日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.

全外显子组测序揭示 HSPA1L 是自发性早产的遗传风险因素

Huusko Johanna M, Karjalainen Minna K, Graham Britney E, Zhang Ge, Farrow Emily G, Miller Neil A, Jacobsson Bo, Eidem Haley R, Murray Jeffrey C, Bedell Bruce, Breheny Patrick, Brown Noah W, Bødker Frans L, Litterman Nadia K, Jiang Pan-Pan, Russell Laura, Hinds David A, Hu Youna, Rokas Antonis, Teramo Kari, Christensen Kaare, Williams Scott M, Rämet Mika, Kingsmore Stephen F, Ryckman Kelli K, Hallman Mikko, Muglia Louis J

Genetic Associations with Gestational Duration and Spontaneous Preterm Birth

遗传因素与妊娠期和自发性早产的关系

Zhang, Ge; Feenstra, Bjarke; Bacelis, Jonas; Liu, Xueping; Muglia, Lisa M; Juodakis, Julius; Miller, Daniel E; Litterman, Nadia; Jiang, Pan-Pan; Russell, Laura; Hinds, David A; Hu, Youna; Weirauch, Matthew T; Chen, Xiaoting; Chavan, Arun R; Wagner, Günter P; Pavličev, Mihaela; Nnamani, Mauris C; Maziarz, Jamie; Karjalainen, Minna K; Rämet, Mika; Sengpiel, Verena; Geller, Frank; Boyd, Heather A; Palotie, Aarno; Momany, Allison; Bedell, Bruce; Ryckman, Kelli K; Huusko, Johanna M; Forney, Carmy R; Kottyan, Leah C; Hallman, Mikko; Teramo, Kari; Nohr, Ellen A; Davey Smith, George; Melbye, Mads; Jacobsson, Bo; Muglia, Louis J

GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci

对自我报告的蚊虫叮咬大小、瘙痒强度和对蚊子的吸引力进行全基因组关联分析表明,免疫相关的易感基因位点参与其中。

Jones, Amy V; Tilley, Mera; Gutteridge, Alex; Hyde, Craig; Nagle, Michael; Ziemek, Daniel; Gorman, Donal; Fauman, Eric B; Chen, Xing; Miller, Melissa R; Tian, Chao; Hu, Youna; Hinds, David A; Cox, Peter; Scollen, Serena

GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning person

对 89,283 名个体进行的全基因组关联研究 (GWAS) 发现了与自我报告为晨型人相关的遗传变异

Hu, Youna; Shmygelska, Alena; Tran, David; Eriksson, Nicholas; Tung, Joyce Y; Hinds, David A

Genome-wide association analysis of pain severity in dysmenorrhea identifies association at chromosome 1p13.2, near the nerve growth factor locus

全基因组关联分析发现,痛经的严重程度与1p13.2染色体上的神经生长因子基因座附近存在关联。

Jones, Amy V; Hockley, James R F; Hyde, Craig; Gorman, Donal; Sredic-Rhodes, Ana; Bilsland, James; McMurray, Gordon; Furlotte, Nicholas A; Hu, Youna; Hinds, David A; Cox, Peter J; Scollen, Serena

Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci

对 128,266 名个体进行的全基因组关联分析发现了新的晨型和睡眠时长相关基因位点

Jones, Samuel E; Tyrrell, Jessica; Wood, Andrew R; Beaumont, Robin N; Ruth, Katherine S; Tuke, Marcus A; Yaghootkar, Hanieh; Hu, Youna; Teder-Laving, Maris; Hayward, Caroline; Roenneberg, Till; Wilson, James F; Del Greco, Fabiola; Hicks, Andrew A; Shin, Chol; Yun, Chang-Ho; Lee, Seung Ku; Metspalu, Andres; Byrne, Enda M; Gehrman, Philip R; Tiemeier, Henning; Allebrandt, Karla V; Freathy, Rachel M; Murray, Anna; Hinds, David A; Frayling, Timothy M; Weedon, Michael N

RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data

RVTESTS:一种高效、全面的罕见变异关联分析工具,使用序列数据进行分析

Zhan, Xiaowei; Hu, Youna; Li, Bingshan; Abecasis, Goncalo R; Liu, Dajiang J

Loss-of-function mutations in APOC3, triglycerides, and coronary disease

APOC3功能丧失突变、甘油三酯和冠心病

Crosby, Jacy; Peloso, Gina M; Auer, Paul L; Crosslin, David R; Stitziel, Nathan O; Lange, Leslie A; Lu, Yingchang; Tang, Zheng-zheng; Zhang, He; Hindy, George; Masca, Nicholas; Stirrups, Kathleen; Kanoni, Stavroula; Do, Ron; Jun, Goo; Hu, Youna; Kang, Hyun Min; Xue, Chenyi; Goel, Anuj; Farrall, Martin; Duga, Stefano; Merlini, Pier Angelica; Asselta, Rosanna; Girelli, Domenico; Olivieri, Oliviero; Martinelli, Nicola; Yin, Wu; Reilly, Dermot; Speliotes, Elizabeth; Fox, Caroline S; Hveem, Kristian; Holmen, Oddgeir L; Nikpay, Majid; Farlow, Deborah N; Assimes, Themistocles L; Franceschini, Nora; Robinson, Jennifer; North, Kari E; Martin, Lisa W; DePristo, Mark; Gupta, Namrata; Escher, Stefan A; Jansson, Jan-Håkan; Van Zuydam, Natalie; Palmer, Colin N A; Wareham, Nicholas; Koch, Werner; Meitinger, Thomas; Peters, Annette; Lieb, Wolfgang; Erbel, Raimund; Konig, Inke R; Kruppa, Jochen; Degenhardt, Franziska; Gottesman, Omri; Bottinger, Erwin P; O'Donnell, Christopher J; Psaty, Bruce M; Ballantyne, Christie M; Abecasis, Goncalo; Ordovas, Jose M; Melander, Olle; Watkins, Hugh; Orho-Melander, Marju; Ardissino, Diego; Loos, Ruth J F; McPherson, Ruth; Willer, Cristen J; Erdmann, Jeanette; Hall, Alistair S; Samani, Nilesh J; Deloukas, Panos; Schunkert, Heribert; Wilson, James G; Kooperberg, Charles; Rich, Stephen S; Tracy, Russell P; Lin, Dan-Yu; Altshuler, David; Gabriel, Stacey; Nickerson, Deborah A; Jarvik, Gail P; Cupples, L Adrienne; Reiner, Alex P; Boerwinkle, Eric; Kathiresan, Sekar

Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol

全外显子组测序可识别与低密度脂蛋白胆固醇相关的罕见和低频编码变异。

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

The benefits of using genetic information to design prevention trials

利用基因信息设计预防试验的益处

Hu, Youna; Li, Li; Ehm, Margaret G; Bing, Nan; Song, Kijoung; Nelson, Matthew R; Talmud, Philippa J; Hingorani, Aroon D; Kumari, Meena; Kivimäki, Mika; Xu, Chun-Fang; Waterworth, Dawn M; Whittaker, John C; Abecasis, Gonçalo R; Spino, Cathie; Kang, Hyun Min