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

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

Doped Biopolymer Composites for Engineered Water Purification: Mechanistic Insights into Multi-Ion Adsorption

用于工程化水净化的掺杂生物聚合物复合材料:多离子吸附的机理研究

Maroulas, Konstantinos N; Tolkou, Athanasia K; Ladomenou, Kalliopi; Drivas, Charalampos; Isaacs, Mark A; Ntougias, Spyridon; Katsoyiannis, Ioannis A; Kyzas, George Z

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

Exclusion-based exome sequencing in critically ill adults 18-40 years old has a 24% diagnostic rate and finds racial disparities in access to genetic testing

对18-40岁危重成年患者进行基于排除法的外显子组测序,诊断率为24%,并发现不同种族在获得基因检测方面存在差异。

Gold, Jessica I; Kripke, Colleen M; Drivas, Theodore G

Digital and AI-assisted multimodal supportive care, combining physical activity, nutrition, and pain management during chemotherapy for advanced pancreatic cancer patients: study protocol of the European multicenter randomized controlled trial of the RELEVIUM project

针对晚期胰腺癌患者,在化疗期间结合体育锻炼、营养和疼痛管理,采用数字化和人工智能辅助的多模式支持性护理:RELEVIUM 项目欧洲多中心随机对照试验的研究方案

Hillen, Barlo; Oestreicher, Gabrielle; Schwab, Lisa; Enders, Kira; Simon, Perikles; Elme, Anneli; Ben-Aharon, Irit; Goshenlago, Tal; Neuzillet, Cindy; Sclafani, Francesco; Beltran, Eva Ester Molina; Schuster, Michael; Doncheva, Hristina; Ruckes, Christian; Karlecik, Michael; Petrowski, Katja; Rosenbaum, David; Diou, Christos; Ballas, Aristotelis; Vlachostergiou, Aggeliki; Mastricci, Davide; Scherrer, Alexander; Pilz, Maximilian; Flechsig, Jonas; Apostolidis, Lazaros; Krooupa, Anna-Maria; Chintha, Sai; Musisi, Isa Wasswa; Tzavara, Nefeli Panagiota; Kakasis, Athanasios; Hadjikypri, Xenia; Karra, Styliani; Chatzipanagiotou, Kyriaki; Drivas, Ioannis; Dacasa, Hugo; Moehler, Markus

The landscape of experimental cardiac arrest research models in rats: a bibliometric analysis of the 100 most cited articles

大鼠实验性心脏骤停研究模型概况:对引用次数最多的100篇文章的文献计量分析

Mavrovounis, Georgios; Mermiri, Maria; Drivas, Ioannis; Drivas, Konstantinos; Kalamatianos, Theodosis; Zarogiannis, Sotirios G; Pantazopoulos, Ioannis

Patient interpretation and implementation of air embolism prevention guidelines in hereditary hemorrhagic telangiectasia (HHT): a survey-based study

遗传性出血性毛细血管扩张症(HHT)患者对空气栓塞预防指南的理解和执行情况:一项基于调查的研究

Wei, Kimberly; Shamimi-Noori, Susan; Drivas, Theodore G; Trerotola, Scott O

The polygenic architecture of hidradenitis suppurativa reveals signaling mechanisms that implicate epithelial remodeling

化脓性汗腺炎的多基因结构揭示了与上皮重塑相关的信号机制

Khan, Atlas; Gould, Poppy A; Luo, Yiming; Prens, Errol P; Wheless, Lee; Hung, Adriana M; Drivas, Theodore G; Ritchie, Marylyn D; Saeidian, Amir Hossein; Hákonarson, Hákon; March, Michael; Dand, Nick; Barker, Jonathan; Simpson, Michael; Saklatvala, Jake; Du-Harpur, Xinyi; Farnood, Shahir; Chung, Raymond; Curtis, Charles J; Lee, Sang Hyuck; Kirby, Brian; Teder-Laving, Maris; Kingo, Külli; Thomas, Laurent F; Løset, Mari; Brumpton, Ben Michael; Hveem, Kristian; Hayes, M Geoffrey; Connolly, John; Mentch, Frank; Sleiman, Patrick; Brown, Kathleen LaRow; Tatonetti, Nicholas; Perez, Olivia D; Braun, Alice; Ripke, Stephan; Gaddam, Sadhana; Oro, Anthony; Redmond, Leah C; Higgins, Claire; Lin, Meng-Ju; Chiu, Ernest S; Lu, Catherine P; Hripcsak, George; Weng, Chunhua; Kiryluk, Krzysztof; Tsoi, Lam C; Gudjonsson, Johann E; van Straalen, Kelsey R; Milner, Joshua D; Petukhova, Lynn

Leveraging Open-Source Large Language Models to Identify Undiagnosed Patients with Rare Genetic Aortopathies

利用开源大型语言模型识别未确诊的罕见遗传性主动脉病患者

Singhal, Pankhuri; Li, Zilinghan; Yang, Ze; Nandi, Tarak; Morse, Colleen; Rodriguez, Zachary; Rodriguez, Alex; Kindratenko, Volodymyr; Sirugo, Giorgio; Pyeritz, Reed E; Drivas, Theodore; Madduri, Ravi; Verma, Anurag

Practice-Based Insights into Adult Genetics: High Diagnostic Yield, Demographic Determinants, and Patterns of Test Utilization in Over 7,000 Patients

基于实践的成人遗传学见解:7000多名患者的高诊断率、人口统计学决定因素和检测利用模式

Gold, Jessica I; Elkaim, Yehuda; Asher, Stephanie; Raper, Anna; Condit, Courtney; Bogus, Zoe; Elysee, Isaac; Hennessy, Laura; Kennedy, Emma; Chai, Teresa; Cohen, Stacey; Gehringer, Brielle N; Gray, Shannon M; Streater, Ala; Toye, Eamon; Kripke, Colleen; Nathanson, Katherine L; Rohanizadegan, Mersedeh; Kallish, Staci; Drivas, Theodore G