Resultats de la cerca - Patrick Turley

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  1. 1
    Education can reduce health differences related to genetic risk of obesity

    Education can reduce health differences related to genetic risk of obesity per Silvia Barcellos, Leandro Carvalho, Patrick Turley

    Publicat 2018
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  2. 2
    Social-Science Genomics: Progress, Challenges, and Future Directions

    Social-Science Genomics: Progress, Challenges, and Future Directions per Daniel J. Benjamin, David Cesarini, Patrick Turley, Alexander I. Young

    Publicat 2024
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  3. 3
    Public views on polygenic screening of embryos

    Public views on polygenic screening of embryos per Michelle N. Meyer, Tammy Tan, Daniel J. Benjamin, David Laibson, Patrick Turley

    Publicat 2023
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  4. 4
    Family-based genome-wide association study designs for increased power and robustness

    Family-based genome-wide association study designs for increased power and robustness per Junming Guan, Tammy Tan, Seyed Moeen Nehzati, Michael Bennett, Patrick Turley, Daniel J. Benjamin, Alexander I. Young

    Publicat 2025
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  5. 5
    Mendelian imputation of parental genotypes for genome-wide estimation of direct and indirect genetic effects

    Mendelian imputation of parental genotypes for genome-wide estimation of direct and indirect genetic effects per Alexander I. Young, Seyed Moeen Nehzati, Chan Wook Lee, Stefania Benónísdóttir, David Cesarini, Daniel J. Benjamin, Patrick Turley, Augustine Kong

    Publicat 2020
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  6. 6
    Mendelian imputation of parental genotypes improves estimates of direct genetic effects

    Mendelian imputation of parental genotypes improves estimates of direct genetic effects per Alexander I. Young, Seyed Moeen Nehzati, Stefania Benónísdóttir, Aysu Okbay, Hariharan Jayashankar, Chan Wook Lee, David Cesarini, Daniel J. Benjamin, Patrick Turley, Augustine Kong

    Publicat 2022
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  7. 7
    Clinical utility of polygenic risk scores for embryo selection: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)

    Clinical utility of polygenic risk scores for embryo selection: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG) per Theresa A. Grebe, George Khushf, John M. Greally, Patrick Turley, Nastaran Foyouzi, Sara Rabin‐Havt, Benjamin E. Berkman, Kathleen Pope, Matteo Vatta, Shagun Kaur

    Publicat 2024
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  8. 8
    Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology

    Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology per Ying Wang, Masahiro Kanai, Taotao Tan, Mireille Kamariza, Kristin Tsuo, Kai Yuan, Wei Zhou, Yukinori Okada, Hailiang Huang, Patrick Turley, Elizabeth G. Atkinson, Alicia R. Martin

    Publicat 2023
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  9. 9
    Imprint of assortative mating on the human genome

    Imprint of assortative mating on the human genome per Loïc Yengo, Matthew R. Robinson, Matthew C. Keller, Kathryn E. Kemper, Yuanhao Yang, Maciej Trzaskowski, Jacob Gratten, Patrick Turley, David Cesarini, Daniel J. Benjamin, Naomi R. Wray, Michael E. Goddard, Jian Yang, Peter M. Visscher

    Publicat 2018
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  10. 10
    Problems with Using Polygenic Scores to Select Embryos

    Problems with Using Polygenic Scores to Select Embryos per Patrick Turley, Michelle N. Meyer, Nancy Wang, David Cesarini, Evelynn M. Hammonds, Alicia R. Martin, Benjamin M. Neale, Heidi L. Rehm, Louise Wilkins‐Haug, Daniel J. Benjamin, Steven E. Hyman, David Laibson, Peter M. Visscher

    Publicat 2021
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  11. 11
    Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries

    Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries per Zhili Zheng, Shouye Liu, Julia Sidorenko, Ying Wang, Tian Lin, Loïc Yengo, Patrick Turley, Alireza Ani, Rujia Wang, Ilja M. Nolte, Harold Snieder, Jian Yang, Naomi R. Wray, Michael E. Goddard, Peter M. Visscher, Jian Zeng

    Publicat 2024
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  12. 12
    Genetic basis of partner choice

    Genetic basis of partner choice per Qinwen Zheng, Sjoerd van Alten, Torkild Hovde Lyngstad, Edoardo Ciscato, Zhongxuan Sun, Jiacheng Miao, Yuchang Wu, Stephen Dorn, Boyan Zheng, Alexandra Havdahl, Elizabeth C. Corfield, Michel G. Nivard, T. J. Galama, Patrick Turley, Pierre‐André Chiappori, Jason M. Fletcher, Qiongshi Lu

    Publicat 2025
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  13. 13
    Multi-trait analysis of genome-wide association summary statistics using MTAG

    Multi-trait analysis of genome-wide association summary statistics using MTAG per Patrick Turley, Raymond K. Walters, Omeed Maghzian, Aysu Okbay, James J. Lee, Mark Alan Fontana, Tuan Anh Nguyen-Viet, Robbee Wedow, Meghan Zacher, Nicholas A. Furlotte, Patrik K. E. Magnusson, Sven Oskarsson, Magnus Johannesson, Peter M. Visscher, David Laibson, David Cesarini, Benjamin M. Neale, Daniel J. Benjamin

    Publicat 2017
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  14. 14
    Wrestling with Social and Behavioral Genomics: Risks, Potential Benefits, and Ethical Responsibility

    Wrestling with Social and Behavioral Genomics: Risks, Potential Benefits, and Ethical Responsibility per Michelle N. Meyer, Paul S. Appelbaum, Daniel J. Benjamin, Shawneequa Callier, Nathaniel Comfort, Dalton Conley, Jeremy Freese, Nanibaa’ A. Garrison, Evelynn M. Hammonds, K. Paige Harden, Sandra Soo‐Jin Lee, Alicia R. Martin, Daphne Oluwaseun Martschenko, Benjamin M. Neale, Rohan H. C. Palmer, James Tabery, Eric Turkheimer, Patrick Turley, Erik Parens

    Publicat 2023
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  15. 15
    Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes

    Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes per Amanda Elliott, Raymond K. Walters, Matti Pirinen, Mitja Kurki, Nella Junna, Jacqueline I. Goldstein, Mary Pat Reeve, Harri Siirtola, Susanna Lemmelä, Patrick Turley, Elisa Lahtela, Juha Mehtonen, Kadri Reis, Abdelrahman G. Elnahas, Anu Reigo, Priit Palta, Tõnu Esko, Reedik Mägi, Andres Metspalu, Mari Nelis, Lili Milani, Georgi Hudjashov, Haari Siirtola, Elisa Lahtinen, Aarno Palotie, Mark J. Daly, Elisabeth Widén

    Publicat 2024
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  16. 16
    Pan-UK Biobank GWAS improves discovery, analysis of genetic architecture, and resolution into ancestry-enriched effects

    Pan-UK Biobank GWAS improves discovery, analysis of genetic architecture, and resolution into ancestry-enriched effects per Konrad J. Karczewski, Rahul Gupta, Masahiro Kanai, Wenhan Lu, Kristin Tsuo, Ying Wang, Raymond K. Walters, Patrick Turley, Shawneequa Callier, Nirav N. Shah, Nikolas Baya, Duncan S. Palmer, Jacqueline I. Goldstein, Gopal Sarma, Matthew Solomonson, Nathan Cheng, Sam Bryant, Claire Churchhouse, Caroline Cusick, Timothy Poterba, John Compitello, Daniel A. King, Wei Zhou, Cotton Seed, Hilary K. Finucane, Mark J. Daly, Benjamin M. Neale, Elizabeth G. Atkinson, Alicia R. Martin

    Publicat 2024
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  17. 17
    Analysis of Shared Heritability in Common Disorders of the Brain

    Analysis of Shared Heritability in Common Disorders of the Brain per Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane, Raymond K. Walters, José Brás, Laramie E. Duncan, Valentina Escott‐Price, Guido J. Falcone, Padhraig Gormley, Rainer Malik, Nikolaos A. Patsopoulos, Stephan Ripke, Zhi Wei, Dongmei Yu, Paul H. Lee, Patrick Turley, Gerome Breen, Tracy Air, Cynthia M. Bulik, Mark J. Daly, Martin Dichgans, Stephen V. Faraone, Rita Guerreiro, Peter Holmans, Kenneth S. Kendler, Bobby P.C. Koeleman, C. Mathews, AL Price, JM Scharf, Pamela Sklar, Julie Williams, Nicholas Wood, Chris Cotsapas, Aarno Palotie, JW Smoller, Patrick F. Sullivan, Jonathan Rosand, Aiden Corvin, BM Neale

    Publicat 2016
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  18. 18
    Genomic analysis of diet composition finds novel loci and associations with health and lifestyle

    Genomic analysis of diet composition finds novel loci and associations with health and lifestyle per S. Fleur W. Meddens, Ronald de Vlaming, Peter N. Bowers, Casper A.P. Burik, Richard Karlsson Linnér, Chan Wook Lee, Aysu Okbay, Patrick Turley, Cornelius A. Rietveld, Mark Alan Fontana, Mohsen Ghanbari, Fumiaki Imamura, George McMahon, Peter J. van der Most, Trudy Voortman, Kaitlin H. Wade, Emma L. Anderson, Kim V.E. Braun, Pauline Emmett, Tõnu Esko, Juan R. González, Jessica C. Kiefte‐de Jong, Claudia Langenberg, Jian’an Luan, Taulant Muka, Susan M. Ring, Fernando Rivadeneira, Harold Snieder, Frank J.A. van Rooij, Bruce H. R. Wolffenbuttel, George Davey Smith, Oscar H. Franco, Nita G. Forouhi, M. Arfan Ikram, André G. Uitterlinden, Jana V. van Vliet‐Ostaptchouk, Nicholas J. Wareham, David Cesarini, K. Paige Harden, James J. Lee, Daniel J. Benjamin, Carson C. Chow, Philipp Koellinger

    Publicat 2020
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  19. 19
    Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity

    Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity per Veera M. Rajagopal, Andrea Ganna, Jonathan R. I. Coleman, Andrea G. Allegrini, Georgios Voloudakis, Jakob Grove, Thomas D. Als, Henriette Thisted Horsdal, Liselotte Petersen, Vivek Appadurai, Andrew J. Schork, Alfonso Buil, Cynthia M. Bulik, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, David M. Hougaard, Ole Mors, Merete Nordentoft, Thomas Werge, Rich Belliveau, Caitlin E. Carey, Felecia Cerrato, Kimberly Chambert, Tracy Air, Mark J. Daly, Ashley Dumont, Jacqueline I. Goldstein, Christine Søholm Hansen, Daniel P. Howrigan, Hailiang Huang, Julian Maller, Alicia R. Martin, Joanna Martin, Manuel Mattheisen, Jennifer L. Moran, Benjamin M. Neale, Jonatan Pallesen, Duncan S. Palmer, Carsten Bcker Pedersen, Marianne Giørtz Pedersen, Timothy Poterba, Stephan Ripke, F. Kyle Satterstrom, Wesley K. Thompson, Patrick Turley, Raymond K. Walters, Preben Bo Mortensen, Gerome Breen, Panos Roussos, Robert Plomin, Esben Agerbo, Anders D. Børglum, Ditte Demontis

    Publicat 2023
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  20. 20
    Common genetic variants associated with cognitive performance identified using the proxy-phenotype method

    Common genetic variants associated with cognitive performance identified using the proxy-phenotype method per Cornelius A. Rietveld, Tõnu Esko, Gail Davies, Tune H. Pers, Patrick Turley, Beben Benyamin, Christopher F. Chabris, Valur Emilsson, Andrew D. Johnson, James J. Lee, Christiaan de Leeuw, Riccardo E. Marioni, Sarah E. Medland, Michael B. Miller, Olga Rostapshova, Sven J. van der Lee, Anna A. E. Vinkhuyzen, Najaf Amin, Dalton Conley, Jaime Derringer, Cornelia M. van Duijn, Rudolf S.N. Fehrmann, Lude Franke, Edward L. Glaeser, Narelle K. Hansell, Caroline Hayward, William G. Iacono, Carla A. Ibrahim‐Verbaas, Vincent W. V. Jaddoe, Juha Karjalainen, David Laibson, Paul Lichtenstein, David C. Liewald, Patrik K. E. Magnusson, Nicholas G. Martin, Matt McGue, George McMahon, Nancy L. Pedersen, Steven Pinker, David J. Porteous, Daniëlle Posthuma, Fernando Rivadeneira, Blair H. Smith, John M. Starr, Henning Tiemeier, Nicholas J. Timpson, Maciej Trzaskowski, André G. Uitterlinden, Frank C. Verhulst, Mary E. Ward, Margaret J. Wright, George Davey Smith, Ian J. Deary, Magnus Johannesson, Robert Plomin, Peter M. Visscher, Daniel J. Benjamin, David Cesarini, Philipp Koellinger

    Publicat 2014
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