Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis (Q35001476)

5 August 2017

title

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

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genome-wide association study

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main subject

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amyotrophic lateral sclerosis

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15

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41

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Sven Cichon

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André Uitterlinden

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Andre G Uitterlinden

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Russell McLaughlin

Russell L McLaughlin

40

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Robin Lemmens

Robin Lemmens

7

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Ammar Al-Chalabi

Ammar Al-Chalabi

49

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Markus M Nöthen

Markus M Nöthen

33

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Lambertus Kiemeney

Lambertus A Kiemeney

37

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Christopher Shaw

Christopher E Shaw

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Albert Hofman

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Albert Hofman

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Agnieszka Slowik

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Vincent Meininger

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Leonard H van den Berg

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Leonard H van den Berg

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Albert C Ludolph

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Wim Robberecht

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Peter M Andersen

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Jan H Veldink

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P Nigel Leigh

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Ina Giegling

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Dan Rujescu

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H-Erich Wichmann

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John H J Wokke

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Stefan Schreiber

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Jonathan D Glass

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John E Landers

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Judith Melki

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R Jeroen Pasterkamp

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Karol Estrada

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Anna Birve

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Barbara Tomik

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Helenius J Schelhaas

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Hylke M Blauw

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Marianne de Visser

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Anneke J van der Kooi

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Anneke J van der Kooi

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Christiaan G J Saris

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Paul W J van Vught

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Ewout J N Groen

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Roel A Ophoff

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Mark H B Huisman

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Caroline Dahlberg

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Perry T C van Doormaal

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Perry T C van Doormaal

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Eric Strengman

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Stefan Waibel

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Sita H H M Vermeulen

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Simon Cronin

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Katsumi Fumoto

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Shaun Purcell

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Pierandrea Muglia

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Robert H Brown

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Machiel J Zwarts

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Michael A van Es

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Corinna Hendrich

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Thomas Meyer

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language of work or name

English

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publication date

6 September 2009

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5 August 2017

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volume

41

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issue

10

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page(s)

1083-1087

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describes a project that uses

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genome-wide association study

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

inferred from title

cites work

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12 December 2020

Large recurrent microdeletions associated with schizophrenia

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12 December 2020

SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

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12 December 2020

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

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12 December 2020

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

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12 December 2020

PopGen: population-based recruitment of patients and controls for the analysis of complex genotype-phenotype relationships

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12 December 2020

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

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12 December 2020

Aberrant morphology and residual transmitter release at the Munc13-deficient mouse neuromuscular synapse

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12 December 2020

A genome-wide investigation of SNPs and CNVs in schizophrenia

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12 December 2020

Whole-genome analysis of sporadic amyotrophic lateral sclerosis

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12 December 2020

Munc13-1 is essential for fusion competence of glutamatergic synaptic vesicles

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12 December 2020

Amyotrophic lateral sclerosis.

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12 December 2020

El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases a

1 reference

12 December 2020

KORA-gen--resource for population genetics, controls and a broad spectrum of disease phenotypes

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12 December 2020

Assessment of clinically silent atherosclerotic disease and established and novel risk factors for predicting myocardial infarction and cardiac death in healthy middle-aged subjects: rationale and design of the Heinz Nixdorf RECALL Study. Risk Facto

1 reference

12 December 2020

The structure of haplotype blocks in the human genome

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12 December 2020

Riluzole for amyotrophic lateral sclerosis (ALS)/motor neuron disease (MND)

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Haploview: analysis and visualization of LD and haplotype maps

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12 December 2020

Practical aspects of imputation-driven meta-analysis of genome-wide association studies

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12 December 2020

Cognitive impairment in amyotrophic lateral sclerosis

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12 December 2020

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

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12 December 2020

British motor neuron disease twin study

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12 December 2020

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer

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12 December 2020

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

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12 December 2020

The Rotterdam Study: objectives and design update

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12 December 2020

Estimation of the multiple testing burden for genomewide association studies of nearly all common variants

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12 December 2020

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

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12 December 2020

On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants

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12 December 2020

The International HapMap Project

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12 December 2020

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

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12 December 2020

Identifiers

DOI

10.1038/NG.442

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5 August 2017

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