Mélanie Parisot

FGF9 and FGF20 Maintain the Stemness of Nephron Progenitors in Mice and Man

Hila Barak, Sung‐Ho Huh, Shuang Chen et al. · Developmental Cell · 2012 · 318 citations · Full text

Life Sciences, Developmental Biology, Nephrology +14

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

Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome

Christelle Arrondel, Sophia Missoury, Rozemarijn Snoek et al. · Nature Communications · 2019 · 100 citations · Full text

Life Sciences, Genetics, Molecular Biology +13

A monocyte/dendritic cell molecular signature of SARS-CoV-2-related multisystem inflammatory syndrome in children with severe myocarditis

Camille de Cevins, Marine Luka, Nikaïa Smith et al. · Med · 2021 · 76 citations · Full text

Medicine, Immunology, Pediatrics +16

Somatic genetic rescue of a germline ribosome assembly defect

Shengjiang Tan, Laëtitia Kermasson, Christine Hilcenko et al. · Nature Communications · 2021 · 74 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17