Camille Humbert

Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humans.

R. Salomon, O. Gribouval, F. Silbermann, 2014, American journal of human genetics.

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

R. Salomon, C. Antignac, S. Saunier, 2017, Journal of the American Society of Nephrology : JASN.

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

P. Shannon, D. Chitayat, S. Saunier, 2019, Human molecular genetics.

Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice.

F. Silbermann, S. Saunier, C. Bole-Feysot, 2017, American journal of human genetics.

Therapeutic potential of extracellular vesicles derived from cardiac progenitor cells in rodent models of chemotherapy-induced cardiomyopathy

P. Croisille, A. Hagège, P. Menasché, 2023, Frontiers in cardiovascular medicine.

Human IFT52 mutations uncover a novel role for the protein in microtubule dynamics 1 and centrosome cohesion 2

S. Saunier, C. Jeanpierre, M. Garfa-Traoré, 2020 .