Author

Michela Biancolella

University of Rome Tor VergataORCID 0000-0002-9376-4231Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Andrea CampanaiD· 1 shared Antonio NovelliiD· 1 shared Dario CocciadiferroiD· 1 shared Francesca LeonardisiD· 1 shared Giuseppe NovelliiD· 1 shared Maria Rosaria D’ApiceiD· 1 shared Massimiliano RaponiiD· 1 shared Massimo AndreoniiD· 1 shared

Activity by Year

2020-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Andrea CampanaORCID

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1 paper

Recent·Most cited

No evidence for allelic association between Covid-19 and ACE2 genetic variants by direct exome sequencing in 99 SARS-CoV-2 positive patients

Antonio Novelli, Michela Biancolella, Paola Borgiani, Dario Cocciadiferro, Vito Luigi Colona, Maria Rosaria D’Apice, Paola Rogliani, Salvatore Zaffina, Francesca Leonardis, Andrea Campana, Massimiliano Raponi, Massimo Andreoni, Sandro Grelli, Giuseppe Novelli

The paper analyzes ACE2 genetic variants in 99 COVID-19 patients using whole-exome sequencing and finds no allelic association with disease severity or sex bias.

Human Genomics · Sep 11, 2020Peer-reviewedGenetic & Genomic Medicine