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

Por Fromer, Menachem, Purcell, Shaun M.
Publicado em 2014

Family-based genetic risk prediction of multifactorial disease

Por Ruderfer, Douglas M, Korn, Joshua, Purcell, Shaun M
Publicado em 2010

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

Por Wray, Naomi R., Purcell, Shaun M., Visscher, Peter M.
Publicado em 2011

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

Por Manoach, Dara S., Pan, Jen Q., Purcell, Shaun M., Stickgold, Robert
Publicado no Biol Psychiatry (2015)

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

Por Lee, Phil H., O'Dushlaine, Colm, Thomas, Brett, Purcell, Shaun M.
Publicado em 2012

Pleiotropy in complex traits: challenges and strategies

Por Solovieff, Nadia, Cotsapas, Chris, Lee, Phil H., Purcell, Shaun M., Smoller, Jordan W.
Publicado em 2013

The Relationship between Sleep Quality and Neurocognition in Bipolar Disorder

Por Russo, Manuela, Mahon, Katie, Shanahan, Megan, Ramjas, Elizabeth, Solon, Carly, Purcell, Shaun M, Burdick, Katherine E
Publicado no J Affect Disord (2015)

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

Por Chang, Christopher C, Chow, Carson C, Tellier, Laurent CAM, Vattikuti, Shashaank, Purcell, Shaun M, Lee, James J
Publicado no Gigascience (2015)

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

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

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

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

STATISTICS FOR X-CHROMOSOME ASSOCIATIONS

Por Özbek, Umut, Lin, Hui-Min, Lin, Yan, Weeks, Daniel E., Chen, Wei, Shaffer, John R., Purcell, Shaun M., Feingold, Eleanor
Publicado no Genet Epidemiol (2018)

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

Por Lee, Phil H., Bergen, Sarah E., Perlis, Roy H., Sullivan, Patrick F., Sklar, Pamela, Smoller, Jordan W., Purcell, Shaun M.
Publicado no Hum Hered (2011)

Pooled Association Tests for Rare Variants in Exon-Resequencing Studies

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

Pooled Association Tests for Rare Variants in Exon-Resequencing Studies

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

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

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

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

Por 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
Publicado em 2009

Testing for an Unusual Distribution of Rare Variants

Por 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.
Publicado em 2011

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

Por 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
Publicado no Eur J Hum Genet (2015)

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

Por 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.
Publicado no Nat Genet (2016)

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

Por 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.
Publicado no Nat Commun (2020)