Kimberly M. Widmeyer, MS, LGC

Licensed Genetic Counselor III, Division of Human Genetics

kimberly.lewis@cchmc.org

About

Masters: Medical Genetics, University of Cincinnati, Cincinnati, OH, 2012,

Services and Specialties

Human Genetics

Publications

Neonatal Inflammatory Skin and Bowel Disease 1 (NISBD1): A Case of ADAM17 Homozygous Mutation. Chang, HR; Bannon, M; Opper, C; Slavotinek, A; Hijazi, G; Widmeyer, KM; Kellner, ES; Iqneibi, M; Bayart, C; Marathe, KS; Bridges, C. Pediatric Dermatology. 2025.

Differences in Prenatal and Postnatal Phenotypic Evaluations in Patients With Congenital Anomalies and Known Genetic Diagnoses. Horton, N; Tolusso, L; Widmeyer, K; He, H; Swarr, DT. Prenatal Diagnosis. 2025; 45(10):1281-1291.

Mosaic X-linked adrenoleukodystrophy in males identified by newborn screening and next-generation sequencing. Keefe, AC; Jensen, DM; Pham, MM; Au, NYT; Beckman, E; Penon-Portmann, M; Shelkowitz, E; Bend, R; Morrow, MM; Kruszka, P; Lund, TC; Eichler, FS; Sun, A; Bennett, JT. npj Genomic Medicine. 2025; 10(1):38.

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(11):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(7):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(3):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(3):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(6):960-970.