메뉴 건너뛰기




Volumn 53, Issue 8, 2014, Pages 910-919

Copy number variation in obsessive-compulsive disorder and tourette syndrome: A cross-disorder study

(121)  McGrath, Lauren M a,c,e   Yu, Dongmei a,e   Marshall, Christian f   Davis, Lea K i   Thiruvahindrapuram, Bhooma f   Li, Bingbin f   Cappi, Carolina j   Gerber, Gloria a   Wolf, Aaron a   Schroeder, Frederick A a   Osiecki, Lisa a   O'Dushlaine, Colm e   Kirby, Andrew a   Illmann, Cornelia a   Haddad, Stephen a   Gallagher, Patience a   Fagerness, Jesen A a   Barr, Cathy L f,g   Bellodi, Laura k   Benarroch, Fortu l   more..


Author keywords

16p13.11; copy number variation; genetics; obsessive compulsive disorder; Tourette syndrome

Indexed keywords

ADULT; ARTICLE; AUTISM; COMORBIDITY; CONTROLLED STUDY; COPY NUMBER VARIATION; DEVELOPMENTAL DISORDER; GENE DELETION; GENE DUPLICATION; GENE LOCUS; GENETIC ASSOCIATION; GENETIC SCREENING; GENOTYPE; GILLES DE LA TOURETTE SYNDROME; HUMAN; MAJOR CLINICAL STUDY; OBSESSIVE COMPULSIVE DISORDER; PHENOTYPE; PRIORITY JOURNAL; SCHIZOPHRENIA; TELOMERE; ADOLESCENT; DIAGNOSTIC AND STATISTICAL MANUAL OF MENTAL DISORDERS; FEMALE; GENETIC PREDISPOSITION; GENETICS; MALE; OBSESSIVE-COMPULSIVE DISORDER; SINGLE NUCLEOTIDE POLYMORPHISM; TOURETTE SYNDROME;

EID: 84904976512     PISSN: 08908567     EISSN: 15275418     Source Type: Journal    
DOI: 10.1016/j.jaac.2014.04.022     Document Type: Article
Times cited : (97)

References (40)
  • 1
    • 63549133694 scopus 로고    scopus 로고
    • The genetics of obsessive-compulsive disorder and Tourette's syndrome: What are the common factors?
    • M.A. Grados The genetics of obsessive-compulsive disorder and Tourette's syndrome: what are the common factors? Curr Psychiatry Rep 11 2009 162 166
    • (2009) Curr Psychiatry Rep , vol.11 , pp. 162-166
    • Grados, M.A.1
  • 2
    • 84887265151 scopus 로고    scopus 로고
    • Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture
    • L.K. Davis, D. Yu, and C.L. Keenan et al. Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture PLoS Genet 9 2013 e1003864
    • (2013) PLoS Genet , vol.9 , pp. 1003864
    • Davis, L.K.1    Yu, D.2    Keenan, C.L.3
  • 3
    • 54049144653 scopus 로고    scopus 로고
    • Copy-number variations associated with neuropsychiatric conditions
    • E.H. Cook Jr., S.W. Scherer, and E.H. Cook Copy-number variations associated with neuropsychiatric conditions Nature 455 2008 919 923
    • (2008) Nature , vol.455 , pp. 919-923
    • Cook, Jr.E.H.1    Scherer, S.W.2    Cook, E.H.3
  • 4
    • 84858434210 scopus 로고    scopus 로고
    • CNVs: Harbingers of a rare variant revolution in psychiatric genetics
    • D. Malhotra, and J. Sebat CNVs: harbingers of a rare variant revolution in psychiatric genetics Cell 148 2012 1223 1241
    • (2012) Cell , vol.148 , pp. 1223-1241
    • Malhotra, D.1    Sebat, J.2
  • 5
    • 84880599004 scopus 로고    scopus 로고
    • Copy number variation: What is it and what has it told us about child psychiatric disorders?
    • A. Thapar, and M. Cooper Copy number variation: what is it and what has it told us about child psychiatric disorders? J Am Acad Child Adolesc Psychiatry 52 2013 772 774
    • (2013) J Am Acad Child Adolesc Psychiatry , vol.52 , pp. 772-774
    • Thapar, A.1    Cooper, M.2
  • 6
    • 84879482530 scopus 로고    scopus 로고
    • Distribution of disease-associated copy number variants across distinct disorders of cognitive development
    • M.F. Pescosolido, E.D. Gamsiz, S. Nagpal, and E.M. Morrow Distribution of disease-associated copy number variants across distinct disorders of cognitive development J Am Acad Child Adolesc Psychiatry 52 2013 414 430.e414
    • (2013) J Am Acad Child Adolesc Psychiatry , vol.52
    • Pescosolido, M.F.1    Gamsiz, E.D.2    Nagpal, S.3    Morrow, E.M.4
  • 8
    • 33845984942 scopus 로고    scopus 로고
    • Obsessive-compulsive disorder, tics and anxiety in 6-year-old twins
    • D. Bolton, F. Rijsdijk, T.G. O'Connor, S. Perrin, and T.C. Eley Obsessive-compulsive disorder, tics and anxiety in 6-year-old twins Psychol Med 37 2007 39 48
    • (2007) Psychol Med , vol.37 , pp. 39-48
    • Bolton, D.1    Rijsdijk, F.2    O'Connor, T.G.3    Perrin, S.4    Eley, T.C.5
  • 10
    • 84855982970 scopus 로고    scopus 로고
    • Prevalence of Tourette syndrome and chronic tics in the population-based Avon Longitudinal Study of Parents and Children cohort
    • J.M. Scharf, L.L. Miller, C.A. Mathews, and Y. Ben-Shlomo Prevalence of Tourette syndrome and chronic tics in the population-based Avon Longitudinal Study of Parents and Children cohort J Am Acad Child Adolesc Psychiatry 51 2012 192 201
    • (2012) J Am Acad Child Adolesc Psychiatry , vol.51 , pp. 192-201
    • Scharf, J.M.1    Miller, L.L.2    Mathews, C.A.3    Ben-Shlomo, Y.4
  • 11
    • 77955507535 scopus 로고    scopus 로고
    • The genetics of obsessive-compulsive disorder: A review
    • D.L. Pauls The genetics of obsessive-compulsive disorder: a review Dialog Clin Neurosci 12 2010 149 163
    • (2010) Dialog Clin Neurosci , vol.12 , pp. 149-163
    • Pauls, D.L.1
  • 12
    • 78650169701 scopus 로고    scopus 로고
    • Familiality of Tourette syndrome, obsessive-compulsive disorder, and attention-deficit/hyperactivity disorder: Heritability analysis in a large sib-pair sample
    • C.A. Mathews, and M.A. Grados Familiality of Tourette syndrome, obsessive-compulsive disorder, and attention-deficit/hyperactivity disorder: heritability analysis in a large sib-pair sample J Am Acad Child Adolesc Psychiatry 50 2011 46 54
    • (2011) J Am Acad Child Adolesc Psychiatry , vol.50 , pp. 46-54
    • Mathews, C.A.1    Grados, M.A.2
  • 13
    • 77953672312 scopus 로고    scopus 로고
    • Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder
    • R. Delorme, D. Moreno-De-Luca, and A. Gennetier et al. Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder BMC Med Genet 11 2010 100
    • (2010) BMC Med Genet , vol.11 , pp. 100
    • Delorme, R.1    Moreno-De-Luca, D.2    Gennetier, A.3
  • 14
    • 84863440382 scopus 로고    scopus 로고
    • Pilot study on HTR2A promoter polymorphism, -1438G/A (rs6311) and a nearby copy number variation showed association with onset and severity in early onset obsessive-compulsive disorder
    • S. Walitza, D.S. Bove, and M. Romanos et al. Pilot study on HTR2A promoter polymorphism, -1438G/A (rs6311) and a nearby copy number variation showed association with onset and severity in early onset obsessive-compulsive disorder J Neural Transm 119 2012 507 515
    • (2012) J Neural Transm , vol.119 , pp. 507-515
    • Walitza, S.1    Bove, D.S.2    Romanos, M.3
  • 15
    • 77952503974 scopus 로고    scopus 로고
    • Tourette syndrome is associated with recurrent exonic copy number variants
    • S.K. Sundaram, A.M. Huq, B.J. Wilson, and H.T. Chugani Tourette syndrome is associated with recurrent exonic copy number variants Neurology 74 2010 1583 1590
    • (2010) Neurology , vol.74 , pp. 1583-1590
    • Sundaram, S.K.1    Huq, A.M.2    Wilson, B.J.3    Chugani, H.T.4
  • 16
    • 84858737859 scopus 로고    scopus 로고
    • Rare copy number variants in Tourette syndrome disrupt genes in histaminergic pathways and overlap with autism
    • T.V. Fernandez, S.J. Sanders, and I.R. Yurkiewicz et al. Rare copy number variants in Tourette syndrome disrupt genes in histaminergic pathways and overlap with autism Biol Psychiatry 71 2012 392 402
    • (2012) Biol Psychiatry , vol.71 , pp. 392-402
    • Fernandez, T.V.1    Sanders, S.J.2    Yurkiewicz, I.R.3
  • 17
    • 84875299901 scopus 로고    scopus 로고
    • CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1
    • A. Nag, E.G. Bochukova, and B. Kremeyer et al. CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1 PLoS One 8 2013 e59061
    • (2013) PLoS One , vol.8 , pp. 59061
    • Nag, A.1    Bochukova, E.G.2    Kremeyer, B.3
  • 18
    • 84878227013 scopus 로고    scopus 로고
    • Genome-wide association study of Tourette's syndrome
    • J.M. Scharf, D. Yu, and C.A. Mathews et al. Genome-wide association study of Tourette's syndrome Mol Psychiatry 18 2013 721 728
    • (2013) Mol Psychiatry , vol.18 , pp. 721-728
    • Scharf, J.M.1    Yu, D.2    Mathews, C.A.3
  • 19
    • 84879422520 scopus 로고    scopus 로고
    • Genome-wide association study of obsessive-compulsive disorder
    • S.E. Stewart, D. Yu, and J.M. Scharf et al. Genome-wide association study of obsessive-compulsive disorder Mol Psychiatry 18 2013 788 798
    • (2013) Mol Psychiatry , vol.18 , pp. 788-798
    • Stewart, S.E.1    Yu, D.2    Scharf, J.M.3
  • 20
    • 77950497675 scopus 로고    scopus 로고
    • A genome-wide association study of alcohol dependence
    • L.J. Bierut, A. Agrawal, and K.K. Bucholz et al. A genome-wide association study of alcohol dependence Proc Natl Acad Sci U S A 107 2010 5082 5087
    • (2010) Proc Natl Acad Sci U S A , vol.107 , pp. 5082-5087
    • Bierut, L.J.1    Agrawal, A.2    Bucholz, K.K.3
  • 21
    • 35948984173 scopus 로고    scopus 로고
    • PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
    • K. Wang, M. Li, and D. Hadley et al. PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data Genome Res 17 2007 1665 1674
    • (2007) Genome Res , vol.17 , pp. 1665-1674
    • Wang, K.1    Li, M.2    Hadley, D.3
  • 22
    • 77954657070 scopus 로고    scopus 로고
    • Functional impact of global rare copy number variation in autism spectrum disorders
    • D. Pinto, A.T. Pagnamenta, and L. Klei et al. Functional impact of global rare copy number variation in autism spectrum disorders Nature 466 2010 368 372
    • (2010) Nature , vol.466 , pp. 368-372
    • Pinto, D.1    Pagnamenta, A.T.2    Klei, L.3
  • 23
    • 79958162661 scopus 로고    scopus 로고
    • Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
    • D. Pinto, K. Darvishi, and X. Shi et al. Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants Nature Biotechnol 29 2011 512 520
    • (2011) Nature Biotechnol , vol.29 , pp. 512-520
    • Pinto, D.1    Darvishi, K.2    Shi, X.3
  • 24
    • 78049303903 scopus 로고    scopus 로고
    • Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: A genome-wide analysis
    • N.M. Williams, I. Zaharieva, and A. Martin et al. Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis Lancet 376 2010 1401 1408
    • (2010) Lancet , vol.376 , pp. 1401-1408
    • Williams, N.M.1    Zaharieva, I.2    Martin, A.3
  • 25
    • 51649107017 scopus 로고    scopus 로고
    • Rare chromosomal deletions and duplications increase risk of schizophrenia
    • Rare chromosomal deletions and duplications increase risk of schizophrenia Nature 455 2008 237 241
    • (2008) Nature , vol.455 , pp. 237-241
  • 26
    • 34548292504 scopus 로고    scopus 로고
    • PLINK: A tool set for whole-genome association and population-based linkage analyses
    • S. Purcell, B. Neale, and K. Todd-Brown et al. PLINK: a tool set for whole-genome association and population-based linkage analyses Am J Hum Genet 81 2007 559 575
    • (2007) Am J Hum Genet , vol.81 , pp. 559-575
    • Purcell, S.1    Neale, B.2    Todd-Brown, K.3
  • 27
    • 79958074870 scopus 로고    scopus 로고
    • Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism
    • S.J. Sanders, A.G. Ercan-Sencicek, and V. Hus et al. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism Neuron 70 2011 863 885
    • (2011) Neuron , vol.70 , pp. 863-885
    • Sanders, S.J.1    Ercan-Sencicek, A.G.2    Hus, V.3
  • 28
    • 80052260252 scopus 로고    scopus 로고
    • A copy number variation morbidity map of developmental delay
    • G.M. Cooper, B.P. Coe, and S. Girirajan et al. A copy number variation morbidity map of developmental delay Nature Genet 43 2011 838 846
    • (2011) Nature Genet , vol.43 , pp. 838-846
    • Cooper, G.M.1    Coe, B.P.2    Girirajan, S.3
  • 29
    • 80052588672 scopus 로고    scopus 로고
    • An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities
    • E.B. Kaminsky, V. Kaul, and J. Paschall et al. An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities Genet Med 13 2011 777 784
    • (2011) Genet Med , vol.13 , pp. 777-784
    • Kaminsky, E.B.1    Kaul, V.2    Paschall, J.3
  • 30
    • 74249088463 scopus 로고    scopus 로고
    • Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies
    • C.G. de Kovel, H. Trucks, and I. Helbig et al. Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies Brain 133 2010 23 32
    • (2010) Brain , vol.133 , pp. 23-32
    • De Kovel, C.G.1    Trucks, H.2    Helbig, I.3
  • 31
    • 77952096810 scopus 로고    scopus 로고
    • Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes
    • E.L. Heinzen, R.A. Radtke, and T.J. Urban et al. Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes Am J Hum Genet 86 2010 707 718
    • (2010) Am J Hum Genet , vol.86 , pp. 707-718
    • Heinzen, E.L.1    Radtke, R.A.2    Urban, T.J.3
  • 32
    • 34447278070 scopus 로고    scopus 로고
    • Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation
    • R. Ullmann, G. Turner, and M. Kirchhoff et al. Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation Hum Mutat 28 2007 674 682
    • (2007) Hum Mutat , vol.28 , pp. 674-682
    • Ullmann, R.1    Turner, G.2    Kirchhoff, M.3
  • 33
    • 64149099583 scopus 로고    scopus 로고
    • DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources
    • H.V. Firth, S.M. Richards, and A.P. Bevan et al. DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources Am J Hum Genet 84 2009 524 533
    • (2009) Am J Hum Genet , vol.84 , pp. 524-533
    • Firth, H.V.1    Richards, S.M.2    Bevan, A.P.3
  • 34
    • 55049107701 scopus 로고    scopus 로고
    • Psychiatric comorbidity in a girl with Saethre-Chotzen syndrome
    • J. Kerbeshian, L.J. Burd, and J.T. Martsolf Psychiatric comorbidity in a girl with Saethre-Chotzen syndrome Psychiatr Genet 18 2008 258 259
    • (2008) Psychiatr Genet , vol.18 , pp. 258-259
    • Kerbeshian, J.1    Burd, L.J.2    Martsolf, J.T.3
  • 35
    • 84856225986 scopus 로고    scopus 로고
    • De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia
    • G. Kirov, A.J. Pocklington, and P. Holmans et al. De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia Mol Psychiatry 17 2012 142 153
    • (2012) Mol Psychiatry , vol.17 , pp. 142-153
    • Kirov, G.1    Pocklington, A.J.2    Holmans, P.3
  • 36
    • 84155191408 scopus 로고    scopus 로고
    • High frequencies of de novo CNVs in bipolar disorder and schizophrenia
    • D. Malhotra, S. McCarthy, and J.J. Michaelson et al. High frequencies of de novo CNVs in bipolar disorder and schizophrenia Neuron 72 2011 951 963
    • (2011) Neuron , vol.72 , pp. 951-963
    • Malhotra, D.1    McCarthy, S.2    Michaelson, J.J.3
  • 38
    • 33747820896 scopus 로고    scopus 로고
    • A patient with both Gilles de la Tourette's syndrome and chromosome 22q11 deletion syndrome: Clue to the genetics of Gilles de la Tourette's syndrome?
    • M.M. Robertson, B.P. Shelley, S. Dalwai, C. Brewer, and H.D. Critchley A patient with both Gilles de la Tourette's syndrome and chromosome 22q11 deletion syndrome: clue to the genetics of Gilles de la Tourette's syndrome? J Psychosom Res 61 2006 365 368
    • (2006) J Psychosom Res , vol.61 , pp. 365-368
    • Robertson, M.M.1    Shelley, B.P.2    Dalwai, S.3    Brewer, C.4    Critchley, H.D.5
  • 39
    • 79957595178 scopus 로고    scopus 로고
    • Tourette syndrome and Klippel-Feil anomaly in a child with chromosome 22q11 duplication
    • R.A. Clarke, Z.M. Fang, A.D. Diwan, and D.L. Gilbert Tourette syndrome and Klippel-Feil anomaly in a child with chromosome 22q11 duplication Case Rep Med 2009 2009 361518
    • (2009) Case Rep Med , vol.2009 , pp. 361518
    • Clarke, R.A.1    Fang, Z.M.2    Diwan, A.D.3    Gilbert, D.L.4
  • 40
    • 77952032690 scopus 로고    scopus 로고
    • Consensus statement: Chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies
    • D.T. Miller, M.P. Adam, and S. Aradhya et al. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies Am J Hum Genet 86 2010 749 764
    • (2010) Am J Hum Genet , vol.86 , pp. 749-764
    • Miller, D.T.1    Adam, M.P.2    Aradhya, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.