Evidence map›Paper›PMID 20062064›Full record

ArticleNature genetics2010

Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk.

Dalemari Crowther-Swanepoel, Peter Broderick, Maria Chiara Di Bernardo, Sara E Dobbins, María Torres, Mahmoud Mansouri, Clara Ruiz-Ponte, Anna Enjuanes, Richard Rosenquist, Angel Carracedo and 25 more

Abstract read
In one paragraph

Article in Nature genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 131 papers, 14 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
131citing papers in PubMed, 14 pooled it
–field-weighted citation impact
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

131 citing papers in PubMed, 14 syntheses or guidelines pooled it.

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71 more citing papers are in PubMed but not listed here.

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

35 authors.

Dalemari Crowther-SwanepoelInstitute of Cancer Research, Sutton, Surrey, UK.
Peter Broderick
Maria Chiara Di Bernardo
Sara E Dobbins
María Torres
Mahmoud Mansouri
Clara Ruiz-Ponte
Anna Enjuanes
Richard Rosenquist
Angel Carracedo
Jesper Jurlander
Elias Campo
Gunnar Juliusson
Emilio Montserrat
Karin E Smedby
Martin J S Dyer
Estella Matutes
Claire Dearden
Nicola J Sunter
Andrew G Hall
Tryfonia Mainou-Fowler
Graham H Jackson
Geoffrey Summerfield
Robert J Harris
Andrew R Pettitt
David J Allsup
James R Bailey
Guy Pratt
Chris Pepper
Chris Fegan
Anton Parker
David Oscier
James M Allan
Daniel Catovsky
Richard S Houlston

Funding

Cancer Research UK A8362Cancer Research UK C1298/A8362Medical Research Council G0000934Medical Research Council MC_U132670597Wellcome TrustWellcome Trust 076113Wellcome Trust 085475
6 · The paper itself

Abstract

To identify new risk variants for chronic lymphocytic leukemia (CLL), we conducted a genome-wide association study of 299,983 tagging SNPs, with validation in four additional series totaling 2,503 cases and 5,789 controls. We identified four new risk loci for CLL at 2q37.3 (rs757978, FARP2; odds ratio (OR) = 1.39; P = 2.11 x 10(-9)), 8q24.21 (rs2456449; OR = 1.26; P = 7.84 x 10(-10)), 15q21.3 (rs7169431; OR = 1.36; P = 4.74 x 10(-7)) and 16q24.1 (rs305061; OR = 1.22; P = 3.60 x 10(-7)). We also found evidence for risk loci at 15q25.2 (rs783540, CPEB1; OR = 1.18; P = 3.67 x 10(-6)) and 18q21.1 (rs1036935; OR = 1.22; P = 2.28 x 10(-6)). These data provide further evidence for genetic susceptibility to this B-cell hematological malignancy.

Indexed as

Genetic Predisposition to DiseaseGenetic VariationAllelesChromosomes, HumanGenetic LociGenome, HumanHumansLeukemia, Lymphocytic, Chronic, B-CellPolymorphism, Single Nucleotide

Identifiers

PMID20062064
PMCPMC5321238

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Registered trials

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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.