Pascal Cousin

A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy

Edwin M. Stone, Andrew Lotery, Francis L. Munier et al. · Nature Genetics · 1999 · 491 citations

Ocular Disease, Retinal Dystrophy, Ophthalmology +8

BIGH3 mutation spectrum in corneal dystrophies.

Francis L. Munier, Béatrice E. Frueh, Philippe Othenin‐Girard et al. · PubMed · 2002 · 255 citations

Defining the RNA polymerase III transcriptome: Genome-wide localization of the RNA polymerase III transcription machinery in human cells

Donatella Canella, Viviane Praz, Jaime H. Reina et al. · Genome Research · 2010 · 185 citations · Full text

Mutation in the Gene for Connexin 30.3 in a Family with Erythrokeratodermia Variabilis

Françoise Macari, Marina Landau, Pascal Cousin et al. · The American Journal of Human Genetics · 2000 · 159 citations · Full text

Biology, Connexin 30.3, Genetics +5

Antibiotic‐associated diarrhoea and Clostridium difficile&gt; <i>in the community</i>

Laurent Beaugerie, Antoine Flahault, Frédéric Barbut et al. · Alimentary Pharmacology & Therapeutics · 2003 · 107 citations · Full text