-
1
-
-
0028212505
-
Factor analysis of symptom subtypes of obsessive compulsive disorder and their relation to personality and tic disorders
-
Baer L. 1994. Factor analysis of symptom subtypes of obsessive compulsive disorder and their relation to personality and tic disorders. J Clin Psychiatry 55 (Suppl): 18-23.
-
(1994)
J Clin Psychiatry
, vol.55
, Issue.SUPPL.
, pp. 18-23
-
-
Baer, L.1
-
2
-
-
0026635532
-
Psychiatric disorders in the families of patients with obsessive-compulsive disorder
-
Bellodi L, Sciuto G, Diaferia G, et al. 1992. Psychiatric disorders in the families of patients with obsessive-compulsive disorder. Psychiatry Res 42:111-120.
-
(1992)
Psychiatry Res
, vol.42
, pp. 111-120
-
-
Bellodi, L.1
Sciuto, G.2
Diaferia, G.3
-
3
-
-
0031846537
-
Hoarding and treatment response in 38 nondepressed subjects with obsessive-compulsive disorder
-
Black DW, Monahan P, Gable J, et al. 1998. Hoarding and treatment response in 38 nondepressed subjects with obsessive-compulsive disorder. J Clin Psychiatry 59:420-425.
-
(1998)
J Clin Psychiatry
, vol.59
, pp. 420-425
-
-
Black, D.W.1
Monahan, P.2
Gable, J.3
-
4
-
-
0035826463
-
Additional evidence that genetic variation of MAO-A gene supports a gender subtype in obsessive-compulsive disorder
-
Camarena B, Rinetti G, Cruz C, et al. 2001. Additional evidence that genetic variation of MAO-A gene supports a gender subtype in obsessive-compulsive disorder. Am J Med Genet 105:279-282.
-
(2001)
Am J Med Genet
, vol.105
, pp. 279-282
-
-
Camarena, B.1
Rinetti, G.2
Cruz, C.3
-
5
-
-
0037390133
-
Association study of heroin dependence and catechol-O-methyltransferase gene
-
Cao L, Li T, Liu X. 2003. Association study of heroin dependence and catechol-O-methyltransferase gene. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 20:127-130.
-
(2003)
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
, vol.20
, pp. 127-130
-
-
Cao, L.1
Li, T.2
Liu, X.3
-
6
-
-
0026410690
-
Clomipramine in the treatment of patients with obsessive-compulsive disorder
-
The Clomipramine Collaborative Study Group.
-
The Clomipramine Collaborative Study Group. 1991, Clomipramine in the treatment of patients with obsessive-compulsive disorder. Arch Gen Psychiatry 48:730-738.
-
(1991)
Arch Gen Psychiatry
, vol.48
, pp. 730-738
-
-
-
7
-
-
6344265879
-
Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): Effects on mRNA, protein, and enzyme activity in postmortem human brain
-
Chen J, Lipska BK, Halim N, et al. 2004. Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): Effects on mRNA, protein, and enzyme activity in postmortem human brain. Am J Hum Genet 75:807-821.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 807-821
-
-
Chen, J.1
Lipska, B.K.2
Halim, N.3
-
8
-
-
0027099746
-
Sertraline in the treatment of obsessive compulsive disorder: Two double-blind, placebo-controlled studies
-
Chouinard G. 1992. Sertraline in the treatment of obsessive compulsive disorder: Two double-blind, placebo-controlled studies. Int Clin Psychopharmacol 7 (Suppl 2): 37-41.
-
(1992)
Int Clin Psychopharmacol
, vol.7
, Issue.SUPPL. 2
, pp. 37-41
-
-
Chouinard, G.1
-
9
-
-
34047121617
-
Factor analysis of the Yale-Brown Obsessive Compulsive Scale in a family study of obsessive-compulsive disorder
-
Cullen B, Brown CH, Riddle MA, et al. 2007. Factor analysis of the Yale-Brown Obsessive Compulsive Scale in a family study of obsessive-compulsive disorder. Depress Anxiety 24:130-138.
-
(2007)
Depress Anxiety
, vol.24
, pp. 130-138
-
-
Cullen, B.1
Brown, C.H.2
Riddle, M.A.3
-
10
-
-
33745636519
-
Association between the dopamine D2 receptor TaqI A2 allele and low activity COMT allele with obsessive-compulsive disorder in males
-
Denys D, Van Nieuwerburgh F, Deforce D, et al. 2006. Association between the dopamine D2 receptor TaqI A2 allele and low activity COMT allele with obsessive-compulsive disorder in males. Eur Neuropsychopharmacol 16:446-450.
-
(2006)
Eur Neuropsychopharmacol
, vol.16
, pp. 446-450
-
-
Denys, D.1
Van Nieuwerburgh, F.2
Deforce, D.3
-
11
-
-
0042472872
-
Lack of association of catechol-O-methyltransferase gene polymorphism in obsessive-compulsive disorder
-
Erdal ME, Tot S, Yazici K, et al. 2003. Lack of association of catechol-O-methyltransferase gene polymorphism in obsessive-compulsive disorder. Depress Anxiety 18:41-45.
-
(2003)
Depress Anxiety
, vol.18
, pp. 41-45
-
-
Erdal, M.E.1
Tot, S.2
Yazici, K.3
-
12
-
-
0037368274
-
Item-by-item factor analysis of the Yale-Brown Obsessive Compulsive Scale Symptom Checklist
-
Feinstein SB, Fallon BA, Petkova E, et al. 2003. Item-by-item factor analysis of the Yale-Brown Obsessive Compulsive Scale Symptom Checklist. J Neuropsychiatry Clin Neurosci 15:187-193.
-
(2003)
J Neuropsychiatry Clin Neurosci
, vol.15
, pp. 187-193
-
-
Feinstein, S.B.1
Fallon, B.A.2
Petkova, E.3
-
13
-
-
38349147050
-
The analytical epidemiology of obsessive-compulsive disorder: Risk factors and correlates
-
Fontenelle LF, Hasler G. 2008. The analytical epidemiology of obsessive-compulsive disorder: Risk factors and correlates. Prog Neuropsychopharmacol Biol Psychiatry 32:1-15.
-
(2008)
Prog Neuropsychopharmacol Biol Psychiatry
, vol.32
, pp. 1-15
-
-
Fontenelle, L.F.1
Hasler, G.2
-
14
-
-
0033995464
-
Association between obsessive-compulsive disorder and polymorphisms of genes encoding components of the serotonergic and dopaminergic pathways
-
Frisch A, Michaelovsky E, Rockah R, et al. 2000. Association between obsessive-compulsive disorder and polymorphisms of genes encoding components of the serotonergic and dopaminergic pathways. Eur Neuropsychopharmacol 10:205-209.
-
(2000)
Eur Neuropsychopharmacol
, vol.10
, pp. 205-209
-
-
Frisch, A.1
Michaelovsky, E.2
Rockah, R.3
-
15
-
-
33646009304
-
COMT genetic variation confers risk for psychotic and affective disorders: A case control study
-
Funke B, Malhotra AK, Finn CT, et al. 2005. COMT genetic variation confers risk for psychotic and affective disorders: A case control study. Behav Brain Funct 1:19.
-
(2005)
Behav Brain Funct
, vol.1
, pp. 19
-
-
Funke, B.1
Malhotra, A.K.2
Finn, C.T.3
-
16
-
-
0026518652
-
Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1-q11.2
-
Grossman MH, Emanuel BS, Budarf ML. 1992. Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1-q11.2. Genomics 12:822-825.
-
(1992)
Genomics
, vol.12
, pp. 822-825
-
-
Grossman, M.H.1
Emanuel, B.S.2
Budarf, M.L.3
-
17
-
-
0033105248
-
No coding variant of the tryptophan hydroxylase gene detected in seasonal affective disorder, obsessive-compulsive disorder, anorexia nervosa, and alcoholism
-
Han L, Nielsen DA, Rosenthal NE, et al. 1999. No coding variant of the tryptophan hydroxylase gene detected in seasonal affective disorder, obsessive-compulsive disorder, anorexia nervosa, and alcoholism. Biol Psychiatry 45:615-619.
-
(1999)
Biol Psychiatry
, vol.45
, pp. 615-619
-
-
Han, L.1
Nielsen, D.A.2
Rosenthal, N.E.3
-
18
-
-
0037043047
-
Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands
-
Hanna GL, Veenstra-VanderWeele J, Cox NJ, et al. 2002. Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands. Am J Med Genet 114:541-552.
-
(2002)
Am J Med Genet
, vol.114
, pp. 541-552
-
-
Hanna, G.L.1
Veenstra-VanderWeele, J.2
Cox, N.J.3
-
19
-
-
33847278836
-
Familiality of factor analysis-derived YBOCS dimensions in OCD-affected sibling pairs from the OCD Collaborative Genetics Study
-
Hasler G, Pinto A, Greenberg BD, et al. 2007. Familiality of factor analysis-derived YBOCS dimensions in OCD-affected sibling pairs from the OCD Collaborative Genetics Study. Biol Psychiatry 61:617-625.
-
(2007)
Biol Psychiatry
, vol.61
, pp. 617-625
-
-
Hasler, G.1
Pinto, A.2
Greenberg, B.D.3
-
20
-
-
33646142054
-
The current status of association studies in obsessive-compulsive disorder
-
Hemmings SM, Stein DJ. 2006. The current status of association studies in obsessive-compulsive disorder. Psychiatr Clin North Am 29:411-444.
-
(2006)
Psychiatr Clin North Am
, vol.29
, pp. 411-444
-
-
Hemmings, S.M.1
Stein, D.J.2
-
21
-
-
0037335412
-
Investigating the role of dopaminergic and serotonergic candidate genes in obsessive-compulsive disorder
-
Hemmings SM, Kinnear CJ, Niehaus DJ, et al. 2003. Investigating the role of dopaminergic and serotonergic candidate genes in obsessive-compulsive disorder. Eur Neuropsychopharmacol 13:93-98.
-
(2003)
Eur Neuropsychopharmacol
, vol.13
, pp. 93-98
-
-
Hemmings, S.M.1
Kinnear, C.J.2
Niehaus, D.J.3
-
22
-
-
33646072813
-
Serotonin transporter promoter gain-of-function genotypes are linked to obsessive-compulsive disorder
-
Hu XZ, Lipsky RH, Zhu G, et al. 2006. Serotonin transporter promoter gain-of-function genotypes are linked to obsessive-compulsive disorder. Am J Hum Genet 78:815-826.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 815-826
-
-
Hu, X.Z.1
Lipsky, R.H.2
Zhu, G.3
-
23
-
-
0001500902
-
Similar and dissimilar manifestations of obsessive-compulsive neuroses in monozygotic twins
-
Inouye E. 1965. Similar and dissimilar manifestations of obsessive-compulsive neuroses in monozygotic twins. Am J Psychiatry 121:1171-1175.
-
(1965)
Am J Psychiatry
, vol.121
, pp. 1171-1175
-
-
Inouye, E.1
-
24
-
-
0030895285
-
Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder
-
Karayiorgou M, Altemus M, Galke BL, et al. 1997. Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder. Proc Natl Acad Sci USA 94:4572-4575.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 4572-4575
-
-
Karayiorgou, M.1
Altemus, M.2
Galke, B.L.3
-
25
-
-
0033135862
-
Family-based association studies support a sexually dimorphic effect of COMT and MAOA on genetic susceptibility to obsessive-compulsive disorder
-
Karayiorgou M, Sobin C, Blundell ML, et al. 1999. Family-based association studies support a sexually dimorphic effect of COMT and MAOA on genetic susceptibility to obsessive-compulsive disorder. Biol Psychiatry 45:1178-1189.
-
(1999)
Biol Psychiatry
, vol.45
, pp. 1178-1189
-
-
Karayiorgou, M.1
Sobin, C.2
Blundell, M.L.3
-
26
-
-
73949160967
-
The role of the COMT Val(158)Met polymorphism in the phenotypic expression of obsessive-compulsive disorder
-
Katerberg H, Cath DC, Denys DA, et al. 2010. The role of the COMT Val(158)Met polymorphism in the phenotypic expression of obsessive-compulsive disorder. Am J Med Genet Part B 153B:167-176.
-
(2010)
Am J Med Genet Part B
, vol.153 B
, pp. 167-176
-
-
Katerberg, H.1
Cath, D.C.2
Denys, D.A.3
-
27
-
-
0030004521
-
Human catechol-O-methyltransferase pharmacogenetics: Description of a functional polymorphism and its potential application to neuropsychiatric disorders
-
Lachman HM, Papolos DF, Saito T, et al. 1996. Human catechol-O-methyltransferase pharmacogenetics: Description of a functional polymorphism and its potential application to neuropsychiatric disorders. Pharmacogenetics 6:243-250.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 243-250
-
-
Lachman, H.M.1
Papolos, D.F.2
Saito, T.3
-
29
-
-
0032879338
-
Use of factor-analyzed symptom dimensions to predict outcome with serotonin reuptake inhibitors and placebo in the treatment of obsessive-compulsive disorder
-
Mataix-Cols D, Rauch SL, Manzo PA, et al. 1999. Use of factor-analyzed symptom dimensions to predict outcome with serotonin reuptake inhibitors and placebo in the treatment of obsessive-compulsive disorder. Am J Psychiatry 156:1409-1416.
-
(1999)
Am J Psychiatry
, vol.156
, pp. 1409-1416
-
-
Mataix-Cols, D.1
Rauch, S.L.2
Manzo, P.A.3
-
30
-
-
0036164142
-
Symptom stability in adult obsessive-compulsive disorder: Data from a naturalistic two-year follow-up study
-
Mataix-Cols D, Rauch SL, Baer L, et al. 2002. Symptom stability in adult obsessive-compulsive disorder: Data from a naturalistic two-year follow-up study. Am J Psychiatry 159:263-268.
-
(2002)
Am J Psychiatry
, vol.159
, pp. 263-268
-
-
Mataix-Cols, D.1
Rauch, S.L.2
Baer, L.3
-
32
-
-
0031802343
-
Evidence for linkage disequilibrium between serotonin transporter protein gene (SLC6A4) and obsessive compulsive disorder
-
McDougle CJ, Epperson CN, Price LH, et al. 1998. Evidence for linkage disequilibrium between serotonin transporter protein gene (SLC6A4) and obsessive compulsive disorder. Mol Psychiatry 3:270-273.
-
(1998)
Mol Psychiatry
, vol.3
, pp. 270-273
-
-
McDougle, C.J.1
Epperson, C.N.2
Price, L.H.3
-
33
-
-
1642503730
-
Association analysis of the catechol-o-methyltransferase (COMT), serotonin transporter (5-HTT) and serotonin 2A receptor (5HT2A) gene polymorphisms with obsessive-compulsive disorder
-
Meira-Lima I, Shavitt RG, Miguita K, et al. 2004. Association analysis of the catechol-o-methyltransferase (COMT), serotonin transporter (5-HTT) and serotonin 2A receptor (5HT2A) gene polymorphisms with obsessive-compulsive disorder. Genes Brain Behav 3:75-79.
-
(2004)
Genes Brain Behav
, vol.3
, pp. 75-79
-
-
Meira-Lima, I.1
Shavitt, R.G.2
Miguita, K.3
-
34
-
-
0030325537
-
DRD2, DRD3 and 5HT2A receptor genes polymorphisms in obsessive-compulsive disorder
-
Nicolini H, Cruz C, Camarena B, et al. 1996. DRD2, DRD3 and 5HT2A receptor genes polymorphisms in obsessive-compulsive disorder. Mol Psychiatry 1:461-465.
-
(1996)
Mol Psychiatry
, vol.1
, pp. 461-465
-
-
Nicolini, H.1
Cruz, C.2
Camarena, B.3
-
35
-
-
0035023438
-
Association between a catechol-o-methyltransferase polymorphism and obsessive-compulsive disorder in the Afrikaner population
-
Niehaus DJ, Kinnear CJ, Corfield VA, et al. 2001. Association between a catechol-o-methyltransferase polymorphism and obsessive-compulsive disorder in the Afrikaner population. J Affect Disord 65:61-65.
-
(2001)
J Affect Disord
, vol.65
, pp. 61-65
-
-
Niehaus, D.J.1
Kinnear, C.J.2
Corfield, V.A.3
-
36
-
-
0027199570
-
Association versus linkage studies in psychosis genetics
-
Nothen MM, Propping P, Fimmers R. 1993. Association versus linkage studies in psychosis genetics. J Med Genet 30:634-637.
-
(1993)
J Med Genet
, vol.30
, pp. 634-637
-
-
Nothen, M.M.1
Propping, P.2
Fimmers, R.3
-
37
-
-
0028134880
-
Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics Initiative
-
discussion 863-4.
-
Nurnberger JI Jr, Blehar MC, Kaufmann CA, et al. 1994. Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics Initiative. Arch Gen Psychiatry 51:849-859; discussion 863-4.
-
(1994)
Arch Gen Psychiatry
, vol.51
-
-
Nurnberger Jr, J.I.1
Blehar, M.C.2
Kaufmann, C.A.3
-
38
-
-
0032541285
-
No association between anxiety disorders and catechol-O-methyltransferase polymorphism
-
Ohara K, Nagai M, Suzuki Y, et al. 1998. No association between anxiety disorders and catechol-O-methyltransferase polymorphism. Psychiatry Res 80:145-148.
-
(1998)
Psychiatry Res
, vol.80
, pp. 145-148
-
-
Ohara, K.1
Nagai, M.2
Suzuki, Y.3
-
40
-
-
34249679268
-
Taboo thoughts and doubt/checking: A refinement of the factor structure for obsessive-compulsive disorder symptoms
-
Pinto A, Eisen JL, Mancebo MC, et al. 2007. Taboo thoughts and doubt/checking: A refinement of the factor structure for obsessive-compulsive disorder symptoms. Psychiatry Res 151:255-258.
-
(2007)
Psychiatry Res
, vol.151
, pp. 255-258
-
-
Pinto, A.1
Eisen, J.L.2
Mancebo, M.C.3
-
41
-
-
34249332777
-
The met(158) allele of catechol-O-methyltransferase (COMT) is associated with obsessive-compulsive disorder in men: Case-control study and meta-analysis
-
Pooley EC, Fineberg N, Harrison PJ. 2007. The met(158) allele of catechol-O-methyltransferase (COMT) is associated with obsessive-compulsive disorder in men: Case-control study and meta-analysis. Mol Psychiatry 12:556-561.
-
(2007)
Mol Psychiatry
, vol.12
, pp. 556-561
-
-
Pooley, E.C.1
Fineberg, N.2
Harrison, P.J.3
-
42
-
-
24044493584
-
COMT Val158Met polymorphism in schizophrenia with obsessive-compulsive disorder: A case-control study
-
Poyurovsky M, Michaelovsky E, Frisch A, et al. 2005. COMT Val158Met polymorphism in schizophrenia with obsessive-compulsive disorder: A case-control study. Neurosci Lett 389:21-24.
-
(2005)
Neurosci Lett
, vol.389
, pp. 21-24
-
-
Poyurovsky, M.1
Michaelovsky, E.2
Frisch, A.3
-
43
-
-
12244264435
-
Genetic power calculator: Design of linkage and association genetic mapping studies of complex traits
-
Purcell S, Cherny SS, Sham PC. 2003. Genetic power calculator: Design of linkage and association genetic mapping studies of complex traits. Bioinformatics 19:149-150.
-
(2003)
Bioinformatics
, vol.19
, pp. 149-150
-
-
Purcell, S.1
Cherny, S.S.2
Sham, P.C.3
-
44
-
-
0036210381
-
Hoarding in obsessive compulsive disorder: Results from a case-control study
-
Samuels J, Bienvenu OJ III, Riddle MA, et al. 2002. Hoarding in obsessive compulsive disorder: Results from a case-control study. Behav Res Ther 40:517-528.
-
(2002)
Behav Res Ther
, vol.40
, pp. 517-528
-
-
Samuels, J.1
Bienvenu III, O.J.2
Riddle, M.A.3
-
45
-
-
0036157565
-
Obsessive-compulsive hoarding: Symptom severity and response to multimodal treatment
-
Saxena S, Maidment KM, Vapnik T, et al. 2002. Obsessive-compulsive hoarding: Symptom severity and response to multimodal treatment. J Clin Psychiatry 63:21-27.
-
(2002)
J Clin Psychiatry
, vol.63
, pp. 21-27
-
-
Saxena, S.1
Maidment, K.M.2
Vapnik, T.3
-
47
-
-
0034606203
-
Association between homozygosity at the COMT gene locus and obsessive compulsive disorder
-
Schindler KM, Richter MA, Kennedy JL, et al. 2000. Association between homozygosity at the COMT gene locus and obsessive compulsive disorder. Am J Med Genet 96:721-724.
-
(2000)
Am J Med Genet
, vol.96
, pp. 721-724
-
-
Schindler, K.M.1
Richter, M.A.2
Kennedy, J.L.3
-
48
-
-
33746545576
-
Genomewide linkage scan for obsessive-compulsive disorder: Evidence for susceptibility loci on chromosomes 3q, 7p, 1q, 15q, and 6q
-
Shugart YY, Samuels J, Willour VL, et al. 2006. Genomewide linkage scan for obsessive-compulsive disorder: Evidence for susceptibility loci on chromosomes 3q, 7p, 1q, 15q, and 6q. Mol Psychiatry 11:763-770.
-
(2006)
Mol Psychiatry
, vol.11
, pp. 763-770
-
-
Shugart, Y.Y.1
Samuels, J.2
Willour, V.L.3
-
49
-
-
0036930448
-
5-HT2A promoter polymorphism -1438G/A in children and adolescents with obsessive-compulsive disorders
-
Walitza S, Wewetzer C, Warnke A, et al. 2002. 5-HT2A promoter polymorphism -1438G/A in children and adolescents with obsessive-compulsive disorders. Mol Psychiatry 7:1054-1057.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 1054-1057
-
-
Walitza, S.1
Wewetzer, C.2
Warnke, A.3
|