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Journal Abstract Search

256 related items for PubMed ID: 11126394

  • 41. A genome wide scan for early onset primary hypertension in Scandinavians.
    von Wowern F, Bengtsson K, Lindgren CM, Orho-Melander M, Fyhrquist F, Lindblad U, Råstam L, Forsblom C, Kanninen T, Almgren P, Burri P, Katzman P, Groop L, Hulthén UL, Melander O.
    Hum Mol Genet; 2003 Aug 15; 12(16):2077-81. PubMed ID: 12913078
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  • 42. Genome wide scan in a Flemish inflammatory bowel disease population: support for the IBD4 locus, population heterogeneity, and epistasis.
    Vermeire S, Rutgeerts P, Van Steen K, Joossens S, Claessens G, Pierik M, Peeters M, Vlietinck R.
    Gut; 2004 Jul 15; 53(7):980-6. PubMed ID: 15194648
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  • 45. 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
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  • 47. A genomewide linkage study of age at onset in schizophrenia.
    Cardno AG, Holmans PA, Rees MI, Jones LA, McCarthy GM, Hamshere ML, Williams NM, Norton N, Williams HJ, Fenton I, Murphy KC, Sanders RD, Gray MY, O'Donovan MC, McGuffin P, Owen MJ.
    Am J Med Genet; 2001 Jul 08; 105(5):439-45. PubMed ID: 11449396
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  • 48. The importance of modelling heterogeneity in complex disease: application to NIMH Schizophrenia Genetics Initiative data.
    Holliday E, Mowry B, Chant D, Nyholt D.
    Hum Genet; 2005 Jul 08; 117(2-3):160-7. PubMed ID: 15843988
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  • 49. Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease.
    Lee JH, Cheng R, Santana V, Williamson J, Lantigua R, Medrano M, Arriaga A, Stern Y, Tycko B, Rogaeva E, Wakutani Y, Kawarai T, St George-Hyslop P, Mayeux R.
    Arch Neurol; 2006 Nov 08; 63(11):1591-8. PubMed ID: 17101828
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  • 50. Genetic linkage mapping for a susceptibility locus to bipolar illness: chromosomes 2, 3, 4, 7, 9, 10p, 11p, 22, and Xpter.
    Detera-Wadleigh SD, Hsieh WT, Berrettini WH, Goldin LR, Rollins DY, Muniec D, Grewal R, Guroff JJ, Turner G, Coffman D.
    Am J Med Genet; 1994 Sep 15; 54(3):206-18. PubMed ID: 7810578
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  • 54. A genome screen of 13 bipolar affective disorder pedigrees provides evidence for susceptibility loci on chromosome 3 as well as chromosomes 9, 13 and 19.
    Badenhop RF, Moses MJ, Scimone A, Mitchell PB, Ewen-White KR, Rosso A, Donald JA, Adams LJ, Schofield PR.
    Mol Psychiatry; 2002 Sep 15; 7(6):594-603. PubMed ID: 12140782
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  • 55. A genome screen of 13 bipolar affective disorder pedigrees provides evidence for susceptibility loci on chromosome 3 as well as chromosomes 9, 13 and 19.
    Badenhop RF, Moses MJ, Scimone A, Mitchell PB, Ewen-White KR, Rosso A, Donald JA, Adams LJ, Schofield PR.
    Mol Psychiatry; 2002 Sep 15; 7(8):851-9. PubMed ID: 12232778
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  • 56. Replication and extension studies of inflammatory bowel disease susceptibility regions confirm linkage to chromosome 6p (IBD3).
    Dechairo B, Dimon C, van Heel D, Mackay I, Edwards M, Scambler P, Jewell D, Cardon L, Lench N, Carey A.
    Eur J Hum Genet; 2001 Aug 15; 9(8):627-33. PubMed ID: 11528509
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  • 57. Sex stratification of an inflammatory bowel disease genome search shows male-specific linkage to the HLA region of chromosome 6.
    Fisher SA, Hampe J, Macpherson AJ, Forbes A, Lennard-Jones JE, Schreiber S, Curran ME, Mathew CG, Lewis CM.
    Eur J Hum Genet; 2002 Apr 15; 10(4):259-65. PubMed ID: 12032734
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  • 58. Genome-wide linkage analysis assessing parent-of-origin effects in the inheritance of type 2 diabetes and BMI in Pima Indians.
    Lindsay RS, Kobes S, Knowler WC, Bennett PH, Hanson RL.
    Diabetes; 2001 Dec 15; 50(12):2850-7. PubMed ID: 11723070
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  • 59. Evidence for the multigenic inheritance of schizophrenia.
    Freedman R, Leonard S, Olincy A, Kaufmann CA, Malaspina D, Cloninger CR, Svrakic D, Faraone SV, Tsuang MT.
    Am J Med Genet; 2001 Dec 08; 105(8):794-800. PubMed ID: 11803533
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  • 60. Genome screen to detect linkage to intracranial aneurysm susceptibility genes: the Familial Intracranial Aneurysm (FIA) study.
    Foroud T, Sauerbeck L, Brown R, Anderson C, Woo D, Kleindorfer D, Flaherty ML, Deka R, Hornung R, Meissner I, Bailey-Wilson JE, Rouleau G, Connolly ES, Lai D, Koller DL, Huston J, Broderick JP, FIA Study Investigators.
    Stroke; 2008 May 08; 39(5):1434-40. PubMed ID: 18323491
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