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

ανά Fromer, Menachem, Purcell, Shaun M.
Έκδοση 2014

Family-based genetic risk prediction of multifactorial disease

ανά Ruderfer, Douglas M, Korn, Joshua, Purcell, Shaun M
Έκδοση 2010

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

ανά Wray, Naomi R., Purcell, Shaun M., Visscher, Peter M.
Έκδοση 2011

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

ανά Manoach, Dara S., Pan, Jen Q., Purcell, Shaun M., Stickgold, Robert
Τόπος έκδοσης Biol Psychiatry (2015)

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

ανά Lee, Phil H., O'Dushlaine, Colm, Thomas, Brett, Purcell, Shaun M.
Έκδοση 2012

Pleiotropy in complex traits: challenges and strategies

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

The Relationship between Sleep Quality and Neurocognition in Bipolar Disorder

ανά Russo, Manuela, Mahon, Katie, Shanahan, Megan, Ramjas, Elizabeth, Solon, Carly, Purcell, Shaun M, Burdick, Katherine E
Τόπος έκδοσης J Affect Disord (2015)

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

ανά Chang, Christopher C, Chow, Carson C, Tellier, Laurent CAM, Vattikuti, Shashaank, Purcell, Shaun M, Lee, James J
Τόπος έκδοσης Gigascience (2015)

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

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

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

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

STATISTICS FOR X-CHROMOSOME ASSOCIATIONS

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

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

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

Pooled Association Tests for Rare Variants in Exon-Resequencing Studies

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

Pooled Association Tests for Rare Variants in Exon-Resequencing Studies

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

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

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

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

ανά 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
Έκδοση 2009

Testing for an Unusual Distribution of Rare Variants

ανά 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.
Έκδοση 2011

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

ανά 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
Τόπος έκδοσης Eur J Hum Genet (2015)

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

ανά 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.
Τόπος έκδοσης Nat Genet (2016)

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

ανά 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.
Τόπος έκδοσης Nat Commun (2020)