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

Concomitant COX-1 and COX-2 suppression is not sufficient to induce enteropathy associated with chronic NSAID use

同时抑制COX-1和COX-2不足以诱发与长期使用非甾体抗炎药相关的肠病。

Barekat, Kayla; Ghosh, Soumita; Herrmann, Christin; Keat, Karl; Assenmacher, Charles-Antoine; Tanes, Ceylan; Wilson, Naomi; Lordan, Ronan; Mrčela, Antonijo; Rauova, Lubica; Sengupta, Arjun; Das, Ujjalkumar Subhash; Joshi, Robin; Friedman, Elliot; Ritchie, Marylyn D; Bittinger, Kyle; Weljie, Aalim; Cadwell, Ken; Bushman, Frederic D; Wu, Gary D; FitzGerald, Garret A; Ricciotti, Emanuela

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

Integrating Imaging-Derived Clinical Endotypes with Plasma Proteomics and External Polygenic Risk Scores Enhances Coronary Microvascular Disease Risk Prediction

将影像衍生的临床内型与血浆蛋白质组学和外部多基因风险评分相结合,可提高冠状动脉微血管疾病风险预测的准确性。

Venkatesh, Rasika; Cherlin, Tess; BioBank, Penn Medicine; Ritchie, Marylyn D; Guerraty, Marie A; Verma, Shefali S

Integrating Polygenic Scores with Clinical, Lifestyle, and Social Risk Factors to Improve Heart Failure Risk Prediction

将多基因评分与临床、生活方式和社会风险因素相结合,以提高心力衰竭风险预测的准确性

Cardone, Katie M; Kim, Dokyoon; Ritchie, Marylyn D

A random-walk-based learning framework to uncover novel gene candidates for Alzheimer's disease therapy

基于随机游走的学习框架,用于发现阿尔茨海默病治疗的新基因候选者

Orlenko, Alena; Li, Binglan; Khanjani, Neda; Venkatesan, Mythreye; Shen, Li; Ritchie, Marylyn D; Wang, Zhiping Paul; Obafemi-Ajayi, Tayo; Moore, Jason H

Evaluating Performance and Agreement of Coronary Heart Disease Polygenic Risk Scores

评估冠心病多基因风险评分的性能和一致性

Abramowitz, Sarah A; Boulier, Kristin; Keat, Karl; Cardone, Katie M; Shivakumar, Manu; DePaolo, John; Judy, Renae; Bermudez, Francisca; Mimouni, Nour; Neylan, Christopher; Kim, Dokyoon; Rader, Daniel J; Ritchie, Marylyn D; Voight, Benjamin F; Pasaniuc, Bogdan; Levin, Michael G; Damrauer, Scott M

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

Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum

心力衰竭的常见变异和罕见变异遗传结构在等位基因频率谱中的分布

Lee, David S M; Cardone, Kathleen M; Zhang, David Y; Tsao, Noah L; Abramowitz, Sarah; Sharma, Pranav; DePaolo, John S; Conery, Mitchell; Aragam, Krishna G; Biddinger, Kiran; Dikilitas, Ozan; Hoffman-Andrews, Lily; Judy, Renae L; Khan, Atlas; Kullo, Iftikhar J; Puckelwartz, Megan J; Reza, Nosheen; Satterfield, Benjamin A; Singhal, Pankhuri; Arany, Zoltan; Cappola, Thomas P; Carruth, Eric D; Day, Sharlene M; Do, Ron; Haggerty, Christopher M; Joseph, Jacob; McNally, Elizabeth M; Nadkarni, Girish; Owens, Anjali T; Rader, Daniel J; Ritchie, Marylyn D; Sun, Yan V; Voight, Benjamin F; Levin, Michael G; Damrauer, Scott M

Mapping rare protein-coding variants on multi-organ imaging traits

将罕见蛋白质编码变异与多器官成像特征联系起来

Fan, Yijun; Chen, Jie; Fan, Zirui; Chirinos, Julio; Stein, Jason L; Sullivan, Patrick F; Wang, Rujin; Nadig, Ajay; Zhang, David Y; Huang, Shuai; Jiang, Zhiwen; Guan, Peter Yi; Qian, Xinjie; Li, Ting; Li, Haoyue; Sun, Zehui; Ritchie, Marylyn D; O'Brien, Joan M; Witschey, Walter; Rader, Daniel J; Li, Tengfei; Zhu, Hongtu; Zhao, Bingxin

A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associations

基因型优先的方法可以识别出高发的NF1致病变异,这些变异与特定的疾病相关。

Safonov, Anton; Nomakuchi, Tomoki T; Chao, Elizabeth; Horton, Carrie; Dolinsky, Jill S; Yussuf, Amal; Richardson, Marcy; Speare, Virginia; Li, Shuwei; Bogus, Zoe C; Bonanni, Maria; Raper, Anna; Odia, Trust; Wubbenhorst, Bradley S; Faulders, Elsa; Schuth, Elisabeth M; Loranger, Kate; Zhang, Jingwen; Scalise, Carly Bess; ElNaggar, Adam; Sha, Youbao; Felker, Stephanie A; Weitzel, Jeffrey; Kallish, Staci; Ritchie, Marylyn D; Nathanson, Katherine L; Drivas, Theodore G