Albert David

Biochemistry, Genetics and Molecular Biology · Life Sciences

55h-index10.3kcitations204works0.32yr avg
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Research Topics

Genomic variations and chromosomal abnormalities(34), Genetics and Neurodevelopmental Disorders(24), Congenital heart defects research(20), Connective tissue disorders research(15), RNA modifications and cancer(12)

Publications202 total

Figures and supplemental materials and methods for Rab35 regulates cell fate within the liver and loss leads to atypical cholangiocyte expansion
Zenodo (CERN European Organization for Nuclear Research)·2026Open Access
Figures and supplemental materials and methods for Rab35 regulates cell fate within the liver and loss leads to atypical cholangiocyte expansion
Zenodo (CERN European Organization for Nuclear Research)·2026Open Access
Quand le management devient patrimoine : défis et enjeux d’une muséalisation
Entreprises et histoire·2024· 1 cited
Table of Contents, Volume 194A, Number 4, April 2024
American Journal of Medical Genetics Part A·2024Open Access
Cat eye syndrome: Clinical, cytogenetics and familial findings in a large cohort of 43 patients highlighting the importance of congenital heart disease and inherited cases
American Journal of Medical Genetics Part A·2023· 10 citedOpen Access
Ce que gérer veut dire. Voyage à travers les dérives et les réinventions de l’entreprise contemporaine (Le Monde 2004-2020)
Revue française de gestion·2022
Les grands auteurs aux frontières du management
EMS Editions eBooks·2022
Les grands auteurs aux frontières du management
EMS Editions eBooks·2022
Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder
Genetics in Medicine·2021· 31 citedOpen Access
Effects of eight neuropsychiatric copy number variants on human brain structure
Translational Psychiatry·2021· 43 citedOpen Access
Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder
2021· 5 citedOpen Access
Climate change adaptation: the case of coastal communities in the Philippines
Journal of the Geographical Institute Jovan Cvijic SASA·2021· 8 citedOpen Access
Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations
UNC Libraries·2020· 1 citedOpen Access
Editorial
Finance Contrôle Stratégie·2020
Théorie de la conception et formation au management de l’innovation : variété des expériences et des impacts
HAL (Le Centre pour la Communication Scientifique Directe)·2019
Developmental trajectories of neuroanatomical alterations associated with the 16p11.2 Copy Number Variations
NeuroImage·2019· 15 citedOpen Access
Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome
npj Genomic Medicine·2019· 3 citedOpen Access
Editorial
Finance Contrôle Stratégie·2019
Deciphering the complexity of the 4q and 10q subtelomeres by molecular combing in healthy individuals and patients with facioscapulohumeral dystrophy
Journal of Medical Genetics·2019· 34 citedOpen Access
Editorial
Finance Contrôle Stratégie·2019
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Frequent Co-authors

Cédric Le Caignec(17), Didier Lacombe(14), Bertrand Isidor(13), Laurence Faivre(10), Valérie Cormier‐Daire(9), Alain Verloès(8), Annick Toutain(8), Dominique Bonneau(7), Sébastien Jacquemont(6), Bruno Delobel(6), Delphine Héron(6), Clarisse Baumann(6), Dominique Gaillard(5), Marion Gérard(5), Geneviève Baujat(5), Cyril Mignot(5), Hubert Journel(5), Hélène Dollfus(5), Valérie Drouin‐Garraud(5), Christel Thauvin‐Robinet(5)