Items where authors include "Hardiman, O"

Article

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

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

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.

Tobin, K, Gilthorpe, MS orcid.org/0000-0001-8783-7695, Rooney, J et al. (4 more authors) (2016) Age-period-cohort analysis of trends in amyotrophic lateral sclerosis incidence. Journal of Neurology, 263 (10). pp. 1919-1926. ISSN 0340-5354

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