Using XHMM software to detect copy number variation in whole-exome sequencing data

le Fromer, Menachem, Purcell, Shaun M.
Foilsithe 2014

Family-based genetic risk prediction of multifactorial disease

le Ruderfer, Douglas M, Korn, Joshua, Purcell, Shaun M
Foilsithe 2010

Synthetic Associations Created by Rare Variants Do Not Explain Most GWAS Results

le Wray, Naomi R., Purcell, Shaun M., Visscher, Peter M.
Foilsithe 2011

Reduced sleep spindles in schizophrenia: A treatable endophenotype that links risk genes to impaired cognition?

le Manoach, Dara S., Pan, Jen Q., Purcell, Shaun M., Stickgold, Robert
Foilsithe in Biol Psychiatry (2015)

INRICH: interval-based enrichment analysis for genome-wide association studies

le Lee, Phil H., O'Dushlaine, Colm, Thomas, Brett, Purcell, Shaun M.
Foilsithe 2012

Pleiotropy in complex traits: challenges and strategies

le Solovieff, Nadia, Cotsapas, Chris, Lee, Phil H., Purcell, Shaun M., Smoller, Jordan W.
Foilsithe 2013

The Relationship between Sleep Quality and Neurocognition in Bipolar Disorder

le Russo, Manuela, Mahon, Katie, Shanahan, Megan, Ramjas, Elizabeth, Solon, Carly, Purcell, Shaun M, Burdick, Katherine E
Foilsithe in J Affect Disord (2015)

Second-generation PLINK: rising to the challenge of larger and richer datasets

le Chang, Christopher C, Chow, Carson C, Tellier, Laurent CAM, Vattikuti, Shashaank, Purcell, Shaun M, Lee, James J
Foilsithe in Gigascience (2015)

Protocol for investigating genetic determinants of posttraumatic stress disorder in women from the Nurses' Health Study II

le Smoller Jordan W, Rich-Edwards Janet, DeVivo Immaculata, Koenen Karestan C, Wright Rosalind J, Purcell Shaun M
Foilsithe 2009-05-01

Protocol for investigating genetic determinants of posttraumatic stress disorder in women from the Nurses' Health Study II

le Koenen, Karestan C, DeVivo, Immaculata, Rich-Edwards, Janet, Smoller, Jordan W, Wright, Rosalind J, Purcell, Shaun M
Foilsithe 2009

STATISTICS FOR X-CHROMOSOME ASSOCIATIONS

le Özbek, Umut, Lin, Hui-Min, Lin, Yan, Weeks, Daniel E., Chen, Wei, Shaffer, John R., Purcell, Shaun M., Feingold, Eleanor
Foilsithe in Genet Epidemiol (2018)

Modifiers and Subtype-Specific Analyses in Whole-Genome Association Studies: A Likelihood Framework

le Lee, Phil H., Bergen, Sarah E., Perlis, Roy H., Sullivan, Patrick F., Sklar, Pamela, Smoller, Jordan W., Purcell, Shaun M.
Foilsithe in Hum Hered (2011)

Pooled Association Tests for Rare Variants in Exon-Resequencing Studies

le Price, Alkes L., Kryukov, Gregory V., de Bakker, Paul I.W., Purcell, Shaun M., Staples, Jeff, Wei, Lee-Jen, Sunyaev, Shamil R.
Foilsithe 2010

Pooled Association Tests for Rare Variants in Exon-Resequencing Studies

le Price, Alkes L., Kryukov, Gregory V., de Bakker, Paul I.W., Purcell, Shaun M., Staples, Jeff, Wei, Lee-Jen, Sunyaev, Shamil R.
Foilsithe 2010

A family-based study of common polygenic variation and risk of schizophrenia

le Ruderfer, Douglas M, Kirov, George, Chambert, Kimberly, Moran, Jennifer L, Owen, Michael J, O’Donovan, Michael C, Sklar, Pamela, Purcell, Shaun M
Foilsithe 2011

Gene Ontology Analysis of GWA Study Data Sets Provides Insights into the Biology of Bipolar Disorder

le Holmans, Peter, Green, Elaine K., Pahwa, Jaspreet Singh, Ferreira, Manuel A.R., Purcell, Shaun M., Sklar, Pamela, Owen, Michael J., O'Donovan, Michael C., Craddock, Nick
Foilsithe 2009

Testing for an Unusual Distribution of Rare Variants

le Neale, Benjamin M., Rivas, Manuel A., Voight, Benjamin F., Altshuler, David, Devlin, Bernie, Orho-Melander, Marju, Kathiresan, Sekar, Purcell, Shaun M., Roeder, Kathryn, Daly, Mark J.
Foilsithe 2011

No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia

le Ruderfer, Douglas M, Lim, Elaine T, Genovese, Giulio, Moran, Jennifer L, Hultman, Christina M, Sullivan, Patrick F, McCarroll, Steven A, Holmans, Peter, Sklar, Pamela, Purcell, Shaun M
Foilsithe in Eur J Hum Genet (2015)

Patterns of genic intolerance of rare copy number variation in 59,898 human exomes

le Ruderfer, Douglas M., Hamamsy, Tymor, Lek, Monkol, Karczewski, Konrad J., Kavanagh, David, Samocha, Kaitlin E., Daly, Mark J., MacArthur, Daniel G., Fromer, Menachem, Purcell, Shaun M.
Foilsithe in Nat Genet (2016)

mTADA is a framework for identifying risk genes from de novo mutations in multiple traits

le Nguyen, Tan-Hoang, Dobbyn, Amanda, Brown, Ruth C., Riley, Brien P., Buxbaum, Joseph D., Pinto, Dalila, Purcell, Shaun M., Sullivan, Patrick F., He, Xin, Stahl, Eli A.
Foilsithe in Nat Commun (2020)