 = Published  = In pre-print
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| Title | DOI | Method | Curator 1 | Curator 2 |
| A Chinese host genetic study discovered IFNs and causality of laboratory traits on COVID-19 severity
|
https://doi.org/10.1016/j.isci.2021.103186 | Microarray, Genome wide association study | fatima | admin |
| A common TMPRSS2 variant has a protective effect against severe COVID-19
|
https://doi.org/10.1016/j.retram.2022.103333 | Genome wide association study | fatima | admin |
| ACE I/D polymorphism in Czech first-wave SARS-CoV-2-positive survivors
|
https://doi.org/10.1016/j.cca.2021.04.024 | PCR based genotyping | fatima | admin |
| ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy
|
https://doi.org/10.18632/aging.103415 | Whole Exome Sequencing and Genome-wide microarray genotyping | tsaone | clherd |
| Allelic Variants Within the ABO Blood Group Phenotype Confer Protection Against Critical COVID-19 Hospital Presentation
|
https://doi.10.3389/fmed.2021.759648 | Genome wide association study | fatima | admin |
| AncestryDNA COVID-19 Host Genetic Study Identifies Three Novel Loci
|
https://doi.org/10.1101/2020.10.06.20205864 | Genome wide association study | jamiem | rachelg |
| Angiotensin-converting enzymes (ACE, ACE2) gene variants and COVID-19 outcome
|
https://doi.org/10.1016/j.gene.2020.145102 | PCR, sequencing | fatima | admin |
| APOE e4 Genotype Predicts Severe COVID-19 in the UK Biobank Community Cohort
|
https://doi.org/10.1093/gerona/glaa131 | Genotype Array | clherd | tsaone |
| Association of Toll-like receptor 7 variants with life-threatening COVID-19 disease in males: findings from a nested case-control study
|
https://doi.org/10.7554/eLife.67569 | LASSO Logistic Regression Analysis | fatima | admin |
| Common genetic variants identify therapeutic targets for COVID-19 and individuals at high risk of severe disease
|
https://doi.org/10.1101/2020.12.14.20248176 | Genome wide association study | fatima | clherd |
| COVID-19 and Genetic Variants of Protein Involved in the SARS-CoV-2 Entry into the Host Cells
|
https://doi.org/10.3390/genes11091010 | Whole exome sequencing | fatima | tsaone |
| Deletion of the NKG2C receptor encoding KLRC2 gene and HLA-E variants are risk factors for severe COVID-19
|
https://doi.org/10.1038/s41436-020-01077-7 | PCR and Sequencing | fatima | admin |
| Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program
|
https://doi.10.3389/fgene.2021.777076 | Genome wide association study | fatima | admin |
| Genetic mechanisms of critical illness in Covid-19
|
https://doi.org/10.1038/s41586-020-03065-y | Microarray, Whole genome sequencing and Genome wide association study | megan | tsaone |
| Genetic risk factors for death with
SARS-CoV-2 from the UK Biobank
|
https://doi.org/10.1101/2020.07.01.20144592 | Genome wide association study, Gene Prediction | tkkalua | clherd |
| Genetic variants are identified to increase risk of COVID-19 related mortality from UK Biobank data
|
https://doi.org/10.1186/s40246-021-00306-7 | Genome wide association study | tkkalua | adele |
| Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease
|
https://doi.org/10.1038/s41588-021-01006-7 | Genome wide association study, Gene Prediction | fatima | admin |
| Genome-wide association study of COVID-19 severity among the Chinese population
|
https://doi.org/10.1038/s41421-021-00318-6 | Genome wide association study | fatima | admin |
| Genomewide association study of severe Covid-19 with respiratory failure
|
https://doi.org/10.1056/NEJMoa2020283 | Microarray, Genome wide association study | laverne1983 | tkkalua |
| Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent
|
https://doi.org/10.3390/life11090921 | Genome wide association study | fatima | admin |
| Host genetic effects in Pneumonia
|
https://doi.org/10.1016/j.ajhg.2020.12.010 | Genome wide association study | fatima | rachelg |
| Host genetic factors of COVID-19 susceptibility and disease severity in a Thai population
|
https://doi.org/10.1038/s10038-021-01009-6 | Microarray and Genome-wide association study | fatima | admin |
| Inborn errors of type I IFN immunity in patients with life-threatening COVID-19
|
https://doi.org/10.1126/science.abd4570 | Whole genome / whole exome sequencing | clherd | fatima |
| Initial study on TMPRSS2 p.Val160Met genetic variant in COVID-19 patients
|
https://doi.org/10.1186/s40246-021-00330-7 | PCR based SNP genotype assay | fatima | admin |
| Initial whole-genome sequencing and analysis of the host genetic contribution to COVID-19 severity and susceptibility
|
https://doi.org/10.1038/s41421-020-00231-4 | Whole genome sequencing and Genome wide association study | fatima | admin |
| Investigation of MBL2 and NOS3 functional gene variants in suspected COVID-
19 PCR (–) patients
|
https://doi.org/10.1080/20477724.2021.1984726 | PCR and RFLP | fatima | admin |
| Is There a Link between Circadian Clock Protein PERIOD 3 (PER3) (rs57875989) Variant and the Severity of COVID-19 Infection?
|
https://doi.org/10.1007/s11596-021-2442-y | PCR based gene polymorphism detection | fatima | admin |
| Japan COVID-19 Task Force: a nation-wide consortium to elucidate host genetics of COVID-19 pandemic in Japan
|
https://doi.org/10.1101/2021.05.17.21256513 | Genome wide association study | clherd | fatima |
| Mannose binding lectin gene 2 (rs1800450) missense variant may contribute to development and severity of COVID-19 infection
|
https://doi.org/10.1016/j.meegid.2021.104717 | PCR based genotyping | fatima | admin |
| Mapping the human genetic architecture of COVID-19
|
https://doi.org/10.1038/s41586-021-03767-x | Genome wide association study | fatima | admin |
| MBL deficiency-causing B allele (rs1800450) as a risk factor for severe COVID-19
|
https://doi.org/10.1016/j.imbio.2021.152136 | PCR and RFLP (Restriction fragment length polymorphism) | fatima | admin |
| Presence of Genetic Variants Among Young Men With Severe COVID-19
|
https://doi.org/10.1001/jama.2020.13719 | Whole exome sequencing | fatima | rachelg |
| Protective Role of a TMPRSS2 Variant on Severe COVID-19 Outcome in Young Males and Elderly Women
|
https://doi.org/10.3390/genes12040596 | Whole exome sequencing | megan | fatima |
| Regulatory Noncoding and Predicted Pathogenic Coding Variants of CCR5 Predispose to Severe COVID-19
|
https://doi.org/10.3390/ijms22105372 | Genome wide association study and Whole exome sequencing | fatima | admin |
| Shared genetic etiology between idiopathic pulmonary fibrosis and
COVID-19 severity
|
https://doi.org/10.1016/j.ebiom.2021.103277 | Genome wide association study, Mendelian randomization | tkkalua | fatima |
| Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males
|
https://doi.org/10.1016/j.ebiom.2021.103246 | PCR, WES and Logistic regression analysis | fatima | admin |
| The MUC5B Promoter Polymorphism Associates With Severe COVID-19 in the European Population
|
https://doi.org/10.3389/fmed.2021.668024 | PCR-based SNP genotyping assay | fatima | admin |
| Trans-ancestry analysis reveals genetic and non-genetic associations with COVID-19
susceptibility and severity
|
https://doi.org/10.1038/s41588-021-00854-7 | Genome wide association study | juanitamellet | laverne1983 |
| Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility
|
https://doi.org/10.1101/2020.08.21.20177246 | Genome wide association study | clherd | jamiem |
| Vitamin D-related polymorphisms
and vitamin D levels as risk
biomarkers of COVID?19 disease
severity
|
https://doi.org/10.1038/s41598-021-99952-z | Microarray | fatima | admin |
| X-linked recessive TLR7 deficiency in 1% of men under 60 years with life-threatening COVID-19
|
https://doi.10.1126/sciimmunol.abl4348. | Whole genome, whole exome sequencing and logistic regression analysis | fatima | admin |
