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Journal Abstract Search

284 related items for PubMed ID: 16923799

  • 1. Evidence for a colorectal cancer susceptibility locus on chromosome 3q21-q24 from a high-density SNP genome-wide linkage scan.
    Kemp Z, Carvajal-Carmona L, Spain S, Barclay E, Gorman M, Martin L, Jaeger E, Brooks N, Bishop DT, Thomas H, Tomlinson I, Papaemmanuil E, Webb E, Sellick GS, Wood W, Evans G, Lucassen A, Maher ER, Houlston RS, ColoRectal tumour Gene Identification (CoRGI) Study Consortium.
    Hum Mol Genet; 2006 Oct 01; 15(19):2903-10. PubMed ID: 16923799
    [Abstract] [Full Text] [Related]

  • 2. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
    Ma DQ, Cuccaro ML, Jaworski JM, Haynes CS, Stephan DA, Parod J, Abramson RK, Wright HH, Gilbert JR, Haines JL, Pericak-Vance MA.
    Mol Psychiatry; 2007 Apr 01; 12(4):376-84. PubMed ID: 17179998
    [Abstract] [Full Text] [Related]

  • 3. Objective prioritization of positional candidate genes at a quantitative trait locus for pre-eclampsia on 2q22.
    Moses EK, Fitzpatrick E, Freed KA, Dyer TD, Forrest S, Elliott K, Johnson MP, Blangero J, Brennecke SP.
    Mol Hum Reprod; 2006 Aug 01; 12(8):505-12. PubMed ID: 16809377
    [Abstract] [Full Text] [Related]

  • 4. Genome-wide linkage analysis for celiac disease in North American families.
    Neuhausen SL, Feolo M, Camp NJ, Farnham J, Book L, Zone JJ.
    Am J Med Genet; 2002 Jul 22; 111(1):1-9. PubMed ID: 12124726
    [Abstract] [Full Text] [Related]

  • 5. Genome-wide linkage analysis for aggressive prostate cancer in Utah high-risk pedigrees.
    Christensen GB, Camp NJ, Farnham JM, Cannon-Albright LA.
    Prostate; 2007 May 01; 67(6):605-13. PubMed ID: 17299800
    [Abstract] [Full Text] [Related]

  • 6. Genome-wide scan for myopia in the Old Order Amish.
    Stambolian D, Ciner EB, Reider LC, Moy C, Dana D, Owens R, Schlifka M, Holmes T, Ibay G, Bailey-Wilson JE.
    Am J Ophthalmol; 2005 Sep 01; 140(3):469-76. PubMed ID: 16084785
    [Abstract] [Full Text] [Related]

  • 7. Genome-wide linkage analysis of ADHD using high-density SNP arrays: novel loci at 5q13.1 and 14q12.
    Romanos M, Freitag C, Jacob C, Craig DW, Dempfle A, Nguyen TT, Halperin R, Walitza S, Renner TJ, Seitz C, Romanos J, Palmason H, Reif A, Heine M, Windemuth-Kieselbach C, Vogler C, Sigmund J, Warnke A, Schäfer H, Meyer J, Stephan DA, Lesch KP.
    Mol Psychiatry; 2008 May 01; 13(5):522-30. PubMed ID: 18301393
    [Abstract] [Full Text] [Related]

  • 8. Localization of a susceptibility locus for hepatocellular carcinoma to chromosome 4q in a hepatitis B hyperendemic area.
    Shih WL, Yu MW, Chen PJ, Yeh SH, Lo MT, Chang HC, Liaw YF, Lin SM, Liu CJ, Lee SD, Lin CL, Hsiao CK, Yang SY, Chen CJ.
    Oncogene; 2006 May 25; 25(22):3219-24. PubMed ID: 16407824
    [Abstract] [Full Text] [Related]

  • 9. Association and linkage of allelic variants of the dopamine transporter gene in ADHD.
    Friedel S, Saar K, Sauer S, Dempfle A, Walitza S, Renner T, Romanos M, Freitag C, Seitz C, Palmason H, Scherag A, Windemuth-Kieselbach C, Schimmelmann BG, Wewetzer C, Meyer J, Warnke A, Lesch KP, Reinhardt R, Herpertz-Dahlmann B, Linder M, Hinney A, Remschmidt H, Schäfer H, Konrad K, Hübner N, Hebebrand J.
    Mol Psychiatry; 2007 Oct 25; 12(10):923-33. PubMed ID: 17579611
    [Abstract] [Full Text] [Related]

  • 10. Identification of a major locus for Paget's disease on chromosome 10p13 in families of British descent.
    Lucas GJ, Riches PL, Hocking LJ, Cundy T, Nicholson GC, Walsh JP, Ralston SH.
    J Bone Miner Res; 2008 Jan 25; 23(1):58-63. PubMed ID: 17907922
    [Abstract] [Full Text] [Related]

  • 11. Deciphering the genetics of hereditary non-syndromic colorectal cancer.
    Papaemmanuil E, Carvajal-Carmona L, Sellick GS, Kemp Z, Webb E, Spain S, Sullivan K, Barclay E, Lubbe S, Jaeger E, Vijayakrishnan J, Broderick P, Gorman M, Martin L, Lucassen A, Bishop DT, Evans DG, Maher ER, Steinke V, Rahner N, Schackert HK, Goecke TO, Holinski-Feder E, Propping P, Van Wezel T, Wijnen J, Cazier JB, Thomas H, Houlston RS, Tomlinson I, CORGI Consortium.
    Eur J Hum Genet; 2008 Dec 25; 16(12):1477-86. PubMed ID: 18628789
    [Abstract] [Full Text] [Related]

  • 12. A genome-wide scan maps a novel high myopia locus to 5p15.
    Lam CY, Tam PO, Fan DS, Fan BJ, Wang DY, Lee CW, Pang CP, Lam DS.
    Invest Ophthalmol Vis Sci; 2008 Sep 25; 49(9):3768-78. PubMed ID: 18421076
    [Abstract] [Full Text] [Related]

  • 13. A genome wide linkage analysis in Swedish families with hereditary non-familial adenomatous polyposis/non-hereditary non-polyposis colorectal cancer.
    Djureinovic T, Skoglund J, Vandrovcova J, Zhou XL, Kalushkova A, Iselius L, Lindblom A.
    Gut; 2006 Mar 25; 55(3):362-6. PubMed ID: 16150854
    [Abstract] [Full Text] [Related]

  • 14. Results of a genome-wide linkage analysis in prostate cancer families ascertained through the ACTANE consortium.
    Edwards S, Meitz J, Eles R, Evans C, Easton D, Hopper J, Giles G, Foulkes WD, Narod S, Simard J, Badzioch M, Mahle L, International ACTANE Consortium.
    Prostate; 2003 Dec 01; 57(4):270-9. PubMed ID: 14601023
    [Abstract] [Full Text] [Related]

  • 15. Comprehensive genetic analysis of seven large families with mismatch repair proficient colorectal cancer.
    Middeldorp A, Jagmohan-Changur SC, van der Klift HM, van Puijenbroek M, Houwing-Duistermaat JJ, Webb E, Houlston R, Tops C, Vasen HF, Devilee P, Morreau H, van Wezel T, Wijnen J.
    Genes Chromosomes Cancer; 2010 Jun 01; 49(6):539-48. PubMed ID: 20222047
    [Abstract] [Full Text] [Related]

  • 16. A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susceptibility locus on chromosome 15q25-26.
    McAuley EZ, Blair IP, Liu Z, Fullerton JM, Scimone A, Van Herten M, Evans MR, Kirkby KC, Donald JA, Mitchell PB, Schofield PR.
    Mol Psychiatry; 2009 May 01; 14(5):492-500. PubMed ID: 18227837
    [Abstract] [Full Text] [Related]

  • 17. A chromosome 14 risk locus for simple phobia: results from a genomewide linkage scan.
    Gelernter J, Page GP, Bonvicini K, Woods SW, Pauls DL, Kruger S.
    Mol Psychiatry; 2003 Jan 01; 8(1):71-82. PubMed ID: 12556910
    [Abstract] [Full Text] [Related]

  • 18. A study comparing precision of the maximum multipoint heterogeneity LOD statistic to three model-free multipoint linkage methods.
    Finch SJ, Chen CH, Gordon D, Mendell NR.
    Genet Epidemiol; 2001 Dec 01; 21(4):315-25. PubMed ID: 11754467
    [Abstract] [Full Text] [Related]

  • 19. A procedure for the detection of linkage with high density SNP arrays in a large pedigree with colorectal cancer.
    Middeldorp A, Jagmohan-Changur S, Helmer Q, van der Klift HM, Tops CM, Vasen HF, Devilee P, Morreau H, Houwing-Duistermaat JJ, Wijnen JT, van Wezel T.
    BMC Cancer; 2007 Jan 12; 7():6. PubMed ID: 17222328
    [Abstract] [Full Text] [Related]

  • 20. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.
    Winkelmann J, Lichtner P, Pütz B, Trenkwalder C, Hauk S, Meitinger T, Strom T, Muller-Myhsok B.
    Mov Disord; 2006 Jan 12; 21(1):28-33. PubMed ID: 16124010
    [Abstract] [Full Text] [Related]

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