(Q30539203)

16 August 2017

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

1 reference

single-nucleotide polymorphism

16 August 2017

1 reference

1 reference

24

1 reference

Christine Van Broeckhoven

PubMed publication ID

24 June 2017

4

John P A Ioannidis

0 references

21

Christine Van Broeckhoven

0 references

Andrea Carmine Belin

Andrea Carmine Belin

7

0 references

George D. Mellick

George D Mellick

16

0 references

Beate Ritz

18

Beate Ritz

1 reference

16 August 2017

17

John G Nutt

1 reference

16 August 2017

20

Caroline M Tanner

1 reference

16 August 2017

8

Stewart A Factor

1 reference

16 August 2017

13

Rejko Krüger

1 reference

16 August 2017

6

Grazia Annesi

1 reference

16 August 2017

23

Karin Wirdefeldt

1 reference

16 August 2017

Georgios M Hadjigeorgiou

10

Georgios M Hadjigeorgiou

1 reference

16 August 2017

29

Thomas A Trikalinos

1 reference

16 August 2017

28

Richard M Myers

1 reference

16 August 2017

Jennifer S. Montimurro

26

Jennifer S Montimurro

1 reference

16 August 2017

19

Ali Samii

1 reference

16 August 2017

3

Haydeh Payami

1 reference

16 August 2017

14

Karen S Marder

1 reference

16 August 2017

Stephen K Van Den Eeden

22

Stephen K Van Den Eeden

1 reference

16 August 2017

9

Carlo Ferrarese

1 reference

16 August 2017

Alexis Elbaz

1

1 reference

16 August 2017

Lorene M Nelson

2

1 reference

16 August 2017

Brian K Fiske

5

1 reference

16 August 2017

Donald S Higgins

11

1 reference

16 August 2017

Hideshi Kawakami

12

1 reference

16 August 2017

Richard P Mayeux

15

1 reference

16 August 2017

Marie Dehem

25

1 reference

16 August 2017

Audrey Southwick

27

1 reference

16 August 2017

1 November 2006

1 reference

16 August 2017

1 reference

16 August 2017

5

1 reference

16 August 2017

11

1 reference

16 August 2017

917-923

1 reference

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

16 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

Genomewide association, Parkinson disease, and PARK10

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

Considerations for genomewide association studies in Parkinson disease

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

A common variant associated with prostate cancer in European and African populations

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

Early extreme contradictory estimates may appear in published research: the Proteus phenomenon in molecular genetics research and randomized trials

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

Complement factor H variant increases the risk of age-related macular degeneration

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

Genome-wide association studies for common diseases and complex traits

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

Prospective Belgian study of neurodegenerative and vascular dementia: APOE genotype effects

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

Quantifying heterogeneity in a meta-analysis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

A brief history of research synthesis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

Parkinson disease in twins: an etiologic study

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

Quantitative synthesis in systematic reviews

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

Implications of small effect sizes of individual genetic variants on the design and interpretation of genetic association studies of complex diseases.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

Evaluating coverage of genome-wide association studies

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

A common genetic variant is associated with adult and childhood obesity

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

Case-control study of environmental risk factors for Parkinson's disease in Belgium

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases I. DNA pooling

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3636768

Polymorphism in semaphorin 5A (Sema5A) gene is not a marker of Parkinson's disease risk

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17052658

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Response from Maraganore et al.

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970579-8

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S1474-4422(06)70579-8

1 reference

release_un7pjdtrifeldamc2dxomefqz4

16 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/un7pjdtrifeldamc2dxomefqz4

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

16 August 2017

PubMed publication ID

17052658

1 reference