Camille Humbert

Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract

Laurence Heidet, Vincent Morinière, C. Henry et al. · Journal of the American Society of Nephrology · 2017 · 123 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice

Lara De Tomasi, Pierre David, Camille Humbert et al. · The American Journal of Human Genetics · 2017 · 114 citations · Full text

Medicine, Genetics, Molecular Genetics +12

Integrin Alpha 8 Recessive Mutations Are Responsible for Bilateral Renal Agenesis in Humans

Camille Humbert, Flora Silbermann, Bharti Morar et al. · The American Journal of Human Genetics · 2014 · 100 citations · Full text

Medicine, Genetics, Molecular Genetics +15

First-in-man use of a cardiovascular cell-derived secretome in heart failure. Case report

Philippe Menasché, Nisa Renault, Albert Hagège et al. · EBioMedicine · 2024 · 34 citations · Full text

Life Sciences, Cardiology, Cell Biology +9

Human IFT52 mutations uncover a novel role for the protein in microtubule dynamics and centrosome cohesion

Marie A. Dupont, Camille Humbert, Céline Huber et al. · Human Molecular Genetics · 2019 · 29 citations

Life Sciences, Cell Biology, Genetics +17