A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease (Q36494703)

14 August 2017

A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease (English)

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14 August 2017

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John P A Ioannidis

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Alexis Brice

10

Christine Van Broeckhoven

Alexis Brice

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5

Christine Van Broeckhoven

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Jessie Theuns

Jessie Theuns

6

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George D. Mellick

George D Mellick

25

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Anna Rita Bentivoglio

Anna Rita Bentivoglio

9

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Matthew J. Farrer

Matthew Farrer

13

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Aldo Quattrone

Aldo Quattrone

29

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Suzanne Lesage

22

Suzanne Lesage

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14 August 2017

4

Thomas Gasser

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14 August 2017

37

Zbigniew Wszolek

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14 August 2017

17

Nobutaka Hattori

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14 August 2017

20

Christine Klein

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14 August 2017

30

Owen A Ross

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28

Alessandro Prigione

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32

Peter A Silburn

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3

Olaf Riess

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1

Rejko Krüger

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14 August 2017

8

Grazia Annesi

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14 August 2017

36

Karin Wirdefeldt

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14 August 2017

Barbara Jasinska-Myga

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Barbara Jasinska-Myga

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2

Manu Sharma

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14 August 2017

Georgios M Hadjigeorgiou

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Georgios M Hadjigeorgiou

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14 August 2017

38

Georgia Xiromerisiou

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27

Grzegorz Opala

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14 August 2017

Demetrius M. Maraganore

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Demetrius M Maraganore

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35

Hiroyuki Tomiyama

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31

Wataru Satake

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14 August 2017

23

Juei-Jueng Lin

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14 August 2017

26

Francesa de Nigris

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14 August 2017

24

Timothy Lynch

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14 August 2017

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Carlo Ferrarese

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14 August 2017

Jan Aasly

7

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14 August 2017

Ana Djarmati

11

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14 August 2017

Alexis Elbaz

12

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14 August 2017

J Mark Gibson

15

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14 August 2017

Eng King Tan

33

1 reference

14 August 2017

Tatsushi Toda

34

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14 August 2017

Genetic Epidemiology of Parkinson's disease consortium

40

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14 August 2017

language of work or name

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24 December 2009

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14 August 2017

Neurobiology of Aging

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14 August 2017

32

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3

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14 August 2017

548.e9-18

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Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease: large-scale collaborative study

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

Validating, augmenting and refining genome-wide association signals

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

STrengthening the REporting of Genetic Association studies (STREGA)--an extension of the STROBE statement

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

Genetic variation of Omi/HtrA2 and Parkinson's disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

Genes mirror geography within Europe

30 September 2017

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

Omi / HtrA2 is relevant to the selective vulnerability of striatal neurons in Huntington's disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

Sequencing analysis of OMI/HTRA2 shows previously reported pathogenic mutations in neurologically normal controls

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

Calibration of credibility of agnostic genome-wide associations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

Uncertainty in heterogeneity estimates in meta-analyses

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

Designing candidate gene and genome-wide case-control association studies.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

Replicating genotype-phenotype associations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

Efficiency and power in genetic association studies

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

PINK1 mutations are associated with sporadic early-onset parkinsonism

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

The complex interplay among factors that influence allelic association.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

Loss of Omi mitochondrial protease activity causes the neuromuscular disorder of mnd2 mutant mice

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

Accumulation of HtrA2/Omi in neuronal and glial inclusions in brains with alpha-synucleinopathies

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson disease

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

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

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724437

10.1016/J.NEUROBIOLAGING.2009.11.021

4 December 2018

Identifiers

DOI

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14 August 2017

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14 August 2017

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