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    Results: 1 to 50 of 197

    1.

    National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health.

    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.

    Ann Intern Med. 2009 Nov 2. [Epub ahead of print] No abstract available. PMID: 19884615 [PubMed - as supplied by publisher]Related articlesFree article

    2.

    PPARG and ADIPOQ gene polymorphisms increase type 2 diabetes mellitus risk in Asian Indian Sikhs: Pro12Ala still remains as the strongest predictor.

    Sanghera DK, Demirci FY, Been L, Ortega L, Ralhan S, Wander GS, Mehra NK, Singh J, Aston CE, Mulvihill JJ, Kamboh IM.

    Metabolism. 2009 Oct 19. [Epub ahead of print]PMID: 19846176 [PubMed - as supplied by publisher]Related articles

    3.

    Risk of cancer among children of cancer patients-A nationwide study in Finland.

    Madanat-Harjuoja LM, Malila N, Lähteenmäki P, Pukkala E, Mulvihill JJ, Boice JD Jr, Sankila R.

    Int J Cancer. 2009 Sep 2. [Epub ahead of print]PMID: 19728329 [PubMed - as supplied by publisher]Related articles

    4.

    NIH State-of-the-Science Conference Statement: Family History and Improving Health.

    Baird MA, Berg AO, 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.

    NIH Consens State Sci Statements. 2009 Aug 26;26(1). [Epub ahead of print]PMID: 19721470 [PubMed - as supplied by publisher]Related articlesFree article

    5.

    Replication of Association Between a Common Variant Near Melanocortin-4 Receptor Gene and Obesity-related Traits in Asian Sikhs.

    Been LF, Nath SK, Ralhan SK, Wander GS, Mehra NK, Singh J, Mulvihill JJ, Sanghera DK.

    Obesity (Silver Spring). 2009 Aug 13. [Epub ahead of print]PMID: 19680233 [PubMed - as supplied by publisher]Related articles

    6.

    Tonic-clonic seizures in a fetus with Pena-Shokeir syndrome.

    Knudtson EJ, Lorenz LB, Wilson PL, McDaniel B, Mulvihill JJ, Dannaway DC.

    J Ultrasound Med. 2009 Aug;28(8):1121-2. No abstract available. PMID: 19643800 [PubMed - indexed for MEDLINE]Related articles

    7.

    Quality assurance in medical and public health genetics services: a systematic review.

    Chou AF, Norris AI, Williamson L, Garcia K, Baysinger J, Mulvihill JJ.

    Am J Med Genet C Semin Med Genet. 2009 Aug 15;151C(3):214-34. Review.PMID: 19621459 [PubMed - indexed for MEDLINE]Related articles

    8.

    Prenatal identification of a novel R937P L1CAM missense mutation.

    Wilson PL, Kattman BB, Mulvihill JJ, Li S, Wilkins J, Wagner AF, Goodman JR.

    Genet Test Mol Biomarkers. 2009 Aug;13(4):515-9.PMID: 19594370 [PubMed - indexed for MEDLINE]Related articles

    9.

    Low adherence to national guidelines for thyroid screening in Down syndrome.

    Fergeson MA, Mulvihill JJ, Schaefer GB, Dehaai KA, Piatt J, Combs K, Bright BC, Neas BR.

    Genet Med. 2009 Jul;11(7):548-51.PMID: 19506481 [PubMed - indexed for MEDLINE]Related articles

    10.

    Evaluating the utility of personal genomic information.

    Foster MW, Mulvihill JJ, Sharp RR.

    Genet Med. 2009 Aug;11(8):570-4.PMID: 19478683 [PubMed - in process]Related articles

    11.

    Population-based clinical epidemiology of familial cancer: lessons for oncologists.

    Winther JF, Mulvihill JJ.

    Lancet Oncol. 2009 May;10(5):439-40. No abstract available. PMID: 19410189 [PubMed - indexed for MEDLINE]Related articles

    12.

    Automated detection and analysis of fluorescent in situ hybridization spots depicted in digital microscopic images of Pap-smear specimens.

    Wang X, Zheng B, Li S, Zhang R, Mulvihill JJ, Chen WR, Liu H.

    J Biomed Opt. 2009 Mar-Apr;14(2):021002.PMID: 19405715 [PubMed - indexed for MEDLINE]Related articles

    13.

    Ovarian failure and reproductive outcomes after childhood cancer treatment: results from the Childhood Cancer Survivor Study.

    Green DM, Sklar CA, Boice JD Jr, Mulvihill JJ, Whitton JA, Stovall M, Yasui Y.

    J Clin Oncol. 2009 May 10;27(14):2374-81. Epub 2009 Apr 13. Review.PMID: 19364956 [PubMed - indexed for MEDLINE]Related articles

    14.

    The Childhood Cancer Survivor Study: a National Cancer Institute-supported resource for outcome and intervention research.

    Robison LL, Armstrong GT, Boice JD, Chow EJ, Davies SM, Donaldson SS, Green DM, Hammond S, Meadows AT, Mertens AC, Mulvihill JJ, Nathan PC, Neglia JP, Packer RJ, Rajaraman P, Sklar CA, Stovall M, Strong LC, Yasui Y, Zeltzer LK.

    J Clin Oncol. 2009 May 10;27(14):2308-18. Epub 2009 Apr 13. Review.PMID: 19364948 [PubMed - indexed for MEDLINE]Related articles

    15.

    Testing the association of novel meta-analysis-derived diabetes risk genes with type II diabetes and related metabolic traits in Asian Indian Sikhs.

    Sanghera DK, Been L, Ortega L, Wander GS, Mehra NK, Aston CE, Mulvihill JJ, Ralhan S.

    J Hum Genet. 2009 Mar;54(3):162-8. Epub 2009 Feb 27.PMID: 19247373 [PubMed - in process]Related articles

    16.

    Radiotherapy for childhood cancer and risk for congenital malformations in offspring: a population-based cohort study.

    Winther JF, Boice JD Jr, Frederiksen K, Bautz A, Mulvihill JJ, Stovall M, Olsen JH.

    Clin Genet. 2009 Jan;75(1):50-6. Epub 2008 Nov 17.PMID: 19021636 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    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.

    Xu W, Lu X, Kim Y, Luo Y, Martin M, Mulvihill JJ, Li S.

    Cancer Genet Cytogenet. 2008 Aug;185(1):43-6.PMID: 18656693 [PubMed - indexed for MEDLINE]Related articles

    18.

    Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk.

    Sanghera DK, Ortega L, Han S, Singh J, Ralhan SK, Wander GS, Mehra NK, Mulvihill JJ, Ferrell RE, Nath SK, Kamboh MI.

    BMC Med Genet. 2008 Jul 3;9:59.PMID: 18598350 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    Automated classification of metaphase chromosomes: optimization of an adaptive computerized scheme.

    Wang X, Zheng B, Li S, Mulvihill JJ, Wood MC, Liu H.

    J Biomed Inform. 2009 Feb;42(1):22-31. Epub 2008 May 21.PMID: 18585097 [PubMed - indexed for MEDLINE]Related articles

    20.

    TCF7L2 polymorphisms are associated with type 2 diabetes in Khatri Sikhs from North India: genetic variation affects lipid levels.

    Sanghera DK, Nath SK, Ortega L, Gambarelli M, Kim-Howard X, Singh JR, Ralhan SK, Wander GS, Mehra NK, Mulvihill JJ, Kamboh MI.

    Ann Hum Genet. 2008 Jul;72(Pt 4):499-509. Epub 2008 Apr 7.PMID: 18397358 [PubMed - indexed for MEDLINE]Related articles

    21.

    A novel subtelomeric translocation t(5;9) and a deletion of the RB1 gene in a patient with acute myeloid leukemia (AML-M0).

    Lee J, Lu X, Shin ES, Kern WF, Mulvihill JJ, Li S.

    Cancer Genet Cytogenet. 2008 Feb;181(1):36-9.PMID: 18262051 [PubMed - indexed for MEDLINE]Related articles

    22.

    De novo three-way chromosome translocation 46,XY,t(4;6;21)(p16;p21.1;q21) in a male with cleidocranial dysplasia.

    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.

    Am J Med Genet A. 2008 Feb 15;146A(4):453-8.PMID: 18203189 [PubMed - indexed for MEDLINE]Related articlesFree article

    23.

    A rule-based computer scheme for centromere identification and polarity assignment of metaphase chromosomes.

    Wang X, Zheng B, Li S, Mulvihill JJ, Liu H.

    Comput Methods Programs Biomed. 2008 Jan;89(1):33-42.PMID: 18082909 [PubMed - indexed for MEDLINE]Related articles

    24.

    Assessing human germ-cell mutagenesis in the Postgenome Era: a celebration of the legacy of William Lawson (Bill) Russell.

    Wyrobek AJ, Mulvihill JJ, Wassom JS, Malling HV, Shelby MD, Lewis SE, Witt KL, Preston RJ, Perreault SD, Allen JW, Demarini DM, Woychik RP, Bishop JB.

    Environ Mol Mutagen. 2007 Mar;48(2):71-95.PMID: 17295306 [PubMed - indexed for MEDLINE]Related articlesFree article

    25.

    Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta.

    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.

    N Engl J Med. 2006 Dec 28;355(26):2757-64.PMID: 17192541 [PubMed - indexed for MEDLINE]Related articlesFree article

    26.

    Investments in cancer genomics: who benefits and who decides.

    Foster MW, Mulvihill JJ, Sharp RR.

    Am J Public Health. 2006 Nov;96(11):1960-4. Epub 2006 Oct 3.PMID: 17018822 [PubMed - indexed for MEDLINE]Related articlesFree article

    27.

    Cryptic and complex chromosomal rearrangements and the deletion of TP53 gene in a patient with leukemic mantle cell lymphoma.

    Zhang L, Kern WF, Yu Z, Mulvihill JJ, Li S.

    Cancer Genet Cytogenet. 2006 Sep;169(2):169-73.PMID: 16938577 [PubMed - indexed for MEDLINE]Related articles

    28.

    Trisomy 1q in a patient with severe aplastic anemia.

    Angelidis P, Kojouri K, Lee J, Kern W, Mulvihill JJ, Li S.

    Cancer Genet Cytogenet. 2006 Aug;169(1):73-5.PMID: 16875941 [PubMed - indexed for MEDLINE]Related articles

    29.

    A computer-aided method to expedite the evaluation of prognosis for childhood acute lymphoblastic leukemia.

    Wang X, Li S, Liu H, Mulvihill JJ, Chen W, Zheng B.

    Technol Cancer Res Treat. 2006 Aug;5(4):429-36.PMID: 16866573 [PubMed - indexed for MEDLINE]Related articles

    30.

    Perform a gene test on every patient: the medical family history revisited.

    Bendure WB, Mulvihill JJ.

    J Okla State Med Assoc. 2006 Feb;99(2):78-83.PMID: 16562397 [PubMed - indexed for MEDLINE]Related articles

    31.

    Ring chromosome 9 [r(9)(p24q34)]: a report of two cases.

    Purandare SM, Lee J, Hassed S, Steele MI, Blackett PR, Mulvihill JJ, Li S.

    Am J Med Genet A. 2005 Oct 15;138A(3):229-35.PMID: 16158426 [PubMed - indexed for MEDLINE]Related articles

    32.

    Ring chromosome 4 in a patient with early onset type 2 diabetes, deafness, and developmental delay.

    Blackett PR, Li S, Mulvihill JJ.

    Am J Med Genet A. 2005 Aug 30;137(2):213-6.PMID: 16082703 [PubMed - indexed for MEDLINE]Related articles

    33.

    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.

    Lee J, Hopcus-Niccum DJ, Mulvihill JJ, Li S.

    Cancer Genet Cytogenet. 2005 Jun;159(2):177-80.PMID: 15899394 [PubMed - indexed for MEDLINE]Related articles

    34.

    A variant t(8;10;21) in a patient with pathological features mimicking atypical chronic myeloid leukemia.

    Lee J, Kern WF, Cain JB, Mulvihill JJ, Li S.

    Cancer Genet Cytogenet. 2005 May;159(1):79-83.PMID: 15860363 [PubMed - indexed for MEDLINE]Related articles

    35.

    Oligogenic combinations associated with breast cancer risk in women under 53 years of age.

    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.

    Hum Genet. 2005 Feb;116(3):208-21. Epub 2004 Dec 21.PMID: 15611867 [PubMed - indexed for MEDLINE]Related articles

    36.

    Down syndrome with pure partial trisomy 21q22 due to a paternal insertion (4;21) uncovered by uncultured amniotic fluid interphase FISH.

    Lee J, Stanley JR, Vaz SA, Mulvihill JJ, Wilson P, Hopcus-Niccum D, Li S.

    Am J Med Genet A. 2005 Jan 15;132A(2):206-8.PMID: 15578618 [PubMed - indexed for MEDLINE]Related articles

    37.

    Dental x-rays and low birth weight.

    Boice JD Jr, Stovall M, Mulvihill JJ, Green DM.

    J Radiol Prot. 2004 Sep;24(3):321-3. No abstract available. PMID: 15511024 [PubMed - indexed for MEDLINE]Related articles

    38.

    Chromosome 2q terminal deletion: report of 6 new patients and review of phenotype-breakpoint correlations in 66 individuals.

    Casas KA, Mononen TK, Mikail CN, Hassed SJ, Li S, Mulvihill JJ, Lin HJ, Falk RE.

    Am J Med Genet A. 2004 Nov 1;130A(4):331-9.PMID: 15386475 [PubMed - indexed for MEDLINE]Related articles

    39.

    Chromosomal abnormalities among offspring of childhood-cancer survivors in Denmark: a population-based study.

    Winther JF, Boice JD Jr, Mulvihill JJ, Stovall M, Frederiksen K, Tawn EJ, Olsen JH.

    Am J Hum Genet. 2004 Jun;74(6):1282-5. Epub 2004 Apr 21.PMID: 15106125 [PubMed - indexed for MEDLINE]Related articlesFree article

    40.

    Leiomyosarcoma of the breast: a pathologic and comparative genomic hybridization study of two cases.

    Lee J, Li S, Torbenson M, Liu QZ, Lind S, Mulvihill JJ, Bane B, Wang J.

    Cancer Genet Cytogenet. 2004 Feb;149(1):53-7.PMID: 15104283 [PubMed - indexed for MEDLINE]Related articles

    41.

    A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome.

    Hassed SJ, Hopcus-Niccum D, Zhang L, Li S, Mulvihill JJ.

    Clin Genet. 2004 May;65(5):400-4.PMID: 15099348 [PubMed - indexed for MEDLINE]Related articles

    42.

    Double trisomy.

    Li S, Hassed S, Mulvihill JJ, Nair AK, Hopcus DJ.

    Am J Med Genet A. 2004 Jan 1;124A(1):96-8. No abstract available. Erratum in: Am J Med Genet A. 2005 Apr 1;134(1):115. PMID: 14679595 [PubMed - indexed for MEDLINE]Related articles

    43.

    Expanding metabolic screening of newborns: can the health care industry do better than public health?

    Mulvihill JJ, Blackett PR, Palmer SE.

    J Okla State Med Assoc. 2003 Oct;96(10):477-81.PMID: 14619602 [PubMed - indexed for MEDLINE]Related articles

    44.

    Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.

    Zhang L, Parkhurst JB, Kern WF, Scott KV, Niccum D, Mulvihill JJ, Li S.

    Chin Med J (Engl). 2003 Sep;116(9):1298-303.PMID: 14527352 [PubMed - indexed for MEDLINE]Related articlesFree article

    45.

    Genetic effects of radiotherapy for childhood cancer.

    Boice JD Jr, Tawn EJ, Winther JF, Donaldson SS, Green DM, Mertens AC, Mulvihill JJ, Olsen JH, Robison LL, Stovall M.

    Health Phys. 2003 Jul;85(1):65-80.PMID: 12852473 [PubMed - indexed for MEDLINE]Related articles

    46.

    Celebrating the structure of DNA: 50 years and beyond.

    Mulvihill JJ.

    J Okla State Med Assoc. 2003 Apr;96(4):184. No abstract available. PMID: 12733207 [PubMed - indexed for MEDLINE]Related articles

    47.

    Identification of t(15;17) and a segmental duplication of chromosome 11q23 in a patient with acute myeloblastic leukemia M2.

    Li S, Zhang L, Kern WF, Andrade D, Forsberg JE, Bates FR, Mulvihill JJ.

    Cancer Genet Cytogenet. 2002 Oct 15;138(2):149-52.PMID: 12505261 [PubMed - indexed for MEDLINE]Related articles

    48.

    Duplication 15q as the sole anomaly in an acute promyelocytic leukemia patient without t(15;17).

    Zhang L, Mulvihill JJ, Kern WF, McMinn J, Li S.

    Cancer Genet Cytogenet. 2002 Oct 1;138(1):17-21.PMID: 12419579 [PubMed - indexed for MEDLINE]Related articles

    49.

    [Cancer in siblings of children with cancer]

    Winther JF, Sankila R, Boice JD Jr, Tulinius H, Bautz A, Barlow L, Glattre E, Langmark F, Möller T, Mulvihill JJ, Olafsdottir GH, Ritvanen A, Olsen JH.

    Ugeskr Laeger. 2002 Jun 3;164(23):3073-9. Danish. PMID: 12082866 [PubMed - indexed for MEDLINE]Related articles

    50.

    Medium chain acyl coenzyme A dehydrogenase (MCAD) deficiency: the case for screening all newborns.

    Alluri VN, Mulvihill JJ.

    J Okla State Med Assoc. 2002 May;95(5):326-8.PMID: 12043106 [PubMed - indexed for MEDLINE]Related articles

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