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4. Significant correlation in linkage signals from genome-wide scans of schizophrenia and schizotypy. Fanous AH, Neale MC, Gardner CO, Webb BT, Straub RE, O'Neill FA, Walsh D, Riley BP, Kendler KS. Mol Psychiatry; 2007 Oct; 12(10):958-65. PubMed ID: 17440434 [Abstract] [Full Text] [Related]
5. 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; 66(10):1058-67. PubMed ID: 19805696 [Abstract] [Full Text] [Related]
6. Suggestive linkage to chromosomal regions 13q31 and 22q12 in families with psychotic bipolar disorder. Potash JB, Zandi PP, Willour VL, Lan TH, Huo Y, Avramopoulos D, Shugart YY, MacKinnon DF, Simpson SG, McMahon FJ, DePaulo JR, McInnis MG. Am J Psychiatry; 2003 Apr; 160(4):680-6. PubMed ID: 12668356 [Abstract] [Full Text] [Related]
9. A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder. DeLisi LE, Shaw SH, Crow TJ, Shields G, Smith AB, Larach VW, Wellman N, Loftus J, Nanthakumar B, Razi K, Stewart J, Comazzi M, Vita A, Heffner T, Sherrington R. Am J Psychiatry; 2002 May; 159(5):803-12. PubMed ID: 11986135 [Abstract] [Full Text] [Related]
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14. Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia. Hamshere ML, Holmans PA, McCarthy GM, Jones LA, Murphy KC, Sanders RD, Gray MY, Zammit S, Williams NM, Norton N, Williams HJ, McGuffin P, O'Donovan MC, Craddock N, Owen MJ, Cardno AG. Am J Med Genet B Neuropsychiatr Genet; 2011 Dec; 156B(8):929-40. PubMed ID: 21960518 [Abstract] [Full Text] [Related]
15. Dissecting the genetic heterogeneity of myopia susceptibility in an Ashkenazi Jewish population using ordered subset analysis. Simpson CL, Wojciechowski R, Ibay G, Stambolian D, Bailey-Wilson JE. Mol Vis; 2011 Dec; 17():1641-51. PubMed ID: 21738393 [Abstract] [Full Text] [Related]
16. Genomewide high-density SNP linkage analysis of 236 Japanese families supports the existence of schizophrenia susceptibility loci on chromosomes 1p, 14q, and 20p. Arinami T, Ohtsuki T, Ishiguro H, Ujike H, Tanaka Y, Morita Y, Mineta M, Takeichi M, Yamada S, Imamura A, Ohara K, Shibuya H, Ohara K, Suzuki Y, Muratake T, Kaneko N, Someya T, Inada T, Yoshikawa T, Toyota T, Yamada K, Kojima T, Takahashi S, Osamu O, Shinkai T, Nakamura M, Fukuzako H, Hashiguchi T, Niwa SI, Ueno T, Tachikawa H, Hori T, Asada T, Nanko S, Kunugi H, Hashimoto R, Ozaki N, Iwata N, Harano M, Arai H, Ohnuma T, Kusumi I, Koyama T, Yoneda H, Fukumaki Y, Shibata H, Kaneko S, Higuchi H, Yasui-Furukori N, Numachi Y, Itokawa M, Okazaki Y, Japanese Schizophrenia Sib-Pair Linkage Group. Am J Hum Genet; 2005 Dec; 77(6):937-44. PubMed ID: 16380906 [Abstract] [Full Text] [Related]
17. Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish families. Venken T, Alaerts M, Souery D, Goossens D, Sluijs S, Navon R, Van Broeckhoven C, Mendlewicz J, Del-Favero J, Claes S. Mol Psychiatry; 2008 Apr; 13(4):442-50. PubMed ID: 17579605 [Abstract] [Full Text] [Related]
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20. A genome-wide linkage study of bipolar disorder and co-morbid migraine: replication of migraine linkage on chromosome 4q24, and suggestion of an overlapping susceptibility region for both disorders on chromosome 20p11. Oedegaard KJ, Greenwood TA, Lunde A, Fasmer OB, Akiskal HS, Kelsoe JR, NIMH Genetics Initiative Bipolar Disorder Consortium. J Affect Disord; 2010 Apr; 122(1-2):14-26. PubMed ID: 19819557 [Abstract] [Full Text] [Related] Page: [Next] [New Search]