Erratum: Findings in an independent sample support an association between bipolar affective disorder and the G72/G30 locus on chromosome 13q33 (Molecular Psychiatry (2004) 9 (87-92) DOI:10.1038/sj.mp.4001453);Findings in an independent sample support an association between bipolar affective disorder and the G72/G30 locus on chromosome 13q33

Molecular Psychiatry

Volumn 9, Issue 1, 2004, Pages 87-92

  Chen, Y S ^a   Akula, N ^b   Detera Wadleigh, S D ^b   Schulze, T G ^b,c   Thomas, J ^b   Potash, J B ^d   DePaulo, J R ^d   Mclnnis, M G ^d   Cox, N J ^a   McMahon, F J ^b  

^a UNIVERSITY OF CHICAGO   (United States)

^b NATIONAL INSTITUTE OF MENTAL HEALTH   (United States)

^c CENTRAL INSTITUTE OF MENTAL HEALTH   (Germany)

^d JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Allele frequency; Genetics; Mood disorder

Indexed keywords

ARTICLE; BIPOLAR DISORDER; CASE CONTROL STUDY; CHROMOSOME 13Q; CONTROLLED STUDY; ETHNIC GROUP; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC MARKER; HAPLOTYPE; HUMAN; MICROSATELLITE MARKER; POLYMORPHIC LOCUS; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 0842264955     PISSN: 13594184     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.mp.4001539     Document Type: Erratum

References (33)

1. Taylor L, Faraone SV, Tsuang MT. Family, twin, and adoption studies of bipolar disease. Curr Psychiatry Rep 2002; 4: 130-133.
2. Prathikanti S, McMahon FJ. Genome scans for susceptibility genes in bipolar affective disorder. Ann Med 2001; 33: 257-262.
3. Craddock N, Dave S, Greening J. Association studies of bipolar disorder. Bipolar Disord 2001; 3: 284-298.
4. Chumakov I, Blumenfeld M, Guerassimenko O, Cavarec L, Palicio M, Abderrahim H et al. Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia. Proc Natl Acad Sci USA 2002; 99; 13675-13680.
5. Detera-Wadleigh SD, Badner JA, Berrettini WH, Yoshikawa T, Goldin LR, Turner G et al. A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2. Proc Natl Acad Sd USA 1999; 96: 5604-5609.
6. Potash JB, Zandi PP, Willour VL, Lan TH, Huo Y, Avramopoulos D et al. Suggestive linkage to chromosomal regions 13q31 and 22q12 in families with psychotic bipolar disorder. Am J Psychiatry 2003; 160: 680-686.
7. Hattori E, Liu C, Badner JA, Bonner TI, Christian SL, Maheshwari M et al. Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series. Am J Hum Genet 2003; 72: 1131-1140.
8. Lander E, Kruglyak L. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet 1995; 11: 241-247.
9. Ardlie KG, Lunetta KL, Seielstad M. Testing for population subdivision and association in four case-control studies. Am J Hum Genet 2002; 71: 304-311.
10. Simpson SG, Folstein SE, Meyers DA, DePaulo JR. Assessment of lineality in bipolar I linkage studies. Am J Psychiatry 1992; 149: 1660-1665.
11. McInnis MG et al. Genome-wide scan of bipolar disorder in 65 pedigrees: supportive evidence for linkage at 8q24, 18q22, 4q32, 2p12, and 13q12. Mol Psychiatry 2003; 8: 288-298.
12. Endicott J, Spitzer RL. A diagnostic interview: the schedule for affective disorders and schizophrenia. Arch Gen Psychiatry 1978; 35: 837-844.
13. Simpson SG, McMahon FJ, McInnis MG, MacKinnon DF, Edwin D, Folstein SE et al. Diagnostic reliability of bipolar II disorder. Arch Gen Psychiatry 2002; 59: 736-740.
14. Egeland JA, Hostetter AM. Amish Study, I: affective disorders among the Amish, 1976-1980. Am JPsychiatry 1983; 140: 56-61.
15. Daussel J, Cann H, Cohen D, Lathrop M, Lalouel JM, While R. Centre d'Etude du Polymorphisme Humain (CEPH): collaborative genetic mapping of the human genome. Genomics 1990; 6: 575-577.
16. Akula N, Chen YS, Hennessy K, Schulze TG, Singh G, McMahon FJ. Utility and accuracy of template-directed dye-terminator incorporation with fluorescence-polarization detection for genotyping single nucleotide polymorphisms. Biotechniques 2002; 32: 1072-1076, 1078.
17. Abecasis GR, Cookson WO. GOLD - graphical overview of linkage disequilibrium. Bioinformatics 2000; 16: 182-183.
18. Excoffier L, Slatkin M. Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population. Mol Biol Evol 1995; 12: 921-927.
19. Devlin B, Risch N. A comparison of linkage disequilibrium measures for fine-scale mapping. Genomics 1995; 29: 311-322.
20. Lewontin RC. On measures of gametic disequilibrium. Genetics 1988; 120: 849-852.
21. Cordell HJ, Clayton DG. A unified stepwise regression procedure for evaluating the relative effecls of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes. Am J Hum Genet 2002; 70: 124-141.
22. Fallin D, Schork NJ. Accuracy of haplotype frequency estimation for biallelic loci, via the expectation-maximization algorithm for unphased diploid genotype data. Am J Hum Genet 2000; 67: 947-959.
23. Kong A, Cox NJ. Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Genet 1997; 61: 1179-1188.
24. Guo SW, Thompson EA. Performing the exact test of Hardy-Weinberg proportion for multiple alleles. Biometrics 1992; 48: 361-372.
25. Pritchard JK, Stephens M, Rosenberg NA, Donnelly P. Association mapping in structured populations. Am J Hum Genet 2000; 67: 170-181.
26. McGinnis R, Shifman S, Darvasi A. Power and efficiency of the TDT and case-control design for association scans. Behav Genet 2002; 32: 135-144.
27. Schulze TG, McMahon FJ. Genetic association mapping at the crossroads: which test and why? Overview and practical guidelines. Am J Med Genet 2002; 114: 1-11.
28. Cardon LR, Palmer LJ. Population stratification and spurious allelic association. Lancet 2003; 361: 598-604.
29. Gordon D, Finch SJ, Nothnagel M, Ott J. Power and sample size calculations for case-control genetic association tests when errors are present: application to single nucleotide polymorphisms. Hum Hered 2002; 54: 22-33.
30. Mitchell AA, Cutler DJ, Chakravarti A. Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/ disequilibrium test. Am J Hum Genet 2003; 72: 598-610.
31. Sun L, Cox NJ, McPeek MS. A statistical method for identification of polymorphisms that explain a linkage result. Am J Hum Genet 2002; 70: 399-411.
32. Long A, Lyman R, Langley C, Mackay T. Two sites in the delta gene region contribute to naturally occurring variation in bristle number in Drosophila melanogaster. Genetics 1998; 149: 999-1017.
33. Drysdale CM, McGraw DW, Stack CB, Stephens JC, Judson RS, Nandabalan K et al. Complex promoter and coding region beta 2-adrenergic receptor haplotypes alter receptor expression and predict in vivo responsiveness. Proc Natl Acad Sci USA 2000; 97: 10483-10488.