Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features. Bonnefond, Amélie; Raimondo, Anne; Stutzmann, Fanny; Ghoussaini, Maya; Ramachandrappa, Shwetha; Bersten, David C.; Durand, Emmanuelle; Vatin, Vincent; Balkau, Beverley; Lantieri, Olivier; Raverdy, Violeta; Pattou, François; Van Hul, Wim; Van Gaal, Luc; Peet, Daniel J.; Weill, Jacques; Miller, Jennifer L.; Horber, Fritz; Goldstone, Anthony P.; Driscoll, Daniel J.; Bruning, John B.; Meyre, David; Whitelaw, Murray L.; Froguel, Philippe. The Journal of Clinical Investigation. 2013; 123: p.3037-3041. doi:10.1172/JCI68035Article