Alice Molle - French Institute of Health and Medical Research

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Papers共 6 篇Author StatisticsCo-AuthorSimilar Experts

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Rare Germline Heterozygous Missense Variants in BRCA1-associated Protein 1, BAP1, Cause a Syndromic Neurodevelopmental Disorder

Sebastien Kury,Frederic Ebstein,Alice Molle,Thomas Besnard,Ming-Kang Lee,Virginie Vignard,Tiphaine Hery,Mathilde Nizon,Grazia M. S. Mancini,Jacques C. Giltay,Benjamin Cogne,Kirsty McWalter,Wallid Deb,Hagar Mor-Shaked,Hong Li,Rhonda E. Schnur,Ingrid M. Wentzensen,Anne-Sophie Denomme-Pichon,Cynthia Fourgeux,Frans W. Verheijen, Eva Faurie,Rachel Schot,Cathy A. Stevens,Daphne J. Smits,Eileen Barr,Ruth Sheffer,Jonathan A. Bernstein, Chandler L. Stimach, Eliana Kovitch,Vandana Shashi,Kelly Schoch, Whitney Smith,Richard H. van Jaarsveld,Anna C. E. Hurst,Kirstin Smith,Evan H. Baugh, Suzanne G. Bohm,Emilie Vyhnalkova,Lukas Ryba,Capucine Delnatte,Juanita Neira,Dominique Bonneau,Annick Toutain,Jill A. Rosenfeld,Severine Audebert-Bellanger,Brigitte Gilbert-Dussardier,Sylvie Odent,Frederic Laumonnier,Seth Berger,Ann C. M. Smith,Franck Bourdeaut,Marc-Henri Stern,Richard Redon,Elke Krueger,Raphael Margueron,Stephane Bezieau,Jeremie Poschmann,Bertrand Isidor

The American Journal of Human Geneticsno. 2 (2022): 361-372

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Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder

American journal of human geneticsno. 5 (2021): 929-941

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Haploinsufficiency of the Sin3/HDAC Corepressor Complex Member SIN3B Causes a Syndromic Intellectual Disability/autism Spectrum Disorder

AMERICAN JOURNAL OF HUMAN GENETICSno. 5 (2021): 929-941

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