2016 publications

Aas, M. et al., 2016. Summaries of plenary, symposia, and oral sessions at the XXII World Congress of Psychiatric Genetics, Copenhagen, Denmark, 12-16 October 2014 [Conference Material]. Psychiatric Genetics 26 (1), pp.1-47. (10.1097/YPG.0000000000000112)
Anderson, J. J. et al., 2016. Gestational influenza and risk of hypomania in young adulthood: prospective birth cohort study. Journal of affective disorders 200 , pp.182-188. (10.1016/j.jad.2016.04.048)
Antonakakis, M. et al., 2016. Altered cross-frequency coupling in resting-state MEG after mild traumatic brain injury. International Journal of Psychophysiology 102 , pp.1-11. (10.1016/j.ijpsycho.2016.02.002)
Bayram-Weston, Z. et al. 2016. Comparison of mHTT antibodies in Huntington's disease mouse models reveal specific binding profiles and steady-state ubiquitin levels with disease development.. PloS One (10.1371/journal.pone.0155834)
Bevan-Jones, R. et al. 2016. Prevalence and correlates of psychotic experiences amongst children of depressed parents. Psychiatry Research 243 , pp.81-86. (10.1016/j.psychres.2016.03.012)
Beyer, S. , Meek, A. and Davies, A. 2016. Supported work experience and its impact on young people with intellectual disabilities, their families and employers. Advances in Mental Health and Intellectual Disabilities 10 (3), pp.207-220. (10.1108/AMHID-05-2014-0015)
Beyer, S. R. 2016. Commentary on 'Employment for all: United States disability policy'. Tizard Learning Disability Review 21 (3), pp.162-164. (10.1108/TLDR-04-2016-0013)
Bigdeli, T. B. et al., 2016. Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 171 (2), pp.276-289. (10.1002/ajmg.b.32402)
Blackmore, E. R. et al., 2016. The effects of trauma history and prenatal affective symptoms on obstetric outcomes. Journal of Traumatic Stress 29 (3), pp.245-252. (10.1002/jts.22095)
Bray, N. J. and Hill, M. 2016. Translating genetic risk loci into molecular risk mechanisms for schizophrenia. Schizophrenia Bulletin 42 (1), pp.5-8. (10.1093/schbul/sbv156)
Breydo, L. et al., 2016. A hyperbranched dopamine-containing PEG-based polymer for the inhibition of a-synuclein fibrillation. Biochemical and Biophysical Research Communications 469 (4), pp.830-835. (10.1016/j.bbrc.2015.12.060)
Brindley, L. et al. 2016. Ipsilateral cortical motor desynchronisation is reduced in benign epilepsy with centro-temporal spikes. Clinical Neurophysiology 127 (2), pp.1147-1159. (10.1016/j.clinph.2015.08.020)
Butterworth, S. E. , Ingram, G. and Robertson, N. 2016. Advances in biomarker research in multiple sclerosis [Journal Club]. Journal of Neurology 263 (3), pp.621-623. (10.1007/s00415-016-8062-y)
Carroll, L. S. et al., 2016. Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutation. Psychiatric Genetics 26 (2), pp.60-65. (10.1097/YPG.0000000000000110)
Casanova Dias, M. , Giacco, D. and Hanon, C. 2016. Early career psychiatrists? preferences on e-learning: viewpoint from the EPA committee on education. European Psychiatry 42 , pp.86-88. (10.1016/j.eurpsy.2016.12.003)
Cauchi, M. and Robertson, N. 2016. CGRP and migraine. Journal of Neurology 263 (1), pp.192-194. (10.1007/s00415-015-8000-4)
Caye, A. et al., 2016. Life span studies of ADHD - conceptual challenges and predictors of persistence and outcome. Current Psychiatry Reports 18 (12) 111. (10.1007/s11920-016-0750-x)
Chan, S. W. et al., 2016. Deactivation in anterior cingulate cortex during facial processing in young individuals with high familial risk and early development of depression: fMRI findings from the Scottish Bipolar Family Study. Journal of Child Psychology and Psychiatry 57 (11), pp.1277-1286. (10.1111/jcpp.12591)
Chatterjee, S. , Humby, T. and Davies, W. 2016. Behavioural and psychiatric phenotypes in men and boys with X-linked ichthyosis: evidence from a worldwide online survey. PLoS ONE 11 (10), pp.e0164417. e0164417. (10.1371/journal.pone.0164417)
Chilton, J. et al., 2016. Galaxy planemo 0.35.0. (10.5281/zenodo.166551)
Cianfaglione, R. et al., 2016. Ageing in Rett syndrome. Journal of Intellectual Disability Research 60 (2), pp.182-190. (10.1111/jir.12228)
Clement, M. et al. 2016. Targeted suppression of autoreactive CD8+ T-cell activation using blocking anti-CD8 antibodies. Scientific Reports 6 35332. (10.1038/srep35332)
Cohen Kadosh, K. et al., 2016. Using real-time fMRI to influence effective connectivity in the developing emotion regulation network. NeuroImage 125 , pp.616-626. (10.1016/j.neuroimage.2015.09.070)
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)
Collishaw, S. et al. 2016. Predictors of mental health resilience in children who have been parentally bereaved by AIDS in urban South Africa. Journal of Abnormal Child Psychology 44 (4), pp.719-730. (10.1007/s10802-015-0068-x)
Collishaw, S. et al. 2016. Mental health resilience in the adolescent offspring of parents with depression: a prospective longitudinal study. Lancet Psychiatry 3 (1), pp.49-57. (10.1016/S2215-0366(15)00358-2)
Cooper, M. et al. 2016. Gaining approvals for mental health research in the NHS. BJPscyh Advances 22 (1), pp.64-72. (10.1192/apt.bp.114.014035)
Corvin, A. and O'Donovan, M. C. 2016. Psychiatric genetics: what's new in 2015?. The Lancet Psychiatry 3 (1), pp.10-12. (10.1016/S2215-0366(15)00571-4)
Cox, W. et al. 2016. Neurofeedback training for alcohol dependence versus treatment as usual: study protocol for a randomized controlled trial. Trials 17 (1), pp.480. (10.1186/s13063-016-1607-7)
D'Angelo, D. et al., 2016. Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities. JAMA Psychiatry 73 (1), pp.20-30. (10.1001/jamapsychiatry.2015.2123)
Davidovich, S. et al., 2016. Do better executive functions buffer the effect of current parental depression on adolescent depressive symptoms?. Journal of Affective Disorders 199 , pp.54-64. (10.1016/j.jad.2016.03.049)
Davies, G. et al., 2016. Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112 151). Molecular Psychiatry 21 (6), pp.758-767. (10.1038/mp.2016.45)
Davies, W. 2016. Insights into rare diseases from social media surveys. Orphanet Journal of Rare Diseases 11 151. (10.1186/s13023-016-0532-x)
de Wit, H. et al., 2016. Psychotic experiences and working memory: a population-based study using signal-detection analysis. PLoS ONE 11 (4) e0153148. (10.1371/journal.pone.0153148)
Dent, C. et al. 2016. Impulsive choices in mice lacking imprinted Nesp55. Genes, Brain and Behavior 15 (8), pp.693-701. (10.1111/gbb.12316)
Di Florio, A. , Munk-Olsen, T. and Bergink, V. 2016. The birth of a psychiatric orphan disorder: postpartum psychosis [Correspondence]. The Lancet Psychiatry 3 (6), pp.502. (10.1016/S2215-0366(16)30037-2)
Dias, M. C. and Jones, I. R. 2016. Perinatal psychiatry. Medicine 44 (12), pp.720-723. (10.1016/j.mpmed.2016.09.006)
Dimitriadis, S. 2016. Identification of infants at high familiar risk for language-learning disorders (LLD) by combining machine learning techniques with EEG-based brain network metrics [Editorial]. Clinical Neurophysiology 127 (7), pp.2692-2694. (10.1016/j.clinph.2016.04.016)
Dimitriadis, S. and Linden, D. E. J. 2016. Modulation of brain criticality via suppression of EEG long-range temporal correlations (LRTCs) in a closed-loop neurofeedback stimulation. Clinical Neurophysiology 127 (8), pp.2878-2881. (10.1016/j.clinph.2016.05.359)
Dimitriadis, S. et al. 2016. Classifying children with reading difficulties from non-impaired readers via symbolic dynamics and complexity analysis of MEG resting-state data. Presented at: 2016 IEEE International Symposium on Signal Processing and Information Technology (ISSPIT) 12-14 December 2016. Signal Processing and Information Technology (ISSPIT), 2016 IEEE International Symposium on. IEEE. , pp.333-336. (10.1109/ISSPIT.2016.7886059)
Dimitriadis, S. et al. 2016. Causal interactions between Frontalθ – Parieto-Occipitalα2 predict performance on a mental arithmetic task. Frontiers in Human Neuroscience 10 454. (10.3389/fnhum.2016.00454)
Dimitriadis, S. et al. 2016. Mnemonic strategy training of the elderly at risk for dementia enhances integration of information processing via cross-frequency coupling. Alzheimer's & Dementia: Translational Research & Clinical Interventions 2 (4), pp.241-249. (10.1016/j.trci.2016.08.004)
Doran, Z. et al., 2016. Managing anti-epileptic drug treatment in adult patients with intellectual disability: a serious conundrum. European Journal of Neurology 23 (7), pp.1152-1157. (10.1111/ene.13016)
Drakesmith, M. et al. 2016. Volumetric, relaxometric and diffusometric correlates of psychotic experiences in a non-clinical sample of young adults. NeuroImage: Clinical 12 , pp.550-558. (10.1016/j.nicl.2016.09.002)
Duarte, R. R. et al., 2016. Genome-wide significant schizophrenia risk variation on chromosome 10q24 is associated with altered cis-regulation of BORCS7, AS3MT, and NT5C2 in the human brain. American Journal of Medical Genetics. Part B 171 (6), pp.806-814. (10.1002/ajmg.b.32445)
Forrester, A. , Valmaggia, L. and Taylor, P. J. 2016. Healthcare services in police custody in England and Wales. BMJ 353. (10.1136/bmj.i1994)
Franke, B. et al., 2016. Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept. Nature Neuroscience 19 (3), pp.420-431. (10.1038/nn.4228)
Fry, A. E. et al. 2016. Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy. BMC Medical Genetics 17 , pp.-. 34. (10.1186/s12881-016-0294-2)
Gage, S. H. , Hickman, M. and Zammit, S. 2016. Association between cannabis and psychosis: epidemiologic evidence. Biological psychiatry 79 (7), pp.549-556. (10.1016/j.biopsych.2015.08.001)
Garfield, A. S. et al., 2016. Increased alternate splicing of Htr2c in a mouse model for Prader-Willi syndrome leads disruption of 5HT2C receptor mediated appetite. Molecular Brain 9 95. (10.1186/s13041-016-0277-4)
Goller, A. et al., 2016. Criminal recidivism of illegal pornography offenders in the overall population - a national cohort study of 4612 offenders in Switzerland. Advances in Applied Sociology 6 (2), pp.48-56. (10.4236/aasoci.2016.62005)
Goodwin, G. et al., 2016. Evidence-based guidelines for treating bipolar disorder: Revised third edition recommendations from the British Association for Psychopharmacology. Journal of Psychopharmacology 30 (6), pp.495-553. (10.1177/0269881116636545)
Habes, I. et al. 2016. fMRI neurofeedback of higher visual areas and perceptual biases. Neuropsychologia 85 , pp.208-215. (10.1016/j.neuropsychologia.2016.03.031)
Hamandi, K. et al. 2016. Non-invasive brain mapping in epilepsy: applications from magnetoencephalography. Journal of Neuroscience Methods 260 , pp.283-291. (10.1016/j.jneumeth.2015.11.012)
Hammerton, G. et al. 2016. Explaining risk for suicidal ideation in adolescent offspring of mothers with depression. Psychological Medicine -London- 46 (2), pp.265-275. (10.1017/S0033291715001671)
Hampel, H. et al., 2016. Precision medicine - the golden gate for detection, treatment and prevention of Alzheimer's disease. Journal of Prevention of Alzheimer's Disease 3 (4), pp.243-259. (10.14283/jpad.2016.112)
Han, J. et al. 2016. Gender differences in CNV burden do not confound schizophrenia CNV associations. Scientific Reports 6 25986. (10.1038/srep25986)
Hannon, E. et al., 2016. Methylation QTLs in the developing brain and their enrichment in schizophrenia risk loci. Nature Neuroscience 19 (1), pp.48-54. (10.1038/nn.4182)
Harding, K. 2016. Book club:the hard problem. Practical Neurology 16 (5), pp.423-423. (10.1136/practneurol-2016-001495)
Harding, K. 2016. Flowers for Algernon. Practical Neurology 16 (1), pp.80-80. (10.1136/practneurol-2015-001346)
Harding, K. and Robertson, N. 2016. Deep brain stimulation for dystonia. Journal of Neurology 263 (5), pp.1045-1046. (10.1007/s00415-016-8137-9)
Harrison, J. and Owen, M. J. 2016. Alzheimer's disease: the amyloid hypothesis on trial. British Journal of Psychiatry 208 (1), pp.1-3. (10.1192/bjp.bp.115.167569)
Holland, D. et al., 2016. Estimating effect sizes and expected replication probabilities from GWAS summary statistics. Frontiers in Genetics 7 15. (10.3389/fgene.2016.00015)
Hrastelj, J. and Robertson, N. 2016. Ice bucket challenge bears fruit for amyotrophic lateral sclerosis. Journal of Neurology 263 (11) 2355. (10.1007/s00415-016-8297-7)
Hubbard, L. et al. 2016. Evidence of common genetic overlap between schizophrenia and cognition. Schizophrenia Bulletin 42 (3), pp.832-842. (10.1093/schbul/sbv168)
Huelga-Suarez, G. et al., 2016. The quest for the Soldier's Rest: Combining anthropological and archaeochemical approaches to study social and occupational diversity in the Medieval graveyard of San Andres de Arroyo (Palencia, Spain). Anthropological Science 124 (3) 161005. (10.1537/ase.161005)
Humby, T. et al. 2016. A pharmacological mouse model suggests a novel risk pathway for postpartum psychosis. Psychoneuroendocrinology 74 , pp.363-370. (10.1016/j.psyneuen.2016.09.019)
Ide, M. et al., 2016. Periodontitis and cognitive decline in Alzheimer's Disease. PLOS ONE 11 (3) e0151081. (10.1371/journal.pone.0151081)
Ihssen, N. , Mussweiler, T. and Linden, D. E. J. 2016. Observing others stay or switch – How social prediction errors are integrated into reward reversal learning. Cognition 153 , pp.19-32. (10.1016/j.cognition.2016.04.012)
Isles, A. R. et al. 2016. Parental origin of interstitial duplications at 15q11.2-q13.3 in schizophrenia and neurodevelopmental disorders. PLoS Genetics 12 (5) e1005993. (10.1371/journal.pgen.1005993)
Jakobsdottir, J. et al., 2016. Rare functional variant in TM2D3 is associated with late-onset Alzheimer's disease. PLoS Genetics 12 (10) e1006327. (10.1371/journal.pgen.1006327)
Jones, H. J. et al., 2016. Phenotypic manifestation of genetic risk for schizophrenia during adolescence in the general population. JAMA Psychiatry 73 (3), pp.221-228. (10.1001/jamapsychiatry.2015.3058)
Jones, H. J. and Zammit, S. 2016. Measures of psychosis proneness and genetic risk for schizophrenia - Reply. JAMA Psychiatry 73 (6), pp.638-639. (10.1001/jamapsychiatry.2016.0241)
Jun, G. et al., 2016. A novel Alzheimer disease locus located near the gene encoding tau protein. Molecular Psychiatry 21 , pp.108-117. (10.1038/mp.2015.23)
Karatzias, T. et al., 2016. An initial psychometric assessment of an ICD-11 based measure of PTSD and complex PTSD (ICD-TQ): evidence of construct validity. Journal of Anxiety Disorders 44 , pp.73-79. (10.1016/j.janxdis.2016.10.009)
Kerr, M. P. 2016. The implications of the new approach to classification: Adults with an intellectual disability. Epilepsy & Behavior 64 (Part B), pp.309-310. (10.1016/j.yebeh.2015.12.016)
Kerr, M. P. et al. 2016. Behavioural disorder in people with an intellectual disability and epilepsy: a report of the Intellectual Disability Task Force of the Neuropsychiatric Commission of ILAE. Epilepsia Open 1 , pp.102-111. (10.1002/epi4.12018)
Khandaker, G. M. et al., 2016. Association between serum C-reactive protein and DSM-IV generalized anxiety disorder in adolescence: Findings from the ALSPAC cohort. Neurobiology of Stress 4 , pp.55-61. (10.1016/j.ynstr.2016.02.003)
Knöchel, C. et al., 2016. Cortical thinning in bipolar disorder and schizophrenia. Schizophrenia Research 172 (1-3), pp.78-85. (10.1016/j.schres.2016.02.007)
Knöchel, C. et al., 2016. White matter abnormalities in the fornix are linked to cognitive performance in SZ but not in BD disorder: An exploratory analysis with DTI deterministic tractography. Journal of affective disorders 201 , pp.64-78. (10.1016/j.jad.2016.03.015)
Lancaster, T. et al. 2016. Associations between polygenic risk for schizophrenia and brain function during probabilistic learning in healthy individuals. Human Brain Mapping 37 (2), pp.491-500. (10.1002/hbm.23044)
Lancaster, T. M. et al. 2016. Polygenic risk of psychosis and ventral striatal activation during reward processing in healthy adolescents. JAMA Psychiatry 73 (8), pp.852-861. (10.1001/jamapsychiatry.2016.1135)
Lawrie, S. M. et al., 2016. Improving classification of psychoses. The Lancet Psychiatry 3 (4), pp.367-374. (10.1016/S2215-0366(15)00577-5)
Lawrie, S. M. et al., 2016. Towards diagnostic markers for the psychoses. The Lancet Psychiatry 3 (4), pp.375-385. (10.1016/S2215-0366(16)00021-3)
Lawton, M. et al., 2016. Equating scores of the University of Pennsylvania smell identification test and sniffin' sticks test in patients with Parkinson's disease. Parkinsonism & Related Disorders 33 , pp.96-101. (10.1016/j.parkreldis.2016.09.023)
Legge, S. et al. 2016. Reasons for discontinuing clozapine: a cohort study of patients commencing treatment. Schizophrenia Research 174 , pp.113-119. (10.1016/j.schres.2016.05.002)
Lelos, M. J. et al. 2016. Direct comparison of rat- and human-derived ganglionic eminence tissue grafts on motor function. Cell Transplantation 25 , pp.665-675. (10.3727/096368915X690297)
Lewis, O. et al. 2016. Chronic, intermittent convection-enhanced delivery devices. Journal of Neuroscience Methods 259 , pp.47-56. (10.1016/j.jneumeth.2015.11.008)
Lubbe, S. et al., 2016. Rare variants analysis of cutaneous malignant melanoma genes in Parkinson's disease. Neurobiology of Aging 48 , pp.222.e1-222.e7. (10.1016/j.neurobiolaging.2016.07.013)
Lubbe, S. J. et al., 2016. Is the MC1R variant p.R160W associated with Parkinson's?. Annals of Neurology 79 (1), pp.159-161. (10.1002/ana.24527)
Lubbe, S. J. et al., 2016. Additional rare variant analysis in Parkinson?s disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance. Human Molecular Genetics 25 (24), pp.5483-5489. (10.1093/hmg/ddw348)
Malek, N. et al., 2016. Vascular disease and vascular risk factors in relation to motor features and cognition in early Parkinson's disease. Movement Disorders 31 (10), pp.1518-1526. (10.1002/mds.26698)
Martin, J. et al. 2016. Association of genetic risk for schizophrenia with nonparticipation over time in a population-based cohort study. American Journal of Epidemiology 183 (12), pp.1149-1158. (10.1093/aje/kww009)
Massey, T. , Pickersgill, T. T. and Peall, K. J. 2016. Nitrous oxide misuse and vitamin B12 deficiency. BMJ Case Reports 215728. (10.1136/bcr-2016-215728)
Massey, T. and Robertson, N. 2016. Zika virus and neurology: proving cause and effect. Journal of Neurology 263 (6), pp.1255-1257. (10.1007/s00415-016-8165-5)
McLauchlan, D. J. and Robertson, N. 2016. Reversing the trend: interventions to treat intracranial haemorrhage associated with anticoagulation. Journal of Neurology 263 (7), pp.1468-1470. (10.1007/s00415-016-8198-9)
McNamara, G. I. et al. 2016. Behavioural abnormalities in a novel mouse model for Silver Russell Syndrome. Human Molecular Genetics 25 (24), pp.5407-5417. (10.1093/hmg/ddw357)
Mehta, D. et al., 2016. Evidence for genetic overlap between schizophrenia and age at first birth in women. JAMA Psychiatry 73 (5), pp.497-505. (10.1001/jamapsychiatry.2016.0129)
Mikkelsen, M. et al., 2016. Quantification of y-aminobutyric acid (GABA) in 1 H MRS volumes composed heterogeneously of grey and white matter. NMR in Biomedicine 29 (11), pp.1644-1655. (10.1002/nbm.3622)
Miller, J. R. C. et al., 2016. RNA-Seq of Huntington's disease patient myeloid cells reveals innate transcriptional dysregulation associated with proinflammatory pathway activation. Human Molecular Genetics 25 (14), pp.2893-2904. (10.1093/hmg/ddw142)
Mitchell, C. J. and Robertson, N. 2016. New ways of looking at an old disease: the reimagination of epilepsy. Journal of Neurology 263 (2), pp.414-416. (10.1007/s00415-016-8025-3)
Mok, K. Y. et al., 2016. Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data. Lancet Neurology 15 (6), pp.585-596. (10.1016/S1474-4422(16)00071-5)
Mole, J. P. et al. 2016. Increased fractional anisotropy in the motor tracts of Parkinson's disease suggests compensatory neuroplasticity or selective neurodegeneration. European Radiology 26 (10), pp.3327-3335. (10.1007/s00330-015-4178-1)
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)
Morgan, C. and Harding, K. 2016. Being mortal. Practical Neurology 16 (2), pp.170-170. (10.1136/practneurol-2016-001386)
Mullins, N. et al., 2016. Polygenic interactions with environmental adversity in the aetiology of major depressive disorder. Psychological Medicine 46 (4), pp.759-770. (10.1017/S0033291715002172)
Munk-Olsen, T. et al., 2016. Perinatal psychiatric episodes: a population-based study on treatment incidence and prevalence. Translational Psychiatry 6 e919. (10.1038/tp.2016.190)
Neal, S. et al., 2016. Exploring the longitudinal association between interventions to support the transition to secondary school and child anxiety. Journal of Adolescence 50 , pp.31-43. (10.1016/j.adolescence.2016.04.003)
Newland, B. et al. 2016. Synthesis of ROS scavenging microspheres from a dopamine containing poly(beta-amino ester) for applications for neurodegenerative disorders. Biomaterials Science 4 (3), pp.400-404. (10.1039/C5BM00542F)
Ng-Knight, T. et al., 2016. A longitudinal study of self-control at the transition to secondary school: Considering the role of pubertal status and parenting. Journal of Adolescence 50 , pp.44-55. (10.1016/j.adolescence.2016.04.006)
Nimmo-Smith, V. et al., 2016. Discrimination, domestic violence, abuse, and other adverse life events in people with epilepsy: Population-based study to assess the burden of these events and their contribution to psychopathology. Epilepsia 57 (11), pp.1870-1878. (10.1111/epi.13561)
Nishi, D. et al., 2016. Adverse childhood experiences, support, and the perception of ability to work in adults with disability. PLoS ONE 11 (7) e0157726. (10.1371/journal.pone.0157726)
Northover, C. et al. 2016. Cortisol levels at baseline and under stress in adolescent males with Attention-Deficit Hyperactivity Disorder, with or without comorbid Conduct Disorder. Psychiatry Research 242 , pp.130-136. (10.1016/j.psychres.2016.05.052)
O'Doherty, S. et al., 2016. Perspectives of family members of people with an intellectual disability to a major reconfiguration of living arrangements for people with intellectual disability in Ireland. Journal of Intellectual Disabilities 20 (2), pp.137-151. (10.1177/1744629516636538)
O'Donovan, M. C. and Owen, M. J. 2016. The implications of the shared genetics of psychiatric disorders. Nature Medicine 22 , pp.1214-1219. (10.1038/nm.4196)
Owen, M. J. and Doherty, J. L. 2016. What can we learn from the high rates of schizophrenia in people with 22q11.2 deletion syndrome?. World Psychiatry 15 (1), pp.23-25. (10.1002/wps.20274)
Owen, M. J. , Sawa, A. and Mortensen, P. B. 2016. Schizophrenia. The Lancet 388 (10039), pp.86-97. (10.1016/S0140-6736(15)01121-6)
Pardinas, A. et al. 2016. Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection. [Online].bioRxiv. (10.1101/068593)Available at: http://dx.doi.org/10.1101/068593.
Peall, K. J. et al. 2016. Psychiatric disorders, myoclonus dystonia and SGCE: an international study. Annals of Clinical and Translational Neurology 3 (1), pp.4-11. (10.1002/acn3.263)
Peall, K. J. and Robertson, N. 2016. Idiopathic rapid eye movement sleep behaviour disorder: a potential gateway to the development of disease-modifying treatments in neurodegenerative disorders. Journal of Neurology 263 (8), pp.1678-1680. (10.1007/s00415-016-8235-8)
Pearson, R. M. et al., 2016. Maternal perinatal mental health and offspring academic achievement at age 16: the mediating role of childhood executive function. Journal of Child Psychology and Psychiatry 57 (4), pp.491-501. (10.1111/jcpp.12483)
Perry, A. et al., 2016. Adverse childhood life events and postpartum psychosis in bipolar disorder. Journal of affective disorders 205 , pp.69-72. (10.1016/j.jad.2016.06.061)
Pers, T. H. et al., 2016. Comprehensive analysis of schizophrenia-associated loci highlights ion channel pathways and biologically plausible candidate causal genes. Human Molecular Genetics 25 (6), pp.1247-1254. (10.1093/hmg/ddw007)
Pickrell, W. O. and Robertson, N. 2016. Stem cell treatment for multiple sclerosis. Journal of Neurology 263 (10), pp.2145-2147. (10.1007/s00415-016-8284-z)
Precious, S. V. et al., 2016. FoxP1 marks medium spiny neurons from precursors to maturity and is required for their differentiation. Experimental Neurology 282 , pp.9-18. (10.1016/j.expneurol.2016.05.002)
Prins, B. P. et al., 2016. Investigating the causal relationship of C-reactive protein with 32 complex somatic and psychiatric outcomes: a large-scale cross-consortium Mendelian randomization study. PLOS Medicine 13 (6) e1001976. (10.1371/journal.pmed.1001976)
Rees, E. et al. 2016. Analysis of intellectual disability copy number variants for association with schizophrenia. JAMA Psychiatry 73 (9), pp.963-969. (10.1001/jamapsychiatry.2016.1831)
Richards, A. et al. 2016. Exome arrays capture polygenic rare variant contributions to schizophrenia. Human Molecular Genetics 25 (5), pp.1001-1007. (10.1093/hmg/ddv620)
Rienecker, K. , Hill, M. and Isles, A. R. 2016. Methods of epigenome editing for probing the function of genomic imprinting. Epigenomics 8 (10), pp.1389-1398. (10.2217/epi-2016-0073)
Riglin, L. et al. 2016. Higher cognitive ability buffers stress-related depressive symptoms in adolescent girls. Development and Psychopathology 28 (1), pp.97-109. (10.1017/S0954579415000310)
Riglin, L. et al. 2016. Association of genetic risk variants with attention-deficit/hyperactivity disorder trajectories in the general population. JAMA Psychiatry 73 (12), pp.1285-1292. (10.1001/jamapsychiatry.2016.2817)
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