Items where authors include "Brunetti, M"

Article

Abed Abud, A, Abi, B, Acciarri, R et al. (1225 more authors) (2022) Separation of track- and shower-like energy deposits in ProtoDUNE-SP using a convolutional neural network. European Physical Journal C, 82 (10). 903. ISSN 1434-6044

Abud, AA, Abi, B, Acciarri, R et al. (1223 more authors) (2022) Scintillation light detection in the 6-m drift-length ProtoDUNE Dual Phase liquid argon TPC. The European Physical Journal C, 82 (7). 618. ISSN 1434-6044

Abud, AA, Abi, B, Acciarri, R et al. (1153 more authors) (2022) Low exposure long-baseline neutrino oscillation sensitivity of the DUNE experiment. Physical Review D, 105 (7). 072006. ISSN 2470-0010

Collaboration, DUNE, Abud, AA, Abi, B et al. (1180 more authors) (2022) Design, construction and operation of the ProtoDUNE-SP Liquid Argon TPC. Journal of Instrumentation, 17 (01). P01005. ISSN 1748-0221

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

Abud, AA, Abi, B, Acciarri, R et al. (1177 more authors) (2021) Searching for solar KDAR with DUNE. Journal of Cosmology and Astroparticle Physics, 2021 (10). 065. ISSN 1475-7516

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

Collaboration, DUNE, Abud, AA, Abi, B et al. (1154 more authors) (2021) Low exposure long-baseline neutrino oscillation sensitivity of the DUNE experiment. arXiv. (Submitted)

Abud, AA, Abi, B, Acciarri, R et al. (1063 more authors) (2021) Deep Underground Neutrino Experiment (DUNE) Near Detector Conceptual Design Report. arXiv. (Submitted)

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)

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

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