NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases (Q28650457)

14

Nathan Pankratz

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Hannah Pliner

Hannah Pliner

26

0 references

Claudia Schulte

Claudia Schulte

13

0 references

Jose Bras

Jose Bras

2

0 references

Vincent Plagnol

Vincent Plagnol

11

0 references

Alan Renton

Alan E Renton

6

0 references

Christina M Lill

Christina M Lill

17

0 references

Maria Martinez

Maria Martinez

29

0 references

Thomas Gasser

30

Thomas Gasser

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Peter Heutink

28

Peter Heutink

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John Anthony Hardy

33

John Hardy

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Rita Guerreiro

9

Rita Guerreiro

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Andrew Singleton

34

Andrew B Singleton

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Bryan Traynor

31

Bryan J Traynor

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Dena G. Hernandez

3

Dena G Hernandez

0 references

Michele T M Hu

1 reference

ORCID Public Data File 2021

Francis Walker

1 reference

ORCID Public Data File 2021

Daniela Berg

1 reference

ORCID Public Data File 2021

Lars Bertram

16

Lars Bertram

0 references

J Raphael Gibbs

12

J Raphael Gibbs

0 references

Connor Edsall

22

Connor Edsall

0 references

Elisa Majounie

5

Elisa Majounie

0 references

Anita L DeStefano

18

Anita L DeStefano

0 references

Margaux F Keller

4

Margaux F Keller

0 references

author name string

Mike A Nalls

1

0 references

Mohamad Saad

7

0 references

Iris Jansen

8

0 references

Steven Lubbe

10

0 references

Margaret Sutherland

15

0 references

Tatiana Faroud

19

0 references

Nicholas Eriksson

20

0 references

Joyce Y Tung

21

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Noah Nichols

23

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Janet Brooks

24

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Chris Letson

27

0 references

Nick Wood

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

32

0 references

language of work or name

English

0 references

publication date

March 2015

0 references

published in

Neurobiology of Aging

0 references

volume

36

0 references

issue

3

0 references

page(s)

1605.e7-12

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317375

An integrated map of genetic variation from 1,092 human genomes

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317375

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=4317375

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=4317375

Web-based genome-wide association study identifies two novel loci and a substantial genetic component 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=4317375

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317375

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317375

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317375

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317375

Cloning of the gene containing mutations that cause PARK8-linked 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=4317375

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317375

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317375

Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317375

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=4317375

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317375

Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317375

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317375

Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317375

Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317375

Locus-specific mutation databases for neurodegenerative brain diseases

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317375

Chromosome 9 ALS and FTD locus is probably derived from a single founder

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317375

Measures of autozygosity in decline: globalization, urbanization, and its implications for medical genetics

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317375

10.1016/J.NEUROBIOLAGING.2014.07.028

3 June 2018

Identifiers

DOI

1 reference

release_lrc53eyndnc6biyhbzvg6e5r3a

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/lrc53eyndnc6biyhbzvg6e5r3a

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

1 reference

PubMed publication ID

25444595

1 reference