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Brian H. Shirts

and economics (choice) institute

41H指数
199论文数
7.6K被引数
收录论文 72
发表时间
Cost-effectiveness of primary care-based risk assessment and hereditary cancer genetic testing基于初级保健的风险评估和遗传性癌症基因检测的成本效益
err2025-12-22
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errOAAI
errBeth Devine; Sanne E. Aalbers; HuiHsuan Chan; Shangqing Jiang; Emerson J. Dusic; Sarah Knerr; Heather M. Harris; Catharine Wang; Barbara M. Norquist; Laurie A. Riemann; Jeannine M. Brant; Brian H. Shirts; Elizabeth M. Swisher
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Imprecision medicine: Systematic gaps in reporting variants of uncertain significance (VUS) and their reclassifications不精确医学:关于不明临床意义变异(VUS)及其重新分类报告的系统化差距
err2025-06-18
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PREAI
errAndrew Folta; Adriana E. Sedeño Cortés; Pankhuri Gupta; Abbye E. McEwen; Eric Y. Kao; Martha Horike-Pyne; Jeremy Stone; Brian H. Shirts; Marianne E. Dubard-Gault; Douglas M. Fowler; Lea M. Starita; Fuki M. Hisama; Andrew B. Stergachis
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Primary care provider practices, attitudes, and confidence with hereditary cancer risk assessment and testing: A mixed methods study初级保健提供者的实践、态度和信心:遗传性癌症风险评估与检测的混合方法研究
err2025-04-01
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errConner, Sarah; Theoryn, Tesla; Dusic, Emerson; Beers, Faith; Knerr, Sarah; Norquist, Barbara; Shirts, Brian H.; Bowen, Deborah; Swisher, Elizabeth M.; Wang, Catharine
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Strategies to Assess Risk for Hereditary Cancer in Primary Care Clinics: A Cluster Randomized Clinical Trial在初级保健诊所中评估遗传性癌症风险的策略:一项整群随机临床试验
err2025-03-07
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errSwisher, Elizabeth M.; Harris, Heather M.; Knerr, Sarah; Theoryn, Tesla N.; Norquist, Barbara M.; Brant, Jeannine; Shirts, Brian H.; Beers, Faith; Cameron, Dalaina; Dusic, Emerson J.; Riemann, Laurie A.; Devine, Beth; Raff, Michael L.; Kadel, Rabindra; Cabral, Howard J.; Wang, Catharine
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A maternal germline mutator phenotype in a family affected by heritable colorectal cancer
err2024-10-15
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errYoung, Candice L.; Beichman, Annabel C.; Mas Ponte, David; Hemker, Shelby L.; Zhu, Luke; Kitzman, Jacob O.; Shirts, Brian H.; Harris, Kelley
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Implementation of population-based risk assessment for hereditary cancer in primary care: Results from the Early Detection of Genetic Risk (EDGE) Trial
err2024-04-05
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PREAI
errSwisher, Elizabeth M.; Harris, Heather M.; Norquist, Barbara M.; Brant, Jeannine; Shirts, Brian; Knerr, Sarah; Dusic, Emerson J.; Beers, Faith; Theoryn, Tesla N.; Cameron, DaLaina; Cabral, Howard; Riemann, Laurie A.; Raff, Michael; Devine, Beth; Bowen, Deborah J.; Wang, Catharine
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Risk perception and intended behavior change after uninformative genetic results for adult-onset hereditary conditions in unselected patients
err2023-09-26
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PREAI
errRao, Nandana D.; King, Kristine M.; Kaganovsky, Jailanie; Hassan, Sajida; Tsinajinne, Darwin; Fullerton, Stephanie M.; Chen, Annie T.; Veenstra, David L.; Shirts, Brian H.
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Current chemoprevention approaches in Lynch syndrome and Familial adenomatous polyposis: a global clinical practice survey
err2023-05-24
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errMraz, Kathryn A.; Hodan, Rachel; Rodgers-Fouche, Linda; Arora, Sanjeevani; Balaguer, Francesc; Guillem, Jose G.; Jeter, Joanne M.; Kanth, Priyanka; Li, Dan; Liska, David; Melson, Joshua; Perez, Kimberly; Ricker, Charite; Shirts, Brian H.; Vilar, Eduardo; Katona, Bryson W.; Dominguez-Valentin, Mev
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Laboratory perspectives in the development of polygenic risk scores for disease: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)
err2023-05-01
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errReddi, Honey V.; Wand, Hannah; Funke, Birgit; Zimmermann, Michael T.; Lebo, Matthew S.; Qian, Emily; Shirts, Brian H.; Zou, Ying S.; Zhang, Bing M.; Rose, Nancy C.; Abu-El-Haija, Aya
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Extended Family Outreach in Hereditary Cancer Using Web-Based Genealogy, Direct-to-Consumer Ancestry Genetics, and Social Media: Mixed Methods Process Evaluation of the ConnectMyVariant Intervention
err2023-04-20
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errChen, Annie T.; Huey, Jennifer; Coe, Sandra; Kaganovsky, Jailanie; Malouf, Emily A.; Evans, Heather; Daker, Jill; Harper, Elizabeth; Fordiani, Olivia; Lowe, Emma E.; Oldroyd, Caileigh McGraw; Price, Ashlyn; Roth, Kristlynn; Stoddard, Julie; Crandell, N.; Shirts, Brian H.
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Optimising clinical care through CDH1-specific germline variant curation: improvement of clinical assertions and updated curation guidelines通过CDH1-specific种系变异管理优化临床护理: 改善临床断言和更新管理指南
err2022-12-07
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errLuo, Xi; Maciaszek, Jamie L.; Thompson, Bryony A.; San Leong, Huei; Dixon, Katherine; Sousa, Sonia; Anderson, Michael; Roberts, Maegan E.; Lee, Kristy; Spurdle, Amanda B.; Mensenkamp, Arjen R.; Brannan, Terra; Pardo, Carolina; Zhang, Liying; Pesaran, Tina; Wei, Sainan; Fasaye, Grace-Ann; Kesserwan, Chimene; Shirts, Brian H.; Davis, Jeremy L.; Oliveira, Carla; Plon, Sharon E.; Schrader, Kasmintan A.; Karam, Rachid
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Laboratory-related outcomes from integrating an accessible delivery model for hereditary cancer risk assessment and genetic testing in populations with barriers to access
err2022-06-01
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errAmendola, Laura M.; Shuster, Elizabeth; Leo, Michael C.; Dorschner, Michael O.; Rolf, Bradley A.; Shirts, Brian H.; Gilmore, Marian J.; Okuyama, Sonia; Zepp, Jamilyn M.; Kauffman, Tia L.; Mittendorf, Kathleen F.; Bellcross, Cecilia; Jenkins, Charisma L.; Joseph, Galen; Riddle, Leslie; Syngal, Sapna; Ukaegbu, Chinedu; Goddard, Katrina A. B.; Wilfond, Benjamin S.; Jarvik, Gail P.
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An algorithm for optimal testing in co-segregation analysis
err2022-04-07
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errBuie, Ronald W.; Ranola, John Michael O.; Chen, Annie T.; Shirts, Brian H.
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Inherited TP53 Variants and Risk of Prostate Cancer
err2022-03-01
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errMaxwell, Kara N.; Cheng, Heather H.; Powers, Jacquelyn; Gulati, Roman; Ledet, Elisa M.; Morrison, Casey; Le, Anh; Hausler, Ryan; Stopfer, Jill; Hyman, Sophie; Kohlmann, Wendy; Naumer, Anne; Vagher, Jennie; Greenberg, Samantha E.; Naylor, Lorraine; Laurino, Mercy; Konnick, Eric Q.; Shirts, Brian H.; AlDubayan, Saud H.; Van Allen, Eliezer M.; Nguyen, Bastien; Vijai, Joseph; Abida, Wassim; Carlo, Maria, I; Dubard-Gault, Marianne; Lee, Daniel J.; Maese, Luke D.; Mandelker, Diana; Montgomery, Bruce; Morris, Michael J.; Nicolosi, Piper; Nussbaum, Robert L.; Schwartz, Lauren E.; Stadler, Zsofia; Garber, Judy E.; Offit, Kenneth; Schiffman, Joshua D.; Nelson, Peter S.; Sartor, Oliver; Walsh, Michael F.; Pritchard, Colin C.
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The utility of CSF-derived cell free DNA in molecular diagnostics for the Megalencephaly-capillary Malformation (MCAP) syndrome: A case report
err2022-03-01
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errChen, Wei-Liang; Timms, Andrew; Pao, Emily; Owens, James; Glass, Ian; Shirts, Brian; Pritchard, Colin; Lockwood, Christina; Mirzaa, Ghayda
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Extending cascade screening using genealogy, DTC genetics and social media - the ConnectMyVariant exploratory pilot study
err2022-03-01
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errChen, Annie; Huey, Jenna; Coe, Sandy; Kaganovsky, Jailanie; Malouf, Emily; Evans, Heather; Daker, Jill; Harper, Elizabeth; Fordiani, Olivia; Lowe, Emma; Oldroyd, Caleigh; Price, Ashlyn; Roth, Kristlynn; Stoddard, Julie; Crandell, Jill; Shirts, Brian
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Molecular diagnosis of childhood immune dysregulation, polyendocrinopathy, and enteropathy, and implications for clinical management
err2022-01-01
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errBaxter, Sarah K.; Walsh, Tom; Casadei, Silvia; Eckert, Mary M.; Allenspach, Eric J.; Hagin, David; Segundo, Gesmar; Lee, Ming K.; Gulsuner, Suleyman; Shirts, Brian H.; Sullivan, Kathleen E.; Keller, Michael D.; Torgerson, Troy R.; King, Mary-Claire
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Harmonizing variant classification for return of results in the All of Us Research Program在全美研究计划中协调变体分类以返回结果
err2021-12-28
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errHarrison, Steven M.; Austin-Tse, Christina A.; Kim, Serra; Lebo, Matthew; Leon, Annette; Murdock, David; Radhakrishnan, Aparna; Shirts, Brian H.; Steeves, Marcie; Venner, Eric; Gibbs, Richard A.; Jarvik, Gail P.; Rehm, Heidi L.
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