(Q45975588)

English

TCF7L2 is associated with high serum triacylglycerol and differentially expressed in adipose tissue in families with familial combined hyperlipidaemia.

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scholarly article

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Europe PubMed Central

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9 January 2020

TCF7L2 is associated with high serum triacylglycerol and differentially expressed in adipose tissue in families with familial combined hyperlipidaemia (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17972059%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

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Christopher Plaisier

2

1 reference

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9 January 2020

Marja-Riitta Taskinen

11

1 reference

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9 January 2020

author name string

A Huertas-Vazquez

1

1 reference

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9 January 2020

D Weissglas-Volkov

3

1 reference

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9 January 2020

J Sinsheimer

4

1 reference

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9 January 2020

S Canizales-Quinteros

5

1 reference

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9 January 2020

I Cruz-Bautista

6

1 reference

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9 January 2020

E Nikkola

7

1 reference

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9 January 2020

M Herrera-Hernandez

8

1 reference

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9 January 2020

A Davila-Cervantes

9

1 reference

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9 January 2020

T Tusie-Luna

10

1 reference

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9 January 2020

C Aguilar-Salinas

12

1 reference

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9 January 2020

P Pajukanta

13

1 reference

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9 January 2020

language of work or name

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publication date

31 October 2007

1 reference

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9 January 2020

1 reference

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9 January 2020

51

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9 January 2020

62-69

1 reference

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9 January 2020

1

1 reference

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9 January 2020

https://scigraph.springernature.com/pub.10.1007/s00125-007-0850-6

0 references

Linkage analysis in the presence of errors III: marker loci and their map as nuisance parameters

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A general test of association for quantitative traits in nuclear families

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common variants in the TCF7L2 gene and predisposition to type 2 diabetes in UK European Whites, Indian Asians and Afro-Caribbean men and women

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

LRP6 mutation in a family with early coronary disease and metabolic risk factors

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms in the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in the Amish: replication and evidence for a role in both insulin secretion and insulin resistance.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of Transcription Factor 7-Like 2 (TCF7L2) Variants With Type 2 Diabetes in a Finnish Sample

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcription Factor TCF7L2 Genetic Study in the French Population: Expression in Human -Cells and Adipose Tissue and Strong Association With Type 2 Diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial combined hyperlipidemia in Mexicans: association with upstream transcription factor 1 and linkage on chromosome 16q24.1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative trait nucleotide analysis using Bayesian model selection.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of TCF7L2 polymorphisms with type 2 diabetes in Mexico City.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association Analysis of 6,736 U.K. Subjects Provides Replication and ConfirmsTCF7L2as a Type 2 Diabetes Susceptibility Gene With a Substantial Effect on Individual Risk

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1).

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High prevalence of low HDL cholesterol concentrations and mixed hyperlipidemia in a Mexican nationwide survey.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Convergence of Wnt, beta-catenin, and cadherin pathways

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common hepatic nuclear factor-4alpha variants are associated with high serum lipid levels and the metabolic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multipoint quantitative-trait linkage analysis in general pedigrees

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The quantitative trait linkage disequilibrium test: a more powerful alternative to the quantitative transmission disequilibrium test for use in the absence of population stratification

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotypes of transcription factor 7-like 2 (TCF7L2) gene and its upstream region are associated with type 2 diabetes and age of onset in Mexican Americans

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

USF1 and dyslipidemias: converging evidence for a functional intronic variant

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcription factor 7-like 2 polymorphisms and type 2 diabetes, glucose homeostasis traits and gene expression in US participants of European and African descent

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family study of serum lipids and lipoproteins in coronary heart-disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome scans provide evidence for low-HDL-C loci on chromosomes 8q23, 16q24.1-24.2, and 20q13.11 in Finnish families

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Wnt/beta-catenin signaling in development and disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variants of transcription factor 7-like 2 (TCF7L2) gene predict conversion to type 2 diabetes in the Finnish Diabetes Prevention Study and are associated with impaired glucose regulation and impaired insulin secretion

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis and classification of diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucose intolerance in familial combined hyperlipidaemia. EUFAM study group

1 reference

https://pubmed.ncbi.nlm.nih.gov/17972059

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00125-007-0850-6

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17972059%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17972059%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

ResearchGate publication ID

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