N. Ravisé

The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1

Ali Benomar, Luc Krols, Giovanni Stévanin et al. · Nature Genetics · 1995 · 160 citations

Life Sciences, Genetics, Molecular Genetics +12

Fine mapping of de novo CMT1A and HNPP rearrangements within CMTIA-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination

Judith Lopes, N. Ravisé, A. Vandenberghe et al. · Human Molecular Genetics · 1998 · 118 citations

Life Sciences, Genetics, Molecular Genetics +14

Spine deformities in Charcot-Marie-Tooth 4C caused by <i>SH3TC2</i> gene mutations

Hamid Azzedine, N. Ravisé, Christophe Verny et al. · Neurology · 2006 · 106 citations

Life Sciences, Genetics, Neurology +17

Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP)

E. Le Guern, F. Sturtz, Michel Gugenheim et al. · Cytogenetics and Cell Genetics · 2008 · 52 citations

Life Sciences, Genetics, Molecular Genetics +17

Chromosome 11q localization of one of the three expected genes for the human α-3-fucosyltransferases, by somatic hybridization

P. Couillin, Rosella Mollicone, M Grisard et al. · Cytogenetics and Cell Genetics · 2008 · 35 citations

Life Sciences, Genetics, Molecular Genetics +5