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European Urology
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October 1, 2018
Personalized Prostate Cancer Screening Based on a Single Midlife Prostate-specific Antigen Measurement
Rebecca E Graff, Linda Kachuri, John S Witte
BMC Proceedings
|
March 1, 2012
Use of principal components to aggregate rare variants in case-control and family-based association studies in the presence of multiple covariates
Rémi Kazma, Thomas J Hoffmann, John S Witte
Epidemiology (Cambridge, Mass.)
|
February 16, 2007
Dissecting effects of complex mixtures: who's afraid of informative priors?
Duncan C Thomas, John S Witte, Sander Greenland
Human Heredity
|
April 19, 2013
Does accounting for gene-environment interactions help uncover association between rare variants and complex diseases?
Rémi Kazma, Niall J Cardin, John S Witte
BMC Proceedings
|
May 10, 2008
An empirical evaluation of the common disease-common variant hypothesis
Gary K Chen, Eric Jorgenson, John S Witte
Genetic Epidemiology
|
September 25, 2004
Increased power for case-control studies of single nucleotide polymorphisms through incorporation of family history and genetic constraints
Deborah Thompson, John S Witte, Martha Slattery, et al.
Epidemiology (Cambridge, Mass.)
|
February 24, 2009
Nutrient pathways and neural tube defects: a semi-Bayesian hierarchical analysis
Suzan L Carmichael, John S Witte, Gary M Shaw
Genetic Epidemiology
|
July 19, 2012
Joint association testing of common and rare genetic variants using hierarchical modeling
Niall J Cardin, Joel A Mefford, John S Witte
Human Heredity
|
November 14, 2003
Haplotype tagging single nucleotide polymorphisms and association studies
Deborah Thompson, Dan Stram, David Goldgar, et al.
Statistics in Medicine
|
July 12, 2002
Analysis of mutational spectra: locating hotspots and clusters of mutations using recursive segmentation
Bonnie A Fijal, Ramana M Idury, John S Witte
Page
of 26
Search research articles
Search
Showing results (31-40 of 256) with videos related to
Sort By:
Page
of 26
European Urology
|
October 1, 2018
Personalized Prostate Cancer Screening Based on a Single Midlife Prostate-specific Antigen Measurement
Rebecca E Graff, Linda Kachuri, John S Witte
BMC Proceedings
|
March 1, 2012
Use of principal components to aggregate rare variants in case-control and family-based association studies in the presence of multiple covariates
Rémi Kazma, Thomas J Hoffmann, John S Witte
Epidemiology (Cambridge, Mass.)
|
February 16, 2007
Dissecting effects of complex mixtures: who's afraid of informative priors?
Duncan C Thomas, John S Witte, Sander Greenland
Human Heredity
|
April 19, 2013
Does accounting for gene-environment interactions help uncover association between rare variants and complex diseases?
Rémi Kazma, Niall J Cardin, John S Witte
BMC Proceedings
|
May 10, 2008
An empirical evaluation of the common disease-common variant hypothesis
Gary K Chen, Eric Jorgenson, John S Witte
Genetic Epidemiology
|
September 25, 2004
Increased power for case-control studies of single nucleotide polymorphisms through incorporation of family history and genetic constraints
Deborah Thompson, John S Witte, Martha Slattery, et al.
Epidemiology (Cambridge, Mass.)
|
February 24, 2009
Nutrient pathways and neural tube defects: a semi-Bayesian hierarchical analysis
Suzan L Carmichael, John S Witte, Gary M Shaw
Genetic Epidemiology
|
July 19, 2012
Joint association testing of common and rare genetic variants using hierarchical modeling
Niall J Cardin, Joel A Mefford, John S Witte
Human Heredity
|
November 14, 2003
Haplotype tagging single nucleotide polymorphisms and association studies
Deborah Thompson, Dan Stram, David Goldgar, et al.
Statistics in Medicine
|
July 12, 2002
Analysis of mutational spectra: locating hotspots and clusters of mutations using recursive segmentation
Bonnie A Fijal, Ramana M Idury, John S Witte
Page
of 26