Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant.
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Nutrition and Cardiovascular Disease: Finding the Perfect Recipe for Cardiovascular HealthGenetics of Type 2 Diabetes in African AmericansGenetic screening for the risk of type 2 diabetes: worthless or valuable?Is genetic testing useful to predict type 2 diabetes?Consistent directions of effect for established type 2 diabetes risk variants across populations: the population architecture using Genomics and Epidemiology (PAGE) ConsortiumAddressing the inter-individual variation in response to consumption of plant food bioactives: Towards a better understanding of their role in healthy aging and cardiometabolic risk reduction.Transferability and fine-mapping of glucose and insulin quantitative trait loci across populations: CARe, the Candidate Gene Association Resource.Comparing a few SNP calling algorithms using low-coverage sequencing data.Personalized nutrition and cardiovascular disease prevention: From Framingham to PREDIMEDGenome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study.An exome sequencing pipeline for identifying and genotyping common CNVs associated with disease with application to psoriasisCharacterization of the transcriptional machinery bound across the widely presumed type 2 diabetes causal variant, rs7903146, within TCF7L2.Association of Type 2 Diabetes Mellitus related SNP genotypes with altered serum adipokine levels and metabolic syndrome phenotypes.Genetic risk assessment of type 2 diabetes-associated polymorphisms in African AmericansPredicting diabetes: our relentless quest for genomic nuggets.Rare variants at 16p11.2 are associated with common variable immunodeficiencyImplication of European-derived adiposity loci in African Americans.A genotype risk score predicts type 2 diabetes from young adulthood: the CARDIA study.TCF7L2 genetic variants modulate the effect of dietary fat intake on changes in body composition during a weight-loss interventionEvaluation of genome-wide association study-identified type 2 diabetes loci in African Americans.Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus StudyGenetics of obesity and type 2 diabetes in African Americans.The association of genetic variants of type 2 diabetes with kidney functionMediterranean diet reduces the adverse effect of the TCF7L2-rs7903146 polymorphism on cardiovascular risk factors and stroke incidence: a randomized controlled trial in a high-cardiovascular-risk population.Genetic susceptibility to type 2 diabetes and obesity: follow-up of findings from genome-wide association studies.T2DM GWAS in the Lebanese population confirms the role of TCF7L2 and CDKAL1 in disease susceptibilityAssociation between transcription factor 7-like 2 rs7903146 polymorphism and diabetic retinopathy in type 2 diabetes mellitus: A meta-analysis.The type 2 diabetes presumed causal variant within TCF7L2 resides in an element that controls the expression of ACSL5.Racial Disparities in the Pathogenesis of Type 2 Diabetes and its Subtypes in the African Diaspora: A New Paradigm.The genomic landscape of African populations in health and disease.Association between type 2 diabetes mellitus-related SNP variants and obesity traits in a Saudi population.Redundant enhancers and causal variants in the TCF7L2 gene.Detection of single nucleotide polymorphisms by PCR conformation-difference gel electrophoresis.Genome-wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans.Ethnicity and cardiovascular health research: pushing the boundaries by including comparison populations in the countries of origin.The TCF7L2 rs7903146 (C/T) polymorphism is associated with risk to type 2 diabetes mellitus in Southern-Brazil.
P2860
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P2860
Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant.
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Resequencing and analysis of v ...... abetes susceptibility variant.
@ast
Resequencing and analysis of v ...... abetes susceptibility variant.
@en
Resequencing and analysis of v ...... abetes susceptibility variant.
@nl
type
label
Resequencing and analysis of v ...... abetes susceptibility variant.
@ast
Resequencing and analysis of v ...... abetes susceptibility variant.
@en
Resequencing and analysis of v ...... abetes susceptibility variant.
@nl
prefLabel
Resequencing and analysis of v ...... abetes susceptibility variant.
@ast
Resequencing and analysis of v ...... abetes susceptibility variant.
@en
Resequencing and analysis of v ...... abetes susceptibility variant.
@nl
P2093
P2860
P356
P1433
P1476
Resequencing and analysis of v ...... abetes susceptibility variant.
@en
P2093
Barry I Freedman
Carl D Langefeld
Donald W Bowden
Jessica M Hester
Maggie C Y Ng
Nicholette D Palmer
S Sandy An
P2860
P304
P356
10.2337/DB10-0134
P407
P577
2010-10-27T00:00:00Z