(Q29417029)

16 April 2017

title

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

1 reference

amyotrophic lateral sclerosis

16 April 2017

main subject

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author

Wim Robberecht

Margaret A. Pericak-Vance

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object named as

Margaret A Pericak-Vance

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Simon Topp

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Russell L McLaughlin

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Bradley N Smith

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Aleksey Shatunov

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Caroline Vance

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Philip van Damme

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Ammar Al-Chalabi

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Orla Hardiman

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Jonathan L Haines

1 reference

16 April 2017

Vincent Meininger

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16 April 2017

Leonard H van den Berg

object named as

Leonard H van den Berg

1 reference

16 April 2017

Gabriele Mora

1 reference

16 April 2017

Adriano Chio

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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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Bryan J Traynor

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Carl D Langefeld

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Miranda C Marion

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Ashley Jones

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Jonathan D Glass

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John E Landers

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Christopher E Shaw

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Judith Melki

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Frank P Diekstra

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Hylke M Blauw

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Evadnie Rampersaud

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Christiaan G Saris

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Paul W van Vught

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Ewout J Groen

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Simon Cronin

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Francois Salachas

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Robert H Brown

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16 April 2017

Michael A van Es

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Kreshnik B Ahmeti

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16 April 2017

Senda Ajroud-Driss

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16 April 2017

Jennifer Armstrong

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16 April 2017

Anne Birve

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16 April 2017

Lucie Bruijn

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16 April 2017

Wenjie Chen

1 reference

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Mary C Comeau

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Athina Soraya Gkazi

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16 April 2017

Josh D Grab

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16 April 2017

Scott Heller

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16 April 2017

Jie Huang

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16 April 2017

Wu-Yen Hung

1 reference

16 April 2017

ITALSGEN consortium

1 reference

16 April 2017

James M Jaworski

1 reference

16 April 2017

Humaira Khan

1 reference

16 April 2017

Jack W Miller

1 reference

16 April 2017

Laurie P Russell

1 reference

16 April 2017

Nailah Siddique

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16 April 2017

Teepu Siddique

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16 April 2017

Robert Sufit

1 reference

16 April 2017

Yi Yang

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16 April 2017

J G Zheng

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16 April 2017

ALSGEN Consortium

1 reference

16 April 2017

publication date

5 September 2012

1 reference

16 April 2017

published in

Neurobiology of Aging

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16 April 2017

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16 April 2017

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16 April 2017

page(s)

357.e7-19

1 reference

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

16 April 2017

cites work

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