Interpretation of genetic association studies in complex disease (Q35082735)

6 August 2017

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title

Interpretation of genetic association studies in complex disease (English)

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6 August 2017

Campbell H

1

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PubMed ID

12629506

6 August 2017

Rudan I

series ordinal

2

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6 August 2017

1 January 2002

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The Pharmacogenomics Journal

6 August 2017

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6 August 2017

2

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6 August 2017

6

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6 August 2017

349-360

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https://scigraph.springernature.com/pub.10.1038/sj.tpj.6500132

6 August 2017

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A full genome scan for late onset Alzheimer's disease.

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Sequence diversity in CYP3A promoters and characterization of the genetic basis of polymorphic CYP3A5 expression

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Association study designs for complex diseases

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Multi-locus nonparametric linkage analysis of complex trait loci with neural networks.

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Searching for genetic determinants in the new millennium

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What is significant in whole-genome linkage disequilibrium studies?

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Significance levels in complex inheritance

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Power calculations for genetic association studies using estimated probability distributions

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Principles of multilevel modelling

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Statistical tests for detection of misspecified relationships by use of genome-screen data

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Genomic control for association studies

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The importance of genealogy in determining genetic associations with complex traits

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Bias and confounding in molecular epidemiological studies: special considerations.

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Factors influencing publication of research results. Follow-up of applications submitted to two institutional review boards

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Replication validity of genetic association studies

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Statistical analysis of case-control studies

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Tests and estimates of allelic association in complex inheritance

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Use of unlinked genetic markers to detect population stratification in association studies.

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Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase

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Induction versus Popper: substance versus semantics

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Are rare variants responsible for susceptibility to complex diseases?

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The problems of using the transmission/disequilibrium test to infer tight linkage

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Characterization of single-nucleotide polymorphisms in coding regions of human genes

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Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis

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Association studies of genetic polymorphisms and complex disease

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Taking a functional genomics approach in molecular medicine

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Measured Haplotype Analysis of the Angiotensin-I Converting Enzyme Gene

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Haplotype tagging for the identification of common disease genes

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Linkage between inherited resistance to activated protein C and factor V gene mutation in venous thrombosis

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7 January 2021

Linkage disequilibrium mapping of complex disease: fantasy or reality?

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7 January 2021

Empirical-Bayes adjustments for multiple comparisons are sometimes useful

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7 January 2021

Large-scale test of hypothesised associations between the angiotensin-converting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 controls. International Studies of Infarct Survival (ISIS) Collaborators

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7 January 2021

Population stratification in epidemiologic studies of common genetic variants and cancer: quantification of bias

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7 January 2021

The replication requirement

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7 January 2021

Integrated designs for gene discovery and characterization

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7 January 2021

Identifiers

DOI

10.1038/SJ.TPJ.6500132

1 reference

PubMed ID

12629506

Dimensions Publication ID

6 August 2017

0 references

1 reference

PubMed ID

12629506