講演情報
[IL1]Is there still a need for clinical geneticists in a new AI world?
Alain Verloes (Department of Genetics, Robert DEBRE University Hospital, Paris, France / European Reference Network for (neuro)developmental anomalies ERN-ITHACA)
Short Biography
Alain Verloes, MD, PhD (born in 1957 in Belgium) is Full Professor of Medical Genetics at Université Paris Cité since 2001. He heads the Clinical Genetics Unit (since 2001) and the Department of Genetics (since 2012) at Robert Debré University Hospital in Paris. He earned his MD at Université libre de Bruxelles in 1982, trained in Paediatrics and Genetics at Université de Liège (Belgium), where he completed a PhD in 1997. From 1989 to 2001, he was Clinical Geneticist, and from 1998 to 2001 Clinical Professor of Genetics at Université de Liège. He led the French Reference Centre for Rare Disorders “Developmental Anomalies and MCA Syndromes – Île-de-France” (2005–2023), has coordinated the European Reference Network ERN-ITHACA on (neuro)developmental disorders since 2019, and co-organises the annual EuroDysmorpho meeting (since 2013) and EuroNDD conference (since 2023). He has served as Editor-in-Chief of the European Journal of Medical Genetics since 2011. His research interests focus on RASopathies, primary microcephalies and the genetic causes of intellectual disability. As of Septembre 2025 he is the author or co-author of 22 book chapters and 547 peer-reviewed articles and letters, with an H-index of 70 (Web of Science).
Alain Verloes, MD, PhD (born in 1957 in Belgium) is Full Professor of Medical Genetics at Université Paris Cité since 2001. He heads the Clinical Genetics Unit (since 2001) and the Department of Genetics (since 2012) at Robert Debré University Hospital in Paris. He earned his MD at Université libre de Bruxelles in 1982, trained in Paediatrics and Genetics at Université de Liège (Belgium), where he completed a PhD in 1997. From 1989 to 2001, he was Clinical Geneticist, and from 1998 to 2001 Clinical Professor of Genetics at Université de Liège. He led the French Reference Centre for Rare Disorders “Developmental Anomalies and MCA Syndromes – Île-de-France” (2005–2023), has coordinated the European Reference Network ERN-ITHACA on (neuro)developmental disorders since 2019, and co-organises the annual EuroDysmorpho meeting (since 2013) and EuroNDD conference (since 2023). He has served as Editor-in-Chief of the European Journal of Medical Genetics since 2011. His research interests focus on RASopathies, primary microcephalies and the genetic causes of intellectual disability. As of Septembre 2025 he is the author or co-author of 22 book chapters and 547 peer-reviewed articles and letters, with an H-index of 70 (Web of Science).
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