(Q34658510)

3 August 2017

title

Comprehensive association testing of common mitochondrial DNA variation in metabolic disease (English)

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3 August 2017

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1

Richa Saxena

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3 August 2017

10

Leif Groop

1 reference

3 August 2017

8

Bo Isomaa

1 reference

3 August 2017

9

Mark J Daly

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3 August 2017

12

David Altshuler

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3 August 2017

6

Joel N Hirschhorn

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3 August 2017

2

Paul I W de Bakker

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3 August 2017

4

Vamsi Mootha

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3 August 2017

Karyn Singer

3

1 reference

3 August 2017

Noel Burtt

series ordinal

5

1 reference

3 August 2017

Daniel Gaudet

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7

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3 August 2017

Kristin G Ardlie

series ordinal

11

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3 August 2017

language of work or name

English

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publication date

24 May 2006

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American Journal of Human Genetics

3 August 2017

published in

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3 August 2017

volume

79

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3 August 2017

issue

1

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3 August 2017

page(s)

54-61

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Mitochondrial medicine: a metabolic perspective on the pathology of oxidative phosphorylation disorders

3 August 2017

cites work

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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Mining disease susceptibility genes through SNP analyses and expression profiling using MALDI-TOF mass spectrometry

7 July 2018

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Impaired mitochondrial activity in the insulin-resistant offspring of patients with type 2 diabetes

7 July 2018

1 reference

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Effects of purifying and adaptive selection on regional variation in human mtDNA.

7 July 2018

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Integrated analysis of protein composition, tissue diversity, and gene regulation in mouse mitochondria

7 July 2018

1 reference

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Coordinated reduction of genes of oxidative metabolism in humans with insulin resistance and diabetes: Potential role of PGC1 and NRF1

7 July 2018

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PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes

7 July 2018

1 reference

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Mitochondrial dysfunction in the elderly: possible role in insulin resistance

7 July 2018

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7 July 2018

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Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

7 July 2018

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Natural selection shaped regional mtDNA variation in humans

7 July 2018

1 reference

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

7 July 2018

1 reference

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Mitochondrial DNA polymorphisms associated with longevity in a Finnish population

7 July 2018

1 reference

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Mitochondrial genotypes and cytochrome b variants associated with longevity or Parkinson's disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

Dysfunction of mitochondria in human skeletal muscle in type 2 diabetes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

Mitochondrial diabetes, DIDMOAD and other inherited diabetes syndromes.

7 July 2018

1 reference

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Inherited variability of the mitochondrial genome and successful aging in humans.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

Mitochondrial involvement in Parkinson's disease, Huntington's disease, hereditary spastic paraplegia and Friedreich's ataxia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

A common mitochondrial DNA variant is associated with insulin resistance in adult life.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

Classification of European mtDNAs from an analysis of three European populations

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

Human brain contains high levels of heteroplasmy in the noncoding regions of mitochondrial DNA.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

Mitochondrial polymorphisms and susceptibility to type 2 diabetes-related traits in Finns

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

Genome-wide strategies for detecting multiple loci that influence complex diseases.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

Deficiency of subsarcolemmal mitochondria in obesity and type 2 diabetes

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

Analysis of European mitochondrial haplogroups with Alzheimer disease risk

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

Mitochondrial DNA polymorphisms as risk factors for Parkinson's disease and Parkinson's disease dementia

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

Mitochondrial DNA haplogroups influence the Friedreich's ataxia phenotype

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

The presence of a common mitochondrial DNA variant is associated with fasting insulin levels in Europeans in Auckland.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

Type 2 diabetes is associated with a common mitochondrial variant: evidence from a population-based case-control study.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

A common mitochondrial DNA variant associated with susceptibility to dilated cardiomyopathy in two different populations

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474138

Association testing in 9,000 people fails to confirm the association of the insulin receptor substrate-1 G972R polymorphism with type 2 diabetes

26 October 2018

1 reference

12 December 2020

Association of the mitochondrial DNA haplogroup J with longevity is population specific

1 reference

12 December 2020

Mitochondrial genotype associated with longevity

1 reference

12 December 2020

Role of the mitochondrial DNA 16184–16193 poly-C tract in type 2 diabetes

1 reference

12 December 2020

A mitochondrial DNA variant associated with left ventricular hypertrophy in diabetes

1 reference

12 December 2020

Mitochondrial DNA polymorphism: its role in longevity of the Irish population

1 reference

12 December 2020

Variation is the spice of life

1 reference

12 December 2020

A combination of three common inherited mitochondrial DNA polymorphisms promotes longevity in Finnish and Japanese subjects

1 reference

12 December 2020

Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease

1 reference

12 December 2020

Altered glycolytic and oxidative capacities of skeletal muscle contribute to insulin resistance in NIDDM

1 reference

12 December 2020

Association testing of variants in the hepatocyte nuclear factor 4alpha gene with risk of type 2 diabetes in 7,883 people

1 reference

12 December 2020

Identifiers

DOI

10.1086/504926

1 reference

3 August 2017

1 reference

3 August 2017

1 reference