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John J Mulvihill

TitleGeorge L Cross Research Professor
InstitutionUniversity of Oklahoma Health Sciences Center
DepartmentDept of Pediatrics
Address1200 N Phillips Ave
Oklahoma City OK 73104-4600
Phone405/271-8685
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    Collapse Research 
    Collapse research activities and funding
    R13CA075223     (MULVIHILL, JOHN J.)May 1, 1997 - Apr 30, 1998
    NIH/NCI
    FAMILIAL CANCER AND PREVENTION
    Role: Principal Investigator

    R01CA075311     (MULVIHILL, JOHN J.)Sep 30, 1997 - Jun 30, 2004
    NIH/NCI
    ECOGENETICS OF PANCREATIC CANCER--FAMILY REGISTRY
    Role: Principal Investigator

    R01CA086771     (MULVIHILL, JOHN J.)Sep 30, 1999 - Aug 31, 2006
    NIH/NCI
    CANCER AND MORTALITY IN NEUROFIBROMATOSIS BY GENOTYPE
    Role: Principal Investigator

    U84DD620160     (MULVIHILL, JOHN J.)Sep 30, 2001 - Sep 29, 2005
    CDC/NCBDD
    Fas neuroldev disorders with children &OR adolescents
    Role: Principal Investigator

    R13CA100429     (MULVIHILL, JOHN J.)Jun 25, 2003 - May 31, 2004
    NIH/NCI
    UICC Intl Conference on Familial Cancer--US Support
    Role: Principal Investigator

    P20RR023477     (MULVIHILL, JOHN J.)Sep 17, 2006 - Jun 30, 2009
    NIH/NCRR
    Oklahoma Planning Grant for Clinical /Translational Scie
    Role: Principal Investigator

    Collapse Bibliographic 
    Collapse selected publications
    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. Mulvihill JJ, Capps B, Joly Y, Lysaght T, Zwart HAE, Chadwick R. Ethical issues of CRISPR technology and gene editing through the lens of solidarity. Br Med Bull. 2017 Jun 01; 122(1):17-29. PMID: 28334154.
      View in: PubMed
    2. Hassed S, Li S, Mulvihill J, Aston C, Palmer S. Adams-Oliver syndrome review of the literature: Refining the diagnostic phenotype. Am J Med Genet A. 2017 Mar; 173(3):790-800. PMID: 28160419.
      View in: PubMed
    3. Jupe ER, Dalessandri KM, Mulvihill JJ, Miike R, Knowlton NS, Pugh TW, Zhao LP, DeFreese DC, Manjeshwar S, Gramling BA, Wiencke JK, Benz CC. A steroid metabolizing gene variant in a polyfactorial model improves risk prediction in a high incidence breast cancer population. BBA Clin. 2014 Dec; 2:94-102. PMID: 26673457; PMCID: PMC4633888.
    4. Kim YM, Lee JY, Xia L, Mulvihill JJ, Li S. Trisomy 8: a common finding in mouse embryonic stem (ES) cell lines. Mol Cytogenet. 2013 Jan 16; 6(1):3. PMID: 23320952; PMCID: PMC3564830.
    5. Saxena R, Saleheen D, Been LF, Garavito ML, Braun T, Bjonnes A, Young R, Ho WK, Rasheed A, Frossard P, Sim X, Hassanali N, Radha V, Chidambaram M, Liju S, Rees SD, Ng DP, Wong TY, Yamauchi T, Hara K, Tanaka Y, Hirose H, McCarthy MI, Morris AP, Basit A, Barnett AH, Katulanda P, Matthews D, Mohan V, Wander GS, Singh JR, Mehra NK, Ralhan S, Kamboh MI, Mulvihill JJ, Maegawa H, Tobe K, Maeda S, Cho YS, Tai ES, Kelly MA, Chambers JC, Kooner JS, Kadowaki T, Deloukas P, Rader DJ, Danesh J, Sanghera DK. Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India. Diabetes. 2013 May; 62(5):1746-55. PMID: 23300278; PMCID: PMC3636649.
    6. Wierenga KJ, Jiang Z, Yang AC, Mulvihill JJ, Tsinoremas NF. A clinical evaluation tool for SNP arrays, especially for autosomal recessive conditions in offspring of consanguineous parents. Genet Med. 2013 May; 15(5):354-60. PMID: 23100014; PMCID: PMC3908554.
    7. Hassed SJ, Wiley GB, Wang S, Lee JY, Li S, Xu W, Zhao ZJ, Mulvihill JJ, Robertson J, Warner J, Gaffney PM. RBPJ mutations identified in two families affected by Adams-Oliver syndrome. Am J Hum Genet. 2012 Aug 10; 91(2):391-5. PMID: 22883147; PMCID: PMC3415535.
    8. Selig BP, Furr JR, Huey RW, Moran C, Alluri VN, Medders GR, Mumm CD, Hallford HG, Mulvihill JJ. Cancer chemotherapeutic agents as human teratogens. Birth Defects Res A Clin Mol Teratol. 2012 Aug; 94(8):626-50. PMID: 22851372.
      View in: PubMed
    9. Mulvihill JJ. Preconception exposure to mutagens: medical and other exposures to radiation and chemicals. J Community Genet. 2012 Jul; 3(3):205-11. PMID: 22752838; PMCID: PMC3419286.
    10. Zhang H, Lu X, Beasley J, Mulvihill JJ, Liu R, Li S, Lee JY. Reversed clinical phenotype due to a microduplication of Sotos syndrome region detected by array CGH: microcephaly, developmental delay and delayed bone age. Am J Med Genet A. 2011 Jun; 155A(6):1374-8. PMID: 21567906.
      View in: PubMed
    11. Been LF, Ralhan S, Wander GS, Mehra NK, Singh J, Mulvihill JJ, Aston CE, Sanghera DK. Variants in KCNQ1 increase type II diabetes susceptibility in South Asians: a study of 3,310 subjects from India and the US. BMC Med Genet. 2011 Jan 24; 12:18. PMID: 21261977; PMCID: PMC3037841.
    12. Sanghera DK, Demirci FY, Been L, Ortega L, Ralhan S, Wander GS, Mehra NK, Singh J, Aston CE, Mulvihill JJ, Kamboh IM. PPARG and ADIPOQ gene polymorphisms increase type 2 diabetes mellitus risk in Asian Indian Sikhs: Pro12Ala still remains as the strongest predictor. Metabolism. 2010 Apr; 59(4):492-501. PMID: 19846176; PMCID: PMC2843807.
    13. Chou AF, Norris AI, Williamson L, Garcia K, Baysinger J, Mulvihill JJ. Quality assurance in medical and public health genetics services: a systematic review. Am J Med Genet C Semin Med Genet. 2009 Aug 15; 151C(3):214-34. PMID: 19621459.
      View in: PubMed
    14. Been LF, Nath SK, Ralhan SK, Wander GS, Mehra NK, Singh J, Mulvihill JJ, Sanghera DK. Replication of association between a common variant near melanocortin-4 receptor gene and obesity-related traits in Asian Sikhs. Obesity (Silver Spring). 2010 Feb; 18(2):425-9. PMID: 19680233.
      View in: PubMed
    15. Knudtson EJ, Lorenz LB, Wilson PL, McDaniel B, Mulvihill JJ, Dannaway DC. Tonic-clonic seizures in a fetus with Pena-Shokeir syndrome. J Ultrasound Med. 2009 Aug; 28(8):1121-2. PMID: 19643800.
      View in: PubMed
    16. Wilson PL, Kattman BB, Mulvihill JJ, Li S, Wilkins J, Wagner AF, Goodman JR. Prenatal identification of a novel R937P L1CAM missense mutation. Genet Test Mol Biomarkers. 2009 Aug; 13(4):515-9. PMID: 19594370.
      View in: PubMed
    17. Fergeson MA, Mulvihill JJ, Schaefer GB, Dehaai KA, Piatt J, Combs K, Bright BC, Neas BR. Low adherence to national guidelines for thyroid screening in Down syndrome. Genet Med. 2009 Jul; 11(7):548-51. PMID: 19506481.
      View in: PubMed
    18. Sanghera DK, Been L, Ortega L, Wander GS, Mehra NK, Aston CE, Mulvihill JJ, Ralhan S. Testing the association of novel meta-analysis-derived diabetes risk genes with type II diabetes and related metabolic traits in Asian Indian Sikhs. J Hum Genet. 2009 Mar; 54(3):162-8. PMID: 19247373.
      View in: PubMed
    19. Xu W, Lu X, Kim Y, Luo Y, Martin M, Mulvihill JJ, Li S. Deletion of 14q24.1 approximately q24.3 in a patient with acute lymphoblastic leukemia: a hidden chromosomal anomaly detected by array-based comparative genomic hybridization. Cancer Genet Cytogenet. 2008 Aug; 185(1):43-6. PMID: 18656693.
      View in: PubMed
    20. Sanghera DK, Ortega L, Han S, Singh J, Ralhan SK, Wander GS, Mehra NK, Mulvihill JJ, Ferrell RE, Nath SK, Kamboh MI. Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk. BMC Med Genet. 2008 Jul 03; 9:59. PMID: 18598350; PMCID: PMC2481250.
    21. Wang X, Zheng B, Li S, Mulvihill JJ, Wood MC, Liu H. Automated classification of metaphase chromosomes: optimization of an adaptive computerized scheme. J Biomed Inform. 2009 Feb; 42(1):22-31. PMID: 18585097; PMCID: PMC2673199.
    22. Purandare SM, Mendoza-Londono R, Yatsenko SA, Napierala D, Scott DA, Sibai T, Casas K, Wilson P, Lee J, Muneer R, Leonard JC, Ramji FG, Lachman R, Li S, Stankiewicz P, Lee B, Mulvihill JJ. De novo three-way chromosome translocation 46,XY,t(4;6;21)(p16;p21.1;q21) in a male with cleidocranial dysplasia. Am J Med Genet A. 2008 Feb 15; 146A(4):453-8. PMID: 18203189; PMCID: PMC2663417.
    23. Lee J, Lu X, Shin ES, Kern WF, Mulvihill JJ, Li S. A novel subtelomeric translocation t(5;9) and a deletion of the RB1 gene in a patient with acute myeloid leukemia (AML-M0). Cancer Genet Cytogenet. 2008 Feb; 181(1):36-9. PMID: 18262051.
      View in: PubMed
    24. Wang X, Zheng B, Li S, Mulvihill JJ, Liu H. A rule-based computer scheme for centromere identification and polarity assignment of metaphase chromosomes. Comput Methods Programs Biomed. 2008 Jan; 89(1):33-42. PMID: 18082909.
      View in: PubMed
    25. Zhang L, Kern WF, Yu Z, Mulvihill JJ, Li S. Cryptic and complex chromosomal rearrangements and the deletion of TP53 gene in a patient with leukemic mantle cell lymphoma. Cancer Genet Cytogenet. 2006 Sep; 169(2):169-73. PMID: 16938577.
      View in: PubMed
    26. Angelidis P, Kojouri K, Lee J, Kern W, Mulvihill JJ, Li S. Trisomy 1q in a patient with severe aplastic anemia. Cancer Genet Cytogenet. 2006 Aug; 169(1):73-5. PMID: 16875941.
      View in: PubMed
    27. Bendure WB, Mulvihill JJ. Perform a gene test on every patient: the medical family history revisited. J Okla State Med Assoc. 2006 Feb; 99(2):78-83. PMID: 16562397.
      View in: PubMed
    28. Purandare SM, Lee J, Hassed S, Steele MI, Blackett PR, Mulvihill JJ, Li S. Ring chromosome 9 [r(9)(p24q34)]: a report of two cases. Am J Med Genet A. 2005 Oct 15; 138A(3):229-35. PMID: 16158426.
      View in: PubMed
    29. Blackett PR, Li S, Mulvihill JJ. Ring chromosome 4 in a patient with early onset type 2 diabetes, deafness, and developmental delay. Am J Med Genet A. 2005 Aug 30; 137(2):213-6. PMID: 16082703.
      View in: PubMed
    30. Lee J, Hopcus-Niccum DJ, Mulvihill JJ, Li S. Cytogenetic and molecular cytogenetic studies of a variant of t(21;22), ins(22;21)(q12;q21q22), with a deletion of the 3' EWSR1 gene in a patient with Ewing sarcoma. Cancer Genet Cytogenet. 2005 Jun; 159(2):177-80. PMID: 15899394.
      View in: PubMed
    31. Lee J, Kern WF, Cain JB, Mulvihill JJ, Li S. A variant t(8;10;21) in a patient with pathological features mimicking atypical chronic myeloid leukemia. Cancer Genet Cytogenet. 2005 May; 159(1):79-83. PMID: 15860363.
      View in: PubMed
    32. Aston CE, Ralph DA, Lalo DP, Manjeshwar S, Gramling BA, DeFreese DC, West AD, Branam DE, Thompson LF, Craft MA, Mitchell DS, Shimasaki CD, Mulvihill JJ, Jupe ER. Oligogenic combinations associated with breast cancer risk in women under 53 years of age. Hum Genet. 2005 Feb; 116(3):208-21. PMID: 15611867.
      View in: PubMed
    33. Lee J, Li S, Torbenson M, Liu QZ, Lind S, Mulvihill JJ, Bane B, Wang J. Leiomyosarcoma of the breast: a pathologic and comparative genomic hybridization study of two cases. Cancer Genet Cytogenet. 2004 Feb; 149(1):53-7. PMID: 15104283.
      View in: PubMed
    34. Mulvihill JJ, Blackett PR, Palmer SE. Expanding metabolic screening of newborns: can the health care industry do better than public health? J Okla State Med Assoc. 2003 Oct; 96(10):477-81. PMID: 14619602.
      View in: PubMed
    35. Mulvihill JJ. Celebrating the structure of DNA: 50 years and beyond. J Okla State Med Assoc. 2003 Apr; 96(4):184. PMID: 12733207.
      View in: PubMed
    36. Li S, Zhang L, Kern WF, Andrade D, Forsberg JE, Bates FR, Mulvihill JJ. Identification of t(15;17) and a segmental duplication of chromosome 11q23 in a patient with acute myeloblastic leukemia M2. Cancer Genet Cytogenet. 2002 Oct 15; 138(2):149-52. PMID: 12505261.
      View in: PubMed
    37. Zhang L, Mulvihill JJ, Kern WF, McMinn J, Li S. Duplication 15q as the sole anomaly in an acute promyelocytic leukemia patient without t(15;17). Cancer Genet Cytogenet. 2002 Oct 01; 138(1):17-21. PMID: 12419579.
      View in: PubMed
    38. Craft M, Mulvihill J. Breast cancer risk: evaluating the risk and role of genetic testing. J Okla State Med Assoc. 2002 Oct; 95(10):663-4; quiz 665-6. PMID: 12420416.
      View in: PubMed
    39. Alluri VN, Mulvihill JJ. Medium chain acyl coenzyme A dehydrogenase (MCAD) deficiency: the case for screening all newborns. J Okla State Med Assoc. 2002 May; 95(5):326-8. PMID: 12043106.
      View in: PubMed
    40. Li S, Stanley JR, Draper ML, Mirabile CP, Coleman FH, Mulvihill JJ. Rapid prenatal diagnosis of trisomies 13, 18, 21 and sex chromosome anomalies by fluorescence in situ hybridization: a year's experience. J Okla State Med Assoc. 2002 Apr; 95(4):244-6. PMID: 11957840.
      View in: PubMed
    41. Zhang L, Mulvihill JJ, Kinasewitz GT, Scott KV, Bates F, Li S. Duplication 15q in a patient with t(8;21) acute myeloblastic leukemia (M2). Cancer Genet Cytogenet. 2002 Mar; 133(2):148-51. PMID: 11943342.
      View in: PubMed
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