Genome-wide association study reveals genetic risk underlying Parkinson's disease (Q24646654)

19

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Thomas Illig

18

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Henry Houlden

20

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Sampath Arepalli

29

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Peter Lichtner

8

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Daniela Berg

6

1 reference

ORCID Public Data File 2021

Rejko Krüger

11

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Günther Deuschl

42

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Katrina Gwinn

31

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Delia Lorenz

41

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Michael Steffens

Michael Steffens

21

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Sonja Scholz

Sonja W Scholz

9

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Claudia Schulte

Claudia Schulte

2

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Jose Bras

Jose M Bras

3

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Honglei Chen

Honglei Chen

43

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Yikyung Park

Yikyung Park

36

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Michael S. Okun

Michael S Okun

22

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Alison Goate

Alison Goate

14

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Stephen Chanock

34

Stephen J Chanock

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Kelly D Foote

Kelly D Foote

25

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Christine Klein

13

Christine Klein

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John Anthony Hardy

45

John A Hardy

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Hubert H Fernandez

26

Hubert H Fernandez

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Mark R Cookson

24

Mark R Cookson

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Joel S Perlmutter

15

Joel Perlmutter

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Xuemei Huang

39

Xuemei Huang

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Andrew Singleton

46

Andrew B Singleton

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Coro Paisán-Ruíz

7

Coro Paisan-Ruiz

0 references

Arthur Schatzkin

35

Arthur Schatzkin

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Olaf Riess

44

Olaf Riess

0 references

Bryan Traynor

27

Bryan J Traynor

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Manu Sharma

4

Manu Sharma

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Dena G. Hernandez

10

Dena G Hernandez

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Stefan Schreiber

28

Stefan Schreiber

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Javier Simón Sánchez

1

Javier Simón-Sánchez

0 references

J Raphael Gibbs

5

J Raphael Gibbs

0 references

Michael Marmot

17

Michael A Nalls

0 references

Albert R Hollenbeck

37

Albert Hollenbeck

0 references

Monica Federoff

12

Monica Federoff

0 references

author name string

Michael Bonin

16

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Brad A Racette

23

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Ryan Zonozi

30

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Marcel van der Brug

32

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Grisel Lopez

33

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Jianjun Gao

38

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Nick W Wood

40

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Thomas Gasser

describes a project that uses

47

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language of work or name

English

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publication date

December 2009

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published in

Nature Genetics

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volume

41

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page(s)

1308-12

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issue

12

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genome-wide association study

1 reference

based on heuristic

inferred from title

cites work

RNA binding activity of the recessive parkinsonism protein DJ-1 supports involvement in multiple cellular pathways

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

High-resolution whole-genome association study of Parkinson disease.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

Haploview: analysis and visualization of LD and haplotype maps

7 April 2017

1 reference

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The International HapMap Project

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

alpha-Synuclein locus triplication causes Parkinson's disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

The structure of haplotype blocks in the human genome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

TAU haplotype and the Saitohin Q7R gene polymorphism do not influence CSF Tau in Alzheimer's disease and are not associated with frontotemporal dementia or Parkinson's disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

SNCA variants are associated with increased risk for multiple system atrophy

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

Linkage disequilibrium and association of MAPT H1 in Parkinson disease

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

Effect of allelic variation at the NACP-Rep1 repeat upstream of the alpha-synuclein gene (SNCA) on transcription in a cell culture luciferase reporter system

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

Missense and splice site mutations in tau associated with FTDP-17: multiple pathogenic mechanisms

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

Collaborative Analysis of α-Synuclein Gene Promoter Variability and Parkinson Disease

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

Association of an extended haplotype in the tau gene with progressive supranuclear palsy.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2787725

28 November 2018

Identifiers

DOI

10.1038/NG.487

1 reference

Dimensions Publication ID

531222

1046211505

0 references

531222

1 reference

1 reference

1 reference