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Volumn 17, Issue 8, 2012, Pages 818-826

Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms

(33)  Badner, J A a   Koller, D b   Foroud, T b   Edenberg, H b   Nurnberger, J I b   Zandi, P P c   Willour, V L c   McMahon, F J d   Potash, J B c   Hamshere, M e   Grozeva, D e   Green, E e   Kirov, G e   Jones, I e   Jones, L f   Craddock, N e   Morris, D g   Segurado, R g   Gill, M g   Sadovnick, D h   more..


Author keywords

bipolar disorder; genome wide linkage analysis; single nucleotide polymorphisms

Indexed keywords

ARTICLE; BIPOLAR DISORDER; CONTROLLED STUDY; EXOME; GENE SEQUENCE; GENETIC ASSOCIATION; GENOTYPE; HUMAN; LINKAGE ANALYSIS; MAJOR DEPRESSION; PARAMETRIC TEST; PEDIGREE ANALYSIS; PRIORITY JOURNAL; RECURRENT DISEASE; SCHIZOAFFECTIVE PSYCHOSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84864343505     PISSN: 13594184     EISSN: 14765578     Source Type: Journal    
DOI: 10.1038/mp.2011.89     Document Type: Article
Times cited : (26)

References (46)
  • 2
    • 0029116941 scopus 로고
    • Complex segregation analyses of old order amish families ascertained through bipolar i individuals
    • Pauls DL, Bailey JN, Carter AS, Allen CR, Egeland JA. Complex segregation analyses of old order Amish families ascertained through bipolar I individuals. Am J Med Genet 1995; 60: 290-297.
    • (1995) Am J Med Genet , vol.60 , pp. 290-297
    • Pauls, D.L.1    Bailey, J.N.2    Carter, A.S.3    Allen, C.R.4    Egeland, J.A.5
  • 4
    • 47749156793 scopus 로고    scopus 로고
    • The genetics of bipolar disorder: Genome 'hot regions,' genes, new potential candidates and future directions
    • DOI 10.1038/mp.2008.29, PII MP200829
    • Serretti A, Mandelli L. The genetics of bipolar disorder: genome 'hot regions,' genes, new potential candidates and future directions. Mol Psychiatry 2008; 13: 742-771. (Pubitemid 352032111)
    • (2008) Molecular Psychiatry , vol.13 , Issue.8 , pp. 742-771
    • Serretti, A.1    Mandelli, L.2
  • 8
    • 70349326121 scopus 로고    scopus 로고
    • A narrow and highly significant linkage signal for severe bipolar disorder in the chromosome 5Q33 region in latin american pedigrees
    • Jasinska AJ, Service S, Jawaheer D, DeYoung J, Levinson M, Zhang Z et al. A narrow and highly significant linkage signal for severe bipolar disorder in the chromosome 5q33 region in Latin American pedigrees. Am J Med Genet B Neuropsychiatr Genet 2009; 150B: 998-1006.
    • (2009) Am J Med Genet B Neuropsychiatr Genet , vol.150 B , pp. 998-1006
    • Jasinska, A.J.1    Service, S.2    Jawaheer, D.3    Deyoung, J.4    Levinson, M.5    Zhang, Z.6
  • 10
    • 11844305917 scopus 로고    scopus 로고
    • Localization of bipolar susceptibility locus by molecular genetic analysis of the chromosome 12q23-q24 region in two pedigrees with bipolar disorder and Darier's disease
    • DOI 10.1176/appi.ajp.162.1.35
    • Green E, Elvidge G, Jacobsen N, Glaser B, Jones I, O'Donovan MC et al. Localization of bipolar susceptibility locus by molecular genetic analysis of the chromosome 12q23-q24 region in two pedigrees with bipolar disorder and Darier's disease. Am J Psychiatry 2005; 162: 35-42. (Pubitemid 40095670)
    • (2005) American Journal of Psychiatry , vol.162 , Issue.1 , pp. 35-42
    • Green, E.1    Elvidge, G.2    Jacobsen, N.3    Glaser, B.4    Jones, I.5    O'Donovan, M.C.6    Kirov, G.7    Owen, M.J.8    Craddock, N.9
  • 12
    • 0002710362 scopus 로고
    • Problems of replicating linkage claims in psychiatry
    • Gershon ES CC (ed) American Psychiatric Press, Inc
    • Suarez BK, V EP, Hampe CL. Problems of replicating linkage claims in psychiatry, In: Gershon ES CC (ed). Genetic Approaches to Mental Disorders. American Psychiatric Press, Inc, 1994, pp. 23-46.
    • (1994) Genetic Approaches to Mental Disorders , pp. 23-46
    • Suarez, B.K.1    Ep, V.2    Hampe, C.L.3
  • 13
    • 65249164859 scopus 로고    scopus 로고
    • Validating, augmenting and refining genome-wide association signals
    • Ioannidis JPA, Thomas G, Daly MJ. Validating, augmenting and refining genome-wide association signals. Nat Rev Genet 2009; 10: 318-329.
    • (2009) Nat Rev Genet , vol.10 , pp. 318-329
    • Ioannidis, J.P.A.1    Thomas, G.2    Daly, M.J.3
  • 14
    • 62549085618 scopus 로고    scopus 로고
    • Human genetic variation and its contribution to complex traits
    • Frazer KA, Murray SS, Schork NJ, Topol EJ. Human genetic variation and its contribution to complex traits. Nat Rev Genet 2009; 10: 241-251.
    • (2009) Nat Rev Genet , vol.10 , pp. 241-251
    • Frazer, K.A.1    Murray, S.S.2    Schork, N.J.3    Topol, E.J.4
  • 15
    • 77952574849 scopus 로고    scopus 로고
    • Uncovering the roles of rare variants in common disease through whole-genome sequencing
    • Cirulli ET, Goldstein DB. Uncovering the roles of rare variants in common disease through whole-genome sequencing. Nat Rev Genet 2010; 11: 415-425.
    • (2010) Nat Rev Genet , vol.11 , pp. 415-425
    • Cirulli, E.T.1    Goldstein, D.B.2
  • 16
    • 84969213492 scopus 로고    scopus 로고
    • Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
    • Consortium WTCC. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 2007; 447: 661-678.
    • (2007) Nature , vol.447 , pp. 661-678
    • Wtcc, C.1
  • 17
    • 50449089356 scopus 로고    scopus 로고
    • Collaborative genome-wide association analysis supports a role for ANK3 and cacna1c in bipolar disorder
    • Ferreira MAR, O'Donovan MC, Meng YA, Jones IR, Ruderfer DM, Jones L et al. Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. Nat Genet 2008; 40: 1056-1058.
    • (2008) Nat Genet , vol.40 , pp. 1056-1058
    • Ferreira, M.A.R.1    O'Donovan, M.C.2    Meng, Y.A.3    Jones, I.R.4    Ruderfer, D.M.5    Jones, L.6
  • 19
    • 38349128462 scopus 로고    scopus 로고
    • A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder
    • Baum AE, Akula N, Cabanero M, Cardona I, Corona W, Klemens B et al. A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder. Mol Psychiatry 2008; 13: 197-207.
    • (2008) Mol Psychiatry , vol.13 , pp. 197-207
    • Baum, A.E.1    Akula, N.2    Cabanero, M.3    Cardona, I.4    Corona, W.5    Klemens, B.6
  • 20
    • 66149092770 scopus 로고    scopus 로고
    • Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry
    • Scott LJ, Muglia P, Kong XQ, Guan W, Flickinger M, Upmanyu R et al. Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. Proc Natl Acad Sci USA 2009; 106: 7501-7506.
    • (2009) Proc Natl Acad Sci USA , vol.106 , pp. 7501-7506
    • Scott, L.J.1    Muglia, P.2    Kong, X.Q.3    Guan, W.4    Flickinger, M.5    Upmanyu, R.6
  • 21
    • 67651158803 scopus 로고    scopus 로고
    • Genome-wide association study of bipolar disorder in European American and African American individuals
    • Smith EN, Bloss CS, Badner JA, Barrett T, Belmonte PL, Berrettini W et al. Genome-wide association study of bipolar disorder in European American and African American individuals. Mol Psychiatry 2009; 14: 755-763.
    • (2009) Mol Psychiatry , vol.14 , pp. 755-763
    • Smith, E.N.1    Bloss, C.S.2    Badner, J.A.3    Barrett, T.4    Belmonte, P.L.5    Berrettini, W.6
  • 22
    • 62849086589 scopus 로고    scopus 로고
    • Findings from bipolar disorder genome-wide association studies replicate in a finnish bipolar family-cohort
    • Ollila HM, Soronen P, Silander K, Palo OM, Kieseppä T, Kaunisto MA et al. Findings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohort. Mol Psychiatry 2009; 14: 351-353.
    • (2009) Mol Psychiatry , vol.14 , pp. 351-353
    • Ollila, H.M.1    Soronen, P.2    Silander, K.3    Palo, O.M.4    Kieseppä, T.5    Kaunisto, M.A.6
  • 32
    • 0032231941 scopus 로고    scopus 로고
    • PedCheck: A program for identification of genotype incompatibilities in linkage analysis
    • DOI 10.1086/301904
    • O'Connell JR, Weeks DE. PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet 1998; 63: 259-266. (Pubitemid 30428342)
    • (1998) American Journal of Human Genetics , vol.63 , Issue.1 , pp. 259-266
    • O'Connell, J.R.1    Weeks, D.E.2
  • 33
    • 0036338150 scopus 로고    scopus 로고
    • Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
    • Abecasis GR, Cherny SS, Cookson WO, Cardon LR. Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 2002; 30: 97-101.
    • (2002) Nat Genet , vol.30 , pp. 97-101
    • Abecasis, G.R.1    Cherny, S.S.2    Cookson, W.O.3    Cardon, L.R.4
  • 34
    • 0033912689 scopus 로고    scopus 로고
    • Statistical tests for detection of misspecified relationships by use of genome-screen data
    • DOI 10.1086/302800
    • 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. (Pubitemid 30470506)
    • (2000) American Journal of Human Genetics , vol.66 , Issue.3 , pp. 1076-1094
    • McPeek, M.S.1    Sun, L.2
  • 35
    • 33746512512 scopus 로고    scopus 로고
    • Principal components analysis corrects for stratification in genome-wide association studies
    • DOI 10.1038/ng1847, PII NG1847
    • Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, Reich D. Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 2006; 38: 904-909. (Pubitemid 44141658)
    • (2006) Nature Genetics , vol.38 , Issue.8 , pp. 904-909
    • Price, A.L.1    Patterson, N.J.2    Plenge, R.M.3    Weinblatt, M.E.4    Shadick, N.A.5    Reich, D.6
  • 36
    • 33751103455 scopus 로고    scopus 로고
    • Multipoint linkage analysis with many multiallelic or dense diallelic markers: Markov chain-Monte Carlo provides practical approaches for genome scans on general pedigrees
    • DOI 10.1086/508472
    • Wijsman EM, Rothstein JH, Thompson EA. Multipoint linkage analysis with many multiallelic or dense diallelic markers: Markov chain-Monte Carlo provides practical approaches for genome scans on general pedigrees. Am J Hum Genet 2006; 79: 846-858. (Pubitemid 44763399)
    • (2006) American Journal of Human Genetics , vol.79 , Issue.5 , pp. 846-858
    • Wijsman, E.M.1    Rothstein, J.H.2    Thompson, E.A.3
  • 37
    • 0030728925 scopus 로고    scopus 로고
    • Allele-sharing models: LOD scores and accurate linkage tests
    • DOI 10.1086/301592
    • Kong A, Cox NJ. Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Genet 1997; 61: 1179-1188. (Pubitemid 27492328)
    • (1997) American Journal of Human Genetics , vol.61 , Issue.5 , pp. 1179-1188
    • Kong, A.1    Cox, N.J.2
  • 39
    • 11144335931 scopus 로고    scopus 로고
    • Robust estimation of critical values for genome scans to detect linkage
    • Bacanu SA. Robust estimation of critical values for genome scans to detect linkage. Genet Epidemiol 2005; 28: 24-32.
    • (2005) Genet Epidemiol , vol.28 , pp. 24-32
    • Bacanu, S.A.1
  • 41
    • 32544437181 scopus 로고    scopus 로고
    • FLOSS: Flexible ordered subset analysis for linkage mapping of complex traits
    • DOI 10.1093/bioinformatics/btk012
    • Browning BL. FLOSS: flexible ordered subset analysis for linkage mapping of complex traits. Bioinformatics 2006; 22: 512-513. (Pubitemid 43231433)
    • (2006) Bioinformatics , vol.22 , Issue.4 , pp. 512-513
    • Browning, B.L.1
  • 42
    • 0035205458 scopus 로고    scopus 로고
    • A robust identity-by-descent procedure using affected sib pairs: Multipoint mapping for complex diseases
    • Liang KY, Chiu YF, Beaty TH. A robust identity-by-descent procedure using affected sib pairs: multipoint mapping for complex diseases. Hum Hered 2001; 51: 64-78.
    • (2001) Hum Hered , vol.51 , pp. 64-78
    • Liang, K.Y.1    Chiu, Y.F.2    Beaty, T.H.3
  • 45
    • 77950587223 scopus 로고    scopus 로고
    • Rare copy number variants: A point of rarity in genetic risk for bipolar disorder and Schizophrenia
    • Grozeva D, Kirov G, Ivanov D, Jones IR, Jones L, Green EK et al. Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and Schizophrenia. Arch Gen Psychiatry 2010; 67: 318-327.
    • (2010) Arch Gen Psychiatry , vol.67 , pp. 318-327
    • Grozeva, D.1    Kirov, G.2    Ivanov, D.3    Jones, I.R.4    Jones, L.5    Green, E.K.6
  • 46
    • 78851471431 scopus 로고    scopus 로고
    • European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2Q14 according to age at onset
    • Mathieu F, Dizier MH, Etain B, Jamain S, Rietschel M, MaierWet al. European collaborative study of early-onset bipolar disorder: evidence for genetic heterogeneity on 2q14 according to age at onset. Am J Med Genet B Neuropsychiatr Genet 2010; 153B: 1425-1433.
    • (2010) Am J Med Genet B Neuropsychiatr Genet , vol.153 B , pp. 1425-1433
    • Mathieu, F.1    Dizier, M.H.2    Etain, B.3    Jamain, S.4    Rietschel, M.5    Maier, W.6


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