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

Por Stewart, William C. L., Cerise, Jane
Publicado em 2013

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

Por Wang, Meng, Stewart, William C. L.
Publicado no Front Genet (2017)

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

Por Greenberg, David A., Stewart, William C. L.
Publicado em 2012

Obtaining Accurate P-values from a Dense SNP Linkage Scan

Por Stewart, William C. L., Subaran, Ryan L.
Publicado em 2012

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

Por Stewart, William C.L., Peljto, Anna L., Greenberg, David A.
Publicado em 2010

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

Por Stewart, William C L, Drill, Esther N, Greenberg, David A
Publicado em 2011

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

Por Subaran, Ryan L, Conte, Juliette M, Stewart, William C L, Greenberg, David A
Publicado no Epilepsia (2015)

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

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

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

Por 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
Publicado em 2007