(Q35221734)

7 August 2017

title

Powerful multilocus tests of genetic association in the presence of gene-gene and gene-environment interactions (English)

1 reference

7 August 2017

5

Sholom Wacholder

0 references

Nilanjan Chatterjee

series ordinal

1

object named as

Nilanjan Chatterjee

1 reference

7 August 2017

4

Ulrike Peters

1 reference

7 August 2017

Zeynep Kalaylioglu

2

1 reference

7 August 2017

Roxana Moslehi

series ordinal

3

1 reference

7 August 2017

language of work or name

English

0 references

publication date

20 October 2006

1 reference

American Journal of Human Genetics

7 August 2017

published in

1 reference

7 August 2017

volume

79

1 reference

7 August 2017

issue

6

1 reference

7 August 2017

page(s)

1002-1016

1 reference

Cigarette smoking, N-acetyltransferase genes and the risk of advanced colorectal adenoma

7 August 2017

cites work

1 reference

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A testing framework for identifying susceptibility genes in the presence of epistasis

13 July 2018

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13 July 2018

1 reference

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A haplotype map of the human genome

13 July 2018

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Nonparametric tests of association of multiple genes with human disease

13 July 2018

1 reference

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Whole-genome patterns of common DNA variation in three human populations

13 July 2018

1 reference

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Genome-wide association studies: theoretical and practical concerns

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Use of unphased multilocus genotype data in indirect association studies

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Mapping complex disease loci in whole-genome association studies

13 July 2018

1 reference

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The International HapMap Project

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Choosing haplotype-tagging SNPS based on unphased genotype data using a preliminary sample of unrelated subjects with an example from the Multiethnic Cohort Study

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Score tests for association between traits and haplotypes when linkage phase is ambiguous

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Gene-environment interaction and affected sib pair linkage analysis

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Association study designs for complex diseases

13 July 2018

1 reference

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A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

13 July 2018

1 reference

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Etiologic and early marker studies in the prostate, lung, colorectal and ovarian (PLCO) cancer screening trial

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease

13 July 2018

1 reference

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Searching for genetic determinants in the new millennium

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Multilocus linkage tests based on affected relative pairs.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

The future of genetic studies of complex human diseases

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Two-trait-locus linkage analysis: a powerful strategy for mapping complex genetic traits

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Statistical methods for linkage analysis of complex traits from high-resolution maps of identity by descent.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Some epistatic two-locus models of disease. I. Relative risks and identity-by-descent distributions in affected sib pairs

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Strategies for studying heterogeneous genetic traits in humans by using a linkage map of restriction fragment length polymorphisms

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Linkage strategies for genetically complex traits. I. Multilocus models

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Effect modification and the limits of biological inference from epidemiologic data.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Genome scans with gene-covariate interaction

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Methods for etiologic and early marker investigations in the PLCO trial.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Genome-wide strategies for detecting multiple loci that influence complex diseases.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Detecting disease associations due to linkage disequilibrium using haplotype tags: a class of tests and the determinants of statistical power

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Sample size calculations for population- and family-based case-control association studies on marker genotypes

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Molecular genetics of human polymorphic N-acetyltransferase: enzymatic analysis of 15 recombinant wild-type, mutant, and chimeric NAT2 allozymes.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Metabolic activation of carcinogenic arylamines by rapid acetylator, slow acetylator, and chimeric recombinant Syrian hamster NAT2 allozymes.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698705

Haplotype tagging for the identification of common disease genes

26 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17186459

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Assessing genomewide statistical significance in linkage studies

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17186459

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/509704

1 reference

7 August 2017

1 reference

7 August 2017

1 reference