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

CYP2D6-Guided Opioid Management and Postoperative Pain Control: A Randomized Clinical Trial

CYP2D6指导的阿片类药物管理和术后疼痛控制:一项随机临床试验

Cavallari, Larisa H; Myers, Rachel A; Chakraborty, Hrishikesh; Skaar, Todd C; Gray, Chancellor F; Baye, Jordan F; Volpi, Simona; Rider, Renee; Cicali, Emily J; Elwood, Erica N; Harris, Elizabeth C; Hines, Lindsay J; Nahid, Noor A; Nguyen, Khoa A; Obeng, Aniwaa Owusu; Parr, J Andrew; Ramos, Michelle A; Orlando, Lori A; Prieto, Hernan A; Sadeghpour, Azita; Singh, Rajbir; Starostik, Petr; Tillman, Emma M; Wyatt, Christina; Horowitz, Carol R; Voora, Deepak; Blake, Kathryn V; Parvataneni, Hari K; Fillingim, Roger B; Dexter, Paul R; Peterson, Josh F; Johnson, Julie A

Genetic Testing for APOL1 in Adults With Hypertension: The GUARDD-US Randomized Clinical Trial

针对高血压成人患者的 APOL1 基因检测:GUARDD-US 随机临床试验

Eadon, Michael T; Cavanaugh, Kerri L; She, Lilin; Steen-Burrell, Kady-Ann; Mohottige, Dinushika; Nadkarni, Girish N; Kitzman, Heather; Chakraborty, Hrishikesh; Empey, Philip E; Limdi, Nita A; Singh, Rajbir; Beasley, Cherry Maynor; Parker, Alexander S; Cicali, Emily J; Ramos, Michelle A; Clermont, Sabrina; Dodgen, Leilani; Elwood, Erica N; Robinson, Mimsie; Umeukeje, Ebele M; Garcia Ortega, Abraham; Shroff, Nandini; Rosenman, Marc B; Nguyen, Khoa A; Volpi, Simona; Rider, Renee; Dexter, Paul R; Skaar, Todd C; Peterson, Josh F; Cavallari, Larisa H; Johnson, Julie A; Wyatt, Christina M; Orlando, Lori A; Cooper-DeHoff, Rhonda M; Horowitz, Carol R

Return of genome-informed risk-assessment results for common conditions to 23,840 adults and children: An eMERGE network study

向 23,840 名成人和儿童反馈常见疾病的基因组信息风险评估结果:一项 eMERGE 网络研究

Lawson, Lucinda P; Prows, Cynthia A; Cortopassi, Josh; Davis, Kyle W; Head, Madilyn; Martin, Lisa J; Perez, Emma F; Sobowale, Agboade; Abul-Husn, Noura S; Bangash, Hana; Bland, Harris T; Bonini, Katherine E; Chisholm, Rex L; Chung, Wendy K; Cimino, James J; Connolly, John J; Crosslin, David R; Freimuth, Robert R; Goff, Blake; Gordon, Adam S; Hakonarson, Hakon; Harr, Margaret H; Henricks, Emma; Hernandez, Valentina; Hoell, Christin; Holm, Ingrid A; Hripcsak, George; Karlson, Elizabeth W; Kenny, Eimear E; Khan, Atlas; Kiryluk, Krzysztof; Kottyan, Leah C; Lennon, Niall J; Limdi, Nita; Linder, Jodell E; Liu, Cong; Manolio, Teri A; Maradik, Mary A; Marathe, Priya N; Maripuri, Devi P; McNally, Elizabeth M; Murphy, Shawn N; Naderian, Mohammadreza; Namjou, Bahram; Odgis, Jacqueline A; Peterson, Josh F; Pineda-Alvarez, Daniel E; Puckelwartz, Megan; Purcell, Jasmine; Rasmussen-Torvik, Laura J; Roden, Dan M; Rosenthal, Elisabeth A; Rowley, Robb; Sabatello, Maya; Scherr, Courtney L; Shaibi, Gabriel Q; Sharp, Richard R; Smoller, Jordan W; Sterling, Rene; Suckiel, Sabrina A; Terek, Shannon; Ting, Yi-Lee; Velez Edwards, Digna R; Walunas, Theresa L; Wei, Wei-Qi; Weng, Chunhua; Wiesner, Georgia L; Xian, Su; Jarvik, Gail P; Kullo, Iftikhar

The Electronic Medical Records and Genomics study: Design and analytic framework for assessing the impact of genome-informed risk assessments

电子病历与基因组学研究:评估基因组信息风险评估影响的设计和分析框架

Limdi, Nita; Beasley, T Mark; Cortopassi, Josh; Davis, Brittney; Bangash, Hana; Chen, Jingheng; Chisholm, Rex L; Chung, Wendy K; Cimino, James J; Connolly, John; Crosslin, David R; Davis, Kyle W; DiVietro, Alanna; Esplin, Edward D; Freimuth, Bob; Gordon, Adam; Hakonarson, Hakon; Hamed, Marwan; He, Megan; Hoell, Christin; Holm, Ingrid; Hripscak, George; Irvin, Margurite R; Jarvik, Gail P; Karavite, Dean; Karlson, Elizabeth W; Kenny, Eimear E; Khan, Atlas; Kiryluk, Krzysztof; Knerr, Sarah; Korf, Bruce; Kottyan, Leah; Kullo, Iftikhar; Larkin, Katie; Lennon, Niall; Linder, Jodell E; Manolio, Teri; Martin, Lisa J; McNally, Elizabeth M; Morse, Jennifer; Murphy, Shawn; Namjou, Bahram; Odgis, Jacqueline A; Orlando, Lori; Pacheco, Jennifer; Peterson, Josh F; Pineda-Alvarez, Daniel E; Prows, Cindy; Puckelwartz, Megan; Purcell, Jasmine; Rasmussen-Torvik, Laura; Rehm, Heidi; Roden, Dan M; Rosenthal, Elisabeth A; Rowley, Robb; Sabatello, Maya; Schaid, Daniel; Sharp, Richard; Smith, Johanna L; Smoller, Jordan W; Soper, Emily R; Sterling, Rene; Suckiel, Sabrina A; Terek, Shannon; Thayer, Jeritt; Ting, Yi-Lee; Tiwari, Hemant; Velez-Edwards, Digna; Wagholikar, Kavishwar B; Walunas, Theresa; Wei, Wei-Qi; Weng, Chunua; Wiesner, Georgia; Abul-Husn, Noura S; Veenstra, David L

Evaluating pregnancy and neonatal outcomes in mothers with genetic disease using electronic health care records

利用电子健康记录评估患有遗传疾病母亲的妊娠和新生儿结局

Tinker, Rory J; Richter, Lucas D; Furuta, Yutaka; Shyr, Cathy; Shirazi, Sherwin M; Sucre, Jennifer; Gatta, Luke A; Phillips, John A 3rd; Peterson, Josh F; Bastarache, Lisa

A Tutorial on the Development of a Physiologically Inspired PKRO Model for Monoclonal Antibodies

关于构建单克隆抗体生理启发式PKRO模型的教程

Kapitanov, Georgi I; Flowers, David; Marcantonio, Diana H; Lezon, Timothy R; Apgar, Josh F; Hua, Fei

Diagnostic Accuracy of Large Language Models for Rare Diseases: A Systematic Review and Meta-Analysis

大型语言模型在罕见病诊断中的准确性:系统评价和荟萃分析

Nguyen, Minh-Ha; Yang, Chih-Ting; Cassini, Thomas A; Ma, Fan; Hamid, Rizwan; Bastarache, Lisa; Peterson, Josh F; Xu, Hua; Li, Lingyao; Ma, Siyuan; Shyr, Cathy

A polygenic score for height identifies an unmeasured genetic predisposition among pediatric patients with idiopathic short stature

身高多基因评分可以识别特发性矮小症患儿中未被测量的遗传易感性。

Shelley, John P; Shi, Mingjian; Peterson, Josh F; Van Driest, Sara L; Simmons, Jill H; Mosley, Jonathan D

Large Language Models for Rare Disease Diagnosis at the Undiagnosed Diseases Network

未确诊疾病网络的大型语言模型用于罕见病诊断

Shyr, Cathy; Cassini, Thomas A; Tinker, Rory J; Byram, Kevin W; Embí, Peter J; Bastarache, Lisa; Peterson, Josh F; Xu, Hua; Hamid, Rizwan

Characterizing trends in clinical genetic testing: A single-center analysis of EHR data from 1.8 million patients over two decades

临床基因检测趋势分析:一项基于20年间180万患者电子病历数据的单中心分析

Bastarache, Lisa; Tinker, Rory J; Schuler, Bryce A; Richter, Lucas; Phillips, John A 3rd; Stead, William W; Hooker, Gillian W; Peterson, Josh F; Ruderfer, Douglas M