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

5 August 2017

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

1 reference

genome-wide association study

5 August 2017

0 references

amyotrophic lateral sclerosis

0 references

1 reference

15

1 reference

5 August 2017

41

1 reference

5 August 2017

32

Sven Cichon

0 references

André Uitterlinden

25

Andre G Uitterlinden

0 references

Russell McLaughlin

Russell L McLaughlin

40

0 references

Robin Lemmens

Robin Lemmens

7

0 references

Ammar Al-Chalabi

Ammar Al-Chalabi

49

0 references

Markus M Nöthen

Markus M Nöthen

33

0 references

Lambertus Kiemeney

Lambertus A Kiemeney

37

0 references

Christopher Shaw

Christopher E Shaw

47

0 references

Albert Hofman

16

Albert Hofman

1 reference

5 August 2017

24

Agnieszka Slowik

1 reference

5 August 2017

44

Vincent Meininger

1 reference

5 August 2017

Leonard H van den Berg

54

Leonard H van den Berg

1 reference

5 August 2017

29

Albert C Ludolph

1 reference

5 August 2017

51

Wim Robberecht

1 reference

5 August 2017

52

Peter M Andersen

1 reference

5 August 2017

2

Jan H Veldink

1 reference

5 August 2017

46

P Nigel Leigh

1 reference

5 August 2017

21

Ina Giegling

1 reference

5 August 2017

19

Dan Rujescu

1 reference

5 August 2017

34

H-Erich Wichmann

1 reference

5 August 2017

38

John H J Wokke

1 reference

5 August 2017

35

Stefan Schreiber

1 reference

5 August 2017

30

Jonathan D Glass

1 reference

5 August 2017

48

John E Landers

1 reference

5 August 2017

45

Judith Melki

1 reference

5 August 2017

43

R Jeroen Pasterkamp

1 reference

5 August 2017

14

Karol Estrada

1 reference

5 August 2017

6

Anna Birve

1 reference

5 August 2017

23

Barbara Tomik

1 reference

5 August 2017

8

Helenius J Schelhaas

1 reference

5 August 2017

4

Hylke M Blauw

1 reference

5 August 2017

12

Marianne de Visser

1 reference

5 August 2017

Anneke J van der Kooi

11

Anneke J van der Kooi

1 reference

5 August 2017

3

Christiaan G J Saris

1 reference

5 August 2017

5

Paul W J van Vught

1 reference

5 August 2017

9

Ewout J N Groen

1 reference

5 August 2017

53

Roel A Ophoff

1 reference

5 August 2017

10

Mark H B Huisman

1 reference

5 August 2017

13

Caroline Dahlberg

1 reference

5 August 2017

Perry T C van Doormaal

18

Perry T C van Doormaal

1 reference

5 August 2017

20

Eric Strengman

1 reference

5 August 2017

27

Stefan Waibel

1 reference

5 August 2017

36

Sita H H M Vermeulen

1 reference

5 August 2017

39

Simon Cronin

1 reference

5 August 2017

42

Katsumi Fumoto

1 reference

5 August 2017

31

Shaun Purcell

1 reference

5 August 2017

22

Pierandrea Muglia

1 reference

5 August 2017

50

Robert H Brown

1 reference

5 August 2017

Michael A van Es

1

1 reference

5 August 2017

Machiel J Zwarts

17

1 reference

5 August 2017

Corinna Hendrich

26

1 reference

5 August 2017

Thomas Meyer

28

1 reference

5 August 2017

language of work or name

English

0 references

publication date

6 September 2009

1 reference

5 August 2017

1 reference

5 August 2017

41

1 reference

5 August 2017

10

1 reference

5 August 2017

1083-1087

1 reference

describes a project that uses

5 August 2017

genome-wide association study

1 reference

https://scigraph.springernature.com/pub.10.1038/ng.442

inferred from title

exact match

0 references

cites work

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

1 reference

12 December 2020

Large recurrent microdeletions associated with schizophrenia

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

A genome-wide investigation of SNPs and CNVs in schizophrenia

1 reference

12 December 2020

Whole-genome analysis of sporadic amyotrophic lateral sclerosis

1 reference

12 December 2020

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

1 reference

12 December 2020

Amyotrophic lateral sclerosis.

1 reference

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

1 reference

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Haploview: analysis and visualization of LD and haplotype maps

1 reference

12 December 2020

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

1 reference

12 December 2020

Cognitive impairment in amyotrophic lateral sclerosis

1 reference

12 December 2020

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

1 reference

12 December 2020

British motor neuron disease twin study

1 reference

12 December 2020

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer

1 reference

12 December 2020

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

1 reference

12 December 2020

The Rotterdam Study: objectives and design update

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

The International HapMap Project

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1038/NG.442

1 reference

5 August 2017

1 reference