(Q33501355)

27 July 2017

Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis (English)

1 reference

genome-wide association study

27 July 2017

0 references

amyotrophic lateral sclerosis

0 references

4

Bryan J Traynor

1 reference

27 July 2017

Qiuying Sha

1

1 reference

27 July 2017

Zhaogong Zhang

series ordinal

2

1 reference

27 July 2017

Jennifer C Schymick

series ordinal

3

1 reference

27 July 2017

Shuanglin Zhang

series ordinal

5

1 reference

27 July 2017

9 September 2009

1 reference

27 July 2017

1 reference

27 July 2017

10

1 reference

27 July 2017

86

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2350-10-86

27 July 2017

0 references

cites work

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752455

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752455

Whole-genome analysis of sporadic amyotrophic lateral sclerosis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752455

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752455

Overcoming the winner's curse: estimating penetrance parameters from case-control data

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752455

Test for interaction between two unlinked loci

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752455

A testing framework for identifying susceptibility genes in the presence of epistasis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752455

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752455

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752455

DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752455

Gene-gene interactions between glutathione-s transferase M1 and matrix metalloproteinase 9 in the formation of hereditary predisposition to chronic obstructive pulmonary disease

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752455

Inference of population structure using multilocus genotype data: linked loci and correlated allele frequencies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752455

Generalized T2 test for genome association studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752455

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752455

Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752455

Some epistatic two-locus models of disease. I. Relative risks and identity-by-descent distributions in affected sib pairs

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752455

Linkage strategies for genetically complex traits. I. Multilocus models

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752455

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

14 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-86

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-86

Mutant dynactin in motor neuron disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-86

Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-86

A novel candidate region for ALS on chromosome 14q11.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-86

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-86

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-86

Susceptibility genes in sporadic ALS: separating the wheat from the chaff by international collaboration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-86

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-86

Glutathione pathway genes and lung cancer risk in young and old populations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-86

Oligogenic combinations associated with breast cancer risk in women under 53 years of age.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-86

Interaction between obesity-susceptibility loci in chromosome regions 2p25-p24 and 13q13-q21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-86

Upward bias in odds ratio estimates from genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-86

A combinatorial searching method for detecting a set of interacting loci associated with complex traits.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-86

Incidence of ALS in Italy: evidence for a uniform frequency in Western countries.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752455

Deletions of the heavy neurofilament subunit tail in amyotrophic lateral sclerosis

31 October 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-86

Polygenic control of hepatocarcinogenesis in Copenhagen x F344 rats

21 January 2018

1 reference

12 December 2020

The Scottish Motor Neuron Disease Register: a prospective study of adult onset motor neuron disease in Scotland. Methodology, demography and clinical features of incident cases in 1989

1 reference

12 December 2020

ALS: life and death in a bad neighborhood

1 reference

12 December 2020

Paraoxonase cluster polymorphisms are associated with sporadic ALS

1 reference

12 December 2020

Paraoxonase gene polymorphisms and sporadic ALS

1 reference

12 December 2020

Five prothrombotic polymorphisms and the prevalence of premature myocardial infarction

1 reference

12 December 2020

SMN genotypes producing less SMN protein increase susceptibility to and severity of sporadic ALS

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2350-10-86

1 reference

27 July 2017

1 reference

27 July 2017

1 reference