Cécile Cazeneuve

Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females

Christel Depienne, Delphine Bouteiller, Boris Keren et al. · PLoS Genetics · 2009 · 371 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

MEFV-Gene Analysis in Armenian Patients with Familial Mediterranean Fever: Diagnostic Value and Unfavorable Renal Prognosis of the M694V Homozygous Genotype—Genetic and Therapeutic Implications

Cécile Cazeneuve, Tamara Sarkisian, Christophe Pécheux et al. · The American Journal of Human Genetics · 1999 · 259 citations · Full text

Medicine, Genetics, Molecular Genetics +8

Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology

Elisa Teyssou, Takahiro Takeda, Vincent Lebon et al. · Acta Neuropathologica · 2013 · 231 citations · Full text

Life Sciences, Molecular Genetics, Neuroscience +12

Identification of MEFV-Independent Modifying Genetic Factors for Familial Mediterranean Fever

Cécile Cazeneuve, Hasmik Ajrapetyan, Stéphanie Papin et al. · The American Journal of Human Genetics · 2000 · 197 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes

Sophie Tézenas du Montcel, Alexandra Dürr, Peter Bauer et al. · Brain · 2014 · 178 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15