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

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DOI: 10.1007/s00439-021-02397-7
Published: 2022 Jan
Container: Human genetics
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1007/s00439-021-02397-7,
  title = {Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity.},
  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 WES/WGS Working Group Within the HGI and GenOMICC Consortium and GEN-COVID Multicenter Study and Mari F and Renieri A and Furini S},
  year = {2022},
  journal = {Human genetics},
  doi = {10.1007/s00439-021-02397-7},
  url = {https://doi.org/10.1007/s00439-021-02397-7}
}

RIS

TY  - JOUR
TI  - Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity.
AU  - Fallerini C
AU  - Picchiotti N
AU  - Baldassarri M
AU  - Zguro K
AU  - Daga S
AU  - Fava F
AU  - Benetti E
AU  - Amitrano S
AU  - Bruttini M
AU  - Palmieri M
AU  - Croci S
AU  - Lista M
AU  - Beligni G
AU  - Valentino F
AU  - Meloni I
AU  - Tanfoni M
AU  - Minnai F
AU  - Colombo F
AU  - Cabri E
AU  - Fratelli M
AU  - Gabbi C
AU  - Mantovani S
AU  - Frullanti E
AU  - Gori M
AU  - Crawley FP
AU  - Butler-Laporte G
AU  - Richards B
AU  - Zeberg H
AU  - Lipcsey M
AU  - Hultström M
AU  - Ludwig KU
AU  - Schulte EC
AU  - Pairo-Castineira E
AU  - Baillie JK
AU  - Schmidt A
AU  - Frithiof R
AU  - WES/WGS Working Group Within the HGI
AU  - GenOMICC Consortium
AU  - GEN-COVID Multicenter Study
AU  - Mari F
AU  - Renieri A
AU  - Furini S
PY  - 2022
JO  - Human genetics
DO  - 10.1007/s00439-021-02397-7
UR  - https://doi.org/10.1007/s00439-021-02397-7
ER  -

APA

C, F., N, P., M, B., K, Z., S, D., F, F., E, B., S, A., M, B., M, P., S, C., M, L., G, B., F, V., I, M., M, T., F, M., F, C., E, C., M, F., C, G., S, M., E, F., M, G., FP, C., G, B., B, R., H, Z., M, L., M, H., KU, L., EC, S., E, P., JK, B., A, S., R, F., HGI, W. W. G. W. T., Consortium, G., Study, G. M., F, M., A, R., & S, F. (2022). Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity.. Human genetics. https://doi.org/10.1007/s00439-021-02397-7

Source records

pubmed · retrieved 2026-09-26T14:26:09.521Z
europe-pmc · retrieved 2026-09-26T14:26:09.513Z