- Medical School - UT Southwestern Medical School (2011-2016)
- Residency - UT Southwestern Medical Center (2016-2018), Pathology
- Fellowship - UT Southwestern Medical Center (2018-2019), Molecular Genetics
- Residency - UT Southwestern Medical Center (2019-2020), Pathology

Jeffrey Sorelle, M.D.
- Pathology
Education & Training
Books & Publications
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Publications
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Real-time resolution of point mutations that cause phenovariance in mice.
Wang T, Zhan X, Bu CH, Lyon S, Pratt D, Hildebrand S, Choi JH, Zhang Z, Zeng M, Wang KW, Turer E, Chen Z, Zhang D, Yue T, Wang Y, Shi H, Wang J, Sun L, SoRelle J, McAlpine W, Hutchins N, Zhan X, Fina M, Gobert R, Quan J, Kreutzer M, Arnett S, Hawkins K, Leach A, Tate C, Daniel C, Reyna C, Prince L, Davis S, Purrington J, Bearden R, Weatherly J, White D, Russell J, Sun Q, Tang M, Li X, Scott L, Moresco EM, McInerney GM, Karlsson Hedestam GB, Xie Y, Beutler B Proceedings of the National Academy of Sciences of the United States of America 2015 Jan -
Clinical Utility of Reinterpreting Previously Reported Genomic Epilepsy Test Results for Pediatric Patients.
SoRelle JA, Thodeson DM, Arnold S, Gotway G, Park JY JAMA pediatrics 2018 Nov e182302 -
Mutual inhibition between Prkd2 and Bcl6 controls T follicular helper cell differentiation.
Misawa T, SoRelle JA, Choi JH, Yue T, Wang KW, McAlpine W, Wang J, Liu A, Tabeta K, Turer EE, Evers B, Nair-Gill E, Poddar S, Su L, Ou F, Yu L, Russell J, Ludwig S, Zhan X, Hildebrand S, Li X, Tang M, Murray AR, Moresco EMY, Beutler B, Science immunology 2020 Jan 5 43 -
Assessment of Interlaboratory Variation in the Interpretation of Genomic Test Results in Patients With Epilepsy.
SoRelle JA, Pascual JM, Gotway G, Park JY, JAMA network open 2020 Apr 3 4 e203812 -
Impact of Hormone Therapy on Laboratory Values in Transgender Patients.
SoRelle JA, Jiao R, Gao E, Veazey J, Frame I, Quinn AM, Day P, Pagels P, Gimpel N, Patel K Clinical chemistry 2019 Jan 65 1 170-179 -
Clinical Validation of a SARS-CoV-2 Real-Time Reverse Transcription PCR Assay Targeting the Nucleocapsid Gene.
SoRelle JA, Frame I, Falcon A, Jacob J, Wagenfuehr J, Mitui M, Park JY, Filkins L, The journal of applied laboratory medicine 2020 Jun -
Different Interpretations of the Same Genetic Data.
SoRelle JA, Gemmell AP, Ross TS, Annals of internal medicine 2020 Jun
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Real-time resolution of point mutations that cause phenovariance in mice.