IGF-I Receptor Mutations Resulting in Intrauterine and Postnatal Growth Retardation

M. Jennifer Abuzzahab, Anke Schneider, Audrey D. Goddard, +11

New England Journal of Medicine

Mutations in the GIGYF2 (TNRC15) Gene at the PARK11 Locus in Familial Parkinson Disease

Corinne Lautier, Stefano Goldwurm, Alexandra Dürr, +5

The American Journal of Human Genetics

Familial Parkinson DiseaseNeurodegenerative DiseasesMendelian DisorderGenetic DisorderParkinson Disease +7

Role of Allelic Variants Gly972Arg of IRS-1 and Gly1057Asp of IRS-2 in Moderate-to-Severe Insulin Resistance of Women With Polycystic Ovary Syndrome

Samira Ait El Mkadem, Corinne Lautier, Françoise Macari, +9

Diabetes

GIGYF2 gene disruption in mice results in neurodegeneration and altered insulin-like growth factor signaling

Barbara Giovannone, William G. Tsiaras, Suzanne de la Monte, +5

Human Molecular Genetics

Complex haplotypes of IRS2 gene are associated with severe obesity and reveal heterogeneity in the effect of Gly1057Asp mutation

Corinne Lautier, Samira Ait El Mkadem, Éric Renard, +4

Human Genetics

ObesityMetabolic SyndromeGenetic DeterminantMetabolic DisorderGenetics +7

Studies of the Variability of the Genes Encoding the Insulin-Like Growth Factor I Receptor and Its Ligand in Relation to Type 2 Diabetes Mellitus1

Søren K. Rasmussen, Corinne Lautier, Lars Hansen, +8

The Journal of Clinical Endocrinology & Metabolism

Adversarial domain translation networks for integrating large-scale atlas-level single-cell datasets

Jia Zhao, Gefei Wang, Jingsi Ming, +162

Nature Computational Science

Artificial IntelligenceEngineeringMachine LearningDeep LearningData Science +8

Association of the FTO gene with obesity and the metabolic syndrome is independent of the IRS-2 gene in the female population of Southern France

Redha Attaoua, Samira Ait El Mkadem, Corinne Lautier, +7

Diabetes & Metabolism

ObesityMetabolic SyndromeMetabolic DisorderGeneticsDiabetes +11

Refinement of genetic localization of the Alström syndrome on chromosome 2p12-13 by linkage analysis in a North African family

Françoise Macari, Corinne Lautier, Anne Girardet, +8

Human Genetics

Alström SyndromeGenetic DisorderNorth African FamilyGeneticsLinkage Analysis +5

Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia

Zeineb Douma, Meriem Dallel, Assila Ben Salem, +6

Gene

InfertilityHormonal ReceptorGeneticsGenetic EpidemiologyReproductive Health +7