(Q38107218)

29 August 2017

title

Genetic and epigenetic studies of amyotrophic lateral sclerosis (English)

1 reference

amyotrophic lateral sclerosis

29 August 2017

main subject

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4

Guy Rouleau

1 reference

29 August 2017

Ammar Al-Chalabi

1

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Teepu Siddique

object named as

Teepu Siddique

5

0 references

Michael J Strong

object named as

Michael Strong

6

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author name string

Shin Kwak

2

1 reference

29 August 2017

Mark Mehler

3

1 reference

29 August 2017

Peter Nigel Leigh

7

1 reference

29 August 2017

publication date

1 May 2013

1 reference

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

29 August 2017

published in

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29 August 2017

volume

14 Suppl 1

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29 August 2017

page(s)

44-52

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Rate of familial amyotrophic lateral sclerosis: a systematic review and meta-analysis

29 August 2017

cites work

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

An estimate of amyotrophic lateral sclerosis heritability using twin data.

21 January 2018

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Clinical genetics of amyotrophic lateral sclerosis: what do we really know?

21 January 2018

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

21 January 2018

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The future of genetic studies of complex human diseases

21 January 2018

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Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

21 January 2018

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TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

21 January 2018

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TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis

21 January 2018

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https://api.crossref.org/works/10.3109%2F21678421.2013.778571

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

21 January 2018

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

21 January 2018

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https://api.crossref.org/works/10.3109%2F21678421.2013.778571

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

21 January 2018

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https://api.crossref.org/works/10.3109%2F21678421.2013.778571

ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis.

21 January 2018

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Mutations of optineurin in amyotrophic lateral sclerosis

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Whole-genome analysis of sporadic amyotrophic lateral sclerosis

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

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

21 January 2018

1 reference

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A high-density genome-wide association screen of sporadic ALS in US veterans

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

A large genome scan for rare CNVs in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

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

21 January 2018

1 reference

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Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

Association of APOE with age at onset of sporadic amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death

21 January 2018

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https://api.crossref.org/works/10.3109%2F21678421.2013.778571

A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS

21 January 2018

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RNA processing defects associated with diseases of the motor neuron

21 January 2018

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https://api.crossref.org/works/10.3109%2F21678421.2013.778571

The evidence for altered RNA metabolism in amyotrophic lateral sclerosis (ALS).

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

RNA metabolism and the pathogenesis of motor neuron diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

Epigenetic principles and mechanisms underlying nervous system functions in health and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

Induced ncRNAs allosterically modify RNA-binding proteins in cis to inhibit transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

Long non-coding RNAs in nervous system function and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

Emerging roles of non-coding RNAs in brain evolution, development, plasticity and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

MicroRNA-206 delays ALS progression and promotes regeneration of neuromuscular synapses in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

Epigenetic regulation of motor neuron cell death through DNA methylation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

Understanding the role of TDP-43 and FUS/TLS in ALS and beyond.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

Glutamate receptors: RNA editing and death of motor neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

Deficient RNA editing of GluR2 and neuronal death in amyotropic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

Induced loss of ADAR2 engenders slow death of motor neurons from Q/R site-unedited GluR2

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

TDP-43 pathology in sporadic ALS occurs in motor neurons lacking the RNA editing enzyme ADAR2.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

Newly identified ADAR-mediated A-to-I editing positions as a tool for ALS research

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2013.778571

10.3109/21678421.2013.778571

21 January 2018

Identifiers

DOI

1 reference

29 August 2017

1 reference