Výsledky vyhledávání - Jared O’Connell

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  1. 1
    Tracking human population structure through time from whole genome sequences

    Tracking human population structure through time from whole genome sequences Autor Ke Wang, Iain Mathieson, Jared O’Connell, Stephan Schiffels

    Vydáno 2020
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  2. 2
    AKT: ancestry and kinship toolkit

    AKT: ancestry and kinship toolkit Autor Rudy Arthur, Ole Schulz-Trieglaff, Anthony J. Cox, Jared O’Connell

    Vydáno 2016
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  3. 3
    NxTrim: optimized trimming of Illumina mate pair reads

    NxTrim: optimized trimming of Illumina mate pair reads Autor Jared O’Connell, Ole Schulz-Trieglaff, Emma Carlson, Matthew M. Hims, Niall Gormley, Anthony J. Cox

    Vydáno 2015
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  4. 4
    An ensemble penalized regression method for multi-ancestry polygenic risk prediction

    An ensemble penalized regression method for multi-ancestry polygenic risk prediction Autor Jingning Zhang, Jianan Zhan, Jin Jin, Cheng Ma, Ruzhang Zhao, Jared O’Connell, Yunxuan Jiang, Bertram L. Koelsch, Haoyu Zhang, Nilanjan Chatterjee

    Vydáno 2024
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  5. 5
    Haplotype estimation for biobank-scale data sets

    Haplotype estimation for biobank-scale data sets Autor Jared O’Connell, Kevin Sharp, Nick Shrine, Louise V. Wain, Ian P. Hall, Martin D. Tobin, Jean‐François Zagury, Olivier Delaneau, Jonathan Marchini

    Vydáno 2016
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  6. 6
    Genome-wide genetic data on ~500,000 UK Biobank participants

    Genome-wide genetic data on ~500,000 UK Biobank participants Autor Clare Bycroft, Colin Freeman, Desislava Petkova, Gavin Band, Lloyd T. Elliott, Kevin Sharp, Allan Motyer, Damjan Vukcevic, Olivier Delaneau, Jared O’Connell, Adrián Cortés, Samantha Welsh, Gil McVean, Stephen Leslie, Peter Donnelly, Jonathan Marchini

    Vydáno 2017
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  7. 7
    The UK Biobank resource with deep phenotyping and genomic data

    The UK Biobank resource with deep phenotyping and genomic data Autor Clare Bycroft, Colin Freeman, Desislava Petkova, Gavin Band, Lloyd T. Elliott, Kevin Sharp, Allan Motyer, Damjan Vukcevic, Olivier Delaneau, Jared O’Connell, Adrián Cortés, Samantha Welsh, A. P. Young, Mark Effingham, Gil McVean, Stephen Leslie, Naomi E. Allen, Peter Donnelly, Jonathan Marchini

    Vydáno 2018
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  8. 8
    Influence of autozygosity on common disease risk across the phenotypic spectrum

    Influence of autozygosity on common disease risk across the phenotypic spectrum Autor Daniel Malawsky, Eva van Walree, Benjamin Meir Jacobs, Teng Hiang Heng, Qin Huang, Ataf Sabir, Saadia Rahman, Saghira Malik Sharif, Ahsan Khan, Maša Umićević Mirkov, Hiroyuki Kuwahara, Xin Gao, Fowzan S. Alkuraya, Daniëlle Posthuma, William G. Newman, Chris Griffiths, Rohini Mathur, David A. van Heel, Sarah Finer, Jared O’Connell, Hilary C. Martin

    Vydáno 2023
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  9. 9
    A General Approach for Haplotype Phasing across the Full Spectrum of Relatedness

    A General Approach for Haplotype Phasing across the Full Spectrum of Relatedness Autor Jared O’Connell, Deepti Gurdasani, Olivier Delaneau, Nicola Pirastu, Sheila Ulivi, Massimiliano Cocca, Michela Traglia, Jie Huang, Jennifer E. Huffman, Igor Rudan, Ruth McQuillan, Ross M. Fraser, Harry Campbell, Ozren Polašek, Gershim Asiki, Kenneth Ekoru, Caroline Hayward, Alan F. Wright, Véronique Vitart, Pau Navarro, Jean-François Zagury, James F. Wilson, Daniela Toniolo, Paolo Gasparini, Nicole Soranzo, Manjinder S. Sandhu, Jonathan Marchini

    Vydáno 2014
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  10. 10
    MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups

    MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups Autor Jin Jin, Jianan Zhan, Jingning Zhang, Ruzhang Zhao, Jared O’Connell, Yunxuan Jiang, Stella Aslibekyan, Adam Auton, Elizabeth Babalola, Robert K. Bell, Jessica Bielenberg, Katarzyna Bryc, Emily Bullis, Daniella Coker, Gabriel Cuéllar-Partida, Devika Dhamija, Sayantan Das, Sarah L. Elson, Nicholas Eriksson, Teresa Filshtein, Alison Fitch, Kipper Fletez‐Brant, Pierre Fontanillas, Will Freyman, Julie M. Granka, Karl Heilbron, Alejandro Hernandez, Barry Hicks, David A. Hinds, Ethan M. Jewett, Yunxuan Jiang, Katelyn Kukar, Alan Kwong, Keng‐Han Lin, Bianca A. Llamas, Maya Lowe, Jey C. McCreight, Matthew H. McIntyre, Steven J. Micheletti, Meghan E. Moreno, Priyanka Nandakumar, Dominique T. Nguyen, Elizabeth S. Noblin, Jared O’Connell, Aaron A. Petrakovitz, G. David Poznik, Alexandra Reynoso, Morgan Schumacher, Anjali J. Shastri, Janie F. Shelton, Jingchunzi Shi, Suyash Shringarpure, Qiaojuan Jane Su, Susana A. Tat, Christophe Toukam Tchakouté, Vinh Tran, Joyce Y. Tung, Xin Wang, Wei Wang, Catherine H. Weldon, Peter Wilton, Corinna D. Wong, Steven Buyske, Christopher R. Gignoux, Christopher A. Haiman, Eimear E. Kenny, Charles Kooperberg, Kari E. North, Bertram L. Koelsch, Genevieve L. Wojcik, Haoyu Zhang, Nilanjan Chatterjee

    Vydáno 2024
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  11. 11
    Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank

    Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank Autor Louise V. Wain, Nick Shrine, S. Miller, Victoria E. Jackson, Ioanna Ntalla, María Soler Artigas, Charlotte K. Billington, Abdul Kader Kheirallah, Richard J. Allen, James P. Cook, Kelly Probert, Ma’en Obeidat, Yohan Bossé, Ke Hao, Dirkje S. Postma, Peter D. Paré, Adaikalavan Ramasamy, Reedik Mägi, Evelin Mihailov, Eva Reinmaa, Erik Melén, Jared O’Connell, Eleni Frangou, Olivier Delaneau, Colin Freeman, Desislava Petkova, Mark I. McCarthy, Ian Sayers, Panos Deloukas, Richard Hubbard, Ian Pavord, Anna Hansell, Neil C. Thomson, Eleftheria Zeggini, Andrew P. Morris, Jonathan Marchini, David P. Strachan, Martin D. Tobin, Ian P. Hall

    Vydáno 2015
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  12. 12
    Genome-wide association and multi-omic analyses reveal ACTN2 as a gene linked to heart failure

    Genome-wide association and multi-omic analyses reveal ACTN2 as a gene linked to heart failure Autor Marios Arvanitis, Emmanouil Tampakakis, Yanxiao Zhang, Wei Wang, Adam Auton, Michelle Agee, Stella Aslibekyan, Robert K. Bell, Katarzyna Bryc, Sarah Clark, Sarah L. Elson, Kipper Fletez‐Brant, Pierre Fontanillas, Nicholas A. Furlotte, Pooja Gandhi, Karl Heilbron, Barry Hicks, David A. Hinds, Karen E. Huber, Ethan M. Jewett, Yunxuan Jiang, Aaron Kleinman, Keng‐Han Lin, Nadia K. Litterman, Jennifer C. McCreight, Matthew H. McIntyre, Kimberly F. McManus, Joanna L. Mountain, Sahar V. Mozaffari, Priyanka Nandakumar, Elizabeth S. Noblin, Carrie A. M. Northover, Jared O’Connell, Steven J. Pitts, G. David Poznik, J. Fah Sathirapongsasuti, Anjali J. Shastri, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Robert J. Tunney, Vladimir Vacic, Xin Wang, Amir S. Zare, Diptavo Dutta, Stephanie Glavaris, Ali R. Keramati, Nilanjan Chatterjee, C. Neil, Bing Ren, Wendy S. Post, Alexis Battle

    Vydáno 2020
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  13. 13
    A population-specific reference panel for improved genotype imputation in African Americans

    A population-specific reference panel for improved genotype imputation in African Americans Autor Jared O’Connell, Taedong Yun, Meghan E. Moreno, Helen Li, Nadia K. Litterman, Alexey Kolesnikov, Elizabeth S. Noblin, Pi-Chuan Chang, Anjali J. Shastri, Elizabeth H. Dorfman, Suyash Shringarpure, Stella Aslibekyan, Elizabeth Babalola, Robert K. Bell, Jessica Bielenberg, Katarzyna Bryc, Emily Bullis, Daniella Coker, Gabriel Cuéllar-Partida, Devika Dhamija, Sayantan Das, Sarah L. Elson, Teresa Filshtein, Kipper Fletez‐Brant, Pierre Fontanillas, Will Freyman, Pooja Gandhi, Karl Heilbron, Alejandro Hernandez, Barry Hicks, David A. Hinds, Ethan M. Jewett, Yunxuan Jiang, Katelyn Kukar, Keng-Han Lin, Maya Lowe, Jey C. McCreight, Matthew H. McIntyre, Steven J. Micheletti, Joanna L. Mountain, Priyanka Nandakumar, Aaron A. Petrakovitz, G. David Poznik, Morgan Schumacher, Janie F. Shelton, Jingchunzi Shi, Christophe Toukam Tchakouté, Vinh Tran, Joyce Y. Tung, Xin Wang, Wei Wang, Catherine H. Weldon, Peter Wilton, Corinna Wong, Adam Auton, Andrew Carroll, Cory Y. McLean

    Vydáno 2021
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  14. 14
    Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways

    Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways Autor Kyoko Watanabe, Philip R. Jansen, Jeanne E. Savage, Priyanka Nandakumar, Xin Wang, Michelle Agee, Stella Aslibekyan, Adam Auton, Robert K. Bell, Katarzyna Bryc, Sarah Clark, Sarah L. Elson, Kipper Fletez‐Brant, Pierre Fontanillas, Nicholas A. Furlotte, Pooja Gandhi, Karl Heilbron, Barry Hicks, Karen E. Huber, Ethan M. Jewett, Yunxuan Jiang, Aaron Kleinman, Keng‐Han Lin, Nadia K. Litterman, Jennifer C. McCreight, Matthew H. McIntyre, Kimberly F. McManus, Joanna L. Mountain, Sahar V. Mozaffari, Elizabeth S. Noblin, Carrie A. M. Northover, Jared O’Connell, Steven J. Pitts, G. David Poznik, J. Fah Sathirapongsasuti, Janie F. Shelton, Jing Shi, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Robert J. Tunney, Vladimir Vacic, Wei Wang, David A. Hinds, Joel Gelernter, Daniel F. Levey, Renato Polimanti, Murray B. Stein, Eus J.W. Van Someren, August B. Smit, Daniëlle Posthuma

    Vydáno 2022
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  15. 15
    A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma

    A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma Autor Mathias Seviiri, Matthew H. Law, Jue‐Sheng Ong, Puya Gharahkhani, Pierre Fontanillas, Stella Aslibekyan, Adam Auton, Elizabeth Babalola, Robert K. Bell, Jessica Bielenberg, Katarzyna Bryc, Emily Bullis, Daniella Coker, Gabriel Cuéllar-Partida, Devika Dhamija, Sayantan Das, Sarah L. Elson, Teresa Filshtein, Kipper Fletez‐Brant, Will Freyman, Pooja Gandhi, Karl Heilbron, Barry Hicks, David A. Hinds, Ethan M. Jewett, Yunxuan Jiang, Katelyn Kukar, Keng‐Han Lin, Maya Lowe, Jey C. McCreight, Matthew H. McIntyre, Steven J. Micheletti, Meghan E. Moreno, Joanna L. Mountain, Priyanka Nandakumar, Elizabeth S. Noblin, Jared O’Connell, Aaron A. Petrakovitz, G. David Poznik, Morgan Schumacher, Anjali J. Shastri, Janie F. Shelton, Jingchunzi Shi, Suyash Shringarpure, Vinh Tran, Joyce Y. Tung, Xin Wang, Wei Wang, Catherine H. Weldon, Peter Wilton, Alejandro Hernandez, Corinna Wong, Christophe Toukam Tchakouté, Catherine M. Olsen, David C. Whiteman, Stuart MacGregor

    Vydáno 2022
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  16. 16
    Genetic determinants of daytime napping and effects on cardiometabolic health

    Genetic determinants of daytime napping and effects on cardiometabolic health Autor Hassan S. Dashti, Iyas Daghlas, Jacqueline M. Lane, Yunru Huang, Miriam S. Udler, Heming Wang, Hanna M. Ollila, Samuel E. Jones, Jaegil Kim, Andrew R. Wood, Michelle Agee, Adam Auton, Robert K. Bell, Katarzyna Bryc, Sarah Clark, Sarah L. Elson, Kipper Fletez‐Brant, Pierre Fontanillas, Nicholas A. Furlotte, Pooja Gandhi, Karl Heilbron, Barry Hicks, David A. Hinds, Karen E. Huber, Ethan M. Jewett, Yunxuan Jiang, Aaron Kleinman, Keng‐Han Lin, Nadia K. Litterman, Marie K. Luff, Jennifer C. McCreight, Matthew H. McIntyre, Kimberly F. McManus, Joanna L. Mountain, Sahar V. Mozaffari, Priyanka Nandakumar, Elizabeth S. Noblin, Carrie A. M. Northover, Jared O’Connell, Aaron A. Petrakovitz, Steven J. Pitts, G. David Poznik, J. Fah Sathirapongsasuti, Anjali J. Shastri, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Robert J. Tunney, Vladimir Vacic, Xin Wang, Amir S. Zare, Michael N. Weedon, Stella Aslibekyan, Marta Garaulet, Richa Saxena

    Vydáno 2021
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  17. 17
    Genome-wide association study of musical beat synchronization demonstrates high polygenicity

    Genome-wide association study of musical beat synchronization demonstrates high polygenicity Autor Maria Niarchou, Daniel E. Gustavson, J. Fah Sathirapongsasuti, Manuel Anglada-Tort, Else Eising, Eamonn Bell, Evonne McArthur, Péter Straub, Stella Aslibekyan, Adam Auton, Robert K. Bell, Katarzyna Bryc, Sarah Clark, Sarah L. Elson, Kipper Fletez‐Brant, Pierre Fontanillas, Nicholas A. Furlotte, Pooja Gandhi, Karl Heilbron, Barry Hicks, Karen E. Huber, Ethan M. Jewett, Yunxuan Jiang, Aaron Kleinman, Keng‐Han Lin, Nadia K. Litterman, Jey C. McCreight, Matthew H. McIntyre, Kimberly F. McManus, Joanna L. Mountain, Sahar V. Mozaffari, Priyanka Nandakumar, Elizabeth S. Noblin, Carrie A. M. Northover, Jared O’Connell, Steven J. Pitts, G. David Poznik, Anjali J. Shastri, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Robert J. Tunney, Vladimir Vacic, Xin Wang, J. Devin McAuley, John A. Capra, Fredrik Ullén, Nicole Creanza, Miriam A. Mosing, David A. Hinds, Lea K. Davis, Nori Jacoby, Reyna L. Gordon

    Vydáno 2022
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  18. 18
    Genetic analysis and natural history of Parkinson’s disease due to the <i>LRRK2</i> G2019S variant

    Genetic analysis and natural history of Parkinson’s disease due to the <i>LRRK2</i> G2019S variant Autor Matthew J. Kmiecik, Steven J. Micheletti, Daniella Coker, Karl Heilbron, Jingchunzi Shi, Keaton Stagaman, Teresa Filshtein Sönmez, Pierre Fontanillas, Suyash Shringarpure, Madeleine Wetzel, Helen Rowbotham, Paul J. Cannon, Janie F. Shelton, David A. Hinds, Joyce Y. Tung, Adam Auton, Elizabeth Babalola, Robert K. Bell, Jessica Bielenberg, Johnathan Bowes, Katarzyna Bryc, Ninad S. Chaudhary, Sayantan Das, Emily DelloRusso, Sarah L. Elson, Nicholas Eriksson, Will Freyman, Julie M. Granka, Alejandro Hernandez, Barry Hicks, Ethan M. Jewett, Yunxuan Jiang, Katelyn Kukar, Alan Kwong, Keng‐Han Lin, Bianca A. Llamas, Maya Lowe, Matthew H. McIntyre, Meghan E. Moreno, Priyanka Nandakumar, Dominique T. Nguyen, Jared O’Connell, Aaron A. Petrakovitz, G. David Poznik, Alexandra Reynoso, Morgan Schumacher, Leah Selcer, Anjali J. Shastri, Qiaojuan Jane Su, Susana A. Tat, Vinh Tran, Xin Wang, Wei Wang, Catherine H. Weldon, Peter Wilton, Corinna D. Wong, Michael V. Holmes, Stella Aslibekyan, Lucy Norcliffe–Kaufmann

    Vydáno 2024
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  19. 19
    Analysis of rare Parkinson’s disease variants in millions of people

    Analysis of rare Parkinson’s disease variants in millions of people Autor Vanessa Pitz, Mary B. Makarious, Sara Bandrés‐Ciga, Hirotaka Iwaki, Stella Aslibekyan, Adam Auton, Elizabeth Babalola, Robert K. Bell, Jessica Bielenberg, Katarzyna Bryc, Emily Bullis, Daniella Coker, Gabriel Cuéllar-Partida, Devika Dhamija, Sayantan Das, Sarah L. Elson, Nicholas Eriksson, Teresa Filshtein, Alison Fitch, Kipper Fletez‐Brant, Pierre Fontanillas, Will Freyman, Julie M. Granka, Alejandro Hernandez, Barry Hicks, David A. Hinds, Ethan M. Jewett, Yunxuan Jiang, Katelyn Kukar, Alan Kwong, Keng‐Han Lin, Bianca A. Llamas, Maya Lowe, Jey C. McCreight, Matthew H. McIntyre, Steven J. Micheletti, Meghan E. Moreno, Priyanka Nandakumar, Dominique T. Nguyen, Elizabeth S. Noblin, Jared O’Connell, Aaron A. Petrakovitz, G. David Poznik, Alexandra Reynoso, Morgan Schumacher, Anjali J. Shastri, Janie F. Shelton, Jingchunzi Shi, Suyash Shringarpure, Qiaojuan Jane Su, Susana A. Tat, Christophe Toukam Tchakouté, Vinh Tran, Joyce Y. Tung, Xin Wang, Wei Wang, Catherine H. Weldon, Peter Wilton, Corinna D. Wong, Andrew Singleton, Mike A. Nalls, Karl Heilbron, Cornelis Blauwendraat

    Vydáno 2024
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  20. 20
    The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease

    The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease Autor William J. Astle, Heather Elding, Tao Jiang, Dave Allen, Dace Ruklisa, Alice Mann, Daniel G. Mead, Heleen Bouman, Fernando Riveros-Mckay, Myrto Kostadima, John Lambourne, Suthesh Sivapalaratnam, Kate Downes, Kousik Kundu, Lorenzo Bomba, Kim Berentsen, John R. Bradley, Louise C. Daugherty, Olivier Delaneau, Kathleen Freson, Stephen F. Garner, Luigi Grassi, José A. Guerrero, Matthias Haimel, Eva M. Janssen‐Megens, Anita Kaan, Mihir Kamat, Bowon Kim, Amit Mandoli, Jonathan Marchini, Joost H.A. Martens, Stuart Meacham, Karyn Mégy, Jared O’Connell, R. Petersen, Nilofar Sharifi, Simon Sheard, James R Staley, Salih Tuna, Martijn van der Ent, Klaudia Walter, Shuang-Yin Wang, Eleanor Wheeler, Steven P. Wilder, Valentina Iotchkova, Carmel Moore, Jennifer Sambrook, Hendrik G. Stunnenberg, Emanuele Di Angelantonio, Stephen Kaptoge, Taco W. Kuijpers, Enrique Carrillo de Santa Pau, David Juan, Daniel Rico, Alfonso Valencia, Lu Chen, Bing Ge, Louella Vasquez, Tony Kwan, Diego Garrido-Martín, Stephen Watt, Ying Yang, Roderic Guigó, Stephan Beck, Dirk S. Paul, Tomi Pastinen, David Bujold, Guillaume Bourque, Mattia Frontini, John Danesh, David J. Roberts, Willem H. Ouwehand, Adam S. Butterworth, Nicole Soranzo

    Vydáno 2016
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