Guilt beyond a reasonable doubt.

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.

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.

Who cites it

76 citing papers in PubMed, 4 syntheses or guidelines pooled it.

1. Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.Nature genetics · 2018
   Pooled it
2. On individual genome-wide association studies and their meta-analysis.Human genetics · 2014
   Pooled it
3. Genome-wide association study of suicide attempts in mood disorder patients.The American journal of psychiatry · 2010
   Pooled it
4. Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controls.Circulation. Cardiovascular genetics · 2010
   Pooled it
5. Genome-wide association study of early-onset and late-onset postpartum depression: the IGEDEPP prospective study.European psychiatry : the journal of the Association of European Psychiatrists · 2024
   Article
6. Use of whole-genome sequence data for fine mapping and genomic prediction of sea louse resistance in Atlantic salmon.Frontiers in genetics · 2024
   Article
7. Precision pharmacotherapy: psychiatry's future direction in preventing, diagnosing, and treating mental disorders.Pharmacogenomics and personalized medicine · 2018
   Review
8. High-Resolution Genetic Maps Identify Multiple Type 2 Diabetes Loci at Regulatory Hotspots in African Americans and Europeans.American journal of human genetics · 2017
   Article
9. The genomic landscape of human immune-mediated diseases.Journal of human genetics · 2015
   Review
10. Specific glial functions contribute to schizophrenia susceptibility.Schizophrenia bulletin · 2014
    Article
11. The major histocompatibility complex: a model for understanding graft-versus-host disease.Blood · 2013
    Review
12. Common variants in adiponectin gene are associated with coronary artery disease and angiographical severity of coronary atherosclerosis in type 2 diabetes.Cardiovascular diabetology · 2013
    Article
13. A diverse array of genetic factors contribute to the pathogenesis of systemic lupus erythematosus.Orphanet journal of rare diseases · 2013
    Review
14. Genetic architectures of psychiatric disorders: the emerging picture and its implications.Nature reviews. Genetics · 2012
    Review
15. Between candidate genes and whole genomes: time for alternative approaches in blood pressure genetics.Current hypertension reports · 2012
    Review
16. Genome-wide association study in RPGRIP1(-/-) dogs identifies a modifier locus that determines the onset of retinal degeneration.Mammalian genome : official journal of the International Mammalian Genome Society · 2012
    Article
17. Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease.Nature genetics · 2011
    Article
18. Design and cohort description of the InterAct Project: an examination of the interaction of genetic and lifestyle factors on the incidence of type 2 diabetes in the EPIC Study.Diabetologia · 2011
    Article
19. Linkage analysis without defined pedigrees.Genetic epidemiology · 2011
    Article
20. Drug resistance in epilepsy and the ABCB1 gene: The clinical perspective.Indian journal of human genetics · 2011
    Article

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

Corrections and comments

• Comment on
  Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.2007
• Comment on
  Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.2007

Authors and funding

2 authors.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

Indexed as