Curriculum Vitae

 

Name:TIMOTHY ATCHISON DONLON


Appointments:

    04/01/86 - 10/31/92    Director, Molecular and Clinical Cytogenetics, Stanford University Hospital

    09/01/88 - 10/31/92     Assistant Professor, Department of Pathology, Stanford University Medical Center

    06/01/88 – 6/1/98        Chairman, Committee on Human Gene Mapping, Chromosome 15  Subcommittee

    12/01/92 - 04/1/98       Director, Molecular & Clinical Cytogenetics, Kapiolani Medical Center

    09/24/93 – 2/1/03        Associate Researcher, Cancer Research Center of Hawaii

    05/01/99 – 4/16/10      Director, Molecular Genetics & Cytogenetics Laboratories, The Queen’s Medical Center

    8/01/93 - 11/1/11           Adjunct Associate Professor, Dept. of Cell & Molecular Biology, University of Hawaii, Manoa

    7/01/01 - 11/1/11           Adjunct Associate Professor, Pathology, University of Hawaii, Manoa

    09/24/93 - 11/1/11        Adjunct Associate Professor, Interdisc. Biomed Sci. Grad. Prog., University of Hawaii, Manoa

    11/01/11 - present        Adjunct Professor, Dept. of Cell & Molecular Biology, University of Hawaii, Manoa

    11/01/11 - present        Adjunct Professor, Pathology, University of Hawaii, Manoa

    11/01/03 - present        Director, Genetics Research Laboratory, Kuakini Medical Center

    12/01/10 - present        Director, Ohana Genetics, Honolulu


Education:

1984  Ph.D.Oregon Health Sciences University (Medical Genetics)

1981  M.S.Portland State University (Biology)

1975  B.S.University of Oregon (Biology)


Postdoctoral Training:

1984-1986Samuel A. Latt, M.D.,  Head, Division of Genetics,  Children's Hospital, Boston


Honors:

1981-1982N.L. Tartar Research Fellowship

1982-1983N.L. Tartar Research Fellowship

1986The Medical Foundation, Boston


Memberships in Professional Societies:

1977- presentAmerican Society of Human Genetics

1978- presentAmerican Association for the Advancement of Science

1993 - presentAmerican College of Medical Genetics

2001 - presentHawaii Society of Clinical Oncology


Certifications:

1987Diplomate, Clinical Cytogenetics; American Board of Medical Genetics

1987Diplomate, Medical Genetics; American Board of Medical Genetics

1993, 2006, 2009Diplomate, Clinical Molecular Genetics, American Board of Medical Genetics


Major Research Interests:

Aging, genomic imprinting and epigenetic modification, cancer genetics, complex genetic disorders, pharmacogenetics, molecular cytogenetics, human microbiomics


JOURNAL ARTICLES:


  1. 1.Magenis RE, Donlon TA, Parks M, Rivas ML, Lovrien E:  Linkage relationships of dominant antithrombin III deficiency and the heterochromatic region of chromosome 1.  Cytogenet. Cell Genet. 22: 327-329, 1978


  1. 2.Magenis RE, Donlon TA, Wyandt HE:  Geimsa-11 staining of chromosome 1: a newly described heteromorphism.  Science 202: 64-65, 1978


  1. 3.Donlon TA, Magenis RE: Structural organization of the heterochromatic region of human chromosome 9 as revealed by Geimsa-11, C-banding, and Lateral Asymmetry techniques.  Chromosoma 84: 353-363, 1981


  1. 4.Magenis RE, Brown MG, Chamberlin J, Donlon TA, Hepburn D, Lamvik N, Lovrien E, Yoshitomi M:  Resolution of breakpoints in a complex rearrangement by use of multiple staining techniques: confirmation of suspected 12p12.3 intraband by deletion dosage effect  LDHB.  Am. J. Med. Genet. 9: 95-103, 1981


  1. 5.Donlon TA, Magenis RE:  Nucleoli and nucleolar organizing regions.  Karyogram (publication of the Assoc. of Cytogenet. Tech.) 7(1): 4-5, 1981


  1. 6.Magenis RE, Donlon TA:  The non-fluorescent human Y chromosome: cytologic evidence of origin.  Hum. Genet. 60: 133-138, 1982


  1. 7.Donlon TA, Litt M, Newcom SR, Magenis RE:  Localization of the restriction fragment length polymorphism D14S1 (pAW101) to chromosome 14q32.1-->32.2.  Am. J. Hum. Genet. 35: 1097-1106, 1983


  1. 8.Donlon TA, Magenis RE:  Methyl green is a substitute for distamycin A in the formation of distamycin A/DAPI C-bands.  Hum. Genet. 65: 144-146, 1983


  1. 9.Sakai K, Kanda N, Shiloh Y, Donlon T, Schreck R, Shipley J, Dryja T, Chaum E, Chaganti RSK, Latt SA:  Molecular and cytologic analysis of DNA amplification in retinoblastoma.  Cancer Genet. Cell Genet. 17: 95-112, 1985


  1. 10.Shiloh Y, Shipley J, Brodeur GM, Bruns G, Korf B, Donlon T, Schreck RR, Seeger R, Sakai K, Latt SA:  Differential amplification, assembly, and relocation of multiple DNA sequences in human neuroblastomas and neuroblastoma cell lines.  Proc. Natl. Acad. Sci. USA 82: 3761-3765, 1985


  1. 11.Ginsberg D, Handin RI, Bonthron DT, Donlon TA, Bruns GA, Latt SA, Orkin SH:  Human von Willebrand factor (vWF): Isolation of complementary DNA (cDNA) clones and chromosomal location.  Science 228: 1401-1406, 1985


  1. 12.Leonard W, Donlon TA, Lebo RV, Greene WC:  Localization of the gene encoding the human Interleukin-2 recepter on chromosome 10.  Science 228: 1547-1549, 1985


  1. 13.Magenis RE, Donlon TA, Tomar DR:  Localization of the ß globin gene to 11p15 by in situ hybridization:  Utilization of chromosome 11 rearrangements.  Hum. Genet. 69: 300-303, 1985


  1. 14.Latt SA, Shiloh Y, Sakai K, Brodeur G, Donlon TA, Korf B, Shipley J, Bruns G, Heartlein M, Kanda N, Kohl N, Alt F, and Seeger R:  Novel DNA rearrangement phenomena associated with DNA amplification in human neuroblastomas and neuroblastoma cell lines.  Prog. Clin. Biol. Res. 209A: 601-612, 1986


  1. 15.Lalande M, Donlon TA, Petersen RA, Liberfarb R, Manter S,  Latt SA:  Molecular detection and differentiation of deletions in band 13q14 in human retinoblastoma.  Cancer Genet.  Cytogenet. 23(2): 151-157, 1986


  1. 16.Müller U, Lalande M, Donlon T, Latt SA:  Moderately repeated DNA-sequences specific for the short arm of the human Y-chromosome are present in XX males and reduced in copy number in an XY female.  Nucl. Acids Res. 14(3):1325-1340, 1986


  1. 17.Donlon TA, Lalande M, Wyman A, Bruns G, Latt SA:  Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome.  Proc. Natl. Acad. Sci. USA 83:4408-4412, 1986


  1. 18.Neve RL, Harris P, Kosik KS, Kurnit DM, and Donlon TA:  Identification of cDNA clones for the human microtubule-associated protein tau and chromosomal localization of the genes for tau and microtubule-associated protein 2.  Brain Research 387(3): 271-280, 1986


  1. 19.Müller U, Donlon TA, Schmid M, Fitch N, Richer C, Lalande M, and Latt SA:  Deletion mapping of the testis determining locus with DNA probes in 46,XX males and in 46,XY and 46,X,dic(Y) females.  Nucl. Acids Res. 14(16): 6489-6505, 1986


  1. 20.Shiloh Y, Donlon TA, Bruns G, Breitman ML, and Tsui LC: Assignment of the human gamma-crystallin gene cluster (CRYG) to the long arm of chromosome 2, region q33-36.  Hum. Genet. 73(1): 17-19, 1986


  1. 21.Latt SA, Lalande M, Donlon TA, Wyman A, Rose E, Shiloh Y, Korf B, Müller U, Sakai K, Kanda N, et al: DNA-based detection of chromosome deletion and amplification: diagnostic and mechanistic significance.  Cold Spring Harbor Symp. Quant. Biol. 51 Pt. 1: 299-307, 1986


  1. 22.Müller U, Donlon TA, Harris P, Rose E, Hoffman E, Bruns GP, and Latt SA:  Highly polymorphic DNA sequences in the distal region of the long arm of chromosome 18.  Cytogenet. Cell Genet. 45(1): 16-20, 1987


  1. 23.Müller U, Donlon TA, Kunkel SM, Lalande M, and Latt SA:  Y-190, a DNA probe for the sensitive detection of Y-derived marker chromosomes and mosaicism.  Hum. Genet. 75: 109-113, 1987


  1. 24.Kaplan LC, Wharton R, Elias E, Mandell F, Donlon T, and Latt SA:  Clinical heterogeneity associated with deletions in the long arm of chromosome 15: report of 3 new cases and their possible genetic significance.  Am. J. Med. Genet. 28: 45-53, 1987


  1. 25.Müller U, Latt SA, and Donlon TA: Y-specific DNA sequences in male patients with 46,XX and 47, XXX karyotypes.  Am. J. Med. Genet. 28(2): 393-401, 1987


  1. 26.Donlon TA: Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman Syndromes.  Hum. Genet. 80: 322-328, 1988


  1. 27.Drucker BJ, Marinola FM, Siao DY, Donlon TA, Bangs CD, and Holder WD, Jr.:  A new human pancreatic carcinoma cell line developed for adoptive immunotherapy studies with lymphokine-activated killer cells in nude mice.  In Vitro Cellul. and Devel. Biol. 24: 1179-1187, 1988


  1. 28. Reeders ST and Donlon TA:  Report on the genetic constitution of chromosome 16.  Cytogenet. Cell Genet.  49 (1-3) p94, 1988


  1. 29.Williams CA, Hendrickson JE, Cantú ES, and Donlon TA:  Angelman syndrome in a daughter with del(15)(q11q13) associated with brachycephaly, hearing loss, enlarged foramen magnum and ataxia in the mother.  Am. J. Med. Genet. 32 (3) 333-8, 1989


  1. 30.Ocrant I, Bangs CD, Johnston KM, Wilson DM, Hintz RL, Rosenfeld RG, and Donlon TA:  Somatic and intellectual development in a patient with 47,XX,psu dic(X)(p11.2) karyotype.  Am. J. Med. Genet. 32:536-539, 1989


  1. 31.Spak DK, Johnston K, and Donlon TA: A non-centromeric C-band variant on chromosome 11q23.2.  J. Med. Genet., J. Med. Genet. 26:532-534, 1989


  1. 32.Müller U, Lalande M, Donlon T, and Heartlein MW: Breakage of the human Y-chromosome short arm between two blocks of tandemly repeated DNA sequences.  Genomics 5:153-156, 1989


  1. 33.Negrin RS, Haeuber DH, Nagler A,  Olds LC, Donlon T,  Souza LM, and Greenberg PL: Treatment of myelodysplastic syndromes with recombinant human granulocyte colony-stimulating factor: A phase I-II trial.  Ann. Int. Med. 110:976-984, 1989


  1. 34.Cox DW and Donlon TA: Report of the committee on the genetic constitution of chromosomes 14 and 15.  Cytogenet. Cell Genet., 51: 280-298, 1989


  1. 35.Mellentin JD, Murre C, Donlon TA, McCaw PS, Smith SD, Carroll AJ, McDonald ME, Baltimore D, and Cleary ML: The gene for an immunoglobulin enhancer-binding protein lies at the site of the t(1;19) chromosomal translocation in acute leukemias.  Science, 246: 379-382, 1989


  1. 36.Donlon TA, Krensky AM, Wallace MR, Collins FS, Lovett M, and Clayberger C: Localization of a human T cell specific gene, RANTES (D17S136E), to chromosome 17q11.2-q12.  Genomics, 6: 548-553, 1990


  1. 37.Hsieh C-L, Donlon TA, Darras BT, Chang DD, Topper JN, Clayton DA, and Francke U:  The gene for the RNA component of the mitochondrial RNA-processing endoribonuclease is located on human chromosome 9p and on mouse chromosome 4.  Genomics, 6: 540-544, 1990


  1. 38.Greenberg P, Negrin R, Nagler A, Vincent M, and Donlon T: Effects of prolonged treatment of myelodysplastic syndromes with recombinant human granulocyte colony-stimulating factor.  Internat. J. Cell Cloning 8: 293-302, 1990


  1. 39.Umetsu DT, Esserman L, Donlon TA, DeKruyff RH, and Levy R:  Induction of proliferation of human follicular (B Type) lymphoma cells by cognate interaction with a CD4+ T cell clone.  J. Immunol., 144: 2550-2557, 1990


  1. 40.Negrin RS, Haeuber DH, Nagler  A,  Kobayashi Y, Sklar J, Donlon T, Vincent M, and Greenberg PL: Maintenance treatment of patients with myelodysplastic syndromes using recombinant human granulocyte colony stimulating factor.  Blood, 76: 36-43, 1990


  1. 41.Donlon TA, Krensky, AM, and Clayberger C: Localization of the human T lymphocyte activation gene 519 (D2S69E) to chromosome 2p12-q11.  Cytogenet. Cell Genet. 53:230-231, 1990


  1. 42.Kupke KG, Lee LV, Viterbo GH, Arancillo J, Donlon T, and Müller U:  X-linked recessive torsion dystonia in the Philippines.  Am. J. Med. Genet., 36:237-242, 1990


  1. 43.Kohler S, Galili N, Sklar JL, Donlon TA, Blume KG, and Cleary ML: Expression of BCR-ABL fusion transcripts following bone marrow transplantation for Philadelphia chromosome-positive leukemia.  Leukemia 4:541-547, 1990


  1. 44.Molina A, Lombard C, Donlon T, Bangs  CD, Dorfman RF:  Immunohistochemical and cytogenetic studies indicate that malignant angioendotheliomatosis is a primary intravascular (angiotropic) lymphoma.  Cancer, 66(3):474-479, 1990


  1. 45.Greenberg P; Negrin R; Nagler A; Souza L; Donlon T:  Effects of treatment of myelodysplastic syndromes with recombinant human granulocyte colony stimulating factor.  Prog. Clin. Biol. Res. 338:151-161, 1990


  1. 46.Nagler A; Ginzton N; Negrin R; Bang D; Donlon T; Greenberg P:  Effects  of  recombinant  human  granulocyte  colony stimulating factor and granulocytemonocyte colony stimulating factor on in vitro hemopoiesis in the myelodysplastic syndromes.  Leukemia  4: 193-202, 1990


  1. 47.Nagler  A, Binet C, Mackichan ML, Negrin R, Bangs C, Donlon T, and Greenberg P: Impact of marrow cytogenetics and morphology on in vitro hematopoiesis in the myelodysplastic syndromes: comparison between recombinant human granulocyte colony-stimulating factor (CSF) and granulocyte-monocyte CSF.  Blood, 76: 1299-1307, 1990


  1. 48.Tkachuk DC, Westbrook CA, Andreeff M, Donlon TA, Cleary ML, Suryanarayan K, Homge M, Redner A, Gray J, and Pinkel D: Detection of bcr-able fusion in chronic myelogenous leukemia by in situ hybridization.  Science 250:  559-562, 1990


  1. 49.Donlon TA and Malcolm S: Report of the committee on the genetic constitution of chromosome 15.  Cytogenet. Cell Genet., 55:189-193, 1990


  1. 50.Comings DE, Muhleman D, Dietz GW, and Donlon TA: Human tryptophan oxygenase localized to 4q31: possible implications for alcoholism and other behavioral disorders.  Genomics 9: 301-308, 1991


  1. 51.Donlon TA and Müller U: Deletion mapping of DNA segments from the Y chromosome long arm and their analysis in an XX male.  Genomics 10(1):51-6, 1991;


  1. 52.Zelenitz AD, Chu G, Galili N, Bangs CD, Horning SJ, Donlon TA, Cleary ML, and Levy R: Enhanced detection of the t(14;18) translocation in malignant lymphoma using pulsed-field gel electrophoresis.  Blood 78(6):1552-60, 1991


  1. 53.Chao NJ, Nademanee AP, Long GD,  Schmidt GM, Donlon TA, Parker P, Slovak ML, Nagasawa LS, Blume KG, Forman SJ: Importance of bone marrow cytogenetic evaluation before autologous bone marrow transplantation for Hodgkin's disease.  J Clin Oncol 9(9):1575-9, 1991


  1. 54.Lambert C, Schultz RA, Smith M, Wagner-McPherson C, McDaniel LD, Donlon T, Stanbridge EJ, Friedberg EC: Functional complementation of ataxia-telangiectasia group D (AT-D) cells by microcell-mediated chromosome transfer and mapping of the AT-D locus to the region 11q22-23.  Proc. Natl. Acad. Sci. 88(13):5907-11, 1991


  1. 55.Donlon TA:  The First International Workshop on Human Chromosome 15 Mapping.  Cytogenet. Cell Genet. 61:161-166, 1992


  1. 56.Özçelik T, Leff S, Robinson W, Donlon T, Lalande M, Sanjines E, Schinzel A, and Francke U:  Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene inthe Prader-Willi critical region.  Nature Genetics 2:265-269, 1992


  1. 57.Sherer SW, Poorkaj P, Allen T, Kim J, Geshuri D, Nunes M, Soder S, Stephens K, Pagon RA, Patton MA, Berg MA, Donlon T, Rivera H, Pfeiffer RA, Naritomi K, Hughes H, Genuardi M, Gurrieri F, Neri G, Lovrien E, Magenis E, Tsui L-C, and Evans JP:  Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1.  Am. J. Hum. Genet. 55 12-20,1994


  1. 58.Malcolm S and Donlon TA: Report and abstracts of the Second International Workshop on Human Chromosome 15 Mapping. England, February 18-20, 1994.  Cytogenet Cell Genet 1994;67(1):1-2


  1. 59. Gabert JA, Lopez M, Bangs CD, Martina N, Donlon TA, Mannoni P, and Lee F:  Characterization of spontaneous factor-independent cell lines derived from human leukemic cell lines TF-1: A dominant event.  Leukemia 8: 1359-1368, 1994


  1. 60.Michaelis RC, Skinner SA, Lethco BA, Simensen RJ, Donlon TA, Tarleton J, and Phelan MC: Deletion involving D15S113 in a mother and son without Angelman syndrome: refinement of the Angelman syndrome critical deletion region.  Am J Med Genet 55:120-126, 1995


  1. 61.Nagler A, MacKichan ML, Negrin RS, Donlon T, and Greenberg PL: Effects of granulocyte colony-stimulating factor therapy on in vitro hemopoiesis in myelodysplastic syndromes.  Leukemia, 9:30-39, 1995


  1. 62.Yancey MK, Hardin EL, Pacheco C, Kuslich CD, and Donlon TA:  Non-mosaic trisomy 16 in a third trimester fetus Obstetrics and Gynecology, 87: 856-860, 1996


  1. 63.Donlon T: Fishing out the Angelman syndrome gene.  Nature Medicine, 3:281, 1997


  1. 64.Hayward A, Ambruso D; Battaglia F, Donlon T, Eddelman K, Giller R, Hobbins J, Hsia YE, Quinones R, Shpall E, Trachtenberg E, and Giardina P: Microchimerism and tolerance following intrauterine transplantation and transfusion for alpha-thalassemia-1. Fetal Diagn. Ther. Jan-Feb;13(1):8-14, 1998


  1. 65.Jordan-Le Saux C, Le Saux O, Donlon T, Boyd CD, and Csiszar K: The human lysyl oxidase-related gene (LOXL2) maps between markers D8S280 and D8S2778 on chromosome 8p21.1-p21.3. Genomics 51(2):305-7, 1998


  1. 66.CD Kuslich, J Kobori, G Mohapatra, C Gregorio-King, and Donlon TA: A Prader-Willi Syndrome Patient with a Balanced de novo Translocation (4;15)(q27;q11.2)pat. Am J Hum Genet, 64(1):70-76, 1999


  1. 67.Hunt JA, Lee L, Donlon TA, and Hsia YE: Determination of the breakpoint of the common a-thalassemia deletion in Filipinos in Hawaii. Brit J Haem 104:284-7, 1999


  1. 68.Morton CC, Christian SL, Donlon TA, Driscoll DJ, Fink JK, Gabriel JM, Gotway G, Greally JM, Hitchins MP, Howard HC, Ji Y, Leonard S, Lerner T, Magenis E, Malcolm S, Ohta T, Rainier S, Rees M, Riley B, Robinson WP, Saitoh S, Schultz R, Sell S, Sharp JD, Talbot C, Trent R, Wevrick R, and Nicholls RD, Report of the fourth international workshop on human chromosome 15 mapping, 1997. Cytogenet. Cell Genet. 84(1-2):11-21, 1999


  1. 69.King TJ, Fukushima LH, Donlon TA, Hieber AD, Shimabukuro KA, Bertram JS: Correlation between growth control, neoplastic potential and endogenous connexin43 expression in HeLa cell lines: implications for tumor progression. Carcinogenesis. 2000 Feb;21(2):311-5.


  1. 70.Pierce LM, Sivaraman L, Chang W, Lum A, Donlon T, Seifried A, Wilkens LR, Lau AF, and Le Marchand L: Relationships of TP53 codon 72 and HRAS1 polymorphisms with lung cancer risk in an ethnically diverse population. Cancer Epidemiology, Biomarkers & Prevention 9:1199-1204, 2000


  1. 71.Goodman MT, McDuffie K, Kolonel LN, Terada K, Donlon TA, Wilkins LR, Guo C, and Le Marchand L: Case-contro study of ov arian cancer and polymorphisms in genes involved in catecholestrogen formation and metabolism.  Cancer Epidemiology, Biomarkers & Prevention 10:209-16, 2001


  1. 72.Goodman MT, McDuffie K, Guo C, Terada K, and Donlon TA: CYP17 genotype and ovarian cancer: a null case-control study. Cancer, Epidemiology, Biomarkers, and Prevention 10(5):563-4, 2001.


  1. 73.Le Marchand L, Hankin JH, Wilkens LR, Pierce LM, Franke A, Kolonel LN, Seifried A, Custer LJ, Chang W, Lum-Jones A, and Donlon T: Combined effects of well-done red meat, smoking, and rapid N-Acetyltransferase 2 and CYP1A2 phenotypes in increasing colorectal cancer risk. Cancer Epidemiology, Biomarkers & Prevention 10: 1259-66, 2001


  1. 74.Goodman MT, McDuffie K, Hernandez B, Wilkens LR, Bertram CC, Killeen J, Le Marchand L, Selhub J, Murphy S, and Donlon TA: Association of methylenetetrahydrofolate reductase polymorphism C677T and dietary folate with the risk of cervical dysplasia. Cancer Epidemiology, Biomarkers & Prevention 10: 1275-80, 2001


  1. 75.Le Marchand L, Donlon T, Lum-Jones A, Seifried A, and Wilkens LR: Association of the hOGG1 Ser326Cys polymorphism with lung cancer risk. Cancer Epidemiology, Biomarkers & Prevention 11:409-12, 2002


  1. 76.Le Marchand L, Donlon T, Seifried A, and Wilkens LR: Red meat intake, CYP2E1 genetic polymorphisms, and colorectal cancer risk. Cancer Epidemiology, Biomarkers & Prevention 11:1019-1024, 2002


  1. 77.Le Marchand L, Donlon T, Seifried A, Kaaks R, Rinaldi S, and Wilkens LR: Association of a common polymorphism in the human GH1 gene with colorectal neoplasia.  J Nat Canc Inst 94(6):454-460, 2002


  1. 78.Le Marchand L, Donlon T, Hankin JH, Kolonel LN, Wilkens LR, and Seifried A: B-vitamin intake, metabolic genes, and colorectal cancer risk (United States). Cancer Causes and Control 13:239-248, 2002


  1. 79.Le Marchand L, Hankin JH, Pierce LM, Sinha R, Nerurkar PV, Franke AA, Wilkens LR, Kolonel LN, Donlon T, Seifried A, Custer LJ, Lum-Jones A, and Chang W, Well-done red meat, metabolic phenotypes and colorectal cancer in Hawaii. Mut Res 506-507:205-14, 2002


  1. 80.Goodman MT, Tung KH, McDuffie K, Wilkens LR, Donlon TA;   Association of Caffeine Intake and CYP1A2 Genotype With Ovarian Cancer. Nutr Cancer 46(1):23-9. 2003


  1. 81.Le Marchand L, Seifried A, Lum-Jones A,  Donlon T, and Wilkens LR: Association of the Cyclin D1 A870G polymorphism with advanced colorectal cancer. JAMA 290 (21):2843-48, 2003


  1. 82.Willcox BJ, Yano K, Chen R, Willcox DC, Rodriguez BL, Masaki KH, Donlon T, Tanaka B, and Curb JD; How Much Should We Eat? The Association Between Energy Intake and Mortality in a 36-Year Follow-Up Study of Japanese-American Men J Geront 59A (8): 789–95, 2004


  1. 83.Donlon TA. Your family history can save your life. Hawaii Med J. Aug;63(8):245-6, 249, 2004


  1. 84.Le Marchand L, Donlon T, Kolonel LN, Henderson BE, and Wilkens LR: Estrogen metabolism-related genes and breast cancer risk: The Multiethnic Cohort Study. Cancer Epidemiology, Biomarkers & Prevention 14(8):1998-2003, 2005


  1. 85.Bangs CD and Donlon TA. Metaphase chromosome preparation from cultured peripheral blood cells. Bangs CD, Donlon TA. Curr Protoc Hum Genet. 2005 May;Chapter 4:Unit 4.1.


  1. 86.Willcox BJ, He Q, Chen R, Yano K, Masaki K, Grove S, Donlon TA, Willcox DC, and Curb JD: Midlife risk factors and healthy survival in men. JAMA 296(19):2343-50, 2006


  1. 87.Curb JD; Ceria-Ulep CD; Rodriguez BL; Grove J, Guralnik J, Willcox BJ; Donlon TA, Masaki KH, Chen R. Performance based measures of physical function for high function populations. J Am Geriatr Soc, 54:737‑42, 2006.


  1. 88.Hsiao CF, Chiu YF, Chiang FT, Ho LT, Lee WJ, Hung YJ, Chen YD, Donlon TA, Jorgenson E, Curb D, Risch N, Hsiung CA; SAPPHIRe Study Group. Genome-wide linkage analysis of lipids in nondiabetic Chinese and Japanese from the SAPPHIRe family study. Am J Hypertens. 2006 Dec;19(12):1270-7.


  1. 89.Chiu YF, Chuang LM, Kao HY, Ho LT, Ting CT, Hung YJ, Chen YD, Donlon T, Curb JD, Quertermous T, Hsiung CA. Bivariate genome-wide scan for metabolic phenotypes in non-diabetic Chinese individuals from the Stanford, Asia and Pacific Program of Hypertension and Insulin Resistance Family Study. Diabetologia. 50(8):1631-40, 2007


  1. 90.Kimbell JL, Koropatnick TA, Grove JS, Huang Y-H, Chiang F-T, Quertermous T, Chen R, Donlon TA, Rodriguez BL, and Curb JD, Absence of evidence for an association between resistin gene variants and insulin resistance in an Asian population with low and high blood pressure. Diabetes Research and Clinical Practice 81(2):231-7, 2008


  1. 91.Willcox BJ, Donlon TA, He Q, Randi Chen R, Grove JS, Yano K, Kamal H. Masaki KH, Willcox DC, Rodriguez B, and Curb JD, FOXO3A genotype is strongly associated with human longevity. Proc Natl Acad Sci U S A. 2008 Sep 16;105(37):13987-92


  1. 92.Koropatnick TA, Kimbell J, Chen R, Grove JS, Donlon TA, Masaki KH, Rodriguez BL, Willcox BJ, Yano K, Curb JD. A prospective study of high-density lipoprotein cholesterol, cholesteryl ester transfer protein gene variants, and healthy aging in very old Japanese-American men. J Gerontol A Biol Sci Med Sci. 63(11):1235-40, 2008


  1. 93.Chang YC, Chiu YF, Shih KC, Lin MW, Sheu WH, Donlon T, Curb JD, Jou YS, Chang TJ, Li HY, Chuang LM. Common PCSK1 Haplotypes Are Associated With Obesity in the Chinese Population. Obesity (Silver Spring). 2009 Oct 29.


  1. 94.Ceria-Ulep CD, Grove J Chen R, Masaki KH, Rodriguez BL, Donlon TA, Guralnik J, WillcoxBJ, Willcox DC, Nigg C, and Curb JD. Physical Aspects of Healthy Aging: Assessments of Three Measures of Balance for Studies in Middle-Aged and Older Adults. Current Gerontology and Geriatrics Research, Volume 2010 (2010), Article ID 849761, 8 pages doi:10.1155/2010/849761


  1. 95.Donlon TA, Curb JD, He Q, Grove JS, Masaki KH, Rodriguez B, Elliott A, Willcox DC, and Willcox BJ. FOXO3 Gene Variants and Human Aging: Coding Variants May Not Be Key Players. J Gerontol A Biol Sci Med Sci. 2012 Mar 28. PMID: 22459618


  1. 96.Chang YC, Chiu YF, Lee IT, Ho LT, Hung YJ, Hsiung CA, Quertermous T, Donlon T, Lee WJ, Lee PC, Chen CH, Mochly-Rosen D, Chuang LM. Common ALDH2 genetic variants predict development of hypertension in the SAPPHIRe prospective cohort: Gene-environmental interaction with alcohol consumption. BMC Cardiovasc Disord. 29;12(1):58, 2012. PMID: 1716177


  1. 97.Morris BJ, Donlon TA, He Q, Grove JS, Masaki KH, Elliott A, Willcox DC, and Willcox BJ, Association Analyses of Insulin Signaling Pathway Gene Polymorphisms With Healthy Aging and Longevity in Americans of Japanese Ancestry. The Journals of Gerontology Series A: Biological Sciences and Medical Sciences 2013; doi: 10.1093/gerona/glt082


  1. 98.Bendjilali N, Hsueh W-C, He Q, Willcox DC, Nievergelt, CM, Donlon TA, Kwok P-Y, Suzuki M, Willcox BJ. Who Are the Okinawans? Ancestry, Genome Diversity, and Implications for the Genetic Study of Human Longevity From a Geographically Isolated Population. J Gerontol A Biol Sci Med Sci. 2014 Jan 20


  1. 99.Morris BJ, Donlon TA, He Q, Grove JS, Masaki KH, Elliott A, Willcox DC, Allsopp R and Willcox BJ. Genetic Analysis of TOR Complex Gene Variation With Human Longevity: A Nested Case–Control Study of American Men of Japanese Ancestry. J Gerontol A Biol Sci Med Sci. 2014 Apr 4. PMID: 24589862


  1. 100.Bell CL, Chen R, Masaki K, Yee P, He Q, Grove J, Donlon T, Curb JD, Willcox DC, Poon LW, Willcox BJ. Late-life factors associated with healthy aging in older men. J Am Geriatr Soc. 2014 May;62(5):880-8. doi: 10.1111/jgs.12796. Epub 2014 Apr 29


  1. 101.He Q, Morris BJ, Grove JS, Petrovitch H, Ross W, Masaki KH, Rodriguez B, Chen R, Donlon TA, Willcox DC, Willcox BJ. Shorter Men Live Longer: Association of Height with Longevity and FOXO3 Genotype in American Men of Japanese Ancestry. PLoS One. 2014 May 7;9(5):e94385. doi: 10.1371/journal.pone.0094385. eCollection 2014. PMID: 24804734



BOOK CHAPTERS:


1.Magenis RE, Brown MG, Donlon T, Olson SB, Sheehy R, Tomar D:  Structural aberrations of the Y chromosome, including the non-fluorescent Y: Cytologic origin and consequences.  In:  Cytogenetics of the Mammalian Y Chromosome.  Progress and Topics in Cytogenetics, AA Sandberg (ed) Alan R Liss, New York, 1986


2.Latt SA, Lalande M, Flint A, Harris P. Muller U, Donlon T, Tatravahi U, Bruns G, Kurnit D, Neve R, and Kunkel L: Metaphase chromosome flow sorting and cloning; rationale, approaches and applications. In: Flow Sorting, Academic Press, New York, 1989


3.Bangs CD and Donlon TA:  Chromosome preparations from cultured peripheral blood cells, pp 4.0.1-4.1.19, In: Current Protocols in Human Genetics, Dracopoli N, Haines J, Korf B, Moir D, Morton C, Seidman C, Seidman J, and Smith D, (eds) John Wiley and Sons, Inc., 1994


4.Donlon TA, Beckmann JS, and Malcolm S:  Report of the committee on the genetic constitution of chromosome 15.  In Chromosome Coordinating Meeting, 1992, Genome Priority Reports, Vol. 1.  AJ Cuticchia, P.L. Pearson, and H.P. Klinger (Eds.) Cytogenetics and Cell Genetics, New York, 1993


5.Donlon TA and Morton CC:  Report of the committee on the genetic constitution of chromosome 15.  In Human Gene Mapping, 1994: A compendium,  AJ Cuticchia (Ed.) The Johns Hopkins University Press, Baltimore, 1995


6.Donlon TA and Morton CC:  Report of the committee on the genetic constitution of chromosome 15.  In Human Gene Mapping, 1995: A compendium,  AJ Cuticchia (Ed.) The Johns Hopkins University Press, Baltimore, 1996


7.Donlon TA: Chromosome 14. In Encyclopedia of Molecular Medicine, TE Creighton (Ed) John Wiley & Sons, Inc., New York, pp 812-15, 2002


  1. 8.Bangs CD and Donlon TA:  Chromosome preparations from cultured peripheral blood cells, pp 4.0.1-4.1.19, In: Current Protocols in Human Genetics, Dracopoli N, Haines J, Korf B, Moir D, Morton C, Seidman C, Seidman J, and Smith D, (eds) John Wiley and Sons, Inc., 1994, revised 2005


  1. 9.Willcox BJ, Suzuki M, Donlon TA, He Q, Grove JS, Masaki KH, and Willcox DC, Optimizing Human Health Span and Life Span Insights From Okinawa and Hawaii, pp 135 – 170, In: Healthy Longevity, A Global Approach, Jean-Marie Robine, Carol Jagger, and Eileen M. Crimmins, (eds) Springer Publishing Co, LLC, 2013



MONOGRAPHS:


1.Donlon TA:  Cytologic characterization of human constitutive heterochromatin.  Master's thesis, Portland State University, 1981


2.Donlon TA:  Molecular and cytogenetic approaches to an understanding of the variability of the human nucleolus organizing region.  Doctoral Thesis, The Oregon Health Sciences University, 1984