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Journal Abstract Search

375 related items for PubMed ID: 11641285

  • 41. Investigation of susceptibility loci identified in the UK rheumatoid arthritis whole-genome scan in a further series of 217 UK affected sibling pairs.
    Eyre S, Barton A, Shephard N, Hinks A, Brintnell W, MacKay K, Silman A, Ollier W, Wordsworth P, John S, Worthington J.
    Arthritis Rheum; 2004 Mar; 50(3):729-35. PubMed ID: 15022312
    [Abstract] [Full Text] [Related]

  • 42. Genome-wide scans reveal quantitative trait Loci on 8p and 13q related to insulin action and glucose metabolism: the San Antonio Family Heart Study.
    Cai G, Cole SA, Freeland-Graves JH, MacCluer JW, Blangero J, Comuzzie AG.
    Diabetes; 2004 May; 53(5):1369-74. PubMed ID: 15111508
    [Abstract] [Full Text] [Related]

  • 43. Evidence for a putative bipolar disorder locus on 2p13-16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21-24, 13q32, 14q21 and 17q11-12.
    Liu J, Juo SH, Dewan A, Grunn A, Tong X, Brito M, Park N, Loth JE, Kanyas K, Lerer B, Endicott J, Penchaszadeh G, Knowles JA, Ott J, Gilliam TC, Baron M.
    Mol Psychiatry; 2003 Mar; 8(3):333-42. PubMed ID: 12660806
    [Abstract] [Full Text] [Related]

  • 44. Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families.
    Wong FK, Hagberg C, Karsten A, Larson O, Gustavsson M, Huggare J, Larsson C, Teh BT, Linder-Aronson S.
    Cleft Palate Craniofac J; 2000 Jul; 37(4):357-62. PubMed ID: 10912714
    [Abstract] [Full Text] [Related]

  • 45. A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder.
    DeLisi LE, Shaw SH, Crow TJ, Shields G, Smith AB, Larach VW, Wellman N, Loftus J, Nanthakumar B, Razi K, Stewart J, Comazzi M, Vita A, Heffner T, Sherrington R.
    Am J Psychiatry; 2002 May; 159(5):803-12. PubMed ID: 11986135
    [Abstract] [Full Text] [Related]

  • 46. Genetic analysis of common factors underlying cardiovascular disease-related traits.
    Liu XQ, Hanley AJ, Paterson AD.
    BMC Genet; 2003 Dec 31; 4 Suppl 1(Suppl 1):S56. PubMed ID: 14975124
    [Abstract] [Full Text] [Related]

  • 47. A genome-wide linkage study of bipolar disorder and co-morbid migraine: replication of migraine linkage on chromosome 4q24, and suggestion of an overlapping susceptibility region for both disorders on chromosome 20p11.
    Oedegaard KJ, Greenwood TA, Lunde A, Fasmer OB, Akiskal HS, Kelsoe JR, NIMH Genetics Initiative Bipolar Disorder Consortium.
    J Affect Disord; 2010 Apr 31; 122(1-2):14-26. PubMed ID: 19819557
    [Abstract] [Full Text] [Related]

  • 48. A genomewide scan identifies two novel loci involved in specific language impairment.
    SLI Consortium.
    Am J Hum Genet; 2002 Feb 31; 70(2):384-98. PubMed ID: 11791209
    [Abstract] [Full Text] [Related]

  • 49. Genome-wide scan for hypertension in Sydney Sibships: the GENIHUSS study.
    Benjafield AV, Wang WY, Speirs HJ, Morris BJ.
    Am J Hypertens; 2005 Jun 31; 18(6):828-32. PubMed ID: 15925743
    [Abstract] [Full Text] [Related]

  • 50. Gene by smoking interaction in hypertension: identification of a major quantitative trait locus on chromosome 15q for systolic blood pressure in Mexican-Americans.
    Montasser ME, Shimmin LC, Hanis CL, Boerwinkle E, Hixson JE.
    J Hypertens; 2009 Mar 31; 27(3):491-501. PubMed ID: 19330903
    [Abstract] [Full Text] [Related]

  • 51. Genome-wide scan of additional Jewish families confirms linkage of a myopia susceptibility locus to chromosome 22q12.
    Stambolian D, Ibay G, Reider L, Dana D, Moy C, Schlifka M, Holmes TN, Ciner E, Bailey-Wilson JE.
    Mol Vis; 2006 Dec 04; 12():1499-505. PubMed ID: 17167407
    [Abstract] [Full Text] [Related]

  • 52. A chromosome 11q quantitative-trait locus influences change of blood-pressure measurements over time in Mexican Americans of the San Antonio Family Heart Study.
    Rutherford S, Cai G, Lopez-Alvarenga JC, Kent JW, Voruganti VS, Proffitt JM, Curran JE, Johnson MP, Dyer TD, Jowett JB, Bastarrachea RA, Atwood LD, Goring HH, Maccluer JW, Moses EK, Blangero J, Comuzzie AG, Cole SA.
    Am J Hum Genet; 2007 Oct 04; 81(4):744-55. PubMed ID: 17846999
    [Abstract] [Full Text] [Related]

  • 53. Genome scan for familial abdominal aortic aneurysm using sex and family history as covariates suggests genetic heterogeneity and identifies linkage to chromosome 19q13.
    Shibamura H, Olson JM, van Vlijmen-Van Keulen C, Buxbaum SG, Dudek DM, Tromp G, Ogata T, Skunca M, Sakalihasan N, Pals G, Limet R, MacKean GL, Defawe O, Verloes A, Arthur C, Lossing AG, Burnett M, Sueda T, Kuivaniemi H.
    Circulation; 2004 May 04; 109(17):2103-8. PubMed ID: 15096456
    [Abstract] [Full Text] [Related]

  • 54. Genome-wide linkage analysis of hemodynamic parameters under mental and physical stress in extended Omani Arab pedigrees: the Oman Family Study.
    Hassan MO, Jaju D, Voruganti VS, Bayoumi RA, Albarwani S, Al-Yahyaee S, Aslani A, Snieder H, Lopez-Alvarenga JC, Al-Anqoudi ZM, Alizadeh BZ, Comuzzie AG.
    Twin Res Hum Genet; 2011 Jun 04; 14(3):257-67. PubMed ID: 21623656
    [Abstract] [Full Text] [Related]

  • 55. Salt susceptibility maps to chromosomes 1 and 17 with sex specificity in the Sabra rat model of hypertension.
    Yagil C, Sapojnikov M, Kreutz R, Katni G, Lindpaintner K, Ganten D, Yagil Y.
    Hypertension; 1998 Jan 04; 31(1):119-24. PubMed ID: 9449402
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  • 57. Genome-wide scan in 124 Indonesian sib-pair families with schizophrenia reveals genome-wide significant linkage to a locus on chromosome 3p26-21.
    IrmansyahDepartment of Psychiatry, Faculty of Medicine, University of Indonesia, Jakarta, Indonesia., Schwab SG, Heriani, Handoko HY, Kusumawardhani A, Widyawati I, Amir N, Nasrun MW, Holmans P, Knapp M, Wildenauer DB.
    Am J Med Genet B Neuropsychiatr Genet; 2008 Oct 05; 147B(7):1245-52. PubMed ID: 18449910
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  • 59. Mapping loci influencing blood pressure in the Framingham pedigrees using model-free LOD score analysis of a quantitative trait.
    Knight J, North BV, Sham PC, Curtis D.
    BMC Genet; 2003 Dec 31; 4 Suppl 1(Suppl 1):S74. PubMed ID: 14975142
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