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Mapping the human genetic architecture of COVID-19

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Mapping the human genetic architecture of COVID-19. / COVID-19 Host Genetics Initiative ; Shih, Barbara.
In: Nature, Vol. 600, 16.12.2021, p. 472-477.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

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COVID-19 Host Genetics Initiative & Shih, B 2021, 'Mapping the human genetic architecture of COVID-19', Nature, vol. 600, pp. 472-477. https://doi.org/10.1038/s41586-021-03767-x

APA

Vancouver

COVID-19 Host Genetics Initiative , Shih B. Mapping the human genetic architecture of COVID-19. Nature. 2021 Dec 16;600:472-477. Epub 2021 Jul 8. doi: 10.1038/s41586-021-03767-x

Author

COVID-19 Host Genetics Initiative ; Shih, Barbara. / Mapping the human genetic architecture of COVID-19. In: Nature. 2021 ; Vol. 600. pp. 472-477.

Bibtex

@article{8ef7426a69204deb9597953ee26e00ae,
title = "Mapping the human genetic architecture of COVID-19",
abstract = "The genetic make-up of an individual contributes to the susceptibility and response to viral infection. Although environmental, clinical and social factors have a role in the chance of exposure to SARS-CoV-2 and the severity of COVID-19, host genetics may also be important. Identifying host-specific genetic factors may reveal biological mechanisms of therapeutic relevance and clarify causal relationships of modifiable environmental risk factors for SARS-CoV-2 infection and outcomes. We formed a global network of researchers to investigate the role of human genetics in SARS-CoV-2 infection and COVID-19 severity. Here we describe the results of three genome-wide association meta-analyses that consist of up to 49,562 patients with COVID-19 from 46 studies across 19 countries. We report 13 genome-wide significant loci that are associated with SARS-CoV-2 infection or severe manifestations of COVID-19. Several of these loci correspond to previously documented associations to lung or autoimmune and inflammatory diseases. They also represent potentially actionable mechanisms in response to infection. Mendelian randomization analyses support a causal role for smoking and body-mass index for severe COVID-19 although not for type II diabetes. The identification of novel host genetic factors associated with COVID-19 was made possible by the community of human genetics researchers coming together to prioritize the sharing of data, results, resources and analytical frameworks. This working model of international collaboration underscores what is possible for future genetic discoveries in emerging pandemics, or indeed for any complex human disease.",
author = "{COVID-19 Host Genetics Initiative} and Barbara Shih",
year = "2021",
month = dec,
day = "16",
doi = "10.1038/s41586-021-03767-x",
language = "English",
volume = "600",
pages = "472--477",
journal = "Nature",
issn = "0028-0836",
publisher = "Nature Publishing Group",

}

RIS

TY - JOUR

T1 - Mapping the human genetic architecture of COVID-19

AU - COVID-19 Host Genetics Initiative

AU - Shih, Barbara

PY - 2021/12/16

Y1 - 2021/12/16

N2 - The genetic make-up of an individual contributes to the susceptibility and response to viral infection. Although environmental, clinical and social factors have a role in the chance of exposure to SARS-CoV-2 and the severity of COVID-19, host genetics may also be important. Identifying host-specific genetic factors may reveal biological mechanisms of therapeutic relevance and clarify causal relationships of modifiable environmental risk factors for SARS-CoV-2 infection and outcomes. We formed a global network of researchers to investigate the role of human genetics in SARS-CoV-2 infection and COVID-19 severity. Here we describe the results of three genome-wide association meta-analyses that consist of up to 49,562 patients with COVID-19 from 46 studies across 19 countries. We report 13 genome-wide significant loci that are associated with SARS-CoV-2 infection or severe manifestations of COVID-19. Several of these loci correspond to previously documented associations to lung or autoimmune and inflammatory diseases. They also represent potentially actionable mechanisms in response to infection. Mendelian randomization analyses support a causal role for smoking and body-mass index for severe COVID-19 although not for type II diabetes. The identification of novel host genetic factors associated with COVID-19 was made possible by the community of human genetics researchers coming together to prioritize the sharing of data, results, resources and analytical frameworks. This working model of international collaboration underscores what is possible for future genetic discoveries in emerging pandemics, or indeed for any complex human disease.

AB - The genetic make-up of an individual contributes to the susceptibility and response to viral infection. Although environmental, clinical and social factors have a role in the chance of exposure to SARS-CoV-2 and the severity of COVID-19, host genetics may also be important. Identifying host-specific genetic factors may reveal biological mechanisms of therapeutic relevance and clarify causal relationships of modifiable environmental risk factors for SARS-CoV-2 infection and outcomes. We formed a global network of researchers to investigate the role of human genetics in SARS-CoV-2 infection and COVID-19 severity. Here we describe the results of three genome-wide association meta-analyses that consist of up to 49,562 patients with COVID-19 from 46 studies across 19 countries. We report 13 genome-wide significant loci that are associated with SARS-CoV-2 infection or severe manifestations of COVID-19. Several of these loci correspond to previously documented associations to lung or autoimmune and inflammatory diseases. They also represent potentially actionable mechanisms in response to infection. Mendelian randomization analyses support a causal role for smoking and body-mass index for severe COVID-19 although not for type II diabetes. The identification of novel host genetic factors associated with COVID-19 was made possible by the community of human genetics researchers coming together to prioritize the sharing of data, results, resources and analytical frameworks. This working model of international collaboration underscores what is possible for future genetic discoveries in emerging pandemics, or indeed for any complex human disease.

U2 - 10.1038/s41586-021-03767-x

DO - 10.1038/s41586-021-03767-x

M3 - Journal article

VL - 600

SP - 472

EP - 477

JO - Nature

JF - Nature

SN - 0028-0836

ER -