Author Search Results

1

Using XHMM software to detect copy number variation in whole-exome sequencing data by Fromer, Menachem, Purcell, Shaun M.

Published 2014

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Sleep and Big Data: harnessing data, technology, and analytics for monitoring sleep and improving diagnostics, prediction, and interventions—an era for Sleep-Omics? by Redline, Susan, Purcell, Shaun M

Published 2021

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Family-based genetic risk prediction of multifactorial disease by Ruderfer, Douglas M, Korn, Joshua, Purcell, Shaun M

Published 2010

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Synthetic Associations Created by Rare Variants Do Not Explain Most GWAS Results by Wray, Naomi R., Purcell, Shaun M., Visscher, Peter M.

Published 2011

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Reduced sleep spindles in schizophrenia: A treatable endophenotype that links risk genes to impaired cognition? by Manoach, Dara S., Pan, Jen Q., Purcell, Shaun M., Stickgold, Robert

Published 2015

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INRICH: interval-based enrichment analysis for genome-wide association studies by Lee, Phil H., O'Dushlaine, Colm, Thomas, Brett, Purcell, Shaun M.

Published 2012

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Pleiotropy in complex traits: challenges and strategies by Solovieff, Nadia, Cotsapas, Chris, Lee, Phil H., Purcell, Shaun M., Smoller, Jordan W.

Published 2013

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8

Second-generation PLINK: rising to the challenge of larger and richer datasets by Chang, Christopher C, Chow, Carson C, Tellier, Laurent CAM, Vattikuti, Shashaank, Purcell, Shaun M, Lee, James J

Published 2015

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Protocol for investigating genetic determinants of posttraumatic stress disorder in women from the Nurses' Health Study II by Koenen, Karestan C, DeVivo, Immaculata, Rich-Edwards, Janet, Smoller, Jordan W, Wright, Rosalind J, Purcell, Shaun M

Published 2009

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STATISTICS FOR X-CHROMOSOME ASSOCIATIONS by Özbek, Umut, Lin, Hui-Min, Lin, Yan, Weeks, Daniel E., Chen, Wei, Shaffer, John R., Purcell, Shaun M., Feingold, Eleanor

Published 2018

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11

Modifiers and Subtype-Specific Analyses in Whole-Genome Association Studies: A Likelihood Framework by Lee, Phil H., Bergen, Sarah E., Perlis, Roy H., Sullivan, Patrick F., Sklar, Pamela, Smoller, Jordan W., Purcell, Shaun M.

Published 2011

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Pooled Association Tests for Rare Variants in Exon-Resequencing Studies by Price, Alkes L., Kryukov, Gregory V., de Bakker, Paul I.W., Purcell, Shaun M., Staples, Jeff, Wei, Lee-Jen, Sunyaev, Shamil R.

Published 2010

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Pooled Association Tests for Rare Variants in Exon-Resequencing Studies by Price, Alkes L., Kryukov, Gregory V., de Bakker, Paul I.W., Purcell, Shaun M., Staples, Jeff, Wei, Lee-Jen, Sunyaev, Shamil R.

Published 2010

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14

A family-based study of common polygenic variation and risk of schizophrenia by Ruderfer, Douglas M, Kirov, George, Chambert, Kimberly, Moran, Jennifer L, Owen, Michael J, O’Donovan, Michael C, Sklar, Pamela, Purcell, Shaun M

Published 2011

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15

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

Published 2009

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16

Testing for an Unusual Distribution of Rare Variants by 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.

Published 2011

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17

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

Published 2016

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18

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

Published 2020

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19

Identifying Relationships among Genomic Disease Regions: Predicting Genes at Pathogenic SNP Associations and Rare Deletions by Raychaudhuri, Soumya, Plenge, Robert M., Rossin, Elizabeth J., Ng, Aylwin C. Y., Purcell, Shaun M., Sklar, Pamela, Scolnick, Edward M., Xavier, Ramnik J., Altshuler, David, Daly, Mark J.

Published 2009

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20

Genetic modifiers and subtypes in schizophrenia: Investigations of age at onset, severity, sex and family history by Bergen, Sarah E., O’Dushlaine, Colm T., Lee, Phil H., Fanous, Ayman H., Ruderfer, Douglas M., Ripke, Stephan, Sullivan, Patrick F., Smoller, Jordan W., Purcell, Shaun M., Corvin, Aiden

Published 2014

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Search Results - Purcell, Shaun M.

Using XHMM software to detect copy number variation in whole-exome sequencing data by Fromer, Menachem, Purcell, Shaun M.

Sleep and Big Data: harnessing data, technology, and analytics for monitoring sleep and improving diagnostics, prediction, and interventions—an era for Sleep-Omics? by Redline, Susan, Purcell, Shaun M

Family-based genetic risk prediction of multifactorial disease by Ruderfer, Douglas M, Korn, Joshua, Purcell, Shaun M

Synthetic Associations Created by Rare Variants Do Not Explain Most GWAS Results by Wray, Naomi R., Purcell, Shaun M., Visscher, Peter M.

Reduced sleep spindles in schizophrenia: A treatable endophenotype that links risk genes to impaired cognition? by Manoach, Dara S., Pan, Jen Q., Purcell, Shaun M., Stickgold, Robert

INRICH: interval-based enrichment analysis for genome-wide association studies by Lee, Phil H., O'Dushlaine, Colm, Thomas, Brett, Purcell, Shaun M.

Pleiotropy in complex traits: challenges and strategies by Solovieff, Nadia, Cotsapas, Chris, Lee, Phil H., Purcell, Shaun M., Smoller, Jordan W.

Second-generation PLINK: rising to the challenge of larger and richer datasets by Chang, Christopher C, Chow, Carson C, Tellier, Laurent CAM, Vattikuti, Shashaank, Purcell, Shaun M, Lee, James J

Protocol for investigating genetic determinants of posttraumatic stress disorder in women from the Nurses' Health Study II by Koenen, Karestan C, DeVivo, Immaculata, Rich-Edwards, Janet, Smoller, Jordan W, Wright, Rosalind J, Purcell, Shaun M

STATISTICS FOR X-CHROMOSOME ASSOCIATIONS by Özbek, Umut, Lin, Hui-Min, Lin, Yan, Weeks, Daniel E., Chen, Wei, Shaffer, John R., Purcell, Shaun M., Feingold, Eleanor

Modifiers and Subtype-Specific Analyses in Whole-Genome Association Studies: A Likelihood Framework by Lee, Phil H., Bergen, Sarah E., Perlis, Roy H., Sullivan, Patrick F., Sklar, Pamela, Smoller, Jordan W., Purcell, Shaun M.

Pooled Association Tests for Rare Variants in Exon-Resequencing Studies by Price, Alkes L., Kryukov, Gregory V., de Bakker, Paul I.W., Purcell, Shaun M., Staples, Jeff, Wei, Lee-Jen, Sunyaev, Shamil R.

Pooled Association Tests for Rare Variants in Exon-Resequencing Studies by Price, Alkes L., Kryukov, Gregory V., de Bakker, Paul I.W., Purcell, Shaun M., Staples, Jeff, Wei, Lee-Jen, Sunyaev, Shamil R.

A family-based study of common polygenic variation and risk of schizophrenia by Ruderfer, Douglas M, Kirov, George, Chambert, Kimberly, Moran, Jennifer L, Owen, Michael J, O’Donovan, Michael C, Sklar, Pamela, Purcell, Shaun M

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

Testing for an Unusual Distribution of Rare Variants by 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.

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

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

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