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

Accelerating Medicines Partnership® Parkinson's Disease Proteomics: A Comprehensive Resource for Advancing Parkinson's Disease Research

加速药物研发伙伴关系®帕金森病蛋白质组学:推进帕金森病研究的综合资源

Dardov, Victoria J; Vasanthakumar, Aparna; Kulkarni, Ameya; Sundararaman, Niveda; Pandey, Rakhi; Bais, Preeti; Van, Jennifer E; Quinton, Maria; Landin, Barry; Vismer, David; Casey, Bradford; Bookman, Matt; Nojopranoto, Willy; Teeple, Erin; Kayatekin, Can; Krishnan, Rajaraman; Hargreaves, Richard; Nagappan, Guhan; Sardi, S Pablo; Pullagura, Sri Ramulu; Swanson-Fischer, Christine

Proteomic signatures of the APOE ε4 and APOE ε2 genetic variants and Alzheimer's disease

APOE ε4 和 APOE ε2 基因变异的蛋白质组学特征与阿尔茨海默病

Lu, Lina; Binette, Alexa Pichet; Hristovska, Ines; Janelidze, Shorena; Smets, Bart; Mayoral, Irene Cumplido; Vasanthakumar, Aparna; Milkovich, Britney; Ossenkoppele, Rik; Krish, Varsha; Imam, Farhad; Palmqvist, Sebastian; Vogel, Jacob; Stomrud, Erik; Hansson, Oskar; Mattsson-Carlgren, Niklas

CYP1B1-RMDN2 Alzheimer's disease endophenotype locus identified for cerebral tau PET

CYP1B1-RMDN2 阿尔茨海默病内表型基因座已通过脑 tau PET 鉴定

Nho, Kwangsik; Risacher, Shannon L; Apostolova, Liana G; Bice, Paula J; Brosch, Jared R; Deardorff, Rachael; Faber, Kelley; Farlow, Martin R; Foroud, Tatiana; Gao, Sujuan; Rosewood, Thea; Kim, Jun Pyo; Nudelman, Kelly; Yu, Meichen; Aisen, Paul; Sperling, Reisa; Hooli, Basavaraj; Shcherbinin, Sergey; Svaldi, Diana; Jack, Clifford R Jr; Jagust, William J; Landau, Susan; Vasanthakumar, Aparna; Waring, Jeffrey F; Doré, Vincent; Laws, Simon M; Masters, Colin L; Porter, Tenielle; Rowe, Christopher C; Villemagne, Victor L; Dumitrescu, Logan; Hohman, Timothy J; Libby, Julia B; Mormino, Elizabeth; Buckley, Rachel F; Johnson, Keith; Yang, Hyun-Sik; Petersen, Ronald C; Ramanan, Vijay K; Ertekin-Taner, Nilüfer; Vemuri, Prashanthi; Cohen, Ann D; Fan, Kang-Hsien; Kamboh, M Ilyas; Lopez, Oscar L; Bennett, David A; Ali, Muhammad; Benzinger, Tammie; Cruchaga, Carlos; Hobbs, Diana; De Jager, Philip L; Fujita, Masashi; Jadhav, Vaishnavi; Lamb, Bruce T; Tsai, Andy P; Castanho, Isabel; Mill, Jonathan; Weiner, Michael W; Saykin, Andrew J

Diversity of CFTR variants across ancestries characterized using 454,727 UK biobank whole exome sequences

利用英国生物银行454,727个全外显子组序列对不同祖先中CFTR变异体的多样性进行了表征

Ideozu, Justin E; Liu, Mengzhen; Riley-Gillis, Bridget M; Paladugu, Sri R; Rahimov, Fedik; Krishnan, Preethi; Tripathi, Rakesh; Dorr, Patrick; Levy, Hara; Singh, Ashvani; Waring, Jeffrey F; Vasanthakumar, Aparna

PINNED: identifying characteristics of druggable human proteins using an interpretable neural network

PINNED:利用可解释神经网络识别可成药的人类蛋白质的特征

Cunningham, Michael; Pins, Danielle; Dezső, Zoltán; Torrent, Maricel; Vasanthakumar, Aparna; Pandey, Abhishek

Editorial: Women in science: Genetics

社论:科学领域的女性:遗传学

de Vasconcellos, Jaira Ferreira; Abedalthagafi, Malak; Calo, Silvia; Dajani, Rana; Dlamini, Zodwa; Hidalgo, Bertha; Le Goff, Carine; Vasanthakumar, Aparna

Association of peripheral blood DNA methylation level with Alzheimer's disease progression

外周血DNA甲基化水平与阿尔茨海默病进展的相关性

Li, Qingqin S; Vasanthakumar, Aparna; Davis, Justin W; Idler, Kenneth B; Nho, Kwangsik; Waring, Jeffrey F; Saykin, Andrew J

Harnessing peripheral DNA methylation differences in the Alzheimer's Disease Neuroimaging Initiative (ADNI) to reveal novel biomarkers of disease

利用阿尔茨海默病神经影像学计划(ADNI)中外周DNA甲基化差异来揭示新的疾病生物标志物

Vasanthakumar, Aparna; Davis, Justin W; Idler, Kenneth; Waring, Jeffrey F; Asque, Elizabeth; Riley-Gillis, Bridget; Grosskurth, Shaun; Srivastava, Gyan; Kim, Sungeun; Nho, Kwangsik; Nudelman, Kelly N H; Faber, Kelley; Sun, Yu; Foroud, Tatiana M; Estrada, Karol; Apostolova, Liana G; Li, Qingqin S; Saykin, Andrew J

Differential translational control of 5' IRE-containing mRNA in response to dietary iron deficiency and acute iron overload

膳食铁缺乏和急性铁过载对含5' IRE的mRNA翻译调控的影响

Garza, Kerry R; Clarke, Stephen L; Ho, Yi-Hsuan; Bruss, Matthew D; Vasanthakumar, Aparna; Anderson, Sheila A; Eisenstein, Richard S

Reduced ITPase activity and favorable IL28B genetic variant protect against ribavirin-induced anemia in interferon-free regimens

ITPase活性降低和有利的IL28B基因变异可预防无干扰素治疗方案中利巴韦林引起的贫血

Vasanthakumar, Aparna; Davis, Justin W; Abunimeh, Manal; Söderholm, Jonas; Zha, Jiuhong; Dumas, Emily O; Cohen, Daniel E; Waring, Jeffrey F; Lagging, Martin