Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure.
He, Karen Y; Wang, Heming; Cade, Brian E; Nandakumar, Priyanka; Giri, Ayush; Ware, Erin B; Haessler, Jeffrey; Liang, Jingjing; Smith, Jennifer A; Franceschini, Nora; Le, Thu H; Kooperberg, Charles; Edwards, Todd L; Kardia, Sharon L R; Lin, Xihong; Chakravarti, Aravinda; Redline, Susan; Zhu, Xiaofeng.
; 13(3): e1006678, 2017 03.
Artigo em Inglês | MEDLINE | ID: mdl-28346479
The genetic architecture of type 2 diabetes.
Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females.
A novel mutation in steroidogenic factor (SF1/NR5A1) gene in a patient with 46 XY DSD without adrenal insufficiency.
Increased burden of cardiovascular disease in carriers of APOL1 genetic variants.
Association between the interleukin-1ß C-511T polymorphism and periodontitis: a meta-analysis in the Chinese population.
Distribution Characteristics and Combined Effect of Polymorphisms Affecting Alcohol Consumption Behaviour in the Hungarian General and Roma Populations.
Genetic study of early-onset Graves' disease in the Chinese Han population.
Distribution of ADH1B genotypes predisposed to enhanced alcohol consumption in the Czech Roma/Gypsy population.