G. Abecasis

发表

Genome-wide analysis in 756,646 individuals provides first genetic evidence that ACE2 expression influences COVID-19 risk and yields genetic risk scores predictive of severe disease

J. Marchini, S. McCarthy, M. Cantor, 2020, medRxiv.

The association between mitochondrial DNA copy number, low-density lipoprotein cholesterol, and cardiovascular disease risk

M. Fornage, A. Reiner, Y. Zhang, 2022, medRxiv.

Rare coding variants in CHRNB2 reduce the likelihood of smoking

J. Marchini, S. Balasubramanian, A. Shuldiner, 2022, Nature Genetics.

A catalog of associations between rare coding variants and COVID-19 outcomes

Alexander Hanbo Li, J. Marchini, J. Szustakowski, 2020, medRxiv : the preprint server for health sciences.

A catalog of associations between rare coding variants and COVID-19 outcomes

Alexander Hanbo Li, J. Marchini, G. Abecasis, 2020, medRxiv.

Exome sequencing of 628,388 individuals identifies common and rare variant associations with clonal hematopoiesis phenotypes

J. Marchini, G. Atwal, Y. Houvras, 2022, medRxiv.

Population-scale analysis of common and rare genetic variation associated with hearing loss in adults

J. Marchini, S. Balasubramanian, S. Mishra, 2021, Communications Biology.

Common genetic variants identify targets for COVID-19 and individuals at 1 high risk of severe disease 2

A. Girshick, D. Rader, C. O'Dushlaine, 2021 .

A catalog of associations between rare coding variants and COVID-19 outcomes

Alexander Hanbo Li, J. Marchini, J. Szustakowski, 2020, medRxiv : the preprint server for health sciences.

Genome-wide analysis in 756,646 individuals provides first genetic evidence that ACE2 expression influences COVID-19 risk and yields genetic risk scores predictive of severe disease

Alexander Hanbo Li, J. Marchini, S. Balasubramanian, 2020, medRxiv.