Loading...

Bryce Mendelsohn, MD, PhD

TitleAssistant Professor
InstitutionUniversity of California San Francisco
DepartmentPediatrics
Address550 16th. Street
San Francisco CA 94158
Phone415-476-3564
vCardDownload vCard

    Collapse Biography 
    Collapse Education and Training
    University of California, San FranciscoResidency School of Medicine
    Collapse Awards and Honors
    Emory University2000Phi Beta Kappa
    Washington University in St. Louis2009Alpha Omega Alpha
    UCSF2013  - 2015Pediatric Scientist Development Program

    Collapse Overview 

    Collapse ORNG Applications 
    Collapse In The News

    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
    List All   |   Timeline
    1. Hirabayashi KE, Moore AT, Mendelsohn B, Taft RJ, Chawla A, Perry D, Henry D, Slavotinek A. Congenital sodium diarrhea and chorioretinal coloboma with optic disc coloboma in a patient with biallelic SPINT2 mutations, including p.(Tyr163Cys). Am J Med Genet A. 2018 Apr; 176(4):997-1000. PMID: 29575628.
      View in: PubMed
    2. Slavotinek A, Risolino M, Losa M, Cho MT, Monaghan KG, Schneidman-Duhovny D, Parisotto S, Herkert JC, Stegmann APA, Miller K, Shur N, Chui J, Muller E, DeBrosse S, Szot JO, Chapman G, Pachter NS, Winlaw DS, Mendelsohn B, Dalton J, Sarafoglou K, Karachunski PI, Lewis JM, Pedro H, Dunwoodie SL, Selleri L, Shieh J. De novo, deleterious sequence variants that alter the transcriptional activity of the homeoprotein PBX1 are associated with intellectual disability and pleiotropic developmental defects. Hum Mol Genet. 2017 Dec 15; 26(24):4849-4860. PMID: 29036646.
      View in: PubMed
    3. Eppley S, Hopkin RJ, Mendelsohn B, Slavotinek AM. Clinical Report: Warsaw Breakage Syndrome with small radii and fibulae. Am J Med Genet A. 2017 Nov; 173(11):3075-3081. PMID: 28960803.
      View in: PubMed
    4. Punwani D, Zhang Y, Yu J, Cowan MJ, Rana S, Kwan A, Adhikari AN, Lizama CO, Mendelsohn B, Fahl SP, Chellappan A, Srinivasan R, Brenner SE, Wiest DL, Puck JM. Multisystem Anomalies in Severe Combined Immunodeficiency with Mutant BCL11B. N Engl J Med. 2016 12 01; 375(22):2165-2176. PMID: 27959755.
      View in: PubMed
    5. Petty EL, Lafon A, Tomlinson SL, Mendelsohn B, Pillus L. Promotion of Cell Viability and Histone Gene Expression by the Acetyltransferase Gcn5 and the Protein Phosphatase PP2A in Saccharomyces cerevisiae. Genetics. 2016 08; 203(4):1693-707. PMID: 27317677; PMCID: PMC4981271 [Available on 08/01/17].
    6. Scott AI, Mendelsohn B, Le A, Cowan TM. The antibiotic cefepime interferes with amino acid analysis by ion-exchange chromatography. Clin Chim Acta. 2016 May 01; 456:149-150. PMID: 26947969.
      View in: PubMed
    7. Pathak D, Shields LY, Mendelsohn B, Haddad D, Lin W, Gerencser AA, Kim H, Brand MD, Edwards RH, Nakamura K. The role of mitochondrially derived ATP in synaptic vesicle recycling. J Biol Chem. 2015 Sep 11; 290(37):22325-36. PMID: 26126824; PMCID: PMC4566209.
    8. Mendelsohn B, Pronold M, Long R, Smaoui N, Slavotinek AM. Advanced bone age in a girl with Wiedemann-Steiner syndrome and an exonic deletion in KMT2A (MLL). Am J Med Genet A. 2014 Aug; 164A(8):2079-83. PMID: 24818805.
      View in: PubMed
    9. Mendelsohn B, Jeng LL, Oberoi S, Klein OD. Dental findings in 14q terminal deletion syndrome. Clin Dysmorphol. 2014 Apr; 23(2):60-2. PMID: 24535103.
      View in: PubMed
    10. Mendelsohn B, Mehta N, Hameed B, Pekmezci M, Packman S, Ralph J. Adult-Onset Fatal Neurohepatopathy in a Woman Caused by MPV17 Mutation. JIMD Rep. 2014; 13:37-41. PMID: 24190800; PMCID: PMC4110326.
    11. Mendelsohn B. A piece of my mind. What is natural? JAMA. 2013 May 01; 309(17):1783-4. PMID: 23632721.
      View in: PubMed
    12. Mendelsohn B, Malone JP, Townsend RR, Gitlin JD. Proteomic analysis of anoxia tolerance in the developing zebrafish embryo. Comp Biochem Physiol Part D Genomics Proteomics. 2009 Mar; 4(1):21-31. PMID: 20403745.
      View in: PubMed
    13. Mendelsohn B, Kassebaum BL, Gitlin JD. The zebrafish embryo as a dynamic model of anoxia tolerance. Dev Dyn. 2008 Jul; 237(7):1780-8. PMID: 18521954; PMCID: PMC3081722.
    14. Mendelsohn B, Gitlin JD. Coordination of development and metabolism in the pre-midblastula transition zebrafish embryo. Dev Dyn. 2008 Jul; 237(7):1789-98. PMID: 18521947.
      View in: PubMed
    15. Madsen EC, Morcos PA, Mendelsohn B, Gitlin JD. In vivo correction of a Menkes disease model using antisense oligonucleotides. Proc Natl Acad Sci U S A. 2008 Mar 11; 105(10):3909-14. PMID: 18316734; PMCID: PMC2268804.
    16. Gansner JM, Mendelsohn B, Hultman KA, Johnson SL, Gitlin JD. Essential role of lysyl oxidases in notochord development. Dev Biol. 2007 Jul 15; 307(2):202-13. PMID: 17543297; PMCID: PMC2467443.
    17. Mendelsohn B, Yin C, Johnson SL, Wilm TP, Solnica-Krezel L, Gitlin JD. Atp7a determines a hierarchy of copper metabolism essential for notochord development. Cell Metab. 2006 Aug; 4(2):155-62. PMID: 16890543.
      View in: PubMed
    18. Mendelsohn B, Li AM, Vargas CA, Riehman K, Watson A, Fridovich-Keil JL. Genetic and biochemical interactions between SCP160 and EAP1 in yeast. Nucleic Acids Res. 2003 Oct 15; 31(20):5838-47. PMID: 14530432; PMCID: PMC219487.