Evidence map›Paper›PMID 30709929›Full record

ArticleCancer research2019

Transcriptome-Wide Association Study Identifies New Candidate Susceptibility Genes for Glioma.

Isabelle Atkins, Ben Kinnersley, Quinn T Ostrom, Karim Labreche, Dora Il'yasova, Georgina N Armstrong, Jeanette E Eckel-Passow, Minouk J Schoemaker, Markus M Nöthen, Jill S Barnholtz-Sloan and 18 more

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
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  14. Integrating genome-wide association and transcriptome prediction model identifies novel target genes for osteoporosis.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2021
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  19. CoMM-SFrontiers in genetics · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

28 authors at 20 institutions in 8 countries.

Isabelle Atkins *Division of Genetics and Epidemiology, The Institute of Cancer Research, London, United Kingdom.
Ben Kinnersley *Division of Genetics and Epidemiology, The Institute of Cancer Research, London, United Kingdom. ben.kinnersely@icr.ac.uk.
Quinn T OstromCase Comprehensive Cancer Center, School of Medicine, Case Western Reserve University, Cleveland, Ohio.ORCID 0000-0003-3469-7558
Karim LabrecheDivision of Genetics and Epidemiology, The Institute of Cancer Research, London, United Kingdom.
Dora Il'yasovaDepartment of Population Health Sciences, School of Public Health, Georgia State University, Atlanta, Georgia.ORCID 0000-0003-4290-6794
Georgina N ArmstrongDepartment of Medicine, Section of Epidemiology and Population Sciences, Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, Texas.
Jeanette E Eckel-PassowDivision of Biomedical Statistics and Informatics, Mayo Clinic College of Medicine, Rochester, Minnesota.
Minouk J SchoemakerDivision of Genetics and Epidemiology, The Institute of Cancer Research, London, United Kingdom.ORCID 0000-0001-8403-2234
Markus M NöthenDepartment of Genomics, Life & Brain Center, University of Bonn, Bonn, Germany.
Jill S Barnholtz-SloanCase Comprehensive Cancer Center, School of Medicine, Case Western Reserve University, Cleveland, Ohio.
Anthony J SwerdlowDivision of Genetics and Epidemiology, The Institute of Cancer Research, London, United Kingdom.ORCID 0000-0001-5550-4159
Matthias SimonDepartment of Neurosurgery, University of Bonn Medical Center, Bonn, Germany.
Preetha RajaramanDivision of Cancer Epidemiology and Genetics, NCI, Bethesda, Maryland.
Stephen J ChanockDivision of Cancer Epidemiology and Genetics, NCI, Bethesda, Maryland.
Joellen ShildkrautDepartment of Public Health Sciences, University of Virginia, Charlottesville, Virginia.
Jonine L BernsteinDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
Per HoffmannDepartment of Genomics, Life & Brain Center, University of Bonn, Bonn, Germany.
Karl-Heinz JöckelInstitute for Medical Informatics, Biometry and Epidemiology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Rose K LaiDepartments of Neurology and Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, California.
Elizabeth B ClausSchool of Public Health, Yale University, New Haven, Connecticut.
Sara H OlsonDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
Christoffer JohansenInstitute of Cancer Epidemiology, Danish Cancer Society, Copenhagen, Denmark.
Margaret R WrenschDepartment of Neurological Surgery, School of Medicine, University of California, San Francisco, San Francisco, California.
Beatrice MelinDepartment of Radiation Sciences, Umeå University, Umeå, Sweden.
Robert B JenkinsDepartment of Laboratory Medicine and Pathology, Mayo Clinic Comprehensive Cancer Center, Mayo Clinic, Rochester, Minnesota.
Marc SansonSorbonne Universités UPMC Univ Paris 06, INSERM CNRS, U1127, UMR 7225, ICM, Paris, France.
Melissa L BondyDepartment of Medicine, Section of Epidemiology and Population Sciences, Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, Texas.
Richard S HoulstonDivision of Genetics and Epidemiology, The Institute of Cancer Research, London, United Kingdom.ORCID 0000-0002-5268-0242
Cancer Research UK · GBBaylor College of Medicine · USCancer Genetics (United States) · USMayo Clinic · USMemorial Sloan Kettering Cancer Center · USBreast Cancer Now · GBBrigham and Women's Hospital · USCase Western Reserve University · USCentre National de la Recherche Scientifique · FRDepartment of Biomedicine Basel · CHDuke University · USEssen University Hospital · DEInstitute of Cancer Research · GBUmeå University · SEUniversity Hospital Bonn · DEUniversity of Bonn · DEUniversity of California, San Francisco · USUniversity of Copenhagen · DKUniversity of Southern California · USUniversity of Virginia · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI DAVID R ROWLEY · 2007 to 2026
$73.9M
GENETIC EPIDEMIOLOGY OF MALIGNANT GLIOMAR01CA052689 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WIENCKE, JOHN K., WRENSCH, MARGARET R. · 1991 to 2015
$20.5M
International Case Control Study of Malignant GliomaR01CA139020 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BONDY, MELISSA L. · 2010 to 2015
$16.0M
Genetic Epidemiology of Glioma International ConsortiumR01CA119215 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BONDY, MELISSA L. · 2006 to 2010
$11.9M
Cancer Research UK A8362NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA125123NCI NIH HHS R01 CA052689NCI NIH HHS R01 CA119215NCI NIH HHS R01 CA139020Wellcome Trust
6 · The paper itself

Abstract

Genome-wide association studies (GWAS) have so far identified 25 loci associated with glioma risk, with most showing specificity for either glioblastoma (GBM) or non-GBM tumors. The majority of these GWAS susceptibility variants reside in noncoding regions and the causal genes underlying the associations are largely unknown. Here we performed a transcriptome-wide association study to search for novel risk loci and candidate causal genes at known GWAS loci using Genotype-Tissue Expression Project (GTEx) data to predict

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideTranscriptomeBiomarkers, TumorCase-Control StudiesGene Expression Regulation, NeoplasticGenome-Wide Association StudyGenotypeGliomaHumansPrognosisQuantitative Trait LociBiomarkers, Tumor

Identifiers

PMID30709929
PMCPMC6522343
OpenAlexW2911609218

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.