BibTex format
@article{Fallerini:2022:10.1007/s00439-021-02397-7,
author = {Fallerini, C and Picchiotti, N and Baldassarri, M and Zguro, K and Daga, S and Fava, F and Benetti, E and Amitrano, S and Bruttini, M and Palmieri, M and Croci, S and Lista, M and Beligni, G and Valentino, F and Meloni, I and Tanfoni, M and Minnai, F and Colombo, F and Cabri, E and Fratelli, M and Gabbi, C and Mantovani, S and Frullanti, E and Gori, M and Crawley, FP and Butler-Laporte, G and Richards, B and Zeberg, H and Lipcsey, M and Hultström, M and Ludwig, KU and Schulte, EC and Pairo-Castineira, E and Baillie, JK and Schmidt, A and Frithiof, R and WESWGS, Working Group Within the HGI and GenOMICC, Consortium and GEN-COVID, Multicenter Study and Mari, F and Renieri, A and Furini, S},
doi = {10.1007/s00439-021-02397-7},
journal = {Human Genetics},
pages = {147--173},
title = {Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity},
url = {http://dx.doi.org/10.1007/s00439-021-02397-7},
volume = {141},
year = {2022}
}