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

Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases

全球多族裔全基因组分析鉴定出与甲状腺癌和良性甲状腺疾病相关的基因和生物学通路

White, Samantha L; Brasher, Maizy S; Pattee, Jack; Zhou, Wei; Chapman, Sinéad; Jee, Yon Ho; Bell, Caitlin C; Jamil, Taylor L; Barrio, Martin; Arehart, Christopher H; Evans, Luke M; Hirbo, Jibril; Cox, Nancy J; Straub, Peter; Namba, Shinichi; Bertucci-Richter, Emily; Guare, Lindsay; Edris, Ahmed; Morris, Sam; Mulford, Ashley J; Zhang, Haoyu; Fennessy, Brian; Tobin, Martin D; Chen, Jing; Williams, Alexander T; John, Catherine; van Heel, David A; Mathur, Rohini; Finer, Sarah; Moksnes, Marta R; Brumpton, Ben M; Åsvold, Bjørn Olav; Peculis, Raitis; Rovite, Vita; Konrade, Ilze; Wang, Ying; Crooks, Kristy; Chavan, Sameer; Fisher, Matthew J; Rafaels, Nicholas; Lin, Meng; Shortt, Jonathan A; Sanders, Alan R; Whiteman, David C; MacGregor, Stuart; Medland, Sarah E; Thorsteinsdóttir, Unnur; Stefánsson, Kári; Karaderi, Tugce; Egan, Kathleen M; Bocklage, Therese; McCrary, Hilary C; Riedlinger, Gregory; Salhia, Bodour; Shriver, Craig; Phan, Minh D; Farlow, Janice L; Edge, Stephen; Kaur, Varinder; Churchman, Michelle L; Rounbehler, Robert J; Brock, Pamela L; Ringel, Matthew D; Pividori, Milton; Schweppe, Rebecca; Raeburn, Christopher D; Walters, Robin G; Chen, Zhengming; Li, Liming; Matsuda, Koichi; Okada, Yukinori; Zöllner, Sebastian; Verma, Anurag; Preuss, Michael H; Kenny, Eimear; Hendricks, Audrey E; Fishbein, Lauren; Kraft, Peter; Daly, Mark J; Neale, Benjamin M; Martin, Alicia R; Cole, Joanne B; Haugen, Bryan R; Gignoux, Christopher R; Pozdeyev, Nikita

Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction.

主动脉狭窄的基因组学和转录组学分析有助于发现治疗靶点和预测疾病。

Small Aeron M, Yang Ta-Yu, Itoh Shinsuke, Thériault Sébastien, Dufresne Line, Kurosawa Ryo, Komuro Issei, Matsuda Koichi, Vy Ha My T, Farber-Eger Eric H, Shaffer Lauren Lee, Boulier Kristin M, Corey Kristin M, Ramaker Megan E, Laporte Fabien, Schott Jean-Jacques, Le Scouarnec Solena, Singh Sasha A, Sonawane Abhijeet R, Smith Harry A, Rafaels Nicholas, Ghouse Jonas, Raja Anna A, Ostrowski Sisse R, Sørensen Erik, Mikkelsen Christina, Pedersen Ole B, Erikstrup Christian, Ullum Henrik, Sveinbjornsson Gardar, Gudbjartsson Daniel F, Abner Erik, Lee Jiwoo, Ganna Andrea, Nowak-Göttl Ulrike, Finer Sarah, Schumacher Johannes, Maj Carlo, Al-Kassou Baravan, Nickenig Georg, Trenkwalder Teresa, Dreβen Martina, Krane Markus, Nöthen Markus M, Moksnes Marta R, Brumpton Ben M, Knight Stacey, Knowlton Kirk U, Nadauld Lincoln, Debiec Radek, Musameh Muntaser D, Braund Peter S, Nelson Christopher P, Czuba Tomasz, Melander Olle, Selvaraj Margaret Sunitha, Koyama Satoshi, Bhukar Rohan, Ruan Yunfeng, Ljungberg Johan, Damrauer Scott M, Levin Michael G, Franke Andre, Berger Klaus, Ruff Christian T, Melloni Giorgio E M, Kamanu Frederick K, Ito Kaoru, Do Ron, Loos Ruth J F, Schunkert Heribert, Wells Quinn S, Shah Svati H, Le Tourneau Thierry, Messika-Zeitoun David, Gignoux Christopher, Bundgaard Henning, Larsson Susanna C, Michaëlsson Karl, Holm Hilma, Helgadottir Anna, Esko Tonu, van Heel David A, Mathieu Patrick, Samani Nilesh J, Smith J Gustav, Söderberg Stefan, Rader Daniel J, Marston Nicholas A, Sabatine Marc S, Pasaniuc Bogdan, Cho Kelly, Wilson Peter W F, O'Donnell Christopher J, Stefansson Kari, Bossé Yohan, Aikawa Elena, Engert James C, Peloso Gina M, Natarajan Pradeep, Thanassoulis George

Polygenic risk score for type 2 diabetes shows context-dependent effects across populations

2型糖尿病的多基因风险评分在不同人群中表现出情境依赖性效应

Guo, Boya; Cai, Yanwei; Kim, Daeeun; Smit, Roelof A J; Wang, Zhe; Iyer, Kruthika R; Hilliard, Austin T; Haessler, Jeffrey; Tao, Ran; Broadaway, K Alaine; Wang, Yujie; Pozdeyev, Nikita; Stæger, Frederik F; Yang, Chaojie; Vanderwerff, Brett; Patki, Amit D; Stalbow, Lauren; Lin, Meng; Rafaels, Nicholas; Shortt, Jonathan; Wiley, Laura; Stanislawski, Maggie; Pattee, Jack; Davis, Lea; Straub, Peter S; Shuey, Megan M; Cox, Nancy J; Lee, Nanette R; Jørgensen, Marit E; Bjerregaard, Peter; Larsen, Christina; Hansen, Torben; Moltke, Ida; Meigs, James B; Stram, Daniel O; Yin, Xianyong; Zhou, Xiang; Chang, Kyong-Mi; Clarke, Shoa L; Guarischi-Sousa, Rodrigo; Lankester, Joanna; Tsao, Philip S; Buyske, Steven; Graff, Mariaelisa; Raffield, Laura M; Sun, Quan; Wilkens, Lynne R; Carlson, Christopher S; Easton, Charles B; Liu, Simin; Manson, JoAnn E; Marchand, Loïc L; Haiman, Christopher A; Mohlke, Karen L; Gordon-Larsen, Penny; Albrechtsen, Anders; Boehnke, Michael; Rich, Stephen S; Manichaikul, Ani; Rotter, Jerome I; Yousri, Noha A; Irvin, Ryan M; Gignoux, Chris; North, Kari E; Loos, Ruth J F; Assimes, Themistocles L; Peters, Ulrike; Kooperberg, Charles; Raghavan, Sridharan; Highland, Heather M; Darst, Burcu F

Prevalence of Actionable Exposures to Pharmacogenetic Medications Among Solid Organ Transplant Recipients in a Population-Scale Biobank

在人群规模生物样本库中,实体器官移植受者接触可采取行动的药物遗传学药物的患病率

Radwan, Alaa; Deininger, Kimberly M; Ambardekar, Amrut V; Anderson, Heather D; Rafaels, Nicholas; Saba, Laura M; The Colorado Center For Personalized Medicine; Aquilante, Christina L

Prediction and Characterization of Genetically Regulated Expression of Target Tissues in Asthma

哮喘靶组织基因调控表达的预测与表征

Slack, Sarah D; Esquinca, Erika; Arehart, Christopher H; Boorgula, Meher Preethi; Szczesny, Brooke; Romero, Alex; Campbell, Monica; Chavan, Sameer; Rafaels, Nicholas; Watson, Harold; Landis, R Clive; Hansel, Nadia N; Rotimi, Charles N; Olopade, Christopher O; Figueiredo, Camila A; Ober, Carole; Liu, Andrew H; Kenny, Eimear E; Kammers, Kai; Ruczinski, Ingo; Taub, Margaret A; Daya, Michelle; Gignoux, Christopher R; Kechris, Katerina; Barnes, Kathleen C; Mathias, Rasika A; Johnson, Randi K

Enabling reproducible type 1 diabetes polygenic risk scoring for clinical and translational applications

实现可重复的 1 型糖尿病多基因风险评分,以用于临床和转化应用

Brasher, Maizy S; Fisher, Matthew J; Wild, Carolina Sanchez; Shortt, Jonathan A; Miller, Krista; Johnson, Randi K; Rafaels, Nicholas M; Kudron, Elizabeth L; Brooks, Ian M; Crooks, Kristy R; Oser, Sean M; Oser, Tamara K; Cole, Joanne B; Wiley, Laura K; Raghavan, Sridharan; Rasouli, Neda; Lin, Meng; Gignoux, Christopher R

Chromosome 21 variants tied to severe asthma exacerbations: A genome-wide association study in a Brazilian population

21号染色体变异与严重哮喘急性发作相关:一项巴西人群的全基因组关联研究

de Santana, Maria B R; Cruz, Álvaro A; Teixeira, Helena M P; Silva, Hatilla Dos S; Abdel-Aziz, Mahmoud I; Hashimoto, Simone; Vijverberg, Susanne J H; Herrera-Luis, Esther; Pino-Yanes, Maria; Burchard, Esteban G; Chung, Kian Fan; Djukanovic, Ratko; Dahlén, Sven-Erik; Adcock, Ian M; Cox, Corey; Brunetti, Tonya; Campbell, Monica; Rafaels, Nicholas; Barnes, Kathleen C; Maitland-van der Zee, Anke H; Figueiredo, Camila A; Costa, Ryan S

Global multi-ancestry genetic study elucidates genes and biological pathways associated with thyroid cancer and benign thyroid diseases

全球多民族遗传学研究阐明了与甲状腺癌和良性甲状腺疾病相关的基因和生物学通路

White, Samantha L; Brasher, Maizy S; Pattee, Jack; Zhou, Wei; Chapman, Sinéad; Jee, Yon Ho; Bell, Caitlin C; Jamil, Taylor L; Barrio, Martin; Hirbo, Jibril; Cox, Nancy J; Straub, Peter; Namba, Shinichi; Bertucci-Richter, Emily; Guare, Lindsay; EdrisMohammed, Ahmed; Morris, Sam; Mulford, Ashley J; Zhang, Haoyu; Fennessy, Brian; Tobin, Martin D; Chen, Jing; Williams, Alexander T; John, Catherine; van Heel, David A; Mathur, Rohini; Finer, Sarah; Moksnes, Marta Riise; Brumpton, Ben; Åsvold, Bjørn Olav; Peculis, Raitis; Rovite, Vita; Konrade, Ilze; Wang, Ying; Crooks, Kristy; Chavan, Sameer; Fisher, Matthew J; Rafaels, Nicholas; Lin, Meng; Shortt, Jonathan; Sanders, Alan R; Whiteman, David; MacGregor, Stuart; Medland, Sarah; Thorsteinsdóttir, Unnur; Stefánsson, Kári; Karaderi, Tugce; Egan, Kathleen M; Bocklage, Therese; McCrary, Hilary C; Riedlingeer, Greg; Salhia, Bodour; Shriver, Craig; Phan, Minh D; Farlow, Janice L; Edge, Stephen; Kaur, Varinder; Churchman, Michelle; Rounbehler, Robert J; Brock, Pamela L; Ringel, Matthew D; Pividori, Milton; Schweppe, Rebecca; Raeburn, Christopher D; Walters, Robin; Chen, Zhengming; Li, Liming; Matsuda, Koichi; Okada, Yukinori; Zoellner, Sebastian; Verma, Anurag; Preuss, Michael; Kenny, Eimear; Hendricks, Audrey; Fishbein, Lauren; Kraft, Peter; Daly, Mark; Neale, Benjamin; Martin, Alicia; Cole, Joanne B; Haugen, Bryan R; Gignoux, Christopher R; Pozdeyev, Nikita

Novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferation

新的祖先特异性原发性开角型青光眼基因位点及其与血管机制和细胞增殖的共同生物学特征

Lo Faro, Valeria; Bhattacharya, Arjun; Zhou, Wei; Zhou, Dan; Wang, Ying; Läll, Kristi; Kanai, Masahiro; Lopera-Maya, Esteban; Straub, Peter; Pawar, Priyanka; Tao, Ran; Zhong, Xue; Namba, Shinichi; Sanna, Serena; Nolte, Ilja M; Okada, Yukinori; Ingold, Nathan; MacGregor, Stuart; Snieder, Harold; Surakka, Ida; Shortt, Jonathan; Gignoux, Chris; Rafaels, Nicholas; Crooks, Kristy; Verma, Anurag; Verma, Shefali S; Guare, Lindsay; Rader, Daniel J; Willer, Cristen; Martin, Alicia R; Brantley, Milam A Jr; Gamazon, Eric R; Jansonius, Nomdo M; Joos, Karen; Cox, Nancy J; Hirbo, Jibril

Building a vertically integrated genomic learning health system: The biobank at the Colorado Center for Personalized Medicine

构建垂直整合的基因组学习健康系统:科罗拉多州个性化医疗中心的生物样本库

Wiley, Laura K; Shortt, Jonathan A; Roberts, Emily R; Lowery, Jan; Kudron, Elizabeth; Lin, Meng; Mayer, David; Wilson, Melissa; Brunetti, Tonya M; Chavan, Sameer; Phang, Tzu L; Pozdeyev, Nikita; Lesny, Joseph; Wicks, Stephen J; Moore, Ethan T; Morgenstern, Joshua L; Roff, Alanna N; Shalowitz, Elise L; Stewart, Adrian; Williams, Cole; Edelmann, Michelle N; Hull, Madelyne; Patton, J Tacker; Axell, Lisen; Ku, Lisa; Lee, Yee Ming; Jirikowic, Jean; Tanaka, Anna; Todd, Emily; White, Sarah; Peterson, Brett; Hearst, Emily; Zane, Richard; Greene, Casey S; Mathias, Rasika; Coors, Marilyn; Taylor, Matthew; Ghosh, Debashis; Kahn, Michael G; Brooks, Ian M; Aquilante, Christina L; Kao, David; Rafaels, Nicholas; Crooks, Kristy R; Hess, Steve; Barnes, Kathleen C; Gignoux, Christopher R