: 10.1038/s41597-022-01265-x

A formalization of one of the main claims of “Overlap of vitamin A and vitamin D target genes with CAKUT-related processes” by Ozisik et al. 2021.

Autori: Friederike Ehrhart, Chris T. Evelo
Pubblicato in: Data Science, Numero 5(1), 2022, Pagina/e 25-27
Editore: IOS Press
DOI: 10.3233/ds-210041

Long-read technologies identify a hidden inverted duplication in a family with choroideremia

Autori: Zeinab Fadaie; Kornelia Neveling; Tuomo Mantere; Ronny Derks; Lonneke Haer-Wigman; Amber den Ouden; Michael Kwint; Luke O’Gorman; Dyon Valkenburg; Carel B. Hoyng; Christian Gilissen; Lisenka E.L.M. Vissers; Marcel R. Nelen; Frans P.M. Cremers; Alexander Hoischen; Susanne Roosing
Pubblicato in: HGG Advances, 2, 1 - 11, Numero 1, 2022
Editore: Science direct
DOI: 10.1016/j.xhgg.2021.100046

A Community-Driven, Openly Accessible Molecular Pathway Integrating Knowledge on Malignant Pleural Mesothelioma

Autori: Marvin Martens; Franziska Kreidl; Friederike Ehrhart; Didier Jean; Merlin Mei; Holly M. Mortensen; Alistair Nash; Penny Nymark; Chris T. Evelo; Ferdinando Cerciello
Pubblicato in: "Frontiers in Oncology, Frontiers, 2022, 12, pp.849640. ⟨10.3389/fonc.2022.849640⟩", Numero 1, 2022
Editore: Frontiers in oncology
DOI: 10.3389/fonc.2022.849640

Beacon v2 and Beacon networks: A “lingua franca” for federated data discovery in biomedical genomics, and beyond

Autori: Jordi Rambla; Michael Baudis; Roberto Ariosa; Tim Beck; Lauren A. Fromont; Arcadi Navarro; Rahel Paloots; Manuel Rueda; Gary Saunders; Babita Singh; John D. Spalding; Juha Törnroos; Claudia Vasallo; Colin D. Veal; Anthony J. Brookes
Pubblicato in: instname:, Numero 1, 2022
Editore: Zurich Open Repository and Archive, University of Zurich
DOI: 10.1002/humu.24369

Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNA.

Autori: Daan H H M Viering; Karl-Peter Schlingmann; Marguerite Hureaux; Tom Nijenhuis; Andrew Mallett; Melanie Chan; André P van Beek; Albertien M. van Eerde; Jean-Marie Coulibaly; Marion Vallet; Stéphane Decramer; Solenne Pelletier; Günter Klaus; Martin Kömhoff; Rolf Beetz; Chirag Patel; Mohan Shenoy; Eric J. Steenbergen; Glenn Anderson; Ernie M.H.F. Bongers; Carsten Bergmann; Daan M. Panneman; Richa
Pubblicato in: VOLUME=33;STARTPAGE=305;ENDPAGE=325;ISSN=1046-6673;TITLE=Journal of the American Society of Nephrology, Numero 1, 2022
Editore: JASN
DOI: 10.1681/asn.2021050596

Systematic Collaborative Reanalysis of Genomic Data Improves Diagnostic Yield in Neurologic Rare Diseases

Autori: Gemma Bullich; Leslie Matalonga; Montserrat Pujadas; Anastasios Papakonstantinou; Davide Piscia; Raúl Tonda; Rafael Artuch; Pia Gallano; Glòria Garrabou; Juan R. González; Daniel Grinberg; Míriam Guitart; Steven Laurie; Conxi Lázaro; Cristina Luengo; Ramon Martí; Montserrat Milà; David Ovelleiro; Genís Parra; Aurora Pujol; Eduardo Tizzano; Alfons Macaya; Francesc Palau; Antònia Ribes; Lui
Pubblicato in: reponame:r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau, Numero 1, 2022
Editore: The journal of molecular diagnostics
DOI: 10.1016/j.jmoldx.2022.02.003

Frameshift mutation S368fs in the gene encoding cytoskeletal β-actin leads to ACTB-associated syndromic thrombocytopenia by impairing actin dynamics

Autori: Johannes N. Greve; Frederic V. Schwäbe; Thomas Pokrant; Jan Faix; Nataliya Di Donato; Manuel H. Taft; Dietmar J. Manstein
Pubblicato in: Crossref, Numero 1, 2022
Editore: Elsevier GmbH
DOI: 10.1016/j.ejcb.2022.151216

Goal-models to support communication, planning and guiding of FAIRification

Autori: Bernab��, C��sar Henrique; Jacobsen, Annika; Queralt Rosinach, N��ria; Bonino da Silva Santos, Luiz Olavo; Silva Souza, V��tor E.; Mons, Barend; Roos, Marco
Pubblicato in: Zenodo, Numero 1, 2021
Editore: Zenodo
DOI: 10.5281/zenodo.5784628

Financing models for sustainable data reuse infrastructure

Autori: Hooft, Rob; Roos, Marco
Pubblicato in: Numero 5, 2023
Editore: Zenodo
DOI: 10.5281/zenodo.7949903

Applying the FAIR Data Principles to the Registry of Vascular Anomalies (VASCA)

Autori: Bruna dos Santos Vieira, Karlijn Groenen, P.A.C. ‘t Hoen, Annika Jacobsen, Marco Roos, Rajaram Kaliyaperumal, Martijn Kersloot, Ronald Cornet, Leo Schultze Kool
Pubblicato in: Studies in Health Technology and Informatics, Numero Volume 271: dHealth 2020 – Biomedical Informatics for Health and Care, 2020, Pagina/e 115 - 116, ISSN 0926-9630
Editore: IOS Press
DOI: 10.3233/shti200085

A FAIR data model for PRISMA (Personalised RISk-based MAmmascreening) Study

Autori: Liao, Xiaofeng; de Jong, Milou; van Damme, Philip; Cornet, Ronald; Dos Santos Vieira, Bruna; Lutomski, Jennifer; Brullemans-Spansier, Mirjam; 't Hoen, Peter
Pubblicato in: Zenodo, Numero 1, 2022
Editore: Zenodo
DOI: 10.5281/zenodo.7029267

Converging pathways found in copy number variation syndromes with high schizophrenia risk

Autori: Friederike Ehrhart, Ana Silva, Therese van Amelsvoort, Emma von Scheibler, Chris Evelo, David E.J. Linden
Pubblicato in: bioRxiv, 2022, Pagina/e United States
Editore: Cold Spring Harbour Laboratory
DOI: 10.1101/2022.02.07.479370

Rare disease education in Europe and beyond: time to act

Autori: Birute Tumiene 1, Harm Peters 2 3, Bela Melegh 4, Borut Peterlin 5, Algirdas Utkus 1 3, Natalja Fatkulina 6, György Pfliegler 7, Holm Graessner 8 9, Sanja Hermanns 8 9, Maurizio Scarpa 10, Jean-Yves Blay 11, Sharon Ashton 12, Lucy McKay 13, Gareth Baynam 14 15 16
Pubblicato in: Orphanet Journal of Rare disease, Numero 19;17(1):441, 2022
Editore: BMC
DOI: 10.1186/s13023-022-02527-y

The impact of dedicated FAIRification stewardship guiding European Reference Networks towards making rare disease resources FAIR

Autori: Inês Henriques; Bruna dos Santos Vieira; César Henriques Bernabé; Shuxin Zhang; Alberto Cámara Ballesteros; Jose Antonio Ramírez García; Joeri van der Velde; Nirupama Benis; Peter 't Hoen; Marco Roos; Annika Jacobsen; Ronald Cornet; Mark Wilkinson; Franz Schaefer; Morris Swertz
Pubblicato in: Numero 9, 2023
Editore: Zenodo
DOI: 10.5281/zenodo.7915232

Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

Autori: Matalonga, Leslie; Hernández-Ferrer, Carles; Piscia, Davide; Schüle, Rebecca; Synofzik, Matthis; Töpf, Ana; Vissers, Lisenka E. L. M.; de Voer, Richarda; Tonda, Raul; Laurie, Steven; Fernandez-Callejo, Marcos; Picó, Daniel; Garcia-Linares, Carles; Papakonstantinou, Anastasios; Corvó, Alberto; Joshi, Ricky; Diez, Hector; Gut, Ivo; Hoischen, Alexander; Graessner, Holm; Beltran, Sergi; Cohen, En
Pubblicato in: European journal of human genetics, Numero 1, 2021
Editore: Eur J Hum Genet
DOI: 10.1038/s41431-021-00852-7

Overview of treatment strategies in paraneoplastic neurological syndromes

Autori: Jeroen Kerstens, Maarten J. Titulaer
Pubblicato in: Handbook of Clinical Neurology, Paraneoplastic Neurologic Disorders, 2024, Pagina/e 97-112, ISSN 0072-9752
Editore: Elsevier
DOI: 10.1016/b978-0-12-823912-4.00015-3

Privacy-Preserving Linkage of Distributed Pseudonymised Datasets in a Virtual European Rare Disease Platform

Autori: Dieter Hayn, Emanuel Sandner, Abishaa Vengadeswaran, Elena-Alexandra Tãtaru, Mark Wilkinson, Marc Hanauer, Karl Kreiner, Guenter Schreier
Pubblicato in: Studies in Health Technology and Informatics, Digital Health and Informatics Innovations for Sustainable Health Care Systems, 2024
Editore: IOS Press
DOI: 10.3233/shti240683

Performance assessment of ontology matching systems for FAIR data

Autori: Philip van Damme; Jesualdo Tomás Fernández-Breis; Nirupama Benis; Jose Antonio Miñarro-Gimenez; Nicolette F. de Keizer; Ronald Cornet
Pubblicato in: Journal of Biomedical Semantics, 13(1):19. BioMed Central Ltd., Numero 1, 2022, ISSN 2041-1480
Editore: Journal of biomedical semantics
DOI: 10.1186/s13326-022-00273-5

Solving unsolved rare neurological diseases—a Solve-RD viewpoint

Autori: Schüle, Rebecca; Timmann, Dagmar; Erasmus, Corrie E.; Reichbauer, Jennifer; Wayand, Melanie; van de Warrenburg, Bart; Schöls, Ludger; Wilke, Carlo; Bevot, Andrea; Zuchner, Stephan; Beltran, Sergi; Laurie, Steven; Matalonga, Leslie; Graessner, Holm; Synofzik, Matthis; Baets, Jonathan; Balicza, Peter; Chinnery, Patrick; Dürr, Alexandra; Haack, Tobias; Hengel, Holger; Horvath, Rita; Houlden, Henry
Pubblicato in: European journal of human genetics, Numero 1, 2021, ISSN 1476-5438
Editore: European Journal of Human Genetics
DOI: 10.1038/s41431-021-00901-1

Possible role for rare TRPM7 variants in patients with hypomagnesaemia with secondary hypocalcaemia

Autori: Rosa Vargas-Poussou; Felix Claverie-Martin; Caroline Prot-Bertoye; Valentina Carotti; Jenny van der Wijst; Ana Perdomo-Ramirez; Gloria M Fraga-Rodriguez; Marguerite Hureaux; Caro Bos; Femke Latta; Pascal Houillier; Joost G J Hoenderop; Jeroen H F de Baaij
Pubblicato in: reponame:r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau, Numero 1, 2022, ISSN 0931-0509
Editore: Oxford University Press
DOI: 10.1093/ndt/gfac182

Applying the FAIR principles to data in a hospital: challenges and opportunities in a pandemic

Autori: Queralt Rosinach, N.; Kaliyaperumal, R.; Bernabe, C.H.; Long, Q.Q.; Joosten, S.A.; Wijk, H.J. van der; Flikkenschild, E.L.A.; Burger, K.; Jacobsen, A.; Mons, B.; Roos, M.; BEAT COVID Grp; COVID-19 LUMC Grp
Pubblicato in: Journal of Biomedical Semantics, 13(1). BMC, Numero 1, 2022, ISSN 2041-1480
Editore: BMC
DOI: 10.1186/s13326-022-00263-7

DMD – BIOMARKERS & OUTCOME MEASURES

Autori: I. Verhaart, P. 'tHoen, M. Roos, E. Vroom
Pubblicato in: Neuromuscular Disorders, Numero 30, 2020, Pagina/e S86, ISSN 0960-8966
Editore: Elsevier BV
DOI: 10.1016/j.nmd.2020.08.137

The de novo FAIRification process of a registry for vascular anomalies

Autori: Karlijn H.J. Groenen, Annika Jacobsen, Martijn G. Kersloot, Bruna Vieira, Esther van Enckevort, Rajaram Kaliyaperumal, Derk L. Arts, Peter A.C. ‘t Hoen, Ronald Cornet, Marco Roos, Leo Schultze Kool
Pubblicato in: Orphanet Journal of Rare Diseases, Numero 16(1), 2021, Pagina/e 376, ISSN 1750-1172
Editore: BioMed Central
DOI: 10.1186/s13023-021-02004-y

Understanding signaling and metabolic paths using semantified and harmonized information about biological interactions

Autori: Ryan A. Miller; Martina Kutmon; Anwesha Bohler; Andra Waagmeester; Chris T. Evelo; Egon Willighagen
Pubblicato in: Plos one, Numero 1, 2022, ISSN 1932-6203
Editore: Public Library of Science
DOI: 10.1101/2020.07.31.230599

The “A” of FAIR – As Open as Possible, as Closed as Necessary

Autori: Annalisa Landi, Mark Thompson, Viviana Giannuzzi, Fedele Bonifazi, Ignasi Labastida, Luiz Olavo Bonino da Silva Santos, Marco Roos
Pubblicato in: Data Intelligence, Numero 2/1-2, 2020, Pagina/e 47-55, ISSN 2641-435X
Editore: The MIT PressJournals
DOI: 10.1162/dint_a_00027

10th European Conference on Rare Diseases & Orphan Products (ECRD 2020)

Autori: Marco Roos, Mark D. Wilkinson, Ronald Cornet, Deborah Mascalzoni, Veronica Popa, Ian Harrow,Claudio Carta, Yaffa R. Rubinstein, Dipak Kalra, Ana Rath, Victoria Hedley, Gülçin Gümüş
Pubblicato in: Orphanet Journal of Rare Diseases, Numero 15/S1, 2020, ISSN 1750-1172
Editore: BioMed Central
DOI: 10.1186/s13023-020-01550-1

Recommendations for whole genome sequencing in diagnostics for rare diseases

Autori: Erika Souche Sergi Beltran, Erwin Brosens, John W Belmont, Magdalena Fossum, Olaf Riess, Christian Gilissen, Amin Ardeshirdavani, Gunnar Houge, Marielle van Gijn , Jill Clayton-Smith , Matthis Synofzik , Nicole de Leeuw, Zandra C Deans, Yasemin Dincer, Sebastian H Eck, Saskia van der Crabben, Meena Balasubramanian, Holm Graessner , Marc Sturm, Helen Firth, Alessandra Ferlini, Rima Nabbout, Elfrid
Pubblicato in: Eur. J. Hum. Genet., Numero Sep;30(9), 2022, Pagina/e 1017-1021, ISSN 1476-5438
Editore: European Journal of Human Genetics
DOI: 10.1038/s41431-022-01113-x

Whole genome sequencing and in vitro splice assays reveal genetic causes for inherited retinal diseases.

Autori: Zeinab Fadaie; Laura Whelan; Tamar Ben-Yosef; Adrian Dockery; Zelia Corradi; Christian Gilissen; Lonneke Haer-Wigman; Jordi Corominas; Galuh D.N. Astuti; Galuh D.N. Astuti; Laura de Rooij; L. Ingeborgh van den Born; Caroline C W Klaver; Caroline C W Klaver; Carel B. Hoyng; Niamh Wynne; Emma Duignan; Paul F. Kenna; Paul F. Kenna; Frans P.M. Cremers; G. Jane Farrar; Susanne Roosing
Pubblicato in: NPJ Genomic Medicine, 6, Numero 1, 2021, ISSN 2056-7944
Editore: Genomic medicine
DOI: 10.1038/s41525-021-00261-1

The Data Use Ontology to streamline responsible access to human biomedical datasets.

Autori: Jonathan Lawson; Moran N. Cabili; Giselle Kerry; Tiffany Boughtwood; Adrian Thorogood; Adrian Thorogood; Pinar Alper; Sarion R. Bowers; Rebecca R. Boyles; Anthony J. Brookes; Matthew Brush; Tony Burdett; Hayley L. Clissold; Stacey Donnelly; Stephanie O. M. Dyke; Mallory A. Freeberg; Melissa Haendel; Chihiro Hata; Petr Holub; Francis Jeanson; Aina Jene; Minae Kawashima; Shuichi Kawashima; Melissa A
Pubblicato in: Cell genome, Numero 1, 2021, ISSN 2666-979X
Editore: Cell genome
DOI: 10.1016/j.xgen.2021.100028

Myopathic mitochondrial DNA depletion syndrome associated with biallelic variants in LIG3.

Autori: Federica Invernizzi; Andrea Legati; Alessia Nasca; Eleonora Lamantea; Barbara Garavaglia; Mirjana Gusic; Robert Kopajtich; Holger Prokisch; Massimo Zeviani; Costanza Lamperti; Daniele Ghezzi
Pubblicato in: Brain, Numero Volume 144, Numero 9, 2021, Pagina/e e74, ISSN 1460-2156
Editore: Oxford academic
DOI: 10.1093/brain/awab238

Adenine base editing efficiently restores the function of Fanconi anemia hematopoietic stem and progenitor cells

Autori: Sebastian M. Siegner; Laura Ugalde; Alexandra Clemens; Laura Garcia-Garcia; Juan A. Bueren; Paula Rio; Mehmet E. Karasu; Jacob E. Corn
Pubblicato in: Nature Communications, 13 (1), Numero 1, 2022, ISSN 2041-1723
Editore: Nature Publishing Group
DOI: 10.3929/ethz-b-000582242

Identifying obstacles hindering the conduct of academic-sponsored trials for drug repurposing on rare-diseases: an analysis of six use cases

Autori: Marta del Álamo; Christoph Bührer; Dirk Fisher; Matthias Griese; Paul Lingor; Giovanni Palladini; Nicolas Sireau; Virginie Hivert; Luca Sangiorgi; Florence Guillot; Juliane Halftermeyer; Lenka Soucková; Kristýna Nosková; Regina Demlová
Pubblicato in: Crossref, Numero 1, 2022, ISSN 1745-6215
Editore: BioMed Central
DOI: 10.1186/s13063-022-06713-y

The COVID-19 epidemiology and monitoring ontology

Autori: Queralt-Rosinach, Núria; Schofield, Paul N.; Hoehndorf, Robert; Weiland, Claus; Schultes, Erik; Bernabé, César H.; Roos, Marco
Pubblicato in: BioHackrXiv, Numero 6, 2021
Editore: BioHackrXiv
DOI: 10.37044/osf.io/n6tcz

Reuse of design pattern measurements for health data.

Autori: Núria Queralt-Rosinach1, Mark Wilkinson2, Rajaram Kaliyaperumal1,César H. Bernabé1, Qinqin Long1, Michel Dumontier3, Paul N. Schofield4andMarco Roos
Pubblicato in: CEUR Workshop Proceedings, 2021, ISSN 1613-0073
Editore: University of Cambridge
DOI: 10.17863/cam.77969

The COVID-19 epidemiology and monitoring ontology

Autori: Queralt-Rosinach, Núria Schofield, Paul Hoehndorf, Robert Weiland, Claus Schultes, Erik Bernabé, César Roos, Marco
Pubblicato in: ISMB 2021, 2021
Editore: Zenodo

Proceedings of the 20th International Vasculitis and ANCA workshop 3-6th April 2022

Autori: Michael Clarkson; Allyson Egan; Mark A Little
Pubblicato in: Zenodo, Numero 58, 2022
Editore: Zenodo
DOI: 10.5281/zenodo.7154405

FAIR metadata, models, and interfaces to support machine-readable data access and use conditions

Autori: null null, Oussama Mohammed Benhamed
Pubblicato in: 2024
Editore: Universidad Politecnica de Madrid - University Library
DOI: 10.20868/upm.thesis.81819

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