المؤلفون: Restuadi, Restuadi, Steyn, Frederik J, Kabashi, Edor, Ngo, Shyuan T, Cheng, Fei-Fei, Nabais, Marta F, Thompson, Mike J, Qi, Ting, Wu, Yang, Henders, Anjali K, Wallace, Leanne, Bye, Chris R, Turner, Bradley J, Ziser, Laura, Mathers, Susan, McCombe, Pamela A, Needham, Merrilee, Schultz, David, Kiernan, Matthew C, van Rheenen, Wouter, van den Berg, Leonard H, Veldink, Jan H, Ophoff, Roel, Gusev, Alexander, Zaitlen, Noah, McRae, Allan F, Henderson, Robert D, Wray, Naomi R, Giacomotto, Jean, Garton, Fleur C

المصدر: Genome Medicine. 14(1)

مصطلحات موضوعية: Biological Sciences, Genetics, Rare Diseases, Neurosciences, Neurodegenerative, Biotechnology, Human Genome, Brain Disorders, ALS, 2.1 Biological and endogenous factors, Aetiology, Neurological, Amyotrophic Lateral Sclerosis, Animals, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Neurodegenerative Diseases, Polymorphism, Single Nucleotide, Zebrafish, Motor neurone disease, MND, Genome-wide association study, Computational biology, Neurodegenerative diseases, Quantitative trait loci, Genes, Regulator, Disease progression, Clinical Sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/5ms535m1Test

المؤلفون: Hop, Paul J., Zwamborn, Ramona A.J., Hannon, Eilis, Shireby, Gemma L., Nabais, Marta F., Walker, Emma M., Rheenen, Wouter van, Vugt, Joke J.F.A. van, Dekker, Annelot M., Westeneng, Henk-Jan, Tazelaar, Gijs H.P., Eijk, Kristel R. van, Moisse, Matthieu, Baird, Denis, Khleifat, Ahmad Al, Iacoangeli, Alfredo, Ticozzi, Nicola, Ratti, Antonia, Cooper-Knock, Jonathan, Morrison, Karen E., Shaw, Pamela J., Nazli Basak, A., Chiò, Adriano, Calvo, Andrea, Moglia, Cristina, Canosa, Antonio, Brunetti, Maura, Grassano, Maurizio, Gotkine, Marc, Lerner, Yossef, Zabari, Michal, Vourc'h, Patrick, Corcia, Philippe, Couratier, Philippe, Mora Pardina, Jesus S., Salas, Teresa, Dion, Patrick, Ross, Jay P., Henderson, Robert D., Mathers, Susan, McCombe, Pamela A., Needham, Merrilee, Nicholson, Garth, Rowe, Dominic B., Pamphlett, Roger, Mather, Karen A., Sachdev, Perminder S., Furlong, Sarah, Garton, Fleur C., Henders, Anjali K., Lin, Tian, Ngo, Shyuan T., Steyn, Frederik J., Wallace, Leanne, Williams, Kelly L., Mitne Neto, Miguel, Cauchi, Ruben J., Blair, Ian P., Kiernan, Matthew C., Drory, Vivian, Povedano, Monica, Carvalho, Mamede de, Pinto, Susana, Weber, Markus, Rouleau, Guy A., Silani, Vincenzo, Landers, John E., Shaw, Christopher E., Andersen, Peter M., McRae, Allan F., van Es, Michael A., Jeroen Pasterkamp, R., Wray, Naomi R., McLaughlin, Russell L., Hardiman, Orla, Kenna, Kevin P., Tsai, Ellen, Runz, Heiko, Al-Chalabi, Ammar, Berg, Leonard H. van den, Damme, Philip Van, Mill, Jonathan, Veldink, Jan H., BIOS Consortium, Brain MEND Consortium

المساهمون: BIOS Consortium, Brain MEND Consortium

مصطلحات موضوعية: Amyotrophic lateral sclerosis -- Diagnosis, Genes, Non-coding RNA, Gene expression, Membrane lipids -- Research

العلاقة: Hop, P. J., Zwamborn, R. A., Hannon, E., Shireby, G. L., Nabais, M. F., Walker, E. M., . & Mill, J. (2022). Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS. Science translational medicine, 14(633), eabj0264.; https://www.um.edu.mt/library/oar/handle/123456789/103515Test

الإتاحة: https://doi.org/10.1126/scitranslmed.abj0264Test
https://www.um.edu.mt/library/oar/handle/123456789/103515Test