Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. (Q29417029)

16 April 2017

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

1 reference

amyotrophic lateral sclerosis

16 April 2017

0 references

author

Wim Robberecht

Margaret A. Pericak-Vance

39

0 references

37

Margaret A Pericak-Vance

0 references

Simon Topp

Simon Topp

49

0 references

Russell McLaughlin

Russell L McLaughlin

32

0 references

Bradley N. Smith

Bradley N Smith

47

0 references

Aleksey Shatunov

Aleksey Shatunov

43

0 references

Caroline Vance

Caroline Vance

51

0 references

Philip Van Damme

Philip van Damme

52

0 references

Ammar Al-Chalabi

Ammar Al-Chalabi

3

0 references

Orla Hardiman

Orla Hardiman

20

0 references

Jonathan L Haines

19

Jonathan L Haines

1 reference

16 April 2017

33

Vincent Meininger

1 reference

16 April 2017

Leonard H van den Berg

53

Leonard H van den Berg

1 reference

16 April 2017

36

Gabriele Mora

1 reference

16 April 2017

11

Adriano Chio

1 reference

16 April 2017

4

Peter M Andersen

1 reference

16 April 2017

56

Jan H Veldink

1 reference

16 April 2017

30

P Nigel Leigh

1 reference

16 April 2017

50

Bryan J Traynor

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29

Carl D Langefeld

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31

Miranda C Marion

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26

Ashley Jones

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16

Jonathan D Glass

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28

John E Landers

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44

Christopher E Shaw

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34

Judith Melki

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14

Frank P Diekstra

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7

Hylke M Blauw

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38

Evadnie Rampersaud

1 reference

16 April 2017

42

Christiaan G Saris

1 reference

16 April 2017

55

Paul W van Vught

1 reference

16 April 2017

18

Ewout J Groen

1 reference

16 April 2017

13

Simon Cronin

1 reference

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41

Francois Salachas

1 reference

16 April 2017

8

Robert H Brown

1 reference

16 April 2017

Kreshnik B Ahmeti

1

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16 April 2017

Senda Ajroud-Driss

2

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16 April 2017

Jennifer Armstrong

5

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16 April 2017

Anne Birve

6

1 reference

16 April 2017

Lucie Bruijn

9

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16 April 2017

Wenjie Chen

10

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16 April 2017

Mary C Comeau

12

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Athina Soraya Gkazi

15

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16 April 2017

Josh D Grab

17

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16 April 2017

Scott Heller

21

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16 April 2017

Jie Huang

22

1 reference

16 April 2017

Wu-Yen Hung

23

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16 April 2017

ITALSGEN consortium

24

1 reference

16 April 2017

James M Jaworski

25

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16 April 2017

Humaira Khan

27

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16 April 2017

Jack W Miller

35

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Laurie P Russell

40

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16 April 2017

Nailah Siddique

45

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16 April 2017

Teepu Siddique

46

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16 April 2017

Robert Sufit

48

1 reference

16 April 2017

Michael A van Es

54

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16 April 2017

Yi Yang

57

1 reference

16 April 2017

J G Zheng

58

1 reference

16 April 2017

ALSGEN Consortium

59

1 reference

16 April 2017

5 September 2012

1 reference

16 April 2017

Neurobiology of Aging

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16 April 2017

34

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16 April 2017

357.e7-19

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16 April 2017

1

1 reference

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

16 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Exome sequencing reveals VCP mutations as a cause of familial ALS

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

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

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

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

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

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

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

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

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Whole-genome analysis of sporadic amyotrophic lateral sclerosis

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

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

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

How common are the "common" neurologic disorders?

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Mutations of optineurin in amyotrophic lateral sclerosis

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

The risk to relatives of patients with sporadic amyotrophic lateral sclerosis

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Keeping up with genetic discoveries in amyotrophic lateral sclerosis: the ALSoD and ALSGene databases

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

An estimate of amyotrophic lateral sclerosis heritability using twin data.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patients

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Genome-wide analysis of genetic loci associated with Alzheimer disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Smoking may be considered an established risk factor for sporadic ALS.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Familial aggregation of amyotrophic lateral sclerosis

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Aggregation of neurodegenerative disease in ALS kindreds

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issues

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Incidence of amyotrophic lateral sclerosis in southern Italy: a population based study.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

The epidemiology of motor neuron diseases: a review of recent studies

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Modelling the effects of penetrance and family size on rates of sporadic and familial disease.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

The sex ratio in amyotrophic lateral sclerosis: A population based study.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Thioredoxin reductase 1 haplotypes modify familial amyotrophic lateral sclerosis onset.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

ALSOD: The Amyotrophic Lateral Sclerosis Online Database

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

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

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

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

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Amyotrophic lateral sclerosis in an urban setting

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Signs and symptoms at diagnosis of amyotrophic lateral sclerosis: a population-based study in southern Italy

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Deletion of the hypoxia-response element in the vascular endothelial growth factor promoter causes motor neuron degeneration.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosis.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Incidence and prevalence of ALS in Ireland, 1995-1997: a population-based study.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839234

Age at onset in sod1-mediated amyotrophic lateral sclerosis shows familiality

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22959728

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Prevalence of SOD1 mutations in the Italian ALS population

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22959728

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.NEUROBIOLAGING.2012.07.017

1 reference

16 April 2017

0 references

1 reference