Complex genetic diseases: controversy over the Croesus code.

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

22 citing papers in PubMed, 89 citations in OpenAlex.

1. The evolution of cancer genomic medicine in Japan and the role of the National Cancer Center Japan.Cancer biology & medicine · 2023
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2. Inbreeding, Native American ancestry and child mortality: linking human selection and paediatric medicine.Human molecular genetics · 2022
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3. Inbreeding among Caribbean Hispanics from the Dominican Republic and its effects on risk of Alzheimer disease.Genetics in medicine : official journal of the American College of Medical Genetics · 2015
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4. Cost-effectiveness of initial diagnostic strategies for pulmonary nodules presenting to thoracic surgeons.The Annals of thoracic surgery · 2014
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5. What is complex about complex disorders?Genome biology · 2012
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6. Genetic variation and its role in malignancy.International journal of biomedical science : IJBS · 2011
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7. Genomic approaches to coronary artery disease.The Indian journal of medical research · 2010
   Review
8. Genome-wide germline analyses on cancer susceptibility and GeMDBJ database: Gastric cancer as an example.Cancer science · 2010
   Review
9. Interpretation of association signals and identification of causal variants from genome-wide association studies.American journal of human genetics · 2010
   Article
10. Genome-wide association studies and the genetic dissection of complex traits.American journal of hematology · 2009
    Review
11. Current and future directions in genomics of amyotrophic lateral sclerosis.Physical medicine and rehabilitation clinics of North America · 2008
    Review
12. Full-exon resequencing reveals toll-like receptor variants contribute to human susceptibility to tuberculosis disease.PloS one · 2007
    Article
13. The role of phospholipases A2 in schizophrenia.Molecular psychiatry · 2006
    Review
14. Predisposition to mouse thymic lymphomas in response to ionizing radiation depends on variant alleles encoding metal-responsive transcription factor-1 (Mtf-1).Oncogene · 2005
    Article
15. The prediction of disease risk in genomic medicine.EMBO reports · 2004
    Article
16. Differential expression of S100 gene family in human esophageal squamous cell carcinoma.Journal of cancer research and clinical oncology · 2004
    Article
17. A systematic approach to the assessment of known TNF-alpha polymorphisms in Graves' disease.Genes and immunity · 2004
    Article
18. Designing a multistage, SNP-based, genome screen for common diseases.Journal of human genetics · 2004
    Article
19. Growing evidence for diabetes susceptibility genes from genome scan data.Current diabetes reports · 2003
    Review
20. New methods for finding disease-susceptibility genes: impact and potential.Genome biology · 2003
    Review

Corrections and comments

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

Authors and funding

2 authors at 1 institution in 1 country.

Funding

No grant is acknowledged in the PubMed record.

Abstract

Indexed as