Centre for Neuropsychiatric Genetics and Genomics

2015 publications

Thapar, A. et al. 2015. Rutter's child and adolescent psychiatry. 6th ed.. Wiley-Blackwell. (10.1002/9781118381953)
Absoud, M. et al., 2015. Protocol for a multicentre randomiSed controlled TRial of IntraVEnous immunoglobulin versus standard therapy for the treatment of transverse myelitis in adults and children (STRIVE). BMJ Open 5 (5) e008312. (10.1136/bmjopen-2015-008312)
Amin, R. and Robertson, N. 2015. Diagnosis and treatment of chronic inflammatory demyelinating polyneuropathy. Journal of Neurology 262 (3), pp.789-791. (10.1007/s00415-015-7667-x)
Andreassen, O. A. et al., 2015. Correction: Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate. PLoS Genetics 11 (11) e1005544. (10.1371/journal.pgen.1005544)
Arber, C. et al., 2015. Activin A directs striatal projection neuron differentiation of human pluripotent stem cells. Development 142 (7), pp.1375-1386. (10.1242/dev.117093)
Arloth, J. et al., 2015. Genetic differences in the immediate transcriptome response to stress predict risk-related brain function and psychiatric disorders. Neuron 86 (5), pp.1189-1202. (10.1016/j.neuron.2015.05.034)
Bayram-Weston, Z. et al. 2015. Similar striatal gene expression profiles in the striatum of the YAC128 and HdhQ150 mouse models of Huntington's disease are not reflected in mutant Huntingtin inclusion prevalence. BMC Genomics 16 , pp.-. 1079. (10.1186/s12864-015-2251-4)
Bisson, J. I. et al. 2015. Post-traumatic stress disorder. BMJ 351 h6161. (10.1136/bmj.h6161)
Bittner, R. A. et al., 2015. The when and where of working memory dysfunction in early-onset schizophrenia - a functional magnetic resonance imaging study. Cerebral Cortex 25 (9), pp.2494-2506. (10.1093/cercor/bhu050)
Bowles, K. R. et al., 2015. Huntingtin subcellular localisation is regulated by Kinase signalling activity in the StHdhQ111 model of HD. PLoS ONE 10 (12) e0144864. (10.1371/journal.pone.0144864)
Bracht, T. , Linden, D. E. J. and Keedwell, P. A. 2015. A review of white matter microstructure alterations of pathways of the reward circuit in depression. Journal of affective disorders 187 , pp.45-53. (10.1016/j.jad.2015.06.041)
Bray, E. , Harding, K. and Hughes, T. 2015. Thinking, fast and slow [Book Review]. Practical Neurology 15 (4), pp.327. (10.1136/practneurol-2015-001218)
Brealy, J. 2015. The relationship between variation in genes, GABA, structure and gamma oscillations in the visual and auditory system of healthy individuals and psychiatric disorder. PhD Thesis , Cardiff University.
Brealy, J. et al. 2015. Increased visual gamma power in schizoaffective bipolar disorder. Psychological Medicine -London- 45 (4), pp.783-794. (10.1017/S0033291714001846)
Bulik-Sullivan, B. K. et al., 2015. LD Score regression distinguishes confounding from polygenicity in genome-wide association studies. Nature Genetics 47 (3), pp.291-295. (10.1038/ng.3211)
Caeyenberghs, K. et al., 2015. Hyperconnectivity in juvenile myoclonic epilepsy: A network analysis. NeuroImage: Clinical 7 , pp.98-104. (10.1016/j.nicl.2014.11.018)
Caseras, X. et al. 2015. Association between genetic risk scoring for schizophrenia and bipolar disorder with regional subcortical volumes. Translational Psychiatry 5 e692. (10.1038/tp.2015.195)
Caseras, X. et al. 2015. Emotion regulation deficits in euthymic bipolar I versus bipolar II disorder: a functional and diffusion-tensor imaging study. Bipolar Disorders 17 (5), pp.461-470. (10.1111/bdi.12292)
Castro, V. M. et al., 2015. Validation of electronic health record phenotyping of bipolar disorder cases and controls. American Journal of Psychiatry 172 (4), pp.363-372. (10.1176/appi.ajp.2014.14030423)
Cianfaglione, R. et al., 2015. A national survey of Rett syndrome: Age, clinical characteristics, current abilities, and health. American Journal of Medical Genetics Part A 167 (7), pp.1493-1500. (10.1002/ajmg.a.37027)
Cianfaglione, R. et al., 2015. A national survey of Rett syndrome: behavioural characteristics. Journal of Neurodevelopmental Disorders 7 11. (10.1186/s11689-015-9104-y)
Cianfaglione, R. et al., 2015. Psychological well-being of mothers and siblings in families of girls and women with Rett Syndrome. Journal of Autism and Developmental Disorders 45 (9), pp.2939-2946. (10.1007/s10803-015-2457-y)
Collier, D. et al., 2015. How can pharmacogenomics biomarkers be translated into patient benefit [Conference Abstract]. European Psychiatry 30 (Suppl1), pp.94-94. (10.1016/S0924-9338(15)30078-X)
Collishaw, S. 2015. Annual Research Review: Secular trends in child and adolescent mental health. Journal of Child Psychology and Psychiatry 56 (3), pp.370-393. (10.1111/jcpp.12372)
Connolly, S. et al., 2015. Investigation of assortative mating in autism spectrum disorders [Conference Abstract]. Human Heredity 79 (1), pp.31-31. A8. (10.1159/000381109)
Cooper, M. , Thapar, A. and Jones, D. K. 2015. ADHD severity is associated with white matter microstructure in the subgenual cingulum. NeuroImage: Clinical 7 , pp.653-660. (10.1016/j.nicl.2015.02.012)
Correia, K. et al., 2015. The Genetic Modifiers of Motor OnsetAge (GeM MOA) Website: Genome-wide Association Analysis for Genetic Modifiers of Huntington's Disease. Journal of Huntington's Disease 4 (3), pp.279-284. (10.3233/JHD-150169)
Creeth, H. et al., 2015. Programming of maternal behaviour by the placenta: A novel animal model. Psychoneuroendocrinology 61 , pp.4. PS1.1.3. (10.1016/j.psyneuen.2015.07.397)
Daley, A. J. et al., 2015. A pragmatic randomized controlled trial to evaluate the effectiveness of a facilitated exercise intervention as a treatment for postnatal depression: the PAM-PeRS trial. Psychological Medicine 45 (11), pp.2413-2425. (10.1017/S0033291715000409)
Daughters, K. et al. 2015. Salivary oxytocin concentrations in males following intranasal administration of oxytocin: a double-blind, cross-over study. PLoS ONE 10 (12) e0145104. (10.1371/journal.pone.0145104)
Davies, F. et al. 2015. "You are just left to get on with it": qualitative study of patient and carer experiences of the transition to secondary progressive multiple sclerosis. BMJ Open 5 (7) e007674. (10.1136/bmjopen-2015-007674)
Davies, J. R. et al. 2015. Behavioural effects of imprinted genes. Current Opinion in Behavioral Sciences 2 , pp.28-33. (10.1016/j.cobeha.2014.07.008)
Davies, J. R. et al. 2015. Calorie seeking, but not hedonic response, contributes to hyperphagia in a mouse model for Prader-Willi syndrome. European Journal of Neuroscience 42 (4), pp.2105-2113. (10.1111/ejn.12972)
Davies, W. and Duncan, L. 2015. Editorial overview: Behavioral genetics. Current Opinion in Behavioral Sciences 2 , pp.v-vii. (10.1016/j.cobeha.2014.12.002)
Dawes, H. et al., 2015. Exercise testing and training in people with Huntington's diseas. Clinical Rehabilitation 29 (2), pp.196-206. (10.1177/0269215514540921)
Desikan, R. S. et al., 2015. Genetic overlap between Alzheimer's Disease and Parkinson's Disease at the MAPT locus. Molecular Psychiatry 20 (12), pp.1588-1595. (10.1038/mp.2015.6)
Desikan, R. S. et al., 2015. Polygenic overlap between C-reactive protein, plasma lipids, and Alzheimer Disease. Circulation 131 (23), pp.2061-2069. (10.1161/CIRCULATIONAHA.115.015489)
Devinsky, O. et al., 2015. Delivery of epilepsy care to adults with intellectual and developmental disabilities. Neurology 85 (17), pp.1512-1521. (10.1212/WNL.0000000000002060)
Di Florio, A. et al. 2015. Bipolar disorder, miscarriage, and termination. Bipolar Disorders 17 (1), pp.102-105. (10.1111/bdi.12217)
Di Florio, A. et al. 2015. Smoking and postpartum psychosis. Bipolar Disorders 17 (5), pp.572-573. (10.1111/bdi.12314)
Drakesmith, M. et al. 2015. Overcoming the effects of false positives and threshold bias in graph theoretical analyses of neuroimaging data. NeuroImage 118 , pp.313-333. (10.1016/j.neuroimage.2015.05.011)
Drakesmith, M. et al. 2015. Schizophrenia-like topological changes in the structural connectome of individuals with subclinical psychotic experiences. Human Brain Mapping 36 (7), pp.2629-2643. (10.1002/hbm.22796)
Escott-Price, V. et al. 2015. No evidence for enrichment in schizophrenia for common allelic associations at imprinted loci. PLoS ONE 10 (12), pp.-. e0144172. (10.1371/journal.pone.0144172)
Escott-Price, V. et al. 2015. Polygenic risk of Parkinson disease is correlated with disease age at onset. Annals of Neurology 77 (4), pp.582-591. (10.1002/ana.24335)
Escott-Price, V. et al. 2015. Common polygenic variation enhances risk prediction for Alzheimer's disease. Brain 138 (12), pp.3673-3684. (10.1093/brain/awv268)
Farrell, M. S. et al., 2015. Evaluating historical candidate genes for schizophrenia. Molecular Psychiatry 20 (5), pp.555-562. (10.1038/mp.2015.16)
Felce, D. J. et al. 2015. Cognitive behavioural anger management intervention for people with intellectual disabilities: costs of intervention and impact on health and social care resource use. Journal of Intellectual Disability Research 59 (1), pp.68-81. (10.1111/jir.12112)
Ferentinos, P. et al., 2015. Familiality and SNP heritability of age at onset and episodicity in major depressive disorder. Psychological Medicine 45 (10), pp.2215-2225. (10.1017/S0033291715000215)
Ferreira, J. J. et al., 2015. Ethyl-eicosapentaenoic acid treatment in Huntington's disease: A placebo-controlled clinical trial. Movement Disorders 30 (10), pp.1426-1429. (10.1002/mds.26308)
Fonville, L. et al., 2015. Psychotic Experiences, Working Memory, and the Developing Brain: A Multimodal Neuroimaging Study. Cerebral Cortex 25 (12), pp.4828-4838. (10.1093/cercor/bhv181)
Fonville, L. et al., 2015. Review of assessment tools for psychotic-like experiences misses the psychosis-like symptoms semi-structured interview (PLIKSi) in ALSPAC. Early Intervention in Psychiatry 11 (3), pp.269-270. (10.1111/eip.12254)
Fung, W. and Robertson, N. 2015. Natalizumab in MS: JC antibody index. Journal of Neurology 262 (2), pp.492-494. (10.1007/s00415-015-7641-7)
Gage, S. H. et al., 2015. Associations of cannabis and cigarette use with depression and anxiety at age 18: findings from the Avon Longitudinal Study of Parents and Children. PLoS ONE 10 (4) e0122896. (10.1371/journal.pone.0122896)
Gordon-Smith, K. et al., 2015. Rapid cycling as a feature of bipolar disorder and comorbid migraine. Journal of Affective Disorders 175 , pp.320. (10.1016/j.jad.2015.01.024)
Green, E. K. et al., 2015. Copy number variation in bipolar disorder. Molecular Psychiatry 21 (1), pp.89-93. (10.1038/mp.2014.174)
Hales, H. et al., 2015. The impact of contact with suicide-related behavior in prison on young offenders. Crisis 36 (1), pp.21-30. (10.1027/0227-5910/a000292)
Hall, J. and Owen, M. J. 2015. Psychiatric classification - a developmental perspective. British Journal of Psychiatry 207 (4), pp.281-282. (10.1192/bjp.bp.114.159996)
Hall, J. et al. 2015. Genetic risk for schizophrenia: convergence on synaptic pathways Involved in plasticity. Biological Psychiatry 77 (1), pp.52-68. (10.1016/j.biopsych.2014.07.011)
Hammerton, G. 2015. Explaining risk for suicide-related behaviour in adolescent offspring of mothers with depression. PhD Thesis , Cardiff University.
Hammerton, G. et al. 2015. Association between maternal depression symptoms across the first eleven years of their child's life and subsequent offspring suicidal ideation. Plos One 10 (7) e0131885. (10.1371/journal.pone.0131885)
Hammerton, G. et al. 2015. Pathways to suicide-related behavior in offspring of mothers with depression: the role of offspring psychopathology. Journal of the American Academy of Child and Adolescent Psychiatry 54 (5), pp.385-393. (10.1016/j.jaac.2015.02.006)
Hammerton, G. et al. 2015. In Reply. Journal of the American Academy of Child & Adolescent Psychiatry 54 (10), pp.868-869. (10.1016/j.jaac.2015.07.012)
Harding, I. and Harding, K. 2015. Michelangelo's finger: an exploration of everyday transcendence. Practical Neurology 15 (6), pp.491-491. (10.1136/practneurol-2015-001312)
Harding, K. and Robertson, N. 2015. HIV-associated neurocognitive disorders. Journal of Neurology 262 (6), pp.1596-1598. (10.1007/s00415-015-7783-7)
Harding, K. E. et al. 2015. Modelling the natural history of primary progressive multiple sclerosis. Journal of Neurology, Neurosurgery and Psychiatry 86 , pp.13-19. (10.1136/jnnp-2014-307791)
Healy, S. , Willis, M. and Robertson, N. P. 2015. Prognosis in multiple sclerosis and the unveiling of pathogenic clues. Journal of Neurology 262 (11), pp.2596-2598. (10.1007/s00415-015-7938-6)
Heckenast, J. R. , Wilkinson, L. S. and Jones, M. W. 2015. Decoding advances in psychiatric genetics: a focus on neural circuits in rodent models. Advances in Genetics 92 , pp.75-106. (10.1016/bs.adgen.2015.09.001)
Heyes, S. et al., 2015. Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders. Progress in Neurobiology 134 , pp.36-54. (10.1016/j.pneurobio.2015.09.002)
Hinton, R. et al., 2015. Preliminary evidence for aortopathy and an x-linked parent-of-origin effect on aortic valve malformation in a mouse model of Turner syndrome. Journal of Cardiovascular Development and Disease 2 (3), pp.190-199. (10.3390/jcdd2030190)
Hirst, C. L. et al., 2015. Acute myeloid leucaemia presenting as a rapidly progressive polyradiculoneuropathy. BMJ Case Reports 2015 , pp.-. bcr2015209556. (10.1136/bcr-2015-209556)
Hodgson, K. , Shelton, K. H. and van den Bree, M. B. 2015. Psychopathology among young homeless people: Longitudinal mental health outcomes for different subgroups. British Journal of Clinical Psychology 54 (3), pp.307-325. (10.1111/bjc.12075)
Holliday, E. and Taylor, P. J. 2015. Consequences for clinicians and mental health services of a homicide by a current or recent patient: A European Union (EU) wide survey. International Journal of Forensic Mental Health 14 (3), pp.218-229. (10.1080/14999013.2015.1075627)
Hosp, F. et al., 2015. Quantitative interaction proteomics of neurodegenerative disease proteins. Cell Reports 11 (7), pp.1134-46. (10.1016/j.celrep.2015.04.030)
Hrastelj, J. and Robertson, N. 2015. Improving survival in amyotrophic lateral sclerosis: future treatments in a modern service. Journal of Neurology 262 (7), pp.1791-1793. (10.1007/s00415-015-7811-7)
Huang, J. et al., 2015. Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel. Nature Communications 6 8111. (10.1038/ncomms9111)
Hung, C. et al., 2015. A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder. BMC Medicine 13 86. (10.1186/s12916-015-0334-3)
Ihssen, N. et al. 2015. Neural mechanisms underlying visual short-term memory gain for temporally distinct objects. Cerebral Cortex 25 (8), pp.2149-2159. (10.1093/cercor/bhu021)
Ingason, A. et al., 2015. Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case?control sample of schizophrenia. Translational Psychiatry 5 (10) e656. (10.1038/tp.2015.151)
Ingram, G. and Robertson, N. P. 2015. Pathophysiology of neuropsychiatric disorders: moving forward. Journal of Neurology 262 (4), pp.1096-1098. (10.1007/s00415-015-7706-7)
Isles, A. R. 2015. 15q maternal duplication and neurodevelopmental disorders; UBE3A is the key. Human Mutation 36 (7), pp.iii. (10.1002/humu.22656)
Isles, A. R. 2015. Neural and behavioral epigenetics; what it is, and what is hype. Genes, Brain and Behavior 14 (1), pp.64-72. (10.1111/gbb.12184)
Ivanov, D. K. et al. 2015. Longevity GWAS using the Drosophila Genetic Reference Panel. Journals of Gerontology, Series A 70 (12), pp.1470-1478. (10.1093/gerona/glv047)
Jackson, C. F. et al., 2015. Non-pharmacological interventions for people with epilepsy and intellectual disabilities. The Cochrane Library (10.1002/14651858.CD005502.pub3)
Jackson, C. F. et al., 2015. Pharmacological interventions for epilepsy in people with intellectual disabilities. Cochrane Database of Systematic Reviews (10.1002/14651858.CD005399.pub3)
Jackson, M. C. et al., 2015. Similarity, not complexity, determines visual working memory performance.. Journal of Experimental Psychology: Learning, Memory, and Cognition 41 (6), pp.1884-1892. (10.1037/xlm0000125)
Jamjoom, A. A. B. et al., 2015. External ventricular drainage: Is it time to look at national practice?. British Journal of Neurosurgery , pp.1. (10.3109/02688697.2014.957162)
Johnstone, M. et al., 2015. Copy number variations in DISC1 and DISC1-interacting partners in major mental illness. Molecular Neuropsychiatry 1 (3), pp.175-190. (10.1159/000438788)
Jones, L. et al. 2015. Convergent genetic and expression data implicate immunity in Alzheimer's disease. Alzheimer's and Dementia 11 (6), pp.658-671. (10.1016/j.jalz.2014.05.1757)
Kavanagh, D. et al., 2015. Schizophrenia genetics: emerging themes for a complex disorder. Molecular Psychiatry 20 (1), pp.72-76. (10.1038/mp.2014.148)
Kerr, M. P. and Linehan, C. 2015. Responding to the needs of people with intellectual disability and epilepsy: Shared priorities. Journal of Intellectual and Developmental Disability 40 (3), pp.248-253. (10.3109/13668250.2015.1059410)
Kilford, E. J. et al., 2015. Affective bias and current, past and future adolescent depression: a familial high risk study. Journal of Affective Disorders 174 , pp.265-271. (10.1016/j.jad.2014.11.046)
Kim, J. et al., 2015. Multivariate clustering of progression profiles reveals different depression patterns in prodromal Huntington disease. Neuropsychology 29 (6), pp.949-960. (10.1037/neu0000199)
Kirov, G. 2015. CNVs in neuropsychiatric disorders. Human Molecular Genetics 24 (R1), pp.R45-R49. (10.1093/hmg/ddv253)
Knöchel, C. et al., 2015. Consolidation time affects performance and neural activity during visual working memory. Psychiatry Research: Neuroimaging 231 (1), pp.33-41. (10.1016/j.pscychresns.2014.10.025)
Knott, S. et al. 2015. Epilepsy and bipolar disorder. Epilepsy & Behavior 52 , pp.267-274. (10.1016/j.yebeh.2015.07.003)
Koelewijn, L. et al. 2015. Resting-state oscillatory dynamics in sensorimotor cortex in benign epilepsy with centro-temporal spikes and typical brain development. Human Brain Mapping 36 (10), pp.3935-3949. (10.1002/hbm.22888)
Koppers, M. et al., 2015. C9orf72 ablation in mice does not cause motor neuron degeneration or motor deficits. Annals of Neurology 78 (3), pp.426-438. (10.1002/ana.24453)
Kun-Rodrigues, C. et al., 2015. A systematic screening to identifyde novomutations causing sporadic early-onset Parkinson's disease. Human Molecular Genetics 24 (23), pp.6711-20. (10.1093/hmg/ddv376)
Lancaster, T. et al. 2015. Replication study implicates COMT val158met polymorphism as a modulator of probabilistic reward learning. Genes, Brain and Behavior 14 (6), pp.486-492. (10.1111/gbb.12228)
Lancaster, T. M. et al. 2015. Alzheimer's disease risk variant in CLU is associated with neural inefficiency in healthy individuals. Alzheimer's and Dementia 11 (10), pp.1144-1152. (10.1016/j.jalz.2014.10.012)
Lawton, M. et al., 2015. A longitudinal model for disease progression was developed and applied to multiple sclerosis. Journal of Clinical Epidemiology 68 (11), pp.1355-1365. (10.1016/j.jclinepi.2015.05.003)
Lee, J. M. et al., 2015. Identification of genetic factors that modify clinical onset of Huntington's disease. Cell 162 (3), pp.516-526. (10.1016/j.cell.2015.07.003)
Lee, S. H. et al., 2015. New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. International Journal of Epidemiology 44 (5), pp.1706-1721. (10.1093/ije/dyv136)
Leonenko, G. M. and Phillips, T. N. 2015. Numerical approximation of high-dimensional Fokker-Planck equations with polynomial coefficients. Journal of computational and applied mathematics 273 , pp.296-312. (10.1016/j.cam.2014.05.024)
Leonpacher, A. K. et al., 2015. Distinguishing bipolar from unipolar depression: the importance of clinical symptoms and illness features. Psychological Medicine 45 (11), pp.2437-2446. (10.1017/S0033291715000446)
Lewis, C. et al., 2015. Internet-based cognitive and behavioural therapies for post-traumatic stress disorder (PTSD) in adults. Cochrane Database of Systematic Reviews (5) CD011710. (10.1002/14651858.CD011710)
Linden, D. E. J. 2015. Moral psychology, vol. 4: free will and moral responsibility. Cognitive Neuropsychiatry 20 (5), pp.469-472. (10.1080/13546805.2015.1073470)
Lipp, I. et al. 2015. The relationship between fearfulness, GABA, and fear-related BOLD responses in the insula. Plos One 10 (3) e0120101. (10.1371/journal.pone.0120101)
Lipp, I. et al. 2015. Agreement and repeatability of vascular reactivity estimates based on a breath-hold task and a resting state scan. NeuroImage 113 , pp.387-396. (10.1016/j.neuroimage.2015.03.004)
Lipp, I. and Tomassini, V. 2015. Neuroplasticity and motor rehabilitation in multiple sclerosis. Frontiers in Neurology 6 00059. (10.3389/fneur.2015.00059)
Liu, D. et al., 2015. Motor onset and diagnosis in Huntington disease using the diagnostic confidence level. Journal of Neurology 262 (12), pp.2691-2698. (10.1007/s00415-015-7900-7)
Lloyd, K. et al., 2015. A national population-based e-cohort of people with psychosis (PsyCymru) linking prospectively ascertained phenotypically rich and genetic data to routinely collected records: Overview, recruitment and linkage. Schizophrenia Research 166 (1-3), pp.131-6. (10.1016/j.schres.2015.05.036)
Loh, P. et al., 2015. Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis. Nature Genetics 47 , pp.1385-1392. (10.1038/ng.3431)
Loohuis, L. M. O. et al., 2015. Genome-wide burden of deleterious coding variants increased in schizophrenia. Nature Communications 6 7501. (10.1038/ncomms8501)
Maier, R. et al., 2015. Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder. American Journal of Human Genetics 96 (2), pp.283-294. (10.1016/j.ajhg.2014.12.006)
Malek, N. et al., 2015. Tracking Parkinson's: study design and baseline patient data. Journal of Parkinson's Disease 5 (4), pp.947-959. (10.3233/JPD-150662)
Mars, B. et al., 2015. Longitudinal symptom course in adults with recurrent depression: Impact on impairment and risk of psychopathology in offspring. Journal of Affective Disorders 182 , pp.32-38. (10.1016/j.jad.2015.04.018)
Martin, J. et al. 2015. The relative contribution of common and rare genetic variants to ADHD. Translational Psychiatry 5 e506. (10.1038/tp.2015.5)
Martin, J. et al. 2015. Neurocognitive abilities in the general population and composite genetic risk scores for attention-deficit hyperactivity disorder. Journal of Child Psychology and Psychiatry 56 (6), pp.648-656. (10.1111/jcpp.12336)
Matsui, J. T. et al., 2015. Prefrontal cortex white matter tracts in prodromal Huntington disease. Human Brain Mapping 36 (10), pp.3717-3732. (10.1002/hbm.22835)
McCourt, A. C. et al., 2015. Characterization of gastric mucosa biopsies reveals alterations in Huntington's Disease. PLoS Currents 1 (10.1371/currents.hd.858b4cc7f235df068387e9c20c436a79)
McLauchlan, D. J. and Robertson, N. 2015. Refining the phenotype of inborn errors of metabolism. Journal of Neurology 262 (10), pp.2396-2398. (10.1007/s00415-015-7917-y)
McManus, I. C. et al., 2015. Doctor, builder, soldier, lawyer, teacher, dancer, shopkeeper, vet: exploratory study of which eleven-year olds would like to become a doctor. BMC Psychology 3 (1) 38. (10.1186/s40359-015-0094-z)
Mencacci, N. et al., 2015. A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystoniaa. American Journal of Human Genetics 96 (6), pp.938-947. (10.1016/j.ajhg.2015.04.008)
Merikangas, A. K. et al., 2015. The phenotypic manifestations of rare genic CNVs in autism spectrum disorder. Molecular Psychiatry 20 (11), pp.1366-1372. (10.1038/mp.2014.150)
Moon, A. et al. 2015. Creatine supplementation in the elderly: is resistance training really needed?. Journal of Nutrition and Health Sciences 2 (2), pp.1-9.
Mort, M. E. et al. 2015. Huntingtin exists as multiple splice forms in human brain. Journal of Huntington's Disease 4 (2), pp.161-171. (10.3233/JHD-150151)
Muthukumaraswamy, S. D. et al. 2015. Evidence that subanesthetic doses of ketamine cause sustained disruptions of NMDA and AMPA-mediated frontoparietal connectivity in humans. Journal of Neuroscience 35 (33), pp.11694-11706. (10.1523/JNEUROSCI.0903-15.2015)
Nalls, M. A. et al., 2015. Genetic risk and age in Parkinson's disease: Continuum not stratum. Movement Disorders 30 (6), pp.850-854. (10.1002/mds.26192)
Nalls, M. A. et al., 2015. Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study. The Lancet Neurology 14 (10), pp.1002-1009. (10.1016/S1474-4422(15)00178-7)
Newland, B. et al. 2015. Prospects for polymer therapeutics in Parkinson's disease and other neurodegenerative disorders. Progress in Polymer Science 44 , pp.79-112. (10.1016/j.progpolymsci.2014.12.002)
Newland, B. et al. 2015. Tackling cell transplantation anoikis: an injectable, shape memory cryogel microcarrier platform material for stem cell and neuronal cell growth. Small 11 (38), pp.5047-5053. (10.1002/smll.201500898)
Niarchou, M. et al. 2015. The clinical presentation of attention deficit-hyperactivity disorder (ADHD) in children with 22q11.2 deletion syndrome. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 168 (8), pp.730-738. (10.1002/ajmg.b.32378)
Niarchou, M. , Zammit, S. and Lewis, G. 2015. The Avon Longitudinal Study of Parents and Children (ALSPAC) birth cohort as a resource for studying psychopathology in childhood and adolescence: a summary of findings for depression and psychosis. Social Psychiatry and Psychiatric Epidemiology 50 (7), pp.1017-1027. (10.1007/s00127-015-1072-8)
Nicol, K. et al., 2015. Childhood trauma, midbrain activation and psychotic symptoms in borderline personality disorder. Translational Psychiatry 5 (5) e559. (10.1038/tp.2015.53)
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