Items where authors include "Riva, N"

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

Gauer, JS orcid.org/0000-0002-0835-639X, Riva, N, Page, EM et al. (4 more authors) (2020) Effect of anticoagulants on fibrin clot structure: A comparison between vitamin K antagonists and factor Xa inhibitors. Research and Practice in Thrombosis and Haemostasis, 4 (8). pp. 1269-1281. ISSN 2475-0379

Bandres‐Ciga, S, Noyce, AJ, Hemani, G et al. (166 more authors) (2019) Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis. Annals of Neurology, 85 (4). pp. 470-481. ISSN 0364-5134

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