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Bioinformatics (Oxford, England)|February 20, 2013
PleioGRiP: genetic risk prediction with pleiotropyStephen W Hartley, Paola SebastianiFrontiers in Genetics|September 14, 2012
Bayesian methods for multivariate modeling of pleiotropic SNP associations and genetic risk predictionStephen W Hartley, Stefano Monti, Ching-Ti Liu, et al.BMC Genetics|December 15, 2010
Clustering by genetic ancestry using genome-wide SNP dataNadia Solovieff, Stephen W Hartley, Clinton T Baldwin, et al.BMC Genetics|December 17, 2008
Imputation of missing genotypes: an empirical evaluation of IMPUTEZhenming Zhao, Nadia Timofeev, Stephen W Hartley, et al.Biorxiv : the Preprint Server for Biology|December 4, 2023
A Simple Strategy for Identifying Conserved Features across Non-independent Omics StudiesEric Reed, Paola SebastianiAmerican Journal of Hematology|May 30, 2012
Genetic modifiers of sickle cell diseaseMartin H Steinberg, Paola SebastianiFrontiers in Genetics|August 24, 2016
Detection of Significant Groups in Hierarchical Clustering by ResamplingPaola Sebastiani, Thomas T PerlsFrontiers in Genetics|December 11, 2012
The genetics of extreme longevity: lessons from the new England centenarian studyPaola Sebastiani, Thomas T PerlsBlood Cells, Molecules & Diseases|May 7, 2011
Ancestry of African Americans with sickle cell diseaseNadia Solovieff, Stephen W Hartley, Clinton T Baldwin, et al.American Journal of Hematology|January 26, 2011
Severe sickle cell anemia is associated with increased plasma levels of TNF-R1 and VCAM-1Daniel A Dworkis, Elizabeth S Klings, Nadia Solovieff, et al.Pageof 23