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

Developing and Assessing a Scalable Digital Health Tool for Pretest Genetic Education in Patients With Early-Onset Colorectal Cancer: Mixed Methods Design

开发和评估一种可扩展的数字健康工具,用于早期结直肠癌患者的基因检测前教育:混合方法设计

Rivera Rivera, Jessica N; Snir, Moran; Simmons, Emilie; Schmidlen, Tara; Sholeh, Misha; Maconi, Melinda Leigh; Geiss, Carley; Fulton, Hayden; Barton, Laura; Gonzalez, Brian D; Permuth, Jennifer; Vadaparampil, Susan

Returning integrated genomic risk and clinical recommendations: The eMERGE study

整合基因组风险和临床建议:eMERGE 研究

Linder, Jodell E; Allworth, Aimee; Bland, Harris T; Caraballo, Pedro J; Chisholm, Rex L; Clayton, Ellen Wright; Crosslin, David R; Dikilitas, Ozan; DiVietro, Alanna; Esplin, Edward D; Forman, Sophie; Freimuth, Robert R; Gordon, Adam S; Green, Richard; Harden, Maegan V; Holm, Ingrid A; Jarvik, Gail P; Karlson, Elizabeth W; Labrecque, Sofia; Lennon, Niall J; Limdi, Nita A; Mittendorf, Kathleen F; Murphy, Shawn N; Orlando, Lori; Prows, Cynthia A; Rasmussen, Luke V; Rasmussen-Torvik, Laura; Rowley, Robb; Sawicki, Konrad Teodor; Schmidlen, Tara; Terek, Shannon; Veenstra, David; Velez Edwards, Digna R; Absher, Devin; Abul-Husn, Noura S; Alsip, Jorge; Bangash, Hana; Beasley, Mark; Below, Jennifer E; Berner, Eta S; Booth, James; Chung, Wendy K; Cimino, James J; Connolly, John; Davis, Patrick; Devine, Beth; Fullerton, Stephanie M; Guiducci, Candace; Habrat, Melissa L; Hain, Heather; Hakonarson, Hakon; Harr, Margaret; Haverfield, Eden; Hernandez, Valentina; Hoell, Christin; Horike-Pyne, Martha; Hripcsak, George; Irvin, Marguerite R; Kachulis, Christopher; Karavite, Dean; Kenny, Eimear E; Khan, Atlas; Kiryluk, Krzysztof; Korf, Bruce; Kottyan, Leah; Kullo, Iftikhar J; Larkin, Katie; Liu, Cong; Malolepsza, Edyta; Manolio, Teri A; May, Thomas; McNally, Elizabeth M; Mentch, Frank; Miller, Alexandra; Mooney, Sean D; Murali, Priyanka; Mutai, Brenda; Muthu, Naveen; Namjou, Bahram; Perez, Emma F; Puckelwartz, Megan J; Rakhra-Burris, Tejinder; Roden, Dan M; Rosenthal, Elisabeth A; Saadatagah, Seyedmohammad; Sabatello, Maya; Schaid, Dan J; Schultz, Baergen; Seabolt, Lynn; Shaibi, Gabriel Q; Sharp, Richard R; Shirts, Brian; Smith, Maureen E; Smoller, Jordan W; Sterling, Rene; Suckiel, Sabrina A; Thayer, Jeritt; Tiwari, Hemant K; Trinidad, Susan B; Walunas, Theresa; Wei, Wei-Qi; Wells, Quinn S; Weng, Chunhua; Wiesner, Georgia L; Wiley, Ken; Peterson, Josh F

Optimizing communication strategies and designing a comprehensive program to facilitate cascade testing for familial hypercholesterolemia

优化沟通策略并设计综合方案,以促进家族性高胆固醇血症的级联检测

Campbell-Salome, Gemme; Jones, Laney K; Walters, Nicole L; Morgan, Kelly M; Brangan, Andrew; Ladd, Ilene G; McGowan, Mary P; Wilemon, Katherine; Schmidlen, Tara J; Simmons, Emilie; Schwartz, Marci L B; McMinn, Megan N; Tricou, Eric; Rahm, Alanna K; Ahmed, Catherine D; Sturm, Amy C

Validation of Pharmacogenomic Interaction Probability (PIP) Scores in Predicting Drug-Gene, Drug-Drug-Gene, and Drug-Gene-Gene Interaction Risks in a Large Patient Population

在大样本患者群体中验证药物基因组学相互作用概率(PIP)评分在预测药物-基因、药物-药物-基因和药物-基因-基因相互作用风险方面的有效性

Ashcraft, Kristine; Grande, Kendra; Bristow, Sara L; Moyer, Nicolas; Schmidlen, Tara; Moretz, Chad; Wick, Jennifer A; Blaxall, Burns C

The Impact of Proband Indication for Genetic Testing on the Uptake of Cascade Testing Among Relatives

先证者基因检测指征对亲属级联检测接受率的影响

Schmidlen, Tara J; Bristow, Sara L; Hatchell, Kathryn E; Esplin, Edward D; Nussbaum, Robert L; Haverfield, Eden V

Developing and Optimizing Innovative Tools to Address Familial Hypercholesterolemia Underdiagnosis: Identification Methods, Patient Activation, and Cascade Testing for Familial Hypercholesterolemia

开发和优化创新工具以解决家族性高胆固醇血症漏诊问题:家族性高胆固醇血症的识别方法、患者激活和级联检测

Campbell-Salome, Gemme; Jones, Laney K; Masnick, Max F; Walton, Nephi A; Ahmed, Catherine D; Buchanan, Adam H; Brangan, Andrew; Esplin, Edward D; Kann, David G; Ladd, Ilene G; Kelly, Melissa A; Kindt, Iris; Kirchner, H Lester; McGowan, Mary P; McMinn, Megan N; Morales, Ana; Myers, Kelly D; Oetjens, Matthew T; Rahm, Alanna Kulchak; Schmidlen, Tara J; Sheldon, Amanda; Simmons, Emilie; Snir, Moran; Strande, Natasha T; Walters, Nicole L; Wilemon, Katherine; Williams, Marc S; Gidding, Samuel S; Sturm, Amy C

Clinical outcomes of a genomic screening program for actionable genetic conditions

针对可干预遗传疾病的基因组筛查项目的临床结果

Buchanan, Adam H; Lester Kirchner, H; Schwartz, Marci L B; Kelly, Melissa A; Schmidlen, Tara; Jones, Laney K; Hallquist, Miranda L G; Rocha, Heather; Betts, Megan; Schwiter, Rachel; Butry, Loren; Lazzeri, Amanda L; Frisbie, Lauren R; Rahm, Alanna Kulchak; Hao, Jing; Willard, Huntington F; Martin, Christa L; Ledbetter, David H; Williams, Marc S; Sturm, Amy C

Pharmacogenomic (PGx) Counseling: Exploring Participant Questions about PGx Test Results

药物基因组学(PGx)咨询:解答参与者关于PGx检测结果的问题

Schmidlen, Tara; Sturm, Amy C; Scheinfeldt, Laura B

Early Outcome Data Assessing Utility of a Post-Test Genomic Counseling Framework for the Scalable Delivery of Precision Health

早期结果数据评估了检测后基因组咨询框架在可扩展精准医疗服务中的实用性

Sturm, Amy C; Schmidlen, Tara; Scheinfeldt, Laura; Hovick, Shelly; McElroy, Joseph P; Toland, Amanda E; Roberts, J Scott; Sweet, Kevin

Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing

将互惠参与模式应用于遗传咨询实践:构建可扩展的基因组咨询和检测服务框架

Schmidlen, Tara; Sturm, Amy C; Hovick, Shelly; Scheinfeldt, Laura; Scott Roberts, J; Morr, Lindsey; McElroy, Joseph; Toland, Amanda E; Christman, Michael; O'Daniel, Julianne M; Gordon, Erynn S; Bernhardt, Barbara A; Ormond, Kelly E; Sweet, Kevin