Rezultati - Colm Ó'Dúshláine

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  1. 1
    INRICH: interval-based enrichment analysis for genome-wide association studies

    INRICH: interval-based enrichment analysis for genome-wide association studies od Sang Hyuck Lee, Colm O’Dushlaine, Brett Thomas, Shaun Purcell

    Izdano 2012
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  2. 2
    The SNP ratio test: pathway analysis of genome-wide association datasets

    The SNP ratio test: pathway analysis of genome-wide association datasets od Colm Ó'Dúshláine, Elaine Kenny, Elizabeth A. Heron, Ricardo Segurado, Michael Gill, Derek W. Morris, Aiden Corvin

    Izdano 2009
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  3. 3
    Pathway Analyses Implicate Glial Cells in Schizophrenia

    Pathway Analyses Implicate Glial Cells in Schizophrenia od Laramie E. Duncan, Peter Holmans, Phil H. Lee, Colm Ó'Dúshláine, Andrew Kirby, Jordan W. Smoller, Döst Öngür, Bruce M. Cohen

    Izdano 2014
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  4. 4
    CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing data

    CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing data od Jonathan S. Packer, Evan K. Maxwell, Colm O’Dushlaine, Alexander Lopez, Frederick E. Dewey, Rostislav Chernomorsky, Aris Baras, John D. Overton, Lukas Habegger, Jeffrey G. Reid

    Izdano 2015
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  5. 5
    Schizophrenia is Associated With an Aberrant Immune Response to Epstein–Barr Virus

    Schizophrenia is Associated With an Aberrant Immune Response to Epstein–Barr Virus od Faith Dickerson, Lorraine Jones‐Brando, Glen Ford, Giulio Genovese, Cassie Stallings, Andrea Origoni, Colm O’Dushlaine, Emily Katsafanas, Kevin Sweeney, Sunil Khushalani, Robert H. Yolken

    Izdano 2018
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  6. 6
    Genetic modifiers and subtypes in schizophrenia: Investigations of age at onset, severity, sex and family history

    Genetic modifiers and subtypes in schizophrenia: Investigations of age at onset, severity, sex and family history od Sarah E. Bergen, Colm O’Dushlaine, Phil H. Lee, Ayman H. Fanous, Douglas M. Ruderfer, Stephan Ripke, Patrick F. Sullivan, Jordan W. Smoller, Shaun Purcell, Aiden Corvin

    Izdano 2014
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  7. 7
    Whole-genome analysis of human embryonic stem cells enables rational line selection based on genetic variation

    Whole-genome analysis of human embryonic stem cells enables rational line selection based on genetic variation od Florian T. Merkle, Sulagna Ghosh, Giulio Genovese, Robert E. Handsaker, Seva Kashin, Daniel Meyer, Konrad J. Karczewski, Colm O’Dushlaine, Carlos N. Pato, Michele T. Pato, Daniel G. MacArthur, Steven A. McCarroll, Kevin Eggan

    Izdano 2022
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  8. 8
    Rare Copy Number Variation in Treatment-Resistant Major Depressive Disorder

    Rare Copy Number Variation in Treatment-Resistant Major Depressive Disorder od Colm Ó'Dúshláine, Stephan Ripke, Douglas M. Ruderfer, Steven P. Hamilton, Maurizio Fava, Dan V. Iosifescu, Isaac S. Kohane, Susanne Churchill, Víctor M. Castro, Caitlin C. Clements, Sarah R. Blumenthal, Shawn N. Murphy, Jordan W. Smoller, Roy H. Perlis

    Izdano 2014
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  9. 9
    Cis-acting regulation of brain-specific ANK3 gene expression by a genetic variant associated with bipolar disorder

    Cis-acting regulation of brain-specific ANK3 gene expression by a genetic variant associated with bipolar disorder od Erroll H. Rueckert, Douglas Barker, Douglas M. Ruderfer, Sarah E. Bergen, Colm O’Dushlaine, Catherine J. Luce, Steven D. Sheridan, Kraig M. Theriault, Kimberly Chambert, Jennifer L. Moran, Shaun Purcell, Jon M. Madison, Stephen J. Haggarty, Pamela Sklar

    Izdano 2012
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  10. 10
    Computationally efficient whole genome regression for quantitative and binary traits

    Computationally efficient whole genome regression for quantitative and binary traits od Joelle Mbatchou, Leland Barnard, Joshua Backman, Anthony Marcketta, Jack A. Kosmicki, Andrey Ziyatdinov, Christian Benner, Colm O’Dushlaine, Mathew Barber, Boris Boutkov, Lukas Habegger, Manuel A. R. Ferreira, Aris Baras, Jeffrey G. Reid, Gonçalo R. Abecasis, Evan K. Maxwell, Jonathan Marchini

    Izdano 2020
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  11. 11
    Computationally efficient whole-genome regression for quantitative and binary traits

    Computationally efficient whole-genome regression for quantitative and binary traits od Joelle Mbatchou, Leland Barnard, Joshua Backman, Anthony Marcketta, Jack A. Kosmicki, Andrey Ziyatdinov, Christian Benner, Colm O’Dushlaine, Mathew Barber, Boris Boutkov, Lukas Habegger, Manuel A. R. Ferreira, Aris Baras, Jeffrey G. Reid, Gonçalo R. Abecasis, Evan K. Maxwell, Jonathan Marchini

    Izdano 2021
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  12. 12
    zCall: a rare variant caller for array-based genotyping

    zCall: a rare variant caller for array-based genotyping od Jacqueline I. Goldstein, Andrew Crenshaw, Jason Carey, George Grant, Jared Maguire, Menachem Fromer, Colm O’Dushlaine, Jennifer L. Moran, Kimberly Chambert, Christine Stevens, Pamela Sklar, Christina M. Hultman, Shaun Purcell, Steven A. McCarroll, Patrick F. Sullivan, Mark J. Daly, Benjamin M. Neale

    Izdano 2012
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  13. 13
    Natural Selection in a Bangladeshi Population from the Cholera-Endemic Ganges River Delta

    Natural Selection in a Bangladeshi Population from the Cholera-Endemic Ganges River Delta od Elinor K. Karlsson, Jason B. Harris, Shervin Tabrizi, Atiqur Rahman, Ilya Shlyakhter, Nick Patterson, Colm O’Dushlaine, S. F. Schaffner, Sameer Gupta, Fahima Chowdhury, Alaullah Sheikh, Ok Sarah Shin, Crystal N. Ellis, Christine Becker, Lynda M. Stuart, Stephen B. Calderwood, Edward T. Ryan, Firdausi Qadri, Pardis C. Sabeti, Regina C. LaRocque

    Izdano 2013
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  14. 14
    The Genetic Structure of the Swedish Population

    The Genetic Structure of the Swedish Population od Keith Humphreys, Alexander Grankvist, Monica Leu, Per Hall, Jianjun Liu, Samuli Ripatti, Karola Rehnström, Leif Groop, Lars Klareskog, Bo Ding, Henrik Grönberg, Jianfeng Xu, Nancy L. Pedersen, Paul Lichtenstein, Morten Mattingsdal, Ole A. Andreassen, Colm O’Dushlaine, Shaun Purcell, Pamela Sklar, Patrick F. Sullivan, Christina M. Hultman, Juni Palmgren, Patrik K. E. Magnusson

    Izdano 2011
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  15. 15
    Cryptic and Complex Chromosomal Aberrations in Early-Onset Neuropsychiatric Disorders

    Cryptic and Complex Chromosomal Aberrations in Early-Onset Neuropsychiatric Disorders od Harrison Brand, Vamsee Pillalamarri, Ryan L. Collins, Stacey Eggert, Colm Ó'Dúshláine, Ellen B. Braaten, Matthew R. Stone, Kimberly Chambert, Nathan D. Doty, Carrie Hanscom, Jill A. Rosenfeld, Hillary L. Ditmars, Jessica E. Blais, Ryan E. Mills, Charles Lee, James F. Gusella, Steven A. McCarroll, Jordan W. Smoller, Michael E. Talkowski, Alysa E. Doyle

    Izdano 2014
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  16. 16
    Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder

    Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder od Sarah E. Bergen, Colm Ó'Dúshláine, Stephan Ripke, P H Lee, Douglas M. Ruderfer, Susanne Akterin, Jennifer L. Moran, Kimberly D. Chambert, Robert E. Handsaker, Lena Backlund, Urban Ösby, Steven A. McCarroll, Mikael Landén, Edward M. Scolnick, Patrik K. E. Magnusson, Paul Lichtenstein, Christina M. Hultman, Shaun Purcell, Pamela Sklar, Patrick F. Sullivan

    Izdano 2012
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  17. 17
    Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study

    Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study od Richard Anney, Jessica Lasky‐Su, Colm Ó'Dúshláine, Elaine Kenny, Benjamin M. Neale, Aisling Mulligan, Barbara Franke, Kaixin Zhou, Wai Chen, Hanna Christiansen, Alejandro Arias Vásquez, Tobias Banaschewski, Jan K. Buitelaar, Richard P. Ebstein, Ana Miranda, Fernando Mulas, Robert D. Oades, Herbert Roeyers, Aribert Rothenberger, Joseph A. Sergeant, Edmund Sonuga‐Barke, Hans‐Christoph Steinhausen, Philip Asherson, Stephen V. Faraone, Michael Gill

    Izdano 2008
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  18. 18
    Inactivating Variants in <i>ANGPTL4</i> and Risk of Coronary Artery Disease

    Inactivating Variants in <i>ANGPTL4</i> and Risk of Coronary Artery Disease od Frederick E. Dewey, Viktoria Gusarova, Colm O’Dushlaine, Omri Gottesman, Jesus Trejos, Charleen Hunt, Cristopher V. Van Hout, Lukas Habegger, David G. Buckler, Ka-Man V. Lai, Joseph B. Leader, Michael F. Murray, Marylyn D. Ritchie, H. Lester Kirchner, David H. Ledbetter, John S. Penn, Alexander Lopez, Ingrid B. Borecki, John D. Overton, Jeffrey G. Reid, David J. Carey, Andrew Murphy, George D. Yancopoulos, Aris Baras, Jesper Gromada, Alan R. Shuldiner

    Izdano 2016
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  19. 19
    Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 Exomes

    Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 Exomes od Jeffrey Staples, Evan K. Maxwell, Nehal Gosalia, Claudia Gonzaga‐Jauregui, Christopher W. Snyder, Alicia Hawes, John S. Penn, Ricardo H. Ulloa, Xiaodong Bai, Alexander Lopez, Cristopher V. Van Hout, Colm O’Dushlaine, Tanya M. Teslovich, Shane McCarthy, Suganthi Balasubramanian, H. Lester Kirchner, Joseph B. Leader, Michael F. Murray, David H. Ledbetter, Alan R. Shuldiner, George D. Yancoupolos, Frederick E. Dewey, David J. Carey, John D. Overton, Aris Baras, Lukas Habegger, Jeffrey G. Reid

    Izdano 2018
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  20. 20
    Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia

    Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia od Jennifer G. Mullé, Ann E. Pulver, John A. McGrath, Paula Wolyniec, Anne Dodd, David J. Cutler, Jonathan Sebat, Dheeraj Malhotra, Gerald Nestadt, Donald F. Conrad, Matthew E. Hurles, C. Barnes, Masashi Ikeda, Nakao Iwata, Douglas F. Levinson, Pablo V. Gejman, Alan R. Sanders, Jubao Duan, Adele A. Mitchell, Inga Peter, Pamela Sklar, Colm Ó'Dúshláine, Detelina Grozeva, Michael O’Donovan, Michael J. Owen, Christina M. Hultman, Anna K. Kähler, Patrick F. Sullivan, George Kirov, Stephen T. Warren

    Izdano 2013
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