Williams, Nigel - Cardiff University

研究领域

My primary research interests focus on the molecular genetic analysis of common neuropsychiatric and neurological disorders, including schizophrenia, attention deficit hyperactivity disorder and Parkinson’s disease.

近期论文

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Lubbe, S.et al. 2016. Additional rare variant analysis in Parkinson?s disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance. Human Molecular Genetics 25(24), pp. 5483-5489. (10.1093/hmg/ddw348) pdf 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) pdf Swallow, D.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) pdf 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 (10.1016/j.parkreldis.2016.09.023) pdf Thapar, A.et al. 2016. Psychiatric gene discoveries shape evidence on ADHD's biology. Molecular Psychiatry 21(9), pp. 1202-1207. (10.1038/mp.2015.163) pdf Mooney, M.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) Mok, K.et al. 2016. Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data. The Lancet Neurology 15(6), pp. 585-596. (10.1016/S1474-4422(16)00071-5) pdf Franke, B.et al. 2016. Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept. Nature Neuroscience 19(3), pp. 420-431. (10.1038/nn.4228) Marshall, C.et al. 2016. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects. Nature Genetics (10.1038/ng.3725) pdf