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

di Fromer, Menachem, Purcell, Shaun M.
Pubblicazione 2014

Family-based genetic risk prediction of multifactorial disease

di Ruderfer, Douglas M, Korn, Joshua, Purcell, Shaun M
Pubblicazione 2010

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

di Wray, Naomi R., Purcell, Shaun M., Visscher, Peter M.
Pubblicazione 2011

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

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

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

di Lee, Phil H., O'Dushlaine, Colm, Thomas, Brett, Purcell, Shaun M.
Pubblicazione 2012

Pleiotropy in complex traits: challenges and strategies

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

The Relationship between Sleep Quality and Neurocognition in Bipolar Disorder

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

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

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

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

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

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

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

STATISTICS FOR X-CHROMOSOME ASSOCIATIONS

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

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

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

Pooled Association Tests for Rare Variants in Exon-Resequencing Studies

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

Pooled Association Tests for Rare Variants in Exon-Resequencing Studies

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

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

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

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

di 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
Pubblicazione 2009

Testing for an Unusual Distribution of Rare Variants

di 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.
Pubblicazione 2011

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

di 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
Pubblicato in Eur J Hum Genet (2015)

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

di 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.
Pubblicato in Nat Genet (2016)

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

di 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.
Pubblicato in Nat Commun (2020)