PubRank

Michael J Owen

Author PubWeight™ 438.92‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. Nat Genet 2009 15.15
2 Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nat Genet 2007 12.62
3 Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Nature 2010 12.27
4 Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nat Genet 2008 10.52
5 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. Nat Genet 2008 10.49
6 Wake-up call for British psychiatry. Br J Psychiatry 2008 10.30
7 Genome-wide analysis of genetic loci associated with Alzheimer disease. JAMA 2010 9.52
8 Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nat Genet 2011 9.23
9 Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet 2013 8.02
10 Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nat Genet 2013 7.44
11 Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. Am J Hum Genet 2003 6.63
12 Microduplications of 16p11.2 are associated with schizophrenia. Nat Genet 2009 6.13
13 Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder. Am J Hum Genet 2009 5.98
14 Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis. Lancet 2010 5.78
15 Synaptic, transcriptional and chromatin genes disrupted in autism. Nature 2014 5.30
16 Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Hum Mol Genet 2007 5.28
17 Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease. Arch Neurol 2007 5.09
18 Support for the involvement of large copy number variants in the pathogenesis of schizophrenia. Hum Mol Genet 2009 4.52
19 The beginning of the end for the Kraepelinian dichotomy. Br J Psychiatry 2005 4.51
20 The Kraepelinian dichotomy - going, going... but still not gone. Br J Psychiatry 2010 4.47
21 Genes for schizophrenia and bipolar disorder? Implications for psychiatric nosology. Schizophr Bull 2005 3.93
22 Genes for schizophrenia? Recent findings and their pathophysiological implications. Lancet 2003 3.61
23 Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth. Am J Hum Genet 2012 3.50
24 Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women. PLoS Genet 2008 3.33
25 Cis-acting variation in the expression of a high proportion of genes in human brain. Hum Genet 2003 3.07
26 Analysis of copy number variations at 15 schizophrenia-associated loci. Br J Psychiatry 2013 3.01
27 Phenotypic and genetic complexity of psychosis. Invited commentary on ... Schizophrenia: a common disease caused by multiple rare alleles. Br J Psychiatry 2007 2.97
28 Rethinking psychosis: the disadvantages of a dichotomous classification now outweigh the advantages. World Psychiatry 2007 2.82
29 Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants. Hum Mol Genet 2007 2.73
30 Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. Am J Hum Genet 2011 2.71
31 Delta-like 1 is necessary for the generation of marginal zone B cells but not T cells in vivo. Nat Immunol 2004 2.63
32 Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorder. Arch Gen Psychiatry 2005 2.58
33 Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease. PLoS One 2010 2.57
34 Agreement between maternal report and antenatal records for a range of pre and peri-natal factors: the influence of maternal and child characteristics. Early Hum Dev 2006 2.56
35 Meta-analysis shows significant association between dopamine system genes and attention deficit hyperactivity disorder (ADHD). Hum Mol Genet 2006 2.48
36 Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. Am J Psychiatry 2012 2.48
37 Paternal age and risk for schizophrenia. Br J Psychiatry 2003 2.34
38 Neurexin 1 (NRXN1) deletions in schizophrenia. Schizophr Bull 2009 2.25
39 Effects of differential genotyping error rate on the type I error probability of case-control studies. Hum Hered 2006 2.21
40 Common variants at VRK2 and TCF4 conferring risk of schizophrenia. Hum Mol Genet 2011 2.21
41 Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. Am J Psychiatry 2012 2.20
42 A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. BMC Med Genomics 2008 2.20
43 Risk of psychopathology in adolescent offspring of mothers with psychopathology and recurrent depression. Br J Psychiatry 2012 2.19
44 Genetic variation of brain-derived neurotrophic factor (BDNF) in bipolar disorder: case-control study of over 3000 individuals from the UK. Br J Psychiatry 2006 2.16
45 A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain. Am J Hum Genet 2003 2.11
46 Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia. Arch Gen Psychiatry 2010 2.11
47 Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome. Proc Natl Acad Sci U S A 2006 2.03
48 Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools. Hum Genet 2002 2.03
49 Adolescent clinical outcomes for young people with attention-deficit hyperactivity disorder. Br J Psychiatry 2010 1.99
50 Pooled DNA genotyping on Affymetrix SNP genotyping arrays. BMC Genomics 2006 1.96
51 Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness. Am J Psychiatry 2011 1.94
52 Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. Am J Hum Genet 2005 1.93
53 Genome-wide association study of schizophrenia in a Japanese population. Biol Psychiatry 2010 1.89
54 De novo rates and selection of schizophrenia-associated copy number variants. Biol Psychiatry 2011 1.87
55 Full genome screen for Alzheimer disease: stage II analysis. Am J Med Genet 2002 1.77
56 The GDP-GTP exchange factor collybistin: an essential determinant of neuronal gephyrin clustering. J Neurosci 2004 1.75
57 Medical disorders in people with recurrent depression. Br J Psychiatry 2008 1.75
58 Glycogen synthase kinase-3beta and tau genes interact in Alzheimer's disease. Ann Neurol 2008 1.74
59 The inter-relatedness and interdependence of mouse T cell receptor gammadelta+ and alphabeta+ cells. Nat Immunol 2003 1.72
60 Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression. Hum Mol Genet 2005 1.72
61 Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries. Hum Mol Genet 2010 1.72
62 DNA pooling as a tool for large-scale association studies in complex traits. Ann Med 2004 1.70
63 Shared polygenic contribution between childhood attention-deficit hyperactivity disorder and adult schizophrenia. Br J Psychiatry 2013 1.70
64 Genetics of psychosis; insights from views across the genome. Hum Genet 2009 1.68
65 Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia. Am J Med Genet B Neuropsychiatr Genet 2006 1.61
66 Phenotypic variations on the theme of CNVs. Nat Genet 2008 1.58
67 No major schizophrenia locus detected on chromosome 1q in a large multicenter sample. Science 2002 1.57
68 Maf promotes osteoblast differentiation in mice by mediating the age-related switch in mesenchymal cell differentiation. J Clin Invest 2010 1.54
69 Family aggregation of high myopia: estimation of the sibling recurrence risk ratio. Invest Ophthalmol Vis Sci 2004 1.50
70 Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease. Nat Genet 2006 1.49
71 Copy number variation in schizophrenia in the Japanese population. Biol Psychiatry 2009 1.49
72 Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13. Arch Gen Psychiatry 2005 1.48
73 The role of the major histocompatibility complex region in cognition and brain structure: a schizophrenia GWAS follow-up. Am J Psychiatry 2013 1.48
74 The ETS transcription factor GABPalpha is essential for early embryogenesis. Mol Cell Biol 2004 1.46
75 Psychosis susceptibility gene ZNF804A and cognitive performance in schizophrenia. Arch Gen Psychiatry 2010 1.46
76 An update on the genetics of schizophrenia. Curr Opin Psychiatry 2006 1.46
77 A genomewide linkage study on suicidality in major depressive disorder confirms evidence for linkage to 2p12. Am J Med Genet B Neuropsychiatr Genet 2010 1.44
78 Catatonia in DSM-5. Schizophr Res 2013 1.43
79 A network of dopaminergic gene variations implicated as risk factors for schizophrenia. Hum Mol Genet 2007 1.43
80 A genome-wide significant linkage for severe depression on chromosome 3: the depression network study. Am J Psychiatry 2011 1.41
81 The genetics of attention deficit hyperactivity disorder. Hum Mol Genet 2005 1.40
82 A replicated molecular genetic basis for subtyping antisocial behavior in children with attention-deficit/hyperactivity disorder. Arch Gen Psychiatry 2008 1.39
83 Genetic overlap between autism, schizophrenia and bipolar disorder. Genome Med 2009 1.37
84 Recent advances in the genetics of schizophrenia. Hum Mol Genet 2003 1.36
85 Chromosome 22 deletion syndrome and schizophrenia. Int Rev Neurobiol 2006 1.35
86 Stressful life events, 5-HTT genotype and risk of depression. Br J Psychiatry 2006 1.34
87 Advances in genetic findings on attention deficit hyperactivity disorder. Psychol Med 2007 1.29
88 Linkage analysis of the genetic loci for high myopia on 18p, 12q, and 17q in 51 U.K. families. Invest Ophthalmol Vis Sci 2004 1.29
89 Finding schizophrenia genes. J Clin Invest 2005 1.28
90 Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia. Schizophr Res 2011 1.28
91 Definition and description of schizophrenia in the DSM-5. Schizophr Res 2013 1.28
92 Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease. Neuromolecular Med 2004 1.26
93 Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria. Biol Psychiatry 2004 1.26
94 Whole genome linkage scan of recurrent depressive disorder from the depression network study. Hum Mol Genet 2005 1.25
95 An international collaborative family-based whole-genome linkage scan for high-grade myopia. Invest Ophthalmol Vis Sci 2009 1.25
96 Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia. Proc Natl Acad Sci U S A 2006 1.25
97 Attenuated psychosis syndrome in DSM-5. Schizophr Res 2013 1.24
98 Is the dysbindin gene (DTNBP1) a susceptibility gene for schizophrenia? Schizophr Bull 2005 1.24
99 A population-based study of shared genetic variation between premorbid IQ and psychosis among male twin pairs and sibling pairs from Sweden. Arch Gen Psychiatry 2012 1.23
100 HTR2A: association and expression studies in neuropsychiatric genetics. Ann Med 2005 1.22
101 Early postnatal death and motor disorders in mice congenitally deficient in calnexin expression. Mol Cell Biol 2002 1.22
102 Logic and justification for dimensional assessment of symptoms and related clinical phenomena in psychosis: relevance to DSM-5. Schizophr Res 2013 1.21
103 Support for neuregulin 1 as a susceptibility gene for bipolar disorder and schizophrenia. Biol Psychiatry 2008 1.20
104 Variation at the DAOA/G30 locus influences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorder. Arch Gen Psychiatry 2006 1.19
105 Genotype effects of CHRNA7, CNR1 and COMT in schizophrenia: interactions with tobacco and cannabis use. Br J Psychiatry 2007 1.19
106 Depression Case Control (DeCC) Study fails to support involvement of the muscarinic acetylcholine receptor M2 (CHRM2) gene in recurrent major depressive disorder. Hum Mol Genet 2009 1.18
107 Cannabis, COMT and psychotic experiences. Br J Psychiatry 2011 1.18
108 Isoform heterogeneity of the human gephyrin gene (GPHN), binding domains to the glycine receptor, and mutation analysis in hyperekplexia. J Biol Chem 2003 1.17
109 Structure of the psychotic disorders classification in DSM-5. Schizophr Res 2013 1.16
110 Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glycine receptor (GLRB). Hum Mol Genet 2002 1.16
111 Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease. Hum Mol Genet 2007 1.16
112 TCF4, schizophrenia, and Pitt-Hopkins Syndrome. Schizophr Bull 2010 1.15
113 Four components describe behavioral symptoms in 1,120 individuals with late-onset Alzheimer's disease. J Am Geriatr Soc 2006 1.15
114 CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. Hum Mol Genet 2013 1.14
115 Is COMT a susceptibility gene for schizophrenia? Schizophr Bull 2007 1.14
116 Schizophrenia: a genetic disorder of the synapse? BMJ 2005 1.14
117 Distribution and expression of picalm in Alzheimer disease. J Neuropathol Exp Neurol 2010 1.13
118 Schizophrenia genetics: new insights from new approaches. Br Med Bull 2009 1.11
119 High loading of polygenic risk for ADHD in children with comorbid aggression. Am J Psychiatry 2013 1.10
120 Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1). Biol Psychiatry 2005 1.10
121 Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations. Schizophr Bull 2014 1.10
122 Support for RGS4 as a susceptibility gene for schizophrenia. Biol Psychiatry 2004 1.10
123 Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk. JAMA Neurol 2013 1.09
124 Targeted disruption of the protein kinase C epsilon gene abolishes the infarct size reduction that follows ischaemic preconditioning of isolated buffer-perfused mouse hearts. Cardiovasc Res 2002 1.09
125 A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia. Hum Mol Genet 2010 1.08
126 Case-control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian population. J Hum Genet 2009 1.08
127 Association analysis of monoamine oxidase A and attention deficit hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet 2003 1.08
128 Strong evidence that GNB1L is associated with schizophrenia. Hum Mol Genet 2007 1.07
129 Identification of novel candidate genes for treatment response to risperidone and susceptibility for schizophrenia: integrated analysis among pharmacogenomics, mouse expression, and genetic case-control association approaches. Biol Psychiatry 2009 1.06
130 SGCE mutations cause psychiatric disorders: clinical and genetic characterization. Brain 2013 1.05
131 Implication of a rare deletion at distal 16p11.2 in schizophrenia. JAMA Psychiatry 2013 1.05
132 Genome-wide association study of multiplex schizophrenia pedigrees. Am J Psychiatry 2012 1.05
133 The effect of age and the H1c MAPT haplotype on MAPT expression in human brain. Neurobiol Aging 2008 1.04
134 Convergent evidence for 2',3'-cyclic nucleotide 3'-phosphodiesterase as a possible susceptibility gene for schizophrenia. Arch Gen Psychiatry 2006 1.04
135 Variation in the protocadherin gamma A gene cluster. Genomics 2003 1.03
136 Misconceptions about gene-environment interactions in psychiatry. Evid Based Ment Health 2010 1.03
137 Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease. Hum Mol Genet 2007 1.03
138 Polymorphisms in the MAOA, MAOB, and COMT genes and aggressive behavior in schizophrenia. Am J Med Genet B Neuropsychiatr Genet 2004 1.03
139 The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease. J Alzheimers Dis 2012 1.02
140 Alzheimer's disease genetics: current knowledge and future challenges. Int J Geriatr Psychiatry 2010 1.02
141 Genomewide association scan of suicidal thoughts and behaviour in major depression. PLoS One 2011 1.02
142 Genetic relationships between schizophrenia, bipolar disorder, and schizoaffective disorder. Schizophr Bull 2014 1.01
143 COL1A1 and COL2A1 genes and myopia susceptibility: evidence of association and suggestive linkage to the COL2A1 locus. Invest Ophthalmol Vis Sci 2009 1.01
144 Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples. Biol Psychiatry 2006 1.00
145 Familiality of symptom dimensions in depression. Arch Gen Psychiatry 2004 1.00
146 No association between schizophrenia and polymorphisms in COMT in two large samples. Am J Psychiatry 2005 1.00
147 Pre-TCR signaling regulates IL-7 receptor alpha expression promoting thymocyte survival at the transition from the double-negative to double-positive stage. Eur J Immunol 2003 0.99
148 Allelic expression of APOE in human brain: effects of epsilon status and promoter haplotypes. Hum Mol Genet 2004 0.99
149 A cross-sectional and a prospective study of thyroid disorders in lithium-treated patients. J Affect Disord 2005 0.98
150 Genetic differences between five European populations. Hum Hered 2010 0.98
151 Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease. Ann Neurol 2006 0.97
152 Genetic variants in the ErbB4 gene are associated with white matter integrity. Psychiatry Res 2011 0.96
153 A neuropsychological investigation of the genome wide associated schizophrenia risk variant NRGN rs12807809. Schizophr Res 2010 0.96
154 Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes. Am J Hum Genet 2013 0.96
155 De novo mutation in schizophrenia. Schizophr Bull 2012 0.95
156 Schizoaffective Disorder in the DSM-5. Schizophr Res 2013 0.95
157 SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype. J Neurol 2014 0.95
158 Association analysis of AKT1 and schizophrenia in a UK case control sample. Schizophr Res 2007 0.95
159 Permutation-based approaches do not adequately allow for linkage disequilibrium in gene-wide multi-locus association analysis. Eur J Hum Genet 2012 0.95
160 Variation in tau isoform expression in different brain regions and disease states. Neurobiol Aging 2013 0.94
161 Influence of NOS1 on verbal intelligence and working memory in both patients with schizophrenia and healthy control subjects. Arch Gen Psychiatry 2009 0.94
162 An association study of common variation at the MAPT locus with late-onset Alzheimer's disease. Am J Med Genet B Neuropsychiatr Genet 2009 0.94
163 Intellectual disability and major psychiatric disorders: a continuum of neurodevelopmental causality. Br J Psychiatry 2012 0.94
164 New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. Int J Epidemiol 2015 0.93
165 Dissecting the genetic heterogeneity of depression through age at onset. Am J Med Genet B Neuropsychiatr Genet 2012 0.93
166 Candidate gene association study of insulin signaling genes and Alzheimer's disease: evidence for SOS2, PCK1, and PPARgamma as susceptibility loci. Am J Med Genet B Neuropsychiatr Genet 2007 0.93
167 Psychopathology and cognition in children with 22q11.2 deletion syndrome. Br J Psychiatry 2013 0.92
168 Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme. Am J Med Genet B Neuropsychiatr Genet 2005 0.92
169 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 0.92
170 No evidence that extended tracts of homozygosity are associated with Alzheimer's disease. Am J Med Genet B Neuropsychiatr Genet 2011 0.91
171 Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease. Hum Genet 2003 0.91
172 Molecular investigation of TBP allele length: a SCA17 cellular model and population study. Neurobiol Dis 2003 0.90
173 Molecular genetic contribution to the developmental course of attention-deficit hyperactivity disorder. Eur Child Adolesc Psychiatry 2008 0.90
174 No evidence for association between polymorphisms in GRM3 and schizophrenia. BMC Psychiatry 2005 0.90
175 Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin. Nat Genet 2004 0.90
176 A multi-center study of ACE and the risk of late-onset Alzheimer's disease. J Alzheimers Dis 2011 0.89
177 Whole genome association study in a homogenous population in Shandong peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia. J Biomed Biotechnol 2009 0.89
178 An examination of single nucleotide polymorphism selection prioritization strategies for tests of gene-gene interaction. Biol Psychiatry 2011 0.89
179 A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk. Hum Mol Genet 2012 0.89
180 Association of serotonin and dopamine gene pathways with behavioral subphenotypes in dementia. Neurobiol Aging 2010 0.88
181 Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study. Am J Med Genet B Neuropsychiatr Genet 2014 0.88
182 No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples. Biol Psychiatry 2005 0.88
183 Schizophrenia and functional polymorphisms in the MAOA and COMT genes: no evidence for association or epistasis. Am J Med Genet 2002 0.88
184 Genotype link with extreme antisocial behavior: the contribution of cognitive pathways. Arch Gen Psychiatry 2010 0.88
185 Association study in the 5q31-32 linkage region for schizophrenia using pooled DNA genotyping. BMC Psychiatry 2008 0.88
186 Psychopathy trait scores in adolescents with childhood ADHD: the contribution of genotypes affecting MAOA, 5HTT and COMT activity. Psychiatr Genet 2009 0.88
187 Clusterin mRNA and protein in Alzheimer's disease. J Alzheimers Dis 2012 0.87
188 Association between a promoter variant in the monoamine oxidase A gene and schizophrenia. Schizophr Res 2003 0.87
189 Genetic abnormalities of chromosome 22 and the development of psychosis. Curr Psychiatry Rep 2004 0.87
190 Schizophrenia two-hit hypothesis in velo-cardio facial syndrome. Am J Med Genet B Neuropsychiatr Genet 2013 0.86
191 Reduced burden of very large and rare CNVs in bipolar affective disorder. Bipolar Disord 2013 0.86
192 Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility. Schizophr Res 2006 0.86
193 Bipolar disorder among an isolated island community in Ethiopia. J Affect Disord 2004 0.86
194 A comparison of four clustering methods for brain expression microarray data. BMC Bioinformatics 2008 0.85
195 Haplotype analysis and a novel allele-sharing method refines a chromosome 4p locus linked to bipolar affective disorder. Biol Psychiatry 2006 0.85
196 The synapse in schizophrenia. Eur J Neurosci 2014 0.85
197 Data and clinical utility should be the drivers of changes to psychiatric classification. Br J Psychiatry 2010 0.84
198 New findings from genetic association studies of schizophrenia. J Hum Genet 2009 0.84
199 No evidence of association between Catechol-O-Methyltransferase (COMT) Val158Met genotype and performance on neuropsychological tasks in children with ADHD: a case-control study. BMC Psychiatry 2004 0.84
200 A single nucleotide polymorphism in CHAT influences response to acetylcholinesterase inhibitors in Alzheimer's disease. Pharmacogenet Genomics 2006 0.83
201 Case-control association study of 65 candidate genes revealed a possible association of a SNP of HTR5A to be a factor susceptible to bipolar disease in Bulgarian population. J Affect Disord 2009 0.83
202 Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples. Am J Med Genet B Neuropsychiatr Genet 2009 0.83
203 Variation at the GABAA receptor gene, Rho 1 (GABRR1) associated with susceptibility to bipolar schizoaffective disorder. Am J Med Genet B Neuropsychiatr Genet 2010 0.83
204 Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1. Hum Mol Genet 2008 0.83
205 Psychopathy traits in adolescents with childhood attention-deficit hyperactivity disorder. Br J Psychiatry 2009 0.82
206 TBP, a polyglutamine tract containing protein, accumulates in Alzheimer's disease. Brain Res Mol Brain Res 2004 0.82
207 Phenotypic variation between parent-offspring trios and non-trios in genetic studies of schizophrenia. J Psychiatr Res 2005 0.82
208 Trajectories of change in self-reported psychotic-like experiences in childhood and adolescence. Schizophr Res 2012 0.82
209 Candidate gene association studies of the alpha 4 (CHRNA4) and beta 2 (CHRNB2) neuronal nicotinic acetylcholine receptor subunit genes in Alzheimer's disease. Neurosci Lett 2004 0.82
210 The internet is parents' main source of information about psychiatric manifestations of 22q11.2 deletion syndrome (22q11.2DS). Eur J Med Genet 2013 0.82
211 Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD. Am J Med Genet B Neuropsychiatr Genet 2004 0.82
212 Familiality of clinical characteristics in schizophrenia. J Psychiatr Res 2002 0.81
213 A family based study implicates solute carrier family 1-member 3 (SLC1A3) gene in attention-deficit/hyperactivity disorder. Biol Psychiatry 2005 0.81
214 Visuospatial working memory in children and adolescents with 22q11.2 deletion syndrome; an fMRI study. J Neurodev Disord 2009 0.81
215 Mosaic copy number variation in schizophrenia. Eur J Hum Genet 2013 0.81
216 Association analysis of the HOPA12bp polymorphism in schizophrenia and manic depressive illness. Am J Med Genet B Neuropsychiatr Genet 2003 0.80
217 Association between TCF4 and schizophrenia does not exert its effect by common nonsynonymous variation or by influencing cis-acting regulation of mRNA expression in adult human brain. Am J Med Genet B Neuropsychiatr Genet 2011 0.80
218 Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31. Bipolar Disord 2009 0.80
219 Linkage disequilibrium mapping of bipolar affective disorder at 12q23-q24 provides evidence for association at CUX2 and FLJ32356. Am J Med Genet B Neuropsychiatr Genet 2005 0.79
220 DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder. PLoS One 2012 0.79
221 The interaction between child maltreatment, adult stressful life events and the 5-HTTLPR in major depression. J Psychiatr Res 2013 0.79
222 Failure to confirm association between PIK4CA and psychosis in 22q11.2 deletion syndrome. Am J Med Genet B Neuropsychiatr Genet 2010 0.78
223 Absence of de novo point mutations in exons of GRIN2B in a large schizophrenia trio sample. Schizophr Res 2012 0.78
224 Memory for new information as a cognitive marker of liability to Alzheimer's disease in a high risk group: a research note. Int J Geriatr Psychiatry 2003 0.78
225 No evidence of association of two 5HT transporter gene polymorphisms and attention deficit hyperactivity disorder. Psychiatr Genet 2003 0.78
226 A regulatory monoamine oxidase a promoter polymorphism and personality traits. Neuropsychobiology 2002 0.78
227 Genome scans and microarrays: converging on genes for schizophrenia? Genome Biol 2002 0.78
228 COMT Val(158) met genotype and striatal D(2/3) receptor binding in adults with 22q11 deletion syndrome. Synapse 2011 0.77
229 Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13? Am J Med Genet B Neuropsychiatr Genet 2008 0.77
230 The future of psychiatric genetics. Ann Med 2003 0.77
231 Molecular genetics and the relationship between epilepsy and psychosis. Br J Psychiatry 2010 0.77
232 The Research Domain Criteria: moving the goalposts to change the game. Br J Psychiatry 2014 0.77
233 Analysis of neurogranin (NRGN) in schizophrenia. Am J Med Genet B Neuropsychiatr Genet 2011 0.77
234 Modeling hydrophobic recovery of electrically discharged polydimethylsiloxane elastomers. J Colloid Interface Sci 2005 0.76
235 Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia. Am J Med Genet B Neuropsychiatr Genet 2011 0.76
236 Mutational analysis of two positional candidate susceptibility genes for bipolar disorder on chromosome 12q23-q24: phenylalanine hydroxylase and human LIM-homeobox LHX5. Psychiatr Genet 2003 0.76
237 Exploring the indirect effects of catechol-O-methyltransferase (COMT) genotype on psychotic experiences through cognitive function and anxiety disorders in a large birth cohort of children. Am J Med Genet B Neuropsychiatr Genet 2014 0.76
238 Genetics and the brain: many pathways to enlightenment. Hum Genet 2009 0.76
239 Analysis of copy number variation using quantitative interspecies competitive PCR. Nucleic Acids Res 2008 0.76
240 Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutation. Psychiatr Genet 2016 0.76
241 Non-random mating, parent-of-origin, and maternal-fetal incompatibility effects in schizophrenia. Schizophr Res 2012 0.76
242 Genetic variation in the seven-pass transmembrane cadherin CELSR1: lack of association with schizophrenia. Psychiatr Genet 2003 0.76
243 No evidence of association between HLA-DRB1 and attention deficit hyperactivity disorder. Psychiatr Genet 2003 0.76
244 The health informatics cohort enhancement project (HICE): using routinely collected primary care data to identify people with a lifetime diagnosis of psychotic disorder. BMC Res Notes 2012 0.75
245 It is time to take a stand for medical research and against terrorism targeting medical scientists. Biol Psychiatry 2008 0.75
246 Specific parental depression symptoms as risk markers for new-onset depression in high-risk offspring. J Clin Psychiatry 2013 0.75
247 Polymorphisms in the phosphate and tensin homolog gene are not associated with late-onset Alzheimer's disease. Neurosci Lett 2006 0.75
248 Major psychiatric disorders and the serotonin transporter gene (SLC6A4): family-based association studies. Psychiatr Genet 2002 0.75