Torthaí cuardaigh - Dan-Yu Lin
- 1 - 15 toradh as 15 á dtaispeáint
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1
Meta-Analysis of Genome-wide Association Studies with Overlapping Subjects de réir Dan-Yu Lin, Patrick F. Sullivan
Foilsithe / Cruthaithe 2009Artigo -
2
A General Framework for Detecting Disease Associations with Rare Variants in Sequencing Studies de réir Dan-Yu Lin, Zheng-Zheng Tang
Foilsithe / Cruthaithe 2011Artigo -
3
Quantitative trait analysis in sequencing studies under trait-dependent sampling de réir Dan-Yu Lin, Donglin Zeng, Zheng-Zheng Tang
Foilsithe / Cruthaithe 2013Artigo -
4
Durability of XBB.1.5 Vaccines against Omicron Subvariants de réir Dan-Yu Lin, Yi Du, Yangjianchen Xu, Sai Paritala, Matthew Donahue, Patrick Maloney
Foilsithe / Cruthaithe 2024Carta -
5
Effectiveness of Covid-19 Vaccines over a 9-Month Period in North Carolina de réir Dan-Yu Lin, Yu Gu, Bradford Wheeler, Hayley A. Young, Shannon T. Holloway, Shadia-Khan Sunny, Zack Moore, Donglin Zeng
Foilsithe / Cruthaithe 2022Artigo -
6
Nirmatrelvir or Molnupiravir Use and Severe Outcomes From Omicron Infections de réir Dan-Yu Lin, Francois Abi Fadel, Shuaiqi Huang, Alex Milinovich, Gretchen L. Sacha, Patricia Bartley, Abhijit Duggal, Xiaofeng Wang
Foilsithe / Cruthaithe 2023Artigo -
7
The association between copy number aberration, DNA methylation and gene expression in tumor samples de réir Wei Sun, Paul A. Bunn, Chong Jin, Paul Little, Vasyl Zhabotynsky, Charles M. Perou, D. Neil Hayes, Mengjie Chen, Dan-Yu Lin
Foilsithe / Cruthaithe 2018Artigo -
8
Genetic Association Analysis under Complex Survey Sampling: The Hispanic Community Health Study/Study of Latinos de réir 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
Foilsithe / Cruthaithe 2014Artigo -
9
Common genetic variation in adiponectin, leptin, and leptin receptor and association with breast cancer subtypes de réir 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
Foilsithe / Cruthaithe 2011Artigo -
10
Outcome prediction models in AQP4-IgG positive neuromyelitis optica spectrum disorders de réir 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
Foilsithe / Cruthaithe 2019Artigo -
11
A randomized, double-blind, placebo-controlled trial of ursodeoxycholic acid in primary biliary cirrhosis de réir 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
Foilsithe / Cruthaithe 1995Artigo -
12
Rare Exome Sequence Variants in <i>CLCN6</i> Reduce Blood Pressure Levels and Hypertension Risk de réir 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
Foilsithe / Cruthaithe 2015Revisão -
13
Genetic analyses of diverse populations improves discovery for complex traits de réir 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
Foilsithe / Cruthaithe 2019Artigo -
14
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture de réir 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
Foilsithe / Cruthaithe 2013Artigo -
15
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol de réir 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
Foilsithe / Cruthaithe 2014Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Medicine
Biology
Genetics
Gene
Internal medicine
Genotype
Single-nucleotide polymorphism
Computational biology
Computer science
Genetic association
Disease
Environmental health
Exome
Exome sequencing
Genome-wide association study
Immunology
Mathematics
Meta-analysis
Mutation
Population
Quantitative trait locus
Statistics
Cancer
Cohort
Confidence interval
Coronavirus disease 2019 (COVID-19)
Endocrinology
Evolutionary biology
Genetic architecture
Genome