These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

249 related items for PubMed ID: 18829870

  • 41. Genomewide linkage scan for myopia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 22q12.
    Stambolian D, Ibay G, Reider L, Dana D, Moy C, Schlifka M, Holmes T, Ciner E, Bailey-Wilson JE.
    Am J Hum Genet; 2004 Sep; 75(3):448-59. PubMed ID: 15273935
    [Abstract] [Full Text] [Related]

  • 42. Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha.
    Carroll LS, Williams NM, Moskvina V, Russell E, Norton N, Williams HJ, Peirce T, Georgieva L, Dwyer S, Grozeva D, Greene E, Farmer A, McGuffin P, Morris DW, Corvin A, Gill M, Rujescu D, Sham P, Holmans P, Jones I, Kirov G, Craddock N, O'Donovan MC, Owen MJ.
    Mol Psychiatry; 2010 Nov; 15(11):1101-11. PubMed ID: 19786960
    [Abstract] [Full Text] [Related]

  • 43. Genome-wide linkage scan, fine mapping, and haplotype analysis in a large, inbred, Arab Israeli pedigree suggest a schizophrenia susceptibility locus on chromosome 20p13.
    Teltsh O, Kanyas K, Karni O, Levi A, Korner M, Ben-Asher E, Lancet D, Hamdan A, Lerer B, Kohn Y.
    Am J Med Genet B Neuropsychiatr Genet; 2008 Mar 05; 147B(2):209-15. PubMed ID: 17823922
    [Abstract] [Full Text] [Related]

  • 44. Allelic and locus heterogeneity in autosomal recessive gelatinous drop-like corneal dystrophy.
    Ren Z, Lin PY, Klintworth GK, Iwata F, Munier FL, Schorderet DF, El Matri L, Theendakara V, Basti S, Reddy M, Hejtmancik JF.
    Hum Genet; 2002 Jun 05; 110(6):568-77. PubMed ID: 12107443
    [Abstract] [Full Text] [Related]

  • 45. Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22.
    Brzustowicz LM, Simone J, Mohseni P, Hayter JE, Hodgkinson KA, Chow EW, Bassett AS.
    Am J Hum Genet; 2004 May 05; 74(5):1057-63. PubMed ID: 15065015
    [Abstract] [Full Text] [Related]

  • 46. Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1.
    Abecasis GR, Burt RA, Hall D, Bochum S, Doheny KF, Lundy SL, Torrington M, Roos JL, Gogos JA, Karayiorgou M.
    Am J Hum Genet; 2004 Mar 05; 74(3):403-17. PubMed ID: 14750073
    [Abstract] [Full Text] [Related]

  • 47.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 48.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 49.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 50. Linkage analysis of schizophrenia to chromosome 15.
    Gejman PV, Sanders AR, Badner JA, Cao Q, Zhang J.
    Am J Med Genet; 2001 Dec 08; 105(8):789-93. PubMed ID: 11803532
    [Abstract] [Full Text] [Related]

  • 51. Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22.
    Brzustowicz LM, Hodgkinson KA, Chow EW, Honer WG, Bassett AS.
    Science; 2000 Apr 28; 288(5466):678-82. PubMed ID: 10784452
    [Abstract] [Full Text] [Related]

  • 52. Pilot study for family-based association analysis of schizophrenia in a Korean population: Analysis for candidate genes positionally on chromosome 18q21.
    Cho MJ, Lee BD, Kim C.
    Asia Pac Psychiatry; 2015 Sep 28; 7(3):268-75. PubMed ID: 25504777
    [Abstract] [Full Text] [Related]

  • 53. Tumor necrosis factor promoter haplotype associated with schizophrenia reveals a linked locus on 1q44.
    Saviouk V, Chow EW, Bassett AS, Brzustowicz LM.
    Mol Psychiatry; 2005 Apr 28; 10(4):375-83. PubMed ID: 15340354
    [Abstract] [Full Text] [Related]

  • 54.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 55. Genomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22.
    Fallin MD, Lasseter VK, Wolyniec PS, McGrath JA, Nestadt G, Valle D, Liang KY, Pulver AE.
    Am J Hum Genet; 2003 Sep 28; 73(3):601-11. PubMed ID: 12929083
    [Abstract] [Full Text] [Related]

  • 56.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 57. Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele.
    Radhakrishna U, Nath SK, McElreavey K, Ratnamala U, Sun C, Maiti AK, Gagnebin M, Béna F, Newkirk HL, Sharp AJ, Everman DB, Murray JC, Schwartz CE, Antonarakis SE, Butler MG.
    J Med Genet; 2012 Apr 28; 49(4):270-6. PubMed ID: 22499347
    [Abstract] [Full Text] [Related]

  • 58. Suggestive evidence for linkage of schizophrenia to markers at chromosome 15q13-14 in Taiwanese families.
    Liu CM, Hwu HG, Lin MW, Ou-Yang WC, Lee SF, Fann CS, Wong SH, Hsieh SH.
    Am J Med Genet; 2001 Dec 08; 105(8):658-61. PubMed ID: 11803511
    [Abstract] [Full Text] [Related]

  • 59. Linkage evidence of schizophrenia to loci near neuregulin 1 gene on chromosome 8p21 in Taiwanese families.
    Liu CM, Hwu HG, Fann CS, Lin CY, Liu YL, Ou-Yang WC, Lee SF.
    Am J Med Genet B Neuropsychiatr Genet; 2005 Apr 05; 134B(1):79-83. PubMed ID: 15704228
    [Abstract] [Full Text] [Related]

  • 60. Novel linkage to chromosome 20p using latent classes of psychotic illness in 270 Irish high-density families.
    Fanous AH, Neale MC, Webb BT, Straub RE, O'Neill FA, Walsh D, Riley BP, Kendler KS.
    Biol Psychiatry; 2008 Jul 15; 64(2):121-7. PubMed ID: 18255048
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 13.