Cyhoeddiadau 2014

Aguirregomozcorta, M. and Robertson, N. 2014. Pregnancy and drug use in neurological disease. Journal of Neurology 261 (4), pp.842-844. (10.1007/s00415-014-7312-0)
Akpudo, H. et al., 2014. Summaries of oral sessions at the XXI World Congress of Psychiatric Genetics, Boston, Massachusetts, 17-21 October 2013. Psychiatric Genetics 24 (4), pp.125-150. (10.1097/YPG.0000000000000043)
Ali, K. and Robertson, N. 2014. Evolving concepts in migraine. Journal of Neurology 261 (5), pp.1046-1048. (10.1007/s00415-014-7348-1)
Amin, R. A. and Robertson, N. 2014. Risk and sub phenotype in Parkinson's disease. Journal of Neurology 261 (1), pp.245-7. (10.1007/s00415-013-7214-6)
Andreasen, J. N. et al., 2014. EQ-5D health utility values in the treatment Of seasonal grass pollen induced rhinoconjunctivitis. Journal of Allergy and Clinical Immunology 133 (2S) AB222. (10.1016/j.jaci.2013.12.793)
Andreassen, O. A. et al., 2014. Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci. Molecular Psychiatry 20 (2), pp.207. (10.1038/mp.2013.195)
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)
Azzopardi, L. et al., 2014. Predicting autoimmunity after alemtuzumab treatment of multiple sclerosis. Journal of Neurology, Neurosurgery & Psychiatry 85 (7), pp.795-98. (10.1136/jnnp-2013-307042)
Bacanu, S. et al., 2014. Functional SNPs are enriched for schizophrenia association signals [Letter]. Molecular Psychiatry 19 (3), pp.276-277. (10.1038/mp.2013.33)
Baker, J. H. et al., 2014. Primary amenorrhea in anorexia nervosa: impact on characteristic masculine and feminine traits. European Eating Disorders Review 22 (1), pp.32-38. (10.1002/erv.2263)
Bannister, C. A. et al. 2014. Automatic development of clinical prediction models with genetic programming: A case study in cardiovascular disease. Value in Health 17 (3), pp.A200-A201. (10.1016/j.jval.2014.03.1171)
Bannister, C. et al. 2014. Can people with type 2 diabetes live longer than people without diabetes? A comparison of all-cause mortality in people initiated with metformin monotherapy or sulfonylurea monotherapy and matched controls without diabetes. Diabetes, Obesity and Metabolism 16 (11), pp.1165-1173. (10.1111/dom.12354)
Bannister, C. et al. 2014. External validation of the UKPDS risk engine in incident type 2 diabetes: a need for new type 2 diabetes-specific risk equations. Diabetes Care 37 (2), pp.537-545. (10.2337/dc13-1159)
Barker, V. et al., 2014. Set shifting and reversal learning in borderline personality disorder. Personality and Mental Health 8 (1), pp.1-13. (10.1002/pmh.1235)
Bebko, G. et al., 2014. Parsing dimensional vs diagnostic category - related patterns of reward circuitry function in behaviorally and emotionally dysregulated youth in the longitudinal assessment of manic symptoms study. JAMA Psychiatry 71 (1), pp.71-80. (10.1001/jamapsychiatry.2013.2870)
Beilina, A. et al., 2014. Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease. Proceedings of the National Academy of Sciences of the United States of America 111 (7), pp.2626-2631. (10.1073/pnas.1318306111)
Benitez, B. A. et al., 2014. Missense variant in TREML2 protects against Alzheimer's disease. Neurobiology of Aging 35 (6), pp.1510.e19-26. (10.1016/j.neurobiolaging.2013.12.010)
Bennett, C. , Bevan-Jones, R. and Smith, D. 2014. Prevention strategies for adolescent depression. Advances in Psychiatric Treatment 20 (2), pp.116-124. (10.1192/apt.bp.112.010314)
Berni, E. et al., 2014. PWE-154 the first evaluation of the relationship between the chronic liver disease questionnaire and the Eq-5d index In hepatic encephalopathy patients treated with Rifaximin-a. Gut 63 (Suppl) A192. (10.1136/gutjnl-2014-307263.414)
Bisson, J. I. 2014. Early responding to traumatic events. British Journal of Psychiatry 204 (5), pp.329-330. (10.1192/bjp.bp.113.136077)
Bowles, K. and Jones, L. 2014. Kinase signalling in Huntington's disease. Journal of Huntington's Disease 3 , pp.89-123. (10.3233/JHD-140106)
Bras, J. et al., 2014. Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies. Human Molecular Genetics 23 (23), pp.6139-6146. (10.1093/hmg/ddu334)
Brown, G. W. et al., 2014. Functional polymorphism in the brain-derived neurotrophic factor gene interacts with stressful life events but not childhood maltreatment in the etiology of depression. Depression and Anxiety 31 (4), pp.326-34. (10.1002/da.22221)
Brydges, N. et al. 2014. Juvenile stress produces long-lasting changes in hippocampal DISC1, GSK3ß and NRG1 expression. Molecular Psychiatry 19 (8), pp.854. (10.1038/mp.2013.193)
Brydges, N. et al. 2014. Prepubertal stress and hippocampal function: Sex-specific effects. Hippocampus 24 (6), pp.684-692. (10.1002/hipo.22259)
Busse, M. et al. 2014. Supporting physical activity engagement in people with Huntington's disease (ENGAGE-HD): study protocol for a randomized controlled feasibility trial. Trials 15 (1) 487. (10.1186/1745-6215-15-487)
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)
Cardno, A. G. and Owen, M. J. 2014. Genetic relationships between schizophrenia, bipolar disorder, and schizoaffective disorder. Schizophrenia Bulletin 40 (3), pp.504-515. (10.1093/schbul/sbu016)
Chase, H. W. et al., 2014. Disrupted posterior cingulate-amygdala connectivity in postpartum depressed women as measured with resting BOLD fMRI. Social Cognitive and Affective Neuroscience 9 (8), pp.1069-75. (10.1093/scan/nst083)
Collett, J. et al., 2014. Insights into gait disorders: walking variability using phase plot analysis, Huntington's Disease. Gait and Posture 40 (4), pp.694-700. (10.1016/j.gaitpost.2014.08.001)
Cooper, M. , Langley, K. and Thapar, A. 2014. Antenatal Acetaminophen use and attention-deficit/hyperactivity disorder. JAMA Pediatrics 168 (4), pp.306-307. (10.1001/jamapediatrics.2013.5292)
Cooper, M. et al. 2014. Autistic traits in children with ADHD index clinical and cognitive problems. European Child & Adolescent Psychiatry 23 (1), pp.23-24. (10.1007/s00787-013-0398-6)
Cooper, M. , Thapar, A. and Jones, D. K. 2014. White matter microstructure predicts autistic traits in attention-deficit/hyperactivity disorder. Journal of Autism and Developmental Disorders 44 (11), pp.2742-2754. (10.1007/s10803-014-2131-9)
Court, H. et al., 2014. Improving the psychometric utility of the hypomania checklist (HCL-32): A Rasch analysis approach. Journal of affective disorders 152-15 , pp.448-53. (10.1016/j.jad.2013.10.014)
Cowley, M. et al., 2014. Developmental programming mediated by complementary roles of imprinted Grb10 in mother and pup. PLoS Biology 12 (2), pp.e1001799. (10.1371/journal.pbio.1001799)
Craddock, N. J. 2014. Social neuroscience: bringing an end to the destructive and misguided "social" versus "biological" in psychiatry. World Psychiatry 13 (2), pp.140-141. (10.1002/wps.20119)
Craddock, N. J. et al. 2014. Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations. Schizophrenia Bulletin 40 (4), pp.729-736. (10.1093/schbul/sbu069)
Craddock, N. J. and Mynors-Wallis, L. 2014. Psychiatric diagnosis: impersonal, imperfect and important. British Journal of Psychiatry 204 (2), pp.93-95. (10.1192/bjp.bp.113.133090)
Craddock, N. J. and Mynors-Wallis, L. 2014. Authors' reply. British Journal of Psychiatry 205 (6), pp.498. (10.1192/bjp.205.6.498)
Crawford, A. A. et al., 2014. Adverse effects from antidepressant treatment: randomised controlled trial of 601 depressed individuals. Psychopharmacology 231 (15), pp.2921-2931. (10.1007/s00213-014-3467-8)
Dascher-Nadel, C. , Rosser, A. E. and Dunnett, S. B. 2014. Repair-HD: Human pluripotent stem cell differentiation, safety, and preparation for therapeutic transplantation in Huntington disease. HD Insights 8 , pp.9-10.
Davies, W. 2014. Sex differences in Attention Deficit Hyperactivity Disorder: Candidate genetic and endocrine mechanisms. Frontiers in Neuroendocrinology 35 (3), pp.331-346. (10.1016/j.yfrne.2014.03.003)
Davies, W. et al. 2014. Genetic and pharmacological modulation of the steroid sulfatase axis improves response control; comparison to drugs used in ADHD. Neuropsychopharmacology 39 , pp.2622-2632. (10.1038/npp.2014.115)
Davis, B. A. and Isles, A. R. 2014. Modelling the genetic contribution to mental illness: a timely end for the psychiatric rodent?. European Journal of Neuroscience 39 (11), pp.1933-1942. (10.1111/ejn.12607)
De Rubeis, S. et al., 2014. Synaptic, transcriptional and chromatin genes disrupted in autism. Nature 515 , pp.209-215. (10.1038/nature13772)
De Santis, S. et al. 2014. Why diffusion tensor MRI does well only some of the time: Variance and covariance of white matter tissue microstructure attributes in the living human brain. NeuroImage 89 , pp.35-44. (10.1016/j.neuroimage.2013.12.003)
de Wit, S. J. et al., 2014. Multicenter voxel-based morphometry mega-analysis of structural brain scans in obsessive-compulsive disorder. American Journal of Psychiatry 171 (3), pp.340-349. (10.1176/appi.ajp.2013.13040574)
Dent, C. and Isles, A. R. 2014. Brain-expressed imprinted genes and adult behaviour: the example of Nesp and Grb10. Mammalian Genome 25 (1-2), pp.87-93. (10.1007/s00335-013-9472-0)
Dent, C. , Isles, A. R. and Humby, T. 2014. Measuring risk-taking in mice: balancing the risk between seeking reward and danger. European Journal of Neuroscience 39 (4), pp.520-530. (10.1111/ejn.12430)
Dent, C. L. and Isles, A. R. 2014. An Overview of measuring impulsive behavior in mice. Current Protocols in Mouse Biology 4 (2), pp.35-45. (10.1002/9780470942390.mo140015)
Di Florio, A. , Craddock, N. J. and van den Bree, M. B. 2014. Alcohol misuse in bipolar disorder. A systematic review and meta-analysis of comorbidity rates. European Psychiatry 29 (3), pp.117-24. (10.1016/j.eurpsy.2013.07.004)
Di Florio, A. et al. 2014. Postpartum bipolar depression in a clinical sample of 1721 parous women with mood disorders [Conference Abstract]. Bipolar Disorders 16 (S1), pp.62-62. (10.1111/bdi.12188)
Di Florio, A. et al. 2014. Mood disorders and parity - A clue to the aetiology of the postpartum trigger. Journal of affective disorders 152-15 , pp.334-339. (10.1016/j.jad.2013.09.034)
Doherty, J. and Owen, M. J. 2014. Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice. Genome Medicine 6 (4) 29. (10.1186/gm546)
Doherty, J. L. and Owen, M. J. 2014. The Research Domain Criteria: moving the goalposts to change the game. British Journal of Psychiatry 204 (3), pp.171-173. (10.1192/bjp.bp.113.133330)
Dong, J. et al., 2014. Susceptibility loci for pigmentation and melanoma in relation to Parkinson's disease. Neurobiology of Aging 35 (6), pp.1512.e5-10. (10.1016/j.neurobiolaging.2013.12.020)
Dorrington, S. et al., 2014. Perinatal maternal life events and psychotic experiences in children at twelve years in a birth cohort study. Schizophrenia Research 152 (1), pp.158-163. (10.1016/j.schres.2013.11.006)
Downing, N. R. et al., 2014. WHODAS 2.0 in prodromal Huntington disease: measures of functioning in neuropsychiatric disease. European Journal of Human Genetics 22 (8), pp.958-63. (10.1038/ejhg.2013.275)
Duncan, L. E. et al., 2014. Pathway analyses implicate glial cells in schizophrenia. PLoS ONE 9 (2), pp.-. e89441. (10.1371/journal.pone.0089441)
Dunnett, S. B. and Rosser, A. E. 2014. Challenges for taking primary and stem cells into clinical neurotransplantation trials for neurodegenerative disease. Neurobiology of Disease 61 , pp.79-89. (10.1016/j.nbd.2013.05.004)
Elsone, L. et al., 2014. Long-term efficacy, tolerability and retention rate of azathioprine in 103 aquaporin-4 antibody-positive neuromyelitis optica spectrum disorder patients: a multicentre retrospective observational study from the UK. Multiple Sclerosis Journal 20 (11), pp.1533-1540. (10.1177/1352458514525870)
Erk, S. et al., 2014. Replication of brain function effects of a genome-wide supported psychiatric risk variant in the CACNA1C gene and new multi-locus effects. NeuroImage 94 , pp.147-154. (10.1016/j.neuroimage.2014.03.007)
Escott-Price, V. et al. 2014. Gene-wide analysis detects two new susceptibility genes for Alzheimer's Disease. PLoS ONE 9 (6) e94661. (10.1371/journal.pone.0094661)
Escott-Price, V. , Ghodsi, M. and Schmidt, K. M. 2014. How allele frequency and study design affect association test statistics with misrepresentation errors. Biostatistics 15 (2), pp.311-326. (10.1093/biostatistics/kxt048)
Esmail, S. and Linden, D. E. J. 2014. Neural networks and neurofeedback in Parkinson's Disease. NeuroRegulation 1 (3-4), pp.240-272. (10.15540/nr.1.3-4.240)
Eyre, O. et al. 2014. Reported child awareness of parental depression. Psychiatric Bulletin 38 (3), pp.122-127. (10.1192/pb.bp.113.044198)
Eyre, O. and Thapar, A. 2014. Common adolescent mental disorders: transition to adulthood. The Lancet 383 (9926), pp.1366. (10.1016/S0140-6736(13)62633-1)
Ferentinos, P. et al., 2014. Investigating the genetic variation underlying episodicity in major depressive disorder: Suggestive evidence for a bipolar contribution. Journal of Affective Disorders 155 , pp.81-89. (10.1016/j.jad.2013.10.027)
Fisher, H. L. et al., 2014. Childhood parasomnias and psychotic experiences at age 12 years in a United Kingdom birth cohort. Sleep 37 (3), pp.475-482. (10.5665/sleep.3478)
Flower, M. D. and Robertson, N. 2014. POLG: a cause of intractable epilepsy. Journal of Neurology 261 (2), pp.446-448. (10.1007/s00415-014-7255-5)
Fogh, I. et al., 2014. A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. Human Molecular Genetics 23 (8), pp.2220-2231. (10.1093/hmg/ddt587)
Forrest, M. et al., 2014. The emerging roles of TCF4 in disease and development. Trends in Molecular Medicine 20 (6), pp.322-331. (10.1016/j.molmed.2014.01.010)
Forty, E. et al. 2014. Comorbid medical illness in bipolar disorder. British Journal of Psychiatry 205 (6), pp.465-472. (10.1192/bjp.bp.114.152249)
Frisullo, G. et al., 2014. Thyroid autoimmunity and dysfunction in multiple sclerosis patients during long-term treatment with interferon beta or glatiramer acetate: an Italian multicenter study. Multiple Sclerosis Journal 20 (9), pp.1265. (10.1177/1352458514521311)
Fromer, M. et al., 2014. De novo mutations in schizophrenia implicate synaptic networks. Nature 506 , pp.179-184. (10.1038/nature12929)
Gage, S. H. et al., 2014. Associations of cannabis and cigarette use with psychotic experiences at age 18: findings from the Avon Longitudinal Study of Parents and Children. Psychological Medicine 44 (16), pp.3435-3444. (10.1017/S0033291714000531)
Geoffroy, P. A. et al., 2014. The arcuate fasciculus in auditory-verbal hallucinations: A meta-analysis of diffusion-tensor-imaging studies. Schizophrenia Research 159 (1), pp.234-237. (10.1016/j.schres.2014.07.014)
Georgieva, L. et al. 2014. De novo CNVs in bipolar affective disorder and schizophrenia. Human Molecular Genetics 23 (24), pp.6677-6683. (10.1093/hmg/ddu379)
Gohier, B. et al., 2014. Genetic modulation of the response bias towards facial displays of anger and happiness. European Psychiatry 29 (4), pp.197-202. (10.1016/j.eurpsy.2013.03.003)
Grundy, G. J. et al., 2014. One ring to bring them all - the role of Ku in mammalian non-homologous end joining. DNA Repair 17 , pp.30-38. (10.1016/j.dnarep.2014.02.019)
Gusareva, E. S. et al., 2014. Genome-wide association interaction analysis for Alzheimer's disease. Neurobiology of Aging 35 (11), pp.2436-2443. (10.1016/j.neurobiolaging.2014.05.014)
Gusev, A. et al., 2014. Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. American Journal of Human Genetics 95 (5), pp.535-552. (10.1016/j.ajhg.2014.10.004)
Haddon, J. E. et al. 2014. Extreme elemental processing in a high schizotypy population: relation to cognitive deficits. The Quarterly Journal of Experimental Psychology 67 (5), pp.918-935. (10.1080/17470218.2013.838281)
Hales, H. et al., 2014. Witnessing suicide-related behavior in prison. Crisis: The Journal of Crisis Intervention and Suicide Prevention 35 (1), pp.10-17. (10.1027/0227-5910/a000223)
Hamandi, K. , Myers, J. and Muthukumaraswamy, S. D. 2014. Tiagabine-induced stupor - More evidence for an encephalopathy [Letter]. Epilepsy & Behavior 31 , pp.196-197. (10.1016/j.yebeh.2013.12.027)
Hammerton, G. , Thapar, A. and Thapar, A. K. 2014. Association between obesity and depressive disorder in adolescents at high risk for depression. International Journal of Obesity 38 , pp.513-519. (10.1038/ijo.2013.133)
Hammerton, G. et al. 2014. Validation of a composite of suicide items from the Mood and Feelings Questionnaire (MFQ) in offspring of recurrently depressed parents. Psychiatry Research 216 (1), pp.82-88. (10.1016/j.psychres.2014.01.040)
Harding, K. and Robertson, N. 2014. Applications of next-generation whole exome sequencing. Journal of Neurology 261 (6), pp.1244-1246. (10.1007/s00415-014-7372-1)
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)
Harold, G. T. and DeGarmo, D. S. 2014. Concerns regarding an evaluation of MTFC-A for adolescents in English care [Letter]. British Journal of Psychiatry 205 (6), pp.498. (10.1192/bjp.205.6.498a)
Harold, G. T. et al. 2014. Maternal caregiving and girls' depressive symptom and antisocial behavior trajectories: An examination among high-risk youth. Development and Psychopathology 26 (4pt2), pp.1461-1475. (10.1017/S095457941400114X)
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)
Hay, D. F. et al. 2014. Precursors to aggression are evident by 6 months of age. Developmental Science 17 (3), pp.471-480. (10.1111/desc.12133)
Hill, M. J. et al. 2014. Transcriptional consequences of schizophrenia candidate miR-137 manipulation in human neural progenitor cells. Schizophrenia Research 153 (1-3), pp.225-230. (10.1016/j.schres.2014.01.034)
Hinney, A. et al., 2014. Genetic variation at theCELF1 (CUGBP, elav-like family member 1 gene) locus is genome-wide associated with Alzheimer's disease and obesity. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 165 (4), pp.283-293. (10.1002/ajmg.b.32234)
Hodgson, K. et al., 2014. Genetic differences in cytochrome P450 enzymes and antidepressant treatment response. Journal of Psychopharmacology 28 (2), pp.133-41. (10.1177/0269881113512041)
Hodgson, K. et al., 2014. Genetic predictors of antidepressant side effects: A grouped candidate gene approach in the Genome-Based Therapeutic Drugs for Depression (GENDEP) study. Journal of Psychopharmacology 28 (2), pp.142-150. (10.1177/0269881113517957)
Hoeffding, L. K. E. et al., 2014. Sequence analysis of 17NRXN1deletions. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 165 (1), pp.52-61. (10.1002/ajmg.b.32204)
Holden, S. E. , Bannister, C. and Currie, C. J. 2014. Mortality after cancer among patients with diabetes mellitus: effect of diabetes duration and treatment: (questionable) classification of diabetic patients based on combination of specific glucose-lowering drugs. Diabetologia 57 (9), pp.2001-2002. (10.1007/s00125-014-3281-1)
Hosang, G. M. et al., 2014. Interaction between stress and the BDNF Val66Met polymorphism in depression: a systematic review and meta-analysis. BMC Medicine 12 (1), pp.7. (10.1186/1741-7015-12-7)
Howard, L. M. et al., 2014. Antenatal and postnatal mental health: summary of updated NICE guidance. BMJ 349 g7394. (10.1136/bmj.g7394)
Hrastelj, J. et al. 2014. Hypercalcaemia mimicking Huntington's disease: lessons learned from delayed diagnosis. The Journal of the Royal College of Physicians of Edinburgh 44 (4), pp.286-288. (10.4997/JRCPE.2014.407)
Hubbard, L. 2014. Common and rare genetic risk factors for schizophrenia and their associations with cognition. PhD Thesis , Cardiff University.
Hughes, A. and Jones, L. 2014. Pathogenic mechanisms in Huntington's disease. In: Bates, G. , Tabrizi, S. and Jones, L. eds. Huntington's Disease, 4th Edition. Oxford University Press
Hughes, A. et al. 2014. B04 Alternative Splicing In Htt [Conference abstract]. Journal of Neurology, Neurosurgery & Psychiatry 85 (Suppl), pp.A10. (10.1136/jnnp-2014-309032.32)
Hughes, A. et al. 2014. Identification of novel alternative splicing events in the Huntingtin gene and assessment of the functional consequences using structural protein homology modelling. Journal of Molecular Biology 426 (7), pp.1428-1438. (10.1016/j.jmb.2013.12.028)
Hughes, T. and Harding, K. 2014. The Curious Incident of the Dog in the Night-time [Book Review]. Practical Neurology 14 (6), pp.451. (10.1136/practneurol-2014-001015)
Hughes, T. and Harding, K. 2014. When the air hits your brain. Practical Neurology 14 (5), pp.364. (10.1136/practneurol-2014-000954)
Hung, C. et al., 2014. Relationship between obesity and the risk of clinically significant depression: Mendelian randomisation study. British Journal of Psychiatry 205 (1), pp.24-28. (10.1192/bjp.bp.113.130419)
Ingram, G. et al. 2014. Complement activation in multiple sclerosis plaques: an immunohistochemical analysis. Acta Neuropathologica Communications 2 53. (10.1186/2051-5960-2-53)
Ingram, G. and Robertson, N. 2014. Accurate diagnosis of inflammatory neuropathies. Journal of Neurology 261 (11), pp.2244-2246. (10.1007/s00415-014-7531-4)
Jackson, M. C. , Linden, D. E. J. and Raymond, J. E. 2014. Angry expressions strengthen the encoding and maintenance of face identity representations in visual working memory. Cognition & Emotion 28 (2), pp.278-97. (10.1080/02699931.2013.816655)
Jamain, S. et al., 2014. Common and rare variant analysis in early-onset bipolar disorder vulnerability. PLoS ONE 9 (8) e104326. (10.1371/journal.pone.0104326)
Jones, I. and McDonald, L. 2014. Living with uncertainty: antidepressants and pregnancy. British Journal of Psychiatry 205 (2), pp.103-104. (10.1192/bjp.bp.113.141713)
Jones, I. R. et al. 2014. Bipolar disorder, affective psychosis, and schizophrenia in pregnancy and the post-partum period. Lancet 384 (9956), pp.1789-1799. (10.1016/S0140-6736(14)61278-2)
Jones, I. R. and Shakespeare, J. 2014. Postnatal depression. British Medical Journal 349 (Aug14) g4500. (10.1136/bmj.g4500)
Jones, K. et al. 2014. Physiotherapy task orientated approach: A case report. Journal of neurology, neurosurgery and psychiatry 85 (1) A68. (10.1136/jnnp-2014-309032.192)
Jones, U. F. et al. 2014. Respiratory function decreases with progression of Huntington's Disease. Journal of Neurology, Neurosurgery & Psychiatry 85 (Suppl), pp.A61-A62. (10.1136/jnnp-2014-309032.173)
Kaehne, A. and Beyer, S. R. 2014. Person-centred reviews as a mechanism for planning the post-school transition of young people with intellectual disability. Journal of Intellectual Disability Research 58 (7), pp.603-613. (10.1111/jir.12058)
Kaye, J. et al., 2014. Managing clinically significant findings in research: the UK10K example. European Journal of Human Genetics 22 (9), pp.1100-1104. (10.1038/ejhg.2013.290)
Kedia, G. et al., 2014. The neural correlates of beauty comparison. Social Cognitive and Affective Neuroscience 9 (5), pp.681-688. (10.1093/scan/nst026)
Kedia, G. , Mussweiler, T. and Linden, D. E. J. 2014. Brain mechanisms of social comparison and their influence on the reward system. NeuroReport 25 (16), pp.1255-1265. (10.1097/WNR.0000000000000255)
Kendler, K. S. and O'Donovan, M. C. 2014. A breakthrough in schizophrenia genetics. JAMA Psychiatry 71 (12), pp.1319-1320. (10.1001/jamapsychiatry.2014.1776)
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)
Kerr, M. P. et al. 2014. A White Paper on the medical and social needs of people with epilepsy and intellectual disability: The Task Force on Intellectual Disabilities and Epilepsy of the International League Against Epilepsy. Epilepsia 55 (12), pp.1902-1906. (10.1111/epi.12848)
Khabirova, E. et al., 2014. The TRiC/CCT chaperone is implicated in Alzheimer's disease based on patient GWAS and an RNAi screen in Aβ-expressing Caenorhabditis elegans. PLoS ONE 9 (7) e102985. (10.1371/journal.pone.0102985)
Khandaker, G. M. et al., 2014. A population-based longitudinal study of childhood neurodevelopmental disorders, IQ and subsequent risk of psychotic experiences in adolescence. Psychological Medicine 44 (15), pp.3229-3238. (10.1017/S0033291714000750)
Khandaker, G. M. et al., 2014. Association of serum interleukin 6 and C-Reactive protein in childhood with depression and psychosis in young adult life: a population-based longitudinal study. JAMA Psychiatry 71 (10), pp.1121-1128. (10.1001/jamapsychiatry.2014.1332)
Khandaker, G. M. et al., 2014. Childhood Epstein-Barr Virus infection and subsequent risk of psychotic experiences in adolescence: A population-based prospective serological study. Schizophrenia Research 158 (1-3), pp.19-24. (10.1016/j.schres.2014.05.019)
Khandaker, G. M. et al., 2014. A population-based study of atopic disorders and inflammatory markers in childhood before psychotic experiences in adolescence. Schizophrenia Research 152 (1), pp.139-45. (10.1016/j.schres.2013.09.021)
Kissell, A. et al. 2014. Disentangling alcohol-related needs among pre-trial prisoners: A longitudinal study. Alcohol and Alcoholism 49 (6), pp.639-644. (10.1093/alcalc/agu056)
Knöchel, C. et al., 2014. Multimodal assessments of the hippocampal formation in schizophrenia and bipolar disorder: evidences from neurobehavioral measures and functional and structural MRI. NeuroImage: Clinical 6 , pp.134-144. (10.1016/j.nicl.2014.08.015)
Kolias, A. G. et al., 2014. Chronic subdural haematoma: How can we improve patient care and outcomes?. British Journal of Neurosurgery 28 (1), pp.136-137. (10.3109/02688697.2013.869555)
Kounali, D. et al., 2014. Common versus psychopathology-specific risk factors for psychotic experiences and depression during adolescence. Psychological Medicine 44 (12), pp.2557-2566. (10.1017/S0033291714000026)
Lancaster, T. et al. 2014. CACNA1C risk variant affects reward responsiveness in healthy individuals. Translational Psychiatry 4 (10) e461. (10.1038/tp.2014.100)
Langley, K. and Thapar, A. 2014. Commentary: Maternal pre-pregnancy BMI and offspring ADHD: a lesson in the importance of testing causal pathways. International Journal of Epidemiology 43 (1), pp.91-93. (10.1093/ije/dyt275)
Lewis, G. et al. 2014. Parent-child hostility and child and adolescent depression symptoms: the direction of effects, role of genetic factors and gender. European Child & Adolescent Psychiatry 23 (5), pp.317-327. (10.1007/s00787-013-0460-4)
Linden, D. E. J. 2014. Brain control: developments in therapy and implications for society. New York: Palgrave Macmillan.
Linden, D. E. J. 2014. Casebook of neuropsychiatry [Book Review]. Cognitive Neuropsychiatry 19 (4), pp.378-380. (10.1080/13546805.2014.893721)
Linden, D. E. J. 2014. Neurofeedback and networks of depression. Dialogues in Clinical Neuroscience 16 (1), pp.103-112.
Linden, D. E. J. 2014. Neuroscience - a historical introduction. Cognitive Neuropsychiatry 19 (5), pp.468-470. (10.1080/13546805.2014.909130)
Linden, S. and Jones, E. 2014. 'Shell shock' revisited: an examination of the case records of the National Hospital in London. Medical History 58 (04), pp.519-545. (10.1017/mdh.2014.51)
Lipp, I. 2014. The role of GABA in fear and its relationship to emotion processing brain networks. PhD Thesis , Cardiff University.
Lipp, I. et al. 2014. Understanding the contribution of neural and physiological signal variation to the low repeatability of emotion-induced BOLD responses. NeuroImage 86 , pp.335-342. (10.1016/j.neuroimage.2013.10.015)
Liu, G. et al., 2014. Cardiovascular disease contributes to Alzheimer's disease: evidence from large-scale genome-wide association studies. Neurobiology of Aging 35 (4), pp.786-92. (10.1016/j.neurobiolaging.2013.10.084)
Lubbe, S. and Morris, H. R. 2014. Recent advances in Parkinson's disease genetics. Journal of Neurology 261 (2), pp.259-66. (10.1007/s00415-013-7003-2)
Luppe, S. and Robertson, N. 2014. MOG-IgG in neuromyelitis optica. Journal of Neurology 261 (3), pp.640-642. (10.1007/s00415-014-7277-z)
Makhashvili, N. et al., 2014. Mental disorders and their association with disability among internally displaced persons and returnees in Georgia. Journal of Traumatic Stress 27 (5), pp.509-518. (10.1002/jts.21949)
Malik, G. and Robertson, N. 2014. Functional neurology: new directions in causes, prognosis and treatment. Journal of Neurology 261 (12), pp.2463-2465. (10.1007/s00415-014-7573-7)
Manrique-Garcia, E. et al., 2014. Prognosis of schizophrenia in persons with and without a history of cannabis use. Psychological Medicine 44 (12), pp.2513-2521. (10.1017/S0033291714000191)
Martin, C. et al. 2014. The inflammatory cytokines: molecular biomarkers for major depressive disorder?. Biomarkers in Medicine 9 (2), pp.169-180. (10.2217/bmm.14.29)
Martin, J. et al. 2014. Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variants. Journal of the American Academy of Child and Adolescent Psychiatry 53 (7), pp.761-770.e26. (10.1016/j.jaac.2014.03.004)
Martin, J. et al. 2014. Factor structure of autistic traits in children with ADHD. Journal of Autism and Developmental Disorders 44 (1), pp.204-215. (10.1007/s10803-013-1865-0)
Martin, J. et al. 2014. Genetic risk for Attention Deficit/Hyperactivity Disorder contributes to neurodevelopmental traits in the general population. Biological Psychiatry 76 (8), pp.664-671. (10.1016/j.biopsych.2014.02.013)
McLauchlan, D. and Robertson, N. 2014. Reducing central nervous system complications associated with the human immunodeficiency virus. Journal of Neurology 261 (9), pp.1842-1845. (10.1007/s00415-014-7466-9)
McNamara, G. 2014. In utero adversity and later life behavioural disorders: the role of Cdkn1c. PhD Thesis , Cardiff University.
McNamara, G. and Isles, A. R. 2014. Influencing the social group: the role of imprinted genes. Advances in Genetics 86 , pp.107-134. (10.1016/B978-0-12-800222-3.00006-1)
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)
Merwood, A. et al., 2014. Genetic associations between the symptoms of Aattention-deficit/hyperactivity disorder and emotional lability in child and adolescent twins. Journal of the American Academy of Child & Adolescent Psychiatry 53 (2), pp.209-220. (10.1016/j.jaac.2013.11.006)
Metzler-Baddeley, C. et al. 2014. Improved executive function and callosal white matter microstructure after rhythmn exercise in Huntington's disease. Journal of Huntington's Disease 3 (3), pp.273-283. (10.3233/JHD-140113)
Miners, S. et al., 2014. Reduced vascular endothelial growth factor and capillary density in the occipital cortex in dementia with Lewy Bodies. Brain Pathology 24 (4), pp.334-343. (10.1111/bpa.12130)
Mok, K. Y. et al., 2014. Polymorphisms in BACE2 may affect the age of onset Alzheimer's dementia in Down syndrome. Neurobiology of Aging 35 (6), pp.1513.e1-5. (10.1016/j.neurobiolaging.2013.12.022)
Monks, S. et al., 2014. Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome. Schizophrenia Research 153 (1-3), pp.231-236. (10.1016/j.schres.2014.01.020)
Morgan, C. J. A. et al., 2014. Long-term heavy ketamine use is associated with spatial memory impairment and altered hippocampal activation. Frontiers in Psychiatry 5 149. (10.3389/fpsyt.2014.00149)
Morris, D. W. et al., 2014. An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis. Human Molecular Genetics 23 (12), pp.3316-3326. (10.1093/hmg/ddu025)
Mukherjee, P. et al., 2014. Altered amygdala connectivity within the social brain in schizophrenia. Schizophrenia Bulletin 40 (1), pp.152-60. (10.1093/schbul/sbt086)
Mulle, J. G. et al., 2014. Reciprocal duplication of the Williams-Beuren Syndrome deletion on chromosome 7q11.23 is associated with schizophrenia. Biological Psychiatry 75 (5), pp.371-7. (10.1016/j.biopsych.2013.05.040)
Mullins, N. et al., 2014. Investigation of blood mRNA biomarkers for suicidality in an independent sample. Translational Psychiatry 4 (10), pp.e474. (10.1038/tp.2014.112)
Mullins, N. et al., 2014. Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: A genome-wide association and polygenic scoring study. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 165 (5), pp.428-437. (10.1002/ajmg.b.32247)
Munafò, M. et al., 2014. Scientific rigor and the art of motorcycle maintenance. Nature Biotechnology 32 (9), pp.871-873. (10.1038/nbt.3004)
Munafò, M. R. , Zammit, S. and Flint, J. 2014. Commentary: Response to commentary by Rutter on Munafo et al. (2014). Journal of Child Psychology and Psychiatry 55 (10), pp.1105-1106. (10.1111/jcpp.12308)
Munafò, M. R. , Zammit, S. and Flint, J. 2014. Practitioner Review: A critical perspective on gene-environment interaction models - what impact should they have on clinical perceptions and practice?. Journal of Child Psychology and Psychiatry 55 (10), pp.1092-1101. (10.1111/jcpp.12261)
Munk-Olsen, T. , Jones, I. R. and Laursen, T. M. 2014. Birth order and postpartum psychiatric disorders. Bipolar Disorders 16 (3), pp.300-7. (10.1111/bdi.12145)
Nalls, M. A. et al., 2014. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. Nature Genetics 46 (9), pp.989-993. (10.1038/ng.3043)
Natsuaki, M. N. et al., 2014. Raised by Depressed Parents: Is it an Environmental Risk?. Clinical Child and Family Psychology Review 17 (4), pp.357-367. (10.1007/s10567-014-0169-z)
Nedopil, N. , Taylor, P. J. and Gunn, J. 2014. Forensic psychiatry in Europe: The perspective of the Ghent Group. International Journal of Psychiatry in Clinical Practice 19 (2), pp.80-83. (10.3109/13651501.2014.967700)
Nelson, A. J. D. et al. 2014. A novel role for the rat retrosplenial cortex in cognitive control. Learning and Memory 21 (2), pp.90-97. (10.1101/lm.032136.113)
Niarchou, M. et al. 2014. Exploring the indirect effects of catechol-O-methyltransferase (COMT) genotype on psychotic experiences through cognitive function and anxiety disorders in a large birth cohort of children. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 165 (5), pp.410-420. (10.1002/ajmg.b.32245)
Niarchou, M. et al. 2014. Psychopathology and cognition in children with 22q11.2 deletion syndrome. British Journal of Psychiatry 204 (1), pp.46-54. (10.1192/bjp.bp.113.132324)
Nicodemus, K. K. et al., 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)
Nicol, K. , Pope, M. and Hall, J. 2014. Facial emotion recognition in borderline personality: An association, with childhood experience. Psychiatry Research 218 (1-2), pp.256-258. (10.1016/j.psychres.2014.04.017)
Nunan, R. et al., 2014. Microglial VPAC1R mediates a novel mechanism of neuroimmune-modulation of hippocampal precursor cells via IL-4 release. Glia 62 (8), pp.1313-1327. (10.1002/glia.22682)
Oertel-Knöchel, V. et al., 2014. Association between symptoms of psychosis and reduced functional connectivity of auditory cortex. Schizophrenia Research 160 (1-3), pp.35-42. (10.1016/j.schres.2014.10.036)
Oertel-Knöchel, V. et al., 2014. Frontal white matter alterations are associated with executive cognitive function in euthymic bipolar patients. Journal of Affective Disorders 155 , pp.223-33. (10.1016/j.jad.2013.11.004)
Oertel-Knöchel, V. et al., 2014. Episodic memory impairments in bipolar disorder are associated with functional and structural brain changes. Bipolar Disorders 16 (8), pp.830-845. (10.1111/bdi.12241)
Olatunji, B. O. et al., 2014. Predicting response to cognitive behavioral therapy in contamination-based obsessive-compulsive disorder from functional magnetic resonance imaging. Psychological Medicine 44 (10), pp.2125-2137. (10.1017/S0033291713002766)
Owen, M. J. 2014. New approaches to psychiatric diagnostic classification. Neuron 84 (3), pp.564-571. (10.1016/j.neuron.2014.10.028)
Palace, J. and Robertson, N. 2014. Modifying disability in progressive multiple sclerosis. Lancet 383 (9936), pp.2189-2191. (10.1016/S0140-6736(13)62641-0)
Pan, L. A. and Phillips, M. L. 2014. Toward identification of neural markers of suicide risk in adolescents. Neuropsychopharmacology 39 (1), pp.236-237. (10.1038/npp.2013.233)
Paulsen, J. S. et al., 2014. Clinical and biomarker changes in premanifest Huntington disease show trial feasibility: A decade of the PREDICT-HD study. Frontiers in Aging Neuroscience 6 78. (10.3389/fnagi.2014.00078)
Peall, K. J. et al. 2014. SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype. Journal of Neurology 261 (12), pp.2296-2304. (10.1007/s00415-014-7488-3)
Peall, K. J. et al. 2014. Benign hereditary chorea related toNKX2.1: expansion of the genotypic and phenotypic spectrum. Developmental Medicine and Child Neurology 56 (7), pp.642-6488. (10.1111/dmcn.12323)
Peall, K. J. et al. 2014. SGCZ mutations are unlikely to be associated with myoclonus dystonia. Neuroscience 272 , pp.88-91. (10.1016/j.neuroscience.2014.04.034)
Peall, K. J. and Robertson, N. 2014. Narcolepsy: environment, genes and treatment. Journal of Neurology 261 (8), pp.1644-1646. (10.1007/s00415-014-7435-3)
Perlman, S. B. et al., 2014. Emotional reactivity and its impact on neural circuitry for attention?emotion interaction in childhood and adolescence. Developmental Cognitive Neuroscience 8 , pp.100. (10.1016/j.dcn.2013.08.005)
Perry, G. et al. 2014. Evidence for increased visual gamma responses in photosensitive epilepsy. Epilepsy Research 108 (6), pp.1076-1086. (10.1016/j.eplepsyres.2014.04.012)
Perry, J. et al. 2014. Contact with primary care: the experience of people with intellectual disabilities. Journal of Applied Research in Intellectual Disabilities 27 (3), pp.200-211. (10.1111/jar.12072)
Pesola, F. , Shelton, K. H. and van den Bree, M. B. M. 2014. Sexual orientation and alcohol problem use among UK adolescents: an indirect link through depressed mood. Addiction 109 (7), pp.1072-1080. (10.1111/add.12528)
Phillips, M. L. and Swartz, H. A. 2014. A critical appraisal of neuroimaging studies of bipolar disorder: toward a new conceptualization of underlying neural circuitry and a road map for future research. American Journal of Psychiatry 171 (8), pp.829-843. (10.1176/appi.ajp.2014.13081008)
Pickrell, O. et al., 2014. Epilepsy prevalence, incidence and socioeconomic deprivation [Conference Abstract]. Journal of Neurology, Neurosurgery & Psychiatry 85 (10), pp.e4.150. (10.1136/jnnp-2014-309236.4)
Pickrell, W. O. et al., 2014. Trends in the first antiepileptic drug prescribed for epilepsy between 2000 and 2010. Seizure - European Journal of Epilepsy 23 (1), pp.77-80. (10.1016/j.seizure.2013.09.007)
Pidsley, R. et al., 2014. Methylomic profiling of human brain tissue supports a neurodevelopmental origin for schizophrenia. Genome Biology 15 (10) 483. (10.1186/s13059-014-0483-2)
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)
Pocklington, A. , O'Donovan, M. C. and Owen, M. J. 2014. The synapse in schizophrenia. European Journal of Neuroscience 39 (7), pp.1059-1067. (10.1111/ejn.12489)
Poole, C. D. et al. 2014. Estimation of health-related utility (EQ-5D index) in subjects with seasonal allergic rhinoconjunctivitis to evaluate health gain associated with sublingual grass allergen immunotherapy. Health and Quality of Life Outcomes 12 (1) 99. (10.1186/1477-7525-12-99)
Poole, C. D. et al. 2014. P451 cost effectiveness of Rifaximin-a in the reduction of recurrence of overt hepatic encephalopathy. Journal of Hepatology 60 (1) S219. (10.1016/S0168-8278(14)60613-9)
Poole, C. D. et al. 2014. PWE-153 cost effectiveness of Rifaximin-a in the reduction of recurrence of overt hepatic encephalopathy. Gut 63 (Suppl) A191. (10.1136/gutjnl-2014-307263.413)
Poulton, R. et al., 2014. Effects of multidimensional treatment foster care on psychotic symptoms in girls. Journal of the American Academy of Child & Adolescent Psychiatry 53 (12), pp.1279-1287. (10.1016/j.jaac.2014.08.014)
Powell, R. et al., 2014. Hyperconnectivity in JME-a network analysis. Journal of Neurology, Neurosurgery & Psychiatry 85 (10), pp.A2. e4. (10.1136/jnnp-2014-309236.5)
Proitsi, P. et al., 2014. Alleles that increase risk for type 2 diabetes mellitus are not associated with increased risk for Alzheimer's disease. Neurobiology of Aging 35 (12) 2883.e3. (10.1016/j.neurobiolaging.2014.07.023)
Proitsi, P. et al., 2014. Genetic predisposition to increased blood cholesterol and triglyceride lipid levels and risk of Alzheimer Disease: a Mendelian Randomization Analysis. Public Library of Science Medicine 11 (9) e1001713. (10.1371/journal.pmed.1001713)
Quinn, L. et al. 2014. Task-specific training in Huntington disease: a randomized controlled feasibility trial. Physical Therapy 94 (11), pp.1555-1568. (10.2522/ptj.20140123)
Radua, J. et al., 2014. COMT Val158Met x SLC6A4 5-HTTLPR interaction impacts on gray matter volume of regions supporting emotion processing. Social Cognitive and Affective Neuroscience 9 (8), pp.1232-8. (10.1093/scan/nst089)
Ramirez, A. et al., 2014. SUCLG2 identified as both a determinator of CSF A 1-42 levels and an attenuator of cognitive decline in Alzheimer's disease. Human Molecular Genetics 23 (24), pp.6644-6658. (10.1093/hmg/ddu372)
Rawal, A. et al., 2014. A longitudinal high-risk study of adolescent anxiety, depression and parent-severity on the developmental course of risk-adjustment. Journal of Child Psychology and Psychiatry 55 (11), pp.1270-1278. (10.1111/jcpp.12279)
Reddington, A. E. , Rosser, A. E. and Dunnett, S. B. 2014. Differentiation of pluripotent stem cells into striatal projection neurons: a pure MSN fate may not be sufficient. Frontiers in Cellular Neuroscience 8 398. (10.3389/fncel.2014.00398)
Rees, E. et al. 2014. CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. Human Molecular Genetics 23 (6), pp.1669-1676. (10.1093/hmg/ddt540)
Rees, E. et al. 2014. Analysis of copy number variations at 15 schizophrenia-associated loci. British Journal of Psychiatry 204 (2), pp.108-114. (10.1192/bjp.bp.113.131052)
Rees, E. et al. 2014. Authors' reply [Letter]. British Journal of Psychiatry 205 (1), pp.78. (10.1192/bjp.205.1.78)
Rice, F. 2014. Prospective and mutual influences of reward processing and emotional disorders in a longitudinal study of the adolescent offspring of depressed parents: the EPAD Cohort. Biological Psychiatry 75 (9), pp.195S. (10.1016/j.biopsych.2014.03.015)
Riglin, L. et al. 2014. The relationship between emotional problems and subsequent school attainment: A meta-analysis. Journal of Adolescence 37 (4), pp.335-346. (10.1016/j.adolescence.2014.02.010)
Rinaldi, F. et al., 2014. Cross-regulation of Connexin43 and β-catenin influences differentiation of human neural progenitor cells. Cell Death and Disease 5 (1) e1017. (10.1038/cddis.2013.546)
Ripke, S. et al., 2014. Biological insights from 108 schizophrenia-associated genetic loci. Nature 511 (7510), pp.421-427. (10.1038/nature13595)
Robertson, N. and Scolding, N. J. 2014. Immune reconstitution and treatment response in multiple sclerosis following alemtuzumab. Neurology 82 (24), pp.2150-2215. (10.1212/WNL.0000000000000530)
Robinson, E. B. et al., 2014. Response to 'Predicting the diagnosis of autism spectrum disorder using gene pathway analysis'. Molecular Psychiatry 19 (8), pp.860-1. (10.1038/mp.2013.125)
Robson, H. et al., 2014. Mismatch negativity (MMN) reveals inefficient auditory ventral stream function in chronic auditory comprehension impairments. Cortex 59 , pp.113-125. (10.1016/j.cortex.2014.07.009)
Rosser, A. E. and Dunnett, S. B. 2014. Cell therapy for Huntington's Disease. Advances in Clinical Neuroscience and Rehabilitation 14 (5), pp.18-21.
Rosser, A. E. and Svendsen, C. N. 2014. Stem cells for cell replacement therapy: A therapeutic strategy for HD?. Movement Disorders 29 (11), pp.1446-1454. (10.1002/mds.26026)
Ruderfer, D. M. et al., 2014. Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia. Molecular Psychiatry 19 (9), pp.1017-1024. (10.1038/mp.2013.138)
Ruiz, A. et al., 2014. Follow-up of loci from the International Genomics of Alzheimer's Disease Project identifies TRIP4 as a novel susceptibility gene. Translational Psychiatry 4 e358. (10.1038/tp.2014.2)
Rutter, M. and Thapar, A. 2014. Genetics of autism spectrum disorders. In: Volkmar, F. R. et al., Handbook of Autism and Pervasive Developmental Disorders. Vol. 1, Hoboken, New Jersey: John Wiley & Sons Inc. , pp.411-423.
Sarrazin, S. et al., 2014. A multicenter tractography study of deep white matter tracts in bipolar I disorder. JAMA Psychiatry 71 (4), pp.388-396. (10.1001/jamapsychiatry.2013.4513)
Saville, C. W. N. et al., 2014. COMT Val158Met genotype is associated with fluctuations in working memory performance: converging evidence from behavioural and single-trial P3b measures. NeuroImage 100 , pp.489-497. (10.1016/j.neuroimage.2014.06.006)
Schepman, K. et al., 2014. Cognitive styles in depressed children with and without comorbid conduct disorder. Journal of Adolescence 37 (5), pp.622-631. (10.1016/j.adolescence.2014.04.004)
Schneider, M. et al., 2014. Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: Results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. American Journal of Psychiatry 171 (6), pp.627-639. (10.1176/appi.ajp.2013.13070864)
Smith, C. G. et al., 2014. Response. Journal of the National Cancer Institute 106 (5), pp.dju087. (10.1093/jnci/dju087)
Sokunbi, M. et al. 2014. Nonlinear complexity analysis of brain fMRI signals in schizophrenia. PLoS ONE 9 (5) e95146. (10.1371/journal.pone.0095146)
Sokunbi, M. et al. 2014. Real-time fMRI brain-computer interface: development of a "motivational feedback" subsystem for the regulation of visual cue reactivity. Frontiers in Behavioral Neuroscience 8 392. (10.3389/fnbeh.2014.00392)
Steer, S. et al., 2014. Epilepsy prevalence and socioeconomic deprivation in England. Epilepsia 55 (10), pp.1634-1641. (10.1111/epi.12763)
Steinberg, S. et al., 2014. Common variant at 16p11.2 conferring risk of psychosis. Molecular Psychiatry 19 (1), pp.108-114. (10.1038/mp.2012.157)
Stewart, J. P. et al., 2014. Seroprevalence of molluscum contagiosum virus in German and UK populations. PLoS ONE 9 (2) e88734. (10.1371/journal.pone.0088734)
Stone, J. M. et al., 2014. Glutamate, N-acetyl aspartate and psychotic symptoms in chronic ketamine users. Psychopharmacology 231 (10), pp.2107-2116. (10.1007/s00213-013-3354-8)
Sullivan, S. A. et al., 2014. Longitudinal associations between adolescent psychotic experiences and depressive symptoms. PLoS ONE 9 (8), pp.e105758. (10.1371/journal.pone.0105758)
Szatkiewicz, J. P. et al., 2014. Copy number variation in schizophrenia in Sweden. Molecular Psychiatry 19 (7), pp.762-773. (10.1038/mp.2014.40)
Tansey, K. et al. 2014. Genetic susceptibility for bipolar disorder and response to antidepressants in major depressive disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 165 (1), pp.77-83. (10.1002/ajmg.b.32210)
Tansey, K. et al. 2014. Copy number variants and therapeutic response to antidepressant medication in major depressive disorder. The Pharmacogenomics Journal 14 (4), pp.395-399. (10.1038/tpj.2013.51)
Thapar, A. K. et al. 2014. Detecting recurrent major depressive disorder within primary care rapidly and reliably using short questionnaire measures. British Journal of General Practice (BJGP) 64 (618), pp.e31-7. (10.3399/bjgp14X676438)
Thapar, A. and Harold, G. T. 2014. Editorial Perspective: Why is there such a mismatch between traditional heritability estimates and molecular genetic findings for behavioural traits?. Journal of Child Psychology and Psychiatry 55 (10), pp.1088-1091. (10.1111/jcpp.12294)
Thomas, R. H. and Robertson, N. 2014. Novel auto-antibody syndromes. Journal of Neurology 261 (10), pp.2043-2045. (10.1007/s00415-014-7497-2)
Thomas, R. H. et al. 2014. A comprehensive neuropsychological description of cognition in drug-refractory juvenile myoclonic epilepsy. Epilepsy & Behavior 36 , pp.124-129. (10.1016/j.yebeh.2014.04.027)
Thompson, P. M. et al., 2014. The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging and Behavior , pp.153-82. (10.1007/s11682-013-9269-5)
Thompson, R. et al., 2014. Caring for a family member with intellectual disability and epilepsy: Practical, social and emotional perspectives. Seizure 23 (10), pp.856-863. (10.1016/j.seizure.2014.07.005)
Timpson, N. J. et al., 2014. A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans. Nature Communications 5 4871. (10.1038/ncomms5871)
Tol, W. A. et al., 2014. World Health Organization guidelines for management of acute stress, PTSD, and bereavement: key challenges on the road ahead. Public Library of Science Medicine 11 (12), pp.e1001769. (10.1371/journal.pmed.1001769)
Torrents-Rodas, D. et al., 2014. Testing the temporal stability of individual differences in the acquisition and generalization of fear. Psychophysiology 51 (7), pp.697-705. (10.1111/psyp.12213)
Trent, S. et al. 2014. Altered brain gene expression but not steroid biochemistry in a genetic mouse model of neurodevelopmental disorder. Molecular Autism 5 (1) 21. (10.1186/2040-2392-5-21)
Uher, R. et al., 2014. An inflammatory biomarker as a differential predictor of outcome of depression treatment with escitalopram and nortriptyline. American Journal of Psychiatry 171 (12), pp.1278-1286. (10.1176/appi.ajp.2014.14010094)
Ul-Haq, Z. et al., 2014. Heaviness, health and happiness: a cross-sectional study of 163066 UK Biobank participants. Journal of Epidemiology and Community Health 68 (4), pp.340-348. (10.1136/jech-2013-203077)
Ul-Haq, Z. et al., 2014. Gender differences in the association between adiposity and probable major depression: a cross-sectional study of 140,564 UK Biobank participants. BMC Psychiatry 14 153. (10.1186/1471-244X-14-153)
Varma, S. et al., 2014. Grainyheadlike 2 distribution reveals novel pathophysiological differences between human idiopathic pulmonary fibrosis and mouse models of pulmonary fibrosis. AJP: Lung Cellular and Molecular Physiology 306 (5), pp.L405-L419. (10.1152/ajplung.00143.2013)
Verrelst, J. et al., 2014. Optimizing LUT-based RTM inversion for semiautomatic mapping of crop biophysical parameters from Sentinel-2 and -3 Data: role of cost functions. IEEE Transactions on Geoscience and Remote Sensing 52 (1), pp.257-269. (10.1109/TGRS.2013.2238242)
Versace, A. et al., 2014. Elevated serum measures of lipid peroxidation and abnormal prefrontal white matter in euthymic bipolar adults: toward peripheral biomarkers of bipolar disorder. Molecular Psychiatry 19 (2), pp.200-208. (10.1038/mp.2012.188)
Waite, A. et al. 2014. Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansion. Neurobiology of Aging 35 (7), pp.1779.e5-1779.e13. (10.1016/j.neurobiolaging.2014.01.016)
Walker, J. et al., 2014. Changes in mental state associated with prison environments: a systematic review. Acta Psychiatrica Scandinavica 129 (6), pp.427-36. (10.1111/acps.12221)
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)
Warnert, E. A. et al. 2014. In vivo assessment of human brainstem cerebrovascular function: a multi-inversion time pulsed arterial spin labelling study. Journal of Cerebral Blood Flow and Metabolism 34 (6), pp.956-963. (10.1038/jcbfm.2014.39)
Willis, M. D. et al. 2014. VGKC-complex antibody encephalitis. QJM: An International Journal of Medicine 107 (8), pp.657-659. (10.1093/qjmed/hcu030)
Willis, M. et al. 2014. Reversible brainstem dysfunction from spinal arterio-venous fistula. Practical Neurology 14 (6), pp.425-428. (10.1136/practneurol-2014-000872)
Willis, M. and Robertson, N. 2014. Drug safety evaluation of alemtuzumab for multiple sclerosis. Expert Opinion on Drug Safety 13 (8), pp.1115-1124. (10.1517/14740338.2014.928691)
Willis, M. and Robertson, N. 2014. Treatment paradigms in multiple sclerosis: who, when and how to treat?. Journal of Neurology 261 (7), pp.1444-1446. (10.1007/s00415-014-7420-x)
Wynford-Thomas, R. et al., 2014. Rarities in neurology: blue rubber bleb naevus syndrome. Practical Neurology 14 (5), pp.360-362. (10.1136/practneurol-2013-000725)
York, J. and Kerr, M. P. 2014. Peri-ictal behavioural change in people with an intellectual disability. Epileptology 2 (1-4), pp.1-5. (10.1016/j.epilep.2014.07.002)
Zammit, S. et al. 2014. Individual- and area-level influence on suicide risk: a multilevel longitudinal study of Swedish schoolchildren. Psychological Medicine 44 (02), pp.267-277. (10.1017/S0033291713000743)

Cyhoeddiadau 2014

Archif cyhoeddiadau

Canolfan ar gyfer Geneteg a Genomeg Niwroseiciatrig

Cysylltwch â ni

Ymweld â Chanolfan ar gyfer Geneteg a Genomeg Niwroseiciatrig