(Q34013806)

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Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study

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scholarly article

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Europe PubMed Central

30 July 2017

Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study (English)

1 reference

Europe PubMed Central

30 July 2017

1 reference

based on heuristic

inferred from title

insulin resistance

1 reference

based on heuristic

inferred from title

James S. Pankow

7

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Europe PubMed Central

30 July 2017

object named as

Charles C Gu

6

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object named as

Treva K Rice

3

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14

object named as

Donna K Arnett

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Europe PubMed Central

30 July 2017

Marguerite R Irvin

1

object named as

Marguerite R Irvin

1 reference

Europe PubMed Central

30 July 2017

8

object named as

Kari E North

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Europe PubMed Central

30 July 2017

Nora Franceschini

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object named as

Nora Franceschini

1 reference

Europe PubMed Central

30 July 2017

10

object named as

Barry I Freedman

1 reference

Europe PubMed Central

30 July 2017

Edmond K. Kabagambe

5

object named as

Edmond K Kabagambe

1 reference

Europe PubMed Central

30 July 2017

author name string

Nathan E Wineinger

2

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Europe PubMed Central

30 July 2017

Nicholas M Pajewski

4

1 reference

Europe PubMed Central

30 July 2017

Jemma B Wilk

9

1 reference

Europe PubMed Central

30 July 2017

Uli Broeckel

12

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Europe PubMed Central

30 July 2017

Hemant K Tiwari

13

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Europe PubMed Central

30 July 2017

language of work or name

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publication date

25 August 2011

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Europe PubMed Central

30 July 2017

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Europe PubMed Central

30 July 2017

6

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Europe PubMed Central

30 July 2017

8

1 reference

Europe PubMed Central

30 July 2017

e24052

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Europe PubMed Central

30 July 2017

copyright license

Creative Commons Attribution 4.0 International

25 August 2011

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April 2022 Public Data File from Crossref

copyright status

0 references

Is diabetes mellitus a continuous spectrum?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3162025

28 July 2018

Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant

1 reference

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Consistent association of type 2 diabetes risk variants found in europeans in diverse racial and ethnic groups

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Genetic structure in African populations: implications for human demographic history

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Mixed linear model approach adapted for genome-wide association studies

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New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

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Diet-induced gene expression of isolated pancreatic islets from a polygenic mouse model of the metabolic syndrome.

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A genome-wide association study of hypertension and blood pressure in African Americans

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Underlying genetic models of inheritance in established type 2 diabetes associations

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Insulin immunoassays in the detection of insulin analogues in factitious hypoglycemia

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Copy-number variations associated with neuropsychiatric conditions

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Extending genome-wide association studies to copy-number variation

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The emerging genetic architecture of type 2 diabetes

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Insulin resistance -- the role of ethnicity: evidence from Caucasian and African cohorts.

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Genomewide rapid association using mixed model and regression: a fast and simple method for genomewide pedigree-based quantitative trait loci association analysis

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Ethnic differences in the frequency of ENPP1/PC1 121Q genetic variant in the Dallas Heart Study cohort

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Detection of large-scale variation in the human genome

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Mice heterozygous for Atp10c, a putative amphipath, represent a novel model of obesity and type 2 diabetes.

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Control of confounding of genetic associations in stratified populations

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Population admixture may appear to mask, change or reverse genetic effects of genes underlying complex traits

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Requirement for the L-type Ca(2+) channel alpha(1D) subunit in postnatal pancreatic beta cell generation

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12 December 2020

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10.1371/JOURNAL.PONE.0024052

1 reference

Europe PubMed Central

30 July 2017

2011PLoSO...624052I

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1 reference

Europe PubMed Central

30 July 2017

1 reference

Europe PubMed Central

30 July 2017

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