Cyhoeddiadau 2016

Mae'r rhestr isod ar gael yn Saesneg yn unig.

Bennasar, M. et al. 2016. Huntington's Disease assessment using tri axis accelerometers. Procedia Computer Science 96 , pp.1193-1201. (10.1016/j.procs.2016.08.163)
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)
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)
Bracht, T. K. et al. 2016. Myelination of the right parahippocampal cingulum is associated with physical activity in young healthy adults. Brain Structure and Function 221 (9), pp.4537-48. (10.1007/s00429-016-1183-3)
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)
Brydges, N. M. 2016. Pre-pubertal stress and brain development in rodents. Current Opinion in Behavioral Sciences 7 , pp.8-14. (10.1016/j.cobeha.2015.08.003)
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)
Carter, E. et al., 2016. An update on the causes, assessment and management of third division sensory trigeminal neuropathies. British Dental Journal 220 (12), pp.627-635. (10.1038/sj.bdj.2016.444)
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)
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)
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)
Corral-Frías, N. S. et al., 2016. COMTVal158Met genotype is associated with reward learning: a replication study and meta-analysis. Genes, Brain and Behavior 15 (5), pp.503-513. (10.1111/gbb.12296)
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)
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 Santis, S. et al. 2016. T1 relaxometry of crossing fibres in the human brain. NeuroImage 141 , pp.133-142. (10.1016/j.neuroimage.2016.07.037)
De Santis, S. , Jones, D. K. and Roebroeck, A. 2016. Including diffusion time dependence in the extra-axonal space improves in vivo estimates of axonal diameter and density in human white matter. NeuroImage 130 , pp.91-103. (10.1016/j.neuroimage.2016.01.047)
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)
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)
Drake, W. M. et al., 2016. A follow-up study of the prevalence of valvular heart abnormalities in hyperprolactinemic patients treated with cabergoline. Journal of Clinical Endocrinology & Metabolism 101 (11), pp.4189-4194. (10.1210/jc.2016-2224)
Drakesmith, M. et al. 2016. Mediation of psychosis risk factors by white-matter microstructure in young adults with psychotic experiences. JAMA Psychiatry 73 (4), pp.396-406. (10.1001/jamapsychiatry.2015.3375)
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)
Falk, A. et al., 2016. Modeling psychiatric disorders: from genomic findings to cellular phenotypes. Molecular Psychiatry 21 (9), pp.1167-1179. (10.1038/mp.2016.89)
Fritz, N. E. et al., 2016. Motor-cognitive dual-task deficits in individuals with early-mid stage Huntington's disease. Gait and Posture 49 , pp.283-289. (10.1016/j.gaitpost.2016.07.014)
Frizzati, A. et al. 2016. Comparable reduction in Zif268 levels and cytochrome oxidase activity in the retrosplenial cortex following mammillothalamic tract lesions. Neuroscience 330 , pp.39-49. (10.1016/j.neuroscience.2016.05.030)
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)
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)
Gennet, N. et al., 2016. FolR1: a novel cell surface marker for isolating midbrain dopamine neural progenitors and nascent dopamine neurons. Scientific Reports 6 32488. (10.1038/srep32488)
Guerreiro, R. et al., 2016. Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases. Neurobiology of Aging 38 214.e7–214.e10. (10.1016/j.neurobiolaging.2015.10.028)
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. Retinotopic fMRI and tumour resection in a case with occipital lobe epilepsy. Seizure - European Journal of Epilepsy 41 , pp.175-178. (10.1016/j.seizure.2016.08.006)
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)
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)
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)
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)
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)
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)
Johnston, J. , Linden, D. E. J. and Van Den Bree, M. B. 2016. Combining stress and dopamine based models of addiction: towards a psycho-neuro-endocrinological theory of addiction. Current Drug Abuse Reviews 9 (1), pp.61-74. (10.2174/1874473709666151209113913)
Jones, C. et al., 2016. The societal cost of Huntington’s disease: are we underestimating the burden?. European Journal of Neurology 23 (10), pp.1588-1590. (10.1111/ene.13107)
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)
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)
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)
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)
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)
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)
Mikkelsen, M. et al. 2016. Comparison of the repeatability of GABA-edited magnetic resonance spectroscopy with and without macromolecule suppression. Magnetic Resonance in Medicine 75 (3), pp.946-953. (10.1002/mrm.25699)
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)
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)
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)
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)
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.
Pascente, R. et al., 2016. Cognitive deficits and brain myo-Inositol are early biomarkers of epileptogenesis in a rat model of epilepsy. Neurobiology of Disease 93 , pp.146-155. (10.1016/j.nbd.2016.05.001)
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)
Prince, L. Y. et al., 2016. Neuromodulation of the feedforward dentate gyrus-CA3 microcircuit. Frontiers in Synaptic Neuroscience 8 32. (10.3389/fnsyn.2016.00032)
Quinn, L. et al. 2016. A randomized, controlled trial of a multi-modal exercise intervention in Huntington's disease. Parkinsonism and Related Disorders 31 , pp.46-52. (10.1016/j.parkreldis.2016.06.023)
Rees, D. A. et al. 2016. White matter microstructure and cognitive function in young women with polycystic ovary syndrome. Journal of Clinical Endocrinology & Metabolism 101 (1), pp.314-323. (10.1210/jc.2015-2318)
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. 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)
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)
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)
Shastin, D. , Zaben, M. and Leach, P. 2016. Life with a cerebrospinal fluid (CSF) shunt. BMJ 355 i5209. (10.1136/bmj.i5209)
Shin, E. et al. 2016. α-Synuclein induced toxicity in brain stem serotonin neurons mediated by an AAV vector driven by the tryptophan hydroxylase promoter. Scientific Reports 6 26285. (10.1038/srep26285)
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)
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)
Stevens, O. A. C. et al., 2016. Miniature standoff Raman probe for neurosurgical applications. Journal of Biomedical Optics 21 (8) 087002. (10.1117/1.JBO.21.8.087002)
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)
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)
Suurland, J. et al., 2016. Parental perceptions of aggressive behavior in preschoolers: Inhibitory control moderates the association with negative emotionality. Child Development 87 (1), pp.256-269. (10.1111/cdev.12455)
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)
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)
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)
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)
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)
Warnert, E. A. H. et al. 2016. The major cerebral arteries proximal to the Circle of Willis contribute to cerebrovascular resistance in humans. Journal of Cerebral Blood Flow and Metabolism 36 (8), pp.1384-1395. (10.1177/0271678X15617952)
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)
Yhnell, E. , Dunnett, S. B. and Brooks, S. P. 2016. A longitudinal motor characterisation of the HdhQ111 mouse model of Huntington's Disease. Journal of Huntington's Disease 5 (2), pp.149-161. (10.3233/JHD-160191)
Yhnell, E. et al. 2016. Cognitive training modifies disease symptoms in a mouse model of Huntington's disease. Experimental Neurology 282 , pp.19-26. (10.1016/j.expneurol.2016.05.008)
Yhnell, E. et al. 2016. L30 Cognitive training improves disease symptoms in a mouse model of huntington's disease. Journal of Neurology, Neurosurgery & Psychiatry 87 (Supp 1), pp.A100-A101. (10.1136/jnnp-2016-314597.285)
Yilmaz, Z. , Egbuniwe, O. and Renton, T. 2016. The detection of small-fiber neuropathies in burning mouth syndrome and latrogenic lingual nerve injuries: Use of quantitative sensory testing. Journal of Oral & Facial Pain and Headache 30 (2), pp.87-98. (10.11607/ofph.1531)
Yilmaz, Z. et al. 2016. A survey of the opinion and experience of UK dentists: part 1: The incidence and cause of Iatrogenic trigeminal nerve injuries related to dental implant surgery. Implant Dentistry 25 (5), pp.638-645. (10.1097/ID.0000000000000472)

Cyhoeddiadau 2016

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