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1. Neurogenetics
: a guide for clinicians
by Wood, Nicholas
2012, ISBN 9780521543729, 252
Progress in genetic knowledge is profoundly affecting medical practice, and no clinical specialty has more diseases associated with genetic mutations than... 
Nervous system | Genetic aspects | Neurogenetics | Diseases
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2. Neurogenetics
: a guide for clinicians
by Wood, N. W. (Nicholas W.)
2012, ISBN 9780521543729
"Progress in genetic knowledge is profoundly affecting medical practice, and no clinical specialty has more diseases associated with genetic mutations than... 
Genetic Testing | genetics | Neurogenetics | Nervous system | Genetic Diseases, Inborn | Genetic aspects | Nervous System Diseases | Diseases | etiology
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3. Full Text Stratification of candidate genes for Parkinson’s disease using weighted protein-protein interaction network analysis
by Ferrari, Raffaele and Kia, Demis A and Tomkins, James E and Hardy, John and Wood, Nicholas W and Lovering, Ruth C and Lewis, Patrick A and Manzoni, Claudia
BMC Genomics, ISSN 1471-2164, 12/2018, Volume 19, Issue 1, pp. 1 - 8
Background Genome wide association studies (GWAS) have helped identify large numbers of genetic loci that significantly associate with increased risk of... 
Parkinson's disease | Seeds | Ontology | Genes | Bias | Risk | Genomes | Autophagy | Data bases | Proteins | Consortia | Mitochondria | Network analysis | Stratification | Movement disorders | Immune response | Neurodegenerative diseases | Health risks | Waste disposal | Loci | Biological activity | Molecular chains | Immune systems | Studies | Hypotheses | Molecular modelling | Acids | Cell death | Protein interaction | Phagocytosis | Dementia | Networks | Pathways | Neurodegeneration | Bioinformatics | Functional genomics | Protein-protein interactions
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4. Full Text Actuators: Tension Pistons: Amplifying Piston Force Using Fluid‐Induced Tension in Flexible Materials (Adv. Funct. Mater. 30/2019)
by Li, Shuguang and Vogt, Daniel M and Bartlett, Nicholas W and Rus, Daniela and Wood, Robert J
Advanced Functional Materials, ISSN 1616-301X, 07/2019, Volume 29, Issue 30, pp. 1970208 - n/a
In article number 1901419 , Shuguang Li, Daniela Rus, Robert J. Wood, and co‐workers propose a new concept for a tension‐driven piston. It utilizes a... 
actuators | pistons | soft robotics | artificial muscles | flexible materials | Actuators | Robotics | Pistons | Rigid structures | Compressibility | Power efficiency
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5. Full Text Association of Multidrug Resistance in Epilepsy with a Polymorphism in the Drug-Transporter Gene ABCB1
by Siddiqui, Asra and Kerb, Reinhold and Weale, Michael E and Brinkmann, Ulrich and Smith, Alice and Goldstein, David B and Wood, Nicholas W and Sisodiya, Sanjay M
The New England Journal of Medicine, ISSN 0028-4793, 04/2003, Volume 348, Issue 15, pp. 1442 - 1448
The cause of drug-resistant epilepsy, a common and debilitating illness affecting one third of patients with epilepsy, is unknown. In this genetic study,... 
CELLS | MEDICINE, GENERAL & INTERNAL | REFRACTORY EPILEPSY | MDR1 GENE | EXPRESSION | HUMAN GENOMIC DIVERSITY | BRAIN | P-GLYCOPROTEIN | Drug Resistance, Multiple - genetics | Genes, MDR | ATP-Binding Cassette, Sub-Family B, Member 1 - genetics | Gene Frequency | Humans | Epilepsy - drug therapy | Epilepsy - genetics | Genotype | Case-Control Studies | Linkage Disequilibrium | Polymorphism, Genetic | Genetic aspects | Drug therapy | Drug resistance | Epilepsy | Neurology | Genotype & phenotype | Automation | Neurosurgery | Drug dosages | Deoxyribonucleic acid--DNA | Index Medicus | Abridged Index Medicus
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6. Full Text Analysis of shared heritability in common disorders of the brain
by Anttila, Verneri and Bulik-Sullivan, Brendan and Finucane, Hilary K and Walters, Raymond K and Bras, Jose and Duncan, Laramie and Escott-Price, Valentina and Falcone, Guido J and Gormley, Padhraig and Malik, Rainer and Patsopoulos, Nikolaos A and Ripke, Stephan and Wei, Zhi and Yu, Dongmei and Lee, Phil H and Turley, Patrick and Grenier-Boley, Benjamin and Chouraki, Vincent and Kamatani, Yoichiro and Berr, Claudine and Letenneur, Luc and Hannequin, Didier and Amouyel, Philippe and Boland, Anne and Deleuze, Jean-François and Duron, Emmanuelle and Vardarajan, Badri N and Reitz, Christiane and Goate, Alison M and Huentelman, Matthew J and Ilyas Kamboh, M and Larson, Eric B and Rogaeva, Ekaterina and George-Hyslop, Peter St and Hakonarson, Hakon and Kukull, Walter A and Farrer, Lindsay A and Barnes, Lisa L and Beach, Thomas G and Yesim Demirci, F and Head, Elizabeth and Hulette, Christine M and Jicha, Gregory A and Kauwe, John S.K and Kaye, Jeffrey A and Leverenz, James B and Levey, Allan I and Lieberman, Andrew P and Pankratz, Vernon S and Poon, Wayne W and Quinn, Joseph F and Saykin, Andrew J and Schneider, Lon S and Smith, Amanda G and Sonnen, Joshua A and Stern, Robert A and Van Deerlin, Vivianna M and Van Eldik, Linda J and Harold, Denise and Russo, Giancarlo and Rubinsztein, David C and Bayer, Anthony and Tsolaki, Magda and Proitsi, Petra and Fox, Nick C and Hampel, Harald and Owen, Michael J and Mead, Simon and Passmore, Peter and Morgan, Kevin and Nöthen, Markus M and Rossor, Martin and Lupton, Michelle K and Hoffmann, Per and Kornhuber, Johannes and Lawlor, Brian and McQuillin, Andrew and Al-Chalabi, Ammar and Bis, Joshua C and Ruiz, Agustin and Boada, Mercè and Seshadri, Sudha and Beiser, Alexa and Rice, Kenneth and Van Der Lee, Sven J and De Jager, Philip L and Geschwind, Daniel H and Riemenschneider, Matthias and Riedel-Heller, Steffi and Rotter, Jerome I and Ransmayr, Gerhard and Hyman, Bradley T and Cruchaga, Carlos and Alegret, Montserrat and Winsvold, Bendik and Palta, Priit and Farh, Kai-How and Cuenca-Leon, Ester and Furlotte, Nicholas and Kurth, Tobias and ... and Brainstorm Consortium and The Brainstorm Consortium
Science, ISSN 0036-8075, 06/2018, Volume 360, Issue 6395, pp. 1313 - 1313
Disorders of the brain can exhibit considerable epidemiological comorbidity and often share symptoms, provoking debate about their etiologic overlap. We... 
ANOREXIA-NERVOSA | POPULATION-BASED TWIN | DEFICIT HYPERACTIVITY DISORDER | LONG-TERM SURVIVAL | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | GENETIC CORRELATIONS | BODY-MASS INDEX | MAJOR DEPRESSIVE DISORDER | BIPOLAR DISORDER | GENOME-WIDE ASSOCIATION | Genetic Variation | Mental Disorders - genetics | Genome-Wide Association Study | Phenotype | Brain Diseases - classification | Quantitative Trait, Heritable | Brain Diseases - diagnosis | Humans | Mental Disorders - classification | Risk Factors | Brain Diseases - genetics | Mental Disorders - diagnosis | Anorexia | Disorders | Cognitive ability | Bipolar disorder | Posttraumatic stress disorder | Mental depression | Epidemiology | Risk factors | Consortia | Proteins | Ischemia | Etiology | Classification | Gilles de la Tourette syndrome | Alzheimer's disease | Neurological disorders | Neurodegenerative diseases | Comorbidity | Behavior disorders | Anorexia nervosa | Risk analysis | Patients | Neurological diseases | Correlation analysis | Heritability | Attention deficit disorder | Headache | Mental disorders | Medical services | Schizophrenia | Risk sharing | Genomes | Heterogeneity | Biological effects | Risk assessment | Stroke | Phenotypes | Migraine | Attention deficit hyperactivity disorder | Eating disorders | Personality | Genetic diversity | Statistics | Activity patterns | Crohn's Disease | Population (statistical) | Scaffolding | Diagnostic systems | Alzheimers disease | Index Medicus | Life Sciences | Human health and pathology | Mental Disorders | Neurons and Cognition | Brain Diseases | Genetics
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7. Full Text Delineating the phenotype of autosomal-recessive HPCA mutations: Not only isolated dystonia
: LETTERS: PUBLISHED ARTICLES
by Balint, Bettina and Charlesworth, Gavin and Erro, Roberto and Wood, Nicholas W and Bhatia, Kailash P
Movement Disorders, ISSN 0885-3185, 04/2019, Volume 34, Issue 4, pp. 589 - 592
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8. Full Text Partial loss‐of‐function of sodium channel SCN8A in familial isolated myoclonus
by Wagnon, Jacy L and Mencacci, Niccolò E and Barker, Bryan S and Wengert, Eric R and Bhatia, Kailash P and Balint, Bettina and Carecchio, Miryam and Wood, Nicholas W and Patel, Manoj K and Meisler, Miriam H
Human Mutation, ISSN 1059-7794, 07/2018, Volume 39, Issue 7, pp. 965 - 969
Variants in the neuronal sodium channel gene SCN8A have been implicated in several neurological disorders. Early infantile epileptic encephalopathy type 13... 
Nav1.6 | movement disorder | myoclonus | sodium channel | DE-NOVO | VARIANTS | DYSTONIA | NA(V)1.6 | MOUSE MUTANT | SEIZURES | GENE | RECURRENT | MUTATION | GENETICS & HEREDITY | EPILEPTIC ENCEPHALOPATHY | Myoclonus - genetics | Seizures - genetics | Humans | Middle Aged | Male | Epilepsy - physiopathology | Intellectual Disability - genetics | Myoclonus - physiopathology | Intellectual Disability - physiopathology | Seizures - physiopathology | Pedigree | Epilepsy - genetics | Female | Heterozygote | NAV1.6 Voltage-Gated Sodium Channel - genetics | Mutation | Child | Loss of Function Mutation - genetics | Medical research | Nervous system diseases | Myoclonus | Analysis | Medicine, Experimental | Genetic aspects | Seizures (Medicine) | Sodium channels | Phenotypes | Channel gating | Epilepsy | Cognitive ability | Neurological diseases | Encephalopathy | Sodium channels (voltage-gated) | Gating | Movement disorders | Seizures | Brief Report | Brief Reports
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9. Full Text Molecular pathogenesis of Parkinson's disease
by Gandhi, S and Wood, NW
HUMAN MOLECULAR GENETICS, ISSN 0964-6906, 10/2005, Volume 14, pp. 2749 - 2755
Parkinson's disease (PD) is a common and incurable neurodegenerative disease, affecting 1% of the population over the age of 65. Despite a well-described... 
COMMON LRRK2 MUTATION | OXIDATIVE DAMAGE | GENE | MITOCHONDRIAL COMPLEX-I | DROSOPHILA MODEL | BIOCHEMISTRY & MOLECULAR BIOLOGY | PROTEASOME | GENETICS & HEREDITY | ALPHA-SYNUCLEIN | DEFICIENT MICE | PATHOLOGY | PROTEIN DJ-1 | Phosphotransferases - metabolism | Animals | Humans | Oxidative Stress - physiology | Ubiquitin - metabolism | Models, Neurological | Mutation | Parkinson Disease - genetics | Proteasome Endopeptidase Complex - metabolism | Mitochondria - physiology | Disease Models, Animal
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10. Full Text Soft Robotics: Increasing the Dimensionality of Soft Microstructures through Injection‐Induced Self‐Folding (Adv. Mater. 38/2018)
by Ranzani, Tommaso and Russo, Sheila and Bartlett, Nicholas W and Wehner, Michael and Wood, Robert J
Advanced Materials, ISSN 0935-9648, 09/2018, Volume 30, Issue 38, pp. 1870282 - n/a
In article number 1802739 , Tommaso Ranzani and co‐workers introduce a manufacturing method that combines multilayer soft lithography, precision laser... 
advanced manufacturing | microfluidics | soft robotics
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11. Full Text Features of GBA-associated Parkinson's disease at presentation in the UK Tracking Parkinson's study
by Malek, Naveed and Weil, Rimona S and Bresner, Catherine and Lawton, Michael A and Grosset, Katherine A and Tan, Manuela and Bajaj, Nin and Barker, Roger A and Burn, David J and Foltynie, Thomas and Hardy, John and Wood, Nicholas W and Ben-Shlomo, Yoav and Williams, Nigel W and Grosset, Donald G and Morris, Huw R and PRoBaND Clinical Consortium and PRoBaND clinical consortium
Journal of Neurology, Neurosurgery and Psychiatry, ISSN 0022-3050, 07/2018, Volume 89, Issue 7, pp. 702 - 709
Objectives To examine the influence of the glucocerebrosidase (GBA) mutation carrier state on age at onset of Parkinson's disease (PD), the motor phenotype and... 
SURGERY | POPULATION | MULTICENTER | COGNITIVE PERFORMANCE | METAANALYSIS | DEMENTIA | PSYCHIATRY | IDENTIFICATION | GLUCOCEREBROSIDASE MUTATIONS | CARRIERS | CLINICAL NEUROLOGY | GENE | HISTORY
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12. Full Text Truncating mutations in SPAST patients are associated with a high rate of psychiatric comorbidities in hereditary spastic paraplegia
by Chelban, Viorica and Tucci, Arianna and Lynch, David S and Polke, James M and Santos, Liana and Jonvik, Hallgeir and Groppa, Stanislav and Wood, Nicholas W and Houlden, Henry
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 08/2017, Volume 88, Issue 8, pp. 681 - 687
BackgroundThe hereditary spastic paraplegias (HSPs) are a rare and heterogeneous group of neurodegenerative disorders that are clinically characterised by... 
SURGERY | AUTISM | PSYCHIATRY | CHROMOSOME 2P | DISORDERS | SPG4 | PARAPARESIS | CLINICAL NEUROLOGY | FAMILY | GENES | AAA PROTEIN | AUTOSOMAL-DOMINANT | SPECTRUM | Spastic Paraplegia, Hereditary - genetics | Spastic Paraplegia, Hereditary - diagnosis | Humans | Middle Aged | Child, Preschool | Infant | Male | Statistics as Topic | Mutation, Missense - genetics | Young Adult | Mental Disorders - genetics | Point Mutation - genetics | DNA Mutational Analysis | Adult | Female | Spastin | Mental Disorders - diagnosis | Child | Infant, Newborn | Introns - genetics | Exons - genetics | Genotype | United Kingdom | Phenotype | Adolescent | Age of Onset | Alleles | Adenosine Triphosphatases - genetics | Codon, Nonsense - genetics | Genetic Carrier Screening | Sequence Deletion - genetics | Gene mutations | Microtubules | Paralysis, Spastic | Causes of | Reports | Genetic aspects | Research | Mental illness | Statistical analysis | Intellectual disabilities | Genes | Bipolar disorder | Patients | Variance analysis | Autism | Neurology | Software | Paralysis | Mutation | Psychiatry | Deoxyribonucleic acid--DNA | Index Medicus | Neurogenetics | 1506
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13. Full Text Is the MC1R variant p.R160W associated with Parkinson's?
by Lubbe, Steven J and Escott‐Price, Valentina and Brice, Alexis and Gasser, Thomas and Hardy, John and Heutink, Peter and Sharma, Manu and Wood, Nicholas W and Nalls, Mike and Singleton, Andrew B and Williams, Nigel M and Morris, Huw R and International Parkinson's Disease Genomics Consortium
Annals of Neurology, ISSN 0364-5134, 01/2016, Volume 79, Issue 1, pp. 159 - 161
Genetic Predisposition to Disease - genetics | Melanoma - genetics | Humans | Receptor, Melanocortin, Type 1 - genetics | Female | Male | Genetic Variation - genetics | Parkinson Disease - genetics | Index Medicus
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14. Full Text Neurodegeneration
by Schapira, Anthony and Wszolek, Zbigniew K and Dawson, Ted M and Wood, Nicholas
2017, 1st ed., ISBN 9780470672686, 347
This book unites the diverse range of complex neurodegenerative diseases into a textbook designed for clinical practice, edited by globally leading authorities... 
Neurology | MEDICAL
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15. Full Text Features of GBA-associated Parkinson’s disease at presentation in the UK Tracking Parkinson’s study
by Malek, Naveed and Weil, Rimona S and Bresner, Catherine and Lawton, Michael A and Grosset, Katherine A and Tan, Manuela and Bajaj, Nin and Barker, Roger A and Burn, David J and Foltynie, Thomas and Hardy, John and Wood, Nicholas W and Ben-Shlomo, Yoav and Williams, Nigel W and Grosset, Donald G and Morris, Huw R
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 07/2018, Volume 89, Issue 7, pp. 702 - 709
ObjectivesTo examine the influence of the glucocerebrosidase (GBA) mutation carrier state on age at onset of Parkinson’s disease (PD), the motor phenotype and... 
Neurosciences | Parkinsons disease | Cognitive ability | Identification | Patients | Meta-analysis | Studies | Psychosis | Neurology | Genotype & phenotype | Anxieties | Mutation | Psychiatry | Dementia | Movement Disorders | 1506
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16. Full Text Delineating the phenotype of autosomal-recessive HPCA mutations: Not only isolated dystonia
by Balint, B and Charlesworth, G and Erro, R and Wood, NW and Bhatia, KP
MOVEMENT DISORDERS, ISSN 0885-3185, 04/2019, Volume 34, Issue 4, pp. 589 - 592
CLINICAL NEUROLOGY | Dystonia - genetics | Dystonic Disorders - genetics | Hippocalcin - genetics | Phenotype | Mutation | Humans | Genetic aspects | Dystonia | Index Medicus
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17.