Jasmine Wong, PhD, MS

Title(s)Associate Professor, Pediatrics
SchoolSchool of Medicine
Address1450 3rd Street
San Francisco CA 94158
Phone415-476-5145
ORCID ORCID Icon0000-0002-2564-8095 Additional info
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    Collapse Biography 
    Collapse Education and Training
    University of California, San FranciscoPostdoctoral FellowPediatrics (hematology/oncology)
    University of TorontoPh.D.Molecular and Medical Genetics
    University of TorontoM.Sc.Molecular and Medical Genetics
    University of WaterlooB.Sc.Biochemistry (Biotechnology option)

    Collapse Overview 

    Collapse Research 
    Collapse Research Activities and Funding
    In Vivo Functional Analysis of Chromosome 7q22 Deletions in Myeloid Malignancies
    NIH/NCI R01CA216352May 22, 2017 - Apr 30, 2022
    Role: Co-Investigator
    Biologic and Preclinical Studies of Myeloid Malignancies
    NIH R50CA211452Sep 15, 2016 - Aug 31, 2021
    Role: Principal Investigator

    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. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. KrasP34R and KrasT58I mutations induce distinct RASopathy phenotypes in mice. JCI Insight. 2020 11 05; 5(21). Wong JC, Perez-Mancera PA, Huang TQ, Kim J, Grego-Bessa J, Del Pilar Alzamora M, Kogan SC, Sharir A, Keefe SH, Morales CE, Schanze D, Castel P, Hirose K, Huang GN, Zenker M, Sheppard D, Klein OD, Tuveson DA, Braun BS, Shannon K. PMID: 32990679; PMCID: PMC7710308.
      View in: PubMed   Mentions: 2     Fields:    Translation:Animals
    2. Genetic disruption of N-RasG12D palmitoylation perturbs hematopoiesis and prevents myeloid transformation in mice. Blood. 2020 05 14; 135(20):1772-1782. Zambetti NA, Firestone AJ, Remsberg JR, Huang BJ, Wong JC, Long AM, Predovic M, Suciu RM, Inguva A, Kogan SC, Haigis KM, Cravatt BF, Shannon K. PMID: 32219446; PMCID: PMC7225687.
      View in: PubMed   Mentions: 4     Fields:    Translation:AnimalsCells
    3. Loss of glucocorticoid receptor expression mediates in vivo dexamethasone resistance in T-cell acute lymphoblastic leukemia. Leukemia. 2020 08; 34(8):2025-2037. Wandler AM, Huang BJ, Craig JW, Hayes K, Yan H, Meyer LK, Scacchetti A, Monsalve G, Dail M, Li Q, Wong JC, Weinberg O, Hasserjian RP, Kogan SC, Jonsson P, Yamamoto K, Sampath D, Nakitandwe J, Downing JR, Zhang J, Aster JC, Taylor BS, Shannon K. PMID: 32066867; PMCID: PMC7440098.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansAnimals
    4. Convergent genetic aberrations in murine and human T lineage acute lymphoblastic leukemias. PLoS Genet. 2019 06; 15(6):e1008168. Huang BJ, Wandler AM, Meyer LK, Dail M, Daemen A, Sampath D, Li Q, Wang X, Wong JC, Nakitandwe J, Downing JR, Zhang J, Taylor BS, Shannon K. PMID: 31199785; PMCID: PMC6594654.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansAnimalsCells
    5. Germline SAMD9 and SAMD9L mutations are associated with extensive genetic evolution and diverse hematologic outcomes. JCI Insight. 2018 07 26; 3(14). Wong JC, Bryant V, Lamprecht T, Ma J, Walsh M, Schwartz J, Del Pilar Alzamora M, Mullighan CG, Loh ML, Ribeiro R, Downing JR, Carroll WL, Davis J, Gold S, Rogers PC, Israels S, Yanofsky R, Shannon K, Klco JM. PMID: 30046003; PMCID: PMC6124395.
      View in: PubMed   Mentions: 28     Fields:    Translation:HumansCells
    6. Functional evidence implicating chromosome 7q22 haploinsufficiency in myelodysplastic syndrome pathogenesis. Elife. 2015 Jul 20; 4. Wong JC, Weinfurtner KM, Alzamora Mdel P, Kogan SC, Burgess MR, Zhang Y, Nakitandwe J, Ma J, Cheng J, Chen SC, Ho TT, Flach J, Reynaud D, Passegué E, Downing JR, Shannon K. PMID: 26193121; PMCID: PMC4569895.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansAnimalsCells
    7. Hematopoiesis and leukemogenesis in mice expressing oncogenic NrasG12D from the endogenous locus. Blood. 2011 Feb 10; 117(6):2022-32. Li Q, Haigis KM, McDaniel A, Harding-Theobald E, Kogan SC, Akagi K, Wong JC, Braun BS, Wolff L, Jacks T, Shannon K. PMID: 21163920; PMCID: PMC3056645.
      View in: PubMed   Mentions: 77     Fields:    Translation:HumansAnimalsCells
    8. Gain of MYC underlies recurrent trisomy of the MYC chromosome in acute promyelocytic leukemia. J Exp Med. 2010 Nov 22; 207(12):2581-94. Jones L, Wei G, Sevcikova S, Phan V, Jain S, Shieh A, Wong JC, Li M, Dubansky J, Maunakea ML, Ochoa R, Zhu G, Tennant TR, Shannon KM, Lowe SW, Le Beau MM, Kogan SC. PMID: 21059853; PMCID: PMC2989761.
      View in: PubMed   Mentions: 40     Fields:    Translation:HumansAnimalsCells
    9. Use of chromosome engineering to model a segmental deletion of chromosome band 7q22 found in myeloid malignancies. Blood. 2010 Jun 03; 115(22):4524-32. Wong JC, Zhang Y, Lieuw KH, Tran MT, Forgo E, Weinfurtner K, Alzamora P, Kogan SC, Akagi K, Wolff L, Le Beau MM, Killeen N, Shannon K. PMID: 20233966; PMCID: PMC2881500.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansAnimalsCells
    10. Tumor suppressor gene inactivation in myeloid malignancies. Best Pract Res Clin Haematol. 2008 Dec; 21(4):601-14. Wong JC, Le Beau MM, Shannon K. PMID: 19041599.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansAnimals
    11. MLL5 contributes to hematopoietic stem cell fitness and homeostasis. Blood. 2009 Feb 12; 113(7):1455-63. Zhang Y, Wong J, Klinger M, Tran MT, Shannon KM, Killeen N. PMID: 18818388; PMCID: PMC2644073.
      View in: PubMed   Mentions: 42     Fields:    Translation:AnimalsCells
    12. Cloning and mutation analysis of ZFP276 as a candidate tumor suppressor in breast cancer. J Hum Genet. 2003; 48(12):668-671. Wong JCY, Gokgoz N, Alon N, Andrulis IL, Buchwald M. PMID: 14605947.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    13. Targeted disruption of exons 1 to 6 of the Fanconi Anemia group A gene leads to growth retardation, strain-specific microphthalmia, meiotic defects and primordial germ cell hypoplasia. Hum Mol Genet. 2003 Aug 15; 12(16):2063-76. Wong JC, Alon N, Mckerlie C, Huang JR, Meyn MS, Buchwald M. PMID: 12913077.
      View in: PubMed   Mentions: 76     Fields:    Translation:AnimalsCells
    14. Disease model: Fanconi anemia. Trends Mol Med. 2002 Mar; 8(3):139-42. Wong JC, Buchwald M. PMID: 11879775.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansAnimals
    15. Cloning and analysis of the mouse Fanconi anemia group A cDNA and an overlapping penta zinc finger cDNA. Genomics. 2000 Aug 01; 67(3):273-83. Wong JC, Alon N, Norga K, Kruyt FA, Youssoufian H, Buchwald M. PMID: 10936049.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansAnimalsCells
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