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John J Mulvihill

TitleProf,George L Cross Rsrch
InstitutionUniversity of Oklahoma Health Sciences Center
DepartmentDept of Pediatrics
AddressOUCPB 12100
1200 N Phillips Ave
Oklahoma City OK 73104
Phone405/271-8685
Fax0
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    Collapse Research 
    Collapse research activities and funding
    R13CA075223     (MULVIHILL, JOHN J.)May 1, 1997 - Apr 30, 1998
    NIH
    FAMILIAL CANCER AND PREVENTION
    Role: Principal Investigator

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

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

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

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

    P20RR023477     (MULVIHILL, JOHN J.)Sep 17, 2006 - Jun 30, 2009
    NIH
    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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    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. Cahalane RM, Barrett HE, Ross AM, Mulvihill JJE, Purtill H, Selvarajah L, O'Brien J, Kavanagh EG, Moloneye MA, Egan SM, Leahy FC, Griffin TP, Islam MN, O'Shea PM, Walsh MT, O'Connor EM. On the association between circulating biomarkers and atherosclerotic calcification in a cohort of arterial disease participants. Nutr Metab Cardiovasc Dis. 2021 05 06; 31(5):1533-1541. PMID: 33810961.
      Citations:    Fields:    Translation:Humans
    2. Capps B, Joly Y, Mulvihill J, Lee WB. The Human Genome Organisation (HUGO) and the 2020 COVID-19 pandemic. Hum Genomics. 2021 02 10; 15(1):12. PMID: 33568209.
      Citations:    Fields:    Translation:HumansPHPublic Health
    3. Biesecker LG, Adam MP, Alkuraya FS, Amemiya AR, Bamshad MJ, Beck AE, Bennett JT, Bird LM, Carey JC, Chung B, Clark RD, Cox TC, Curry C, Dinulos MBP, Dobyns WB, Giampietro PF, Girisha KM, Glass IA, Graham JM, Gripp KW, Haldeman-Englert CR, Hall BD, Innes AM, Kalish JM, Keppler-Noreuil KM, Kosaki K, Kozel BA, Mirzaa GM, Mulvihill JJ, Nowaczyk MJM, Pagon RA, Retterer K, Rope AF, Sanchez-Lara PA, Seaver LH, Shieh JT, Slavotinek AM, Sobering AK, Stevens CA, Stevenson DA, Tan TY, Tan WH, Tsai AC, Weaver DD, Williams MS, Zackai E, Zarate YA. A dyadic approach to the delineation of diagnostic entities in clinical genomics. Am J Hum Genet. 2021 01 07; 108(1):8-15. PMID: 33417889.
      Citations: 1     Fields:    Translation:Humans
    4. Schoch K, Esteves C, Bican A, Spillmann R, Cope H, McConkie-Rosell A, Walley N, Fernandez L, Kohler JN, Bonner D, Reuter C, Stong N, Mulvihill JJ, Novacic D, Wolfe L, Abdelbaki A, Toro C, Tifft C, Malicdan M, Gahl W, Liu P, Newman J, Goldstein DB, Hom J, Sampson J, Wheeler MT, Cogan J, Bernstein JA, Adams DR, McCray AT, Shashi V. Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science. Genet Med. 2021 02; 23(2):259-271. PMID: 33093671.
      Citations:    Fields:    
    5. Mulvihill JJ. The joy and duty of a marginal teratologist. Birth Defects Res. 2020 07 15; 112(12):918-928. PMID: 32459072.
      Citations:    Fields:    
    6. Kenborg L, Duun-Henriksen AK, Dalton SO, Bidstrup PE, Doser K, Rugbjerg K, Pedersen C, Krøyer A, Johansen C, Andersen KK, Østergaard JR, Hove H, Sørensen SA, Riccardi VM, Mulvihill JJ, Winther JF. Multisystem burden of neurofibromatosis 1 in Denmark: registry- and population-based rates of hospitalizations over the life span. Genet Med. 2020 06; 22(6):1069-1078. PMID: 32107470.
      Citations:    Fields:    Translation:Humans
    7. Capps B, Chadwick R, Joly Y, Lysaght T, Mills C, Mulvihill JJ, Zwart H. Statement on bioinformatics and capturing the benefits of genome sequencing for society. Hum Genomics. 2019 05 29; 13(1):24. PMID: 31142362.
      Citations:    Fields:    Translation:Humans
    8. Silverman EK, Allard P, Loscalzo J, Mulvihill JJ, Korrick SA. Reported environmental exposures are inversely associated with obtaining a genetic diagnosis in the Undiagnosed Diseases Network. . 2019 06; 179(6):958-965. PMID: 30903737.
      Citations:    
    9. Splinter K, Adams DR, Bacino CA, Bellen HJ, Bernstein JA, Cheatle-Jarvela AM, Eng CM, Esteves C, Gahl WA, Hamid R, Jacob HJ, Kikani B, Koeller DM, Kohane IS, Lee BH, Loscalzo J, Luo X, McCray AT, Metz TO, Mulvihill JJ, Nelson SF, Palmer CGS, Phillips JA, Pick L, Postlethwait JH, Reuter C, Shashi V, Sweetser DA, Tifft CJ, Walley NM, Wangler MF, Westerfield M, Wheeler MT, Wise AL, Worthey EA, Yamamoto S, Ashley EA. Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease. N Engl J Med. 2018 11 29; 379(22):2131-2139. PMID: 30304647.
      Citations: 55     Fields:    Translation:HumansAnimals
    10. Chou AF, Mulvihill J, Kaye C, Mann S, Williams MS, Williamson L. Developing a genetic services assessment tool to inform quality improvement efforts in state genetic service delivery. Genet Med. 2019 04; 21(4):955-964. PMID: 30214070.
      Citations: 1     Fields:    Translation:Humans
    11. Nielsen BF, Schmidt AA, Mulvihill JJ, Frederiksen K, Tawn EJ, Stovall M, Johansen C, Boice JD, Winther JF. Chromosomal Abnormalities in Offspring of Young Cancer Survivors: A Population-Based Cohort Study in Denmark. J Natl Cancer Inst. 2018 05 01; 110(5):534-538. PMID: 29228263.
      Citations: 2     Fields:    Translation:Humans
    12. Capps B, Chadwick R, Joly Y, Mulvihill JJ, Lysaght T, Zwart H. Falling giants and the rise of gene editing: ethics, private interests and the public good. Hum Genomics. 2017 08 29; 11(1):20. PMID: 28851444.
      Citations: 6     Fields:    Translation:Humans
    13. 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 06 01; 122(1):17-29. PMID: 28334154.
      Citations: 11     Fields:    Translation:HumansCells
    14. Malinowski AK, Ananth CV, Catalano P, Hines EP, Kirby RS, Klebanoff MA, Mulvihill JJ, Simhan H, Hamilton CM, Hendershot TP, Phillips MJ, Kilpatrick LA, Maiese DR, Ramos EM, Wright RJ, Dolan SM. Research standardization tools: pregnancy measures in the PhenX Toolkit. Am J Obstet Gynecol. 2017 09; 217(3):249-262. PMID: 28578176.
      Citations: 1     Fields:    Translation:Humans
    15. Hassed S, Li S, Mulvihill J, Aston C, Palmer S. Adams-Oliver syndrome review of the literature: Refining the diagnostic phenotype. . 2017 Mar; 173(3):790-800. PMID: 28160419.
      Citations:    
    16. Ramoni RB, Mulvihill JJ, Adams DR, Allard P, Ashley EA, Bernstein JA, Gahl WA, Hamid R, Loscalzo J, McCray AT, Shashi V, Tifft CJ, Wise AL. The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease. Am J Hum Genet. 2017 02 02; 100(2):185-192. PMID: 28157539.
      Citations: 50     Fields:    Translation:Humans
    17. Bowdin S, Gilbert A, Bedoukian E, Carew C, Adam MP, Belmont J, Bernhardt B, Biesecker L, Bjornsson HT, Blitzer M, D'Alessandro LC, Deardorff MA, Demmer L, Elliott A, Feldman GL, Glass IA, Herman G, Hindorff L, Hisama F, Hudgins L, Innes AM, Jackson L, Jarvik G, Kim R, Korf B, Ledbetter DH, Li M, Liston E, Marshall C, Medne L, Meyn MS, Monfared N, Morton C, Mulvihill JJ, Plon SE, Rehm H, Roberts A, Shuman C, Spinner NB, Stavropoulos DJ, Valverde K, Waggoner DJ, Wilkens A, Cohn RD, Krantz ID. Recommendations for the integration of genomics into clinical practice. Genet Med. 2016 11; 18(11):1075-1084. PMID: 27171546.
      Citations: 47     Fields:    Translation:Humans
    18. Gahl WA, Mulvihill JJ, Toro C, Markello TC, Wise AL, Ramoni RB, Adams DR, Tifft CJ. The NIH Undiagnosed Diseases Program and Network: Applications to modern medicine. Mol Genet Metab. 2016 Apr; 117(4):393-400. PMID: 26846157.
      Citations: 49     Fields:    Translation:Humans
    19. Pathak A, Seipel K, Pemov A, Dewan R, Brown C, Ravichandran S, Luke BT, Malasky M, Suman S, Yeager M, Gatti RA, Caporaso NE, Mulvihill JJ, Goldin LR, Pabst T, McMaster ML, Stewart DR. Whole exome sequencing reveals a C-terminal germline variant in CEBPA-associated acute myeloid leukemia: 45-year follow up of a large family. Haematologica. 2016 07; 101(7):846-52. PMID: 26721895.
      Citations: 7     Fields:    Translation:HumansCells
    20. Scheuner MT, Peredo J, Benkendorf J, Bowdish B, Feldman G, Fleisher L, Mulvihill JJ, Watson M, Herman GE, Evans J. Reporting genomic secondary findings: ACMG members weigh in. Genet Med. 2015 Jan; 17(1):27-35. PMID: 25394173.
      Citations: 22     Fields:    Translation:Humans
    21. 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.
      Citations:    
    22. Walsh MT, Cunnane EM, Mulvihill JJ, Akyildiz AC, Gijsen FJ, Holzapfel GA. Uniaxial tensile testing approaches for characterisation of atherosclerotic plaques. J Biomech. 2014 Mar 03; 47(4):793-804. PMID: 24508324.
      Citations: 23     Fields:    Translation:Humans
    23. Zhao W, Niu G, Shen B, Zheng Y, Gong F, Wang X, Lee J, Mulvihill JJ, Chen X, Li S. High-resolution analysis of copy number variants in adults with simple-to-moderate congenital heart disease. . 2013 Dec; 161A(12):3087-94. PMID: 24115576.
      Citations:    
    24. 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.
      Citations:    
    25. 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.
      Citations: 65     Fields:    Translation:Humans
    26. 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.
      Citations: 26     Fields:    Translation:Humans
    27. 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.
      Citations: 43     Fields:    Translation:HumansCells
    28. 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.
      Citations: 6     Fields:    Translation:Humans
    29. 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.
      Citations:    
    30. Signorello LB, Mulvihill JJ, Green DM, Munro HM, Stovall M, Weathers RE, Mertens AC, Whitton JA, Robison LL, Boice JD. Congenital anomalies in the children of cancer survivors: a report from the childhood cancer survivor study. J Clin Oncol. 2012 Jan 20; 30(3):239-45. PMID: 22162566.
      Citations: 26     Fields:    Translation:Humans
    31. Winther JF, Olsen JH, Wu H, Shyr Y, Mulvihill JJ, Stovall M, Nielsen A, Schmiegelow M, Boice JD. Genetic disease in the children of Danish survivors of childhood and adolescent cancer. J Clin Oncol. 2012 Jan 01; 30(1):27-33. PMID: 22124106.
      Citations: 19     Fields:    Translation:Humans
    32. 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. . 2011 Jun; 155A(6):1374-8. PMID: 21567906.
      Citations:    
    33. Been LF, Hatfield JL, Shankar A, Aston CE, Ralhan S, Wander GS, Mehra NK, Singh JR, Mulvihill JJ, Sanghera DK. A low frequency variant within the GWAS locus of MTNR1B affects fasting glucose concentrations: genetic risk is modulated by obesity. Nutr Metab Cardiovasc Dis. 2012 Nov; 22(11):944-51. PMID: 21558052.
      Citations: 14     Fields:    Translation:Humans
    34. 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.
      Citations: 26     Fields:    Translation:Humans
    35. Winther JF, Boice JD, Christensen J, Frederiksen K, Mulvihill JJ, Stovall M, Olsen JH. Hospitalizations among children of survivors of childhood and adolescent cancer: a population-based cohort study. Int J Cancer. 2010 Dec 15; 127(12):2879-87. PMID: 21351267.
      Citations: 10     Fields:    Translation:Humans
    36. Signorello LB, Mulvihill JJ, Green DM, Munro HM, Stovall M, Weathers RE, Mertens AC, Whitton JA, Robison LL, Boice JD. Stillbirth and neonatal death in relation to radiation exposure before conception: a retrospective cohort study. Lancet. 2010 Aug 21; 376(9741):624-30. PMID: 20655585.
      Citations: 37     Fields:    Translation:HumansPHPublic Health
    37. Wang X, Zheng B, Li S, Mulvihill JJ, Chen X, Liu H. Automated identification of abnormal metaphase chromosome cells for the detection of chronic myeloid leukemia using microscopic images. J Biomed Opt. 2010 Jul-Aug; 15(4):046026. PMID: 20799828.
      Citations:    Fields:    Translation:HumansCells
    38. Wang X, Zheng B, Zhang RR, Li S, Chen X, Mulvihill JJ, Lu X, Pang H, Liu H. Automated analysis of fluorescent in situ hybridization (FISH) labeled genetic biomarkers in assisting cervical cancer diagnosis. Technol Cancer Res Treat. 2010 Jun; 9(3):231-42. PMID: 20441233.
      Citations: 3     Fields:    Translation:Humans
    39. Berg AO, Baird MA, Botkin JR, Driscoll DA, Fishman PA, Guarino PD, Hiatt RA, Jarvik GP, Millon-Underwood S, Morgan TM, Mulvihill JJ, Pollin TI, Schimmel SR, Stefanek ME, Vollmer WM, Williams JK. National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health. Ann Intern Med. 2009 Dec 15; 151(12):872-7. PMID: 19884615.
      Citations: 76     Fields:    Translation:Humans
    40. 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.
      Citations: 27     Fields:    Translation:Humans
    41. Berg AO, Baird MA, Botkin JR, Driscoll DA, Fishman PA, Guarino PD, Hiatt RA, Jarvik GP, Millon-Underwood S, Morgan TM, Mulvihill JJ, Pollin TI, Schimmel SR, Stefanek ME, Vollmer WM, Williams JK. National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health: August 24-26, 2009. NIH Consens State Sci Statements. 2009 Aug 26; 26(1):1-19. PMID: 19721470.
      Citations: 9     Fields:    Translation:Humans
    42. 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.
      Citations: 3     Fields:    Translation:HumansPHPublic Health
    43. 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.
      Citations: 15     Fields:    Translation:Humans
    44. 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.
      Citations: 1     Fields:    Translation:Humans
    45. Foster MW, Mulvihill JJ, Sharp RR. Evaluating the utility of personal genomic information. Genet Med. 2009 Aug; 11(8):570-4. PMID: 19478683.
      Citations: 72     Fields:    Translation:Humans
    46. 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.
      Citations: 1     Fields:    Translation:Humans
    47. 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.
      Citations: 4     Fields:    Translation:HumansPHPublic Health
    48. Green DM, Sklar CA, Boice JD, Mulvihill JJ, Whitton JA, Stovall M, Yasui Y. Ovarian failure and reproductive outcomes after childhood cancer treatment: results from the Childhood Cancer Survivor Study. J Clin Oncol. 2009 May 10; 27(14):2374-81. PMID: 19364956.
      Citations: 116     Fields:    Translation:Humans
    49. Wang X, Zheng B, Li S, Zhang R, Mulvihill JJ, Chen WR, Liu H. Automated detection and analysis of fluorescent in situ hybridization spots depicted in digital microscopic images of Pap-smear specimens. J Biomed Opt. 2009 Mar-Apr; 14(2):021002. PMID: 19405715.
      Citations: 4     Fields:    Translation:Humans
    50. 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.
      Citations: 19     Fields:    Translation:Humans
    51. Winther JF, Boice JD, Frederiksen K, Bautz A, Mulvihill JJ, Stovall M, Olsen JH. Radiotherapy for childhood cancer and risk for congenital malformations in offspring: a population-based cohort study. Clin Genet. 2009 Jan; 75(1):50-6. PMID: 19021636.
      Citations: 21     Fields:    Translation:HumansPHPublic Health
    52. Wang X, Zheng B, Li S, Mulvihill JJ, Liu H. Development and Assessment of an Integrated Computer-Aided Detection Scheme for Digital Microscopic Images of Metaphase Chromosomes. J Electron Imaging. 2008 Oct 01; 17(4). PMID: 23087585.
      Citations:    
    53. 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.
      Citations: 1     Fields:    Translation:HumansCells
    54. 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.
      Citations: 109     Fields:    Translation:Humans
    55. 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.
      Citations: 7     Fields:    Translation:HumansCells
    56. Sanghera DK, Nath SK, Ortega L, Gambarelli M, Kim-Howard X, Singh JR, Ralhan SK, Wander GS, Mehra NK, Mulvihill JJ, Kamboh MI. TCF7L2 polymorphisms are associated with type 2 diabetes in Khatri Sikhs from North India: genetic variation affects lipid levels. Ann Hum Genet. 2008 Jul; 72(Pt 4):499-509. PMID: 18397358.
      Citations: 17     Fields:    Translation:Humans
    57. 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. . 2008 Feb 15; 146A(4):453-8. PMID: 18203189.
      Citations:    
    58. 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.
      Citations: 1     Fields:    Translation:HumansCells
    59. 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.
      Citations: 5     Fields:    Translation:HumansCells
    60. Barnes AM, Chang W, Morello R, Cabral WA, Weis M, Eyre DR, Leikin S, Makareeva E, Kuznetsova N, Uveges TE, Ashok A, Flor AW, Mulvihill JJ, Wilson PL, Sundaram UT, Lee B, Marini JC. Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta. N Engl J Med. 2006 Dec 28; 355(26):2757-64. PMID: 17192541.
      Citations: 107     Fields:    Translation:HumansCells
    61. Foster MW, Mulvihill JJ, Sharp RR. Investments in cancer genomics: who benefits and who decides. Am J Public Health. 2006 Nov; 96(11):1960-4. PMID: 17018822.
      Citations:    Fields:    Translation:Humans
    62. 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.
      Citations: 2     Fields:    Translation:Humans
    63. McCay T, Mulvihill J, Leonard JC. Multifocal melorheostosis. Clin Nucl Med. 2006 Aug; 31(8):504-5. PMID: 16855446.
      Citations: 1     Fields:    Translation:Humans
    64. Wang X, Li S, Liu H, Mulvihill JJ, Chen W, Zheng B. A computer-aided method to expedite the evaluation of prognosis for childhood acute lymphoblastic leukemia. Technol Cancer Res Treat. 2006 Aug; 5(4):429-36. PMID: 16866573.
      Citations: 2     Fields:    Translation:HumansCells
    65. 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.
      Citations: 1     Fields:    Translation:HumansCells
    66. 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.
      Citations: 2     Fields:    Translation:Humans
    67. 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. . 2005 Oct 15; 138A(3):229-35. PMID: 16158426.
      Citations:    
    68. Blackett PR, Li S, Mulvihill JJ. Ring chromosome 4 in a patient with early onset type 2 diabetes, deafness, and developmental delay. . 2005 Aug 30; 137(2):213-6. PMID: 16082703.
      Citations:    
    69. 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.
      Citations: 2     Fields:    Translation:HumansCells
    70. 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.
      Citations:    Fields:    Translation:HumansCells
    71. Lee J, Stanley JR, Vaz SA, Mulvihill JJ, Wilson P, Hopcus-Niccum D, Li S. Down syndrome with pure partial trisomy 21q22 due to a paternal insertion (4;21) uncovered by uncultured amniotic fluid interphase FISH. . 2005 Jan 15; 132A(2):206-8. PMID: 15578618.
      Citations:    
    72. 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.
      Citations: 17     Fields:    Translation:Humans
    73. Casas KA, Mononen TK, Mikail CN, Hassed SJ, Li S, Mulvihill JJ, Lin HJ, Falk RE. Chromosome 2q terminal deletion: report of 6 new patients and review of phenotype-breakpoint correlations in 66 individuals. . 2004 Nov 01; 130A(4):331-9. PMID: 15386475.
      Citations:    
    74. Hassed SJ, Hopcus-Niccum D, Zhang L, Li S, Mulvihill JJ. A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome. Clin Genet. 2004 May; 65(5):400-4. PMID: 15099348.
      Citations: 24     Fields:    Translation:HumansCells
    75. Winther JF, Boice JD, Mulvihill JJ, Stovall M, Frederiksen K, Tawn EJ, Olsen JH. Chromosomal abnormalities among offspring of childhood-cancer survivors in Denmark: a population-based study. Am J Hum Genet. 2004 Jun; 74(6):1282-5. PMID: 15106125.
      Citations: 32     Fields:    Translation:Humans
    76. 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.
      Citations: 4     Fields:    Translation:HumansCells
    77. Li S, Hassed S, Mulvihill JJ, Nair AK, Hopcus DJ. Double trisomy. . 2004 Jan 01; 124A(1):96-8. PMID: 14679595.
      Citations:    
    78. 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.
      Citations:    Fields:    Translation:HumansPHPublic Health
    79. Zhang L, Parkhurst JB, Kern WF, Scott KV, Niccum D, Mulvihill JJ, Li S. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia. Chin Med J (Engl). 2003 Sep; 116(9):1298-303. PMID: 14527352.
      Citations: 1     Fields:    Translation:HumansCells
    80. Boice JD, Tawn EJ, Winther JF, Donaldson SS, Green DM, Mertens AC, Mulvihill JJ, Olsen JH, Robison LL, Stovall M. Genetic effects of radiotherapy for childhood cancer. Health Phys. 2003 Jul; 85(1):65-80. PMID: 12852473.
      Citations: 33     Fields:    Translation:HumansPHPublic Health
    81. Mulvihill JJ. Celebrating the structure of DNA: 50 years and beyond. J Okla State Med Assoc. 2003 Apr; 96(4):184. PMID: 12733207.
      Citations:    Fields:    Translation:Cells
    82. 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.
      Citations: 2     Fields:    Translation:HumansCells
    83. 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.
      Citations:    Fields:    Translation:HumansCells
    84. 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.
      Citations:    Fields:    Translation:Humans
    85. Winther JF, Sankila R, Boice JD, Tulinius H, Bautz A, Barlow L, Glattre E, Langmark F, Möller T, Mulvihill JJ, Olafsdottir GH, Ritvanen A, Olsen JH. [Cancer in siblings of children with cancer]. Ugeskr Laeger. 2002 Jun 03; 164(23):3073-9. PMID: 12082866.
      Citations:    Fields:    Translation:Humans
    86. 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.
      Citations:    Fields:    Translation:HumansPHPublic Health
    87. 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.
      Citations:    Fields:    Translation:Humans
    88. Robison LL, Mertens AC, Boice JD, Breslow NE, Donaldson SS, Green DM, Li FP, Meadows AT, Mulvihill JJ, Neglia JP, Nesbit ME, Packer RJ, Potter JD, Sklar CA, Smith MA, Stovall M, Strong LC, Yasui Y, Zeltzer LK. Study design and cohort characteristics of the Childhood Cancer Survivor Study: a multi-institutional collaborative project. Med Pediatr Oncol. 2002 Apr; 38(4):229-39. PMID: 11920786.
      Citations: 279     Fields:    Translation:Humans
    89. 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.
      Citations:    Fields:    Translation:HumansCells
    90. Winther JF, Sankila R, Boice JD, Tulinius H, Bautz A, Barlow L, Glattre E, Langmark F, Möller TR, Mulvihill JJ, Olafsdottir GH, Ritvanen A, Olsen JH. Cancer in siblings of children with cancer in the Nordic countries: a population-based cohort study. Lancet. 2001 Sep 01; 358(9283):711-7. PMID: 11551577.
      Citations: 13     Fields:    Translation:HumansPHPublic Health
    91. Foster MW, Sharp RR, Mulvihill JJ. Pharmacogenetics, race, and ethnicity: social identities and individualized medical care. Ther Drug Monit. 2001 Jun; 23(3):232-8. PMID: 11360031.
      Citations: 1     Fields:    Translation:Humans
    92. Jupe ER, Badgett AA, Neas BR, Craft MA, Mitchell DS, Resta R, Mulvihill JJ, Aston CE, Thompson LF. Single nucleotide polymorphism in prohibitin 3' untranslated region and breast-cancer susceptibility. Lancet. 2001 May 19; 357(9268):1588-9. PMID: 11377649.
      Citations: 25     Fields:    Translation:HumansCells
    93. Boice JD, Robison LL, Mertens A, Stovall M, Green DM, Mulvihill JJ. Stillbirths and male irradiation. J Radiol Prot. 2000 Sep; 20(3):321-2. PMID: 11008937.
      Citations: 2     Fields:    Translation:HumansPHPublic Health
    94. Banke MG, Mulvihill JJ, Aston CE. Inheritance of pancreatic cancer in pancreatic cancer-prone families. Med Clin North Am. 2000 May; 84(3):677-90, x-xi. PMID: 10872424.
      Citations: 8     Fields:    Translation:Humans
    95. Mulvihill JJ, Berg K. Permanent Committee of the International Congress of Human Genetics. Am J Med Genet. 1998 Sep 01; 79(2):79-81. PMID: 9741463.
      Citations:    Fields:    Translation:Humans
    96. Pollack IF, Colak A, Fitz C, Wiener E, Moreland M, Mulvihill JJ. Surgical management of spinal cord compression from plexiform neurofibromas in patients with neurofibromatosis 1. Neurosurgery. 1998 Aug; 43(2):248-55; discussion 255-6. PMID: 9696077.
      Citations: 3     Fields:    Translation:Humans
    97. Lin AY, Nutman TB, Kaslow D, Mulvihill JJ, Fontaine L, White BJ, Knutsen T, Theil KS, Raghuprasad PK, Goldstein AM, Tucker MA. Familial eosinophilia: clinical and laboratory results on a U.S. kindred. Am J Med Genet. 1998 Mar 19; 76(3):229-37. PMID: 9508242.
      Citations: 10     Fields:    Translation:HumansCells
    98. Mulvihill JJ. Encomium: Robert Warwick Miller: mentor, synthesizer, and international interdisciplinary initiator. Am J Med Genet. 1998 Feb 26; 76(1):1-8. PMID: 9508057.
      Citations:    Fields:    Translation:Humans
    99. Byrne J, Rasmussen SA, Steinhorn SC, Connelly RR, Myers MH, Lynch CF, Flannery J, Austin DF, Holmes FF, Holmes GE, Strong LC, Mulvihill JJ. Genetic disease in offspring of long-term survivors of childhood and adolescent cancer. Am J Hum Genet. 1998 Jan; 62(1):45-52. PMID: 9443870.
      Citations: 39     Fields:    Translation:HumansCells
    100. Nwokoro NA, Korytkowski MT, Rose S, Gorin MB, Penles Stadler M, Witchel SF, Mulvihill JJ. Spectrum of malignancy and premalignancy in Carney syndrome. Am J Med Genet. 1997 Dec 31; 73(4):369-77. PMID: 9415461.
      Citations: 3     Fields:    Translation:Humans
    101. Mulvihill JJ, Ferrell RE, Carty SE, Tisherman SE, Zbar B. Familial pheochromocytoma due to mutant von Hippel-Lindau disease gene. Arch Intern Med. 1997 Jun 23; 157(12):1390-1. PMID: 9201016.
      Citations: 3     Fields:    Translation:Humans
    102. Rubinstein WS, Wenger SL, Hoffman RM, Auerbach AD, Mulvihill JJ. Interstitial lung disease in an adult with Fanconi anemia: clues to the pathogenesis. Am J Med Genet. 1997 Mar 31; 69(3):315-9. PMID: 9096763.
      Citations:    Fields:    Translation:Humans
    103. Muenke M, Gripp KW, McDonald-McGinn DM, Gaudenz K, Whitaker LA, Bartlett SP, Markowitz RI, Robin NH, Nwokoro N, Mulvihill JJ, Losken HW, Mulliken JB, Guttmacher AE, Wilroy RS, Clarke LA, Hollway G, Adès LC, Haan EA, Mulley JC, Cohen MM, Bellus GA, Francomano CA, Moloney DM, Wall SA, Wilkie AO, et al. A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome. Am J Hum Genet. 1997 Mar; 60(3):555-64. PMID: 9042914.
      Citations: 84     Fields:    Translation:HumansCells
    104. Nwokoro NA, Mulvihill JJ. Cholesterol and bile acid replacement therapy in children and adults with Smith-Lemli-Opitz (SLO/RSH) syndrome. Am J Med Genet. 1997 Jan 31; 68(3):315-21. PMID: 9024566.
      Citations: 27     Fields:    Translation:HumansCTClinical Trials
    105. Lazebnik N, McPherson E, Rittmeyer LJ, Mulvihill JJ. The floating harbor syndrome with cardiac septal defect. Am J Med Genet. 1996 Dec 18; 66(3):300-2. PMID: 8985491.
      Citations: 1     Fields:    Translation:Humans
    106. Allen A, Anderson B, Andrews L, Beckwith J, Bowman J, Cook-Deegan R, Cox D, Duster T, Eisenberg R, Fine B, Holtzman N, King P, Kitcher P, McInerney J, McKusick V, Mulvihill J, Murray J, Murray R, Murray T, Nelkin D, Rapp R, Saxton M, Wexler N. The Bell Curve: statement by the NIH-DOE Joint Working Group on the Ethical, Legal, and Social Implications of Human Genome Research. Am J Hum Genet. 1996 Aug; 59(2):487-8. PMID: 8755944.
      Citations: 1     Fields:    Translation:Humans
    107. Pollack IF, Shultz B, Mulvihill JJ. The management of brainstem gliomas in patients with neurofibromatosis 1. Neurology. 1996 Jun; 46(6):1652-60. PMID: 8649565.
      Citations: 27     Fields:    Translation:Humans
    108. Nelen MR, Padberg GW, Peeters EA, Lin AY, van den Helm B, Frants RR, Coulon V, Goldstein AM, van Reen MM, Easton DF, Eeles RA, Hodgsen S, Mulvihill JJ, Murday VA, Tucker MA, Mariman EC, Starink TM, Ponder BA, Ropers HH, Kremer H, Longy M, Eng C. Localization of the gene for Cowden disease to chromosome 10q22-23. Nat Genet. 1996 May; 13(1):114-6. PMID: 8673088.
      Citations: 128     Fields:    Translation:HumansCells
    109. Zbar B, Kishida T, Chen F, Schmidt L, Maher ER, Richards FM, Crossey PA, Webster AR, Affara NA, Ferguson-Smith MA, Brauch H, Glavac D, Neumann HP, Tisherman S, Mulvihill JJ, Gross DJ, Shuin T, Whaley J, Seizinger B, Kley N, Olschwang S, Boisson C, Richard S, Lips CH, Lerman M, et al. Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan. Hum Mutat. 1996; 8(4):348-57. PMID: 8956040.
      Citations: 112     Fields:    Translation:Humans
    110. Benichou J, Gail MH, Mulvihill JJ. Graphs to estimate an individualized risk of breast cancer. J Clin Oncol. 1996 Jan; 14(1):103-10. PMID: 8558184.
      Citations: 12     Fields:    Translation:HumansPHPublic Health
    111. Andersson HC, Parry DM, Mulvihill JJ. Lymphangiosarcoma in late-onset hereditary lymphedema: case report and nosological implications. Am J Med Genet. 1995 Mar 13; 56(1):72-5. PMID: 7747790.
      Citations: 4     Fields:    Translation:Humans
    112. Nwokoro NA, Hyde B, Mulvihill JJ. Smith-Lemli-Opitz syndrome: biochemical before clinical diagnosis; early dietary management. Am J Med Genet. 1994 May 01; 50(4):375-6. PMID: 8209919.
      Citations: 1     Fields:    Translation:Humans
    113. Ron E, Tarone RE, Modan B, Chaki R, Alfandary E, Parry DM, Makar M, Setlow N, Mulvihill JJ, Miller RW, et al. In vitro radiosensitivity of fibroblasts from thyroid and skin cancer patients treated with X-rays for tinea capitis. Cancer Epidemiol Biomarkers Prev. 1994 Apr-May; 3(3):229-32. PMID: 8019372.
      Citations:    Fields:    Translation:HumansCells
    114. Ramsey-Goldman R, Mientus JM, Kutzer JE, Mulvihill JJ, Medsger TA. Pregnancy outcome in women with systemic lupus erythematosus treated with immunosuppressive drugs. J Rheumatol. 1993 Jul; 20(7):1152-7. PMID: 8371208.
      Citations: 12     Fields:    Translation:Humans
    115. Lin AE, McPherson E, Nwokoro NA, Clemens M, Losken HW, Mulvihill JJ. Further delineation of the Baller-Gerold syndrome. Am J Med Genet. 1993 Feb 15; 45(4):519-24. PMID: 8465861.
      Citations: 6     Fields:    Translation:Humans
    116. Nicholson HS, Mulvihill JJ. Late effects of therapy in survivors of childhood and adolescent osteosarcoma. Cancer Treat Res. 1993; 62:45-8. PMID: 8096758.
      Citations: 1     Fields:    Translation:Humans
    117. Winn DM, Li FP, Robison LL, Mulvihill JJ, Daigle AE, Fraumeni JF. A case-control study of the etiology of Ewing's sarcoma. Cancer Epidemiol Biomarkers Prev. 1992 Nov-Dec; 1(7):525-32. PMID: 1302564.
      Citations: 11     Fields:    Translation:Humans
    118. Steele MW, Wenger SL, Deka R, Mulvihill JJ, Sukarachana K. Genetic analyses on a set of parasitic conjoined twins. Am J Med Genet. 1992 Apr 01; 42(6):856. PMID: 1554027.
      Citations:    Fields:    Translation:Humans
    119. Epstein ND, Fananapazir L, Lin HJ, Mulvihill J, White R, Lalouel JM, Lifton RP, Nienhuis AW, Leppert M. Evidence of genetic heterogeneity in five kindreds with familial hypertrophic cardiomyopathy. Circulation. 1992 Feb; 85(2):635-47. PMID: 1735158.
      Citations: 17     Fields:    Translation:HumansCells
    120. Wertz DC, Fletcher JC, Mulvihill JJ. Medical geneticists confront ethical dilemmas: cross-cultural comparisons among 18 nations. Am J Hum Genet. 1990 Jun; 46(6):1200-13. PMID: 2339711.
      Citations: 14     Fields:    Translation:Humans
    121. Basta M, Morton NE, Mulvihill JJ, Radovanovic Z, Radojicic C, Marinkovic D. Inheritance of acute appendicitis: familial aggregation and evidence of polygenic transmission. Am J Hum Genet. 1990 Feb; 46(2):377-82. PMID: 2301403.
      Citations: 5     Fields:    Translation:Humans
    122. Mulvihill JJ. Sentinel and other mutational effects in offspring of cancer survivors. Prog Clin Biol Res. 1990; 340C:179-86. PMID: 2381923.
      Citations: 3     Fields:    Translation:HumansCellsPHPublic Health
    123. Gail MH, Brinton LA, Byar DP, Corle DK, Green SB, Schairer C, Mulvihill JJ. Projecting individualized probabilities of developing breast cancer for white females who are being examined annually. J Natl Cancer Inst. 1989 Dec 20; 81(24):1879-86. PMID: 2593165.
      Citations: 785     Fields:    Translation:Humans
    124. Mulvihill JJ. Prospects for cancer control and prevention through genetics. Clin Genet. 1989 Nov; 36(5):313-9. PMID: 2689001.
      Citations: 1     Fields:    Translation:Humans
    125. Bale AE, Bale SJ, Murli H, Ivett J, Mulvihill JJ, Parry DM. Sister chromatid exchange and chromosome fragility in the nevoid basal cell carcinoma syndrome. Cancer Genet Cytogenet. 1989 Oct 15; 42(2):273-9. PMID: 2507127.
      Citations: 1     Fields:    Translation:HumansCells
    126. Mulvihill JJ, Kaiser-Kupfer MI. Niikawa-Kuroki (Kabuki make-up) syndrome. Am J Med Genet. 1989 Jul; 33(3):425. PMID: 2801782.
      Citations:    Fields:    Translation:Humans
    127. Mulvihill JJ, Byrne J. Genetic counseling of the cancer survivor. Semin Oncol Nurs. 1989 Feb; 5(1):29-35. PMID: 2646665.
      Citations: 2     Fields:    Translation:HumansAnimals
    128. Seizinger BR, Farmer GE, Haines JL, Ozelius LJ, Anderson K, Korf BR, Parry DM, Pericak-Vance MA, Mulvihill JJ, Menon A, et al. Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1). Am J Hum Genet. 1989 Jan; 44(1):30-2. PMID: 2491778.
      Citations: 4     Fields:    Translation:HumansCells
    129. Goldgar DE, Green P, Parry DM, Mulvihill JJ. Multipoint linkage analysis in neurofibromatosis type I: an international collaboration. Am J Hum Genet. 1989 Jan; 44(1):6-12. PMID: 2491784.
      Citations: 46     Fields:    Translation:HumansCells
    130. Mulvihill JJ. Narrowing the scope of the journal? Am J Hum Genet. 1988 Aug; 43(2):219. PMID: 17948589.
      Citations:    Fields:    
    131. Parry DM, Mulvihill JJ, Miller RW, Berg K, Carter CL. Strategies for controlling cancer through genetics. Cancer Res. 1987 Dec 15; 47(24 Pt 1):6814-7. PMID: 3315192.
      Citations: 6     Fields:    Translation:Humans
    132. Byrne J, Mulvihill JJ, Myers MH, Connelly RR, Naughton MD, Krauss MR, Steinhorn SC, Hassinger DD, Austin DF, Bragg K, et al. Effects of treatment on fertility in long-term survivors of childhood or adolescent cancer. N Engl J Med. 1987 Nov 19; 317(21):1315-21. PMID: 3683460.
      Citations: 52     Fields:    Translation:Humans
    133. Parry DM, Berg K, Mulvihill JJ, Carter CL, Miller RW. Strategies for controlling cancer through genetics: report of a workshop. Am J Hum Genet. 1987 Jul; 41(1):63-9. PMID: 3605097.
      Citations: 2     Fields:    Translation:Humans
    134. Caporaso N, Greene MH, Tsai S, Pickle LW, Mulvihill JJ. Cytogenetics in hereditary malignant melanoma and dysplastic nevus syndrome: is dysplastic nevus syndrome a chromosome instability disorder? Cancer Genet Cytogenet. 1987 Feb; 24(2):299-314. PMID: 3791179.
      Citations: 4     Fields:    Translation:HumansCells
    135. Parry DM, Mulvihill JJ, Tsai SE, Kaiser-Kupfer MI, Cowan JM. SC phocomelia syndrome, premature centromere separation, and congenital cranial nerve paralysis in two sisters, one with malignant melanoma. Am J Med Genet. 1986 Aug; 24(4):653-72. PMID: 3740099.
      Citations: 12     Fields:    Translation:HumansCells
    136. Holmes GE, Baker A, Hassanein RS, Bovee EC, Mulvihill JJ, Myers MH, Holmes FF. The availability of insurance to long-time survivors of childhood cancer. Cancer. 1986 Jan 01; 57(1):190-3. PMID: 3940618.
      Citations: 6     Fields:    Translation:Humans
    137. Spence MA, Parry DM, Bader JL, Marazita ML, Bocian M, Funderburk SJ, Mulvihill JJ, Sparkes RS. Genetic linkage analysis of neurofibromatosis. Ann N Y Acad Sci. 1986; 486:287-92. PMID: 3105393.
      Citations: 2     Fields:    Translation:HumansCells
    138. Danforth DN, Tamarkin L, Mulvihill JJ, Bagley CS, Lippman ME. Plasma melatonin and the hormone-dependency of human breast cancer. J Clin Oncol. 1985 Jul; 3(7):941-8. PMID: 4020407.
      Citations: 9     Fields:    Translation:Humans
    139. Bale AE, Drum MA, Parry DM, Mulvihill JJ. Familial Sotos syndrome (cerebral gigantism): craniofacial and psychological characteristics. Am J Med Genet. 1985 Apr; 20(4):613-24. PMID: 2581446.
      Citations: 6     Fields:    Translation:Humans
    140. Kao YS, Kao-Shan CS, Knutsen T, Whang-Peng J, Mulvihill JJ. Neurofibromatosis: no chromosomal defect by prophase banding technique. Cancer Genet Cytogenet. 1984 Nov; 13(3):281-2. PMID: 6437664.
      Citations: 3     Fields:    Translation:Humans
    141. Maron BJ, Nichols PF, Pickle LW, Wesley YE, Mulvihill JJ. Patterns of inheritance in hypertrophic cardiomyopathy: assessment by M-mode and two-dimensional echocardiography. Am J Cardiol. 1984 Apr 01; 53(8):1087-94. PMID: 6538384.
      Citations: 40     Fields:    Translation:Humans
    142. McKeen EA, Hanson MR, Mulvihill JJ, Glaubiger DL. Birth defects with Ewing's sarcoma. N Engl J Med. 1983 Dec 15; 309(24):1522. PMID: 6646179.
      Citations: 4     Fields:    Translation:Humans
    143. Mulvihill JJ, Czeizel A. International Commission for Protection against Environmental Mutagens and Carcinogens. ICPEMC Working Paper 5/6. Perspectives in mutation epidemiology, 6. A 1983 view of sentinel phenotypes. Mutat Res. 1983 Dec; 123(3):345-61. PMID: 6358880.
      Citations: 4     Fields:    Translation:HumansCells
    144. Goffman TE, Mulvihill JJ, Carney DN, Triche TJ, Whang-Peng J. Fatal hypereosinophilia with chromosome 15q- in a patient with multiple primary and familial neoplasms. Cancer Genet Cytogenet. 1983 Mar; 8(3):197-202. PMID: 6297705.
      Citations: 1     Fields:    Translation:HumansCells
    145. Mulvihill JJ, Safyer AW, Bening JK. Prevention in familial breast cancer: counseling and prophylactic mastectomy. Prev Med. 1982 Sep; 11(5):500-11. PMID: 7156060.
      Citations: 2     Fields:    Translation:Humans
    146. Goffman TE, Hassinger DD, Mulvihill JJ. Familial respiratory tract cancer. Opportunities for research and prevention. JAMA. 1982 Feb 19; 247(7):1020-3. PMID: 7057577.
      Citations: 1     Fields:    Translation:HumansCells
    147. Hope DG, Mulvihill JJ. Malignancy in neurofibromatosis. Adv Neurol. 1981; 29:33-56. PMID: 6798842.
      Citations: 32     Fields:    Translation:Humans
    148. Blatt J, Mulvihill JJ, Ziegler JL, Young RC, Poplack DG. Pregnancy outcome following cancer chemotherapy. Am J Med. 1980 Dec; 69(6):828-32. PMID: 7446548.
      Citations: 17     Fields:    Translation:Humans
    149. Hassinger DD, Mulvihill JJ, Chandler JB. Aarskog's syndrome with Hirschsprung's disease, midgut malrotation, and dental anomalies. J Med Genet. 1980 Jun; 17(3):235-8. PMID: 7401138.
      Citations: 4     Fields:    Translation:Humans
    150. Blattner WA, McGuire DB, Mulvihill JJ, Lampkin BC, Hananian J, Fraumeni JF. Genealogy of cancer in a family. JAMA. 1979 Jan 19; 241(3):259-61. PMID: 281540.
      Citations: 9     Fields:    Translation:Humans
    151. Blattner WA, Lubiniecki AS, Mulvihill JJ, Lalley P, Fraumeni JF. Genetics of SV40 T-antigen expression: studies of twins, heritable syndromes and cancer families. Int J Cancer. 1978 Sep 15; 22(3):231-8. PMID: 212368.
      Citations: 5     Fields:    Translation:HumansAnimalsCells
    152. Parry DM, Safyer AW, Mulvihill JJ. Waardenburg-like features with cataracts, small head size, joint abnormalities, hypogonadism, and osteosarcoma. J Med Genet. 1978 Feb; 15(1):66-9. PMID: 273099.
      Citations: 2     Fields:    Translation:Humans
    153. Mulvihill JJ, Gralnick HR, Whang-Peng J, Leventhal BG. Multiple childhood osteosarcomas in an American Indian family with erythroid macrocytosis and skeletal anomalies. Cancer. 1977 Dec; 40(6):3115-22. PMID: 201363.
      Citations: 5     Fields:    Translation:HumansCells
    154. Mulvihill JJ, McKeen EA. Discussion: genetics of multiple primary tumors: a clinical etiologic approach illustrated by three patients. Cancer. 1977 Oct; 40(4 Suppl):1867-71. PMID: 907990.
      Citations: 6     Fields:    Translation:Humans
    155. Mulvihill JJ, Klimas JT, Stokes DC, Risemberg HM. Fetal alcohol syndrome: seven new cases. Am J Obstet Gynecol. 1976 Aug 01; 125(7):937-41. PMID: 941948.
      Citations: 2     Fields:    Translation:Humans
    156. Mulvihill JJ. Host factors in human lung tumors: an example of ecogenetics in oncology. J Natl Cancer Inst. 1976 Jul; 57(1):3-7. PMID: 1003506.
      Citations: 5     Fields:    Translation:Humans
    157. Mulvihill JJ, Smith DW. Another disorder with prenatal shortness of stature and premature aging. Birth Defects Orig Artic Ser. 1975; 11(2):368-70. PMID: 1227552.
      Citations: 5     Fields:    Translation:Humans
    158. Mulvihill JJ, Mulvihill CG, Neill CA. Letter: Congenital heart defects and prenatal sex hormones. Lancet. 1974 Jun 08; 1(7867):1168. PMID: 4136887.
      Citations:    Fields:    Translation:Humans
    159. Mulvihill JJ. Caffeine as teratogen and mutagen. Teratology. 1973 Aug; 8(1):69-72. PMID: 4737491.
      Citations: 2     Fields:    Translation:HumansAnimals
    160. Wertelecki W, Fraumeni JF, Mulvihill JJ. Nongonadal neoplasia in Turner's syndrome. Cancer. 1970 Aug; 26(2):485-8. PMID: 4318552.
      Citations: 5     Fields:    Translation:Humans
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