Kimberly Kripps, M.D.

- B.S., 2009, University of Washington
- M.D., 2014, Medical College of Wisconsin
Residency
- Phoenix Children’s Hospital and Maricopa Medical Center Pediatric Residency Program, Phoenix, AZ
- University of Colorado Clinical Genetics and Metabolism Residency Program, Aurora, CO
Fellowship
- University of Colorado Medical Biochemical Genetics Fellowship Program, Aurora, CO

Selected for the Travel Award for poster
Selected to give a podium presentation of project on Mucolipidosis Type IV at the MCW Pathways Scholarship Forum, 2013
Recipient of the Washington Scholars Scholarship, 2005-2009

Publications

Kripps K and McCandless S. Book Chapter: Genetics, including Inborn Errors of Metabolism. Klaus and Fanaroff, Care of the High Risk Neonate, 7th Ed.
Emrick, LT, Rosenfeld JA, Lalani SR, Jain M, Desai NK, Larson A, Kripps K, et al. "Microdeletions Excluding Ywhae and Pafah1b1 Cause a Unique Leukoencephalopathy: Further Delineation of the 17p13.3 Microdeletion Spectrum." Genet Med 2019;21(7): 1652-56. https://doi.org/10.1038/s41436-018-0358-0.
Shireman LM, Kripps KA, Balogh LM, Conner KP, Whittington D, Atkins WM. Glutathione transferase A4-4 resists adduction by 4-hydroxynonenal. Arch Biochem Biophys. 2010;504(2):182-9.
Balogh LM, Le Trong I, Kripps KA, Tars K, Stenkamp RE, Mannervik B, and Atkins WM. Structural Analysis of a Glutathione Transferase A1-1 Mutant Tailored for High Catalytic Efficiency with Toxic Alkenals. Biochemistry. 2009;48:7698-7704.