RMND1 and PLN variants are the underlying cause of Perrault-like syndrome and cardiac anomalies in a patient. Du, X; Barnett, CL; Widmeyer, KM; Wang, X; Brightman, DS; Noonan, CW; Weaver, KN; Hopkin, RJ; Wu, Y. Clinical Case Reports. 2024; 12:e9537.

14q22.3 duplication including OTX2 in a girl with medulloblastoma: A case report with literature review. Blake, C; Widmeyer, K; DAquila, K; Mochizuki, A; Smolarek, TA; Pillay-Smiley, N; Kim, SY. American Journal of Medical Genetics, Part A. 2024; 194:e63604.

Preparedness and training of genetic counselors practicing in inpatient settings. Mancl, N; Myers, MF; Miller, EM; Jackson, F; Widmeyer, K. Journal of Genetic Counseling. 2024; 33:539-553.

Factors that influence the management recommendations breast surgeons provide to women with pathogenic variants in moderate penetrance breast cancer susceptibility genes. Vanderwal, A; Lewis, J; Basil, J; Atzinger, C; Widmeyer, K. Journal of Genetic Counseling. 2023; 32:674-684.

Factors that impact risk management decisions among women with pathogenic variants in moderate penetrance genes associated with hereditary breast cancer. Napoli, M; Lewis, J; Hopper, J; Widmeyer, K. Journal of Genetic Counseling. 2020; 29:960-970.