(Q47989626)

7 February 2018

title

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

1 reference

7 February 2018

0 references

0 references

1 reference

Jukka S Moilanen

0 references

Arto Mannermaa

1 reference

7 February 2018

Hilkka Soininen

1 reference

7 February 2018

Jaana Autere

1 reference

7 February 2018

Saara Finnilä

1 reference

7 February 2018

Päivi Hartikainen

1 reference

7 February 2018

Merja Hallikainen

1 reference

7 February 2018

Kari Majamaa

1 reference

7 February 2018

publication date

24 April 2004

1 reference

7 February 2018

published in

Human Genetics

1 reference

7 February 2018

volume

115

1 reference

7 February 2018

issue

1 reference

7 February 2018

page(s)

29-35

1 reference

7 February 2018

Statistical method for testing the neutral mutation hypothesis by DNA polymorphism

cites work

1 reference

12 December 2020

On the number of segregating sites in genetical models without recombination

1 reference

12 December 2020

Atypical parkinsonism in a family of Portuguese ancestry: absence of CAG repeat expansion in the MJD1 gene

1 reference

12 December 2020

Mitochondrial oxidative phosphorylation defects in Parkinson's disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Statistical tests of neutrality of mutations

1 reference

12 December 2020

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

1 reference

12 December 2020

Human mitochondrial complex I in health and disease

1 reference

12 December 2020

Mitochondrial genotype associated with longevity

1 reference

12 December 2020

Statistical Tests of Neutrality of Mutations Against Population Growth, Hitchhiking and Background Selection

1 reference

12 December 2020

Human mtDNA haplogroups associated with high or reduced spermatozoa motility

1 reference

12 December 2020

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

1 reference

12 December 2020

Chronic systemic pesticide exposure reproduces features of Parkinson's disease

1 reference

12 December 2020

Mitochondrial genome variation and the origin of modern humans

1 reference

12 December 2020

Parkinson's Disease Society Brain Bank, London: overview and research

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 DNA transmission of the mitochondrial defect in Parkinson's disease

1 reference

12 December 2020

Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

1 reference

12 December 2020

Does nonneutral evolution shape observed patterns of DNA variation in animal mitochondrial genomes?

1 reference

12 December 2020

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

1 reference

12 December 2020

Mitochondrial DNA variation in human evolution and disease

1 reference

12 December 2020

Cortical Lewy body pathology in the diagnosis of dementia

1 reference

12 December 2020

Mitochondrial complex I deficiency in Parkinson's disease

1 reference

12 December 2020

Phylogenetic network for European mtDNA.

1 reference

12 December 2020

Apoptosis in Parkinson's disease: signals for neuronal degradation

1 reference

12 December 2020

Transmembrane topology of the NuoL, M and N subunits of NADH:quinone oxidoreductase and their homologues among membrane-bound hydrogenases and bona fide antiporters

1 reference

12 December 2020

The epidemiology of pathogenic mitochondrial DNA mutations

1 reference

12 December 2020

Inhibition of NADH-linked oxidation in brain mitochondria by 1-methyl-4-phenyl-pyridine, a metabolite of the neurotoxin, 1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine

1 reference

12 December 2020

Statistical tests of selective neutrality in the age of genomics

1 reference

12 December 2020

PAML: a program package for phylogenetic analysis by maximum likelihood

1 reference

12 December 2020

Classification of European mtDNAs from an analysis of three European populations

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

1994 William Allan Award Address. Mitochondrial DNA variation in human evolution, degenerative disease, and aging

1 reference

12 December 2020

Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.

1 reference

12 December 2020

Properties of statistical tests of neutrality for DNA polymorphism data

1 reference

12 December 2020

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

1 reference

12 December 2020

Estimating synonymous and nonsynonymous substitution rates under realistic evolutionary models

1 reference

12 December 2020

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

1 reference

12 December 2020

Increased variation in mtDNA in patients with familial sensorineural hearing impairment

1 reference

12 December 2020

Parkinson disease: analysis of mitochondrial DNA in monozygotic twins

1 reference

12 December 2020

10.1007/S00439-004-1123-9

Identifiers

DOI

1 reference

7 February 2018

1 reference

7 February 2018