Cyhoeddiadau 2016

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)
Riglin, L. et al. 2016. Profiling depression in childhood and adolescence: the role of conduct problems. Journal of Child Psychology and Psychiatry 57 (4), pp.481-490. (10.1111/jcpp.12465)
Rodríguez Cruz, P. M. et al., 2016. Time and region-specific season of birth effects in multiple sclerosis in the United Kingdom. JAMA Neurology 73 (8), pp.954-960. (10.1001/jamaneurol.2016.1463)
Roiser, J. P. et al., 2016. Minimum statistical standards for submissions to Neuroimage: Clinical [Editorial]. NeuroImage: Clinical 12 , pp.1045-1047. (10.1016/j.nicl.2016.08.002)
Rucker, J. J. et al., 2016. Phenotypic association analyses with copy number variation in recurrent depressive disorder. Biological Psychiatry 79 (4), pp.329-336. (10.1016/j.biopsych.2015.02.025)
Scholz, B. et al., 2016. The regulation of cytokine networks in hippocampal CA1 differentiates extinction from those required for the maintenance of contextual fear memory after recall. PLoS ONE 11 (5) e0153102. (10.1371/journal.pone.0153102)
Scott, R. A. et al., 2016. A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease. Science Translational Medicine 8 (341) 341ra76. (10.1126/scitranslmed.aad3744)
Sellers, R. et al. 2016. Examining whether offspring psychopathology influences illness course in mothers with recurrent depression using a high-risk longitudinal sample. Journal of Abnormal Psychology 125 (2), pp.256-266. (10.1037/abn0000080)
Siebald, C. et al., 2016. Association between childhood psychiatric disorders and psychotic experiences in adolescence: A population-based longitudinal study. Comprehensive Psychiatry 69 , pp.45-52. (10.1016/j.comppsych.2016.05.004)
Sims, R. and Williams, J. 2016. Defining the genetic architecture of Alzheimer's Disease: where next. Neurodegenerative Diseases 16 (1-2)(10.1159/000440841)
Singh, T. et al., 2016. Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders. Nature Neuroscience 19 , pp.571-577. (10.1101/036384)
Singh, T. et al., 2016. Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders. Nature Neuroscience 19 (4), pp.571-577. (10.1038/nn.4267)
Smith, D. J. et al., 2016. Genome-wide analysis of over 106,000 individuals identifies 9 neuroticism-associated loci. Molecular Psychiatry 21 , pp.749-757. (10.1038/mp.2016.49)
Stephan, K. E. et al., 2016. Charting the landscape of priority problems in psychiatry, part 1: classification and diagnosis. The Lancet Psychiatry 3 (1), pp.77-83. (10.1016/S2215-0366(15)00361-2)
Stephan, K. E. et al., 2016. Charting the landscape of priority problems in psychiatry, part 2: pathogenesis and aetiology. The Lancet Psychiatry 3 (1), pp.84-90. (10.1016/S2215-0366(15)00360-0)
Stergiakouli, E. , Thapar, A. and Davey Smith, G. 2016. Association of acetaminophen use during pregnancy with behavioral problems in childhood. JAMA Pediatrics 170 (10), pp.964-970. (10.1001/jamapediatrics.2016.1775)
Steventon, J. et al. 2016. Longitudinal in vivo MRI in a Huntington's disease mouse model: global atrophy in the absence of white matter microstructural damage. Scientific Reports 6 32423. (10.1038/srep32423)
Steventon, J. et al. 2016. Robust MR-based approaches to quantifying white matter structure and structure/function alterations in Huntington's disease. Journal of Neuroscience Methods 265 , pp.2-12. (10.1016/j.jneumeth.2015.08.027)
Straccia, M. et al., 2016. Human t-DARPP is induced during striatal development. Neuroscience 333 , pp.320-330. (10.1016/j.neuroscience.2016.07.022)
Strehlow, V. et al., 2016. Generalized epilepsy and myoclonic seizures in 22q11.2 deletion syndrome. Molecular Syndromology 7 (4), pp.239-246. (10.1159/000448445)
Subramanian, L. et al. 2016. Clinical improvements following bilateral anterior capsulotomy in treatment-resistant depression. Psychological Medicine 47 (6), pp.1097-1106. (10.1017/S0033291716003159)
Subramanian, L. et al. 2016. Functional magnetic resonance imaging neurofeedback-guided motor imagery training and motor training for Parkinson's Disease: randomized trial. Frontiers in Behavioral Neuroscience 10 111. (10.3389/fnbeh.2016.00111)
Sullivan, S. A. et al., 2016. A longitudinal investigation of childhood communication ability and adolescent psychotic experiences in a community sample. Schizophrenia Research 173 (1-2), pp.54-61. (10.1016/j.schres.2016.03.005)
Swallow, D. M. A. et al., 2016. Statins are underused in recent-onset Parkinson's disease with increased vascular risk: findings from the UK Tracking Parkinson's and Oxford Parkinson's Disease Centre (OPDC) discovery cohorts. Journal of Neurology, Neurosurgery & Psychiatry 87 (11), pp.1183-1190. (10.1136/jnnp-2016-313642)
Tallantyre, E. C. , Wardle, M. and Robertson, N. 2016. How to run a multiple sclerosis relapse clinic. Practical Neurology 16 (1), pp.62-69. (10.1136/practneurol-2015-001214)
Tansey, K. E. et al. 2016. Common alleles contribute to schizophrenia in CNV carriers. Molecular Psychiatry 21 , pp.1085-1089. (10.1038/mp.2015.143)
Telezhkin, V. et al., 2016. Forced cell-cycle exit and modulation of GABAA, CREB and GSK3β signaling promote functional maturation of induced pluripotent stem cell-derived neurons. American Journal of Physiology - Cell Physiology ajpcell.00166.2015. (10.1152/ajpcell.00166.2015)
Thapar, A. et al. 2016. Psychiatric gene discoveries shape evidence on ADHD's biology. Molecular Psychiatry 21 , pp.1202-1207. (10.1038/mp.2015.163)
Thapar, A. et al. 2016. Identifying key parent-reported symptoms for detecting depression in high risk adolescents. Psychiatry Research 242 , pp.210-217. (10.1016/j.psychres.2016.05.025)
Thapar, A. and Cooper, M. 2016. Attention deficit hyperactivity disorder. Lancet 387 (10024), pp.1240-1250. (10.1016/S0140-6736(15)00238-X)
Thomas, R. S. et al. 2016. Decreasing the expression of PICALM reduces endocytosis and the activity of β-secretase: implications for Alzheimer's disease. BMC Neuroscience 17 50. (10.1186/s12868-016-0288-1)
Thomas, R. H. and Robertson, N. 2016. The consequences of valproate exposure in utero. Journal of Neurology 263 (9), pp.1887-1889. (10.1007/s00415-016-8269-y)
Thomas, R. H. and Robertson, N. 2016. What can rare variant genetics tell us about cognition and intellectual difficulties?. Journal of Neurology 263 (12), pp.2565-2566. (10.1007/s00415-016-8326-6)
Thomson, P. A. et al., 2016. Balanced translocation linked to psychiatric disorder, glutamate, and cortical structure/function. npj Schizophrenia 2 16024. (10.1038/npjschz.2016.24)
Tilling, K. et al., 2016. Modelling disease progression in relapsing?remitting onset multiple sclerosis using multilevel models applied to longitudinal data from two natural history cohorts and one treated cohort. Health Technology Assessment 20 (81)(10.3310/hta20810)
Tomassini, V. et al. 2016. The effect of inflammation and its reduction on brain plasticity in multiple sclerosis: MRI evidence. Human Brain Mapping 37 (7), pp.2431-2445. (10.1002/hbm.23184)
Townhill, J. et al. 2016. Using Actiwatch to monitor circadian rhythm disturbance in Huntington' disease: A cautionary note. Journal of Neuroscience Methods 265 , pp.13-18. (10.1016/j.jneumeth.2016.01.009)
van Goozen, S. H. M. et al. 2016. Identifying mechanisms that underlie links between COMT genotype and aggression in male adolescents with ADHD. Journal of Child Psychology and Psychiatry 57 (4), pp.472-480. (10.1111/jcpp.12464)
Waite, A. J. et al. 2016. Myoclonus dystonia and muscular dystrophy: ɛ-sarcoglycan is part of the dystrophin-associated protein complex in brain. Movement Disorders 31 (11), pp.1694-1703. (10.1002/mds.26738)
Walton, C. and Kerr, M. P. 2016. Prader Willi syndrome: systematic review of the prevalence and nature of presentation of unipolar depression. Advances in Mental Health and Intellectual Disabilities 10 (3), pp.172-184. (10.1108/AMHID-08-2015-0037)
Walton, C. and Kerr, M. 2016. Severe intellectual disability: systematic review of the prevalence and nature of presentation of unipolar depression. Journal of Applied Research in Intellectual Disabilities 29 (5), pp.395-408. (10.1111/jar.12203)
Wang, Y. et al., 2016. Leveraging genomic annotations and pleiotropic enrichment for improved replication rates in schizophrenia GWAS. PLoS Genetics 12 (1) e1005803. (10.1371/journal.pgen.1005803)
Watkins, L. M. et al., 2016. Complement is activated in progressive multiple sclerosis cortical grey matter lesions. Journal of Neuroinflammation 13 161. (10.1186/s12974-016-0611-x)
Whitton, L. et al., 2016. Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 171 (8), pp.1170-1179. (10.1002/ajmg.b.32503)
Williams, C. J. et al., 2016. Cluster of atypical adult Guillain-Barré syndrome temporally associated with neurological illness due to EV-D68 in children, South Wales, United Kingdom, October 2015 to January 2016. Eurosurveillance 21 (4) 30119. (10.2807/1560-7917.ES.2016.21.4.30119)
Willis, M. et al. 2016. Alemtuzumab for multiple sclerosis: Long term follow-up in a multi-centre cohort. Multiple Sclerosis Journal 22 (9), pp.1215-1223. 1352458515614092. (10.1177/1352458515614092)
Willis, M. et al. 2016. Alemtuzumab-induced remission of multiple sclerosis-associated uveitis. International Ophthalmology (10.1007/s10792-016-0370-9)
Willis, M. and Robertson, N. 2016. Alemtuzumab for multiple sclerosis. Current Neurology and Neuroscience Reports 16 84. (10.1007/s11910-016-0685-y)
Witczak, J. et al. 2016. Predicting malignancy in thyroid nodules: feasibility of a predictive model integrating clinical, biochemical, and ultrasound characteristics. Thyroid Research 9 (1) 4. (10.1186/s13044-016-0033-y)
Yhnell, E. , Dunnett, S. and Brooks, S. 2016. A longitudinal operant assessment of cognitive and behavioural changes in the HdhQ111 mouse model of Huntington's Disease. PLoS ONE 11 (10) e0164072. (10.1371/journal.pone.0164072)
Zacharopoulos, G. et al. 2016. A hedonism hub in the human brain. Cerebral Cortex 26 (10), pp.3921-3927. (10.1093/cercor/bhw197)
Zutt, R. et al., 2016. Distribution and coexistence of myoclonus and dystonia as clinical predictors of SGCE mutation status: a pilot study. Frontiers in Neurology 7 72. (10.3389/fneur.2016.00072)

Cyhoeddiadau 2016

Archif cyhoeddiadau

Canolfan ar gyfer Geneteg a Genomeg Niwroseiciatrig

Cysylltwch â ni

Ymweld â Chanolfan ar gyfer Geneteg a Genomeg Niwroseiciatrig