Julia Meyer, PhD

Title(s)Associate Specialist, Pediatrics
SchoolSchool of Medicine
Address1450 3rd Street
San Francisco CA 94158
Phone415-514-9389
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    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. Molecular and phenotypic diversity of CBL-mutated juvenile myelomonocytic leukemia. Haematologica. 2022 01 01; 107(1):178-186. Hecht A, Meyer JA, Behnert A, Wong E, Chehab F, Olshen A, Hechmer A, Aftandilian C, Bhat R, Choi SW, Chonat S, Farrar JE, Fluchel M, Frangoul H, Han JH, Kolb EA, Kuo DJ, MacMillan ML, Maese L, Maloney KW, Narendran A, Oshrine B, Schultz KR, Sulis ML, Van Mater D, Tasian SK, Hofmann WK, Loh ML, Stieglitz E. PMID: 33375775; PMCID: PMC8719097.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    2. Association of Combined Focal 22q11.22 Deletion and IKZF1 Alterations With Outcomes in Childhood Acute Lymphoblastic Leukemia. JAMA Oncol. 2021 Oct 01; 7(10):1521-1528. Mangum DS, Meyer JA, Mason CC, Shams S, Maese LD, Gardiner JD, Downie JM, Pei D, Cheng C, Gleason A, Luo M, Pui CH, Aplenc R, Hunger SP, Loh M, Greaves M, Trede N, Raetz E, Frazer JK, Mullighan CG, Engel ME, Miles RR, Rabin KR, Schiffman JD. PMID: 34410295; PMCID: PMC8377604.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    3. Genome-wide DNA methylation analysis pre- and post-lenalidomide treatment in patients with myelodysplastic syndrome with isolated deletion (5q). Ann Hematol. 2021 Jun; 100(6):1463-1471. Hecht A, Meyer JA, Jann JC, Sockel K, Giagounidis A, Götze KS, Letsch A, Haase D, Schlenk RF, Haferlach T, Schafhausen P, Bug G, Lübbert M, Thol F, Büsche G, Schuler E, Nowak V, Obländer J, Fey S, Müller N, Metzgeroth G, Hofmann WK, Germing U, Nolte F, Reinwald M, Nowak D. PMID: 33903952; PMCID: PMC8116243.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCellsCTClinical Trials
    4. International Consensus Definition of DNA Methylation Subgroups in Juvenile Myelomonocytic Leukemia. Clin Cancer Res. 2021 01 01; 27(1):158-168. Schönung M, Meyer J, Nöllke P, Olshen AB, Hartmann M, Murakami N, Wakamatsu M, Okuno Y, Plass C, Loh ML, Niemeyer CM, Muramatsu H, Flotho C, Stieglitz E, Lipka DB. PMID: 33139265; PMCID: PMC7785676.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    5. Feasibility of monitoring peripheral blood to detect emerging clones in children with acute lymphoblastic leukemia†. Pediatr Blood Cancer. 2020 07; 67(7):e28306. Saliba J, Evensen NA, Meyer JA, Newman D, Nersting J, Narang S, Ma X, Schmiegelow K, Carroll WL. PMID: 32391957.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    6. Fusion driven JMML: a novel CCDC88C-FLT3 fusion responsive to sorafenib identified by RNA sequencing. Leukemia. 2020 02; 34(2):662-666. Chao AK, Meyer JA, Lee AG, Hecht A, Tarver T, Van Ziffle J, Koegel AK, Golden C, Braun BS, Sweet-Cordero EA, Smith CC, Dvorak CC, Loh ML, Stieglitz E. PMID: 31511612; PMCID: PMC6995757.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansAnimalsCells
    7. Mechanisms of NT5C2-Mediated Thiopurine Resistance in Acute Lymphoblastic Leukemia. Mol Cancer Ther. 2019 10; 18(10):1887-1895. Moriyama T, Liu S, Li J, Meyer J, Zhao X, Yang W, Shao Y, Heath R, Hnízda A, Carroll WL, Yang JJ. PMID: 31358663; PMCID: PMC6774896.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    8. Molecular assessment of pretransplant chemotherapy in the treatment of juvenile myelomonocytic leukemia. Pediatr Blood Cancer. 2019 11; 66(11):e27948. Hecht A, Meyer J, Chehab FF, White KL, Magruder K, Dvorak CC, Loh ML, Stieglitz E. PMID: 31347788; PMCID: PMC6754267.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    9. Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome. Am J Hum Genet. 2019 06 06; 104(6):1223-1232. Capri Y, Flex E, Krumbach OHF, Carpentieri G, Cecchetti S, Lißewski C, Rezaei Adariani S, Schanze D, Brinkmann J, Piard J, Pantaleoni F, Lepri FR, Goh ES, Chong K, Stieglitz E, Meyer J, Kuechler A, Bramswig NC, Sacharow S, Strullu M, Vial Y, Vignal C, Kensah G, Cuturilo G, Kazemein Jasemi NS, Dvorsky R, Monaghan KG, Vincent LM, Cavé H, Verloes A, Ahmadian MR, Tartaglia M, Zenker M. PMID: 31130282; PMCID: PMC6562003.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansCells
    10. MSH6 haploinsufficiency at relapse contributes to the development of thiopurine resistance in pediatric B-lymphoblastic leukemia. Haematologica. 2018 05; 103(5):830-839. Evensen NA, Madhusoodhan PP, Meyer J, Saliba J, Chowdhury A, Araten DJ, Nersting J, Bhatla T, Vincent TL, Teachey D, Hunger SP, Yang J, Schmiegelow K, Carroll WL. PMID: 29449434; PMCID: PMC5927991.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansAnimalsCells
    11. Splice site mutation in factor X gene manifesting as severe intracranial haemorrhage in neonatal period with a challenging treatment course. Haemophilia. 2017 03; 23(2):e138-e140. Madhusoodhan PP, Lu BY, Chen J, Jones CL, Meyer JA, Roman EA, Nardi M, Carroll WL, Bhatla T. PMID: 27995737.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    12. Genomic characterization of pediatric B-lymphoblastic lymphoma and B-lymphoblastic leukemia using formalin-fixed tissues. Pediatr Blood Cancer. 2017 Jul; 64(7). Meyer JA, Zhou D, Mason CC, Downie JM, Rodic V, Abromowitch M, Wistinghausen B, Termuhlen AM, Angiolillo AL, Perkins SL, Lones MA, Barnette P, Schiffman JD, Miles RR. PMID: 27957801.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    13. Genomic Characterization of Poorly Differentiated Neuroendocrine Carcinoma in a Pediatric Patient. J Pediatr Hematol Oncol. 2016 Jan; 38(1):e21-5. Bhatla T, Dandekar S, Lu BY, Wang J, Han E, Bitterman D, Jones CL, Evensen NA, Magid M, Meyer JA, Carroll WL. PMID: 26558807; PMCID: PMC4681625.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    14. A six gene expression signature defines aggressive subtypes and predicts outcome in childhood and adult acute lymphoblastic leukemia. Oncotarget. 2015 Jun 30; 6(18):16527-42. Wang J, Mi JQ, Debernardi A, Vitte AL, Emadali A, Meyer JA, Charmpi K, Ycart B, Callanan MB, Carroll WL, Khochbin S, Rousseaux S. PMID: 26001296; PMCID: PMC4599287.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansCells
    15. State of the art discovery with tumor profiling in pediatric oncology. Am Soc Clin Oncol Educ Book. 2015; e601-7. Carroll WL, Raetz E, Meyer J. PMID: 25993229.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    16. The biology of relapsed acute lymphoblastic leukemia: opportunities for therapeutic interventions. J Pediatr Hematol Oncol. 2014 Aug; 36(6):413-8. Bhatla T, Jones CL, Meyer JA, Vitanza NA, Raetz EA, Carroll WL. PMID: 24942023; PMCID: PMC4264573.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansPHPublic Health
    17. Ikaros deletions in BCR-ABL-negative childhood acute lymphoblastic leukemia are associated with a distinct gene expression signature but do not result in intrinsic chemoresistance. Pediatr Blood Cancer. 2014 Oct; 61(10):1779-85. Vitanza NA, Zaky W, Blum R, Meyer JA, Wang J, Bhatla T, Morrison DJ, Raetz EA, Carroll WL. PMID: 24976218; PMCID: PMC4217284.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    18. Screening for gene mutations: will identification of NT5C2 mutations help predict the chance of relapse in acute lymphoblastic leukemia? Expert Rev Hematol. 2013 Jun; 6(3):223-4. Meyer JA, Carroll WL, Bhatla T. PMID: 23782074; PMCID: PMC4117397.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    19. HMGA1 overexpression correlates with relapse in childhood B-lineage acute lymphoblastic leukemia. Leuk Lymphoma. 2013 Nov; 54(11):2565-7. Roy S, Di Cello F, Kowalski J, Hristov AC, Tsai HL, Bhojwani D, Meyer JA, Carroll WL, Belton A, Resar LM. PMID: 23472968; PMCID: PMC5036165.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    20. Relapse-specific mutations in NT5C2 in childhood acute lymphoblastic leukemia. Nat Genet. 2013 Mar; 45(3):290-4. Meyer JA, Wang J, Hogan LE, Yang JJ, Dandekar S, Patel JP, Tang Z, Zumbo P, Li S, Zavadil J, Levine RL, Cardozo T, Hunger SP, Raetz EA, Evans WE, Morrison DJ, Mason CE, Carroll WL. PMID: 23377183; PMCID: PMC3681285.
      View in: PubMed   Mentions: 138     Fields:    Translation:HumansCells
    21. Integrated genomic analysis of relapsed childhood acute lymphoblastic leukemia reveals therapeutic strategies. Blood. 2011 Nov 10; 118(19):5218-26. Hogan LE, Meyer JA, Yang J, Wang J, Wong N, Yang W, Condos G, Hunger SP, Raetz E, Saffery R, Relling MV, Bhojwani D, Morrison DJ, Carroll WL. PMID: 21921043; PMCID: PMC3217405.
      View in: PubMed   Mentions: 106     Fields:    Translation:HumansCells
    22. Genomic profiling in Down syndrome acute lymphoblastic leukemia identifies histone gene deletions associated with altered methylation profiles. Leukemia. 2011 Oct; 25(10):1555-63. Loudin MG, Wang J, Leung HC, Gurusiddappa S, Meyer J, Condos G, Morrison D, Tsimelzon A, Devidas M, Heerema NA, Carroll AJ, Plon SE, Hunger SP, Basso G, Pession A, Bhojwani D, Carroll WL, Rabin KR. PMID: 21647151; PMCID: PMC4107887.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansCells
    23. Identification of an ICP27-responsive element in the coding region of a herpes simplex virus type 1 late gene. J Virol. 2010 Mar; 84(6):2707-18. Sedlackova L, Perkins KD, Meyer J, Strain AK, Goldman O, Rice SA. PMID: 20042503; PMCID: PMC2826072.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansAnimalsCells
    24. Rearrangement of CRLF2 in B-progenitor- and Down syndrome-associated acute lymphoblastic leukemia. Nat Genet. 2009 Nov; 41(11):1243-6. Mullighan CG, Collins-Underwood JR, Phillips LA, Loudin MG, Liu W, Zhang J, Ma J, Coustan-Smith E, Harvey RC, Willman CL, Mikhail FM, Meyer J, Carroll AJ, Williams RT, Cheng J, Heerema NA, Basso G, Pession A, Pui CH, Raimondi SC, Hunger SP, Downing JR, Carroll WL, Rabin KR. PMID: 19838194; PMCID: PMC2783810.
      View in: PubMed   Mentions: 241     Fields:    Translation:HumansAnimalsCells
    25. The MMSET protein is a histone methyltransferase with characteristics of a transcriptional corepressor. Blood. 2008 Mar 15; 111(6):3145-54. Marango J, Shimoyama M, Nishio H, Meyer JA, Min DJ, Sirulnik A, Martinez-Martinez Y, Chesi M, Bergsagel PL, Zhou MM, Waxman S, Leibovitch BA, Walsh MJ, Licht JD. PMID: 18156491; PMCID: PMC2265454.
      View in: PubMed   Mentions: 92     Fields:    Translation:HumansAnimalsCells
    26. NOM1 targets protein phosphatase I to the nucleolus. J Biol Chem. 2008 Jan 04; 283(1):398-404. Gunawardena SR, Ruis BL, Meyer JA, Kapoor M, Conklin KF. PMID: 17965019.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansAnimalsCells
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