C. Lautier

发表

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

C. Lautier, S. A. E. Mkadem, E. Renard, 2003, Human Genetics.

PORTABILITY OF GWAS RESULTS BETWEEN ETHNIC POPULATIONS: GENETIC MARKERS FOR POLYCYSTIC OVARY SYNDROME (PCOS) IN MEDITERRANEAN AREA.

C. Lautier, F. Grigorescu, Z. Douma, 2019, Acta endocrinologica.

Mouse lemur, a new animal model to investigate cardiac pacemaker activity in primates

C. Lautier, N. Lamb, F. Pifferi, 2022, bioRxiv.

Lessons from the analysis of nonhuman primates for understanding human aging and neurodegenerative diseases

Jean-Michel Verdier, Gina Devau, S. Trouche, 2015, Front. Neurosci..

Mouse lemur, a new animal model to investigate cardiac pacemaker activity in primates

C. Lautier, N. Lamb, F. Pifferi, 2022, bioRxiv.

Sex-specific patterns of age-related cerebral atrophy in a nonhuman primate Microcebus murinus

C. Lautier, E. Zimmermann, Daniel Schmidtke, 2020, Neurobiology of Aging.

BRANCHED CHAIN AMINO ACIDS AT THE EDGE BETWEEN MENDELIAN AND COMPLEX DISORDERS.

C. Lautier, F. Grigorescu, S. Haydar, 2018, Acta Endocrinologica.

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

Justus M. Kebschull, Trygve E Bakken, Gabrielle J. Loeb, 2022, Nature Computational Science.

Studies of the variability of the genes encoding the insulin-like growth factor I receptor and its ligand in relation to type 2 diabetes mellitus.

T. Hansen, O. Pedersen, C. Lautier, 2000, The Journal of clinical endocrinology and metabolism.

IGF-I receptor mutations resulting in intrauterine and postnatal growth retardation.

C. Lautier, F. Grigorescu, W. Kiess, 2003, The New England journal of medicine.

Identification by RT-PCR and immunolocalization of arginine vasopressin in rat pancreas.

C. Lautier, F. Grigorescu, J. Serrano, 1999, Diabetes & metabolism.

Identification of two novel insulin receptor mutations, Asp59Gly and Leu62Pro, in type A syndrome of extreme insulin resistance.

C. Lautier, E. Renard, J. Brun, 1997, Biochemical and biophysical research communications.

Complex haplotypes of IRS 2 gene are associated with severe obesity and reveal heterogeneity in the effect of Gly 1057 Asp mutation

C. Lautier, S. A. E. Mkadem, E. Renard, 2022 .

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

C. Lautier, S. M. de la Monte, J. Klysik, 2009, Human molecular genetics.

HOW GENETICISTS CONTRIBUTE TO UNDERSTANDING OF COVID-19 DISEASE PATHOGENICITY.

C. Lautier, F. Grigorescu, 2020, Acta endocrinologica.

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

C. Lautier, E. Renard, F. Grigorescu, 1998, Human Genetics.

Fine-scale haplotype mapping of MUT, AACS, SLC6A15 and PRKCA genes indicates association with insulin resistance of metabolic syndrome and relationship with branched chain amino acid metabolism or regulation

J. Robine, E. Khusnutdinova, C. Lautier, 2019, PloS one.

MOLECULAR GENETICS STRATEGIES TO IDENTIFY VASOTOCIN CODING SEQUENCES IN HUMANS: FAMILY- SPECIFIC APPROACH USING GENOMIC DNA AND FETAL TISSUES mRNAs

C. Lautier, F. Grigorescu, C. Badiu, 2005 .

35th Annual meeting of the European Association for the Study of Diabetes. Brussels, Belgium, 28 September-2 October, 1999. Abstracts.

Thomas J. Smith, B. M. Rasmussen, V. C. Phan, 1999, Diabetologia.

Branched-Chain Amino Acid Database Integrated in MEDIPAD Software as a Tool for Nutritional Investigation of Mediterranean Populations

E. Khusnutdinova, C. Lautier, F. Grigorescu, 2018, Nutrients.

GIGYF 2 gene disruption in mice results in neurodegeneration and altered insulin-like growth factor signaling

C. Lautier, J. Klysik, Robert J. Smith, 2009 .

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.

C. Lautier, E. Renard, J. Gris, 2001, Diabetes.

Association of ATF5 Gene with Metabolic Syndrome and Insulin Resistance in Mediterranean Populations

C. Lautier, F. Grigorescu, A. Tsatsoulis, 2018, Diabetes.

Follow-up study of two sisters with type A syndrome of severe insulin resistance gives a new insight into PCOS pathogenesis in relation to puberty and pregnancy outcome: a case report.

A. Vambergue, C. Lautier, F. Grigorescu, 2006, Human reproduction.

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

C. Lautier, F. Grigorescu, Z. Douma, 2020, Gene.

Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson disease.

C. Lautier, A. Dürr, A. Brice, 2008, American journal of human genetics.

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.

C. Lautier, E. Renard, J. Brun, 2009, Diabetes & metabolism.

Characterization of cardiac pacemaker activity in the primate lemur Microcebus murinus.

C. Lautier, F. Pifferi, Anne Fernandez, 2021 .

Characterization of sinoatrial automaticity in Microcebus murinus to study the effect of aging on cardiac activity and the correlation with longevity

C. Lautier, N. Lamb, F. Pifferi, 2023, Scientific Reports.