(Q42974496)

12 November 2017

Associating mitochondrial DNA variation with complex traits (English)

1 reference

12 November 2017

0 references

1 reference

4

Patrick F Chinnery

1 reference

12 November 2017

Joanna L Elson

1

1 reference

12 November 2017

Kari Majamaa

series ordinal

2

1 reference

12 November 2017

Neil Howell

series ordinal

3

1 reference

12 November 2017

language of work or name

English

0 references

publication date

1 February 2007

1 reference

American Journal of Human Genetics

12 November 2017

1 reference

12 November 2017

80

1 reference

12 November 2017

2

1 reference

12 November 2017

378-82; author reply 382-3

1 reference

Comprehensive association testing of common mitochondrial DNA variation in metabolic disease

12 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785337

Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785337

A reanalysis of the indirect evidence for recombination in human mitochondrial DNA.

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785337

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

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785337

Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785337

Mitochondrial DNA haplogroups do not play a role in the variable phenotypic presentation of the A3243G mutation

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785337

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

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785337

Phylogenetic network for European mtDNA.

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785337

Analysis of European mtDNAs for recombination

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785337

The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785337

Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484.

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785337

Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785337

Mitochondrial DNA sequence variation in human evolution and disease.

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785337

The power to detect disease associations with mitochondrial DNA haplogroups

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785337

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

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785337

Analysis of European mitochondrial haplogroups with Alzheimer disease risk

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785337

Leber's hereditary optic neuropathy: the spectrum of mitochondrial DNA mutations in Iranian patients.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785337

Mitochondrial DNA haplogroup distribution within Leber hereditary optic neuropathy pedigrees

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785337

Phylogenetic network and physicochemical properties of nonsynonymous mutations in the protein-coding genes of human mitochondrial DNA.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785337

Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunction

16 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17304709

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Does the mitochondrial genome play a role in the etiology of Alzheimer's disease?

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17304709

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17304709

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/511652

1 reference

12 November 2017

1 reference

12 November 2017

PubMed publication ID

17304709

1 reference