(Q35671414)

9 August 2017

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study (English)

1 reference

genome-wide association study

9 August 2017

0 references

amyotrophic lateral sclerosis

0 references

author

Orla Hardiman

13

1 reference

9 August 2017

15

1 reference

9 August 2017

Kin Mok

2

0 references

Bradley N. Smith

Bradley Smith

5

0 references

Aleksey Shatunov

Aleksey Shatunov

1

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Caroline Vance

Caroline Vance

6

0 references

Stephen J. Newhouse

Stephen Newhouse

3

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Michael E. Weale

Michael E Weale

4

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Vincenzo Silani

Vincenzo Silani

20

0 references

Ammar Al-Chalabi

Ammar Al-Chalabi

37

0 references

Pamela Shaw

Pamela J Shaw

35

0 references

Isabella Fogh

Isabella Fogh

19

0 references

Christopher Shaw

Christopher E Shaw

36

0 references

Karen E Morrison

Karen E Morrison

34

0 references

John Anthony Hardy

30

John Hardy

1 reference

9 August 2017

24

Vincent Meininger

1 reference

9 August 2017

Leonard H van den Berg

10

Leonard H van den Berg

1 reference

9 August 2017

11

Wim Robberecht

1 reference

9 August 2017

21

Adriano Chiò

1 reference

9 August 2017

18

Peter M Andersen

1 reference

9 August 2017

8

Jan H Veldink

1 reference

9 August 2017

29

P Nigel Leigh

1 reference

9 August 2017

22

Bryan J Traynor

1 reference

9 August 2017

26

Peter McGuffin

1 reference

9 August 2017

27

Jonathan D Glass

1 reference

9 August 2017

25

John E Landers

1 reference

9 August 2017

23

Judith Melki

1 reference

9 August 2017

17

Olubunmi Abel

1 reference

9 August 2017

28

Hardev Pall

1 reference

9 August 2017

31

Robert H Brown

1 reference

9 August 2017

Lauren Johnson

7

1 reference

9 August 2017

Michael A van Es

9

1 reference

9 August 2017

Philip Van Damme

12

1 reference

9 August 2017

Anne E Farmer

14

1 reference

9 August 2017

Amy W Butler

16

1 reference

9 August 2017

John F Powell

32

1 reference

9 August 2017

Richard W Orrell

33

1 reference

9 August 2017

1 October 2010

1 reference

9 August 2017

1 reference

9 August 2017

9

1 reference

9 August 2017

10

1 reference

9 August 2017

986-994

1 reference

describes a project that uses

9 August 2017

genome-wide association study

1 reference

An estimate of amyotrophic lateral sclerosis heritability using twin data.

inferred from title

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

FuncBase: a resource for quantitative gene function annotation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Rare variants create synthetic genome-wide associations

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Analysis of genome-wide copy number variation in Irish and Dutch ALS populations

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

PLINK: a tool set for whole-genome association and population-based linkage analyses

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Whole-genome analysis of sporadic amyotrophic lateral sclerosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

A new multipoint method for genome-wide association studies by imputation of genotypes

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Population structure and eigenanalysis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Principal components analysis corrects for stratification in genome-wide association studies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

The International HapMap Project

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Genome-wide association study of major recurrent depression in the U.K. population.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

A genome-wide association study of sporadic ALS in a homogenous Irish population.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Three families with amyotrophic lateral sclerosis and frontotemporal dementia with evidence of linkage to chromosome 9p.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Prevalence and patterns of cognitive impairment in sporadic ALS.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Characterization of amyotrophic lateral sclerosis and frontotemporal dementia

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Association of the dystrobrevin binding protein 1 gene (DTNBP1) in a bipolar case-control study (BACCS)

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

Amyotrophic lateral sclerosis in an urban setting

23 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

ALSOD: The Amyotrophic Lateral Sclerosis Online Database

23 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257853

No association of DPP6 with amyotrophic lateral sclerosis in an Italian population

7 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20801717

12 December 2020

inferred from PubMed ID database lookup

A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20801717

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1016/S1474-4422(10)70197-6

1 reference

release_ohsp2dhgfjddtec6acmzwqq2z4

9 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ohsp2dhgfjddtec6acmzwqq2z4

24 November 2022

mapped directly with Wikidata item

PMCID

3257853

1 reference

9 August 2017

1 reference