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

по Fromer, Menachem, Purcell, Shaun M.
Опубликовано 2014

Family-based genetic risk prediction of multifactorial disease

по Ruderfer, Douglas M, Korn, Joshua, Purcell, Shaun M
Опубликовано 2010

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

по Wray, Naomi R., Purcell, Shaun M., Visscher, Peter M.
Опубликовано 2011

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

по Manoach, Dara S., Pan, Jen Q., Purcell, Shaun M., Stickgold, Robert
Опубликовано в: Biol Psychiatry (2015)

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

по Lee, Phil H., O'Dushlaine, Colm, Thomas, Brett, Purcell, Shaun M.
Опубликовано 2012

Pleiotropy in complex traits: challenges and strategies

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

The Relationship between Sleep Quality and Neurocognition in Bipolar Disorder

по Russo, Manuela, Mahon, Katie, Shanahan, Megan, Ramjas, Elizabeth, Solon, Carly, Purcell, Shaun M, Burdick, Katherine E
Опубликовано в: J Affect Disord (2015)

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

по Chang, Christopher C, Chow, Carson C, Tellier, Laurent CAM, Vattikuti, Shashaank, Purcell, Shaun M, Lee, James J
Опубликовано в: Gigascience (2015)

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

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

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

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

STATISTICS FOR X-CHROMOSOME ASSOCIATIONS

по Özbek, Umut, Lin, Hui-Min, Lin, Yan, Weeks, Daniel E., Chen, Wei, Shaffer, John R., Purcell, Shaun M., Feingold, Eleanor
Опубликовано в: Genet Epidemiol (2018)

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

по Lee, Phil H., Bergen, Sarah E., Perlis, Roy H., Sullivan, Patrick F., Sklar, Pamela, Smoller, Jordan W., Purcell, Shaun M.
Опубликовано в: Hum Hered (2011)

Pooled Association Tests for Rare Variants in Exon-Resequencing Studies

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

Pooled Association Tests for Rare Variants in Exon-Resequencing Studies

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

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

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

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

по 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
Опубликовано 2009

Testing for an Unusual Distribution of Rare Variants

по 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.
Опубликовано 2011

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

по 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
Опубликовано в: Eur J Hum Genet (2015)

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

по 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.
Опубликовано в: Nat Genet (2016)

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

по 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.
Опубликовано в: Nat Commun (2020)