Low-frequency variants in HMGA1 are not associated with type 2 diabetes risk (Q40666739)

22 September 2017

Low-frequency variants in HMGA1 are not associated with type 2 diabetes risk (English)

1 reference

22 September 2017

9

1 reference

22 September 2017

18

1 reference

22 September 2017

19

1 reference

22 September 2017

Odile Poulain-Godefroy

Odile Poulain-Godefroy

12

0 references

Peter Jacobson

Peter Jacobson

15

0 references

Mario Falchi

Mario Falchi

5

0 references

François Pattou

Francois Pattou

11

0 references

Michel Marre

Michel Marre

21

0 references

Philippe Froguel

Philippe Froguel

22

0 references

DIAGRAM Consortium

24

DIAGRAM Consortium

1 reference

22 September 2017

6

Andrew P Morris

1 reference

22 September 2017

Marcel Marquez

1

1 reference

22 September 2017

Marlène Huyvaert

2

1 reference

22 September 2017

John R B Perry

3

1 reference

22 September 2017

Richard D Pearson

4

1 reference

22 September 2017

Sidonie Vivequin

7

1 reference

22 September 2017

Stéphane Lobbens

8

1 reference

22 September 2017

Stefan Gaget

10

1 reference

22 September 2017

Guillaume Charpentier

13

1 reference

22 September 2017

Lena M S Carlsson

14

1 reference

22 September 2017

Lars Sjöström

16

1 reference

22 September 2017

Olivier Lantieri

17

1 reference

22 September 2017

Beverley Balkau

20

1 reference

22 September 2017

Stéphane Cauchi

23

1 reference

22 September 2017

language of work or name

English

0 references

publication date

30 December 2011

1 reference

22 September 2017

1 reference

22 September 2017

61

1 reference

22 September 2017

524-530

1 reference

22 September 2017

2

1 reference

Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported

22 September 2017

start time

27 August 2021

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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1 reference

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Pseudogene-mediated posttranscriptional silencing of HMGA1 can result in insulin resistance and type 2 diabetes.

22 September 2017

1 reference

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The genetics of insulin resistance: Where's Waldo?

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Uncovering the roles of rare variants in common disease through whole-genome sequencing

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Finding the missing heritability of complex diseases

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

HMGA1 is induced by Wnt/beta-catenin pathway and maintains cell proliferation in gastric cancer

22 September 2017

1 reference

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Common vs. rare allele hypotheses for complex diseases

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

The cAMP-HMGA1-RBP4 system: a novel biochemical pathway for modulating glucose homeostasis

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Interrogating type 2 diabetes genome-wide association data using a biological pathway-based approach

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Next-generation DNA sequencing

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Next-generation DNA sequencing methods

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

New gene variants alter type 2 diabetes risk predominantly through reduced beta-cell function

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Common and rare variants in multifactorial susceptibility to common diseases

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Family-based association tests for genomewide association scans

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

A genome-wide association study identifies novel risk loci for type 2 diabetes

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Effects of low dose ramipril on cardiovascular and renal outcomes in patients with type 2 diabetes and raised excretion of urinary albumin: randomised, double blind, placebo controlled trial (the DIABHYCAR study).

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

An octamer motif is required for activation of the inducible nitric oxide synthase promoter in pancreatic beta-cells

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Measuring inconsistency in meta-analyses

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

A nucleoprotein complex containing Sp1, C/EBP beta, and HMGI-Y controls human insulin receptor gene transcription

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Accurate assessment of beta-cell function: the hyperbolic correction

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

HMGI/Y proteins: flexible regulators of transcription and chromatin structure

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Are rare variants responsible for susceptibility to complex diseases?

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

The non-insulin-dependent diabetes, hypertension, microalbuminuria or proteinuria, cardiovascular events, and ramipril (DIABHYCAR) study: design, organization, and patient recruitment. DIABHYCAR Study Group

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Regulation of DNA-dependent activities by the functional motifs of the high-mobility-group chromosomal proteins

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Familiality of physical and metabolic characteristics that predict the development of non-insulin-dependent diabetes mellitus in Pima Indians.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

The insulin receptor: molecular biology and transmembrane signaling

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Mutations in the insulin receptor gene

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Transcriptional regulation of human insulin receptor gene by the high-mobility group protein HMGI(Y).

22 September 2017

1 reference

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Insulin resistance or insulin deficiency. Which is the primary cause of NIDDM?

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

1000 genomes: a world of variation

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Functional variants of the HMGA1 gene and type 2 diabetes mellitus

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

HMGA1 protein is a positive regulator of the insulin-like growth factor-I receptor gene.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Random-effects model for meta-analysis of clinical trials: an update

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Evaluating coverage of genome-wide association studies

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Lack of the architectural factor HMGA1 causes insulin resistance and diabetes in humans and mice

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Candidate-gene approaches for studying complex genetic traits: practical considerations

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Insulin sensitivity and insulin secretion in monozygotic and dizygotic twins.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Insulin sensitivity indices obtained from oral glucose tolerance testing: comparison with the euglycemic insulin clamp.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Familiality of quantitative metabolic traits in Finnish families with non-insulin-dependent diabetes mellitus. Finland-United States Investigation of NIDDM Genetics (FUSION) Study investigators.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

The 30 minute insulin incremental response in an oral glucose tolerance test as a measure of insulin secretion.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

Power in the phenotypic extremes: a simulation study of power in discovery and replication of rare variants

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266400

HMGA1, a novel locus for type 2 diabetes mellitus

2 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22210315

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Determinants and nature of dietary underreporting in a free-living population: the Fleurbaix Laventie Ville Santé (FLVS) study

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22210315

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Heritability of pancreatic beta-cell function among nondiabetic members of Caucasian familial type 2 diabetic kindreds

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22210315

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.2337/DB11-0728

1 reference

22 September 2017

1 reference

22 September 2017

1 reference