A. Brioschi
University Hospital of Lausanne
1 Papers
A. Brioschi is an academic researcher from University Hospital of Lausanne. The author has contributed to research in topics: Genome-wide association study & Missing heritability problem. The author has an hindex of 1, co-authored 1 publications.
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Papers
A new highly penetrant form of obesity due to deletions on chromosome 16p11.2
Robin G. Walters,Sébastien Jacquemont,Armand Valsesia,Armand Valsesia,Armand Valsesia,A J de Smith,Danielle Martinet,Johanna C. Andersson,Mario Falchi,Fei Chen,Joris Andrieux,Stéphane Lobbens,Bruno Delobel,Fanny Stutzmann,J. S. El-Sayed Moustafa,Jean-Claude Chèvre,C. Lecoeur,Vincent Vatin,Sonia Bouquillon,Jessica L. Buxton,Odile Boute,Muriel Holder-Espinasse,Jean-Marie Cuisset,Marie-Pierre Lemaitre,Anne-Emmanuelle Ambresin,A. Brioschi,Muriel Gaillard,Vittorio Giusti,Florence Fellmann,Alessandra Ferrarini,Nouchine Hadjikhani,Nouchine Hadjikhani,Dominique Campion,Audrey Guilmatre,Alice Goldenberg,Nadège Calmels,Jean-Louis Mandel,C Le Caignec,Albert David,Bertrand Isidor,Marie-Pierre Cordier,Sophie Dupuis-Girod,Audrey Labalme,Damien Sanlaville,M. Béri-Dexheimer,Philippe Jonveaux,B. Leheup,Katrin Õunap,Elena G. Bochukova,Elana Henning,Julia M. Keogh,Richard J. Ellis,Kay D. MacDermot,M. M. van Haelst,Catherine Vincent-Delorme,Ghislaine Plessis,R. Touraine,Anne Philippe,Valérie Malan,Michèle Mathieu-Dramard,Jean Chiesa,Bettina Blaumeiser,R. F. Kooy,Robert Caiazzo,Robert Caiazzo,Marie Pigeyre,B. Balkau,Robert Sladek,Sven Bergmann,Sven Bergmann,Vincent Mooser,Dawn M. Waterworth,Alexandre Reymond,Peter Vollenweider,Gérard Waeber,Ants Kurg,Priit Palta,Tõnu Esko,Tõnu Esko,Andres Metspalu,Andres Metspalu,Mari Nelis,Mari Nelis,Paul Elliott,A.-L. Hartikainen,Mark I. McCarthy,Mark I. McCarthy,Leena Peltonen,Leena Peltonen,Lena M. S. Carlsson,Peter Jacobson,Lars Sjöström,Ni Huang,Matthew E. Hurles,Stephen O'Rahilly,I. S. Farooqi,Katrin Männik,Marjo-Riitta Järvelin,Marjo-Riitta Järvelin,François Pattou,François Pattou,David Meyre,Andrew Walley,Lachlan J. M. Coin,Alexandra I. F. Blakemore,Philippe Froguel,Philippe Froguel,Jacques S. Beckmann,Jacques S. Beckmann +108 more
TL;DR: A highly penetrant form of obesity is reported, initially observed in 31 subjects who were heterozygous for deletions of at least 593 kilobases at 16p11.2 and whose ascertainment included cognitive deficits, which highlights a promising strategy for identifying missing heritability in obesity and other complex traits.