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Loris McGavran

TitleAsst Professor-Clinical
InstitutionUniversity of Colorado Denver - Anschutz Medical Campus
DepartmentSOM-Pathology
Phone303/724-5711

    Collapse Bibliographic 
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Sanmann JN, McGavran L, Patil SR. In Memoriam: Warren G. Sanger, PhD (October 6, 1945-February 5, 2015). Cancer Genet. 2015 Apr; 208(4):105-6. PMID: 26180852.
      View in: PubMed
    2. Liang X, Branchford B, Greffe B, McGavran L, Carstens B, Meltesen L, Albano EA, Quinones R, Cook B, Graham DK. Dual ALK and MYC rearrangements leading to an aggressive variant of anaplastic large cell lymphoma. J Pediatr Hematol Oncol. 2013 Jul; 35(5):e209-13. PMID: 23619105.
      View in: PubMed
    3. Liang X, Jones A, Giller RH, Swisshelm K, McGavran L, Meltesen L, Carstens B, McGranahan AN, Albano EA. Primary high-grade B-cell lymphoma of the breast with concurrent IGH-BCL2 and MYC-IGL translocations in an adolescent patient. Pediatr Dev Pathol. 2011 Sep-Oct; 14(5):402-6. PMID: 21491965.
      View in: PubMed
    4. Taylor MR, Jirikowic J, Wells C, Springer M, McGavran L, Lunt B, Swisshelm K. High prevalence of array comparative genomic hybridization abnormalities in adults with unexplained intellectual disability. Genet Med. 2010 Jan; 12(1):32-8. PMID: 20009761.
      View in: PubMed
    5. Porter CC, Liang X, Gralla J, McGavran L, Albano EA. BCL6 expression correlates with monomorphic histology in children with posttransplantation lymphoproliferative disease. J Pediatr Hematol Oncol. 2008 Sep; 30(9):684-8. PMID: 18776761; PMCID: PMC2652168.
    6. Zhong CH, Prima V, Liang X, Frye C, McGavran L, Meltesen L, Wei Q, Boomer T, Varella-Garcia M, Gump J, Hunger SP. E2A-ZNF384 and NOL1-E2A fusion created by a cryptic t(12;19)(p13.3; p13.3) in acute leukemia. Leukemia. 2008 Apr; 22(4):723-9. PMID: 18185522.
      View in: PubMed
    7. Heerema NA, Raimondi SC, Anderson JR, Biegel J, Camitta BM, Cooley LD, Gaynon PS, Hirsch B, Magenis RE, McGavran L, Patil S, Pettenati MJ, Pullen J, Rao K, Roulston D, Schneider NR, Shuster JJ, Sanger W, Sutcliffe MJ, van Tuinen P, Watson MS, Carroll AJ. Specific extra chromosomes occur in a modal number dependent pattern in pediatric acute lymphoblastic leukemia. Genes Chromosomes Cancer. 2007 Jul; 46(7):684-93. PMID: 17431878.
      View in: PubMed
    8. Gheorghe G, Albano EA, Porter CC, McGavran L, Wei Q, Meltesen L, Danielson SM, Liang X. Posttransplant Hodgkin lymphoma preceded by polymorphic posttransplant lymphoproliferative disorder: report of a pediatric case and review of the literature. J Pediatr Hematol Oncol. 2007 Feb; 29(2):112-6. PMID: 17279008.
      View in: PubMed
    9. Myers JB, Dall'Era J, Odom LF, McGavran L, Lovell MA, Furness P. Teratoid Wilms' tumor, an important variant of nephroblastoma. J Pediatr Urol. 2007 Aug; 3(4):282-6. PMID: 18947756.
      View in: PubMed
    10. Kleinschmidt-DeMasters BK, Meltesen L, McGavran L, Lillehei KO. Characterization of glioblastomas in young adults. Brain Pathol. 2006 Oct; 16(4):273-86. PMID: 17107596.
      View in: PubMed
    11. Popesco MC, Maclaren EJ, Hopkins J, Dumas L, Cox M, Meltesen L, McGavran L, Wyckoff GJ, Sikela JM. Human lineage-specific amplification, selection, and neuronal expression of DUF1220 domains. Science. 2006 Sep 01; 313(5791):1304-7. PMID: 16946073.
      View in: PubMed
    12. Chung CH, Ely K, McGavran L, Varella-Garcia M, Parker J, Parker N, Jarrett C, Carter J, Murphy BA, Netterville J, Burkey BB, Sinard R, Cmelak A, Levy S, Yarbrough WG, Slebos RJ, Hirsch FR. Increased epidermal growth factor receptor gene copy number is associated with poor prognosis in head and neck squamous cell carcinomas. J Clin Oncol. 2006 Sep 01; 24(25):4170-6. PMID: 16943533.
      View in: PubMed
    13. Keating AK, Salzberg DB, Sather S, Liang X, Nickoloff S, Anwar A, Deryckere D, Hill K, Joung D, Sawczyn KK, Park J, Curran-Everett D, McGavran L, Meltesen L, Gore L, Johnson GL, Graham DK. Lymphoblastic leukemia/lymphoma in mice overexpressing the Mer (MerTK) receptor tyrosine kinase. Oncogene. 2006 Oct 05; 25(45):6092-100. PMID: 16652142.
      View in: PubMed
    14. Trobaugh-Lotrario AD, Kletzel M, Quinones RR, McGavran L, Proytcheva MA, Hunger SP, Malcolm J, Schissel D, Hild E, Giller RH. Monosomy 7 associated with pediatric acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS): successful management by allogeneic hematopoietic stem cell transplant (HSCT). Bone Marrow Transplant. 2005 Jan; 35(2):143-9. PMID: 15558042.
      View in: PubMed
    15. Fortna A, Kim Y, MacLaren E, Marshall K, Hahn G, Meltesen L, Brenton M, Hink R, Burgers S, Hernandez-Boussard T, Karimpour-Fard A, Glueck D, McGavran L, Berry R, Pollack J, Sikela JM. Lineage-specific gene duplication and loss in human and great ape evolution. PLoS Biol. 2004 Jul; 2(7):E207. PMID: 15252450; PMCID: PMC449870.
    16. Liu L, McGavran L, Lovell MA, Wei Q, Jamieson BA, Williams SA, Dirks NN, Danielson MS, Dubie LM, Liang X. Nonpositive terminal deoxynucleotidyl transferase in pediatric precursor B-lymphoblastic leukemia. Am J Clin Pathol. 2004 Jun; 121(6):810-5. PMID: 15198352.
      View in: PubMed
    17. Tsai AC, Gibby T, Beischel L, McGavran L, Johnson JP. A child with Angelman syndrome and trisomy 13 findings due to associated paternal UPD 15 and segmental UPD 13. Am J Med Genet A. 2004 Apr 15; 126A(2):208-12. PMID: 15057988.
      View in: PubMed
    18. Liang X, Meech SJ, Odom LF, Bitter MA, Ryder JW, Hunger SP, Lovell MA, Meltesen L, Wei Q, Williams SA, Hutchinson RN, McGavran L. Assessment of t(2;5)(p23;q35) translocation and variants in pediatric ALK+ anaplastic large cell lymphoma. Am J Clin Pathol. 2004 Apr; 121(4):496-506. PMID: 15080301.
      View in: PubMed
    19. Lear-Kaul KC, Yoon HR, Kleinschmidt-DeMasters BK, McGavran L, Singh M. Her-2/neu status in breast cancer metastases to the central nervous system. Arch Pathol Lab Med. 2003 Nov; 127(11):1451-7. PMID: 14567724.
      View in: PubMed
    20. Casillas JN, Woods WG, Hunger SP, McGavran L, Alonzo TA, Feig SA. Prognostic implications of t(10;11) translocations in childhood acute myelogenous leukemia: a report from the Children's Cancer Group. J Pediatr Hematol Oncol. 2003 Aug; 25(8):594-600. PMID: 12902910.
      View in: PubMed
    21. Silliman CC, Tyson RW, Wei Q, Karrer FG, Davies SM, Blake M, McGavran L. Acute Philadelphia chromosome-positive leukemia in an adolescent boy after liver transplantation. J Pediatr Hematol Oncol. 2003 Jul; 25(7):565-8. PMID: 12847326.
      View in: PubMed
    22. Thomas JA, Johnson J, Peterson Kraai TL, Wilson R, Tartaglia N, LeRoux J, Beischel L, McGavran L, Hagerman RJ. Genetic and clinical characterization of patients with an interstitial duplication 15q11-q13, emphasizing behavioral phenotype and response to treatment. Am J Med Genet A. 2003 Jun 01; 119A(2):111-20. PMID: 12749048.
      View in: PubMed
    23. Fleitz JM, Wootton-Gorges SL, Wyatt-Ashmead J, McGavran L, Koyle M, West DC, Kurzrock EA, Martin KW, Odom LF. Renal cell carcinoma in long-term survivors of advanced stage neuroblastoma in early childhood. Pediatr Radiol. 2003 Aug; 33(8):540-5. PMID: 12748834.
      View in: PubMed
    24. Tsai CH, Graw SL, McGavran L. 8p23 duplication reconsidered: is it a true euchromatic variant with no clinical manifestation? J Med Genet. 2002 Oct; 39(10):769-74. PMID: 12362038; PMCID: PMC1734989.
    25. Orr LC, Fleitz J, McGavran L, Wyatt-Ashmead J, Handler M, Foreman NK. Cytogenetics in pediatric low-grade astrocytomas. Med Pediatr Oncol. 2002 Mar; 38(3):173-7. PMID: 11836716.
      View in: PubMed
    26. Wyatt-Ashmead J, Kleinschmidt-DeMasters BK, Hill DA, Mierau GW, McGavran L, Thompson SJ, Foreman NK. Rhabdoid glioblastoma. Clin Neuropathol. 2001 Nov-Dec; 20(6):248-55. PMID: 11758780.
      View in: PubMed
    27. Wyatt-Ashmead J, Kleinschmidt-DeMasters B, Mierau GW, Malkin D, Orsini E, McGavran L, Foreman NK. Choroid plexus carcinomas and rhabdoid tumors: phenotypic and genotypic overlap. Pediatr Dev Pathol. 2001 Nov-Dec; 4(6):545-9. PMID: 11826360.
      View in: PubMed
    28. Gump J, McGavran L, Wei Q, Hunger SP. Analysis of TP53 mutations in relapsed childhood acute lymphoblastic leukemia. J Pediatr Hematol Oncol. 2001 Oct; 23(7):416-9. PMID: 11878574.
      View in: PubMed
    29. Varella-Garcia M, Hogan CJ, Odom LF, Murata-Collins JL, Ai H, Chen L, Richkind K, Paskulin G, Andreeff M, Brizard A, McGavran L, Gemmill RM, Berger R, Drabkin HA. Minimal residual disease (MRD) in remission t(8;21) AML and in vivo differentiation detected by FISH and CD34+ cell sorting. Leukemia. 2001 Sep; 15(9):1408-14. PMID: 11516101.
      View in: PubMed
    30. Meech SJ, McGavran L, Odom LF, Liang X, Meltesen L, Gump J, Wei Q, Carlsen S, Hunger SP. Unusual childhood extramedullary hematologic malignancy with natural killer cell properties that contains tropomyosin 4--anaplastic lymphoma kinase gene fusion. Blood. 2001 Aug 15; 98(4):1209-16. PMID: 11493472.
      View in: PubMed
    31. Wyatt-Ashmead J, Bao L, Eilert RE, Gibbs P, Glancy G, McGavran L. Primary aneurysmal bone cysts: 16q22 and/or 17p13 chromosome abnormalities. Pediatr Dev Pathol. 2001 Jul-Aug; 4(4):418-9. PMID: 11441369.
      View in: PubMed
    32. Boomer T, Varella-Garcia M, McGavran L, Meltesen L, Olsen AS, Hunger SP. Detection of E2A translocations in leukemias via fluorescence in situ hybridization. Leukemia. 2001 Jan; 15(1):95-102. PMID: 11243406.
      View in: PubMed
    33. Gore L, Ess J, Bitter MA, McGavran L, Meltesen L, Wei Q, Hunger SP. Protean clinical manifestations in children with leukemias containing MLL-AF10 fusion. Leukemia. 2000 Dec; 14(12):2070-5. PMID: 11187895.
      View in: PubMed
    34. Kadan-Lottick NS, Stork L, Ruyle SZ, Koyle M, Hunger SP, McGavran L. Cytogenetic abnormalities in a case of botryoid rhabdomyosarcoma. Med Pediatr Oncol. 2000 Apr; 34(4):293-5. PMID: 10742076.
      View in: PubMed
    35. Bilir BM, Guinette D, Karrer F, Kumpe DA, Krysl J, Stephens J, McGavran L, Ostrowska A, Durham J. Hepatocyte transplantation in acute liver failure. Liver Transpl. 2000 Jan; 6(1):32-40. PMID: 10648575.
      View in: PubMed
    36. Maloney K, McGavran L, Murphy J, Odom L, Stork L, Wei Q, Hunger S. TEL-AML1 fusion identifies a subset of children with standard risk acute lymphoblastic leukemia who have an excellent prognosis when treated with therapy that includes a single delayed intensification. Leukemia. 1999 Nov; 13(11):1708-12. PMID: 10557042.
      View in: PubMed
    37. Mierau GW, Tyson RW, McGavran L, Parker NB, Partington MD. Astroblastoma: ultrastructural observations on a case of high-grade type. Ultrastruct Pathol. 1999 Sep-Oct; 23(5):325-32. PMID: 10582270.
      View in: PubMed
    38. Maloney KW, McGavran L, Odom LF, Hunger SP. Acquisition of p16(INK4A) and p15(INK4B) gene abnormalities between initial diagnosis and relapse in children with acute lymphoblastic leukemia. Blood. 1999 Apr 01; 93(7):2380-5. PMID: 10090949.
      View in: PubMed
    39. Hunger SP, McGavran L, Meltesen L, Parker NB, Kassenbrock CK, Bitter MA. Oncogenesis in utero: fetal death due to acute myelogenous leukaemia with an MLL translocation. Br J Haematol. 1998 Nov; 103(2):539-42. PMID: 9827932.
      View in: PubMed
    40. Silliman CC, McGavran L, Wei Q, Miller LA, Li S, Hunger SP. Alternative splicing in wild-type AF10 and CALM cDNAs and in AF10-CALM and CALM-AF10 fusion cDNAs produced by the t(10;11)(p13-14;q14-q21) suggests a potential role for truncated AF10 polypeptides. Leukemia. 1998 Sep; 12(9):1404-10. PMID: 9737689.
      View in: PubMed
    41. Maloney KW, McGavran L, Odom LF, Hunger SP. Different patterns of homozygous p16INK4A and p15INK4B deletions in childhood acute lymphoblastic leukemias containing distinct E2A translocations. Leukemia. 1998 Sep; 12(9):1417-21. PMID: 9737691.
      View in: PubMed
    42. Paskulin GA, Philips G, Morgan R, Sandberg A, Richkind K, Borovik C, McGavran L, Rabinovich N, Dietz-Band J, Erickson P, Drabkin H, Varella-Garcia M. Pre-clinical evaluation of probes to detect t(8;21) AML minimal residual disease by fluorescence in situ hybridization. Genes Chromosomes Cancer. 1998 Feb; 21(2):144-51. PMID: 9491326.
      View in: PubMed
    43. Hunger SP, Sun T, Boswell AF, Carroll AJ, McGavran L. Hyperdiploidy and E2A-PBX1 fusion in an adult with t(1;19)+ acute lymphoblastic leukemia: case report and review of the literature. Genes Chromosomes Cancer. 1997 Dec; 20(4):392-8. PMID: 9408756.
      View in: PubMed
    44. Wachtel SS, Sammons D, Manley M, Wachtel G, Twitty G, Utermohlen J, Phillips OP, Shulman LP, Taron DJ, Müller UR, Koeppen P, Ruffalo TM, Addis K, Porreco R, Murata-Collins J, Parker NB, McGavran L. Fetal cells in maternal blood: recovery by charge flow separation. Hum Genet. 1996 Aug; 98(2):162-6. PMID: 8698333.
      View in: PubMed
    45. Thomas JA, Manchester DK, Prescott KE, Milner R, McGavran L, Cohen MM. Hunter-McAlpine craniosynostosis phenotype associated with skeletal anomalies and interstitial deletion of chromosome 17q. Am J Med Genet. 1996 Apr 24; 62(4):372-5. PMID: 8723067.
      View in: PubMed
    46. Roulston D, Anastasi J, Rudinsky R, Nucifora G, Zeleznik-Le N, Rowley JD, McGavran L, Tsuchida M, Hayashi Y. Therapy-related acute leukemia associated with t(11q23) after primary acute myeloid leukemia with t(8;21): a report of two cases. Blood. 1995 Nov 01; 86(9):3613-4. PMID: 7579475.
      View in: PubMed
    47. Prall JA, McGavran L, Greffe BS, Partington MD. Intracranial malignant germ cell tumor and the Klinefelter syndrome. Case report and review of the literature. Pediatr Neurosurg. 1995; 23(4):219-24. PMID: 8835213.
      View in: PubMed
    48. Porreco RP, Harshbarger B, McGavran L. Rapid cytogenetic assessment of fetal blood samples. Obstet Gynecol. 1993 Aug; 82(2):242-6. PMID: 8336872.
      View in: PubMed
    49. Silliman CC, Mierau GW, Strain JD, White Y, McNeely L, Wilson H, McGavran L, Cullen JW. Peripheral neuroepithelioma of the soft tissues. A retrospective analysis of fifteen pediatric patients. Am J Pediatr Hematol Oncol. 1993 Aug; 15(3):299-305. PMID: 8328643.
      View in: PubMed
    50. Staley LW, Hull CE, Mazzocco MM, Thibodeau SN, Snow K, Wilson VL, Taylor A, McGavran L, Weiner D, Riddle J, et al. Molecular-clinical correlations in children and adults with fragile X syndrome. Am J Dis Child. 1993 Jul; 147(7):723-6. PMID: 8322740.
      View in: PubMed
    51. Poole SR, Smith AC, Hays T, McGavran L, Auerbach AD. Monozygotic twin girls with congenital malformations resembling fanconi anemia. Am J Med Genet. 1992 Apr 01; 42(6):780-4. PMID: 1554014.
      View in: PubMed
    52. Brandom WF, McGavran L, Bistline RW, Bloom AD. Sister chromatid exchanges and chromosome aberration frequencies in plutonium workers. Int J Radiat Biol. 1990 Jul; 58(1):195-207. PMID: 1973437.
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    53. Timmons CF, McGavran L, Unterkircher L, Beckwith JB, Wilson HL. Hyperdiploidy including trisomy 8 in a cystic partially differentiated nephroblastoma. Cancer Genet Cytogenet. 1989 Aug; 41(1):79-85. PMID: 2548706.
      View in: PubMed
    54. Hagerman R, Berry R, Jackson AW, Campbell J, Smith AC, McGavran L. Institutional screening for the fragile X syndrome. Am J Dis Child. 1988 Nov; 142(11):1216-21. PMID: 3177330.
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    55. Waldstein G, McGavran L. Four-year experience with rapid bone marrow chromosome analyses in newborns. Arch Pathol Lab Med. 1987 Aug; 111(8):703-7. PMID: 3632283.
      View in: PubMed
    56. Favara BE, Mierau GW, McCarthy RC, Waldstein G, McGavran L. The leukemias of childhood. Perspect Pediatr Pathol. 1987; 9:75-132. PMID: 3547311.
      View in: PubMed
    57. Berry R, Smith AC, McGavran L, O'Hanlon K. Cytogenetic studies in patients with multiple anomalies with or without mental retardation. Birth Defects Orig Artic Ser. 1987; 23(6):100-10. PMID: 3435749.
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    58. Smith AC, McGavran L, Robinson J, Waldstein G, Macfarlane J, Zonona J, Reiss J, Lahr M, Allen L, Magenis E. Interstitial deletion of (17)(p11.2p11.2) in nine patients. Am J Med Genet. 1986 Jul; 24(3):393-414. PMID: 2425619.
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    59. Heideman RL, McGavran L, Waldstein G. Nephroblastomatosis and deletion of 11p. The potential etiologic relationship to subsequent Wilms' tumor. Am J Pediatr Hematol Oncol. 1986; 8(3):231-4. PMID: 3021014.
      View in: PubMed
    60. Hagerman RJ, Jackson AW, Levitas A, Braden M, McBogg P, Kemper M, McGavran L, Berry R, Matus I, Hagerman PJ. Oral folic acid versus placebo in the treatment of males with the fragile X syndrome. Am J Med Genet. 1986 Jan-Feb; 23(1-2):241-62. PMID: 3513567.
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    61. Hagerman RJ, Van Housen K, Smith AC, McGavran L. Consideration of connective tissue dysfunction in the fragile X syndrome. Am J Med Genet. 1984 Jan; 17(1):111-21. PMID: 6711590.
      View in: PubMed
    62. Morgan RT, Woods LK, Moore GE, McGavran L, Quinn LA, Semple TU. A human gallbladder adenocarcinoma cell line. In Vitro. 1981 Jun; 17(6):503-10. PMID: 7262900.
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    63. Morgan RT, Woods LK, Moore GE, Quinn LA, McGavran L, Gordon SG. Human cell line (COLO 357) of metastatic pancreatic adenocarcinoma. Int J Cancer. 1980 May 15; 25(5):591-8. PMID: 6989766.
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