(Q37027318)

17 August 2017

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Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease (English)

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17 August 2017

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1 reference

1 reference

David J Burn

13

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John Anthony Hardy

11

object named as

John Hardy

1 reference

17 August 2017

9

Roger A Barker

1 reference

17 August 2017

10

Andrew B Singleton

1 reference

17 August 2017

14

Patrick F Chinnery

1 reference

17 August 2017

1

Gavin Hudson

1 reference

17 August 2017

Mike Nalls

2

1 reference

17 August 2017

Jonathan R Evans

3

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17 August 2017

David P Breen

4

1 reference

17 August 2017

Sophie Winder-Rhodes

5

1 reference

17 August 2017

Karen E Morrison

6

1 reference

17 August 2017

Huw R Morris

7

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17 August 2017

Caroline H Williams-Gray

8

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17 August 2017

Nicholas E Wood

12

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17 August 2017

language of work or name

English

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publication date

3 May 2013

1 reference

17 August 2017

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17 August 2017

80

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17 August 2017

22

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17 August 2017

2042-2048

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Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

Genome-wide association study reveals genetic risk underlying Parkinson's disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

alpha-Synuclein is differentially expressed in mitochondria from different rat brain regions and dose-dependently down-regulates complex I activity

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

PLINK: a tool set for whole-genome association and population-based linkage analyses

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

Mitochondrial 16S rRNA gene encodes a functional peptide, a potential drug for Alzheimer's disease and target for cancer therapy

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

Evidence for in vivo production of Humanin peptide, a neuroprotective factor against Alzheimer's disease-related insults

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

Chronic systemic pesticide exposure reproduces features of Parkinson's disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

alpha-synuclein promotes mitochondrial deficit and oxidative stress

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

Evidence of active nerve cell degeneration in the substantia nigra of humans years after 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine exposure

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

Classification of European mtDNAs from an analysis of three European populations

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

Functional mitochondria are required for alpha-synuclein toxicity in aging yeast.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

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

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3716399

Mitochondrial DNA polymorphisms and haplogroups in Parkinson's disease and control individuals with a similar genetic background

4 September 2018

1 reference

12 December 2020

1 reference

12 December 2020

1 reference

12 December 2020

mt4216C variant in linkage with the mtDNA TJ cluster may confer a susceptibility to mitochondrial dysfunction resulting in an increased risk of Parkinson's disease in the Irish

1 reference

12 December 2020

Mitochondrial polymporphisms in Parkinson's Disease

1 reference

12 December 2020

Mitochondrial complex I deficiency in Parkinson's disease

1 reference

12 December 2020

Mitochondrial DNA and survival after sepsis: a prospective study

1 reference

12 December 2020

Mitochondrial DNA mutations in complex I and tRNA genes in Parkinson's disease

1 reference

12 December 2020

10.1212/WNL.0B013E318294B434

Identifiers

DOI

1 reference

17 August 2017

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17 August 2017

1 reference