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Genomics
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January 10, 2013
Pathway-based genetic analysis of preterm birth
Alper Uzun, Andrew T Dewan, Sorin Istrail, et al.
Molecular Human Reproduction
|
November 28, 2012
Association between the SERPINE1 (PAI-1) 4G/5G insertion/deletion promoter polymorphism (rs1799889) and pre-eclampsia: a systematic review and meta-analysis
Linlu Zhao, Michael B Bracken, Andrew T Dewan, et al.
Bioinformatics (Oxford, England)
|
July 23, 2018
MendelProb: probability and sample size calculations for Mendelian studies of exome and whole genome sequence data
Zongxiao He, Lu Wang, Andrew T DeWan, et al.
BMC Infectious Diseases
|
June 23, 2018
Identification of genetic variants associated with dengue or West Nile virus disease: a systematic review and meta-analysis
Megan E Cahill, Samantha Conley, Andrew T DeWan, et al.
Human Molecular Genetics
|
June 1, 2026
Identification of multi-omic pleiotropy factors for peripheral artery disease
Jiaqi Hu, Cassius I Ochoa Chaar, Hongyu Zhao, et al.
BMC Genomics
|
March 6, 2025
The case-only design is a powerful approach to detect interactions but should be used with caution
Rui Dong, Gao T Wang, Andrew T DeWan, et al.
Briefings in Bioinformatics
|
July 9, 2024
LDER-GE estimates phenotypic variance component of gene-environment interactions in human complex traits accurately with GE interaction summary statistics and full LD information
Zihan Dong, Wei Jiang, Hongyu Li, et al.
Environmental Epidemiology (Philadelphia, Pa.)
|
November 7, 2025
The role of cardiovascular disease as a mediator in mitigating the impact of ambient PM<sub>2.5</sub> on dementia risk
Chengyi Lin, Yechi Zhang, Andrew T DeWan, et al.
Vaccines
|
December 11, 2020
In-Depth Analysis of Genetic Variation Associated with Severe West Nile Viral Disease
Megan E Cahill, Mark Loeb, Andrew T Dewan, et al.
BMC Proceedings
|
March 1, 2012
Disease risk prediction with rare and common variants
Chengqing Wu, Kyle M Walsh, Andrew T Dewan, et al.
Page
of 10
Search research articles
Search
Showing results (21-30 of 97) with videos related to
Sort By:
Page
of 10
Genomics
|
January 10, 2013
Pathway-based genetic analysis of preterm birth
Alper Uzun, Andrew T Dewan, Sorin Istrail, et al.
Molecular Human Reproduction
|
November 28, 2012
Association between the SERPINE1 (PAI-1) 4G/5G insertion/deletion promoter polymorphism (rs1799889) and pre-eclampsia: a systematic review and meta-analysis
Linlu Zhao, Michael B Bracken, Andrew T Dewan, et al.
Bioinformatics (Oxford, England)
|
July 23, 2018
MendelProb: probability and sample size calculations for Mendelian studies of exome and whole genome sequence data
Zongxiao He, Lu Wang, Andrew T DeWan, et al.
BMC Infectious Diseases
|
June 23, 2018
Identification of genetic variants associated with dengue or West Nile virus disease: a systematic review and meta-analysis
Megan E Cahill, Samantha Conley, Andrew T DeWan, et al.
Human Molecular Genetics
|
June 1, 2026
Identification of multi-omic pleiotropy factors for peripheral artery disease
Jiaqi Hu, Cassius I Ochoa Chaar, Hongyu Zhao, et al.
BMC Genomics
|
March 6, 2025
The case-only design is a powerful approach to detect interactions but should be used with caution
Rui Dong, Gao T Wang, Andrew T DeWan, et al.
Briefings in Bioinformatics
|
July 9, 2024
LDER-GE estimates phenotypic variance component of gene-environment interactions in human complex traits accurately with GE interaction summary statistics and full LD information
Zihan Dong, Wei Jiang, Hongyu Li, et al.
Environmental Epidemiology (Philadelphia, Pa.)
|
November 7, 2025
The role of cardiovascular disease as a mediator in mitigating the impact of ambient PM<sub>2.5</sub> on dementia risk
Chengyi Lin, Yechi Zhang, Andrew T DeWan, et al.
Vaccines
|
December 11, 2020
In-Depth Analysis of Genetic Variation Associated with Severe West Nile Viral Disease
Megan E Cahill, Mark Loeb, Andrew T Dewan, et al.
BMC Proceedings
|
March 1, 2012
Disease risk prediction with rare and common variants
Chengqing Wu, Kyle M Walsh, Andrew T Dewan, et al.
Page
of 10