Olivier Lantieri

Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes

Inês Barroso, Beverley Balkau, Philippe Froguel, 2012, Nature Genetics.

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Thomas Meitinger, Inês Barroso, Peter Kraft, 2010, Nature Genetics.

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Thomas Meitinger, Inês Barroso, Peter Kraft, 2011, Nature Genetics.

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Dan M Roden, Beverley Balkau, Pierre Lindenbaum, 2013, Nature Genetics.

Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features.

Beverley Balkau, Philippe Froguel, David Meyre, 2013, The Journal of clinical investigation.

Type 2 diabetes-related genetic risk scores associated with variations in fasting plasma glucose and development of impaired glucose homeostasis in the prospective DESIR study

Beverley Balkau, Philippe Froguel, Amélie Bonnefond, 2014, Diabetologia.