Population genetic approaches to neurological disease: Parkinson's disease as an example (Q36226918)

12 August 2017

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title

Population genetic approaches to neurological disease: Parkinson's disease as an example (English)

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12 August 2017

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W Gilks

5

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Michael E. Weale

object named as

M Weale

4

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D.G. Healy

3

object named as

D G Healy

1 reference

12 August 2017

S Gandhi

1

1 reference

12 August 2017

P M Abou-Sleiman

2

1 reference

12 August 2017

K Ahmadi

6

1 reference

12 August 2017

D B Goldstein

7

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12 August 2017

N W Wood

8

1 reference

12 August 2017

language of work or name

English

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publication date

1 August 2005

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Philosophical Transactions of the Royal Society B

12 August 2017

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12 August 2017

360

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12 August 2017

1460

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12 August 2017

1573-1578

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A common LRRK2 mutation in idiopathic Parkinson's disease

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

Mathematical assumptions versus biological reality: myths in affected sib pair linkage analysis

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

Novel PINK1 mutations in early-onset parkinsonism

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

PINK1 mutations are associated with sporadic early-onset parkinsonism

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

Smoking and Parkinson's disease: systematic review of prospective studies

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

Identifying candidate causal variants responsible for altered activity of the ABCB1 multidrug resistance gene

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

Occupational and environmental risk factors for Parkinson's disease

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

Molecular Pathways of Neurodegeneration in Parkinson's Disease

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

Haplotype blocks and linkage disequilibrium in the human genome

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

Further studies in xenobiotic metabolism and Parkinson's disease.

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

Pathophysiology and biochemistry of dyskinesia: clues for the development of non-dopaminergic treatments

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

Permanent human parkinsonism due to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP): seven cases

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

Homozygous PINK1 C-terminus mutation causing early-onset parkinsonism.

1 October 2017

1 reference

Crossref

https://api.crossref.org/works/10.1098%2FRSTB.2005.1687

Prevalence of Parkinson's disease in the elderly: The Rotterdam Study

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1098%2FRSTB.2005.1687

A single-nucleotide polymorphism tagging set for human drug metabolism and transport

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569523

Familial aggregation of early- and late-onset Parkinson's disease

5 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16096106

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16096106

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1098/RSTB.2005.1687

1 reference

release_aucdqrph3neurpf5qwtafft7ye

12 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/aucdqrph3neurpf5qwtafft7ye

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

12 August 2017

PubMed publication ID

16096106

1 reference