Correcting for a potential bias in the pedigree disequilibrium test.

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

64 citing papers in PubMed.

1. Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in attention-deficit/hyperactivity disorder.Molecular psychiatry · 2005
   Trial
2. Analysis of the RELN gene as a genetic risk factor for autism.Molecular psychiatry · 2005
   Trial
3. A comparison of popular TDT-generalizations for family-based association analysis.Genetic epidemiology · 2019
   Article
4. A Pragmatic Test for Detecting Association between a Dichotomous Trait and the Genotypes of Affected Families, Controls and Independent Cases.Frontiers in genetics · 2017
   Article
5. On the validity of within-nuclear-family genetic association analysis in samples of extended families.Statistical applications in genetics and molecular biology · 2015
   Article
6. The power comparison of the haplotype-based collapsing tests and the variant-based collapsing tests for detecting rare variants in pedigrees.BMC genomics · 2014
   Article
7. Evaluating power and type 1 error in large pedigree analyses of binary traits.PloS one · 2013
   Article
8. Lack of association between autism and four heavy metal regulatory genes.Neurotoxicology · 2011
   Article
9. Association of alcohol dehydrogenase genes with alcohol-related phenotypes in a Native American community sample.Alcoholism, clinical and experimental research · 2011
   Article
10. Ablation of Mrds1/Ofcc1 induces hyper-γ-glutamyl transpeptidasemia without abnormal head development and schizophrenia-relevant behaviors in mice.PloS one · 2011
    Article
11. Association and gene-gene interaction of SLC6A4 and ITGB3 in autism.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2010
    Article
12. GABRR1 and GABRR2, encoding the GABA-A receptor subunits rho1 and rho2, are associated with alcohol dependence.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2010
    Article
13. Infantile hypertrophic pyloric stenosis: evaluation of three positional candidate genes, TRPC1, TRPC5 and TRPC6, by association analysis and re-sequencing.Human genetics · 2009
    Article
14. Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14.Epilepsy research · 2009
    Article
15. A generalized family-based association test for dichotomous traits.American journal of human genetics · 2009
    Article
16. Evidence for association between polymorphisms in the cannabinoid receptor 1 (CNR1) gene and cannabis dependence.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2009
    Article
17. A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.Annals of human genetics · 2009
    Article
18. Genetic variation in the serotonin 2A receptor and suicidal ideation in a sample of 270 Irish high-density schizophrenia families.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2009
    Article
19. Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis.Human genetics · 2009
    Article
20. Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestry.BMC medical genetics · 2009
    Article

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

Corrections and comments

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  A test for linkage and association in general pedigrees: the pedigree disequilibrium test.2000

Authors and funding

3 authors.

Funding

Abstract

PubMed holds no abstract for this paper.

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