Works matching AU Purcell, Shaun M.


Results: 39
    1

    Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.

    Published in:
    Nature, 2009, v. 460, n. 7256, p. 748, doi. 10.1038/nature08185
    By:
    • Purcell, Shaun M.;
    • Wray, Naomi R.;
    • Stone, Jennifer L.;
    • Visscher, Peter M.;
    • O'Donovan, Michael C.;
    • Sullivan, Patrick F.;
    • Sklar, Pamela;
    • Purcell (Leader), Shaun M.;
    • Ruderfer, Douglas M.;
    • McQuillin, Andrew;
    • Morris, Derek W.;
    • O’Dushlaine, Colm T.;
    • Corvin, Aiden;
    • Holmans, Peter A.;
    • O’Donovan, Michael C.;
    • Macgregor, Stuart;
    • Gurling, Hugh;
    • Blackwood, Douglas H. R.;
    • Craddock, Nick J.;
    • Gill, Michael
    Publication type:
    Article
    2
    3

    Statistics for X‐chromosome associations.

    Published in:
    Genetic Epidemiology, 2018, v. 42, n. 6, p. 539, doi. 10.1002/gepi.22132
    By:
    • Özbek, Umut;
    • Lin, Hui‐Min;
    • Lin, Yan;
    • Weeks, Daniel E.;
    • Chen, Wei;
    • Shaffer, John R.;
    • Purcell, Shaun M.;
    • Feingold, Eleanor
    Publication type:
    Article
    4

    Genome-wide association analysis of composite sleep health scores in 413,904 individuals.

    Published in:
    Communications Biology, 2025, v. 8, n. 1, p. 1, doi. 10.1038/s42003-025-07514-0
    By:
    • Goodman, Matthew O.;
    • Faquih, Tariq;
    • Paz, Valentina;
    • Nagarajan, Pavithra;
    • Lane, Jacqueline M.;
    • Spitzer, Brian;
    • Maher, Matthew;
    • Chung, Joon;
    • Cade, Brian E.;
    • Purcell, Shaun M.;
    • Zhu, Xiaofeng;
    • Noordam, Raymond;
    • Phillips, Andrew J. K.;
    • Kyle, Simon D.;
    • Spiegelhalder, Kai;
    • Weedon, Michael N.;
    • Lawlor, Deborah A.;
    • Rotter, Jerome I.;
    • Taylor, Kent D.;
    • Isasi, Carmen R.
    Publication type:
    Article
    5
    6

    Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep.

    Published in:
    PLoS Genetics, 2019, v. 15, n. 4, p. 1, doi. 10.1371/journal.pgen.1007739
    By:
    • Lee, Jiwon;
    • Gleason, Kevin J.;
    • Gottlieb, Daniel J.;
    • Cade, Brian E.;
    • Purcell, Shaun M.;
    • Wang, Heming;
    • Saxena, Richa;
    • Redline, Susan;
    • Sofer, Tamar;
    • Below, Jennifer E.;
    • Cai, Jianwen;
    • Evans, Daniel S.;
    • Stone, Katie L.;
    • Tranah, Gregory J.;
    • Frazier-Wood, Alexis C.;
    • Gharib, Sina A.;
    • Hillman, David R.;
    • Lederer, David J.;
    • Loredo, Jose S.;
    • Mei, Hao
    Publication type:
    Article
    7

    Rare chromosomal deletions and duplications increase risk of schizophrenia.

    Published in:
    Nature, 2008, v. 455, n. 7210, p. 237, doi. 10.1038/nature07239
    By:
    • Stone, Jennifer L.;
    • O’Donovan, Michael C.;
    • Gurling, Hugh;
    • Kirov, George K.;
    • Blackwood, Douglas H. R.;
    • Corvin, Aiden;
    • Craddock, Nick J.;
    • Gill, Michael;
    • Hultman, Christina M.;
    • Lichtenstein, Paul;
    • McQuillin, Andrew;
    • Pato, Carlos N.;
    • Ruderfer, Douglas M.;
    • Owen, Michael J.;
    • St Clair, David;
    • Sullivan, Patrick F.;
    • Sklar, Pamela;
    • Purcell (Leader), Shaun M.;
    • Korn, Joshua;
    • Macgregor, Stuart
    Publication type:
    Article
    8
    9

    Mosaic copy number variation in schizophrenia.

    Published in:
    European Journal of Human Genetics, 2013, v. 21, n. 9, p. 1007, doi. 10.1038/ejhg.2012.287
    By:
    • Ruderfer, Douglas M;
    • Chambert, Kim;
    • Moran, Jennifer;
    • Talkowski, Michael;
    • Chen, Elizabeth S;
    • Gigek, Carolina;
    • Gusella, James F;
    • Blackwood, Douglas H;
    • Corvin, Aiden;
    • Gurling, Hugh M;
    • Hultman, Christina M;
    • Kirov, George;
    • Magnusson, Patrick;
    • O'Donovan, Michael C;
    • Owen, Michael J;
    • Pato, Carlos;
    • St Clair, David;
    • Sullivan, Patrick F;
    • Purcell, Shaun M;
    • Sklar, Pamela
    Publication type:
    Article
    10

    Exome sequencing and the genetic basis of complex traits.

    Published in:
    Nature Genetics, 2012, v. 44, n. 6, p. 623, doi. 10.1038/ng.2303
    By:
    • Kiezun, Adam;
    • Garimella, Kiran;
    • Do, Ron;
    • Stitziel, Nathan O;
    • Neale, Benjamin M;
    • McLaren, Paul J;
    • Gupta, Namrata;
    • Sklar, Pamela;
    • Sullivan, Patrick F;
    • Moran, Jennifer L;
    • Hultman, Christina M;
    • Lichtenstein, Paul;
    • Magnusson, Patrik;
    • Lehner, Thomas;
    • Shugart, Yin Yao;
    • Price, Alkes L;
    • de Bakker, Paul I W;
    • Purcell, Shaun M;
    • Sunyaev, Shamil R
    Publication type:
    Article
    11

    Extremely low-coverage sequencing and imputation increases power for genome-wide association studies.

    Published in:
    Nature Genetics, 2012, v. 44, n. 6, p. 631, doi. 10.1038/ng.2283
    By:
    • Pasaniuc, Bogdan;
    • Rohland, Nadin;
    • McLaren, Paul J;
    • Garimella, Kiran;
    • Zaitlen, Noah;
    • Li, Heng;
    • Gupta, Namrata;
    • Neale, Benjamin M;
    • Daly, Mark J;
    • Sklar, Pamela;
    • Sullivan, Patrick F;
    • Bergen, Sarah;
    • Moran, Jennifer L;
    • Hultman, Christina M;
    • Lichtenstein, Paul;
    • Magnusson, Patrik;
    • Purcell, Shaun M;
    • Haas, David W;
    • Liang, Liming;
    • Sunyaev, Shamil
    Publication type:
    Article
    12

    Testing for an Unusual Distribution of Rare Variants.

    Published in:
    PLoS Genetics, 2011, v. 7, n. 3, p. 1, doi. 10.1371/journal.pgen.1001322
    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.
    Publication type:
    Article
    13
    14
    15

    Exome Sequencing of Familial Bipolar Disorder.

    Published in:
    2016
    By:
    • Goes, Fernando S.;
    • Pirooznia, Mehdi;
    • Parla, Jennifer S.;
    • Kramer, Melissa;
    • Ghiban, Elena;
    • Mavruk, Senem;
    • Yun-Ching Chen;
    • Monson, Eric T.;
    • Willour, Virginia L.;
    • Karchin, Rachel;
    • Flickinger, Matthew;
    • Locke, Adam E.;
    • Levy, Shawn E.;
    • Scott, Laura J.;
    • Boehnke, Michael;
    • Stahl, Eli;
    • Moran, Jennifer L.;
    • Hultman, Christina M.;
    • Landén, Mikael;
    • Purcell, Shaun M.
    Publication type:
    journal article
    16

    Common Variants on Xq28 Conferring Risk of Schizophrenia in Han Chinese.

    Published in:
    2014
    By:
    • Wong, Emily H.M.;
    • So, Hon-Cheong;
    • Li, Miaoxin;
    • Wang, Quang;
    • Butler, Amy W.;
    • Paul, Basil;
    • Wu, Hei-Man;
    • Hui, Tomy C.K.;
    • Choi, Siu-Chung;
    • So, Man-Ting;
    • Garcia-Barcelo, Maria-Mercè;
    • McAlonan, Grainne M.;
    • Chen, Eric Y.H.;
    • Cheung, Eric F.C.;
    • Chan, Raymond C.K.;
    • Purcell, Shaun M.;
    • Cherny, Stacey S.;
    • Chen, Ronald R.L.;
    • Li, Tao;
    • Sham, Pak-Chung
    Publication type:
    Journal Article
    17

    Common Variants on Xq28 Conferring Risk of Schizophrenia in Han Chinese.

    Published in:
    Schizophrenia Bulletin, 2014, v. 40, n. 4, p. 777, doi. 10.1093/schbul/sbt104
    By:
    • Wong, Emily H.M.;
    • So, Hon-Cheong;
    • Li, Miaoxin;
    • Wang, Quang;
    • Butler, Amy W.;
    • Paul, Basil;
    • Wu, Hei-Man;
    • Hui, Tomy C.K.;
    • Choi, Siu-Chung;
    • So, Man-Ting;
    • Garcia-Barcelo, Maria-Mercè;
    • McAlonan, Grainne M.;
    • Chen, Eric Y.H.;
    • Cheung, Eric F.C.;
    • Chan, Raymond C.K.;
    • Purcell, Shaun M.;
    • Cherny, Stacey S.;
    • Chen, Ronald R.L.;
    • Li, Tao;
    • Sham, Pak-Chung
    Publication type:
    Article
    18

    A framework for the interpretation of de novo mutation in human disease.

    Published in:
    Nature Genetics, 2014, v. 46, n. 9, p. 944, doi. 10.1038/ng.3050
    By:
    • Samocha, Kaitlin E;
    • Robinson, Elise B;
    • Sanders, Stephan J;
    • Stevens, Christine;
    • Sabo, Aniko;
    • McGrath, Lauren M;
    • Kosmicki, Jack A;
    • Rehnström, Karola;
    • Mallick, Swapan;
    • Kirby, Andrew;
    • Wall, Dennis P;
    • MacArthur, Daniel G;
    • Gabriel, Stacey B;
    • DePristo, Mark;
    • Purcell, Shaun M;
    • Palotie, Aarno;
    • Boerwinkle, Eric;
    • Buxbaum, Joseph D;
    • Cook, Edwin H;
    • Gibbs, Richard A
    Publication type:
    Article
    19

    Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.

    Published in:
    Nature Genetics, 2013, v. 45, n. 9, p. 984, doi. 10.1038/ng.2711
    By:
    • Lee, S Hong;
    • Ripke, Stephan;
    • Neale, Benjamin M;
    • Faraone, Stephen V;
    • Purcell, Shaun M;
    • Perlis, Roy H;
    • Mowry, Bryan J;
    • Thapar, Anita;
    • Goddard, Michael E;
    • Witte, John S;
    • Absher, Devin;
    • Agartz, Ingrid;
    • Akil, Huda;
    • Amin, Farooq;
    • Andreassen, Ole A;
    • Anjorin, Adebayo;
    • Anney, Richard;
    • Anttila, Verneri;
    • Arking, Dan E;
    • Asherson, Philip
    Publication type:
    Article
    20
    21
    22

    The Genomic Psychiatry Cohort: Partners in Discovery.

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 4, p. 306, doi. 10.1002/ajmg.b.32160
    By:
    • Pato, Michele T.;
    • Sobell, Janet L.;
    • Medeiros, Helena;
    • Abbott, Colony;
    • Sklar, Brooke M.;
    • Buckley, Peter F.;
    • Bromet, Evelyn J.;
    • Escamilla, Michael A.;
    • Fanous, Ayman H.;
    • Lehrer, Douglas S.;
    • Macciardi, Fabio;
    • Malaspina, Dolores;
    • McCarroll, Steve A.;
    • Marder, Stephen R.;
    • Moran, Jennifer;
    • Morley, Christopher P.;
    • Nicolini, Humberto;
    • Perkins, Diana O.;
    • Purcell, Shaun M.;
    • Rapaport, Mark H.
    Publication type:
    Article
    23
    24
    25

    A multivariate test of association.

    Published in:
    Bioinformatics, 2009, v. 25, n. 1, p. 132, doi. 10.1093/bioinformatics/btn563
    By:
    • Ferreira, Manuel A. R.;
    • Purcell, Shaun M.
    Publication type:
    Article
    26

    Genetic Association Analysis of 300 Genes Identifies a Risk Haplotype in SLC18A2 for Post-traumatic Stress Disorder in Two Independent Samples.

    Published in:
    Neuropsychopharmacology, 2014, v. 39, n. 8, p. 1872, doi. 10.1038/npp.2014.34
    By:
    • Solovieff, Nadia;
    • Roberts, Andrea L;
    • Ratanatharathorn, Andrew;
    • Haloosim, Michelle;
    • De Vivo, Immaculata;
    • King, Anthony P;
    • Liberzon, Israel;
    • Aiello, Allison;
    • Uddin, Monica;
    • Wildman, Derek E;
    • Galea, Sandro;
    • Smoller, Jordan W;
    • Purcell, Shaun M;
    • Koenen, Karestan C
    Publication type:
    Article
    27

    Causal Association Between Subtypes of Excessive Daytime Sleepiness and Risk of Cardiovascular Diseases.

    Published in:
    Journal of the American Heart Association, 2023, v. 12, n. 24, p. 1, doi. 10.1161/JAHA.122.030568
    By:
    • Goodman, Matthew O.;
    • Dashti, Hassan S.;
    • Lane, Jacqueline M.;
    • Windred, Daniel P.;
    • Burns, Angus;
    • Jones, Samuel E.;
    • Sofer, Tamar;
    • Purcell, Shaun M.;
    • Xiaofeng Zhu;
    • Ollila, Hanna M.;
    • Kyle, Simon D.;
    • Spiegelhalder, Kai;
    • Peker, Yuksel;
    • Huang, Tianyi;
    • Cain, Sean W.;
    • Phillips, Andrew J. K.;
    • Saxena, Richa;
    • Rutter, Martin K.;
    • Redline, Susan;
    • Heming Wang
    Publication type:
    Article
    28
    29

    Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program.

    Published in:
    Genome Medicine, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13073-021-00917-8
    By:
    • Cade, Brian E.;
    • Lee, Jiwon;
    • Sofer, Tamar;
    • Wang, Heming;
    • Zhang, Man;
    • Chen, Han;
    • Gharib, Sina A.;
    • Gottlieb, Daniel J.;
    • Guo, Xiuqing;
    • Lane, Jacqueline M.;
    • Liang, Jingjing;
    • Lin, Xihong;
    • Mei, Hao;
    • Patel, Sanjay R.;
    • Purcell, Shaun M.;
    • Saxena, Richa;
    • Shah, Neomi A.;
    • Evans, Daniel S.;
    • Hanis, Craig L.;
    • Hillman, David R.
    Publication type:
    Article
    30
    31

    Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders.

    Published in:
    Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0497-y
    By:
    • Nguyen, Hoang T.;
    • Bryois, Julien;
    • Kim, April;
    • Dobbyn, Amanda;
    • Huckins, Laura M.;
    • Munoz-Manchado, Ana B.;
    • Ruderfer, Douglas M.;
    • Genovese, Giulio;
    • Fromer, Menachem;
    • Xinyi Xu;
    • Pinto, Dalila;
    • Linnarsson, Sten;
    • Verhage, Matthijs;
    • Smit, August B.;
    • Hjerling-Leffler, Jens;
    • Buxbaum, Joseph D.;
    • Hultman, Christina;
    • Sklar, Pamela;
    • Purcell, Shaun M.;
    • Lage, Kasper
    Publication type:
    Article
    32

    AI-Driven sleep staging from actigraphy and heart rate.

    Published in:
    PLoS ONE, 2023, v. 18, n. 5, p. 1, doi. 10.1371/journal.pone.0285703
    By:
    • Song, Tzu-An;
    • Chowdhury, Samadrita Roy;
    • Malekzadeh, Masoud;
    • Harrison, Stephanie;
    • Hoge, Terri Blackwell;
    • Redline, Susan;
    • Stone, Katie L.;
    • Saxena, Richa;
    • Purcell, Shaun M.;
    • Dutta, Joyita
    Publication type:
    Article
    33
    34

    The Genetic Structure of the Swedish Population.

    Published in:
    PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0022547
    By:
    • Humphreys, Keith;
    • Grankvist, Alexander;
    • Leu, Monica;
    • Hall, Per;
    • Liu, Jianjun;
    • Ripatti, Samuli;
    • Rehnström, Karola;
    • Groop, Leif;
    • Klareskog, Lars;
    • Ding, Bo;
    • Grönberg, Henrik;
    • Xu, Jianfeng;
    • Pedersen, Nancy L.;
    • Lichtenstein, Paul;
    • Mattingsdal, Morten;
    • Andreassen, Ole A.;
    • O'Dushlaine, Colm;
    • Purcell, Shaun M.;
    • Sklar, Pamela;
    • Sullivan, Patrick F.
    Publication type:
    Article
    35

    A polygenic burden of rare disruptive mutations in schizophrenia.

    Published in:
    Nature, 2014, v. 506, n. 7487, p. 185, doi. 10.1038/nature12975
    By:
    • Purcell, Shaun M.;
    • Moran, Jennifer L.;
    • Fromer, Menachem;
    • Ruderfer, Douglas;
    • Solovieff, Nadia;
    • Roussos, Panos;
    • O'Dushlaine, Colm;
    • Chambert, Kimberly;
    • Bergen, Sarah E.;
    • Kähler, Anna;
    • Duncan, Laramie;
    • Stahl, Eli;
    • Genovese, Giulio;
    • Fernández, Esperanza;
    • Collins, Mark O.;
    • Komiyama, Noboru H.;
    • Choudhary, Jyoti S.;
    • Magnusson, Patrik K. E.;
    • Banks, Eric;
    • Shakir, Khalid
    Publication type:
    Article
    36

    Upregulated heme biosynthesis increases obstructive sleep apnea severity: a pathway-based Mendelian randomization study.

    Published in:
    Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-05415-4
    By:
    • Wang, Heming;
    • Kurniansyah, Nuzulul;
    • Cade, Brian E.;
    • Goodman, Matthew O.;
    • Chen, Han;
    • Gottlieb, Daniel J.;
    • Gharib, Sina A.;
    • Purcell, Shaun M.;
    • Lin, Xihong;
    • Saxena, Richa;
    • Zhu, Xiaofeng;
    • Durda, Peter;
    • Tracy, Russel;
    • Liu, Yongmei;
    • Taylor, Kent D.;
    • Johnson, W. Craig;
    • Gabriel, Stacey;
    • Smith, Joshua D.;
    • Aguet, François;
    • Ardlie, Kirstin
    Publication type:
    Article
    37
    38

    Sleep Architecture, Obstructive Sleep Apnea, and Cognitive Function in Adults.

    Published in:
    JAMA Network Open, 2023, v. 6, n. 7, p. e2325152, doi. 10.1001/jamanetworkopen.2023.25152
    By:
    • Pase, Matthew P.;
    • Harrison, Stephanie;
    • Misialek, Jeffrey R.;
    • Kline, Christopher E.;
    • Cavuoto, Marina;
    • Baril, Andree-Ann;
    • Yiallourou, Stephanie;
    • Bisson, Alycia;
    • Himali, Dibya;
    • Leng, Yue;
    • Yang, Qiong;
    • Seshadri, Sudha;
    • Beiser, Alexa;
    • Gottesman, Rebecca F.;
    • Redline, Susan;
    • Lopez, Oscar;
    • Lutsey, Pamela L.;
    • Yaffe, Kristine;
    • Stone, Katie L.;
    • Purcell, Shaun M.
    Publication type:
    Article
    39