Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive ImpairmentsClaire S. Leblond, Tobias M. Boeckers, Laurence Perrin et al.|PLoS Genetics|2014Cited by 672
French multi-centric study of 2000 amniotic fluid interphase FISH analyses from high-risk pregnancies and review of the literatureIsabelle Luquet, Brigitte Benzacken, Francine Mugneret et al.|Annales de Génétique|2002Cited by 20
Clinical relevance of 8q23, 15q13 and 18q21 SNP genotyping to evaluate colorectal cancer riskStéphanie Baert‐Desurmont, Agnès Hardouin, Chrystelle Colas et al.|European Journal of Human Genetics|2015Cited by 17
Gene‐ and pathway‐level analyses of <scp>iCOGS</scp> variants highlight novel signaling pathways underlying familial breast cancer susceptibilityChristine Lonjou, Fabienne Lesueur, Séverine Eon‐Marchais et al.|International Journal of Cancer|2020Cited by 6
<i>ACTB</i> deletions or single-nucleotide loss-of-function variants: expansion and further delineation of the phenotype and review of the literatureMarion Lesieur‐Sebellin, Valérie Malan, Kristen Wigby et al.|Journal of Medical Genetics|2025Cited by 0