Sandrine Barbaux

Donor splice-site mutations in WT1 are responsible for Frasier syndrome

Sandrine Barbaux, Patrick Niaudet, Marie-Claire Gübler et al. · Nature Genetics · 1997 · 742 citations

Mendelian Disorder, Genetic Disorder, Genetics +6

The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations

Derval J. Gaughan, Leo A. J. Kluijtmans, Sandrine Barbaux et al. · Atherosclerosis · 2001 · 272 citations

Biochemistry, Plasma Homocysteine Concentrations, Genetics +9

High frequency of well-defined Y-chromosome deletions in idiopathic Sertoli cell-only syndrome

C. Foresta, Alberto Ferlin, Andrea Garolla et al. · Human Reproduction · 1998 · 262 citations · Full text

Genetic Analysis of the Interleukin-18 System Highlights the Role of the Interleukin-18 Gene in Cardiovascular Disease

Laurence Tiret, Tiphaine Godefroy, Edith Lubos et al. · Circulation · 2005 · 230 citations

Maternal Genetic Effects, Exerted by Genes Involved in Homocysteine Remethylation, Influence the Risk of Spina Bifida

Marie-Therese Doolin, Sandrine Barbaux, Maeve McDonnell et al. · The American Journal of Human Genetics · 2002 · 146 citations · Full text

Biology, Homocysteine Remethylation, Natural Sciences +11