1996 William Allan Award Address. Algorithms and inferences: the challenge of multifactorial diseases.

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

13 citing papers in PubMed.

1. Presidential address: Six open questions to genetic epidemiologists.Genetic epidemiology · 2019
   Article
2. A novel germline mutation in BAP1 predisposes to familial clear-cell renal cell carcinoma.Molecular cancer research : MCR · 2013
   Article
3. GIGI: an approach to effective imputation of dense genotypes on large pedigrees.American journal of human genetics · 2013
   Article
4. Controlling the proportion of false positives in multiple dependent tests.Genetics · 2004
   Article
5. Search for genetic factors predisposing to atherogenic dyslipidemia.BMC genetics · 2003
   Article
6. Genome-wide screen for heavy alcohol consumption.BMC genetics · 2003
   Article
7. Evidence for a locus (IDDM16) in the immunoglobulin heavy chain region on chromosome 14q32.3 producing susceptibility to type 1 diabetes.Genes and immunity · 2002
   Article
8. A genomewide scan for loci involved in attention-deficit/hyperactivity disorder.American journal of human genetics · 2002
   Article
9. Interpretation of genetic association studies in complex disease.The pharmacogenomics journal · 2002
   Review
10. Genome-wide scans of three independent sets of 90 Irish multiplex schizophrenia families and follow-up of selected regions in all families provides evidence for multiple susceptibility genes.Molecular psychiatry · 2002
    Article
11. Chromosome 6p influences on different dyslexia-related cognitive processes: further confirmation.American journal of human genetics · 2000
    Article
12. Sampling strategies for model free linkage analyses of quantitative traits: implications for sib pair studies of reading and spelling disabilities to minimize the total study cost.European child & adolescent psychiatry · 1999
    Article
13. Blood pressure and survival of a chromosome 7 congenic strain bred from Dahl rats.Mammalian genome : official journal of the International Mammalian Genome Society · 1997
    Article

Corrections and comments

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

Authors and funding

1 author.

Funding

Abstract

PubMed holds no abstract for this paper.

Indexed as