2017 publications
- Abdul Rahim, M. I. and Thomas, R. H. 2017. Gamification of medication adherence in epilepsy. Seizure - European Journal of Epilepsy 52 , pp.11-14. (10.1016/j.seizure.2017.09.008)
- Absoud, M. et al., 2017. A multicentre randomiSed controlled TRial of IntraVEnous immunoglobulin compared with standard therapy for the treatment of transverse myelitis in adults and children (STRIVE). Health Technology Assessment 21 31. (10.3310/hta21310)
- Abu-Akel, A. et al., 2017. Autistic and schizotypal traits and global functioning in bipolar I disorder. Journal of affective disorders 207 , pp.268-275. (10.1016/j.jad.2016.09.059)
- Adam, M. A. and Isles, A. R. 2017. EHMT1/GLP; biochemical function and association with brain disorders. Epigenomes 1 (3) 15. (10.3390/epigenomes1030015)
- Agha, S. S. et al. 2017. Maternal psychopathology and offspring clinical outcome: a four-year follow-up of boys with ADHD. European Child and Adolescent Psychiatry 26 (2), pp.253-262. (10.1007/s00787-016-0873-y)
- Al-Ansari, A. and Robertson, N. 2017. Creutzfeldt-Jacob disease: new directions in diagnosis and therapeutics. Journal of Neurology 264 (5), pp.1029-1031. (10.1007/s00415-017-8473-4)
- Allardyce, J. et al. 2017. Psychosis and the level of mood incongruence in Bipolar Disorder are related to genetic liability for Schizophrenia. [Online].bioRxiv. Available at: http://dx.doi.org/10.1101/160119.
- Andreassen, O. A. et al., 2017. Cortical abnormalities in bipolar disorder: An MRI analysis of 6,503 individuals from the ENIGMA-Bipolar Disorder Working Group. Molecular Psychiatry 23 , pp.932-942. (10.1038/mp.2017.73)
- Antonakakis, M. et al., 2017. Reconfiguration of dominant coupling modes in mild traumatic brain injury mediated by δ-band activity: a resting state MEG study. Neuroscience 356 , pp.275-286. (10.1016/j.neuroscience.2017.05.032)
- Bassett, A. S. et al., 2017. Rare genome-wide copy number variation and expression of schizophrenia in 22q11.2 deletion syndrome. American Journal of Psychiatry 174 (11), pp.1054-1063. (10.1176/appi.ajp.2017.16121417)
- Benson, M. A. et al., 2017. Ryanodine receptors are part of the myospryn complex in cardiac muscle. Scientific Reports 7 (1) 6312. (10.1038/s41598-017-06395-6)
- Bevan Jones, R. et al. 2017. Translation: From bench to brain – Using the visual arts and metaphors to engage and educate. Research for All 1 (2), pp.265-283. (10.18546/RFA.01.2.04)
- Bevan-Jones, R. et al. 2017. Psychoeducational interventions in adolescent depression: A systematic review. Patient Education and Counseling (10.1016/j.pec.2017.10.015)
- Beyer, S. 2017. Economic impact of inclusion in the open labour market for persons with disabilities. Éditions universitaires européennes.
- Beyer, S. and Beyer, A. 2017. A systematic review of the literature on the benefits for employers of employing people with learning disabilities. Technical Report.
- Bhugra, D. et al., 2017. The WPA-Lancet Psychiatry Commission on the future of psychiatry. The Lancet Psychiatry 4 (10), pp.775-818. (10.1016/S2215-0366(17)30333-4)
- Bigdeli, T. B. et al., 2017. Genetic effects influencing risk for major depressive disorder in China and Europe. Translational Psychiatry 7 (3), pp.e1074. (10.1038/tp.2016.292)
- Blokland, G. A. M. et al., 2017. Heritability of neuropsychological measures in Schizophrenia and non-psychiatric populations: a systematic review and meta-analysis. Schizophrenia Bulletin 43 (4), pp.788-800. (10.1093/schbul/sbw146)
- Bowles, K. R. et al. 2017. SMAD transcription factors are altered in cell models of HD and regulate HTT expression. Cellular Signalling 31 , pp.1-14. (10.1016/j.cellsig.2016.12.005)
- Casanova Dias, M. et al. 2017. Equipping doctors for global health challenges. Journal of the Royal Society of Medicine 110 (1), pp.5-8. (10.1177/0141076816686349)
- Chao, M. J. et al., 2017. Haplotype-based stratification of Huntington's disease. European Journal of Human Genetics 25 , pp.1202-1209. (10.1038/ejhg.2017.125)
- Charney, A. W. et al., 2017. Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder. Translational Psychiatry 7 (1), pp.e993. (10.1038/tp.2016.242)
- Chawner, S. et al. 2017. Childhood cognitive development in 22q11.2 deletion syndrome: case–control study. British Journal of Psychiatry 211 (4), pp.223-230. (10.1192/bjp.bp.116.195651)
- Clifton, N. E. et al. 2017. Schizophrenia copy number variants and associative learning. Molecular Psychiatry 22 (2), pp.178-182. (10.1038/mp.2016.227)
- Connolly, S. et al., 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)
- Copeland, L. et al. 2017. Measurement of side effects of anti-epileptic drugs (AEDs) in adults with intellectual disability: A systematic review. Seizure - European Journal of Epilepsy 51 , pp.61-73. (10.1016/j.seizure.2017.07.013)
- 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)
- Cosgrove, D. et al., 2017. Cognitive characterization of schizophrenia risk variants involved in synaptic transmission: evidence of CACNA1C's role in working memory. Neuropsychopharmacology 42 , pp.2612-2622. (10.1038/npp.2017.123)
- Crawshaw, A. and Harding, K. 2017. A portrait of the brain by Adam Zeman [Book Club]. Practical Neurology 17 , pp.419-419. (10.1136/practneurol-2017-001746)
- Crawshaw, A. and Harding, K. 2017. The Selfish Gene. Practical Neurology 17 (3), pp.244. (10.1136/practneurol-2017-001645)
- Crawshaw, A. A. and Robertson, N. P. 2017. The role of TSPO PET in assessing neuroinflammation. Journal of Neurology 264 (8), pp.1825-1827. (10.1007/s00415-017-8565-1)
- Davies, W. 2017. Understanding the pathophysiology of postpartum psychosis: challenges and new approaches. World Journal of Psychiatry 7 (2), pp.77-88. http://dx.doi.org/10.5498/wjp.v7.i2.77. (10.5498/wjp.v7.i2.77)
- De Giglio, L. et al., 2017. Effect on cognition of estroprogestins combined with Interferon beta in multiple sclerosis: analysis of secondary outcomes from a randomized controlled trial. CNS Drugs 31 (2), pp.161-168. (10.1007/s40263-016-0401-0)
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- Di Florio, A. et al. 2017. The impact of education, country, race and ethnicity on the self-report of postpartum depression using the Edinburgh Postnatal Depression Scale. Psychological Medicine 47 (5), pp.787-799. (10.1017/S0033291716002087)
- Dimitriadis, S. 2017. A high performing EEG approach for the automated scoring of the sleep stages of neonates. Clinical Neurophysiology 128 (6), pp.1039-1040. (10.1016/j.clinph.2017.04.001)
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- Direk, N. et al., 2017. An analysis of two genome-wide association meta-analyses identifies a new locus for broad depression phenotype. Biological Psychiatry 82 (5), pp.322-329. (10.1016/j.biopsych.2016.11.013)
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- Fernández, E. et al., 2017. Arc requires PSD95 for assembly into postsynaptic complexes involved with neural dysfunction and intelligence. Cell Reports 21 (3), pp.679-691. (10.1016/j.celrep.2017.09.045)
- Fonferko-Shadrach, B. et al., 2017. Validating epilepsy diagnoses in routinely collected data. Seizure 52 , pp.195-196. (10.1016/j.seizure.2017.10.008)
- Fovet, T. et al., 2017. Serious games: the future of psychotherapy? proposal of an integrative model. Psychotherapy and Psychosomatics 86 (3), pp.187-188. (10.1159/000460256)
- Fraguas, D. et al., 2017. Mental disorders of known aetiology and precision medicine in psychiatry: a promising but neglected alliance [Editorial]. Psychological Medicine 47 (2), pp.193-197. (10.1017/S0033291716001355)
- Gage, S. H. et al., 2017. Assessing causality in associations between cannabis use and schizophrenia risk: a two-sample Mendelian randomization study. Psychological Medicine 47 (5), pp.971-980. (10.1017/S0033291716003172)
- Gage, S. H. et al., 2017. Investigating causality in associations between smoking initiation and schizophrenia using Mendelian randomization. Scientific Reports 7 40653. (10.1038/srep40653)
- García-González, J. et al., 2017. Pharmacogenetics of antidepressant response: a polygenic approach. Progress in Neuro-Psychopharmacology and Biological Psychiatry 75 , pp.128-134. (10.1016/j.pnpbp.2017.01.011)
- Giegling, I. et al., 2017. Genetics of schizophrenia: A consensus paper of the WFSBP task force on genetics. World Journal of Biological Psychiatry 18 (7), pp.492-505. (10.1080/15622975.2016.1268715)
- Gomes, C. et al., 2017. Phenotyping the ancient world: the physical appearance and ancestry of very degraded samples from a chalcolithic human remains. Forensic Science International: Genetics Supplement Series 6 , pp.e484-e486. (10.1016/j.fsigss.2017.09.188)
- Gordon-Smith, K. et al., 2017. Changes to the diagnostic criteria for bipolar disorder in DSM-5 make little difference to lifetime diagnosis: findings from the U.K. Bipolar Disorder Research Network (BDRN) study. American Journal of Psychiatry 174 (8), pp.803. (10.1176/appi.ajp.2017.17010109)
- Green, E. K. et al., 2017. Genome-wide significant locus for Research Diagnostic Criteria Schizoaffective Disorder Bipolar type. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 174 (8), pp.767-771. (10.1002/ajmg.b.32572)
- Green, T. , Naylor, P. and Davies, W. 2017. Attention Deficit Hyperactivity Disorder (ADHD) in phenotypically-similar neurogenetic conditions: Turner syndrome and the RASopathies. Journal of Neurodevelopmental Disorders 9 (25), pp.794-802. (10.1186/s11689-017-9205-x)
- Greene, C. et al., 2017. Dose-dependent expression of claudin-5 is a modifying factor in schizophrenia. Molecular Psychiatry 23 , pp.2156-2166. (10.1038/mp.2017.156)
- Grütz, K. et al., 2017. Faithful SGCE imprinting in iPSC-derived cortical neurons: an endogenous cellular model of myoclonus-dystonia. Scientific Reports 7 41156. (10.1038/srep41156)
- Gur, R. et al., 2017. A neurogenetic model for the study of schizophrenia spectrum disorders: The International 22q11.2 Deletion Syndrome Brain Behavior Consortium. Molecular Psychiatry 22 , pp.1664-1672.
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- Hakobyan, S. et al. 2017. Plasma complement biomarkers distinguish multiple sclerosis and neuromyelitis optica spectrum disorder. Multiple Sclerosis Journal 23 (7), pp.946-955. 135245851666900. (10.1177/1352458516669002)
- Hampel, H. et al., 2017. A precision medicine initiative for Alzheimer's disease: the road ahead to biomarker-guided integrative disease modeling. Climacteric 20 (2), pp.107-118. (10.1080/13697137.2017.1287866)
- Handley, J. D. et al., 2017. On the road again: assessing driving ability in patients with neurological conditions. Practical Neurology 17 (3)(10.1136/practneurol-2017-001601)
- Hannon, E. et al., 2017. Pleiotropic effects of trait-associated genetic variation on DNA methylation: utility for refining GWAS loci. American Journal of Human Genetics 100 (6), pp.954-959. (10.1016/j.ajhg.2017.04.013)
- Harding, K. and Robertson, N. 2017. Epidemiology of progressive multiple sclerosis. In: Wilkins, A. ed. Progressive Multiple Sclerosis. Springer. , pp.31-47. (10.1007/978-3-319-65921-3_2)
- Harding, K. et al. 2017. Seasonal variation in multiple sclerosis relapse. Journal of Neurology 264 (6), pp.1059-1067. (10.1007/s00415-017-8485-0)
- Harrison, J. R. 2017. Improving inpatient care for older adults: implementing dementia commissioning for quality and innovation (CQUIN). BMJ Quality Improvement Reports 6 (1), pp.u212202.w4875. (10.1136/bmjquality.u212202.w4875)
- Harvey, E. et al., 2017. Potency of human cardiosphere-derived cells from patients with ischemic heart disease is associated with robust vascular supportive ability. Stem Cells Translational Medicine 6 (5), pp.1399-1411. (10.1002/sctm.16-0229)
- Hayes, J. F. et al., 2017. Childhood interleukin-6, C-reactive protein and atopic disorders as risk factors for hypomanic symptoms in young adulthood: a longitudinal birth cohort study. Psychological Medicine 47 (1), pp.1-11. (10.1017/S0033291716001574)
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- Hensman Moss, D. J. et al., 2017. Huntington's disease blood and brain show a common gene expression pattern and share an immune signature with Alzheimer's disease. Scientific Reports 7 , pp.-. 44849. (10.1038/srep44849)
- Hensman Moss, D. J. et al., 2017. Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study. Lancet Neurology 16 (9), pp.701-711. (10.1016/S1474-4422(17)30161-8)
- Hill, M. et al. 2017. Knockdown of the schizophrenia susceptibility gene TCF4 alters gene expression and proliferation of progenitor cells from the developing human neocortex. Journal of Psychiatry & Neuroscience 42 (3), pp.181-188. 160073. (10.1503/jpn.160073)
- Holmans, P. A. , Massey, T. H. and Jones, L. 2017. Genetic modifiers of Mendelian disease: Huntington's disease and the trinucleotide repeat disorders. Human Molecular Genetics 26 (R2), pp.R83-R90. (10.1093/hmg/ddx261)
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- Hughes, E. and Thomas, R. H. 2017. Epilepsy treatment priorities: answering the questions that matter. Journal of Neurology, Neurosurgery, and Psychiatry 88 (11), pp.999-1001. (10.1136/jnnp-2016-315135)
- Humby, T. et al. 2017. A genetic variant within STS previously associated with inattention in boys with Attention Deficit Hyperactivity Disorder is associated with enhanced cognition in healthy adult males. Brain and Behavior 7 (3) e00646. (10.1002/brb3.646)
- Hyland, P. et al., 2017. Validation of Posttraumatic Stress Disorder (PTSD) and Complex-PTSD using the International Trauma Questionnaire. Acta Psychiatrica Scandinavica 136 (3), pp.313-322. (10.1111/acps.12771)
- Jamjoom, A. A. B. et al., 2017. Prospective, multicentre study of external ventricular drainage-related infections in the UK and Ireland. Journal of Neurology, Neurosurgery & Psychiatry (10.1136/jnnp-2017-316415)
- Jansen, I. E. et al., 2017. Establishing the role of rare coding variants in known Parkinson's disease risk loci. Neurobiology of Aging 59 , pp.220.e11-220.e18. (10.1016/j.neurobiolaging.2017.07.009)
- Jeong, Y. H. et al., 2017. Tdp-43 cryptic exons are highly variable between cell types. Molecular Neurodegeneration 12 (10.1186/s13024-016-0144-x)
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