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De novo variants in RNF213 are associated with a clinical spectrum ranging from Leigh syndrome to early-onset stroke.
Brunet T, Zott B, Lieftüchter V, Lenz D, Schmidt A, Peters P, Kopajtich R, Zaddach M, Zimmermann H, Hüning I, Ballhausen D, Staufner C, Bianzano A, Hughes J, Taylor RW, McFarland R, Devlin A, Mihaljević M, Barišić N, Rohlfs M, Wilfling S, Sondheimer N, Hewson S, Marinakis NM, Kosma K, Traeger-Synodinos J, Elbracht M, Begemann M, Trepels-Kottek S, Hasan D, Scala M, Capra V, Zara F, van der Ven AT, Driemeyer J, Apitz C, Krämer J, Strong A, Hakonarson H, Watson D, Mayr JA, Prokisch H, Meitinger T, Borggraefe I, Spiegler J, Baric I, Paolini M, Gerstl L, Wagner M. Brunet T, et al. Among authors: watson d. Genet Med. 2024 Feb;26(2):101013. doi: 10.1016/j.gim.2023.101013. Epub 2023 Nov 1. Genet Med. 2024. PMID: 37924258
Strong damped Lyman-α absorption in young star-forming galaxies at redshifts 9 to 11.
Heintz KE, Watson D, Brammer G, Vejlgaard S, Hutter A, Strait VB, Matthee J, Oesch PA, Jakobsson P, Tanvir NR, Laursen P, Naidu RP, Mason CA, Killi M, Jung I, Hsiao TY, Abdurro'uf, Coe D, Haro PA, Finkelstein SL, Toft S. Heintz KE, et al. Among authors: watson d. Science. 2024 May 24;384(6698):890-894. doi: 10.1126/science.adj0343. Epub 2024 May 23. Science. 2024. PMID: 38781391
Levelling the playing field through the London Network of the UK clinical trials accelerator platform.
Matthews J, Dobra R, Wilson G, Allen L, Bossley C, Brendell R, Brugha R, Brown D, Brown S, Cadiente S, Cameron L, Davies G, Dawson C, Elborn S, Hughes D, Longmate J, Macedo P, Pappas L, Pao C, Round C, Ruiz G, Saunders C, Shafi N, Simmonds N, Waller M, Watson D, Davies JC. Matthews J, et al. Among authors: watson d. Contemp Clin Trials Commun. 2024 Apr 26;39:101301. doi: 10.1016/j.conctc.2024.101301. eCollection 2024 Jun. Contemp Clin Trials Commun. 2024. PMID: 38711836 Free PMC article.
4,181 results