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Detecting haplotype effects in genomewide association studies

Genetic epidemiology, 2007-12, Vol.31 (8), p.803-812

2007

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1400 DISCOVERY OF A DIRECT ASSOCIATION BETWEEN PRIMARY BILIARY CIRRHOSIS AND LOW BONE MASS: IDENTIFICATION OF TNFSF11/RANKL AS A RISK LOCUS FOR PATIENTS WITH PBC

Journal of hepatology, 2012-04, Vol.56, p.S550-S551

2012

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High risk of HIV-1 infection for first-born twins

The Lancet (British edition), 1991-12, Vol.338 (8781), p.1471-1475

1991

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Genetic variants in the folate metabolic pathway genes predict cutaneous melanoma‐specific survival

British journal of dermatology (1951), 2020-10, Vol.183 (4), p.719-728

2020

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Entropy-based information gain approaches to detect and to characterize gene-gene and gene-environment interactions/correlations of complex diseases

Genetic epidemiology, 2011-11, Vol.35 (7), p.706-721

2011

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Association of primary biliary cirrhosis with variants in the CLEC16A, SOCS1, SPIB and SIAE immunomodulatory genes

Genes and immunity, 2012-06, Vol.13 (4), p.328-335

2012

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A Major Lung Cancer Susceptibility Locus Maps to Chromosome 6q23–25

American journal of human genetics, 2004-09, Vol.75 (3), p.460-474

2004

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Innovations in risk-stratification and treatment of Veterans with oropharynx cancer; roadmap of the 2019 Field Based Meeting

Oral oncology, 2020-03, Vol.102, p.104440-104440, Article 104440

2020

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Robust variance-components approach for assessing genetic linkage in pedigrees

American journal of human genetics, 1994-03, Vol.54 (3), p.535-543

AMOS, C. I

1994

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Shared susceptibility variations in autoimmune diseases: a brief perspective on common issues

Genes and immunity, 2009-01, Vol.10 (1), p.1-4

2009

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A susceptibility locus on chromosome 6q greatly increases risk lung cancer risk among light and never smokers

Cancer research (Chicago, Ill.), 2010-03, Vol.70 (6), p.2359-2367

2010

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Relationship between plasma carotenoids and prostate cancer

Nutrition and cancer, 2005-01, Vol.53 (2), p.127-134

2005

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Genetic linkage methods for quantitative traits

Statistical methods in medical research, 2001-02, Vol.10 (1), p.3-25

2001

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Effect of Box-Cox Transformation on Power of Haseman-Elston and Maximum-Likelihood Variance Components Tests to Detect Quantitative Trait Loci

Human Heredity, 2003-01, Vol.55 (2/3), p.108-116

2003

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Assessing linkage on chromosome 5 using components of variance approach: Univariate versus multivariate

Genetic epidemiology, 1997, Vol.14 (6), p.773-778

1997

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Comparison of model-free linkage mapping strategies for the study of a complex trait

Genetic epidemiology, 1997, Vol.14 (6), p.743-748

1997

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Testing for Linkage under Robust Genetic Models

Human heredity, 1999-06, Vol.49 (3), p.146-153

1999

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Assessing linkage of monoamine oxidase B in a genome-wide scan using a univariate variance components approach

Genetic epidemiology, 1999, Vol.17 (S1), p.S49-S54

1999

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A genome-wide search for susceptibility genes linked to alcohol dependence

Genetic epidemiology, 1999, Vol.17 (S1), p.S295-S300

1999

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Refined mapping of the gene causing familial mediterranean fever, by linkage and homozygosity studies

American journal of human genetics, 1993-08, Vol.53 (2), p.451-461

1993

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Estimating the Strength of Genetic Effects: A Comparison of Maximum Likelihood and Transmission Disequilibrium Methods in the Study of Ankylosing Spondylitis

Human immunology, 1997-09, Vol.57 (1), p.44-50

1997

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Testing for Linkage underRobust Genetic Models

Human heredity, 1999-01, Vol.49 (3), p.146-153

1999

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Preliminary evaluation of linkage between chromosome 1p markers and nevus densities in the Utah data

Cytogenetic and genome research, 1992, Vol.59 (2-3), p.173-175

1992

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4 Primary immunodeficiency mutation databases

Advances in Genetics, 2001, Vol.43, p.103-188

2001

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Detecting haplotype effects in genomewide association studies

1400 DISCOVERY OF A DIRECT ASSOCIATION BETWEEN PRIMARY BILIARY CIRRHOSIS AND LOW BONE MASS: IDENTIFICATION OF TNFSF11/RANKL AS A RISK LOCUS FOR PATIENTS WITH PBC

High risk of HIV-1 infection for first-born twins

Genetic variants in the folate metabolic pathway genes predict cutaneous melanoma‐specific survival

Entropy-based information gain approaches to detect and to characterize gene-gene and gene-environment interactions/correlations of complex diseases

Association of primary biliary cirrhosis with variants in the CLEC16A, SOCS1, SPIB and SIAE immunomodulatory genes

A Major Lung Cancer Susceptibility Locus Maps to Chromosome 6q23–25

Innovations in risk-stratification and treatment of Veterans with oropharynx cancer; roadmap of the 2019 Field Based Meeting

Robust variance-components approach for assessing genetic linkage in pedigrees

Shared susceptibility variations in autoimmune diseases: a brief perspective on common issues

A susceptibility locus on chromosome 6q greatly increases risk lung cancer risk among light and never smokers

Relationship between plasma carotenoids and prostate cancer

Genetic linkage methods for quantitative traits

Effect of Box-Cox Transformation on Power of Haseman-Elston and Maximum-Likelihood Variance Components Tests to Detect Quantitative Trait Loci

Assessing linkage on chromosome 5 using components of variance approach: Univariate versus multivariate

Comparison of model-free linkage mapping strategies for the study of a complex trait

Testing for Linkage under Robust Genetic Models

Assessing linkage of monoamine oxidase B in a genome-wide scan using a univariate variance components approach

A genome-wide search for susceptibility genes linked to alcohol dependence

Refined mapping of the gene causing familial mediterranean fever, by linkage and homozygosity studies

Estimating the Strength of Genetic Effects: A Comparison of Maximum Likelihood and Transmission Disequilibrium Methods in the Study of Ankylosing Spondylitis

Testing for Linkage underRobust Genetic Models

Preliminary evaluation of linkage between chromosome 1p markers and nevus densities in the Utah data

4 Primary immunodeficiency mutation databases

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