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Kimberly A. Kripps

Observed names: K Kripps, Kimberly A Kripps, Kimberly Kripps, KimberlyA. Kripps
ORCID: 0000-0002-1343-9974
Observed ORCID: 0000-0002-1343-9974
OpenAlex ID: A5026928142
Substrate Specificity Combined with Stereopromiscuity in Glutathione Transferase A4-4-Dependent Metabolism of 4-Hydroxynonenal
2010 · Larissa M. Balogh, Isolde Le Trong, et al. · Biochemistry · 46
Successful liver transplantation in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)
2020 · KimberlyA. Kripps, Warapan Nakayuenyongsuk, et al. · Molecular Genetics and Metabolism · 38
Methionine synthase deficiency: Variable clinical presentation and benefit of early diagnosis and treatment
2021 · Kimberly A. Kripps, Leighann Sremba, et al. · Journal of Inherited Metabolic Disease · 29
Loss of FOCAD, operating via the SKI messenger RNA surveillance pathway, causes a pediatric syndrome with liver cirrhosis
2022 · Ricardo Moreno Traspas, Tze Shin Teoh, et al. · Nature Genetics · 28
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Structural Analysis of a Glutathione Transferase A1-1 Mutant Tailored for High Catalytic Efficiency with Toxic Alkenals
2009 · Larissa M. Balogh, Isolde Le Trong, et al. · Biochemistry · 25
Glutathione transferase A4-4 resists adduction by 4-hydroxynonenal
2010 · Laura M. Shireman, Kimberly A. Kripps, et al. · Archives of Biochemistry and Biophysics · 24
Microdeletions excluding YWHAE and PAFAH1B1 cause a unique leukoencephalopathy: further delineation of the 17p13.3 microdeletion spectrum
2018 · Lisa T. Emrick, Jill A. Rosenfeld, et al. · Genetics in Medicine · 15
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REVIEW: Practical strategies to maintain anabolism by intravenous nutritional management in children with inborn metabolic diseases
2021 · Kimberly A. Kripps, Peter R. Baker, et al. · Molecular Genetics and Metabolism · 13
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Feasibility of newborn screening for pyridoxine-dependent epilepsy
2024 · Kristine Pauly, Michael Woontner, et al. · Molecular Genetics and Metabolism · 10
A novel acceptor stem variant in mitochondrial tRNATyr impairs mitochondrial translation and is associated with a severe phenotype
2020 · Kimberly A. Kripps, Marisa W. Friederich, et al. · Molecular Genetics and Metabolism · 7
Rubella virus‐associated necrotizing granulomatous inflammation with extensive eyelid, ocular, and orbital involvement
2023 · Matthew A. Pimentel, Donna H. Kim, et al. · Pediatric Dermatology · 3
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The clinical utility of functional testing in fibroblasts to diagnose primary mitochondrial disease
2026 · Johan L.K. Van Hove, Marisa W. Friederich, et al. · medRxiv · 1
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P.48 Severe variant for pyridoxine dependent epilepsy found in the Micronesian population: a case study
2024 · L Sliwoski, S Van Calcar, et al. · Molecular Genetics and Metabolism · 1
A Novel Intronic Pathogenic Variant in STAR With a Dominant Negative Mechanism Causes Attenuated Lipoid Congenital Adrenal Hyperplasia
2021 · Erin Finn, Kimberly Kripps, et al. · Journal of Investigative Medicine High Impact Case Reports · 1
Unusual Neuroimaging in a Case of Rapidly Progressive Juvenile-Onset Krabbe Disease
2020 · Kimberly Kripps, Janell Kierstein, et al. · Journal of Child Neurology · 1
Comprehensive functional testing in fibroblasts has strong utility to diagnose mitochondrial disease
2026 · Johan L K Van Hove, Marisa W Friederich, et al. · EMBO Molecular Medicine
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Novel SUCLG1 Variants in a Patient with Fatal Neonatal Onset Succinyl-Coa Ligase Deficiency
2025 · Devlynne S. Ondusko, Lauren Culbertson, et al. · Journal of Pediatric Genetics
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Pyridoxine Dependent Epilepsy: Identification of a Founder Variant in the Micronesian Population With Severe Features
2023 · Kimberly Kripps, Cary Harding, et al. · Molecular Genetics and Metabolism
Anabolism: Practical Strategies
2022 · Kimberly A. Kripps, Johan L. K. Van Hove · Springer eBooks
Urea Cycle Disorders in Children
2021 · Kimberly A. Kripps, Derek A. Wong, et al. · Cambridge University Press eBooks
Contributors
2020 · Isabella Peixoto de Barcelos, Marni J. Falk, et al. · Elsevier eBooks
Works count: 21
Citation count: 242
H-index: 9
I10-index: 9
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