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Scientific Reports|October 19, 2024
The role of genetically predicted serum iron levels on neurodegenerative and cardiovascular traitsWiame Belbellaj, Frida Lona-Durazo, Cinzia Bodano, et al.Nature Communications|January 20, 2016
Genomic signals of migration and continuity in Britain before the Anglo-SaxonsRui Martiniano, Anwen Caffell, Malin Holst, et al.Nature Communications|November 17, 2015
Upper Palaeolithic genomes reveal deep roots of modern EurasiansEppie R Jones, Gloria Gonzalez-Fortes, Sarah Connell, et al.NAR Genomics and Bioinformatics|February 8, 2021
Cross-reactive probes on Illumina DNA methylation arrays: a large study on ALS shows that a cautionary approach is warranted in interpreting epigenome-wide association studiesPaul J Hop, Ramona A J Zwamborn, Eilis J Hannon, et al.Neurobiology of Aging|December 15, 2022
Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosisGijs H P Tazelaar, Paul J Hop, Meinie Seelen, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 13, 2025
Oligogenic structure of amyotrophic lateral sclerosis has genetic testing, counselling and therapeutic implicationsAlfredo Iacoangeli, Allison A Dilliott, Ahmad Al Khleifat, et al.Neurobiology of Aging|October 22, 2018
Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohortGijs H P Tazelaar, Annelot M Dekker, Joke J F A van Vugt, et al.Brain Communications|September 21, 2020
ATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalizationGijs H P Tazelaar, Steven Boeynaems, Mathias De Decker, et al.Biorxiv : the Preprint Server for Biology|December 9, 2024
Sex-specific DNA methylation differences in Amyotrophic lateral sclerosisOlivia A Grant, Alfredo Iacoangeli, Ramona A J Zwamborn, et al.Human Molecular Genetics|August 6, 2010
A large genome scan for rare CNVs in amyotrophic lateral sclerosisHylke M Blauw, Ammar Al-Chalabi, Peter M Andersen, et al.Pageof 8