Marc Delpech

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

Catherine Dodé, Jacqueline Levilliers, Jean‐Michel Dupont et al. · Nature Genetics · 2003 · 825 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +3

Association of TNF2, a TNF-α Promoter Polymorphism, With Septic Shock Susceptibility and Mortality

Jean‐Paul Mira, Alain Cariou, Franck Grall et al. · JAMA · 1999 · 740 citations

Acute Lung Injury, Immunology, Genetic Epidemiology +19

Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2

Catherine Dodé, Luís Teixeira, Jacqueline Levilliers et al. · PLoS Genetics · 2006 · 451 citations · Full text

Kallmann Syndrome Combines, Human Growth, Genetics +21

New Mutations of CIAS1 That Are Responsible for Muckle-Wells Syndrome and Familial Cold Urticaria: A Novel Mutation Underlies Both Syndromes

Catherine Dodé, Nathalie Le Dû, Laurence Cuisset et al. · The American Journal of Human Genetics · 2002 · 298 citations · Full text

Muckle-wells Syndrome, New Mutations, Mendelian Disorder +7

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 · 258 citations · Full text

Diagnostic Virology, Armenian Patients, Medicine +8