(Q37198961)

18 August 2017

Phactr2 and Parkinson's disease (English)

1 reference

18 August 2017

1 reference

12

Ryan J Uitti

1 reference

18 August 2017

13

Zbigniew K Wszolek

1 reference

18 August 2017

Kristoffer Haugarvoll

6

object named as

Kristoffer Haugarvoll

1 reference

18 August 2017

15

Owen A Ross

1 reference

18 August 2017

14

Matthew J Farrer

1 reference

18 August 2017

3

Michael G Heckman

1 reference

18 August 2017

4

Nancy N Diehl

1 reference

18 August 2017

10

Alex Rajput

1 reference

18 August 2017

11

Michele L Rajput

1 reference

18 August 2017

9

Timothy Lynch

1 reference

18 August 2017

Christian Wider

1

1 reference

18 August 2017

Sarah J Lincoln

2

1 reference

18 August 2017

Jeremy T Stone

5

1 reference

18 August 2017

Jan O Aasly

7

1 reference

18 August 2017

J Mark Gibson

8

1 reference

18 August 2017

language of work or name

English

0 references

publication date

10 February 2009

1 reference

18 August 2017

3

1 reference

based on heuristic

inferred from page(s)

published in

Neuroscience Letters

1 reference

18 August 2017

453

1 reference

18 August 2017

1

1 reference

18 August 2017

9-11

1 reference

Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684848

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684848

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684848

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684848

Phactrs 1-4: A family of protein phosphatase 1 and actin regulatory proteins

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684848

Diagnostic criteria for Parkinson disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684848

Amyloid fibrils in hereditary cerebral hemorrhage with amyloidosis of Icelandic type is a variant of gamma-trace basic protein (cystatin C)

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684848

Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684848

Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684848

Genomewide association, Parkinson disease, and PARK10

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684848

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

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684848

Considerations for genomewide association studies in Parkinson disease

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684848

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

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684848

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

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684848

Evidence of linkage and association on chromosome 20 for late-onset Alzheimer disease.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684848

A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan

3 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19429005

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.NEULET.2009.02.009

1 reference

18 August 2017

1 reference

18 August 2017

1 reference