scispace - formally typeset
L

Luisa Benussi

Researcher at University of Brescia

Publications -  551
Citations -  18162

Luisa Benussi is an academic researcher from University of Brescia. The author has contributed to research in topics: Large Hadron Collider & Frontotemporal dementia. The author has an hindex of 58, co-authored 525 publications receiving 13817 citations. Previous affiliations of Luisa Benussi include University of Verona & Sacred Heart Hospital.

Papers
More filters
Journal ArticleDOI

Search for a low-mass τ−τ+ resonance in association with a bottom quark in proton-proton collisions at s√ = 13 TeV

Albert M. Sirunyan, +2336 more
TL;DR: In this paper, a general search is presented for a low-mass τ−τ+ resonance produced in association with a bottom quark, based on proton-proton collision data at a center-of-mass energy of 13 TeV collected by the CMS experiment at the LHC, corresponding to an integrated luminosity of 35.9 fb−1.
Journal ArticleDOI

Molecular Pathways Bridging Frontotemporal Lobar Degeneration and Psychiatric Disorders

TL;DR: It is believed that prevention and therapy of psychiatric and neurological disorders could be achieved enhancing both BDNF and progranulin levels thanks to drug discovery efforts.
Journal ArticleDOI

Measurement of the associated production of a Z boson with charm or bottom quark jets in proton-proton collisions at $\sqrt{s}=$ 13 TeV

Albert M. Sirunyan, +2293 more
- 19 Aug 2020 - 
TL;DR: The first measurements of the cross section ratios at 13-TeV were made in this article, where a Z boson with at least one charm or bottom quark jet was measured in proton-proton collisions at s=13TeV.
Journal ArticleDOI

Search for new phenomena in final states with two opposite-charge, same-flavor leptons, jets, and missing transverse momentum in pp collisions at root s=13TeV

Albert M. Sirunyan, +2215 more
Journal ArticleDOI

Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort

Jan Verheijen, +70 more
TL;DR: Target resequencing of TBK1 in patients with clinical diagnosis of early onset Alzheimer's disease and a positive family history of ALS found only 1 LoF mutation, not indicative of a significant role forTBK1 mutations in EOAD, and the association between common variants in TBk1, disease risk and reduced TBK 1 expression warrants follow-up in FTD/ALS cohorts.