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Shannon K McDonnell

Showing results (1-10 of 116) with videos related to

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Genetic Epidemiology|February 12, 2019
Familial recurrence risk with varying amount of family historyDaniel J Schaid, Shannon K McDonnell, Stephen N Thibodeau
American Journal of Human Genetics|March 30, 2022
Polygenic risk for prostate cancer: Decreasing relative risk with age but little impact on absolute riskDaniel J Schaid, Jason P Sinnwell, Anthony Batzler, et al.
Genetic Epidemiology|May 8, 2013
Multiple genetic variant association testing by collapsing and kernel methods with pedigree or population structured dataDaniel J Schaid, Shannon K McDonnell, Jason P Sinnwell, et al.
Biorxiv : the Preprint Server for Biology|October 10, 2024
Fine Mapping Regulatory Variants by Characterizing Native CpG Methylation with Nanopore Long-Read SequencingYijun Tian, Shannon K McDonnell, Lang Wu, et al.
Human Genetics|July 12, 2013
Detecting genomic clustering of risk variants from sequence data: cases versus controlsDaniel J Schaid, Jason P Sinnwell, Shannon K McDonnell, et al.
HGG Advances|October 19, 2025
Fine mapping regulatory variants by characterizing native CpG methylation with nanopore long-read sequencingYijun Tian, Shannon K McDonnell, Lang Wu, et al.
American Journal of Human Genetics|October 22, 2002
Caution on pedigree haplotype inference with software that assumes linkage equilibriumDaniel J Schaid, Shannon K McDonnell, Liang Wang, et al.
Genetics|September 23, 2016
Incorporating Functional Annotations for Fine-Mapping Causal Variants in a Bayesian Framework Using Summary StatisticsWenan Chen, Shannon K McDonnell, Stephen N Thibodeau, et al.
American Journal of Human Genetics|March 24, 2005
Nonparametric tests of association of multiple genes with human diseaseDaniel J Schaid, Shannon K McDonnell, Scott J Hebbring, et al.
Genetic Epidemiology|December 30, 2009
Estimation of genotype relative risks from pedigree data by retrospective likelihoodsDaniel J Schaid, Shannon K McDonnell, Shaun M Riska, et al.
Pageof 12

Showing results (1-10 of 116) with videos related to

Sort By:
Pageof 12
Genetic Epidemiology|February 12, 2019
Familial recurrence risk with varying amount of family historyDaniel J Schaid, Shannon K McDonnell, Stephen N Thibodeau
American Journal of Human Genetics|March 30, 2022
Polygenic risk for prostate cancer: Decreasing relative risk with age but little impact on absolute riskDaniel J Schaid, Jason P Sinnwell, Anthony Batzler, et al.
Genetic Epidemiology|May 8, 2013
Multiple genetic variant association testing by collapsing and kernel methods with pedigree or population structured dataDaniel J Schaid, Shannon K McDonnell, Jason P Sinnwell, et al.
Biorxiv : the Preprint Server for Biology|October 10, 2024
Fine Mapping Regulatory Variants by Characterizing Native CpG Methylation with Nanopore Long-Read SequencingYijun Tian, Shannon K McDonnell, Lang Wu, et al.
Human Genetics|July 12, 2013
Detecting genomic clustering of risk variants from sequence data: cases versus controlsDaniel J Schaid, Jason P Sinnwell, Shannon K McDonnell, et al.
HGG Advances|October 19, 2025
Fine mapping regulatory variants by characterizing native CpG methylation with nanopore long-read sequencingYijun Tian, Shannon K McDonnell, Lang Wu, et al.
American Journal of Human Genetics|October 22, 2002
Caution on pedigree haplotype inference with software that assumes linkage equilibriumDaniel J Schaid, Shannon K McDonnell, Liang Wang, et al.
Genetics|September 23, 2016
Incorporating Functional Annotations for Fine-Mapping Causal Variants in a Bayesian Framework Using Summary StatisticsWenan Chen, Shannon K McDonnell, Stephen N Thibodeau, et al.
American Journal of Human Genetics|March 24, 2005
Nonparametric tests of association of multiple genes with human diseaseDaniel J Schaid, Shannon K McDonnell, Scott J Hebbring, et al.
Genetic Epidemiology|December 30, 2009
Estimation of genotype relative risks from pedigree data by retrospective likelihoodsDaniel J Schaid, Shannon K McDonnell, Shaun M Riska, et al.
Pageof 12