Evidence map›Paper›PMID 24149102›Full record

SynthesisNature communications2013

Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma.

Matthew Frampton, Miguel Inacio da Silva Filho, Peter Broderick, Hauke Thomsen, Asta Försti, Jayaram Vijayakrishnan, Rosie Cooke, Victor Enciso-Mora, Per Hoffmann, Markus M Nöthen and 15 more

Open access · bronzeAbstract readMeta-Analysis
In one paragraph

Synthesis in Nature communications, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 7 pooled it
4.7field-weighted citation impact, top 5% 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

38 citing papers in PubMed, 7 syntheses or guidelines pooled it, 69 citations in OpenAlex.

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  8. Characterization of Genetic Etiologic Factors for Pediatric Acute Lymphoblastic Leukemia in Large Childhood Cancer Survivorship Cohorts.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2026
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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

25 authors at 8 institutions in 4 countries.

Matthew FramptonDivision of Genetics and Epidemiology, Institute of Cancer Research, Sutton, Surrey SM2 5NG, UK.
Miguel Inacio da Silva Filho
Peter Broderick
Hauke Thomsen
Asta Försti
Jayaram Vijayakrishnan
Rosie Cooke
Victor Enciso-Mora
Per Hoffmann
Markus M Nöthen
Amy Lloyd
Amy Holroyd
Lewin Eisele
Karl-Heinz Jöckel
Sabine Ponader
Elke Pogge von Strandmann
Tracy Lightfoot
Eve Roman
Annette Lake
Dorothy Montgomery
Ruth F Jarrett
Anthony J Swerdlow
Andreas Engert
Kari Hemminki
Richard S Houlston
Institute of Cancer Research · GBGerman Cancer Research Center · DEMRC University of Glasgow Centre for Virus Research · GBUniversity Hospital Cologne · DEUniversity of Bonn · DEUniversity of Duisburg-Essen · DEUniversity of York · GBLund University · SE

Funding

Cancer Research UK C1298/A8362Medical Research Council G0000934Wellcome TrustWellcome Trust 068545/Z/02Wellcome Trust 076113Wellcome Trust 085475
6 · The paper itself

Abstract

In addition to HLA, recent genome-wide association studies (GWASs) of Hodgkin's lymphoma (HL) have identified susceptibility loci for HL at 2p16.1, 8q24.21 and 10p14. In this study, we perform a GWAS meta-analysis with published GWAS (totalling 1,465 cases and 6,417 controls of European background), and follow-up the most significant association signals in 2,024 cases and 1,853 controls. A combined analysis identifies new HL susceptibility loci mapping to 3p24.1 (rs3806624; P=1.14 × 10(-12), odds ratio (OR)=1.26) and 6q23.3 (rs7745098; P=3.42 × 10(-9), OR=1.21). rs3806624 localizes 5' to the EOMES (eomesodermin) gene within a p53 response element affecting p53 binding. rs7745098 maps intergenic to HBS1L and MYB, a region previously associated with haematopoiesis. These findings provide further insight into the genetic and biological basis of inherited susceptibility to HL.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideCase-Control StudiesChromosomes, Human, Pair 3Chromosomes, Human, Pair 6Gene ExpressionGene FrequencyGenetic LociGenome-Wide Association StudyHodgkin DiseaseHumansOdds RatioT-Box Domain ProteinsTumor Suppressor Protein p53White PeopleEOMES protein, humanT-Box Domain ProteinsTumor Suppressor Protein p53

Identifiers

PMID24149102
PMCPMC5053363
OpenAlexW1976676411

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.