Результати пошуку - Priyanka Nandakumar

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  1. 1
    Biophysical and structural considerations for protein sequence evolution

    Biophysical and structural considerations for protein sequence evolution за авторством Johan A. Grahnen, Priyanka Nandakumar, Jan Kubelka, David A. Liberles

    Опубліковано 2011
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  2. 2
    MicroRNAs in the miR-17 and miR-15 families are downregulated in chronic kidney disease with hypertension

    MicroRNAs in the miR-17 and miR-15 families are downregulated in chronic kidney disease with hypertension за авторством Priyanka Nandakumar, Adrienne Tin, Megan L. Grove, Jianzhong Ma, Eric Boerwinkle, Josef Coresh, Aravinda Chakravarti

    Опубліковано 2017
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  3. 3
    Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation

    Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation за авторством Thomas J. Hoffmann, Georg Ehret, Priyanka Nandakumar, Dilrini K. Ranatunga, Catherine Schaefer, Pui‐Yan Kwok, Carlos Iribarren, Aravinda Chakravarti, Neil Risch

    Опубліковано 2016
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  4. 4
    Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett’s oesophagus and provides insights into clinical heterogeneity in reflux diagnosis

    Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett’s oesophagus and provides insights into clinical heter... за авторством Jue‐Sheng Ong, Jiyuan An, Xikun Han, Matthew H. Law, Priyanka Nandakumar, Johannes Schumacher, Ines Gockel, Anne C. Böhmer, Janusz Jankowski, Claire Palles, Catherine M. Olsen, Rachel Ε. Neale, Rebecca C. Fitzgerald, Aaron P. Thrift, Thomas L. Vaughan, Matthew F. Buas, David A Hinds, Puya Gharahkhani, Bradley J. Kendall, Stuart MacGregor

    Опубліковано 2021
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  5. 5
    <i>Trans</i>-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease

    <i>Trans</i>-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease за авторством Clara Sze-Man Tang, Hongsheng Gui, Ashish Kapoor, Jeong‐Hyun Kim, Berta Luzón‐Toro, Anna Pelet, Grzegorz Burzynski, Francesca Lantieri, Man-Ting So, Courtney Berrios, Hyoung Doo Shin, Raquel M. Fernández, Thuy-Linh Le, Joanne Verheij, Ivana Matera, Stacey S. Cherny, Priyanka Nandakumar, Hyun Sub Cheong, Guillermo Antiñolo, Jeanne Amiel, Jeong-Meen Seo, Dae Yeon Kim, Jung-Tak Oh, Stanislas Lyonnet, Salud Borrego, Isabella Ceccherini, Robert M.W. Hofstra, Aravinda Chakravarti, Hyun‐Young Kim, Pak C. Sham, Paul Tam, Maria‐Mercè Garcia‐Barceló

    Опубліковано 2016
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  6. 6
    Insights into the genetic basis of retinal detachment

    Insights into the genetic basis of retinal detachment за авторством Thibaud Boutin, David G. Charteris, Aman Chandra, Susan Campbell, Caroline Hayward, Archie Campbell, Priyanka Nandakumar, David A. Hinds, Danny Mitry, Véronique Vitart, Michelle Agee, Babak Alipanahi, Adam Auton, Robert K. Bell, Katarzyna Bryc, Sarah L. Elson, Pierre Fontanillas, Nicholas A. Furlotte, Barry Hicks, Karen E. Huber, Ethan M. Jewett, Yunxuan Jiang, Aaron Kleinman, Keng‐Han Lin, Nadia K. Litterman, Matthew H. McIntyre, Kimberly F. McManus, Joanna L. Mountain, Elizabeth S. Noblin, Carrie A. M. Northover, Steven J. Pitts, G. David Poznik, J. Fah Sathirapongsasuti, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Vladimir Vacic, Xin Wang, Catherine H. Wilson

    Опубліковано 2019
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  7. 7
    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 за авторством 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

    Опубліковано 2020
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  8. 8
    A population-specific reference panel for improved genotype imputation in African Americans

    A population-specific reference panel for improved genotype imputation in African Americans за авторством 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

    Опубліковано 2021
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  9. 9
    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 за авторством 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

    Опубліковано 2022
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  10. 10
    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 за авторством 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

    Опубліковано 2022
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  11. 11
    Genetic determinants of daytime napping and effects on cardiometabolic health

    Genetic determinants of daytime napping and effects on cardiometabolic health за авторством 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

    Опубліковано 2021
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  12. 12
    Genome-wide association study of musical beat synchronization demonstrates high polygenicity

    Genome-wide association study of musical beat synchronization demonstrates high polygenicity за авторством 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

    Опубліковано 2022
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  13. 13
    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 за авторством 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

    Опубліковано 2024
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  14. 14
    Analysis of rare Parkinson’s disease variants in millions of people

    Analysis of rare Parkinson’s disease variants in millions of people за авторством 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

    Опубліковано 2024
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  15. 15
    Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction

    Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction за авторством Barbara Schormair, Chen Zhao, Steven Bell, Maria Didriksen, Muhammad Sulaman Nawaz, Nathalie Schandra, Ambra Stefani, Birgit Högl, Yves Dauvilliers, Cornelius G. Bachmann, David Kemlink, Karel Šonka, Walter Paulus, Claudia Trenkwalder, Wolfgang H. Oertel, Magdolna Hornyak, Maris Teder‐Laving, Andres Metspalu, Georgios M. Hadjigeorgiou, Olli Polo, Ingo Fietze, Owen A. Ross, Zbigniew K. Wszołek, Abubaker Ibrahim, Melanie Bergmann, Volker Kittke, Philip Harrer, Joseph Dowsett, Sofiène Chenini, Sisse Rye Ostrowski, Erik Sørensen, Christian Erikstrup, Ole Birger Pedersen, Mie Topholm Bruun, Kaspar René Nielsen, Adam S. Butterworth, Nicole Soranzo, Willem H. Ouwehand, David J. Roberts, John Danesh, Brendan Burchell, Nicholas A. Furlotte, Priyanka Nandakumar, Amélie Bonnefond, Louis Potier, Christopher J. Earley, William G. Ondo, Lan Xiong, Alex Désautels, Markus Perola, Pavel Vodička, Christian Dina, Monika Stoll, André Franke, Wolfgang Lieb, Alexandre F.R. Stewart, Svati H. Shah, Christian Gieger, Annette Peters, David B. Rye, Guy A. Rouleau, Klaus Berger, Hreinn Stefánsson, Henrik Ullum, Hreinn Stefánsson, David A. Hinds, Emanuele Di Angelantonio, Konrad Oexle, Juliane Winkelmann

    Опубліковано 2024
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  16. 16
    Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy

    Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy за авторством Kristi Krebs, Jonas Bovijn, Neil S. Zheng, Maarja Lepamets, Jenny C. Censin, Tuuli Jürgenson, Dage Särg, Erik Abner, Triin Laisk, Yang Luo, Line Skotte, Frank Geller, Bjarke Feenstra, Wei Wang, Adam Auton, Soumya Raychaudhuri, Tõnu Esko, Andres Metspalu, Sven Laur, Dan M. Roden, Wei‐Qi Wei, Michael V. Holmes, Cecilia M. Lindgren, Elizabeth J. Phillips, Reedik Mägi, Lili Milani, João Fadista, Michelle Agee, Stella Aslibekyan, Robert K. Bell, Katarzyna Bryc, Sarah K. 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

    Опубліковано 2020
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  17. 17
    A new method for multiancestry polygenic prediction improves performance across diverse populations

    A new method for multiancestry polygenic prediction improves performance across diverse populations за авторством Haoyu Zhang, Jianan Zhan, Jin Jin, Jingning Zhang, Wenxuan Lu, Ruzhang Zhao, Thomas U. Ahearn, Zhi Yu, Jared O’Connell, Yunxuan Jiang, Tony Chen, Dayne Okuhara, 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, 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, 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, Montserrat García‐Closas, Xihong Lin, Bertram L. Koelsch, Nilanjan Chatterjee

    Опубліковано 2023
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  18. 18
    MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups

    MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups за авторством 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

    Опубліковано 2024
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  19. 19
    Genetic analyses identify widespread sex-differential participation bias

    Genetic analyses identify widespread sex-differential participation bias за авторством Nicola Pirastu, Mattia Cordioli, Priyanka Nandakumar, Gianmarco Mignogna, Abdel Abdellaoui, Benjamin Hollis, Masahiro Kanai, Veera M. Rajagopal, Pietro Della Briotta Parolo, Nikolas Baya, Caitlin E. Carey, Juha Karjalainen, Thomas D. Als, Matthijs D. van der Zee, Felix R. Day, Ken K. Ong, 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, Karen E. Huber, Ethan M. Jewett, Yunxuan Jiang, Aaron Kleinman, Keng‐Han Lin, Nadia K. Litterman, Marie K. Luff, Matthew H. McIntyre, Kimberly F. McManus, Joanna L. Mountain, Sahar V. Mozaffari, Elizabeth S. Noblin, Carrie A. M. Northover, Jared O’Connell, Aaron A. Petrakovitz, Steven J. Pitts, G. David Poznik, J. Fah Sathirapongsasuti, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Robert J. Tunney, Vladimir Vacic, Xin Wang, Amir Zare, Preben Bo Mortensen, Ole Mors, Thomas Werge, Merete Nordentoft, David M. Hougaard, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Takayuki Morisaki, Eco J. C. de Geus, Rino Bellocco, Yukinori Okada, Anders D. Børglum, Peter K. Joshi, Adam Auton, David A. Hinds, Benjamin M. Neale, Raymond K. Walters, Michel G. Nivard, John R. B. Perry, Andrea Ganna

    Опубліковано 2021
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  20. 20
    CADM2 is implicated in impulsive personality and numerous other traits by genome- and phenome-wide association studies in humans and mice

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    Опубліковано 2023
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    Artigo
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