Research Topics
Genomes and Genes
| Michael J OwenSummaryAffiliation: Cardiff University Country: UK Publications
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Detail Information
Publications
Recent advances in the genetics of schizophreniaMichael C O'Donovan
Department of Psychological Medicine, University of Wales College of Medicine, Cardiff
Hum Mol Genet 12:R125-33. 2003....
No association between schizophrenia and polymorphisms in COMT in two large samplesHywel J Williams
Department of Psychological Medicine, Henry Wellcome Building for Biomedical Research, Cardiff University, Heath Park, Cardiff, CF14 4XN, UK
Am J Psychiatry 162:1736-8. 2005..The authors examined these hypotheses...
Convergent evidence for 2',3'-cyclic nucleotide 3'-phosphodiesterase as a possible susceptibility gene for schizophreniaTimothy R Peirce
Department of Psychological Medicine, School of Medicine, Cardiff University, Cardiff, Wales
Arch Gen Psychiatry 63:18-24. 2006..However, it is unclear whether the observed changes in the schizophrenic brain are primary or secondary...
Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibilityBeate Glaser
Department of Psychological Medicine, Cardiff University, Heath Park, Cardiff, UK, and Department of Psychiatry, Royal College of Surgeons in Ireland, Education and Research Centre, Beaumont Hospital, Dublin, Ireland
Schizophr Res 87:21-7. 2006..Our data do not support the hypothesis that an interaction between these genes influences susceptibility to schizophrenia...
Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorderElaine K Green
Department of Psychological Medicine and Biostatics and Bioinformatics Unit, University of Wales College of Medicine, Cardiff
Arch Gen Psychiatry 62:642-8. 2005..The most consistent finding has been that one particular haplotype (the "core" haplotype) is overrepresented in cases compared with control subjects...
Linkage disequilibrium mapping of bipolar affective disorder at 12q23-q24 provides evidence for association at CUX2 and FLJ32356Beate Glaser
Department of Psychological Medicine, University of Wales College of Medicine, Heath Park, Cardiff CF4 4XN, Wales, UK
Am J Med Genet B Neuropsychiatr Genet 132:38-45. 2005..Our data provide evidence for association between bipolar mood disorder and markers on chromosome 12q23-q24 but need replication in independent samples...
Genotype effects of CHRNA7, CNR1 and COMT in schizophrenia: interactions with tobacco and cannabis useStanley Zammit
Department of Psychological Medicine, Cardiff University, Heath Park, Cardiff, UK
Br J Psychiatry 191:402-7. 2007..Genetic variations might modify associations between schizophrenia and cannabis or tobacco use...
No evidence for association between polymorphisms in GRM3 and schizophreniaNadine Norton
Department of Psychological Medicine, Wales School of Medicine, Henry Wellcome Building, Cardiff University, Heath Park, Cardiff, UK
BMC Psychiatry 5:23. 2005..Three studies have previously reported data that were interpreted by the authors as supportive of association between schizophrenia and polymorphisms in the gene encoding the metabotropic glutamate receptor GRM3...
No evidence of association of two 5HT transporter gene polymorphisms and attention deficit hyperactivity disorderKate Langley
Department of Psychological Medicine, University of Wales College of Medicine, Cardiff, UK
Psychiatr Genet 13:107-10. 2003..In an attempt to replicate these findings, we examined this polymorphism and a variable number tandem repeat in the second intron of 5-HTT for association with ADHD...
Support for RGS4 as a susceptibility gene for schizophreniaNigel M Williams
Department of Psychological Medicine, University of Wales College of Medicine, Cardiff, United Kingdom
Biol Psychiatry 55:192-5. 2004..Although the original report was highly suggestive, a limitation was that the study was conducted on rather small samples...
A family based study implicates solute carrier family 1-member 3 (SLC1A3) gene in attention-deficit/hyperactivity disorderDarko Turic
Department of Psychological Medicine, Cardiff University, School of Medicine, Heath Park, Cardiff, United Kingdom
Biol Psychiatry 57:1461-6. 2005..SLC1A3 is thus both a functional and positional candidate gene for ADHD...
Phenotypic variation between parent-offspring trios and non-trios in genetic studies of schizophreniaStanley Zammit
Department of Psychological Medicine, Cardiff University, Heath Park, Cardiff, CF14 4XN, UK
J Psychiatr Res 40:622-6. 2006....
Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from BulgariaGeorge Kirov
Department of Psychological Medicine, University of Wales College of Medicine, Cardiff, United Kingdom
Biol Psychiatry 55:971-5. 2004..We tried to replicate these findings in a sample of 488 parent-proband trios recruited in Bulgaria. Probands had a diagnosis of schizophrenia (n = 441) or schizoaffective disorder (n = 47)...
Localization of bipolar susceptibility locus by molecular genetic analysis of the chromosome 12q23-q24 region in two pedigrees with bipolar disorder and Darier's diseaseElaine Green
Department of Psychological Medicine, University of Wales College of Medicine, Heath Park, Cardiff, Wales, UK
Am J Psychiatry 162:35-42. 2005..Further molecular genetic analysis of this region is required to identify the gene(s)...
Polymorphisms in the MAOA, MAOB, and COMT genes and aggressive behavior in schizophreniaStanley Zammit
Department of Psychological Medicine, University of Wales College of Medicine, Cardiff CF14 4XN, Wales, United Kingdom
Am J Med Genet B Neuropsychiatr Genet 128:19-20. 2004..These results fail to support the theory that functional polymorphisms within the MAOA, MAOB, or COMT genes, as determinants of catecholamine enzymatic activity, are risk factors for aggressive behavior...
Four components describe behavioral symptoms in 1,120 individuals with late-onset Alzheimer's diseasePaul Hollingworth
Department of Psychological Medicine, Cardiff University School of Medicine, Heath Park, Cardiff, United Kingdom
J Am Geriatr Soc 54:1348-54. 2006..CONCLUSION: Four behavioral components were identified that were comparable with those observed previously. Future analysis of these components will strengthen understanding of the underlying pathology of behavioral symptoms and AD...
Identification of loci associated with schizophrenia by genome-wide association and follow-upMichael C O'Donovan
Department of Psychological Medicine, School of Medicine, Cardiff University, Cardiff, UK
Nat Genet 40:1053-5. 2008..Meta-analysis provided strongest evidence for association around ZNF804A (P = 1.61 x 10(-7)) and this strengthened when the affected phenotype included bipolar disorder (P = 9.96 x 10(-9))...
Allelic expression of APOE in human brain: effects of epsilon status and promoter haplotypesNicholas J Bray
Department of Psychological Medicine, School of Medicine, Cardiff University, Cardiff, UK
Hum Mol Genet 13:2885-92. 2004..02). Our data indicate that, in human brain, most of the cis-acting variance in APOE expression is accounted for by the epsilon4 haplotype, but there are additional, small, cis-acting influences associated with promoter genotype...
No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samplesBeate Glaser
Department of Psychological Medicine, Cardiff University, Cardiff, United Kingdom
Biol Psychiatry 58:78-80. 2005..It has been recently reported that a functional variant in the ZDHHC8 gene encoding a putative palmitoyltransferase directly confers susceptibility to schizophrenia in females ()...
A single nucleotide polymorphism in CHAT influences response to acetylcholinesterase inhibitors in Alzheimer's diseaseDenise Harold
Department of Psychological Medicine, Cardiff University, Cardiff, UK
Pharmacogenet Genomics 16:75-7. 2006..Treatment with acetylcholinesterase (AChE) inhibitors aims to reverse this deficit and does ameliorate the decline in cognition in some AD patients, although response is variable...
Support for the involvement of large copy number variants in the pathogenesis of schizophreniaGeorge Kirov
Department of Psychological Medicine, Cardiff University, Heath Park, Cardiff, UK
Hum Mol Genet 18:1497-503. 2009..2 and schizophrenia (P = 0.026). This study confirms the involvement of rare CNVs in the pathogenesis of schizophrenia and contributes to the growing list of specific CNVs that are implicated...
A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brainNicholas J Bray
Department of Psychological Medicine, University of Wales College of Medicine, Cardiff, CF14 4XN, Wales, UK
Am J Hum Genet 73:152-61. 2003....
Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexiaNatalie Cope
Department of Psychological Medicine, Wales College of Medicine, Cardiff University, Cardiff, United Kingdom
Am J Hum Genet 76:581-91. 2005..006 in trios; 1-degree-of-freedom tests). Our data strongly implicate KIAA0319 as a susceptibility gene for dyslexia. The gene product is expressed in brain, but its specific function is currently unknown...
Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's diseaseDenise Harold
Department of Psychological Medicine, University of Wales College of Medicine, CF14 4XN, Cardiff, UK
Hum Genet 113:258-67. 2003..Levels of linkage disequilibrium were generally low across the CHAT locus but two of the coding variants, D7N and A120T, proved to be in complete linkage disequilibrium...
Advances in genetic findings on attention deficit hyperactivity disorderAnita Thapar
Department of Psychological Medicine, School of Medicine, Cardiff University, Cardiff, UK
Psychol Med 37:1681-92. 2007....
Association analysis of the HOPA12bp polymorphism in schizophrenia and manic depressive illnessGeorge Kirov
Neuropsychiatric Genetics Unit, Department of Psychological Medicine, University of Wales College of Medicine, Tenovus Building, Heath Park, Cardiff CF144 4XN, Wales, UK
Am J Med Genet B Neuropsychiatr Genet 118:16-9. 2003..6%, P = 0.6. We conclude that the HOPA polymorphism is unlikely to be a major risk factor in the pathogenesis of these major psychiatric disorders although there could be a small effect in schizophrenia...
Association analysis of monoamine oxidase A and attention deficit hyperactivity disorderDeborah C Lawson
Department of Psychologycal Medicine, University of Wales College of Medicine, Cardiff, United Kingdom
Am J Med Genet B Neuropsychiatr Genet 116:84-9. 2003..0, 95% CI = 1.09, 3.5), and TDT analysis indicated a statistical trend toward association. Our findings highlight the importance of phenotype definition and the need for the MAOA VNTR to be further examined...
Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31Marian L Hamshere
Department of Psychological Medicine, The Henry Wellcome Building for Biomedical Research in Wales, Cardiff, CF14 4XN, UK
Bipolar Disord 11:610-20. 2009..Findings in recent association studies at two specific genes suggest that the occurrence of mood-incongruent psychotic features may indicate a relatively homogeneous subset of the bipolar phenotype. We examined this hypothesis...
Schizophrenia and functional polymorphisms in the MAOA and COMT genes: no evidence for association or epistasisNadine Norton
Department of Psychological Medicine, University of Wales College of Medicine, Heath Park, Cardiff CF4 4XN, UK
Am J Med Genet 114:491-6. 2002..Our data, therefore, do not support the hypothesis that genetic variation in MAOA and COMT is involved individually or in combination in the etiology of schizophrenia...
Psychopathy traits in adolescents with childhood attention-deficit hyperactivity disorderTom Fowler
Department of Psychological Medicine, Cardiff University, Cardiff, UK
Br J Psychiatry 194:62-7. 2009..Children with attention-deficit hyperactivity disorder (ADHD) are thought to be at higher risk of psychopathy. Early biological and social adversity may contribute to this risk...
No evidence of association between Catechol-O-Methyltransferase (COMT) Val158Met genotype and performance on neuropsychological tasks in children with ADHD: a case-control studySophie Mills
Department of Psychological Medicine, University of Wales College of Medicine, Cardiff, CF14 4XN, UK
BMC Psychiatry 4:15. 2004..Two studies showed that subjects with the low activity Met allele performed better on the Wisconsin Card Sorting Test (WCST) and another study found an effect on processing speed and attention...
Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1)Rachel Raybould
Department of Psychological Medicine, Wales College of Medicine, Cardiff University, Cardiff, Wales, UK
Biol Psychiatry 57:696-701. 2005..We previously reported that variation at a specific 3-locus haplotype influences susceptibility to schizophrenia in a large United Kingdom (UK) Caucasian case-control sample...
The genetic deconstruction of psychosisMichael J Owen
Department of Psychological Medicine, The School of Medicine, Cardiff University, Cardiff, UK
Schizophr Bull 33:905-11. 2007....
An update on the genetics of schizophreniaNadine Norton
Department of Psychological Medicine, Wales School of Medicine, Cardiff University, Heath Park, Cardiff, UK
Curr Opin Psychiatry 19:158-64. 2006..This paper reviews recent molecular genetic studies of schizophrenia and evaluates claims implicating specific genes as susceptibility loci...
Molecular genetic contribution to the developmental course of attention-deficit hyperactivity disorderKate Langley
Department of Psychological Medicine, School of Medicine, Cardiff University, Heath Park, Cardiff, CF14 4XN, UK
Eur Child Adolesc Psychiatry 18:26-32. 2009....
Dysbindin-1 and schizophrenia: from genetics to neuropathologyMichael J Owen
Department of Psychological Medicine, University of Wales College of Medicine, Cardiff, United Kingdom
J Clin Invest 113:1255-7. 2004..Further studies of dysbindin-1 and the proteins with which it interacts can be expected to throw light on the pathogenesis of schizophrenia...
DNA pooling as a tool for large-scale association studies in complex traitsNadine Norton
Department of Psychological Medicine, University of Wales College of Medicine, Cardiff, UK
Ann Med 36:146-52. 2004..Here, we consider the main points in study design, and illustrate the application of pooling using psychiatric phenotypes as an example...
A comparison of four clustering methods for brain expression microarray dataAlexander L Richards
Department of Psychological Medicine, School of Medicine, University Hospital Wales, Heath Park, Cardiff, Wales, UK
BMC Bioinformatics 9:490. 2008..The results are compared on speed, gene coverage and GO enrichment. The effects of combining the clusters produced by each method are also assessed...
Finding schizophrenia genesGeorge Kirov
Department of Psychological Medicine, Wales College of Medicine, Cardiff University, Cardiff, United Kingdom
J Clin Invest 115:1440-8. 2005..These findings are grounds for optimism that insight into genetic factors associated with schizophrenia will help further our understanding of this disease and contribute to the development of new ways to treat it...
Familiality of symptom dimensions in depressionAnia Korszun
Department of Psychological Medicine, University of Wales College of Medicine, Cardiff, United Kingdom
Arch Gen Psychiatry 61:468-74. 2004..A dimensional rather than a categorical approach to depressive phenotype definition may be more useful for identification of susceptibility genes...
New findings from genetic association studies of schizophreniaHywel J Williams
Department of Psychological Medicine, School of Medicine, Cardiff Universty, Heath Park, Cardiff, UK
J Hum Genet 54:9-14. 2009....
Genetic abnormalities of chromosome 22 and the development of psychosisNigel M Williams
Department of Psychological Medicine, Henry Wellcome Building for Biomedical Research, University of Wales College of Medicine, Cardiff CF14 4XN, Wales, UK
Curr Psychiatry Rep 6:176-82. 2004..However, although a number of genes have been implicated as possible schizophrenia susceptibility loci, further confirmatory studies are required...
Chromosome 22 deletion syndrome and schizophreniaNigel M Williams
Department of Psychological Medicine, Henry Wellcome Building for Biomedical Research, College of Medicine, Cardiff University, Cardiff, United Kingdom
Int Rev Neurobiol 73:1-27. 2006
Analysis of copy number variation using quantitative interspecies competitive PCRNigel M Williams
Department of Psychological Medicine, Wales School of Medicine, Cardiff University, Heath Park, Cardiff CF14 4XN, UK
Nucleic Acids Res 36:e112. 2008....
Association analysis of AKT1 and schizophrenia in a UK case control sampleNadine Norton
Department of Psychological Medicine, Wales School of Medicine, Henry Wellcome Building, Cardiff University, Heath Park, Cardiff CF14 4XN, UK
Schizophr Res 93:58-65. 2007..Examination of our own data and those of other groups leads us to conclude that overall, the evidence for association of AKT1 as a susceptibility gene for schizophrenia is weakly positive, but not yet convincing...
Genetics of psychosis; insights from views across the genomeMichael C O'Donovan
Department of Psychological Medicine and Neurology, MRC Centre for Neuropsychiatric Genetics and Genomics, School of Medicine, Heath Park, Cardiff CF23 6BQ, UK
Hum Genet 126:3-12. 2009..They also provide grounds for optimism that larger studies will reveal more about the origins of these disorders, although currently, very little of the genetic risk of either disorder is explained...
Genetic overlap between autism, schizophrenia and bipolar disorderLiam S Carroll
MRC Centre for Neuropsychiatric Genetics and Genomics, Department of Psychological Medicine and Neurology, Cardiff University, Henry Wellcome Building, Heath Park, Cardiff CF14 4XN, UK
Genome Med 1:102. 2009....
Variation at the GABAA receptor gene, Rho 1 (GABRR1) associated with susceptibility to bipolar schizoaffective disorderElaine K Green
Department of Psychological Medicine and Neurology, MRC Centre for Neuropsychiatric Genetics and Genomics, School of Medicine, Cardiff University, Heath Park, Cardiff, United Kingdom
Am J Med Genet B Neuropsychiatr Genet 153:1347-9. 2010..Here we provide suggestive evidence implicating a sixth member of the gene family, GABRR1 (gene-wide Pā=ā0.0058; experiment-wide corrected significance Pā=ā0.052)...
Strong evidence that GNB1L is associated with schizophreniaNigel M Williams
Department of Psychological Medicine, Wales School of Medicine, Cardiff University, Heath Park, Cardiff CF14 4XN, UK
Hum Mol Genet 17:555-66. 2008..However, other explanations are possible, and further analyses will be required to clarify the correct functional mechanism...
Is the dysbindin gene (DTNBP1) a susceptibility gene for schizophrenia?Nigel M Williams
Department of Psychological Medicine, Cardiff University, UK
Schizophr Bull 31:800-5. 2005....
The future of psychiatric geneticsMarianne B M van den Bree
Department of Psychological Medicine, University of Wales, College of Medicine, Heath Park, Cardiff CF14 4XN, UK
Ann Med 35:122-34. 2003..In this article, we consider the difficulties that complex diseases pose to genetic research, discuss progress and make suggestions regarding future directions...
HTR2A: association and expression studies in neuropsychiatric geneticsNadine Norton
Department of Psychological Medicine, Henry Wellcome Building, Wales School of Medicine, Heath Park, Cardiff CF14 4XN, UK
Ann Med 37:121-9. 2005..In this review we examine and summarize these findings in various neuropsychiatric phenotypes...
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysisNigel M Williams
MRC Centre in Neuropsychiatric Genetics and Genomics and Department of Psychological Medicine and Neurology, Cardiff University School of Medicine, Cardiff, UK
Lancet 376:1401-8. 2010..We aimed to establish whether burden of CNVs was increased in ADHD, and to investigate whether identified CNVs were enriched for loci previously identified in autism and schizophrenia...
Genome scans and microarrays: converging on genes for schizophrenia?Nigel M Williams
Department of Psychological Medicine, Neuropsychiatric Genetics Unit, University of Wales College of Medicine, Cardiff, CF14 4XN, UK
Genome Biol 3:REVIEWS1011. 2002..Microarray expression analysis may identify new candidate genes and pathways, and a number of intriguing preliminary findings have already been reported...
Bipolar disorder among an isolated island community in EthiopiaAbebaw Fekadu
Department of Psychological Medicine, University of Wales College Medicine, Cardiff, UK
J Affect Disord 80:1-10. 2004..The Zeway islanders have lived in geographic and cultural isolation for over three centuries...
Memory for new information as a cognitive marker of liability to Alzheimer's disease in a high risk group: a research noteFrances Rice
Department of Psychological Medicine, 4th Floor, University of Wales College of Medicine, Heath Park, Cardiff CF14 4XN, Wales, UK
Int J Geriatr Psychiatry 18:155-60. 2003..The development of Alzheimer's disease (AD) is often insidious and there is evidence that pre-morbid neuropsychological deficits exist...
Genomic approaches to schizophreniaMichael J Owen
Department of Psychological Medicine, School of Medicine, Wales College of Medicine, Heath Park, Cardiff, United Kingdom
Clin Ther 27:S2-7. 2005..However, like other common disorders, the mode of transmission is complex and probably reflects oligogenic inheritance against a polygenic background...
Cis-acting variation in the expression of a high proportion of genes in human brainNicholas J Bray
Department of Psychological Medicine, University of Wales College of Medicine, Heath Park, Cardiff, CF14 4XN, UK
Hum Genet 113:149-53. 2003....
Universal, robust, highly quantitative SNP allele frequency measurement in DNA poolsNadine Norton
Department of Psychological Medicine, University of Wales College of Medicine, Heath Park, Cardiff CF14 4XN, UK
Hum Genet 110:471-8. 2002..Our assay conditions are generalisable, universal, robust and, therefore, for the first time, permit high-throughput association analysis at a realistic cost...
Paternal age and risk for schizophreniaStanley Zammit
Department of Psychological Medicine, University of Wales College of Medicine, Cardiff, UK
Br J Psychiatry 183:405-8. 2003....
Wake-up call for British psychiatryNick Craddock
Department of Psychological Medicine, Medical School, Cardiff University, Heath Park, Cardiff, UK
Br J Psychiatry 193:6-9. 2008..On the 200th birthday of psychiatry, it is fitting to reconsider the specialty's core values and renew efforts to use psychiatric skills for the maximum benefit of patients...
Mutational analysis of two positional candidate susceptibility genes for bipolar disorder on chromosome 12q23-q24: phenylalanine hydroxylase and human LIM-homeobox LHX5Elaine K Green
Molecular Psychiatry Group, Division of Neuroscience, University of Birmingham, Queen Elizabeth Psychiatric Hospital, Birmingham, UK
Psychiatr Genet 13:97-101. 2003..1; pedigree 5501, maximum LOD=3.6)...
Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's diseaseYonghong Li
Celera, 1401 Harbor Bay Parkway, Alameda, CA 94502, USA
Hum Mol Genet 17:759-67. 2008..These data implicate NEDD9 as a novel susceptibility gene for LOAD and possibly PD...
A replicated molecular genetic basis for subtyping antisocial behavior in children with attention-deficit/hyperactivity disorderAvshalom Caspi
Medical Research Council Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, King s College London, London, England
Arch Gen Psychiatry 65:203-10. 2008..Attention-deficit/hyperactivity disorder (ADHD) is a heterogeneous neurodevelopmental disorder that in some cases is accompanied by antisocial behavior...
Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in womenSagiv Shifman
Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kindgdom
PLoS Genet 4:e28. 2008..58 (p = 8.8 x 10(-7); p = 1.6 x 10(-5) for gene-sex interaction). The female-specific association between RELN and schizophrenia is one of the few examples of a replicated sex-specific genetic association in any disease...
Association study in the 5q31-32 linkage region for schizophrenia using pooled DNA genotypingIrina Zaharieva
Department of Psychological Medicine, School of Medicine, Cardiff University, Heath Park, Cardiff CF14 4XN, UK
BMC Psychiatry 8:11. 2008..Several linkage studies suggest that chromosome 5q31-32 might contain risk loci for schizophrenia (SZ). We wanted to identify susceptibility genes for schizophrenia within this region...
Common variants near MC4R are associated with fat mass, weight and risk of obesityRuth J F Loos
MRC Epidemiology Unit, Addenbrooke s Hospital, Cambridge CB2 0QQ, UK
Nat Genet 40:768-75. 2008....
Support for neuregulin 1 as a susceptibility gene for bipolar disorder and schizophreniaLyudmila Georgieva
Department of Psychological Medicine, School of Medicine, Cardiff University, Heath Park, Cardiff CF14 4XN, United Kingdom
Biol Psychiatry 64:419-27. 2008..We wished to investigate further the involvement of NRG1 in schizophrenia and bipolar disorder...
Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer diseaseHao Li
GlaxoSmithKline, Research Triangle Park, North Carolina, USA
Arch Neurol 65:45-53. 2008..To identify single-nucleotide polymorphisms (SNPs) associated with risk and age at onset of Alzheimer disease (AD) in a genomewide association study of 469 438 SNPs...
Rare chromosomal deletions and duplications increase risk of schizophreniaJennifer L Stone
Nature 455:237-41. 2008..Our results provide strong support for a model of schizophrenia pathogenesis that includes the effects of multiple rare structural variants, both genome-wide and at specific loci...
Major psychiatric disorders and the serotonin transporter gene (SLC6A4): family-based association studiesAlbena Dimitrova
Department of Medical Genetics, Medical University Sofia, University Hospital Maichin Dom, Sofia, Bulgaria
Psychiatr Genet 12:137-41. 2002..2). The VNTR polymorphism in the 5-HTT gene does not appear to be a major risk factor for increasing susceptibility to major psychiatric disorders...
Genes for schizophrenia? Recent findings and their pathophysiological implicationsPaul J Harrison
University of Oxford Department of Psychiatry, Neurosciences Building, Warneford Hospital, OX3 7JX, Oxford, UK
Lancet 361:417-9. 2003..Confirmation that any of the genes is a true susceptibility gene for schizophrenia could trigger the same rapid therapeutic progress as has occurred recently in Alzheimer's disease...
Association between a promoter variant in the monoamine oxidase A gene and schizophreniaErik G Jonsson
Department of Clinical Neuroscience, Psychiatry Section, HUBIN project, Karolinska Institute and Hospital, R5 00, SE 171 76 Stockholm, Sweden
Schizophr Res 61:31-7. 2003..05). In women, no significant differences were found. The present results support the involvement of the MAOA gene in men with schizophrenia in the investigated Swedish population but should be interpreted with caution until replicated...
Genetic variation in the seven-pass transmembrane cadherin CELSR1: lack of association with schizophreniaLyudmila Georgieva
Department of Medical Genetics, Medical University Sofia, Sofia, Bulgaria
Psychiatr Genet 13:103-6. 2003..31, a region in which evidence for linkage to schizophrenia has been reported. The gene has an unusually large first exon of 3544 nucleotides, which encodes the signal peptide and all nine ectodomains in the protein...
A network of dopaminergic gene variations implicated as risk factors for schizophreniaMichael E Talkowski
Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA
Hum Mol Genet 17:747-58. 2008..Our data suggest that a network of dopaminergic polymorphisms increase risk for SZ...
Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset ADAmanda J Myers
Department of Psychiatry, Washington University School of Medicine, St Louis, Missouri, USA
Am J Med Genet B Neuropsychiatr Genet 124:29-37. 2004..Eight polymorphisms spanning the entire gene were examined using case control (CC) and family-based association methods. No association was observed by any method making it unlikely that variation in PLAU explains our linkage data...
Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophreniaLyudmila Georgieva
Department of Psychological Medicine, Cardiff University School of Medicine, Heath Park, Cardiff CF14 4XN, United Kingdom
Proc Natl Acad Sci U S A 103:12469-74. 2006..Our data provide strong convergent evidence that variation in OLIG2 confers susceptibility to schizophrenia alone and as part of a network of genes implicated in oligodendrocyte function...
Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's diseaseScott Smemo
Department of Psychiatry, Washington University School of Medicine, 660 S Euclid Street, St Louis, MO 63110, USA
Ann Neurol 59:21-6. 2006..We did not find any evidence that this single nucleotide polymorphism, or any of six others tested in UBQLN1, increases risk for LOAD...
Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13Marian L Hamshere
Department of Psychological Medicine, School of Medicine, Cardiff University, Wales
Arch Gen Psychiatry 62:1081-8. 2005..Follow-up of this region should use samples enriched for cases of schizoaffective disorder. Our findings have similar implications for the search for genetic variation on chromosome 22q11 that influences susceptibility to psychosis...
Effects of differential genotyping error rate on the type I error probability of case-control studiesValentina Moskvina
Bioinformatics and Biostatistics Unit, School of Medicine, Wales College of Medicine, Cardiff University, Cardiff, UK
Hum Hered 61:55-64. 2006....
Variation at the DAOA/G30 locus influences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorderNigel M Williams
Department of Psychological Medicine and Biostatistics and Bioinformatics Unit, Wales School of Medicine, Cardiff University
Arch Gen Psychiatry 63:366-73. 2006..Variation at the DAOA/G30 locus has been described to be associated with both schizophrenia and bipolar disorder, but there is little consistency between studies of the tested polymorphisms or variants showing association...
Polymorphisms in the phosphate and tensin homolog gene are not associated with late-onset Alzheimer's diseaseGillian Hamilton
MRC Centre for Neurodegeneration Research, Department of Neuroscience, Institute of Psychiatry, Kings College London, Denmark Hill, London SE5 8AF, UK
Neurosci Lett 401:77-80. 2006..Our results suggest that it is unlikely that genetic variation within the PTEN gene contributes to risk of LOAD...
Pooled DNA genotyping on Affymetrix SNP genotyping arraysGeorge Kirov
Department of Psychological Medicine, Henry Wellcome Building, Cardiff University, Heath Park, Cardiff CF14 4XN, UK
BMC Genomics 7:27. 2006..However, thus far, this conclusion is based upon published data concerning only a small number of SNPs...
Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophreniaNadine Norton
Department of Psychological Medicine, Wales School of Medicine, Heath Park, Cardiff CF14 4XN, Wales, UK
Am J Med Genet B Neuropsychiatr Genet 141:96-101. 2006....
Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variantsAndrew Grupe
Celera Diagnostics, 1401 Harbor Bay Parkway, Alameda, CA 94502, USA
Hum Mol Genet 16:865-73. 2007..This is a missense mutation in the galanin-like peptide precursor gene (P = 0.00005, OR = 1.2, false positive rate = 0.87)...
Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expressionNicholas J Bray
Department of Psychological Medicine, School of Medicine, Cardiff University, Heath Park, UK
Hum Mol Genet 14:1947-54. 2005..Our data indicate that variation in the DTNBP1 gene confers susceptibility to schizophrenia through reduced expression, and that this, therefore, represents a primary aetiological mechanism in the disorder...
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 diseaseVictoria Busby
Department of Neuroscience, Institute of Psychiatry, De Crespigny Park, London SE5 8AF, United Kingdom
Neuromolecular Med 5:133-46. 2004..None of these SNPs was associated with disease. Although an excellent candidate, we conclude that CTNNA3 is unlikely to account for the AD susceptibility locus on chromosome 10...
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variantsPaul R Burton
Genetic Epidemiology Group, Department of Health Sciences, University of Leicester, Adrian Building, University Road, Leicester LE1 7RH, UK
Nat Genet 39:1329-37. 2007....
Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's diseaseMarian L Hamshere
Biostatistics and Bioinformatics Unit, School of Medicine, Cardiff University, Heath Park, Cardiff CF14 4XN, UK
Hum Mol Genet 16:2703-12. 2007..Where samples overlapped, the genotyping consistency was high, estimated to average at 97.3%. Our large-scale linkage analysis consolidates clear evidence for a susceptibility locus for LOAD on 10q21.2...
No major schizophrenia locus detected on chromosome 1q in a large multicenter sampleDouglas F Levinson
Department of Psychiatry, University of Pennsylvania, Philadelphia, PA 19104, USA
Science 296:739-41. 2002..If schizophrenia susceptibility genes are present on chromosome 1q, their population-wide genetic effects are likely to be small...
Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzymePetra Nowotny
Department of Psychiatry, Washington University School of Medicine, St Louis, MO 63110, USA
Am J Med Genet B Neuropsychiatr Genet 136:62-8. 2005..Although our results are not universally negative, we were unable to replicate the results of previous studies and conclude that common variants or haplotypes of these variants in IDE are not major risk factors for LOAD...
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetesEleftheria Zeggini
Oxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Churchill Hospital, Oxford, OX3 7LJ, UK
Science 316:1336-41. 2007..The regions identified underscore the importance of pathways influencing pancreatic beta cell development and function in the etiology of type 2 diabetes...
Candidate gene association study of insulin signaling genes and Alzheimer's disease: evidence for SOS2, PCK1, and PPARgamma as susceptibility lociGillian Hamilton
MRC Centre for Neurodegeneration Research, Department of Neuroscience, Institute of Psychiatry, Kings College London, Denmark Hill, London, UK
Am J Med Genet B Neuropsychiatr Genet 144:508-16. 2007..In particular, our data suggest that the effect of variants within these genes might be influenced by gender...
Is COMT a susceptibility gene for schizophrenia?Hywel J Williams
Department of Psychological Medicine, School of Medicine, Cardiff Uniiversity, Henry Wellcome Building, Health Park, Cardiff CF14 4XN, UK
Schizophr Bull 33:635-41. 2007....
Genetic variation of brain-derived neurotrophic factor (BDNF) in bipolar disorder: case-control study of over 3000 individuals from the UKElaine K Green
Department of Psychological Medicine, Henry Wellcome Building, Wales College of Medicine, Cardiff University, Heath Park, Cardiff CF4 4XN, Wales, UK
Br J Psychiatry 188:21-5. 2006..Three family-based studies have shown association of the common Valine (Val) allele of the Val66Met polymorphism of the BDNF gene with susceptibility to bipolar disorder...
