Common and Unique Genetic Background between Attention-Deficit/Hyperactivity Disorder and Excessive Body Weight.
Genes
Dmitrzak-Weglarz, Monika M; Paszynska, Elzbieta E; Bilska, Karolina K; Szczesniewska, Paula P; Bryl, Ewa E; Duda, Joanna J; Dutkiewicz, Agata A; Tyszkiewicz-Nwafor, Marta M; Czerski, Piotr P; Hanc, Tomasz T; Slopien, Agnieszka A
NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study.
Prevalence of loss-of-function FTO mutations in lean and obese individuals.
Diabetes
Meyre, David D; Proulx, Karine K; Kawagoe-Takaki, Hiroko H; Vatin, Vincent V; Gutiérrez-Aguilar, Ruth R; Lyon, Debbie D; Ma, Marcella M; Choquet, Helene H; Horber, Fritz F; Van Hul, Wim W; Van Gaal, Luc L; Balkau, Beverley B; Visvikis-Siest, Sophie S; Pattou, François F; Farooqi, I Sadaf IS; Saudek, Vladimir V; O'Rahilly, Stephen S; Froguel, Philippe P; Sedgwick, Barbara B; Yeo, Giles S H GS