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Journal Abstract Search

202 related items for PubMed ID: 19118813

  • 1. Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia.
    Chen PL, Avramopoulos D, Lasseter VK, McGrath JA, Fallin MD, Liang KY, Nestadt G, Feng N, Steel G, Cutting AS, Wolyniec P, Pulver AE, Valle D.
    Am J Hum Genet; 2009 Jan; 84(1):21-34. PubMed ID: 19118813
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  • 2. Common genetic variation in Neuregulin 3 (NRG3) influences risk for schizophrenia and impacts NRG3 expression in human brain.
    Kao WT, Wang Y, Kleinman JE, Lipska BK, Hyde TM, Weinberger DR, Law AJ.
    Proc Natl Acad Sci U S A; 2010 Aug 31; 107(35):15619-24. PubMed ID: 20713722
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  • 3. Identification and functional studies of regulatory variants responsible for the association of NRG3 with a delusion phenotype in schizophrenia.
    Zeledón M, Eckart N, Taub M, Vernon H, Szymanksi M, Wang R, Chen PL, Nestadt G, McGrath JA, Sawa A, Pulver AE, Avramopoulos D, Valle D.
    Mol Neuropsychiatry; 2015 May 31; 1(1):36-46. PubMed ID: 26528484
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  • 4. Neuregulin 3 does not confer risk for schizophrenia and smooth pursuit eye movement abnormality in a Korean population.
    Pasaje CF, Bae JS, Park BL, Cheong HS, Kim JH, Park TJ, Lee JS, Kim Y, Park CS, Kim BJ, Cha B, Kim JW, Choi WH, Shin TM, Choi IG, Hwang J, Shin HD, Woo SI.
    Genes Brain Behav; 2011 Nov 31; 10(8):828-33. PubMed ID: 21762460
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  • 5. Neuregulin 3 (NRG3) as a susceptibility gene in a schizophrenia subtype with florid delusions and relatively spared cognition.
    Morar B, Dragović M, Waters FA, Chandler D, Kalaydjieva L, Jablensky A.
    Mol Psychiatry; 2011 Aug 31; 16(8):860-6. PubMed ID: 20548296
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  • 7. Neuregulin 3 genetic variations and susceptibility to schizophrenia in a Chinese population.
    Wang YC, Chen JY, Chen ML, Chen CH, Lai IC, Chen TT, Hong CJ, Tsai SJ, Liou YJ.
    Biol Psychiatry; 2008 Dec 15; 64(12):1093-6. PubMed ID: 18708184
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  • 10. Genome scan of Han Chinese schizophrenia families from Taiwan: confirmation of linkage to 10q22.3.
    Faraone SV, Hwu HG, Liu CM, Chen WJ, Tsuang MM, Liu SK, Shieh MH, Hwang TJ, Ou-Yang WC, Chen CY, Chen CC, Lin JJ, Chou FH, Chueh CM, Liu WM, Hall MH, Su J, Van Eerdewegh P, Tsuang MT.
    Am J Psychiatry; 2006 Oct 15; 163(10):1760-6. PubMed ID: 17012687
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  • 11. Temporal, Diagnostic, and Tissue-Specific Regulation of NRG3 Isoform Expression in Human Brain Development and Affective Disorders.
    Paterson C, Wang Y, Hyde TM, Weinberger DR, Kleinman JE, Law AJ.
    Am J Psychiatry; 2017 Mar 01; 174(3):256-265. PubMed ID: 27771971
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  • 12. Consistently replicating locus linked to migraine on 10q22-q23.
    Anttila V, Nyholt DR, Kallela M, Artto V, Vepsäläinen S, Jakkula E, Wennerström A, Tikka-Kleemola P, Kaunisto MA, Hämäläinen E, Widén E, Terwilliger J, Merikangas K, Montgomery GW, Martin NG, Daly M, Kaprio J, Peltonen L, Färkkilä M, Wessman M, Palotie A.
    Am J Hum Genet; 2008 May 01; 82(5):1051-63. PubMed ID: 18423523
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  • 16. Susceptibility genes for age-related maculopathy on chromosome 10q26.
    Jakobsdottir J, Conley YP, Weeks DE, Mah TS, Ferrell RE, Gorin MB.
    Am J Hum Genet; 2005 Sep 01; 77(3):389-407. PubMed ID: 16080115
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  • 17. Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis.
    Holliday EG, McLean DE, Nyholt DR, Mowry BJ.
    Arch Gen Psychiatry; 2009 Oct 01; 66(10):1058-67. PubMed ID: 19805696
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  • 19. The genetics of symptom-based phenotypes: toward a molecular classification of schizophrenia.
    DeRosse P, Lencz T, Burdick KE, Siris SG, Kane JM, Malhotra AK.
    Schizophr Bull; 2008 Nov 01; 34(6):1047-53. PubMed ID: 18628273
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