(Q36145972)

12 August 2017

0 references

Genome-wide association study identifies multiple susceptibility loci for glioma (English)

1 reference

genome-wide association study

12 August 2017

0 references

1 reference

19

Mark Lathrop

1 reference

12 August 2017

12

Sarah J Fleming

0 references

Ben Kinnersley

Ben Kinnersley

1

0 references

Minouk J Schoemaker

Minouk J Schoemaker

Stefanie Heilmann-Heimbach

11

0 references

Stefanie Heilmann

14

0 references

Richard Houlston

Richard S Houlston

23

0 references

Markus M Nöthen

Markus M Nöthen

17

0 references

Anthony Swerdlow

Anthony Swerdlow

18

0 references

Peter Broderick

5

Peter Broderick

1 reference

12 August 2017

16

Heinz-Erich Wichmann

1 reference

12 August 2017

15

Stefan Schreiber

1 reference

12 August 2017

Jayaram Vijayakrishnan

6

Jayaram Vijayakrishnan

1 reference

12 August 2017

2

Marianne Labussière

1 reference

12 August 2017

3

Amy Holroyd

1 reference

12 August 2017

Anna Luisa Di Stefano

4

Anna-Luisa Di Stefano

1 reference

12 August 2017

7

Karima Mokhtari

1 reference

12 August 2017

8

Jean-Yves Delattre

1 reference

12 August 2017

9

Konstantinos Gousias

1 reference

12 August 2017

10

Johannes Schramm

1 reference

12 August 2017

13

Stefan Herms

1 reference

12 August 2017

20

Matthias Simon

1 reference

12 August 2017

21

Melissa Bondy

1 reference

12 August 2017

22

Marc Sanson

1 reference

12 August 2017

language of work or name

English

0 references

publication date

1 October 2015

1 reference

full work available at URL

12 August 2017

http://eprints.whiterose.ac.uk/109630/

content deliverer

White Rose Research Online

copyright license

Creative Commons Attribution 4.0 International

0 references

published in

Nature Communications

1 reference

12 August 2017

6

1 reference

12 August 2017

1

1 reference

30 June 2019

page(s)

8559

1 reference

Creative Commons Attribution 4.0 International

12 August 2017

start time

1 October 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

genome-wide association study

1 reference

based on heuristic

inferred from title

exact match

https://scigraph.springernature.com/pub.10.1038/ncomms9559

0 references

cites work

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2 October 2017

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Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk

2 October 2017

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2 October 2017

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2 October 2017

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A general framework for estimating the relative pathogenicity of human genetic variants

2 October 2017

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2 October 2017

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Super-enhancers in the control of cell identity and disease

2 October 2017

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Transcriptome and genome sequencing uncovers functional variation in humans

2 October 2017

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Systematic identification of trans eQTLs as putative drivers of known disease associations

2 October 2017

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Low penetrance susceptibility to glioma is caused by the TP53 variant rs78378222.

2 October 2017

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The Subread aligner: fast, accurate and scalable read mapping by seed-and-vote

2 October 2017

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Integrative analysis of complex cancer genomics and clinical profiles using the cBioPortal

2 October 2017

1 reference

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Deciphering the 8q24.21 association for glioma

2 October 2017

1 reference

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Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia

2 October 2017

1 reference

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Annotation of functional variation in personal genomes using RegulomeDB

2 October 2017

1 reference

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Mapping cis- and trans-regulatory effects across multiple tissues in twins

2 October 2017

1 reference

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Recurrent mutations of MYD88 and TBL1XR1 in primary central nervous system lymphomas

2 October 2017

1 reference

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Vti1a identifies a vesicle pool that preferentially recycles at rest and maintains spontaneous neurotransmission

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

Mutations in POLR3A and POLR3B encoding RNA Polymerase III subunits cause an autosomal-recessive hypomyelinating leukoencephalopathy

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

PHLDA1 is a crucial negative regulator and effector of Aurora A kinase in breast cancer

2 October 2017

1 reference

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The variant call format and VCFtools

2 October 2017

1 reference

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Chromosome 7p11.2 (EGFR) variation influences glioma risk

2 October 2017

1 reference

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A map of human genome variation from population-scale sequencing

2 October 2017

1 reference

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Familial aggregation of glioma: a pooled analysis

2 October 2017

1 reference

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i-GSEA4GWAS: a web server for identification of pathways/gene sets associated with traits by applying an improved gene set enrichment analysis to genome-wide association study

2 October 2017

1 reference

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Meta-analysis and imputation refines the association of 15q25 with smoking quantity

2 October 2017

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A method and server for predicting damaging missense mutations

2 October 2017

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Targeted capture and massively parallel sequencing of 12 human exomes

2 October 2017

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Genome-wide association study identifies five susceptibility loci for glioma

2 October 2017

1 reference

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Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility

2 October 2017

1 reference

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A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

2 October 2017

1 reference

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Brain tumor epidemiology: consensus from the Brain Tumor Epidemiology Consortium

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

Identification of low penetrance alleles for lung cancer: the GEnetic Lung CAncer Predisposition Study (GELCAPS).

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

The expanding RNA polymerase III transcriptome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

National study of colorectal cancer genetics

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

The INTERPHONE study: design, epidemiological methods, and description of the study population

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

The 2007 WHO classification of tumours of the central nervous system

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

A new multipoint method for genome-wide association studies by imputation of genotypes

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

Genome-wide association study of prostate cancer identifies a second risk locus at 8q24

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

Population structure and eigenanalysis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

ZW10 function in mitotic checkpoint control, dynein targeting and membrane trafficking: is dynein the unifying theme?

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

PopGen: population-based recruitment of patients and controls for the analysis of complex genotype-phenotype relationships

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

Population structure, differential bias and genomic control in a large-scale, case-control association study

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

The v-SNARE Vti1a regulates insulin-stimulated glucose transport and Acrp30 secretion in 3T3-L1 adipocytes

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

KORA-gen--resource for population genetics, controls and a broad spectrum of disease phenotypes

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

Distribution and intensity of constraint in mammalian genomic sequence

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

The SU.VI.MAX Study: a randomized, placebo-controlled trial of the health effects of antioxidant vitamins and minerals

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

Measuring inconsistency in meta-analyses

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

Assessment of clinically silent atherosclerotic disease and established and novel risk factors for predicting myocardial infarction and cardiac death in healthy middle-aged subjects: rationale and design of the Heinz Nixdorf RECALL Study. Risk Facto

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

The structure of haplotype blocks in the human genome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

A polymorphic variant in the human electron transfer flavoprotein alpha-chain (alpha-T171) displays decreased thermal stability and is overrepresented in very-long-chain acyl-CoA dehydrogenase-deficient patients with mild childhood presentation.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

Crystal structure of the BTB domain from PLZF

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

Rearrangements of the retinoic acid receptor alpha and promyelocytic leukemia zinc finger genes resulting from t(11;17)(q23;q21) in a patient with acute promyelocytic leukemia

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

Acyl-CoA dehydrogenases, electron transfer flavoprotein and electron transfer flavoprotein dehydrogenase

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

Glutaric acidemia type II. Heterogeneity in beta-oxidation flux, polypeptide synthesis, and complementary DNA mutations in the alpha subunit of electron transfer flavoprotein in eight patients

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

The immunohistochemical differential diagnosis of microcystic adnexal carcinoma, desmoplastic trichoepithelioma and morpheaform basal cell carcinoma using BerEP4 and stem cell markers.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

Isocitrate dehydrogenase 1 codon 132 mutation is an important prognostic biomarker in gliomas.

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

Familial risks in nervous-system tumours: a histology-specific analysis from Sweden and Norway

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

BAC array CGH distinguishes mutually exclusive alterations that define clinicogenetic subtypes of gliomas.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4600760

Polygenes, risk prediction, and targeted prevention of breast cancer

23 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26424050

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1 reference

https://pubmed.ncbi.nlm.nih.gov/26424050

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NCOMMS9559

1 reference

Dimensions Publication ID

12 August 2017

0 references

0 references

0 references

0 references

1 reference

12 August 2017

PubMed publication ID

26424050

1 reference