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Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 7, 2016
Numerous Brugada syndrome-associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortalityJonas Ghouse, Christian T Have, Morten W Skov, et al.Liver International : Official Journal of the International Association for the Study of the Liver|May 20, 2023
An adult-based genetic risk score for liver fat associates with liver and plasma lipid traits in children and adolescentsYun Huang, Sara E Stinson, Helene Baek Juel, et al.The American Journal of Clinical Nutrition|December 25, 2009
TCF7L2 rs7903146-macronutrient interaction in obese individuals' responses to a 10-wk randomized hypoenergetic dietKatrine Grau, Stephane Cauchi, Claus Holst, et al.Human Genetics|August 3, 2007
Polymorphisms in the 3' UTR in the neurocalcin delta gene affect mRNA stability, and confer susceptibility to diabetic nephropathyMasumi Kamiyama, Masaaki Kobayashi, Shin-ichi Araki, et al.Diabetologia|April 29, 2021
Physical activity attenuates postprandial hyperglycaemia in homozygous TBC1D4 loss-of-function mutation carriersTheresia M Schnurr, Emil Jørsboe, Alexandra Chadt, et al.Plos One|October 29, 2014
Interaction between genetic predisposition to adiposity and dietary protein in relation to subsequent change in body weight and waist circumferenceMikkel Z Ankarfeldt, Sofus C Larsen, Lars Ängquist, et al.Science (New York, N.Y.)|September 19, 2015
Greenlandic Inuit show genetic signatures of diet and climate adaptationMatteo Fumagalli, Ida Moltke, Niels Grarup, et al.Nature Communications|January 14, 2026
Identification of modifiable plasma protein markers of cardiometabolic risk in children and adolescents with obesitySara Elizabeth Stinson, Yun Huang, Roman Thielemann, et al.Diabetologia|June 22, 2018
Identification of novel high-impact recessively inherited type 2 diabetes risk variants in the Greenlandic populationNiels Grarup, Ida Moltke, Mette K Andersen, et al.European Heart Journal|July 11, 2015
Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT intervalJonas Ghouse, Christian Theil Have, Peter Weeke, et al.Pageof 57