Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...
Ergebnis 22 von 649
Human molecular genetics, 2022-11, Vol.31 (23), p.3945-3966
2022

Details

Autor(en) / Beteiligte
Titel
Detailed stratified GWAS analysis for severe COVID-19 in four European populations
Ist Teil von
  • Human molecular genetics, 2022-11, Vol.31 (23), p.3945-3966
Ort / Verlag
England: Oxford University Press
Erscheinungsjahr
2022
Link zum Volltext
Quelle
Oxford Journals 2020 Medicine
Beschreibungen/Notizen
  • Given the highly variable clinical phenotype of Coronavirus disease 2019 (COVID-19), a deeper analysis of the host genetic contribution to severe COVID-19 is important to improve our understanding of underlying disease mechanisms. Here, we describe an extended genome-wide association meta-analysis of a well-characterized cohort of 3255 COVID-19 patients with respiratory failure and 12 488 population controls from Italy, Spain, Norway and Germany/Austria, including stratified analyses based on age, sex and disease severity, as well as targeted analyses of chromosome Y haplotypes, the human leukocyte antigen region and the SARS-CoV-2 peptidome. By inversion imputation, we traced a reported association at 17q21.31 to a ~0.9-Mb inversion polymorphism that creates two highly differentiated haplotypes and characterized the potential effects of the inversion in detail. Our data, together with the 5th release of summary statistics from the COVID-19 Host Genetics Initiative including non-Caucasian individuals, also identified a new locus at 19q13.33, including NAPSA, a gene which is expressed primarily in alveolar cells responsible for gas exchange in the lung.
Sprache
Englisch
Identifikatoren
ISSN: 0964-6906, 1460-2083
eISSN: 1460-2083
DOI: 10.1093/hmg/ddac158
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9703941

Weiterführende Literatur

Empfehlungen zum selben Thema automatisch vorgeschlagen von bX