Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS. (Q34235637)

31 July 2017

Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS. (English)

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amyotrophic lateral sclerosis

31 July 2017

1 reference

12

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19

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14

Andre G Uitterlinden

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Wouter van Rheenen

3

Wouter van Rheenen

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Aleksey Shatunov

Aleksey Shatunov

22

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Ammar Al-Chalabi

Ammar Al-Chalabi

25

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Lude Franke

Lude Franke

4

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Christopher Shaw

Christopher E Shaw

23

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Albert Hofman

13

Albert Hofman

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31 July 2017

18

Vincent Meininger

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31 July 2017

Leonard H van den Berg

27

Leonard H van den Berg

1 reference

31 July 2017

15

Wim Robberecht

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16

Peter M Andersen

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28

Jan H Veldink

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31 July 2017

24

P Nigel Leigh

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20

John E Landers

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17

Judith Melki

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1

Frank P Diekstra

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11

Karol Estrada

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8

Hylke M Blauw

1 reference

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2

Christiaan G J Saris

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7

Paul W J van Vught

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31 July 2017

9

Ewout J N Groen

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26

Roel A Ophoff

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21

Robert H Brown

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Ritsert C Jansen

5

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31 July 2017

Michael A van Es

6

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31 July 2017

Steve Horvath

10

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31 July 2017

language of work or name

English

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publication date

11 April 2012

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31 July 2017

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7

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4

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e35333

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Creative Commons Attribution 4.0 International

31 July 2017

start time

11 April 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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

1 reference

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Chromosome 9 ALS and FTD locus is probably derived from a single founder

28 July 2018

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Nuclear accumulation of stress response mRNAs contributes to the neurodegeneration caused by Fragile X premutation rCGG repeats

28 July 2018

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

28 July 2018

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Energy metabolism in amyotrophic lateral sclerosis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

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

28 July 2018

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

28 July 2018

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Analysis of SNPs with an effect on gene expression identifies UBE2L3 and BCL3 as potential new risk genes for Crohn's disease

28 July 2018

1 reference

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

28 July 2018

1 reference

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Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

Multiple common variants for celiac disease influencing immune gene expression

28 July 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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

Genetic control of human brain transcript expression in Alzheimer disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

Mapping complex disease traits with global gene expression

28 July 2018

1 reference

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

28 July 2018

1 reference

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

28 July 2018

1 reference

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Screening for replication of genome-wide SNP associations in sporadic ALS

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

Genetical genomics: spotlight on QTL hotspots

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

Using gene expression to investigate the genetic basis of complex disorders

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

Capturing heterogeneity in gene expression studies by surrogate variable analysis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

Whole-genome analysis of sporadic amyotrophic lateral sclerosis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

Sequence polymorphisms cause many false cis eQTLs

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

Principal components analysis corrects for stratification in genome-wide association studies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

Clinical and molecular diagnosis of cerebrotendinous xanthomatosis with a review of the mutations in the CYP27A1 gene.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

Genome-wide associations of gene expression variation in humans

28 July 2018

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An integrative genomics approach to infer causal associations between gene expression and disease

28 July 2018

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Haploview: analysis and visualization of LD and haplotype maps

28 July 2018

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Detection of large-scale variation in the human genome

28 July 2018

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A comparison of normalization methods for high density oligonucleotide array data based on variance and bias

28 July 2018

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Power and sample size calculations. A review and computer program

28 July 2018

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Mutations in the bile acid biosynthetic enzyme sterol 27-hydroxylase underlie cerebrotendinous xanthomatosis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

Genetics of motor neuron disorders: new insights into pathogenic mechanisms

28 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035333

No evidence of association of FLJ10986 and ITPR2 with ALS in a large German cohort.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035333

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035333

Genetical genomics: the added value from segregation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035333

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035333

Unusual cerebrotendinous xanthomatosis with fronto-temporal dementia phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035333

Lower serum lipid levels are related to respiratory impairment in patients with ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035333

System-wide molecular evidence for phenotypic buffering in Arabidopsis

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035333

Genetics of sporadic amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

BLAT—The BLAST-Like Alignment Tool

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

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

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324559

Analysis ofFGGYas a risk factor for sporadic amyotrophic lateral sclerosis

28 October 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035333

Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22509407

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Dyslipidemia is a protective factor in amyotrophic lateral sclerosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22509407

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0035333

1 reference

31 July 2017

0 references

1 reference

31 July 2017

1 reference