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

door Stewart, William C. L., Cerise, Jane
Gepubliceerd in 2013

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

door Wang, Meng, Stewart, William C. L.
Gepubliceerd in Front Genet (2017)

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

door Greenberg, David A., Stewart, William C. L.
Gepubliceerd in 2012

Obtaining Accurate P-values from a Dense SNP Linkage Scan

door Stewart, William C. L., Subaran, Ryan L.
Gepubliceerd in 2012

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

door Stewart, William C.L., Peljto, Anna L., Greenberg, David A.
Gepubliceerd in 2010

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

door Stewart, William C L, Drill, Esther N, Greenberg, David A
Gepubliceerd in 2011

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

door Vieland, Veronica J., Seok, Sang-Cheol, Stewart, William C. L.
Gepubliceerd in PLoS One (2020)

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

door Zhou, Xiaofei, Wang, Meng, Zhang, Han, Stewart, William C. L., Lin, Shili
Gepubliceerd in BMC Proc (2018)

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

door Subaran, Ryan L, Conte, Juliette M, Stewart, William C L, Greenberg, David A
Gepubliceerd in Epilepsia (2015)

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

door Pathak, Shilpa, Miller, James, Morris, Emily C, Stewart, William C L, Greenberg, David A
Gepubliceerd in Epilepsia (2018)

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

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

Brd2 haploinsufficiency extends lifespan and healthspan in C57B6/J mice

door Pathak, Shilpa, Stewart, William C. L., Burd, Christin E., Hester, Mark E., Greenberg, David A.
Gepubliceerd in PLoS One (2020)

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

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

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

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

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

door 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
Gepubliceerd in J R Soc Interface (2019)

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

door 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
Gepubliceerd in 2007