Whiwon相关文献与解析，生知库 | 链接生命科学的每一步

Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational study

了解基因组学次要发现对临床护理和患者体验的影响：一项前瞻性观察研究方案

doi:10.1136/bmjopen-2025-115821

Assamad, Daniel; Hansen, Abigail; Fooks, Katharine; Luca, Stephanie; Venkataramanan, Viji; Hsue, Erin; Shickh, Salma; Yan, Joyce; Wu, Vercancy; Badalato, Lauren; Balci, Tugce B; Beausejour Ladouceur, Virginie; Chad, Lauren; Chisholm, Caitlin; Gillespie, Meredith K; Huang, Lijia; Jarinova, Olga; Lau, Lynette; Lee, Whiwon; Mackley, Michael P; Marshall, Christian R; Mendoza-Londono, Roberto; Morel, Chantal F; Richer, Julie; Sawyer, Sarah; Stavropoulos, Dimitri J; Szuto, Anna; Tarnopolsky, Mark; Villani, Anita; Zahavich, Laura; Somerville, Martin J; Boycott, Kym M; Ungar, Wendy J; Hayeems, Robin Z

发表日期：2026

文献求助收藏

What are patient perspectives on privacy and trust in digital genomic tools? A qualitative study

患者对数字基因组工具的隐私和信任有何看法？一项定性研究

期刊:Journal of Genetic Counseling

影响因子:1.9

doi:10.1002/jgc4.70025

Jha, Vedika; Saeedi, Saumeh; Clausen, Marc; Assamad, Daniel; Grewal, Sonya; Hirjikaka, Daena; Lee, Whiwon; Luca, Stephanie; Shaw, Angela; Hayeems, Robin; Bombard, Yvonne

发表日期：2025

文献求助收藏

Finding the sweet spot: a qualitative study exploring patients' acceptability of chatbots in genetic service delivery

寻找最佳平衡点：一项探索患者对基因服务中聊天机器人接受度的定性研究

期刊:Human Genetics

影响因子:3.6

doi:10.1007/s00439-022-02512-2

Luca, Stephanie; Clausen, Marc; Shaw, Angela; Lee, Whiwon; Krishnapillai, Suvetha; Adi-Wauran, Ella; Faghfoury, Hanna; Costain, Gregory; Jobling, Rebekah; Aronson, Melyssa; Liston, Eriskay; Silver, Josh; Shuman, Cheryl; Chad, Lauren; Hayeems, Robin Z; Bombard, Yvonne

发表日期：2023

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Genetic counselors' response types to prenatal patient deferring or attributing religious/spiritual statements: An exploratory study of US genetic counselors

美国遗传咨询师对产前患者推迟或归因于宗教/精神因素的陈述的反应类型：一项探索性研究

期刊:Journal of Genetic Counseling

影响因子:1.9

doi:10.1002/jgc4.1634

Sitaula, Alina; Veach, Patricia McCarthy; MacFarlane, Ian M; Lee, Whiwon; Redlinger-Grosse, Krista

发表日期：2023

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Comparing genome sequencing technologies to improve rare disease diagnostics: a protocol for the evaluation of a pilot project, Genome-wide Sequencing Ontario

比较基因组测序技术以改进罕见病诊断：一项试点项目评估方案，安大略省全基因组测序

期刊:

影响因子:

doi:10.9778/cmajo.20210272

Hayeems, Robin Z; Marshall, Christian R; Gillespie, Meredith K; Szuto, Anna; Chisholm, Caitlin; Stavropoulos, Dimitri J; Venkataramanan, Viji; Tsiplova, Kate; Sawyer, Sarah; Price, E Magda; Lau, Lynette; Khan, Reem; Lee, Whiwon; Huang, Lijia; Jarinova, Olga; Ungar, Wendy J; Mendoza-Londono, Roberto; Somerville, Martin J; Boycott, Kym M

Sequencing

发表日期：2022

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Genome sequencing identifies a rare case of moderate Zellweger spectrum disorder caused by a PEX3 defect: Case report and literature review

基因组测序发现了一例由 PEX3 缺陷引起的罕见中度 Zellweger 谱系障碍病例：病例报告及文献综述

期刊:Molecular Genetics and Metabolism Reports

影响因子:1.9

doi:10.1016/j.ymgmr.2020.100664

Lee, Whiwon; Costain, Gregory; Blaser, Susan; Walker, Susan; Marshall, Christian R; Gonorazky, Hernan; Inbar-Feigenberg, Michal

发表日期：2020

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The role of race and ethnicity in views toward and participation in genetic studies and precision medicine research in the United States: A systematic review of qualitative and quantitative studies

种族和民族在美国对基因研究和精准医学研究的看法和参与度中所起的作用：一项对定性和定量研究的系统性综述

期刊:Molecular Genetics & Genomic Medicine

影响因子:1.6

doi:10.1002/mgg3.1099

Fisher, Elena R; Pratt, Rebekah; Esch, Riley; Kocher, Megan; Wilson, Katie; Lee, Whiwon; Zierhut, Heather A

发表日期：2020

文献求助收藏

Next generation sequencing for clinical diagnostics: Five year experience of an academic laboratory

用于临床诊断的下一代测序：一家学术实验室的五年经验

期刊:Molecular Genetics and Metabolism Reports

影响因子:1.9

doi:10.1016/j.ymgmr.2019.100464

Hartman, Paige; Beckman, Kenneth; Silverstein, Kevin; Yohe, Sophia; Schomaker, Matthew; Henzler, Christine; Onsongo, Getiria; Lam, Ham Ching; Munro, Sarah; Daniel, Jerry; Billstein, Bradley; Deshpande, Archana; Hauge, Adam; Mroz, Pawel; Lee, Whiwon; Holle, Jennifer; Wiens, Katie; Karnuth, Kylene; Kemmer, Teresa; Leary, Michaela; Michel, Stephen; Pohlman, Laurie; Thayanithy, Venugopal; Nelson, Andrew; Bower, Matthew; Thyagarajan, Bharat

发表日期：2019

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Integrating paediatric subspecialists into the delivery of genomic medicine: A qualitative study

将儿科专科医生纳入基因组医学服务：一项定性研究

Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational study

了解基因组学次要发现对临床护理和患者体验的影响：一项前瞻性观察研究方案

What are patient perspectives on privacy and trust in digital genomic tools? A qualitative study

患者对数字基因组工具的隐私和信任有何看法？一项定性研究

Finding the sweet spot: a qualitative study exploring patients' acceptability of chatbots in genetic service delivery

寻找最佳平衡点：一项探索患者对基因服务中聊天机器人接受度的定性研究

Genetic counselors' response types to prenatal patient deferring or attributing religious/spiritual statements: An exploratory study of US genetic counselors

美国遗传咨询师对产前患者推迟或归因于宗教/精神因素的陈述的反应类型：一项探索性研究

Comparing genome sequencing technologies to improve rare disease diagnostics: a protocol for the evaluation of a pilot project, Genome-wide Sequencing Ontario

比较基因组测序技术以改进罕见病诊断：一项试点项目评估方案，安大略省全基因组测序

Genome sequencing identifies a rare case of moderate Zellweger spectrum disorder caused by a PEX3 defect: Case report and literature review

基因组测序发现了一例由 PEX3 缺陷引起的罕见中度 Zellweger 谱系障碍病例：病例报告及文献综述

The role of race and ethnicity in views toward and participation in genetic studies and precision medicine research in the United States: A systematic review of qualitative and quantitative studies

种族和民族在美国对基因研究和精准医学研究的看法和参与度中所起的作用：一项对定性和定量研究的系统性综述

Next generation sequencing for clinical diagnostics: Five year experience of an academic laboratory

用于临床诊断的下一代测序：一家学术实验室的五年经验