Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population (Q28943392)

ORCID Public Data File 2021

Joseph H. Lee

object named as

Joseph H. Lee

16

1 reference

ORCID Public Data File 2021

Miguel Verbitsky

3

object named as

Miguel Verbitsky

1 reference

14 March 2017

4

Sergey Kisselev

1 reference

14 March 2017

11

Blair Ford

1 reference

14 March 2017

14

Karen Marder

1 reference

14 March 2017

8

Lucien J. Cote

1 reference

14 March 2017

15

Lorraine N. Clark

1 reference

14 March 2017

10

Cheryl Waters

1 reference

14 March 2017

Xinmin Liu

1

1 reference

14 March 2017

Rong Cheng

2

1 reference

14 March 2017

Andrew Browne

5

1 reference

14 March 2017

Helen Mejia-Sanatana

6

1 reference

14 March 2017

Howard Andrews

describes a project that uses

9

1 reference

14 March 2017

3 August 2011

1 reference

14 March 2017

1 reference

14 March 2017

12

1 reference

14 March 2017

104

1 reference

14 March 2017

genome-wide association study

1 reference

based on heuristic

inferred from title

exact match

https://scigraph.springernature.com/pub.10.1186/1471-2350-12-104

0 references

cites work

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Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease

16 March 2017

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Interaction of dopamine D1 receptor with N-ethylmaleimide-sensitive factor is important for the membrane localization of the receptor

16 March 2017

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Abraham's children in the genome era: major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern Ancestry

16 March 2017

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Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update

16 March 2017

1 reference

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Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease

16 March 2017

1 reference

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

16 March 2017

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Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

16 March 2017

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

16 March 2017

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16 March 2017

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

16 March 2017

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

16 March 2017

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16 March 2017

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Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

16 March 2017

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Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

16 March 2017

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Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

16 March 2017

1 reference

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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.

16 March 2017

1 reference

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Genomewide association study for onset age in Parkinson disease

7 April 2017

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Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

7 April 2017

1 reference

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7 April 2017

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A common inversion under selection in Europeans

7 April 2017

1 reference

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Genetic variability at the PARK16 locus

7 April 2017

1 reference

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Dimerization of dopamine D1 and D3 receptors in the regulation of striatal function.

3 June 2018

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A network of G-protein signaling pathways control neuronal activity in C. elegans

3 June 2018

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Genomewide association study for susceptibility genes contributing to familial Parkinson disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166909

Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166909

Fourteen novel human members of mitochondrial solute carrier family 25 (SLC25) widely expressed in the central nervous system.

3 June 2018

1 reference

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3 June 2018

1 reference

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Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population

3 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-104

A genetic profile of contemporary Jewish populations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-104

LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-104

Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-104

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-104

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

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21812969

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

NSF--fusion and beyond

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21812969

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2350-12-104

1 reference

Dimensions Publication ID

3719277

1004621362

0 references

3719277

1 reference

1 reference

1 reference