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1دورية أكاديمية
المؤلفون: Sarah Opie-Martin, Alfredo Iacoangeli, Simon D. Topp, Olubunmi Abel, Keith Mayl, Puja R. Mehta, Aleksey Shatunov, Isabella Fogh, Harry Bowles, Naomi Limbachiya, Thomas P. Spargo, Ahmad Al-Khleifat, Kelly L. Williams, Jennifer Jockel-Balsarotti, Taha Bali, Wade Self, Lyndal Henden, Garth A. Nicholson, Nicola Ticozzi, Diane McKenna-Yasek, Lu Tang, Pamela J. Shaw, Adriano Chio, Albert Ludolph, Jochen H. Weishaupt, John E. Landers, Jonathan D. Glass, Jesus S. Mora, Wim Robberecht, Philip Van Damme, Russell McLaughlin, Orla Hardiman, Leonard van den Berg, Jan H. Veldink, Phillippe Corcia, Zorica Stevic, Nailah Siddique, Vincenzo Silani, Ian P. Blair, Dong-sheng Fan, Florence Esselin, Elisa de la Cruz, William Camu, Nazli A. Basak, Teepu Siddique, Timothy Miller, Robert H. Brown, Ammar Al-Chalabi, Christopher E. Shaw
المصدر: Nature Communications, Vol 15, Iss 1, Pp 1-2 (2024)
مصطلحات موضوعية: Science
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2041-1723
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2دورية أكاديميةThe SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration
المؤلفون: Sarah Opie-Martin, Alfredo Iacoangeli, Simon D. Topp, Olubunmi Abel, Keith Mayl, Puja R. Mehta, Aleksey Shatunov, Isabella Fogh, Harry Bowles, Naomi Limbachiya, Thomas P. Spargo, Ahmad Al-Khleifat, Kelly L. Williams, Jennifer Jockel-Balsarotti, Taha Bali, Wade Self, Lyndal Henden, Garth A. Nicholson, Nicola Ticozzi, Diane McKenna-Yasek, Lu Tang, Pamela J. Shaw, Adriano Chio, Albert Ludolph, Jochen H. Weishaupt, John E. Landers, Jonathan D. Glass, Jesus S. Mora, Wim Robberecht, Philip Van Damme, Russell McLaughlin, Orla Hardiman, Leonard van den Berg, Jan H. Veldink, Phillippe Corcia, Zorica Stevic, Nailah Siddique, Vincenzo Silani, Ian P. Blair, Dong-sheng Fan, Florence Esselin, Elisa de la Cruz, William Camu, Nazli A. Basak, Teepu Siddique, Timothy Miller, Robert H. Brown, Ammar Al-Chalabi, Christopher E. Shaw
المصدر: Nature Communications, Vol 13, Iss 1, Pp 1-9 (2022)
مصطلحات موضوعية: Science
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2041-1723
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3دورية أكاديمية
المؤلفون: Olubunmi Abel, John F Powell, Peter M Andersen, Ammar Al-Chalabi
المصدر: PLoS ONE, Vol 8, Iss 6, p e64899 (2013)
وصف الملف: electronic resource
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المؤلفون: John Powell, Olubunmi Abel, Ammar Al-Chalabi, Peter M. Andersen
المصدر: Human Mutation; Vol 33
مصطلحات موضوعية: medicine.medical_specialty, Information Storage and Retrieval, Biology, User-Computer Interface, 03 medical and health sciences, Superoxide Dismutase-1, 0302 clinical medicine, Physical medicine and rehabilitation, Databases, Genetic, Genetics, medicine, Humans, Genetic Predisposition to Disease, Amyotrophic lateral sclerosis, Genetic Association Studies, Genetics (clinical), 030304 developmental biology, Internet, 0303 health sciences, Geography, Superoxide Dismutase, Amyotrophic Lateral Sclerosis, Computational Biology, medicine.disease, 3. Good health, Phenotype, Mutation, Medical genetics, Age of onset, 030217 neurology & neurosurgery
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المؤلفون: Christina M. Lill, Lars Bertram, Olubunmi Abel, Ammar Al-Chalabi
المصدر: Amyotrophic Lateral Sclerosis; Vol 12
مصطلحات موضوعية: Databases, Factual, Genotype, Biology, computer.software_genre, 03 medical and health sciences, symbols.namesake, User-Computer Interface, 0302 clinical medicine, medicine, Humans, Genetic Predisposition to Disease, Amyotrophic lateral sclerosis, Genotyping, 030304 developmental biology, 0303 health sciences, Database, Genetic heterogeneity, Amyotrophic Lateral Sclerosis, Family aggregation, General Medicine, medicine.disease, 3. Good health, Phenotype, Neurology, Mutation, Mendelian inheritance, symbols, Neurology (clinical), computer, 030217 neurology & neurosurgery, Diffi cult, Software
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المؤلفون: Bradley N. Smith, Cathryn M. Lewis, John Hardy, Wim Robberecht, Christopher Shaw, Stephen Newhouse, Adriano Chiò, Isabella Fogh, Aleksey Shatunov, Richard W. Orrell, Olubunmi Abel, Vincenzo Silani, Peter M. Andersen, Michael A van Es, Peter McGuffin, P. Nigel Leigh, John Powell, Karen E. Morrison, Leonard H. van den Berg, Jonathan D. Glass, Caroline Vance, Kin Y. Mok, Robert H. Brown, Pamela J. Shaw, John Landers, Jan H. Veldink, Ammar Al-Chalabi, Bryan J. Traynor, Anne Farmer, Lauren Johnson, Hardev Pall, Vincent Meininger, Orla Hardiman, Michael E. Weale, Philip Van Damme, Amy W. Butler, Judith Melki
المصدر: Lancet Neurology
Shatunov, A, Mok, K, Newhouse, S, Weale, M E, Smith, B, Vance, C, Johnson, L, Veldink, J H, van Es, M A, van den Berg, L H, Robberecht, W, Van Damme, P, Hardiman, O, Farmer, A E, Lewis, C M, Butler, A W, Abel, O, Andersen, P M, Fogh, I, Silani, V, Chiò, A, Traynor, B J, Melki, J, Meininger, V, Landers, J E, McGuffin, P, Glass, J D, Pall, H, Leigh, P N, Hardy, J, Brown, R H, Powell, J F, Orrell, R W, Morrison, K E, Shaw, P J, Shaw, C E & Al-Chalabi, A 2010, ' Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries : a genome-wide association study ', Lancet Neurology, vol. 9, no. 10, pp. 986-94 . https://doi.org/10.1016/S1474-4422(10)70197-6مصطلحات موضوعية: medicine.medical_specialty, Internationality, Population, Clinical Neurology, Locus (genetics), Single-nucleotide polymorphism, Genome-wide association study, Polymorphism, Single Nucleotide, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Fast track — Articles, medicine, Humans, Amyotrophic lateral sclerosis, education, Aged, 030304 developmental biology, Genetic association, Aged, 80 and over, Genetics, 0303 health sciences, education.field_of_study, business.industry, Amyotrophic Lateral Sclerosis, Odds ratio, Middle Aged, medicine.disease, United Kingdom, United States, 3. Good health, Europe, Case-Control Studies, Frontotemporal Dementia, Neurology (clinical), Chromosomes, Human, Pair 9, business, Motor neurone disease, 030217 neurology & neurosurgery, Genome-Wide Association Study
وصف الملف: application/pdf
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المؤلفون: Peter M Andersen, Ashley R. Jones, Olubunmi Abel, John Powell, Ammar Al-Chalabi, Aleksey Shatunov
المصدر: JMIR mHealth and uHealth, Vol 1, Iss 2, p e18 (2013)
JMIR mHealth and uHealthمصطلحات موضوعية: amyotrophic lateral sclerosis, Computer science, Health Informatics, Information technology, Web-bases, computer.software_genre, frontotemporal dementia, 03 medical and health sciences, 0302 clinical medicine, Computer Systems, medicine, genetics, Amyotrophic lateral sclerosis, mobile website, app, database, 030304 developmental biology, Genetics, Original Paper, 0303 health sciences, Database, bioinformatics, medicine.disease, T58.5-58.64, 3. Good health, ALSoD, Datorsystem, Smartphone app, Public aspects of medicine, RA1-1270, computer, 030217 neurology & neurosurgery
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcad6629b66d2bd7816aa3298f37f1d9
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-142770 -
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المؤلفون: Pamela J. Shaw, Aleksey Shatunov, Ammar Al-Chalabi, John Powell, Vladimir L. Buchman, Johnathan Cooper-Knock, Kirsten M. Scott, Ione O.C. Woollacott, Ashley R. Jones, Cathryn M. Lewis, Peter McGuffin, Olubunmi Abel, P. Nigel Leigh, Anne Farmer, Karen E. Morrison, Christopher Shaw, Rubika Balendra, Bradley N. Smith, William Sproviero, Catherine M. Ellis
المصدر: Neurobiology of Aging
Neurobiology of Aging; Vol 34مصطلحات موضوعية: Aging, Genotype, Neuroscience(all), Population, Clinical Neurology, Locus (genetics), Genome-wide association study, Biology, TARDBP, 03 medical and health sciences, 0302 clinical medicine, C9orf72, Genetics, medicine, Humans, GWAS, Amyotrophic lateral sclerosis, Allele, education, Alleles, 030304 developmental biology, Residual association, 0303 health sciences, education.field_of_study, C9orf72 Protein, General Neuroscience, Amyotrophic Lateral Sclerosis, Proteins, Hexanucleotide repeat mutation, medicine.disease, Molecular biology, 3. Good health, Ageing, Genetic Loci, Mutation, Neurology (clinical), Geriatrics and Gerontology, Trinucleotide Repeat Expansion, Trinucleotide repeat expansion, Genetics Reports Abstract, 030217 neurology & neurosurgery, Genome-Wide Association Study, Developmental Biology
وصف الملف: application/octet-stream
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المؤلفون: Peter M. Andersen, Ammar Al-Chalabi, John Powell, Olubunmi Abel
المصدر: PLoS ONE; Vol 8
PLoS ONE
PLoS ONE, Vol 8, Iss 6, p e64899 (2013)مصطلحات موضوعية: Neurologi, lcsh:Medicine, Biological Data Management, Disease, Biology, Bioinformatics, TARDBP, Statistics, Nonparametric, Motor Neuron Diseases, 03 medical and health sciences, 0302 clinical medicine, Credibility, Genetics, medicine, Humans, Genetic Predisposition to Disease, Amyotrophic lateral sclerosis, Allele, lcsh:Science, Alleles, Genetic Association Studies, 030304 developmental biology, Computational Neuroscience, Clinical Genetics, 0303 health sciences, Models, Statistical, Multidisciplinary, Models, Genetic, lcsh:R, Amyotrophic Lateral Sclerosis, Computational Biology, Reproducibility of Results, Human Genetics, Neurodegenerative Diseases, Evidence-based medicine, VAPB, medicine.disease, 3. Good health, Neurology, Ranking, Genetics of Disease, Medicine, lcsh:Q, 030217 neurology & neurosurgery, Research Article, Neuroscience
وصف الملف: application/pdf
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المؤلفون: Ammar Al-Chalabi, P. Anderson, John Powell, Olubunmi Abel
المصدر: Journal of Neurology, Neurosurgery & Psychiatry. 81:e65-e65
مصطلحات موضوعية: Genetics, Database, business.industry, Genetic variants, computer.software_genre, Psychiatry and Mental health, Resource (project management), Documentation, Research community, Mutation (genetic algorithm), Central repository, Medicine, Analysis software, Surgery, Neurology (clinical), business, computer, Genetic association