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

URL الوصول: https://doaj.org/article/8e0ad59b00f44e48822c11311414e619

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

URL الوصول: https://doaj.org/article/3a2b8e9a76094f53a4b32e441bb751a4

المؤلفون: Olubunmi Abel, John F Powell, Peter M Andersen, Ammar Al-Chalabi

المصدر: PLoS ONE, Vol 8, Iss 6, p e64899 (2013)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC3674010?pdf=render; https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/7e5025af61b84f529541bceeb3963e80

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

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40cc12260ede382a2d0431adc34d9007
https://doi.org/10.1002/humu.22157

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

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc3e19bdd506a597de5463ce67fd460b

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)70197-6

مصطلحات 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

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6f49011e47a3d731c1d1a93bf661bb4
https://doi.org/10.1016/s1474-4422(10)70197-6

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 uHealth

مصطلحات 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

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 34

مصطلحات 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

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f82174bbb934ff78ca7a31a29a28029

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

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30a91e612930c07069b1c74d9bf9c272

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

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::dc4e81c6c236eae2043f0d39c71a24e0
https://doi.org/10.1136/jnnp.2010.226340.192