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Genetic Epidemiology
|
March 12, 2005
Reduction of selection bias in genomewide studies by resampling
Lei Sun, Shelley B Bull
Statistics in Medicine
|
March 25, 2023
Penalized maximum likelihood inference under the mixture cure model in sparse data
Changchang Xu, Shelley B Bull
BMC Proceedings
|
March 1, 2012
Are quantitative trait-dependent sampling designs cost-effective for analysis of rare and common variants?
Yildiz E Yilmaz, Shelley B Bull
Genetic Epidemiology
|
December 16, 2005
Validity, efficiency, and robustness of a family-based test of association
Juan Pablo Lewinger, Shelley B Bull
Human Heredity
|
December 22, 2012
Cumulative meta-analysis for genetic association: when is a new study worthwhile?
Michael A Rotondi, Shelley B Bull
BMC Proceedings
|
March 1, 2012
Two-stage study designs combining genome-wide association studies, tag single-nucleotide polymorphisms, and exome sequencing: accuracy of genetic effect estimates
Laura L Faye, Shelley B Bull
Journal of Cardiovascular Translational Research
|
June 26, 2012
Does familial clustering of risk factors for long-term diabetic complications leave any place for genes that act independently?
Andrew D Paterson, Shelley B Bull
American Journal of Human Genetics
|
December 8, 2004
Corrections to the parameterization of constraints on allele sharing in sibling pairs alter covariate-parameter estimates but not sharing-probability estimates or power of tests for linkage
Celia M T Greenwood, Shelley B Bull
Genetic Epidemiology
|
December 13, 2005
Fine mapping by linkage and association in nuclear family and case-control designs
Shelley B Bull, Sally John, Laurent Briollais
BMC Proceedings
|
May 10, 2008
Application of bivariate mixed counting process models to genetic analysis of rheumatoid arthritis severity
Rinku Sutradhar, Dushanthi Pinnaduwage, Shelley B Bull
Page
of 12
Search research articles
Search
Showing results (1-10 of 115) with videos related to
Sort By:
Page
of 12
Genetic Epidemiology
|
March 12, 2005
Reduction of selection bias in genomewide studies by resampling
Lei Sun, Shelley B Bull
Statistics in Medicine
|
March 25, 2023
Penalized maximum likelihood inference under the mixture cure model in sparse data
Changchang Xu, Shelley B Bull
BMC Proceedings
|
March 1, 2012
Are quantitative trait-dependent sampling designs cost-effective for analysis of rare and common variants?
Yildiz E Yilmaz, Shelley B Bull
Genetic Epidemiology
|
December 16, 2005
Validity, efficiency, and robustness of a family-based test of association
Juan Pablo Lewinger, Shelley B Bull
Human Heredity
|
December 22, 2012
Cumulative meta-analysis for genetic association: when is a new study worthwhile?
Michael A Rotondi, Shelley B Bull
BMC Proceedings
|
March 1, 2012
Two-stage study designs combining genome-wide association studies, tag single-nucleotide polymorphisms, and exome sequencing: accuracy of genetic effect estimates
Laura L Faye, Shelley B Bull
Journal of Cardiovascular Translational Research
|
June 26, 2012
Does familial clustering of risk factors for long-term diabetic complications leave any place for genes that act independently?
Andrew D Paterson, Shelley B Bull
American Journal of Human Genetics
|
December 8, 2004
Corrections to the parameterization of constraints on allele sharing in sibling pairs alter covariate-parameter estimates but not sharing-probability estimates or power of tests for linkage
Celia M T Greenwood, Shelley B Bull
Genetic Epidemiology
|
December 13, 2005
Fine mapping by linkage and association in nuclear family and case-control designs
Shelley B Bull, Sally John, Laurent Briollais
BMC Proceedings
|
May 10, 2008
Application of bivariate mixed counting process models to genetic analysis of rheumatoid arthritis severity
Rinku Sutradhar, Dushanthi Pinnaduwage, Shelley B Bull
Page
of 12