Items where authors include "Al-Chalabi, A"
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Škorić-Milosavljević, D, Tadros, R, Bosada, FM et al. (77 more authors) (2022) Common genetic variants contribute to risk of transposition of the great arteries. Circulation Research, 130 (2). pp. 166-180. ISSN 0009-7330
Kliest, T, Van Eijk, RPA, Al-Chalabi, A et al. (54 more authors) (2022) Clinical trials in pediatric ALS : a TRICALS feasibility study. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 23 (7-8). pp. 481-488. ISSN 2167-8421
van Rheenen, W, van der Spek, RAA, Bakker, MK et al. (279 more authors) (2021) Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. Nature Genetics, 53 (12). pp. 1636-1648. ISSN 1061-4036
Johnson, JO, Chia, R, Miller, DE et al. (295 more authors) (2021) Association of variants in the SPTLC1 gene with juvenile amyotrophic lateral sclerosis. JAMA Neurology, 78 (10). pp. 1236-1248. ISSN 2168-6149
Nabais, MF, Laws, SM, Lin, T et al. (67 more authors) (2021) Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders. Genome Biology, 22. 90. ISSN 1474-760X
Cooper-Knock, J orcid.org/0000-0002-0873-8689, Zhang, S, Kenna, KP et al. (51 more authors) (2020) Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk Gene. Cell Reports, 33 (9). 108456. ISSN 2211-1247
Lahrouchi, N, Tadros, R, Crotti, L et al. (103 more authors) (2020) Transethnic genome-wide association study provides insights in the genetic architecture and heritability of Long QT syndrome. Circulation, 142 (4). pp. 324-338. ISSN 0009-7322
Janel, JO, Chia, R, Kumaran, R et al. (50 more authors) (2019) Mutations in the sphingolipid pathway gene SPTLC1 are a cause of amyotrophic lateral sclerosis. SSRN. (Submitted)
Nicolas, A, Kenna, KP, Renton, AE et al. (210 more authors) (2018) Genome-wide Analyses Identify KIF5A as a Novel ALS Gene. Neuron, 97 (6). 1268-1283.e6.
van Rheenen, W, Shatunov, A, Dekker, AM et al. (180 more authors) (2016) Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. Nature Genetics. ISSN 1546-1718