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Hepatitis C Virus Core Antigen (HCVAg): an affordable assay to monitor the efficacy of treatment in DAAs era.
New Microbiol. 2021 Apr;44(2):89-94. Epub 2021 May 21.
New Microbiol. 2021.
PMID: 34151994
Free article.
Staphylococcus aureus vaccine preclinical and clinical development: current state of the art.
Redi D, Raffaelli CS, Rossetti B, De Luca A, Montagnani F.
Redi D, et al. Among authors: raffaelli cs.
New Microbiol. 2018 Jul;41(3):208-213. Epub 2018 Jun 6.
New Microbiol. 2018.
PMID: 29874390
Free article.
Review.
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Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity.
Fallerini C, Picchiotti N, Baldassarri M, Zguro K, Daga S, Fava F, Benetti E, Amitrano S, Bruttini M, Palmieri M, Croci S, Lista M, Beligni G, Valentino F, Meloni I, Tanfoni M, Minnai F, Colombo F, Cabri E, Fratelli M, Gabbi C, Mantovani S, Frullanti E, Gori M, Crawley FP, Butler-Laporte G, Richards B, Zeberg H, Lipcsey M, Hultström M, Ludwig KU, Schulte EC, Pairo-Castineira E, Baillie JK, Schmidt A, Frithiof R; WES/WGS Working Group Within the HGI; GenOMICC Consortium; GEN-COVID Multicenter Study; Mari F, Renieri A, Furini S.
Fallerini C, et al.
Hum Genet. 2022 Jan;141(1):147-173. doi: 10.1007/s00439-021-02397-7. Epub 2021 Dec 10.
Hum Genet. 2022.
PMID: 34889978
Free PMC article.
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Rare variants in Toll-like receptor 7 results in functional impairment and downregulation of cytokine-mediated signaling in COVID-19 patients.
Mantovani S, Daga S, Fallerini C, Baldassarri M, Benetti E, Picchiotti N, Fava F, Gallì A, Zibellini S, Bruttini M, Palmieri M, Croci S, Amitrano S, Alaverdian D, Capitani K, Furini S, Mari F, Meloni I; GEN-COVID Multicenter Study; Frullanti E, Mondelli MU, Renieri A.
Mantovani S, et al.
Genes Immun. 2022 Feb;23(1):51-56. doi: 10.1038/s41435-021-00157-1. Epub 2021 Dec 24.
Genes Immun. 2022.
PMID: 34952932
Free PMC article.
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An explainable model of host genetic interactions linked to COVID-19 severity.
Onoja A, Picchiotti N, Fallerini C, Baldassarri M, Fava F; GEN-COVID Multicenter Study; Colombo F, Chiaromonte F, Renieri A, Furini S, Raimondi F.
Onoja A, et al.
Commun Biol. 2022 Oct 26;5(1):1133. doi: 10.1038/s42003-022-04073-6.
Commun Biol. 2022.
PMID: 36289370
Free PMC article.
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Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder.
Bergantini L, Baldassarri M, d'Alessandro M, Brunelli G, Fabbri G, Zguro K, Degl'Innocenti A; GEN-COVID Multicenter study; Fallerini C, Bargagli E, Renieri A.
Bergantini L, et al.
Respir Res. 2023 Jun 16;24(1):158. doi: 10.1186/s12931-023-02458-7.
Respir Res. 2023.
PMID: 37328761
Free PMC article.
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A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death.
Minnai F, Biscarini F, Esposito M, Dragani TA, Bujanda L, Rahmouni S, Alarcón-Riquelme ME, Bernardo D, Carnero-Montoro E, Buti M, Zeberg H, Asselta R, Romero-Gómez M; GEN-COVID Multicenter Study; Fernandez-Cadenas I, Fallerini C, Zguro K, Croci S, Baldassarri M, Bruttini M, Furini S, Renieri A, Colombo F.
Minnai F, et al.
Sci Rep. 2024 Feb 6;14(1):3000. doi: 10.1038/s41598-024-53310-x.
Sci Rep. 2024.
PMID: 38321133
Free PMC article.
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Impairment of PI3K/AKT and WNT/β-catenin pathways in bone marrow mesenchymal stem cells isolated from patients with myelodysplastic syndromes.
Falconi G, Fabiani E, Fianchi L, Criscuolo M, Raffaelli CS, Bellesi S, Hohaus S, Voso MT, D'Alò F, Leone G.
Falconi G, et al. Among authors: raffaelli cs.
Exp Hematol. 2016 Jan;44(1):75-83.e1-4. doi: 10.1016/j.exphem.2015.10.005. Epub 2015 Oct 28.
Exp Hematol. 2016.
PMID: 26521017
Free article.
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