Showing results (91-100 of 181) with videos related to

Sort By:
Pageof 19
International Journal of Obesity (2005)|May 18, 2018
Fine-mapping of 98 obesity loci in Mexican childrenHsin Yen Liu, Akram Alyass, Arkan Abadi, et al.
Plos One|April 7, 2016
Risk Alleles in/near ADCY5, ADRA2A, CDKAL1, CDKN2A/B, GRB10, and TCF7L2 Elevate Plasma Glucose Levels at Birth and in Early Childhood: Results from the FAMILY StudyZahra N Sohani, Sonia S Anand, Sebastien Robiou-du-Pont, et al.
BMJ Open|December 13, 2017
Rationale and design of GENEiUS: a prospective observational study on the genetic and environmental determinants of body mass index evolution in Canadian undergraduate studentsRita E Morassut, Christine Langlois, Akram Alyass, et al.
Human Molecular Genetics|March 8, 2008
R125W coding variant in TBC1D1 confers risk for familial obesity and contributes to linkage on chromosome 4p14 in the French populationDavid Meyre, Morgane Farge, Cécile Lecoeur, et al.
Plos One|July 5, 2013
Causal relationship between adiponectin and metabolic traits: a Mendelian randomization study in a multiethnic populationAndrew Mente, David Meyre, Matthew B Lanktree, et al.
Obesity (Silver Spring, Md.)|July 2, 2011
Common variants in FTO, MC4R, TMEM18, PRL, AIF1, and PCSK1 show evidence of association with adult obesity in the Greek populationKonstantinos Rouskas, Anastasia Kouvatsi, Konstantinos Paletas, et al.
The Journal of Clinical Psychiatry|December 31, 2015
Obesity genes and risk of major depressive disorder in a multiethnic population: a cross-sectional studyZainab Samaan, Yvonne K Lee, Hertzel C Gerstein, et al.
Scientific Reports|October 27, 2016
Evaluating the transferability of 15 European-derived fasting plasma glucose SNPs in Mexican children and adolescentsChristine Langlois, Arkan Abadi, Jesus Peralta-Romero, et al.
Scientific Reports|March 3, 2017
Genetic contribution to lipid levels in early life based on 158 loci validated in adults: the FAMILY studyShanice Christie, Sébastien Robiou-du-Pont, Sonia S Anand, et al.
Obesity (Silver Spring, Md.)|September 20, 2014
Identification of two novel loss-of-function SIM1 mutations in two overweight children with developmental delayLouise Montagne, Anne Raimondo, Bruno Delobel, et al.
Pageof 19