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

Racial and socioeconomic disparities in genetic evaluation and testing in the adult patient population

成人患者群体中基因评估和检测的种族和社会经济差异

Gold, Jessica I; Elkaim, Yehuda; Gold, Nina B; Asher, Stephanie; Raper, Anna; Condit, Courtney; Bogus, Zoe; Elysee, Isaac; Hennessy, Laura; Kennedy, Emma; Briere, Lauren C; Sweetser, David A; Kripke, Colleen; Verma, Anurag; Salmasian, Hojjat; Landry, Latrice; Nathanson, Katherine L; Kallish, Staci; Drivas, Theodore G

Electronic Health Records to Test Multimorbidity Influences to Plasma Biomarker Interpretation for Alzheimer's Disease

利用电子健康记录检验多种疾病共存对阿尔茨海默病血浆生物标志物解读的影响

Cousins, Katheryn A Q; Boyle, Rory; Morse, Colleen; Verma, Anurag; Brown, Christopher A; O'Brien, Kyra S; Serper, Marina; Dehghani, Nadia; McMillan, Corey T; Lee, Edward B; Shaw, Leslie M; Wolk, David A

DRIVE-KG: Enhancing variant-phenotype association discovery in understudied complex diseases using heterogeneous knowledge graphs

DRIVE-KG:利用异构知识图谱增强对研究不足的复杂疾病中变异-表型关联的发现

Rajagopalan, Ananya; Nguyen, Tram Anh; Guare, Lindsay A; Rico, Andre Luis Garao; Venkatesh, Rasika; Caruth, Lannawill; Genetics Center, Regeneron; Medicine BioBank, Penn; Verma, Anurag; Ritchie, Marylyn D; Hall, Molly A; Romano, Joseph D; Setia-Verma, Shefali

Protein nano-bioactives against microgravity-induced endothelial dysfunction

蛋白质纳米生物活性物质对抗微重力诱导的内皮功能障碍

Kabir, Anisha; B, Mukilarasi; Manohar, Anagha; Gadani, Maulesh; Sinha, Anurag Kumar; Sharma, Payal; Verma, Anurag; Selvaraj, Vimalraj; Sudhakar, Swathi

SAIGE-GPU: accelerating genome- and phenome-wide association studies using GPUs

SAIGE-GPU:利用GPU加速全基因组和全表型关联研究

Rodriguez, Alex; Kim, Youngdae; Nandi, Tarak Nath; Keat, Karl; Kumar, Rachit; Conery, Mitchell; Bhukar, Rohan; Liu, Molei; Hessington, John; Maheshwari, Ketan; Begoli, Edmon; Tourassi, Georgia; Muralidhar, Sumitra; Natarajan, Pradeep; Voight, Benjamin F; Cho, Kelly; Gaziano, John Michael; Damrauer, Scott M; Liao, Katherine P; Zhou, Wei; Huffman, Jennifer E; Verma, Anurag; Madduri, Ravi K

An African ancestry-specific nonsense variant in CD36 is associated with a higher risk of dilated cardiomyopathy

CD36基因中一种非洲裔特异性无义变异与扩张型心肌病风险升高相关。

Huffman, Jennifer E; Gaziano, Liam; Al Sayed, Zeina R; Judy, Renae L; Raffield, Laura M; Biddinger, Kiran J; Charest, Brian; Chopra, Anant; Gagnon, David; Guo, Xiuqing; Koledova, Vera; Levin, Michael G; Min, Yuan-I; Pirruccello, James P; Reza, Nosheen; Ruan, Richard; Verma, Shefali Setia; Venkatesh, Bharath Ambale; Verma, Anurag; Yao, Jie; Carr, John Jeffrey; Casas, Juan P; Cho, Kelly; Lima, Joao A C; Post, Wendy S; Rader, Daniel J; Ritchie, Marylyn D; Shah, Amil; Taylor, Kent D; Terry, James G; Rich, Stephen S; O'Donnell, Christopher J; Phillips, Lawrence S; Lunetta, Kathryn L; Rotter, Jerome I; Wilson, Peter W F; Gaziano, J Michael; Damrauer, Scott M; Sun, Yan V; Ellinor, Patrick T; Joseph, Jacob; Aragam, Krishna G

Genetically-determined variation in CRP impacts disease activity assessment in rheumatoid arthritis

遗传决定的CRP变异会影响类风湿性关节炎的疾病活动度评估

Riley, Thomas R; Wheeler, Austin M; Cannon, Grant W; Sauer, Brian; Wysham, Katherine D; England, Bryant R; Wipfler, Kristin; Michaud, Kaleb; March, Michael; Damrauer, Scott M; Verma, Anurag; George, Michael D; Mikuls, Ted R; Baker, Joshua F

Reduced order computational fluid dynamic simulations in the thoracic aorta are associated with disease recorded in a medical biobank

胸主动脉的降阶计算流体动力学模拟与医学生物样本库中记录的疾病相关

Sokolow, Ryan; Bhattacharya, Anindro; Kissas, Georgios; Thompson, Elizabeth W; Beeche, Cameron; Swago, Sophia; Zhang, David; Viswanadha, Mukund; Morse, Colleen; Chirinos, Julio; Damrauer, Scott; Verma, Anurag; Perdikaris, Paris; Rader, Daniel J; Witschey, Walter R

Rapid identification and phenotyping of nonalcoholic fatty liver disease patients using a machine-based approach in diverse healthcare systems

利用基于机器的方法在不同的医疗保健系统中快速识别和表型分析非酒精性脂肪肝患者

Basile, Anna O; Verma, Anurag; Tang, Leigh Anne; Serper, Marina; Scanga, Andrew; Farrell, Ava; Destin, Brittney; Carr, Rotonya M; Anyanwu-Ofili, Anuli; Rajagopal, Gunaretnam; Krikhely, Abraham; Bessler, Marc; Reilly, Muredach P; Ritchie, Marylyn D; Tatonetti, Nicholas P; Wattacheril, Julia