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Elisa Benetti
Elisa Benetti
Università degli Studi di Siena, Siena, Italy
Verified email at hsr.it
Title
Cited by
Cited by
Year
ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population
E Benetti, R Tita, O Spiga, A Ciolfi, G Birolo, A Bruselles, G Doddato, ...
European Journal of Human Genetics 28 (11), 1602-1614, 2020
2702020
Whole-genome sequencing reveals host factors underlying critical COVID-19
A Kousathanas, E Pairo-Castineira, K Rawlik, A Stuckey, CA Odhams, ...
Nature 607 (7917), 97-103, 2022
2222022
Association of Toll-like receptor 7 variants with life-threatening COVID-19 disease in males: findings from a nested case-control study
C Fallerini, S Daga, S Mantovani, E Benetti, N Picchiotti, D Francisci, ...
elife 10, e67569, 2021
1742021
A first update on mapping the human genetic architecture of COVID-19
Writing group lead Andrews Shea J. 6 Kanai Masahiro 3 Cordioli Mattia 7, ...
Nature 608 (7921), E1-E10, 2022
912022
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases
B Zurek, K Ellwanger, LELM Vissers, R Schüle, M Synofzik, A Töpf, ...
European journal of human genetics 29 (9), 1325-1331, 2021
672021
Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males
M Baldassarri, N Picchiotti, F Fava, C Fallerini, E Benetti, S Daga, ...
EBioMedicine 65, 2021
592021
Protective Role of a TMPRSS2 Variant on Severe COVID-19 Outcome in Young Males and Elderly Women
M Monticelli, B Hay Mele, E Benetti, C Fallerini, M Baldassarri, S Furini, ...
Genes 12 (4), 596, 2021
492021
Rare variants in Toll-like receptor 7 results in functional impairment and downregulation of cytokine-mediated signaling in COVID-19 patients
S Mantovani, S Daga, C Fallerini, M Baldassarri, E Benetti, N Picchiotti, ...
Genes & Immunity 23 (1), 51-56, 2022
452022
Solving patients with rare diseases through programmatic reanalysis of genome-phenome data
L Matalonga, C Hernández-Ferrer, D Piscia, R Schüle, M Synofzik, A Töpf, ...
European Journal of Human Genetics 29 (9), 1337-1347, 2021
422021
Employing a systematic approach to biobanking and analyzing clinical and genetic data for advancing COVID-19 research
S Daga, C Fallerini, M Baldassarri, F Fava, F Valentino, G Doddato, ...
European Journal of Human Genetics 29 (5), 745-759, 2021
392021
Clinical and molecular characterization of COVID-19 hospitalized patients
E Benetti, A Giliberti, A Emiliozzi, F Valentino, L Bergantini, C Fallerini, ...
Plos one 15 (11), e0242534, 2020
362020
New candidates for autism/intellectual disability identified by whole-exome sequencing
LP Bruno, G Doddato, F Valentino, M Baldassarri, R Tita, C Fallerini, ...
International journal of molecular sciences 22 (24), 13439, 2021
322021
The polymorphism L412F in TLR3 inhibits autophagy and is a marker of severe COVID-19 in males
S Croci, MA Venneri, S Mantovani, C Fallerini, E Benetti, N Picchiotti, ...
Autophagy 18 (7), 1662-1672, 2022
312022
Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity
C Fallerini, N Picchiotti, M Baldassarri, K Zguro, S Daga, F Fava, E Benetti, ...
Human genetics 141 (1), 147-173, 2022
312022
New frontiers to cure Alport syndrome: COL4A3 and COL4A5 gene editing in podocyte-lineage cells
S Daga, F Donati, K Capitani, S Croci, R Tita, A Giliberti, F Valentino, ...
European Journal of Human Genetics 28 (4), 480-490, 2020
302020
SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues
M D’Antonio, JP Nguyen, TD Arthur, H Matsui, BM Neale, M Daly, ...
Cell reports 37 (7), 2021
272021
Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders
F Mochel, A Rastetter, B Ceulemans, K Platzer, S Yang, DN Shinde, ...
Brain 143 (12), 3564-3573, 2020
272020
Pathogen-sugar interactions revealed by universal saturation transfer analysis
CJ Buchanan, B Gaunt, PJ Harrison, Y Yang, J Liu, A Khan, AM Giltrap, ...
Science 377 (6604), eabm3125, 2022
262022
Exome sequencing in 200 intellectual disability/autistic patients: New candidates and atypical presentations
F Valentino, LP Bruno, G Doddato, A Giliberti, R Tita, S Resciniti, ...
Brain Sciences 11 (7), 936, 2021
222021
Severe COVID-19 in Hospitalized Carriers of Single CFTR Pathogenic Variants
M Baldassarri, F Fava, C Fallerini, S Daga, E Benetti, K Zguro, S Amitrano, ...
Journal of personalized medicine 11 (6), 558, 2021
192021
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