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Journal Abstract Search

281 related items for PubMed ID: 18449910

  • 41.
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  • 42. Expanded genome scan in extended families with age-related macular degeneration.
    Barral S, Francis PJ, Schultz DW, Schain MB, Haynes C, Majewski J, Ott J, Acott T, Weleber RG, Klein ML.
    Invest Ophthalmol Vis Sci; 2006 Dec; 47(12):5453-9. PubMed ID: 17122136
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  • 44. A discordant sib-pair linkage analysis of age-related macular degeneration.
    Santangelo SL, Yen CH, Haddad S, Fagerness J, Huang C, Seddon JM.
    Ophthalmic Genet; 2005 Jun; 26(2):61-7. PubMed ID: 16020308
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  • 46. Genome-wide linkage analysis replicates susceptibility locus for fasting plasma triglycerides: NHLBI Family Heart Study.
    Arnett DK, Miller MB, Coon H, Ellison RC, North KE, Province M, Leppert M, Eckfeldt JH.
    Hum Genet; 2004 Nov; 115(6):468-74. PubMed ID: 15375693
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  • 47. Significant linkage on chromosome 10p in families with bulimia nervosa.
    Bulik CM, Devlin B, Bacanu SA, Thornton L, Klump KL, Fichter MM, Halmi KA, Kaplan AS, Strober M, Woodside DB, Bergen AW, Ganjei JK, Crow S, Mitchell J, Rotondo A, Mauri M, Cassano G, Keel P, Berrettini WH, Kaye WH.
    Am J Hum Genet; 2003 Jan; 72(1):200-7. PubMed ID: 12476400
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  • 48. Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.
    Suarez BK, Duan J, Sanders AR, Hinrichs AL, Jin CH, Hou C, Buccola NG, Hale N, Weilbaecher AN, Nertney DA, Olincy A, Green S, Schaffer AW, Smith CJ, Hannah DE, Rice JP, Cox NJ, Martinez M, Mowry BJ, Amin F, Silverman JM, Black DW, Byerley WF, Crowe RR, Freedman R, Cloninger CR, Levinson DF, Gejman PV.
    Am J Hum Genet; 2006 Feb; 78(2):315-33. PubMed ID: 16400611
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  • 49. Strong evidence for a novel schizophrenia risk locus on chromosome 1p31.1 in homogeneous pedigrees from Tamil Nadu, India.
    Holliday EG, Nyholt DR, Tirupati S, John S, Ramachandran P, Ramamurti M, Ramadoss AJ, Jeyagurunathan A, Kottiswaran S, Smith HJ, Filippich C, Nertney DA, Nancarrow DJ, Hayward NK, Watkins WS, Jorde LB, Thara R, Mowry BJ.
    Am J Psychiatry; 2009 Feb; 166(2):206-15. PubMed ID: 18829870
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  • 50. Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib-pair linkage analysis.
    Schwab SG, Albus M, Hallmayer J, Hönig S, Borrmann M, Lichtermann D, Ebstein RP, Ackenheil M, Lerer B, Risch N.
    Nat Genet; 1995 Nov; 11(3):325-7. PubMed ID: 7581458
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  • 51. Genome-wide scan for type 1 diabetic nephropathy in the Finnish population reveals suggestive linkage to a single locus on chromosome 3q.
    Osterholm AM, He B, Pitkaniemi J, Albinsson L, Berg T, Sarti C, Tuomilehto J, Tryggvason K.
    Kidney Int; 2007 Jan; 71(2):140-5. PubMed ID: 17021601
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  • 52. A genome-wide significant linkage for severe depression on chromosome 3: the depression network study.
    Breen G, Webb BT, Butler AW, van den Oord EJ, Tozzi F, Craddock N, Gill M, Korszun A, Maier W, Middleton L, Mors O, Owen MJ, Cohen-Woods S, Perry J, Galwey NW, Upmanyu R, Craig I, Lewis CM, Ng M, Brewster S, Preisig M, Rietschel M, Jones L, Knight J, Rice J, Muglia P, Farmer AE, McGuffin P.
    Am J Psychiatry; 2011 Aug; 168(8):840-7. PubMed ID: 21572164
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  • 57. 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; 12(4):376-84. PubMed ID: 17179998
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  • 58. Linkage of familial schizophrenia to chromosome 13q32.
    Brzustowicz LM, Honer WG, Chow EW, Little D, Hogan J, Hodgkinson K, Bassett AS.
    Am J Hum Genet; 1999 Oct; 65(4):1096-103. PubMed ID: 10486329
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  • 59.
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  • 60. 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]

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