Výsledky vyhledávání - Dan-Yu Lin

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  1. 1
    Meta-Analysis of Genome-wide Association Studies with Overlapping Subjects

    Meta-Analysis of Genome-wide Association Studies with Overlapping Subjects Autor Dan-Yu Lin, Patrick F. Sullivan

    Vydáno 2009
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    Artigo
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  2. 2
    A General Framework for Detecting Disease Associations with Rare Variants in Sequencing Studies

    A General Framework for Detecting Disease Associations with Rare Variants in Sequencing Studies Autor Dan-Yu Lin, Zheng-Zheng Tang

    Vydáno 2011
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    Artigo
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  3. 3
    Quantitative trait analysis in sequencing studies under trait-dependent sampling

    Quantitative trait analysis in sequencing studies under trait-dependent sampling Autor Dan-Yu Lin, Donglin Zeng, Zheng-Zheng Tang

    Vydáno 2013
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  4. 4
    Durability of XBB.1.5 Vaccines against Omicron Subvariants

    Durability of XBB.1.5 Vaccines against Omicron Subvariants Autor Dan-Yu Lin, Yi Du, Yangjianchen Xu, Sai Paritala, Matthew Donahue, Patrick Maloney

    Vydáno 2024
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    Carta
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  5. 5
    Effectiveness of Covid-19 Vaccines over a 9-Month Period in North Carolina

    Effectiveness of Covid-19 Vaccines over a 9-Month Period in North Carolina Autor Dan-Yu Lin, Yu Gu, Bradford Wheeler, Hayley A. Young, Shannon T. Holloway, Shadia-Khan Sunny, Zack Moore, Donglin Zeng

    Vydáno 2022
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  6. 6
    Nirmatrelvir or Molnupiravir Use and Severe Outcomes From Omicron Infections

    Nirmatrelvir or Molnupiravir Use and Severe Outcomes From Omicron Infections Autor Dan-Yu Lin, Francois Abi Fadel, Shuaiqi Huang, Alex Milinovich, Gretchen L. Sacha, Patricia Bartley, Abhijit Duggal, Xiaofeng Wang

    Vydáno 2023
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  7. 7
    The association between copy number aberration, DNA methylation and gene expression in tumor samples

    The association between copy number aberration, DNA methylation and gene expression in tumor samples Autor Wei Sun, Paul A. Bunn, Chong Jin, Paul Little, Vasyl Zhabotynsky, Charles M. Perou, D. Neil Hayes, Mengjie Chen, Dan-Yu Lin

    Vydáno 2018
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  8. 8
    Genetic Association Analysis under Complex Survey Sampling: The Hispanic Community Health Study/Study of Latinos

    Genetic Association Analysis under Complex Survey Sampling: The Hispanic Community Health Study/Study of Latinos Autor Dan-Yu Lin, Ran Tao, William D. Kalsbeek, Donglin Zeng, Franklyn Gonzalez, Lindsay Fernández‐Rhodes, Mariaelisa Graff, Gary G. Koch, Kari E. North, Gerardo Heiss

    Vydáno 2014
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  9. 9
    Common genetic variation in adiponectin, leptin, and leptin receptor and association with breast cancer subtypes

    Common genetic variation in adiponectin, leptin, and leptin receptor and association with breast cancer subtypes Autor Sarah J. Nyante, Marilie D. Gammon, Jay S. Kaufman, Jeannette T. Bensen, Dan Yu Lin, Jill S. Barnholtz‐Sloan, Yi‐Juan Hu, Qianchuan He, Jingchun Luo, Robert C. Millikan

    Vydáno 2011
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  10. 10
    Outcome prediction models in AQP4-IgG positive neuromyelitis optica spectrum disorders

    Outcome prediction models in AQP4-IgG positive neuromyelitis optica spectrum disorders Autor Jacqueline Palace, Dan-Yu Lin, Donglin Zeng, Masoud Majed, Liene Elsone, Shahd Hamid, Silvia Messina, Tatsuro Misu, Jessica Sagen, Daniel Whittam, Yoshiki Takai, Maria Isabel Leite, Brian G. Weinshenker, Philippe Cabre, Anu Jacob, Ichiro Nakashima, Kazuo Fujihara, Sean J. Pittock

    Vydáno 2019
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  11. 11
    A randomized, double-blind, placebo-controlled trial of ursodeoxycholic acid in primary biliary cirrhosis

    A randomized, double-blind, placebo-controlled trial of ursodeoxycholic acid in primary biliary cirrhosis Autor Burton Combes, Robert L. Carithers, Willis C. Maddrey, Dan-Yu Lin, Mary F. McDonald, Donald E. Wheeler, Edwin H. Eigenbrodt, Santiago J. Muñoz, Raphael Rubin, Guadalupe Garcı́a-Tsao, Gregory F. Bonner, A. Brian West, James L. Boyer, Velimir A. Luketic, Mitchell L. Shiffman, Scott A. Mills, Marion G. Peters, Heather M. White, Rowen K. Zetterman, Stephen S. Rossi, Alan F. Hofmann, Rodney S. Markin

    Vydáno 1995
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  12. 12
    Rare Exome Sequence Variants in <i>CLCN6</i> Reduce Blood Pressure Levels and Hypertension Risk

    Rare Exome Sequence Variants in <i>CLCN6</i> Reduce Blood Pressure Levels and Hypertension Risk Autor Bing Yu, Sara L. Pulit, Shih-Jen Hwang, Jennifer A. Brody, Najaf Amin, Paul L. Auer, Joshua C. Bis, Eric Boerwinkle, Gregory L. Burke, Aravinda Chakravarti, Adolfo Correa, Albert W. Dreisbach, Oscar H. Franco, Georg Ehret, Nora Franceschini, Albert Hofman, Dan-Yu Lin, Ginger Metcalf, Solomon K. Musani, Donna M. Muzny, Walter Palmas, Leslie J. Raffel, Alex P. Reiner, Kenneth Rice, Jerome I. Rotter, Narayanan Veeraraghavan, Ervin R. Fox, Xiuqing Guo, Kari E. North, Richard A. Gibbs, Cornelia M. van Duijn, Bruce M. Psaty, Daniel Levy, Christopher Newton‐Cheh, Alanna C. Morrison

    Vydáno 2015
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    Revisão
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  13. 13
    Genetic analyses of diverse populations improves discovery for complex traits

    Genetic analyses of diverse populations improves discovery for complex traits Autor Genevieve L. Wojcik, Mariaelisa Graff, Katherine K. Nishimura, Ran Tao, Jeffrey Haessler, Christopher R. Gignoux, Heather M. Highland, Yesha Patel, Elena P. Sorokin, Christy L. Avery, Gillian M. Belbin, Stephanie A. Bien, Iona Cheng, Sinéad Cullina, Chani J. Hodonsky, Yao Hu, Laura M. Huckins, Janina M. Jeff, Anne E. Justice, Jonathan Kocarnik, Unhee Lim, Bridget M. Lin, Yingchang Lu, Sarah C. Nelson, Sung-Shim L. Park, Hannah Poisner, Michael Preuß, Melissa A. Richard, Claudia Schurmann, Veronica Wendy Setiawan, Alexandra Sockell, Karan Vahi, Marie Verbanck, Abhishek Vishnu, Ryan W. Walker, Kristin L. Young, Niha Zubair, Victor Acuña-Alonso, José Luis Ambite, Kathleen C. Barnes, Eric Boerwinkle, Erwin P. Böttinger, Carlos D. Bustamante, Christian Caberto, Samuel Canizales‐Quinteros, Matthew P. Conomos, Ewa Deelman, Ron Do, Kimberly F. Doheny, Lindsay Fernández‐Rhodes, Myriam Fornage, Benyam Hailu, Gerardo Heiss, Brenna M. Henn, Lucia A. Hindorff, Rebecca D. Jackson, Cecelia Laurie, Cathy C. Laurie, Yuqing Li, Dan-Yu Lin, Andrés Moreno‐Estrada, Girish N. Nadkarni, Paul J. Norman, Loreall Pooler, Alexander P. Reiner, Jane Romm, Chiara Sabatti, Karla Sandoval, Xin Sheng, Eli A. Stahl, Daniel O. Stram, Timothy A. Thornton, Christina L. Wassel, Lynne R. Wilkens, Cheryl A. Winkler, Sachi Yoneyama, Steven Buyske, Christopher A. Haiman, Charles Kooperberg, Loı̈c Le Marchand, Ruth J. F. Loos, Tara C. Matise, Kari E. North, Ulrike Peters, Eimear E. Kenny, Christopher S. Carlson

    Vydáno 2019
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  14. 14
    Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

    Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture Autor Sonja I. Berndt, Stefan Gustafsson, Reedik Mägi, Andrea Ganna, Eleanor Wheeler, Mary F. Feitosa, Anne E. Justice, Keri L. Monda, Damien C. Croteau‐Chonka, Felix R. Day, Tõnu Esko, Tove Fall, Teresa Ferreira, Davide Gentilini, Anne Jackson, Jian’an Luan, Joshua C. Randall, Sailaja Vedantam, Cristen J. Willer, Thomas W. Winkler, Andrew R. Wood, Tsegaselassie Workalemahu, Yi‐Juan Hu, Sang Lee, Liming Liang, Dan-Yu Lin, Josine L. Min, Benjamin M. Neale, Guðmar Þorleifsson, Jian Yang, Eva Albrecht, Najaf Amin, Jennifer L. Bragg‐Gresham, Gemma Cadby, Martin den Heijer, Niina Eklund, Krista Fischer, Anuj Goel, Jouke‐Jan Hottenga, Jennifer E. Huffman, Ivonne Jarick, Åsa Johansson, Toby Johnson, Stavroula Kanoni, Marcus E. Kleber, Inke R. König, Kati Kristiansson, Zoltán Kutalik, Claudia Lamina, Cécile Lecœur, Li Guo, Massimo Mangino, Wendy L. McArdle, Carolina Medina‐Gómez, Martina Müller‐Nurasyid, Julius S. Ngwa, Ilja M. Nolte, Lavinia Paternoster, Sonali Pechlivanis, Markus Perola, Marjolein J. Peters, Michael Preuß, Lynda M. Rose, Jianxin Shi, Dmitry Shungin, Albert V. Smith, Rona J. Strawbridge, Ida Surakka, Alexander Teumer, Mieke D. Trip, Jonathan P. Tyrer, Jana V. van Vliet‐Ostaptchouk, Liesbeth Vandenput, Lindsay L. Waite, Wei Zhao, Devin Absher, Folkert W. Asselbergs, Mustafa Atalay, Antony Attwood, Anthony J. Balmforth, Hanneke Basart, John Beilby, Lori L. Bonnycastle, Paolo Brambilla, Marcel Bruinenberg, Harry Campbell, Daniel I. Chasman, Peter S. Chines, Francis S. Collins, John Connell, William Cookson, Ulf dé Fairé, Femmie de Vegt, Mariano Dei, Maria Dimitriou, Sarah Edkins, Karol Estrada, David M. Evans, Martin Farrall, Maurizio Ferrario

    Vydáno 2013
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  15. 15
    Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

    Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol Autor Leslie A. Lange, Youna Hu, He Zhang, Chenyi Xue, Ellen M. Schmidt, Zheng-Zheng Tang, Chris Bizon, Ethan M. Lange, Joshua D. Smith, Emily H. Turner, Goo Jun, Hyun Min Kang, Gina M. Peloso, Paul L. Auer, Kuo-ping Li, Jason Flannick, Ji Zhang, Christian Fuchsberger, Kyle J. Gaulton, Cecilia M. Lindgren, Adam E. Locke, Alisa K. Manning, Xueling Sim, Manuel A. Rivas, Oddgeir L. Holmen, Omri Gottesman, Yingchang Lu, Douglas M. Ruderfer, Eli A. Stahl, Qing Duan, Yun Li, Peter Durda, Shuo Jiao, Aaron Isaacs, Albert Hofman, Joshua C. Bis, Adolfo Correa, Michael Griswold, Jóhanna Jakobsdóttir, Albert V. Smith, Pamela J. Schreiner, Mary F. Feitosa, Qunyuan Zhang, Jennifer E. Huffman, Jacy R. Crosby, Christina L. Wassel, Ron Do, Nora Franceschini, Lisa W. Martin, Jennifer G. Robinson, Themistocles L. Assimes, David R. Crosslin, Elisabeth A. Rosenthal, Michael Y. Tsai, Mark J. Rieder, Deborah Farlow, Aaron R. Folsom, Thomas Lumley, Ervin R. Fox, Christopher S. Carlson, Ulrike Peters, Rebecca D. Jackson, Cornelia M. van Duijn, André G. Uitterlinden, Daniel Levy, Jerome I. Rotter, Herman A. Taylor, Vilmundur Guðnason, David S. Siscovick, Myriam Fornage, Ingrid B. Borecki, Caroline Hayward, Igor Rudan, Y. Eugene Chen, Erwin P. Böttinger, Ruth J. F. Loos, Pål Sætrom, Kristian Hveem, Michael Boehnke, Leif Groop, Mark I. McCarthy, Thomas Meitinger, Christie M. Ballantyne, Stacey Gabriel, Christopher J. O’Donnell, Wendy S. Post, Kari E. North, Alexander P. Reiner, Eric Boerwinkle, Bruce M. Psaty, David Altshuler, Sekar Kathiresan, Dan-Yu Lin, Gail P. Jarvik, L. Adrienne Cupples, Charles Kooperberg, James G. Wilson, Deborah A. Nickerson, Gonçalo R. Abecasis, Stephen S. Rich

    Vydáno 2014
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