Cargando…
Integrative genomics analysis reveals a 21q22.11 locus contributing risk to COVID-19
The systematic identification of host genetic risk factors is essential for the understanding and treatment of coronavirus disease 2019 (COVID-19). By performing a meta-analysis of two independent genome-wide association summary datasets (N = 680 128), a novel locus at 21q22.11 was identified to be...
Autores principales: | Ma, Yunlong, Huang, Yukuan, Zhao, Sen, Yao, Yinghao, Zhang, Yaru, Qu, Jia, Wu, Nan, Su, Jianzhong |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8136003/ https://www.ncbi.nlm.nih.gov/pubmed/33949668 http://dx.doi.org/10.1093/hmg/ddab125 |
Ejemplares similares
-
Detection of 21q11.2‐q22.11 deletions in a fetus by NIPT
por: Zheng, Yunyun, et al.
Publicado: (2019) -
Monosomy chromosome 21 compensated by 21q22.11q22.3 duplication in a case with small size and minor anomalies
por: Su, Meng, et al.
Publicado: (2018) -
A de novo 2.78-Mb duplication on chromosome 21q22.11 implicates candidate genes in the partial trisomy 21 phenotype
por: Weisfeld-Adams, James D, et al.
Publicado: (2016) -
A de novo 2.78-Mb duplication on chromosome 21q22.11 implicates candidate genes in the partial trisomy 21 phenotype
por: Weisfeld-Adams, James D, et al.
Publicado: (2017) -
Abstract No. : ABS2211
por: Raja, Thanigai
Publicado: (2022)