Valérie Benoît

Deletion of KDM6A, a Histone Demethylase Interacting with MLL2, in Three Patients with Kabuki Syndrome

Damien Lederer, Bernard Grisart, M. Cristina Digilio et al. · The American Journal of Human Genetics · 2011 · 371 citations · Full text

Novel <i><scp>KDM6A</scp></i> (<scp>UTX</scp>) mutations and a clinical and molecular review of the X‐linked Kabuki syndrome (<scp>KS2</scp>)

Siddharth Banka, Damien Lederer, Valérie Benoît et al. · Clinical Genetics · 2014 · 134 citations · Full text

De novo, heterozygous, loss‐of‐function mutations in <i>SYNGAP1</i> cause a syndromic form of intellectual disability

Michael Parker, Alan Fryer, Deborah Shears et al. · American Journal of Medical Genetics Part A · 2015 · 121 citations · Full text

NF-κB-dependent MnSOD expression protects adenocarcinoma cells from TNF-α-induced apoptosis

Sylvie Delhalle, Valérie Deregowski, Valérie Benoît et al. · Oncogene · 2002 · 111 citations

Inflammation, Nf-κb-dependent Mnsod Expression, Medicine +9

HUWE1 variants cause dominant X-linked intellectual disability: a clinical study of 21 patients

Stéphanie Moortgat, Siren Berland, Ingvild Aukrust et al. · European Journal of Human Genetics · 2017 · 98 citations · Full text