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Journal of Community Genetics|November 28, 2016
A novel approach to screening for familial hypercholesterolemia in a large public venueMegan Campbell, Jessa Humanki, Heather ZierhutAmerican Journal of Medical Genetics. Part A|July 30, 2015
Canaries in the coal mine: Personal and professional impact of undergoing whole genome sequencing on medical professionalsHeather Zierhut, Patricia McCarthy Veach, Bonnie LeRoyGenetics in Medicine : Official Journal of the American College of Medical Genetics|June 17, 2022
A scoping review of interventions increasing screening and diagnosis of familial hypercholesterolemiaAmanda Polanski, Ellory Wolin, Megan Kocher, et al.Journal of Genetic Counseling|March 15, 2017
Seekers, Finders, Settlers, and Stumblers: Identifying the Career Paths of Males in the Genetic Counseling ProfessionAnthony Chen, Pat McCarthy Veach, Cheri Schoonveld, et al.Journal of Clinical Lipidology|March 1, 2020
Pediatric cholesterol screening practices in 9- to 11-year-olds in a large midwestern primary care settingCarly Allen-Tice, Julia Steinberger, Kari Murdy, et al.Journal of Genetic Counseling|January 31, 2026
Navigating identity and professional life: A qualitative study of LGBTQ+ genetic counselors' workplace experiencesKayla L Nelson, Kimberly Zayhowski, Ian M MacFarlaneJournal of Genetic Counseling|January 24, 2024
The State of National Institute of Health Awards for funding genetic counseling research, resources, and training over the past decadeHeather Zierhut, Samantha Betterman, Megan Kocher, et al.Journal of Genetic Counseling|December 11, 2024
Evaluating genetic counseling session duration: A scoping review of patient care time, influencing factors, and impact on patient outcomesEmily Glanton, Megan Kocher, Molly Bostrom, et al.Journal of Genetic Counseling|September 25, 2023
Genetic counseling processes and strategies for racially and ethnically diverse populations: A systematic reviewMrunmayee Shete, Megan Kocher, Rebekah Pratt, et al.American Journal of Medical Genetics. Part A|October 8, 2016
Phenotypic variability in patients with Fanconi anemia and biallelic FANCF mutationsRebecca Tryon, Heather Zierhut, Margaret L MacMillan, et al.Pageof 8