O46: GenIDA, an international participatory database to better characterize comorbidities of genetic forms of intellectual disability: insights on Koolen-de Vries syndrome
| Main Authors: | , , , , , , , , , , , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2023-01-01
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| Series: | Genetics in Medicine Open |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2949774423006994 |
| _version_ | 1797341958961627136 |
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| author | Pauline Burger Florent Colin Axelle Strehle Timothée Mazzucotelli Nicole Collot Ariane Bouman Daphna Landau Prat David Geneviève Valentin Ruault Roseline Caumes Thomas Smol Jamal Ghoumid Joost Kummeling Charlotte Ockeloen Tjitske Kleefstra Pierre Parrend Amélie Piton David Koolen Jean-Louis Mandel |
| author_facet | Pauline Burger Florent Colin Axelle Strehle Timothée Mazzucotelli Nicole Collot Ariane Bouman Daphna Landau Prat David Geneviève Valentin Ruault Roseline Caumes Thomas Smol Jamal Ghoumid Joost Kummeling Charlotte Ockeloen Tjitske Kleefstra Pierre Parrend Amélie Piton David Koolen Jean-Louis Mandel |
| author_sort | Pauline Burger |
| collection | DOAJ |
| first_indexed | 2024-03-08T10:25:33Z |
| format | Article |
| id | doaj.art-4b842162beb74c9ea0073327de69ce27 |
| institution | Directory Open Access Journal |
| issn | 2949-7744 |
| language | English |
| last_indexed | 2024-03-08T10:25:33Z |
| publishDate | 2023-01-01 |
| publisher | Elsevier |
| record_format | Article |
| series | Genetics in Medicine Open |
| spelling | doaj.art-4b842162beb74c9ea0073327de69ce272024-01-27T07:10:46ZengElsevierGenetics in Medicine Open2949-77442023-01-0111100699O46: GenIDA, an international participatory database to better characterize comorbidities of genetic forms of intellectual disability: insights on Koolen-de Vries syndromePauline Burger0Florent Colin1Axelle Strehle2Timothée Mazzucotelli3Nicole Collot4Ariane Bouman5Daphna Landau Prat6David Geneviève7Valentin Ruault8Roseline Caumes9Thomas Smol10Jamal Ghoumid11Joost Kummeling12Charlotte Ockeloen13Tjitske Kleefstra14Pierre Parrend15Amélie Piton16David Koolen17Jean-Louis Mandel18Institut de Génétique et de Biologie Moléculaire et Cellulaire, Université de Strasbourg, INSERM, Illkirch, FranceInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Université de Strasbourg, INSERM, Illkirch, FranceInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Université de Strasbourg, INSERM, Illkirch, FranceInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Université de Strasbourg, INSERM, Illkirch, FranceInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Université de Strasbourg, INSERM, Illkirch, FranceDepartment of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, RadboudUMC, Nijmegen, The NetherlandsGoldschleger Eye Institute, Sheba Medical Center, Tel Hashomer, Israel; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, IsraelUniversité de Montpellier, CHU Montpellier, CLAD Sud Languedoc-Roussillon, INSERM, Montpellier, FranceUniversité de Montpellier, CHU Montpellier, CLAD Sud Languedoc-Roussillon, INSERM, Montpellier, FranceClinique de Génétique, CHU Lille, Lille, FranceInstitut de Génétique Médicale, CHU Lille, Lille, FranceClinique de Génétique, CHU Lille, Lille, FranceDepartment of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, RadboudUMC, Nijmegen, The NetherlandsDepartment of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, RadboudUMC, Nijmegen, The NetherlandsDepartment of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, RadboudUMC, Nijmegen, The NetherlandsICube, Université de Strasbourg, Strasbourg, France; EPITA, Strasbourg, FranceIGBMC INSERM, Illkirch; Laboratoire de diagnostic génétique, IGMA, HUS, StrasbourgDepartment of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, RadboudUMC, Nijmegen, The NetherlandsInstitut Universitaire de France; IGBMC, Université de Strasbourg, INSERM, Illkirch, France; Université de Strasbourghttp://www.sciencedirect.com/science/article/pii/S2949774423006994 |
| spellingShingle | Pauline Burger Florent Colin Axelle Strehle Timothée Mazzucotelli Nicole Collot Ariane Bouman Daphna Landau Prat David Geneviève Valentin Ruault Roseline Caumes Thomas Smol Jamal Ghoumid Joost Kummeling Charlotte Ockeloen Tjitske Kleefstra Pierre Parrend Amélie Piton David Koolen Jean-Louis Mandel O46: GenIDA, an international participatory database to better characterize comorbidities of genetic forms of intellectual disability: insights on Koolen-de Vries syndrome Genetics in Medicine Open |
| title | O46: GenIDA, an international participatory database to better characterize comorbidities of genetic forms of intellectual disability: insights on Koolen-de Vries syndrome |
| title_full | O46: GenIDA, an international participatory database to better characterize comorbidities of genetic forms of intellectual disability: insights on Koolen-de Vries syndrome |
| title_fullStr | O46: GenIDA, an international participatory database to better characterize comorbidities of genetic forms of intellectual disability: insights on Koolen-de Vries syndrome |
| title_full_unstemmed | O46: GenIDA, an international participatory database to better characterize comorbidities of genetic forms of intellectual disability: insights on Koolen-de Vries syndrome |
| title_short | O46: GenIDA, an international participatory database to better characterize comorbidities of genetic forms of intellectual disability: insights on Koolen-de Vries syndrome |
| title_sort | o46 genida an international participatory database to better characterize comorbidities of genetic forms of intellectual disability insights on koolen de vries syndrome |
| url | http://www.sciencedirect.com/science/article/pii/S2949774423006994 |
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