Erratum: Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: Evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22 (Molecular Psychiatry (2005) 10, (831-841) DOI: 10.1038/sj.mp.4001684);Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: Evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22

Molecular Psychiatry

Volumn 10, Issue 9, 2005, Pages 831-841

  Lambert, D ^a   Middle, F ^b   Hamshere, M L ^c   Segurado, R ^a   Raybould, R ^c   Corvin, A ^a   Green, E ^c   O'Mahony, E ^a   Nikolov, I ^c   Mulcahy, T ^a   Haque, S ^b   Bort, S ^a   Bennett, P ^b   Norton, N ^c   Owen, M J ^c   Kirov, G ^c   Lendon, C ^b   Jones, L ^b   Jones, I ^c   Holmans, P ^c   Gill, M ^a   Craddock, N ^c   more..

^a TRINITY COLLEGE DUBLIN   (Ireland)

^b UNIVERSITY OF BIRMINGHAM   (United Kingdom)

^c CARDIFF UNIVERSITY   (United Kingdom)

Author keywords

Genetics; Genome scan; Linkage; LOD score; Manic depressive; Microsatellite repeats

Indexed keywords

ARTICLE; BIPOLAR DISORDER; CHROMOSOME 10P; CHROMOSOME 18P; CHROMOSOME 4Q; CHROMOSOME 6Q; CHROMOSOME 9P; CONTROLLED STUDY; FAMILY; FEMALE; GENDER; GENE LOCUS; GENETIC LINKAGE; GENETIC SCREENING; GENOME ANALYSIS; HUMAN; HUMAN GENOME; MAJOR CLINICAL STUDY; MALE; MAXIMUM LIKELIHOOD METHOD; MICROSATELLITE MARKER; PRIORITY JOURNAL; SCHIZOPHRENIA; SCORING SYSTEM; SIBLING; X CHROMOSOME; CHROMOSOME 10; CHROMOSOME 18; CHROMOSOME 4; CHROMOSOME 6; CHROMOSOME 9; CHROMOSOME MAP; CLINICAL TRIAL; GENETIC MARKER; GENETICS; GENOME; MULTICENTER STUDY; PARENT; PEDIGREE;

BIPOLAR DISORDER; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 10; CHROMOSOMES, HUMAN, PAIR 18; CHROMOSOMES, HUMAN, PAIR 4; CHROMOSOMES, HUMAN, PAIR 6; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; GENETIC MARKERS; GENETIC SCREENING; GENOME, HUMAN; HUMANS; LOD SCORE; MALE; PARENTS; PEDIGREE; SIBLINGS;

EID: 25444446614     PISSN: 13594184     EISSN: 14765578     Source Type: Journal    
DOI: 10.1038/sj.mp.4001917     Document Type: Erratum

References (53)

1. Goodwin FK, Jamison KR. Manic-Depressive Illness. Oxford University Press: New York, Oxford, 1990.
2. Craddock N, Jones I. Genetics of bipolar disorder. J Med Genet 1999; 36: 585-594.
3. Baron M. Linkage mapping of bipolar affective disorder. Am J Med Genet 2000; 96: 881-883.
4. Craddock N, Khodel V, Van Eerdewegh P, Reich T. Mathematical limits of multilocus models: the genetic transmission of bipolar disorder. Am J Hum Genet 1995; 57: 690-702.
5. Badner JA, Gershon ES. Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia. Mol Psychiatry 2002; 7: 405-411.
6. Segurado R, Detera-Wadleigh SD, Levinson DF, Lewis CM, Gill M, Nurnberger Jr JI et al. Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: bipolar disorder. Am J Hum Genet 2003; 73: 49-62.
7. Lewis CM, Levinson DF, Wise LH, DeLisi LE, Straub RE, Hovatta I et al. Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia. Am J Hum Genet 2003; 73: 34-48.
8. Craddock N, O'Donovan MC, Owen MJ. Genetics of schizophrenia and bipolar disorder: dissecting psychosis. J Med Genet 2005; 42: 288-299.
9. Dick DM, Foroud T, Flury L, Bowman ES, Miller MJ, Rau NL et al. Genome wide linkage analyses of bipolar disorder: a new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative. Am J Hum Genet 2003; 73: 107-114, (Erratum 73: 979).
10. Holmans P, Craddock N. Efficient strategies for genome scanning using maximum-likelihood affected-sib-pair analysis. Am J Hum Genet 1997; 60: 657-666.
11. Bennett P, Segurado R, Jones I, Bort S, McCandless F, Lambert D et al. The Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: first stage report. Mol Psychiatry 2002; 7: 189-200.
12. APA. Diagnostic and Statistical Manual for Mental Disorders Fourth Edition (DSM-IV), 4th ed. American Psychiatric Press, Inc.: Washington, DC, USA, 1994.
13. Wing JK, Babor T, Brugha T, Burke J, Cooper JE, Giel R et al. SCAN. Schedules for clinical assessment in neuropsychiatry. Arch Gen Psychiatry 1990; 47: 589-593.
14. Cohen J. Weighted kappa: nominal scale agreement with provision for scaled disagreement or partial credit. Psychol Bull 1968; 70: 213-220.
15. Ott J. Analysis of Human Genetic Linkage, Revised Edition. Johns Hopkins University Press: Baltimore, 1991.
16. Lander ES, Green P. Construction of multilocus genetic linkage maps in humans. Proc Natl Acad Sci USA 1987; 84: 2363-2367.
17. Matise TC, Gitlin JA. MAP-O-MAT: marker-based linkage mapping on the World Wide Web. Am J Hum Genet 1999; 65: A435.
18. Fenton I, Sandkuijl LA. MEGABASE/PKD: a genetic database for polycystic kidney disease. Contrib Nephrol 1992; 97: 118-127.
19. O'Connell JR, Weeks DE. PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet 1998; 63: 259-266.
20. Göring HH, Ott J. Relationship estimation in affected sib pair analysis of late-onset diseases. Eur J Hum Genet 1997; 5: 69-77.
21. Boehnke M, Cox NJ. Accurate inference of relationships in sib-pair linkage studies. Am J Hum Genet 1997; 61: 423-429.
22. Broman KW, Weber JL. Estimation of pairwise relationships in the presence of genotyping errors. Am J Hum Genet 1998; 63: 1563-1564.
23. McPeek MS, Sun L. Statistical tests for detection of misspecified relationships by use of genome-screen data. Am J Hum Genet 2000; 66: 1076-1094.
24. Abecasis GR, Cherny SS, Cookson WO, Cardon LR. GRR: graphical representation of relationship errors. Bioinformatics 2001; 17: 742-743.
25. Holmans P. Asymptotic properties of affected-sib-pair linkage analysis. Am J Hum Genet 1993; 52: 362-374.
26. Holmans P, Clayton D. Efficiency of typing unaffected relatives in an affected-sib-pair linkage study with single-locus and multiple tightly linked markers. Am J Hum Genet 1995; 57: 1221-1232.
27. Kruglyak L, Lander ES. Complete multipoint sib-pair analysis of qualitative and quantitative traits. Am J Hum Genet 1995; 57: 439-454.
28. Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES. Parametric and nonparametric linkage analysis: a unified multipoint approach. Am J Hum Genet 1996; 58: 1347-1363.
29. Rice JP, Rochberg N, Neuman RJ, Saccone NL, Liu KY, Zhang X et al. Covariates in linkage analysis. Genet Epidemiol 1999; 17(Suppl 1): S691-S695.
30. Holmans P. Detecting gene-gene interactions using affected sib pair analysis with covariates. Hum Hered 2002; 53: 92-102.
31. Lander E, Kruglyak L. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet 1995; 11: 241-247.
32. Risch N. Linkage strategies for genetically complex traits. I. Multilocus models. Am J Hum Genet 1990; 46: 222-228.
33. Middleton FA, Pato MT, Gentile KL, Morley CP, Zhao X, Eisener AF et al. Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22. Am J Hum Genet 2004; 74: 886-897.
34. Schulze TG, Buervenich S, Badner JA, Steele CJ, Detera-Wadleigh SD, Dick D et al. Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees. Biol Psychiatry 2004; 56: 18-23.
35. Pato CN, Pato MT, Kirby A, Petryshen TL, Medeiros H, Carvalho C et al. Genome-wide scan in Portuguese Island families implicates multiple loci in bipolar disorder: fine mapping adds support on chromosomes 6 and 11. Am J Med Genet 2004; 127B: 30-34.
36. Ewald H, Flint T, Kruse TA, Mors O. A genome-wide scan shows significant linkage between bipolar disorder and chromosome 12q24.3 and suggestive linkage to chromosomes 1p22-21, 4p16, 6q14-22, 10q26 and 16p13.3. Mol Psychiatry 2002; 7: 734-744.
37. McInnis MG, Dick DM, Willour VL, Avramopoulos D, MacKinnon DF, Simpson SG et al. Genome-wide scan and conditional analysis in bipolar disorder: evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar pedigrees. Biol Psychiatry 2003; 54: 1265-1273.
38. Maes M, Goossens F, Scharpe S, Meltzer HY, D'Hondt P, Cosyns P. Lower serum prolyl endopeptidase enzyme activity in major depression: further evidence that peptidases play a role in the pathophysiology of depression. Biol Psychiatry 1994; 35: 545-552.
39. Maes M, Goossens F, Scharpe S, Calabrese J, Desnyder R, Meltzer HY. Alterations in plasma prolyl endopeptidase activity in depression, mania, and schizophrenia: effects of antidepressants, mood stabilizers, and antipsychotic drugs. Psychiatry Res 1995; 58: 217-225.
40. Williams RS, Cheng L, Mudge AW, Harwood AJ. A common mechanism of action for three mood-stabilizing drugs. Nature 2002; 417: 292-295.
41. Williams RS, Eames M, Ryves WJ, Viggars J, Harwood AJ. Loss of a prolyl oligopeptidase confers resistance to lithium by elevation of inositol (1,4,5) trisphosphate. EMBO J 1999; 18: 2734-2745.
42. Murai KK, Pasquale EB. Can Eph receptors stimulate the mind? Neuron 2002; 33: 159-162.
43. Gerlai R, McNamara A. Anesthesia induced retrograde amnesia is ameliorated by ephrinA5-IgG in mice: EphA receptor tyrosine kinases are involved in mammalian memory. Behav Brain Res 2000; 108: 133-143.
44. Murai KK, Pasquale EB. Eph receptors, ephrins, and synaptic function. Neuroscientist 2004; 10: 1-11.
45. 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 Sci USA 1999; 96: 5604-5609.
46. Kelsoe JR, Spence MA, Loetscher E, Foguet M, Sadovnick AD, Remick RA et al. A genome survey indicates a possible susceptibility locus for bipolar disorder on chromosome 22. Proc Natl Acad Sci USA 2001; 98: 585-590.
47. Badenhop RF, Moses MJ, Scimone A, Mitchell PB, Ewen KR, Rosso A et al. A genome screen of a large bipolar affective disorder pedigree supports evidence for a susceptibility locus on chromosome 13q. Mol Psychiatry 2001; 6: 396-403.
48. Liu J, Juo SH, Dewan A, Grunn A, Tong X, Brito M et al. Evidence for a putative bipolar disorder locus on 2p13-16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21-24, 13q32, 14q21 and 17q11-12. Mol Psychiatry 2003; 8: 333-342.
49. Shaw SH, Mroczkowski-Parker Z, Shekhtman T, Alexander M, Remick RA, Sadovnick AD et al. Linkage of a bipolar disorder susceptibility locus to human chromosome 13q32 in a new pedigree series. Mol Psychiatry 2003; 8: 558-564.
50. 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.
51. Liu C, Badner JA, Christian SL, Guroff JJ, Detera-Wadleigh SD, Gershon ES. Fine mapping supports previous linkage evidence for a bipolar disorder susceptibility locus on 13q32. Am J Med Genet 2001; 105: 375-380.
52. Berrettini W. Evidence for shared susceptibility in bipolar disorder and schizophrenia. Am J Med Genet 2003; 123C: 59-64.
53. Evans DM, Cardon LR. Guidelines for genotyping in genomewide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps. Am J Hum Genet 2004; 75: 687-692.