Eliane Khallouf

Identification of the gene altered in Berardinelli–Seip congenital lipodystrophy on chromosome 11q13

Jocelyne Magré, Marc Délepine, Eliane Khallouf et al. · Nature Genetics · 2001 · 744 citations

Genetic Disorder, Genetics, Pathology +7

Seipin deficiency alters fatty acid Δ9 desaturation and lipid droplet formation in Berardinelli-Seip congenital lipodystrophy

Emilie Boutet, Haquima El Mourabit, Matthieu Prot et al. · Biochimie · 2009 · 149 citations

Lipid Analysis, Metabolic Syndrome, Developmental Biology +10

Human peroxisome proliferator-activated receptor-gamma2: genetic mapping, identification of a variant in the coding sequence, and exclusion as the gene responsible for lipoatrophic diabetes.

Corinne Vigouroux, Lluís Fajas, Eliane Khallouf et al. · Diabetes · 1998 · 76 citations · Full text

Metabolic Syndrome, Diabetes Management, Diabetes Epidemiology +14

Higher Adiponectin Levels in Patients with Berardinelli-Seip Congenital Lipodystrophy due to Seipin as compared with 1-Acylglycerol-3-Phosphate-<i>O</i>-Acyltransferase-2 Deficiency

Bárbara Antuna-Puente, Emilie Boutet, Corinne Vigouroux et al. · The Journal of Clinical Endocrinology & Metabolism · 2010 · 54 citations · Full text

Genetic Exclusion of 14 Candidate Genes in Lipoatropic Diabetes Using Linkage Analysis in 10 Consanguineous Families¹

Corinne Vigouroux, Eliane Khallouf, Charlotte Bourut et al. · The Journal of Clinical Endocrinology & Metabolism · 1997 · 26 citations · Full text