Increasing the power of association studies with affected families, unrelated cases and controls

ανά Stewart, William C. L., Cerise, Jane
Έκδοση 2013

A Pragmatic Test for Detecting Association between a Dichotomous Trait and the Genotypes of Affected Families, Controls and Independent Cases

ανά Wang, Meng, Stewart, William C. L.
Τόπος έκδοσης Front Genet (2017)

How should we be searching for genes for common epilepsy? A critique and a prescription

ανά Greenberg, David A., Stewart, William C. L.
Έκδοση 2012

Obtaining Accurate P-values from a Dense SNP Linkage Scan

ανά Stewart, William C. L., Subaran, Ryan L.
Έκδοση 2012

Multiple Subsampling of Dense SNP Data Localizes Disease Genes with Increased Precision

ανά Stewart, William C.L., Peljto, Anna L., Greenberg, David A.
Έκδοση 2010

Finding disease genes: a fast and flexible approach for analyzing high-throughput data

ανά Stewart, William C L, Drill, Esther N, Greenberg, David A
Έκδοση 2011

A new linear regression-like residual for survival analysis, with application to genome wide association studies of time-to-event data

ανά Vieland, Veronica J., Seok, Sang-Cheol, Stewart, William C. L.
Τόπος έκδοσης PLoS One (2020)

Logistic Bayesian LASSO for detecting association combining family and case-control data

ανά Zhou, Xiaofei, Wang, Meng, Zhang, Han, Stewart, William C. L., Lin, Shili
Τόπος έκδοσης BMC Proc (2018)

Pathogenic EFHC1 mutations are tolerated in healthy individuals dependent on reported ancestry

ανά Subaran, Ryan L, Conte, Juliette M, Stewart, William C L, Greenberg, David A
Τόπος έκδοσης Epilepsia (2015)

DNA methylation of the BRD2 promoter is associated with Juvenile Myoclonic Epilepsy in Caucasians

ανά Pathak, Shilpa, Miller, James, Morris, Emily C, Stewart, William C L, Greenberg, David A
Τόπος έκδοσης Epilepsia (2018)

Mutations in bacterial genes induce unanticipated changes in the relationship between bacterial pathogens in experimental otitis media

ανά Lakhani, Vinal, Tan, Li, Mukherjee, Sayak, Stewart, William C. L., Swords, W. Edward, Das, Jayajit
Τόπος έκδοσης R Soc Open Sci (2018)

Brd2 haploinsufficiency extends lifespan and healthspan in C57B6/J mice

ανά Pathak, Shilpa, Stewart, William C. L., Burd, Christin E., Hester, Mark E., Greenberg, David A.
Τόπος έκδοσης PLoS One (2020)

Prediction of Short-Term Neonatal Complications in Preterm Infants Using Exome-Wide Genetic Variation and Gestational Age: A Pilot Study

ανά Stewart, William C L., Gnona, Komla M., White, Peter, Kelly, Ben, Klebanoff, Mark, Buhimschi, Irina A., Nelin, Leif D.
Τόπος έκδοσης Pediatr Res (2020)

Novel loci interacting epistatically with Bone Morphogenetic Protein Receptor 2 cause familial pulmonary arterial hypertension

ανά Rodriguez-Murillo, Laura, Subaran, Ryan, Stewart, William C. L., Pramanik, Sreemanta, Marathe, Sudhir, Barst, Robyn J., Chung, Wendy K., Greenberg, David A.
Έκδοση 2009

Mathematical modelling identifies the role of adaptive immunity as a key controller of respiratory syncytial virus in cotton rats

ανά Wethington, Darren, Harder, Olivia, Uppulury, Karthik, Stewart, William C. L., Chen, Phylip, King, Tiffany, Reynolds, Susan D., Perelson, Alan S., Peeples, Mark E., Niewiesk, Stefan, Das, Jayajit
Τόπος έκδοσης J R Soc Interface (2019)

A second-generation combined linkage–physical map of the human genome

ανά Matise, Tara C., Chen, Fang, Chen, Wenwei, De La Vega, Francisco M., Hansen, Mark, He, Chunsheng, Hyland, Fiona C.L., Kennedy, Giulia C., Kong, Xiangyang, Murray, Sarah S., Ziegle, Janet S., Stewart, William C.L., Buyske, Steven
Έκδοση 2007