A novel method to identify gene-gene effects in nuclear families: the MDR-PDT. (Q34479246)

2 August 2017

title

A novel method to identify gene-gene effects in nuclear families: the MDR-PDT. (English)

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2 August 2017

5

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2 August 2017

2

Ritchie MD

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2 August 2017

Martin ER

1

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2 August 2017

Hahn L

series ordinal

3

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2 August 2017

Kang S

series ordinal

4

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2 August 2017

publication date

1 February 2006

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2 August 2017

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2 August 2017

volume

30

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2 August 2017

issue

2

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2 August 2017

page(s)

111-123

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Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

2 August 2017

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MDR and PRP: A Comparison of Methods for High-Order Genotype-Phenotype Associations

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7 January 2021

Multifactor-dimensionality reduction shows a two-locus interaction associated with Type 2 diabetes mellitus.

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An application of conditional logistic regression and multifactor dimensionality reduction for detecting gene-gene interactions on risk of myocardial infarction: the importance of model validation

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Tree and spline based association analysis of gene-gene interaction models for ischemic stroke

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Detecting epistatic interactions contributing to quantitative traits

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Fine mapping of the -T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigrees

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Multifactor dimensionality reduction software for detecting gene-gene and gene-environment interactions

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Genotype‐based association test for general pedigrees: The genotype‐PDT

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Interaction between the alpha-T catenin gene (VR22) and APOE in Alzheimer's disease

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Computational analysis of gene-gene interactions using multifactor dimensionality reduction

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A global view of epistasis

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New strategies for identifying gene-gene interactions in hypertension

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Traversing the conceptual divide between biological and statistical epistasis: systems biology and a more modern synthesis

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A combinatorial partitioning method to identify multilocus genotypic partitions that predict quantitative trait variation

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"Are we there yet?": Deciding when one has demonstrated specific genetic causation in complex diseases and quantitative traits.

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An association study of the N-methyl-D-aspartate receptor NR1 subunit gene (GRIN1) and NR2B subunit gene (GRIN2B) in schizophrenia with universal DNA microarray

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7 January 2021

Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer

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Power of multifactor dimensionality reduction for detecting gene-gene interactions in the presence of genotyping error, missing data, phenocopy, and genetic heterogeneity

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Testing linkage disequilibrium in sibships

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7 January 2021

Susceptibility and modifier genes in Portuguese transthyretin V30M amyloid polyneuropathy: complexity in a single-gene disease

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Renin-angiotensin system gene polymorphisms and atrial fibrillation

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Embryonic-endometrial interactions at implantation in humans

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7 January 2021

Identifiers

DOI

10.1002/GEPI.20128

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2 August 2017

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