Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease (Q29614900)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19915576

30 April 2017

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genome-wide association study

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author name string

Satake W

1

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Nakabayashi Y

2

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Mizuta I

3

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Hirota Y

4

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Ito C

5

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Kubo M

6

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Kawaguchi T

7

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Tsunoda T

8

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Watanabe M

9

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Takeda A

10

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Tomiyama H

11

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Nakashima K

12

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Hasegawa K

13

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Obata F

14

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Yoshikawa T

15

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Kawakami H

16

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Sakoda S

17

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Yamamoto M

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Hattori N

19

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Murata M

20

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Nakamura Y

21

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Toda T

22

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language of work or name

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publication date

December 2009

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30 April 2017

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volume

41

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issue

12

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page(s)

1303-7

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describes a project that uses

30 April 2017

genome-wide association study

1 reference

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

inferred from title

cites work

1 reference

12 December 2020

Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease.

1 reference

12 December 2020

A genome-wide association study of global gene expression

1 reference

12 December 2020

Physiological functions of cyclic ADP-ribose and NAADP as calcium messengers

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A haplotype map of the human genome

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12 December 2020

Multiple regions of alpha-synuclein are associated with Parkinson's disease

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12 December 2020

A common LRRK2 mutation in idiopathic Parkinson's disease

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12 December 2020

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

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12 December 2020

Common variants of LRRK2 are not associated with sporadic Parkinson's disease

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12 December 2020

SLC41A1 is a novel mammalian Mg2+ carrier

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12 December 2020

alpha-Synuclein promoter confers susceptibility to Parkinson's disease.

1 reference

12 December 2020

The structure of haplotype blocks in the human genome

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12 December 2020

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

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12 December 2020

Genetic and environmental factors in the cause of Parkinson's disease

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12 December 2020

alpha-Synuclein locus triplication causes Parkinson's disease

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12 December 2020

Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

1 reference

12 December 2020

Molecular cloning of a mammalian nuclear phosphoprotein NUCKS, which serves as a substrate for Cdk1 in vivo

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12 December 2020

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12 December 2020

Multiple candidate gene analysis identifies alpha-synuclein as a susceptibility gene for sporadic Parkinson's disease

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12 December 2020

Crystallographic studies on human BST-1/CD157 with ADP-ribosyl cyclase and NAD glycohydrolase activities

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12 December 2020

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

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12 December 2020

Coupled oscillator model of the dopaminergic neuron of the substantia nigra

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12 December 2020

Haploview: analysis and visualization of LD and haplotype maps

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Cloning and chromosome assignment to 1q32 of a human cDNA (RAB7L1) encoding a small GTP-binding protein, a member of the RAS superfamily

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12 December 2020

'Rejuvenation' protects neurons in mouse models of Parkinson's disease

1 reference

12 December 2020

Role of the tau gene region chromosome inversion in progressive supranuclear palsy, corticobasal degeneration, and related disorders

1 reference

12 December 2020

Prevalence of parkinsonism and Parkinson's disease in Europe: the EUROPARKINSON Collaborative Study. European Community Concerted Action on the Epidemiology of Parkinson's disease

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12 December 2020

Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity

1 reference

12 December 2020

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

1 reference

12 December 2020

Identification of a mammalian H(+)-myo-inositol symporter expressed predominantly in the brain

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12 December 2020

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

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12 December 2020

Disappearance of high-incidence amyotrophic lateral sclerosis and parkinsonism-dementia on Guam

1 reference

12 December 2020

Tau gene and Parkinson's disease: a case-control study and meta-analysis

1 reference

12 December 2020

Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews

1 reference

12 December 2020

Kinase activity of mutant LRRK2 mediates neuronal toxicity

1 reference

12 December 2020

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

1 reference

12 December 2020

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

1 reference

12 December 2020

Calcium, ageing, and neuronal vulnerability in Parkinson's disease

1 reference

12 December 2020

Genetics of Parkinson disease: paradigm shifts and future prospects.

1 reference

12 December 2020

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.485

7 January 2021

inferred from DOI database lookup

Identifiers

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19915576

30 April 2017

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

432541

Dimensions Publication ID

1018183324

0 references

OpenCitations bibliographic resource ID

432541

1 reference