Mélanie Letexier

Integrated analysis of somatic mutations and focal copy-number changes identifies key genes and pathways in hepatocellular carcinoma

Cécile Guichard, Giuliana Amaddeo, Sandrine Imbeaud et al. · Nature Genetics · 2012 · 1.4K citations · Full text

Medicine, Molecular Genetics, Oncology +14

Recurrent AAV2-related insertional mutagenesis in human hepatocellular carcinomas

Jean‐Charles Nault, Shalini Datta, Sandrine Imbeaud et al. · Nature Genetics · 2015 · 480 citations

Life Sciences, Molecular Biology, Molecular Genetics +14

Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases

Isabelle Audo, Kinga M. Bujakowska, Thierry Léveillard et al. · Orphanet Journal of Rare Diseases · 2012 · 172 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Whole-Exome Sequencing Identifies LRIT3 Mutations as a Cause of Autosomal-Recessive Complete Congenital Stationary Night Blindness

Christina Zeitz, Samuel G. Jacobson, Christian Hamel et al. · The American Journal of Human Genetics · 2012 · 138 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness

Isabelle Audo, Kinga M. Bujakowska, Elise Orhan et al. · The American Journal of Human Genetics · 2012 · 134 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11