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Sabrina Malone-Jenkins
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Sabrina Malone-Jenkins, MD

Languages spoken: English

  • Sabrina Malone Jenkins, MD is an Assistant Professor of Pediatrics at the Ï㽶ÊÓƵ of Utah in the Division of Neonatology. She provides care to critically ill infants in the Newborn Intensive Care Units at Primary Children’s Medical Center, the Ï㽶ÊÓƵ of Utah Medical Center, and Intermountain Medical Center. Her clinical interests include improving neonatal nutrition and genetic testing in the NICU.

    Specialties

    Board Certification

    American Board of Pediatrics (Pediatrics)
    American Board of Pediatrics (Sub: Neonatal-Perinatal Medicine)

  • Sabrina Malone Jenkins, MD is an Assistant Professor of Pediatrics at the Ï㽶ÊÓƵ of Utah in the Division of Neonatology. She provides care to critically ill infants in the Newborn Intensive Care Units at Primary Children’s Medical Center, the Ï㽶ÊÓƵ of Utah Medical Center, and Intermountain Medical Center. Her clinical interests include improving neonatal nutrition and genetic testing in the NICU.

    Board Certification and Academic Information

    Academic Departments Pediatrics -Primary
    Academic Divisions Neonatology
    Board Certification
    American Board of Pediatrics (Pediatrics)
    American Board of Pediatrics (Sub: Neonatal-Perinatal Medicine)

    Education history

    Fellowship Neonatal-Perinatal Medicine - Ï㽶ÊÓƵ of Utah Fellow
    Pediatrics - Ï㽶ÊÓƵ of Nebraska Medical Center/Creighton Ï㽶ÊÓƵ Medical Center Resident
    Professional Medical Ross Ï㽶ÊÓƵ School of Medicine M.D.
    Nutritional Sciences - Ï㽶ÊÓƵ of Florida B.S.

    Selected Publications

    Journal Article

    1. Callahan KP, Radack J, Wojcik MH, Jenkins SM, Nye RT, Skraban C, Wild KT, Feudtner C (2022). Hospital-level variation in genetic testing in children's hospitals' neonatal intensive care units from 2016 to 2021spital-level variation in genetic testing in children's hospitals' neonatal intensive care units from 2016 to 2021. Genet Med, 25(3), 100357.
    2. Nicholas T, Al-Sweel N, Farrell A, Mao R, Bayrak-Toydemir P, Miller C, Bentley D, Palmquist R, Moore B, Hernandez E, Cormier M, Fredrickson E, Noble K, Rynearson S, Holt C, Karren MA, Bonkowsky J, Tristani-Firouzi M, Yandell M, Marth G, Quinlan A, Brunelli L, Toydemir R, Shayota B, Carey J, Boyden S, Malone Jenkins S (2022). Comprehensive variant calling from whole-genome sequencing identifies a complex inversion that disrupts ZFPM2 in familial congenital diaphragmatic hernia. Mol Genet Genomics, e1888, doi: 10.1002/mgg3.1888. Epub ahead of print. PMID: 35119225.
    3. Palmquist R, Malone Jenkins S co-first author, Bentley D, Miller C, Rong M, Meibos B, Bayrak-Toydemir P, Tvrdik T, Nadauld L, Bleyl S, Chowdhury S, Ostrander B, Flores-Daboub J, Longo N, Tristani-Firouzi M, Hobbs C, Bonkowsky J and Brunelli L (2022). Evaluating Use of Changing Technologies for Rapid Next Generation Sequencing in Pediatrics. Pediatr Res, doi: 10.1038/s41390-022-01965-5. Epub ahead of print. PMID: 35115709.
    4. Ward A, Velinder M, Di Sera T, Ekawake A, Malone Jenkins S, Moore B, Mao R, Bayrak-Toydemir P, Marth G (2022). Clin.iobio: A Collaborative Diagnostic Workflow to Enable Team-Based Precision Genomics. J Pers Med, 12(1), 73.
    5. Malone Jenkins S, Palmquist R, Kapron A, Torr C, Best D, Karren M, Brunelli L, Yandell M, Tristani-Firouzi M, Dimmock D, Watts B, Botkin J, Johnson A, Bonkowsky J (2021). Addressing ethical and laboratory challenges for initiation of a rapid whole genome sequencing program. J Clin Transl Sci, 5(1), e177.
    6. Brunelli L, Jenkins SM co-first authors, Gudgeon JM, Bleyl SB, Miller CE, Tvrdik T, Dames SA, Ostrander B, Daboub JAF, Zielinski BA, Zinkhan EK, Underhill HR, Wilson T, Bonkowsky JL, Yost CC, Botto LD, Jenkins J, Pysher TJ, Bayrak-Toydemir P, Mao R (2019). Targeted gene panel sequencing for the rapid diagnosis of acutely ill infants. Mol Genet Genomic Med, 7(7), e00796. ()
    7. Brunelli L, Mao R, Jenkins SM, Bleyl SB, Dames SA, Miller CE, Ostrander B, Tvrdik T, Andrews S, Flores J, Patel S, Gudgeon JM, Schaefer S (2017). A rapid gene sequencing panel strategy to facilitate precision neonatal medicine. Am J Med Genet A, 173(7), 1979-1982. ()

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