(Q42418561)

30 October 2017

Genomewide association, Parkinson disease, and PARK10 (English)

1 reference

30 October 2017

1 reference

1

1 reference

30 October 2017

Andrew J Whittle

7

0 references

Kristoffer Haugarvoll

object named as

Kristoffer Haugarvoll

2

0 references

Mathias Toft

object named as

Mathias Toft

18

0 references

Ryan J Uitti

17

object named as

Ryan J Uitti

1 reference

30 October 2017

16

Zbigniew K Wszolek

1 reference

30 October 2017

3

Owen A Ross

1 reference

30 October 2017

9

Mary M Hulihan

1 reference

30 October 2017

10

Michael G Heckman

1 reference

30 October 2017

14

David Gosal

1 reference

30 October 2017

15

Timothy Lynch

1 reference

30 October 2017

Jeremy T Stone

4

1 reference

30 October 2017

Nicole M Milkovic

5

1 reference

30 October 2017

Stephanie A Cobb

6

1 reference

30 October 2017

Sarah J Lincoln

8

1 reference

30 October 2017

Linda R White

11

1 reference

30 October 2017

Jan O Aasly

12

1 reference

30 October 2017

J Mark Gibson

13

1 reference

30 October 2017

language of work or name

English

0 references

publication date

1 June 2006

1 reference

American Journal of Human Genetics

30 October 2017

1 reference

30 October 2017

78

1 reference

30 October 2017

1084-8; author reply 1092-4

1 reference

30 October 2017

6

1 reference

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

30 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474105

Pathophysiology, pleiotrophy and paradigm shifts: genetic lessons from Parkinson's disease

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474105

Complement factor H polymorphism in age-related macular degeneration

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474105

Complement factor H polymorphism and age-related macular degeneration

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474105

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

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474105

Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474105

Genome-wide association studies: theoretical and practical concerns

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474105

Genome-wide association studies for common diseases and complex traits

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474105

Linkage disequilibrium and association of MAPT H1 in Parkinson disease

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474105

Haploview: analysis and visualization of LD and haplotype maps

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474105

The future of association studies: gene-based analysis and replication

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474105

The structure of haplotype blocks in the human genome

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474105

Age at onset in two common neurodegenerative diseases is genetically controlled

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474105

Estimating Scandinavian and Gaelic ancestry in the male settlers of Iceland

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474105

Diagnostic criteria for Parkinson disease

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474105

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

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474105

A metric linkage disequilibrium map of a human chromosome.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474105

A susceptibility gene for late-onset idiopathic Parkinson's disease

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474105

What makes a good genetic association study?

1 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16685661

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/504728

1 reference

release_kapbfp4phjennabkiqfaoz2wjm

30 October 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/kapbfp4phjennabkiqfaoz2wjm

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

30 October 2017

1 reference