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BMC Proceedings
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December 17, 2016
Comparison of parametric and machine methods for variable selection in simulated Genetic Analysis Workshop 19 data
Emily R Holzinger, Silke Szymczak, James Malley, et al.
European Journal of Human Genetics : EJHG
|
September 6, 2012
Genetic heterogeneity in Finnish hereditary prostate cancer using ordered subset analysis
Claire L Simpson, Cheryl D Cropp, Tiina Wahlfors, et al.
BMC Proceedings
|
March 1, 2012
Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression
Heejong Sung, Yoonhee Kim, Juanliang Cai, et al.
BMC Proceedings
|
March 1, 2012
Performance of random forests and logic regression methods using mini-exome sequence data
Yoonhee Kim, Qing Li, Cheryl D Cropp, et al.
The Oncologist
|
March 3, 2012
Racial disparities in the association between variants on 8q24 and prostate cancer: a systematic review and meta-analysis
Sarah M Troutman, Tristan M Sissung, Cheryl D Cropp, et al.
Molecular Pharmaceutics
|
December 28, 2012
Gene expression profiling of transporters in the solute carrier and ATP-binding cassette superfamilies in human eye substructures
Amber Dahlin, Ethan Geier, Sophie L Stocker, et al.
Clinical and Translational Science
|
August 25, 2021
Efficacy of personal pharmacogenomic testing as an educational tool in the pharmacy curriculum: A nonblinded, randomized controlled trial
Chloe Grace, Marti M Larriva, Heidi E Steiner, et al.
The American Journal of Clinical Nutrition
|
October 20, 2018
The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population
Barry Shane, Faith Pangilinan, James L Mills, et al.
International Journal of Cancer
|
January 6, 2011
Genome-wide linkage scan for prostate cancer susceptibility in Finland: evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21-q22
Cheryl D Cropp, Claire L Simpson, Tiina Wahlfors, et al.
Human Molecular Genetics
|
October 18, 2017
The FUT2 secretor variant p.Trp154Ter influences serum vitamin B12 concentration via holo-haptocorrin, but not holo-transcobalamin, and is associated with haptocorrin glycosylation
Aneliya Velkova, Jennifer E L Diaz, Faith Pangilinan, et al.
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of 4
Search research articles
Search
Showing results (11-20 of 32) with videos related to
Sort By:
Page
of 4
BMC Proceedings
|
December 17, 2016
Comparison of parametric and machine methods for variable selection in simulated Genetic Analysis Workshop 19 data
Emily R Holzinger, Silke Szymczak, James Malley, et al.
European Journal of Human Genetics : EJHG
|
September 6, 2012
Genetic heterogeneity in Finnish hereditary prostate cancer using ordered subset analysis
Claire L Simpson, Cheryl D Cropp, Tiina Wahlfors, et al.
BMC Proceedings
|
March 1, 2012
Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression
Heejong Sung, Yoonhee Kim, Juanliang Cai, et al.
BMC Proceedings
|
March 1, 2012
Performance of random forests and logic regression methods using mini-exome sequence data
Yoonhee Kim, Qing Li, Cheryl D Cropp, et al.
The Oncologist
|
March 3, 2012
Racial disparities in the association between variants on 8q24 and prostate cancer: a systematic review and meta-analysis
Sarah M Troutman, Tristan M Sissung, Cheryl D Cropp, et al.
Molecular Pharmaceutics
|
December 28, 2012
Gene expression profiling of transporters in the solute carrier and ATP-binding cassette superfamilies in human eye substructures
Amber Dahlin, Ethan Geier, Sophie L Stocker, et al.
Clinical and Translational Science
|
August 25, 2021
Efficacy of personal pharmacogenomic testing as an educational tool in the pharmacy curriculum: A nonblinded, randomized controlled trial
Chloe Grace, Marti M Larriva, Heidi E Steiner, et al.
The American Journal of Clinical Nutrition
|
October 20, 2018
The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population
Barry Shane, Faith Pangilinan, James L Mills, et al.
International Journal of Cancer
|
January 6, 2011
Genome-wide linkage scan for prostate cancer susceptibility in Finland: evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21-q22
Cheryl D Cropp, Claire L Simpson, Tiina Wahlfors, et al.
Human Molecular Genetics
|
October 18, 2017
The FUT2 secretor variant p.Trp154Ter influences serum vitamin B12 concentration via holo-haptocorrin, but not holo-transcobalamin, and is associated with haptocorrin glycosylation
Aneliya Velkova, Jennifer E L Diaz, Faith Pangilinan, et al.
Page
of 4