Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease (Q33548162)

28 July 2017

title

Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease (English)

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28 July 2017

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9

Tatiana Foroud

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Nathan Pankratz

2

object named as

Nathan Pankratz

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Francis Walker

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ORCID Public Data File 2021

Michael W. Pauciulo

4

object named as

Michael W Pauciulo

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28 July 2017

5

Cheryl A Halter

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28 July 2017

6

Alice Rudolph

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Parkinson Study Group - PROGENI Investigators

28 July 2017

10

object named as

Parkinson Study Group-PROGENI Investigators

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28 July 2017

David K Simon

1

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28 July 2017

Diane K Kissell

3

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28 July 2017

Ronald F Pfeiffer

7

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28 July 2017

William C Nichols

8

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28 July 2017

publication date

1 April 2010

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28 July 2017

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28 July 2017

volume

11

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28 July 2017

page(s)

53

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Genomewide association study for susceptibility genes contributing to familial Parkinson disease

28 July 2017

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28 July 2018

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28 July 2018

Whole-genome genotyping

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Dominant inheritance of premature ovarian failure associated with mutant mitochondrial DNA polymerase gamma.

28 July 2018

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Implications of genetics on the diagnosis and care of patients with Parkinson disease

28 July 2018

1 reference

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

28 July 2018

1 reference

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Mitochondrial ND5 mutations in idiopathic Parkinson's disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858137

High frequency of mitochondrial complex I mutations in Parkinson's disease and aging

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858137

Somatic mitochondrial DNA mutations in cortex and substantia nigra in aging and Parkinson's disease

28 July 2018

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Prenatal exposure to the bacteriotoxin lipopolysaccharide leads to long-term losses of dopamine neurons in offspring: a potential, new model of Parkinson's disease

28 July 2018

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The rotenone model of Parkinson's disease: genes, environment and mitochondria

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858137

Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858137

Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858137

Segregation analysis of Parkinson disease revealing evidence for a major causative gene.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858137

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858137

In utero bacterial endotoxin exposure causes loss of tyrosine hydroxylase neurons in the postnatal rat midbrain.

28 July 2018

1 reference

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Gender ratio differences between Parkinson's disease patients and their affected relatives

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858137

Association between early-onset Parkinson's disease and mutations in the parkin gene

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858137

Matrilineal inheritance of complex I dysfunction in a multigenerational Parkinson's disease family

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858137

Mitochondrial DNA transmission of the mitochondrial defect in Parkinson's disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858137

Mitochondrial DNA polymorphisms in pathologically proven Parkinson's disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858137

Maternal inheritance in Parkinson's disease

28 July 2018

1 reference

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Origin and functional consequences of the complex I defect in Parkinson's disease

28 July 2018

1 reference

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Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

28 July 2018

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The Familial Occurrence of Parkinson's Disease Lack of Evidence for Maternal Inheritance

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858137

The etiology of Parkinson's disease with emphasis on the MPTP story

28 July 2018

1 reference

https://api.crossref.org/works/10.1186/1471-2350-11-53

Parkinson syndrome, neuropathy, and myopathy caused by the mutation A8344G (MERRF) in tRNALys

21 January 2018

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https://api.crossref.org/works/10.1186/1471-2350-11-53

Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.

21 January 2018

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https://api.crossref.org/works/10.1186/1471-2350-11-53

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

21 January 2018

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

21 January 2018

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A mitochondrial etiology of neurodegenerative diseases: evidence from Parkinson's disease

21 January 2018

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Interrater reliability of the Unified Parkinson's Disease Rating Scale motor examination.

21 January 2018

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Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD.

21 January 2018

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Frequency of LRRK2 mutations in early- and late-onset Parkinson disease

21 January 2018

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A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy

21 January 2018

1 reference

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A genetic study of Parkinson's disease.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858137

31 October 2018

1 reference

12 December 2020

Familial multisystem degeneration with parkinsonism associated with the 11778 mitochondrial DNA mutation

1 reference

12 December 2020

Maternal effect on Parkinson's disease

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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 encephalopathy with multiple mitochondrial DNA deletions: a report of two families and two sporadic cases with unusual clinical and neuropathological features

1 reference

12 December 2020

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

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12 December 2020

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12 December 2020

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

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12 December 2020

Sequence analysis of the entire mitochondrial genome in Parkinson's disease

1 reference

12 December 2020

Abnormalities of the electron transport chain in idiopathic Parkinson's disease

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12 December 2020

Mitochondrial complex I deficiency in Parkinson's disease

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12 December 2020

Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish family

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2350-11-53

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Dimensions Publication ID

28 July 2017

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28 July 2017

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