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Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

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Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies (English)

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Parkinson's disease

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genome-wide association study

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Vincent Plagnol

3

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Vincent Plagnol

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Vincent

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Plagnol

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PubMed publication ID

20 October 2023

16

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Alexis Brice

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Alexis

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Brice

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20 October 2023

Kári Stefánsson

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Kári Stefánsson

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Kári

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Stefánsson

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20 October 2023

Claudia Schulte

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Claudia Schulte

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Claudia

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Schulte

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20 October 2023

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Maria Martinez

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Maria

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Martinez

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20 October 2023

Nicholas W. Wood

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Nicholas W Wood

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Nicholas W

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Wood

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20 October 2023

10

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Suzanne Lesage

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Suzanne

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Lesage

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20 October 2023

John Anthony Hardy

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John Hardy

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John

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Hardy

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20 October 2023

15

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Peter Heutink

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Peter

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Heutink

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20 October 2023

Andrew Singleton

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Andrew B Singleton

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Andrew B

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Singleton

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20 October 2023

5

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Manu Sharma

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Manu

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Sharma

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20 October 2023

Dena G. Hernandez

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Dena G Hernandez

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Dena G

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Hernandez

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PubMed publication ID

20 October 2023

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ORCID Public Data File 2021

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ORCID Public Data File 2021

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ORCID Public Data File 2021

Una-Marie Sheerin

6

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Una-Marie Sheerin

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Una-Marie

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Sheerin

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20 October 2023

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Michael A Nalls

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Michael A

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Nalls

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20 October 2023

Mohamad Saad

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Mohamad

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Saad

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20 October 2023

J Simón-Sánchez

8

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J

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Simón-Sánchez

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20 October 2023

Sigurlaug Sveinbjörnsdóttir

11

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Sigurlaug

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Sveinbjörnsdóttir

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PubMed publication ID

20 October 2023

Thomas Gasser

17

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Thomas

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Gasser

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20 October 2023

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publication date

19 February 2011

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377

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9766

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Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain

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7 April 2017

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

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7 April 2017

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

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7 April 2017

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

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7 April 2017

The NCBI dbGaP database of genotypes and phenotypes

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The autosomal recessive juvenile Parkinson disease gene product, parkin, interacts with and ubiquitinates synaptotagmin XI

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7 April 2017

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

1 reference

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7 April 2017

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

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7 April 2017

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

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7 April 2017

METAL: fast and efficient meta-analysis of genomewide association scans

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7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696507

7 April 2017

Genotype imputation

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7 April 2017

Genome-wide association study confirms extant PD risk loci among the Dutch

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27 September 2017

Towards a complete resolution of the genetic architecture of disease

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The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression

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STK39 polymorphisms and blood pressure: an association study in British Caucasians and assessment of cis-acting influences on gene expression

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Epistasis among HLA-DRB1, HLA-DQA1, and HLA-DQB1 loci determines multiple sclerosis susceptibility

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From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.

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Genomewide association study for susceptibility genes contributing to familial Parkinson disease

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Huntingtin-interacting protein 1 influences worm and mouse presynaptic function and protects Caenorhabditis elegans neurons against mutant polyglutamine toxicity.

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Heterogeneity in meta-analyses of genome-wide association investigations

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Common and well-documented HLA alleles: report of the Ad-Hoc committee of the american society for histocompatiblity and immunogenetics

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Overcoming the winner's curse: estimating penetrance parameters from case-control data

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An inflammatory pathomechanism for Parkinson's disease?

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Screening for mutations in synaptotagmin XI in Parkinson's disease.

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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

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Parkinson's disease and dementia with Lewy bodies: a difference in dose?

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7 January 2021

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10.1016/S0140-6736(10)62345-8

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