Dr Richard Anney

(he/him)

PhD FHEA

2024

• Caseras, X. et al. 2024. Common risk alleles for schizophrenia within the major histocompatibility complex predict white matter microstructure. Translational Psychiatry 14, article number: 194. (10.1038/s41398-024-02910-2)

2023

• Guintivano, J. et al. 2023. Meta-analyses of genome-wide association studies for postpartum depression. The American Journal of Psychiatry 180(12), pp. 884-895. (10.1176/appi.ajp.20230053)
• Caseras, X., Legge, S., Bracher-Smith, M., Anney, R., Owen, M., Escott-Price, V. and Kirov, G. 2023. Copy Number Variants increasing risk for schizophrenia: shared and distinct effects on brain morphometry and cognitive performance. Biological Psychiatry: Global Open Science 3(4), pp. 902-911. (10.1016/j.bpsgos.2022.10.006)
• Weavers, B. et al. 2023. Characterising depression trajectories in young people at high familial risk of depression. Journal of Affective Disorders 337, pp. 66-74. (10.1016/j.jad.2023.05.063)
• Lewis, K., Martin, J., Gregory, A. M., Anney, R., Thapar, A. and Langley, K. 2023. Sleep disturbances in ADHD: Investigating the contribution of polygenic liability for ADHD and sleep-related phenotypes. European Child and Adolescent Psychiatry 32, pp. 1253-1261. (10.1007/s00787-021-01931-2)
• Rolland, T. et al. 2023. Phenotypic effects of genetic variants associated with autism. Nature Medicine 29(7), pp. 1671-1680. (10.1038/s41591-023-02408-2)
• Lynham, A. J. et al. 2023. DRAGON-Data: A platform and protocol for integrating genomic and phenotypic data across large psychiatric cohorts. BJPsych Open 9(2), article number: e32. (10.1192/bjo.2022.636)
• Martin, J. et al. 2023. Investigating direct and indirect genetic effects in attention-deficit/hyperactivity disorder using parent-offspring trios. Biological Psychiatry 93(1), pp. 37-44. (10.1016/j.biopsych.2022.06.008)

2022

• Pat, N., Yue, W., Anney, R., Riglin, L., Thapar, A. and Argyris, S. 2022. Longitudinally stable, brain-based predictive models mediate the relationships between childhood cognition and socio-demographic, psychological and genetic factors.. Human Brain Mapping 43(18), pp. 5520-5542. (10.1002/hbm.26027)
• Hamshere, M. L., Files, C., Davies, W. and Anney, R. 2022. Embedding genomic research into teaching practice: the rewards and potential pitfalls. Genetics Society News 87, pp. 30-31.
• Pat, N., Riglin, L., Anney, R., Wang, Y., Barch, D., Thapar, A. and Stringaris, A. 2022. Motivation and cognitive abilities as mediators between polygenic scores and psychopathology in children. Journal of the American Academy of Child and Adolescent Psychiatry 61(6), pp. 782-795., article number: e3. (10.1016/j.jaac.2021.08.019)
• Chambers, T. et al. 2022. Genetic common variants associated with cerebellar volume and their overlap with mental disorders: a study on 33,265 individuals from the UK-Biobank. Molecular Psychiatry 27, pp. 2282-2290. (10.1038/s41380-022-01443-8)

2021

• Weavers, B. et al. 2021. The antecedents and outcomes of persistent and remitting adolescent depressive symptom trajectories: a longitudinal, population-based English study. The Lancet Psychiatry 8(12), pp. 1053-1061. (10.1016/S2215-0366(21)00281-9)
• Hall, L. S. et al. 2021. Cis-effects on gene expression in the human prenatal brain associated with genetic risk for neuropsychiatric disorders. Molecular Psychiatry 26, pp. 2082-2088. (10.1038/s41380-020-0743-3)
• Powell, V., Martin, J., Thapar, A., Rice, F. and Anney, R. 2021. Investigating regions of shared genetic variation in attention deficit/hyperactivity disorder and major depressive disorder: a GWAS meta-analysis. Scientific Reports 11, article number: 7353. (10.1038/s41598-021-86802-1)
• Chambers, T. et al. 2021. Effects of thyroid status on regional brain volumes: a diagnostic and genetic imaging study in UK Biobank. Journal of Clinical Endocrinology and Metabolism 106(3), pp. 688-696. (10.1210/clinem/dgaa903)
• Demontis, D. et al. 2021. Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder. Nature Communications 12(1), article number: 576. (10.1038/s41467-020-20443-2)
• Chawner, S. et al. 2021. A genetics-first approach to dissecting the heterogeneity of autism: phenotypic comparison of autism risk copy number variants. American Journal of Psychiatry 178(1), pp. 77-86. (10.1176/appi.ajp.2020.20010015)

2020

• Powell, V. et al. 2020. What explains the link between childhood ADHD and adolescent depression? Investigating the role of peer relationships and academic attainment. European Child and Adolescent Psychiatry 29, pp. 1581-1591. (10.1007/s00787-019-01463-w)
• Grama, S. et al. 2020. Polygenic risk for schizophrenia and subcortical brain anatomy in the UK Biobank cohort. Translational Psychiatry 10, article number: 309. (10.1038/s41398-020-00940-0)
• Riglin, L. et al. 2020. Using genetics to examine a general liability to childhood psychopathology. Behavior Genetics 50, pp. 213-220. (10.1007/s10519-019-09985-4)

2019

• Lee, P. H. et al. 2019. Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders. Cell 179(7), pp. 1469-1482.e11. (10.1016/j.cell.2019.11.020)
• Underwood, J., Kendall, K., Berrett, J., Lewis, C., Anney, R., Van den Bree, M. and Hall, J. 2019. Autism spectrum disorder diagnosis in adults: phenotype and genotype findings from a clinically derived cohort. British Journal of Psychiatry 215(5), pp. 647-653. (10.1192/bjp.2019.30)
• Connolly, S., Anney, R., Gallagher, L. and Heron, E. 2019. Evidence of assortative mating in autism spectrum disorder. Biological Psychiatry 86(4), pp. 286-293. (10.1016/j.biopsych.2019.04.014)
• Pain, O. et al. 2019. Novel insight into the etiology of autism spectrum disorder gained by integrating expression data with genome-wide association statistics. Biological Psychiatry 86(4), pp. 265-273. (10.1016/j.biopsych.2019.04.034)
• Underwood, J., Kendall, K., Berrett, J., Anney, R., Bree, M. V. D. and Hall, J. 2019. SA20COPY Number variants and polygenic risk scores in adults with autism spectrum disorder (ASD): results from the NCMH adult ASD cohort. European Neuropsychopharmacology 29(S4), pp. S1198-S1199. (10.1016/j.euroneuro.2018.08.242)
• Gorman, K. M. et al. 2019. Bi-allelic loss-of-function CACNA1B mutations in progressive epilepsy-dyskinesia. American Journal of Human Genetics 104(5), pp. 948-956. (10.1016/j.ajhg.2019.03.005)
• Rice, F., Riglin, L., Thapar, A. K., Heron, J., Anney, R., O'Donovan, M. C. and Thapar, A. 2019. Characterizing developmental trajectories and the role of neuropsychiatric genetic risk variants in early-onset depression. JAMA Psychiatry 76(3), pp. 306-313. (10.1001/jamapsychiatry.2018.3338)
• Grove, J. et al. 2019. Identification of common genetic risk variants for autism spectrum disorder. Nature Genetics 51, pp. 431-444. (10.1038/s41588-019-0344-8)
• O'Brien, H. et al. 2019. Sex differences in gene expression in the human fetal brain. [Online]. bioRxiv. (10.1101/483636) Available at: https://doi.org/10.1101/483636

2018

• Demontis, D. et al. 2018. Discovery of the first genome-wide significant risk loci for attention-deficit/hyperactivity disorder. Nature Genetics 51, pp. 63-75. (10.1038/s41588-018-0269-7)
• Anttila, V. et al. 2018. Analysis of shared heritability in common disorders of the brain. Science 360(6395), article number: eaap8757. (10.1126/science.aap8757)
• Martin, J. et al. 2018. A genetic investigation of sex bias in the prevalence of attention-deficit/hyperactivity disorder. Biological Psychiatry 83(12), pp. 1044-1053. (10.1016/j.biopsych.2017.11.026)
• Cosgrove, D. et al. 2018. Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177(3), pp. 369-376. (10.1002/ajmg.b.32620)

2017

• Lim, E. T. et al. 2017. Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder. Nature Neuroscience 20(9), pp. 1217-1224. (10.1038/nn.4598)
• Weiner, D. J. et al. 2017. Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders. Nature Genetics 49(7), pp. 978-985. (10.1038/ng.3863)
• Hendricks, A. E. et al. 2017. Rare variant analysis of human and rodent obesity genes in individuals with severe childhood obesity. Scientific Reports 7, article number: 4394. (10.1038/s41598-017-03054-8)
• Vorstman, J. A. S., Parr, J. R., Moreno-De-Luca, D., Anney, R., Nurnberger Jr, J. I. and Hallmayer, J. F. 2017. Autism genetics: opportunities and challenges for clinical translation. Nature Reviews Genetics 18(6), pp. 362-376. (10.1038/nrg.2017.4)
• The Autism Spectrum Disorders Working Group of The Psychiatric G, ., Anney, R. J. L. and Holmans, P. 2017. Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. Molecular Autism 8, article number: 21. (10.1186/s13229-017-0137-9)
• Connolly, S., Anney, R., Gallagher, L. and Heron, E. A. 2017. A genome-wide investigation into parent-of-origin effects in autism spectrum disorder identifies previously associated genes including SHANK3. European Journal of Human Genetics 25(2), pp. 234-239. (10.1038/ejhg.2016.153)
• Cosgrove, D. et al. 2017. MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls. Translational Psychiatry 7(1), pp. e1012. (10.1038/tp.2016.286)

2016

• Mooney, M. A. et al. 2016. Pathway analysis in attention deficit hyperactivity disorder: an ensemble approach. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 171(6), pp. 815-826. (10.1002/ajmg.b.32446)
• Coleman, C. et al. 2016. Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci. European Journal of Human Genetics 24(2), pp. 291-297. (10.1038/ejhg.2015.87)

2015

• Merikangas, A. K. et al. 2015. The phenotypic manifestations of rare genic CNVs in autism spectrum disorder. Molecular Psychiatry 20(11), pp. 1366-1372. (10.1038/mp.2014.150)
• Walter, K. et al. 2015. The UK10K project identifies rare variants in health and disease. Nature 526, pp. 82-90. (10.1038/nature14962)
• Ning, Z. et al. 2015. Regulation of SPRY3 by X chromosome and PAR2-linked promoters in an autism susceptibility region. Human Molecular Genetics 24(18), pp. 5126-5141. (10.1093/hmg/ddv231)
• Huang, J. et al. 2015. Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel. Nature Communications 6, article number: 8111. (10.1038/ncomms9111)
• Schmidts, M. et al. 2015. TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport. Nature Communications 6, article number: 7074. (10.1038/ncomms8074)
• Connolly, S., Anney, R., Gallagher, L. and Heron, E. 2015. Investigation of assortative mating in autism spectrum disorders [Conference Abstract]. Human Heredity 79(1), pp. 31-31., article number: A8. (10.1159/000381109)
• O'Dushlaine, C. et al. 2015. Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. Nature Neuroscience 18(2), pp. 199-209. (10.1038/nn.3922)

2014

• Timpson, N. J. et al. 2014. A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans. Nature Communications 5, article number: 4871. (10.1038/ncomms5871)
• Merikangas, A. K. et al. 2014. The phenotypic manifestations of rare CNVs in schizophrenia. Schizophrenia Research 158(1-3), pp. 255-260. (10.1016/j.schres.2014.06.016)
• Kenny, E. M. et al. 2014. Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders. Molecular Psychiatry 19(8), pp. 872-879. (10.1038/mp.2013.127)
• Anney, R. et al. 2014. Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies. The Lancet Neurology 13(9), pp. 893-903. (10.1016/S1474-4422(14)70171-1)
• Nicodemus, K. K., Hargreaves, A., Morris, D., Anney, R., Gill, M., Corvin, A. and Donohoe, G. 2014. Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway. JAMA Psychiatry 71(7), pp. 778-785. (10.1001/jamapsychiatry.2014.528)
• Hargreaves, A. et al. 2014. The one and the many: effects of the cell adhesion molecule pathway on neuropsychological function in psychosis. Psychological Medicine 44(10), pp. 2177-2187. (10.1017/S0033291713002663)
• Nicodemus, K. K., Hargreaves, A., Morris, D., Anney, R., Gill, M., Corvin, A. and Donohoe, G. 2014. Variability inworking memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway. JAMA Psychiatry 71(7), pp. 778-785. (10.1001/jamapsychiatry.2014.528)
• Waltes, R. et al. 2014. Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders. Human Genetics 133(6), pp. 781-792. (10.1007/s00439-013-1416-y)
• Buxbaum, J. D. et al. 2014. The autism simplex collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses. Molecular Autism 5, pp. 34. (10.1186/2040-2392-5-34)
• Pinto, D. et al. 2014. Convergence of genes and cellular pathways dysregulated in autism spectrum disorders. American Journal of Human Genetics 94(5), pp. 677-694. (10.1016/j.ajhg.2014.03.018)
• Hart, A. B. et al. 2014. Genetic variation associated with euphorigenic effects of d-amphetamine is associated with diminished risk for schizophrenia and attention deficit hyperactivity disorder. Proceedings of the National Academy of Sciences 111(16), pp. 5968-5973. (10.1073/pnas.1318810111)

2013

• Lee, S. et al. 2013. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics 45(9), pp. 984-994. (10.1038/ng.2711)
• Hamshere, M. L. et al. 2013. High loading of polygenic risk for ADHD in children with comorbid aggression. American Journal of Psychiatry 170(8), pp. 909-916. (10.1176/appi.ajp.2013.12081129)
• Merikangas, A., Heron, E., Anney, R., Corvin, A. and Gallagher, L. 2013. Risk factors and clinical correlates of CNVs associated with autism spectrum disorders: evidence for joint contribution of genetic and environmental risk factors [Conference Abstract]. European Child & Adolescent Psychiatry 22(Suppl2), pp. S188-S188. (10.1007/s00787-013-0423-9)
• Smoller, J. W. et al. 2013. Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. The Lancet 381(9875), pp. 1371-1379. (10.1016/S0140-6736(12)62129-1)
• Quinn, E. M. et al. 2013. Development of strategies for SNP detection in RNA-seq data: application to lymphoblastoid cell lines and evaluation using 1000 genomes data. PLoS ONE 8(3), article number: e58815. (10.1371/journal.pone.0058815)
• Mulligan, A. et al. 2013. Home environment: association with hyperactivity/impulsivity in children with ADHD and their non-ADHD siblings. Child Care Health and Development 39(2), pp. 202-212. (10.1111/j.1365-2214.2011.01345.x)
• Vorstman, J. A. S. et al. 2013. No evidence that common genetic risk variation is shared between schizophrenia and autism. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 162B(1), pp. 55-60. (10.1002/ajmg.b.32121)

2012

• Holt, R. et al. 2012. CNVs leading to fusion transcripts in individuals with autism spectrum disorder. European Journal of Human Genetics 20(11), pp. 1141-1147. (10.1038/ejhg.2012.73)
• Quinn, E. M., Hill, M., Anney, R., Gill, M., Corvin, A. P. and Morris, D. W. 2012. Evidence for cis-acting regulation of ANK3 and CACNA1C gene expression [Erratum]. Bipolar Disorders 14(7), pp. 792-792. (10.1111/bdi.12020)
• Anney, R. et al. 2012. Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Human Molecular Genetics 21(21), pp. 4781-4792. (10.1093/hmg/dds301)
• Casey, J. P. et al. 2012. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Human Genetics 131(4), pp. 565-579. (10.1007/s00439-011-1094-6)
• Williams, N. M. et al. 2012. Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. American Journal of Psychiatry 169(2), pp. 195-204. (10.1176/appi.ajp.2011.11060822)
• Elia, J. et al. 2012. Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder. Nature Genetics 44(1), pp. 78-84. (10.1038/ng.1013)

2011

• Hill, M. J. et al. 2011. Allelic expression imbalance of the schizophrenia susceptibility gene CHI3L1: evidence of cis-acting variation and tissue specific regulation. Psychiatric Genetics 21(6), pp. 281-286. (10.1097/YPG.0b013e328348045b)
• Anney, R. et al. 2011. Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders. European Journal of Human Genetics 19(10), pp. 1082-1089. (10.1038/ejhg.2011.75)
• Sonuga-Barke, E. J. S. et al. 2011. A functional variant of the serotonin transporter gene (SLC6A4) moderates impulsive choice in attention-deficit/hyperactivity disorder boys and siblings. Biological psychiatry 70(3), pp. 230-236. (10.1016/j.biopsych.2011.01.040)
• Tansey, K. E., Hill, M. J., Cochrane, L. E., Gill, M., Anney, R. and Gallagher, L. 2011. Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism. Molecular Autism 2(1), pp. 3. (10.1186/2040-2392-2-3)
• Rizzi, T. S. et al. 2011. The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156B(2), pp. 145-157. (10.1002/ajmg.b.31149)

2010

• Cochrane, L. E., Tansey, K. E., Gill, M., Gallagher, L. and Anney, R. 2010. Lack of association between markers in the ITGA3, ITGAV, ITGA6 and ITGB3 and autism in an Irish sample. Autism Research 3(6), pp. 342-344. (10.1002/aur.157)
• Merikangas, A. K., Heron, E. A., Anney, R., Corvin, A. P. and Gallagher, L. 2010. Investigating the association between rare copy number variation and developmental anomalies in autism spectrum disorders [Conference Abstract]. Genetic Epidemiology 34(8), pp. 929-929. (10.1002/gepi.20553)
• Anney, R. et al. 2010. A genome-wide scan for common alleles affecting risk for autism. Human Molecular Genetics 19(20), pp. 4072-4082. (10.1093/hmg/ddq307)
• Hill, M., Anney, R., Gill, M. and Hawi, Z. 2010. Functional analysis of intron 8 and 3 ' UTR variable number of tandem repeats of SLC6A3: differential activity of intron 8 variants. Pharmacogenomics Journal 10(5), pp. 442-447. (10.1038/tpj.2009.66)
• Sobanski, E. et al. 2010. Emotional lability in children and adolescents with attention deficit/hyperactivity disorder (ADHD): clinical correlates and familial prevalence. Journal of Child Psychology and Psychiatry 51(8), pp. 915-923. (10.1111/j.1469-7610.2010.02217.x)
• Pinto, D. et al. 2010. Functional impact of global rare copy number variation in autism spectrum disorders. Nature 466(7304), pp. 368-372. (10.1038/nature09146)
• Nijmeijer, J. S. et al. 2010. Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach. Journal of the American Academy of Child & Adolescent Psychiatry 49(7), pp. 675-685. (10.1016/j.jaac.2010.03.015)
• Quinn, E. M., Hill, M., Anney, R., Gill, M., Corvin, A. P. and Morris, D. W. 2010. Evidence for cis-acting regulation of ANK3 and CACNA1C gene expression. Bipolar Disorders 12(4), pp. 440-445. (10.1111/j.1399-5618.2010.00817.x)
• Tansey, K. E. et al. 2010. Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: Genetic and molecular studies. Neuroscience Letters 474(3), pp. 163-167. (10.1016/j.neulet.2010.03.035)
• Lasky-Su, J. et al. 2010. On genome-wide association studies for family-based designs: an integrative analysis approach combining ascertained family samples with unselected controls. American Journal of Human Genetics 86(4), pp. 573-580. (10.1016/j.ajhg.2010.02.019)
• Olsson, C. A. et al. 2010. Prospects for epigenetic research within cohort studies of psychological disorder: A pilot investigation of a peripheral cell marker of epigenetic risk for depression. Biological Psychology 83(2), pp. 159-165. (10.1016/j.biopsycho.2009.12.003)
• Hawi, Z. et al. 2010. ADHD and DAT1: further evidence of paternal over-transmission of risk alleles and haplotype. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B(1), pp. 97-102. (10.1002/ajmg.b.30960)
• Neale, B. M. et al. 2010. Case-control genome-wide association study of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child & Adolescent Psychiatry 49(9), pp. 906-920. (10.1016/j.jaac.2010.06.007)
• Neale, B. M. et al. 2010. Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child & Adolescent Psychiatry 49(9), pp. 884-897. (10.1016/j.jaac.2010.06.008)

2009

• Sonuga-Barke, E. J. S. et al. 2009. Dopamine and serotonin transporter genotypes moderate sensitivity to maternal expressed emotion: the case of conduct and emotional problems in attention deficit/hyperactivity disorder. Journal of Child Psychology and Psychiatry 50(9), pp. 1052-1063. (10.1111/j.1469-7610.2009.02095.x)
• Anney, R. and Lasky-Su, J. 2009. S.18.05 Molecular-genetics of aggression and antisocial behaviour in clinical populations [Conference abstract]. European Neuropsychopharmacology 19, pp. S203-S203. (10.1016/S0924-977X(09)70264-0)
• Conroy, J. et al. 2009. Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B(4), pp. 535-544. (10.1002/ajmg.b.30854)
• Mulligan, A. et al. 2009. Autism symptoms in attention-deficit/hyperactivity disorder: a familial trait which correlates with conduct, oppositional defiant, language and motor disorders. Journal of Autism and Developmental Disorders 39(2), pp. 197-209. (10.1007/s10803-008-0621-3)

2008

• Lasky-Su, J. et al. 2008. Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B(8), pp. 1345-1354. (10.1002/ajmg.b.30867)
• Brookes, K. J. et al. 2008. Association of ADHD with genetic variants in the 5'-region of the dopamine transporter gene: evidence for allelic heterogeneity. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B(8), pp. 1519-1523. (10.1002/ajmg.b.30782)
• Anney, R. et al. 2008. Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B(8), pp. 1369-1378. (10.1002/ajmg.b.30871)
• Neale, B. M. et al. 2008. Genome-wide association scan of attention deficit hyperactivity disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B(8), pp. 1337-1344. (10.1002/ajmg.b.30866)
• Anney, R. et al. 2008. Parent of Origin Effects in Attention/Deficit Hyperactivity Disorder (ADHD): Analysis of Data From the International Multicenter ADHD Genetics (IMAGE) Program. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B(8), pp. 1495-1500. (10.1002/ajmg.b.30659)
• Xu, X. et al. 2008. Replication of a Rare Protective Allele in the Noradrenaline Transporter Gene and ADHD. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B(8), pp. 1564-1567. (10.1002/ajmg.b.30872)
• Sonuga-Barke, E. J. S. et al. 2008. Does Parental Expressed Emotion Moderate Genetic Effects in ADHD? An Exploration Using a Genome Wide Association Scan. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B(8), pp. 1359-1368. (10.1002/ajmg.b.30860)
• Lasky-Su, J. et al. 2008. Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B(8), pp. 1355-1358. (10.1002/ajmg.b.30869)
• Anney, R. et al. 2008. Non-random error in genotype calling procedures: implications for family-based and case-control genome-wide association studies. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B(8), pp. 1379-1386. (10.1002/ajmg.b.30836)
• Oades, R. D. et al. 2008. The influence of serotonin- and other genes on impulsive behavioral aggression and cognitive impulsivity in children with attention-deficit/hyperactivity disorder (ADHD): Findings from a family-based association test (FBAT) analysis. Behavioral and Brain Functions : BBF 4, pp. 48. (10.1186/1744-9081-4-48)
• Xu, X. et al. 2008. No association between two polymorphisms of the Serotonin Transporter Gene and combined type Attention Deficit Hyperactivity Disorder. American Journal of Medical Genetics. Part B 147B(7), pp. 1306-1309. (10.1002/ajmg.b.30737)
• Zhou, K. et al. 2008. Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings. Biological psychiatry 64(7), pp. 571-576. (10.1016/j.biopsych.2008.02.024)
• Altink, M. E. et al. 2008. The dopamine receptor D4 7-repeat allele and prenatal smoking in ADHD-affected children and their unaffected siblings: no gene-environment interaction. Journal of Child Psychology and Psychiatry 49(10), pp. 1053-1060. (10.1111/j.1469-7610.2008.01998.x)
• Sonuga-Barke, E. J. S. et al. 2008. Intelligence in DSM-IV combined type attention-deficit/hyperactivity disorder is not predicted by either dopamine receptor/transporter genes or other previously identified risk alleles for attention-deficit/hyperactivity disorder [Erratum]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B(5), pp. 670-670. (10.1002/ajmg.b.30820)
• Asherson, P. et al. 2008. A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16. Molecular Psychiatry 13(5), pp. 514-521. (10.1038/sj.mp.4002140)
• Sonuga-Barke, E. J. S. et al. 2008. Intelligence in DSM-IV combined type attention-deficit/hyperactivity disorder is not predicted by either dopamine receptor/transporter genes or other previously identified risk alleles for attention-deficit/hyperactivity disorder. American Journal of Medical Genetics. Part B 147B(3), pp. 316-319. (10.1002/ajmg.b.30596)

2007

• Olsson, C. A., Byrnes, G. B., Anney, R., Collins, V., Hemphill, S. A., Williamson, R. and Patton, G. C. 2007. COMT Val(158)Met and 5HTTLPR functional loci interact to predict persistence of anxiety across adolescence: results from the Victorian Adolescent Health Cohort Study. Genes Brain and Behavior 6(7), pp. 647-652. (10.1111/j.1601-183X.2007.00313.x)
• Anney, R., Lotfi-Miri, M., Olsson, C. A., Reid, S. C., Hemphill, S. A. and Patton, G. C. 2007. Variation in the gene coding for the M5 Muscarinic receptor (CHRM5) influences cigarette dose but is not associated with dependence to drugs of addiction: evidence from a prospective population based cohort study of young adults. BMC Genetics 8, pp. 46. (10.1186/1471-2156-8-46)

2006

• Brookes, K. et al. 2006. The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes. Molecular Psychiatry 11(12), pp. 934-953. (10.1038/sj.mp.4001869)
• Anney, R. et al. 2006. Epigenetic effects in ADHD: Parent-of-origin effects in image sample [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141B(7), pp. 736-737. (10.1002/ajmg.b.30408)
• Mulligan, A., Anney, R., Chen, W., Butler, L., Fitzgerald, M. and Gill, M. 2006. Autistic symptoms in ADHD- A report from the International Multi-Center ADHD Gene Project (IMAGE) [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141B(7), pp. 687-687. (10.1002/ajmg.b.30408)

2005

• Olsson, C., Byrnes, G., Lotfi-Miri, M., Collins, V., Williamson, R., Patton, C. and Anney, R. 2005. Association between 5-HTTLPR genotypes and persisting patterns of anxiety and alcohol use: results from a 10-year longitudinal study of adolescent mental health. Molecular Psychiatry 10(9), pp. 868-876. (10.1038/sj.mp.4001677)
• Olsson, C., Anney, R., Lotfi-Miri, M., Byrnes, G., Williamson, R. and Patton, G. 2005. Association between the COMT Val158Met polymorphism and propensity to anxiety in an Australian population-based longitudinal study of adolescent health. Psychiatric Genetics 15(2), pp. 109-115.
• Staddon, S. et al. 2005. Association between dopamine D3 receptor gene polymorphisms and schizophrenia in an isolate population. Schizophrenia Research 73(1), pp. 49-54. (10.1016/j.schres.2004.06.011)

2002

• Anney, R. et al. 2002. Characterisation, mutation detection, and association analysis of alternative promoters and 5' UTRs of the human dopamine D3 receptor gene in schizophrenia. Molecular psychiatry 7(5), pp. 493-502. (10.1038/sj.mp.4001003)