(Q28602162)

3

object named as

Dena G Hernandez

0 references

Margaux F Keller

2

object named as

Margaux F Keller

0 references

author name string

Mike A Nalls

1

0 references

Lan Chen

4

0 references

David J Stone

NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases

5

0 references

language of work or name

English

0 references

publication date

January 2016

0 references

published in

Movement Disorders

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volume

31

0 references

issue

1

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page(s)

79-85

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cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724309

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724309

A large study reveals no association between APOE and Parkinson's disease

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724309

A two-stage meta-analysis identifies several new loci for Parkinson's disease

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724309

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724309

A haplotype map of the human genome

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724309

A common LRRK2 mutation in idiopathic Parkinson's disease

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724309

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724309

GCTA: a tool for genome-wide complex trait analysis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724309

Integrating common and rare genetic variation in diverse human populations

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724309

Comparing the areas under two or more correlated receiver operating characteristic curves: a nonparametric approach

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724309

Genetic insights into common pathways and complex relationships among immune-mediated diseases

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724309

The Parkinson Progression Marker Initiative (PPMI).

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724309

The MoCA: well-suited screen for cognitive impairment in Parkinson disease.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724309

Role of DaTSCAN and clinical diagnosis in Parkinson disease.

29 September 2017

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FMDS.26374

Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FMDS.26374

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26268663