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Sergio Daga

Observed names: Daga Sergio, Daga, Sergio, S Daga, S. Daga, Sergio Daga (11283239)
ORCID: 0000-0002-6419-9456
Observed ORCID: 0000-0002-6419-9456
OpenAlex ID: A5014816362
Mapping the human genetic architecture of COVID-19
2021 · COVID-19 Host Genetics Initiative, COVID-19 Host Genetics InitiativeLeadership, et al. · Nature · 983
Whole-genome sequencing reveals host factors underlying critical COVID-19
2022 · Athanasios Kousathanas, Erola Pairo-Castineira, et al. · Nature · 327
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ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population
2020 · Elisa Benetti, Rossella Tita, et al. · European Journal of Human Genetics · 263
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Association of Toll-like receptor 7 variants with life-threatening COVID-19 disease in males: findings from a nested case-control study
2021 · Chiara Fallerini, Sergio Daga, et al. · eLife · 198
A first update on mapping the human genetic architecture of COVID-19
2022 · COVID-19 Host Genetics Initiative, COVID-19 Host Genetics Initiative, et al. · Nature · 181
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Digenic Alport Syndrome
2022 · Judy Savige, Alessandra Renieri, et al. · Clinical Journal of the American Society of Nephrology · 69
Rare variants in Toll-like receptor 7 results in functional impairment and downregulation of cytokine-mediated signaling in COVID-19 patients
2021 · Stefania Mantovani, Sergio Daga, et al. · Genes and Immunity · 69
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Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males
2021 · Margherita Baldassarri, Nicola Picchiotti, et al. · EBioMedicine · 62
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Pathogen-sugar interactions revealed by universal saturation transfer analysis
2022 · Charles J. Buchanan, Ben Gaunt, et al. · Science · 56
New frontiers to cure Alport syndrome: COL4A3 and COL4A5 gene editing in podocyte-lineage cells
2019 · Sergio Daga, Francesco Donati, et al. · European Journal of Human Genetics · 53
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iPSC-derived neurons profiling reveals GABAergic circuit disruption and acetylated α-tubulin defect which improves after iHDAC6 treatment in Rett syndrome
2018 · Elisa Landucci, Margherita Brindisi, et al. · Experimental Cell Research · 52
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Employing a systematic approach to biobanking and analyzing clinical and genetic data for advancing COVID-19 research
2021 · Sergio Daga, Chiara Fallerini, et al. · European Journal of Human Genetics · 46
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SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues
2021 · Matteo D’Antonio, Jennifer P. Nguyen, et al. · Cell Reports · 45
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The polymorphism L412F in TLR3 inhibits autophagy and is a marker of severe COVID-19 in males
2021 · Susanna Croci, Mary Anna Venneri, et al. · Autophagy · 44
The 2019 and 2021 International Workshops on Alport Syndrome
2022 · Sergio Daga, Jie Ding, et al. · European Journal of Human Genetics · 37
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Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity
2021 · Chiara Fallerini, Nicola Picchiotti, et al. · Human Genetics · 37
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Severe COVID-19 in Hospitalized Carriers of Single CFTR Pathogenic Variants
2021 · Margherita Baldassarri, Francesca Fava, et al. · Journal of Personalized Medicine · 25
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Non-collagen genes role in digenic Alport syndrome
2019 · S. Daga, C. Fallerini, et al. · BMC Nephrology · 23
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Urine-derived podocytes-lineage cells: A promising tool for precision medicine in Alport Syndrome
2017 · Sergio Daga, Margherita Baldassarri, et al. · Human Mutation · 23
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High rate of HDR in gene editing of p.(Thr158Met) MECP2 mutational hotspot
2020 · Susanna Croci, Miriam Lucia Carriero, et al. · European Journal of Human Genetics · 20
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Post-Mendelian Genetic Model in COVID-19
2021 · Nicola Picchiotti, Elisa Benetti, et al. · Cardiology and Cardiovascular Medicine · 16
SELP Asp603Asn and severe thrombosis in COVID-19 males
2021 · Chiara Fallerini, Sergio Daga, et al. · Journal of Hematology & Oncology · 15
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AAV-mediated FOXG1 gene editing in human Rett primary cells
2020 · Susanna Croci, Miriam Lucia Carriero, et al. · European Journal of Human Genetics · 15
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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
2023 · Laura Bergantini, Margherita Baldassarri, et al. · Respiratory Research · 13
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Slowly progressive autosomal dominant Alport Syndrome due to COL4A3 splicing variant
2024 · Sergio Daga, Lorenzo Loberti, et al. · European Journal of Human Genetics · 9
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Works count: 52
Citation count: 2,746
H-index: 20
I10-index: 24
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