Holly K Tabor

Publication Activity (10 Years)

Years Active: 2015-2022
Publications (10 Years): 12

Top Topics

High Throughput Sequencing

Human Immunodeficiency Virus

Top Venues

Journal of medical Internet research

Genetics in medicine : official journal of the American College of Medical Genetics

Journal of genetic counseling

Annals of the American Thoracic Society

This page only lists publications with an associated author ORCID identifier.

Publications

Megan Yabumoto, Emily Miller, Anoushka Rao, Holly K Tabor, Kelly E Ormond, Meghan C Halley
Perspectives of Rare Disease Social Media Group Participants on Engaging With Genetic Counselors: Mixed Methods Study. Journal of medical Internet research 24 (12) (2022)
Megan Yabumoto, Emily Miller, Anoushka Rao, Holly K Tabor, Kelly E Ormond, Meghan C Halley
Perspectives of Rare Disease Social Media Group Participants on Engaging With Genetic Counselors: Mixed Methods Study. Journal of medical Internet research 24 (12) (2022)
Megan Yabumoto, Emily Miller, Anoushka Rao, Holly K Tabor, Kelly E Ormond, Meghan C Halley
Perspectives of Rare Disease Social Media Group Participants on Engaging With Genetic Counselors: Mixed Methods Study. Journal of medical Internet research 24 (12) (2022)
Megan Yabumoto, Emily Miller, Anoushka Rao, Holly K Tabor, Kelly E Ormond, Meghan C Halley
Perspectives of Rare Disease Social Media Group Participants on Engaging With Genetic Counselors: Mixed Methods Study. Journal of medical Internet research 24 (12) (2022)
Megan Yabumoto, Emily Miller, Anoushka Rao, Holly K Tabor, Kelly E Ormond, Meghan C Halley
Perspectives of Rare Disease Social Media Group Participants on Engaging With Genetic Counselors: Mixed Methods Study. Journal of medical Internet research 24 (12) (2022)
Megan Yabumoto, Emily Miller, Anoushka Rao, Holly K Tabor, Kelly E Ormond, Meghan C Halley
Perspectives of Rare Disease Social Media Group Participants on Engaging With Genetic Counselors: Mixed Methods Study. Journal of medical Internet research 24 (12) (2022)
Heather A Dron, Daiana Bucio, Jennifer L Young, Holly K Tabor, Mildred K Cho
Latinx attitudes, barriers, and experiences with genetic counseling and testing: A systematic review. Journal of genetic counseling (2022)
Alexander A Iyer, Julie R Barzilay, Holly K Tabor
Patient and family social media use surrounding a novel treatment for a rare genetic disease: a qualitative interview study. Genetics in medicine : official journal of the American College of Medical Genetics 22 (11) (2020)
Craig P Hersh, Issssswan M Adcock, Juan C Celedón, Michael H Cho, David Chistopher Christiani, Blanca E Himes, Naftali Kaminski, Rasika A Mathias, Deborah A Meyers, John Quackenbush, Susan Redline, Katrina A Steiling, Holly K Tabor, Martin D Tobin, Mark M Wurfel, Ivana V Yang, Gerard H Koppelmann
High-Throughput Sequencing in Respiratory, Critical Care, and Sleep Medicine Research. An Official American Thoracic Society Workshop Report. Annals of the American Thoracic Society 16 (1) (2020)
Abby D'Angelo, Kelly E Ormond, David Magnus, Holly K Tabor
Assessing genetic counselors' experiences with physician aid-in-dying and practice implications. Journal of genetic counseling 28 (1) (2019)
Krysta S Barton, Andrew Wingerson, Julie R Barzilay, Holly K Tabor
"Before Facebook and before social media…we did not know anybody else that had this": parent perspectives on internet and social media use during the pediatric clinical genetic testing process. Journal of community genetics 10 (3) (2018)
Holly K Tabor, Seema M Jamal, Joon-Ho Yu, Julia M Crouch, Aditi G Shankar, Karin M Dent, Nick Anderson, Damon A Miller, Brett T Futral, Michael J Bamshad
My46: a Web-based tool for self-guided management of genomic test results in research and clinical settings. Genetics in medicine : official journal of the American College of Medical Genetics 19 (4) (2016)
Jessica Xiao-Ling Chong, Joon-Ho Yu, Peter Lorentzen, Karen M Park, Seema M Jamal, Holly K Tabor, Anita Rauch, Margarita Sifuentes Saenz, Eugen Boltshauser, Karynne E Patterson, Deborah A Nickerson, Michael J Bamshad
Gene discovery for Mendelian conditions via social networking: de novo variants in KDM1A cause developmental delay and distinctive facial features. Genetics in medicine : official journal of the American College of Medical Genetics 18 (8) (2015)