On the public citation graph

AncestryDNA COVID-19 Host Genetic Study Identifies Three Novel Loci

0 signed · 94 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/jama.2020.13719openalex-snapshot
Presence of Genetic Variants Among Young Men With Severe COVID-19
inferredcites →https://doi.org/10.1001/jama.2020.5394openalex-snapshot
Baseline Characteristics and Outcomes of 1591 Patients Infected With SARS-CoV-2 Admitted to ICUs of the Lombardy Region, Italy
inferredcites →https://doi.org/10.1001/jama.2020.6775openalex-snapshot
Presenting Characteristics, Comorbidities, and Outcomes Among 5700 Patients Hospitalized With COVID-19 in the New York City Area
inferredcites →https://doi.org/10.1002/gepi.20303openalex-snapshot
Estimation of the multiple testing burden for genomewide association studies of nearly all common variants
inferredcites →https://doi.org/10.1002/gepi.20398openalex-snapshot
Quantifying and correcting for the winner's curse in genetic association studies
inferredcites →https://doi.org/10.1016/j.ajhg.2010.11.011openalex-snapshot
GCTA: A Tool for Genome-wide Complex Trait Analysis
inferredcites →https://doi.org/10.1016/j.ajhg.2011.02.002openalex-snapshot
Estimating Missing Heritability for Disease from Genome-wide Association Studies
inferredcites →https://doi.org/10.1016/j.chom.2013.04.011openalex-snapshot
Quantitative Phosphoproteomics Reveals Extensive Cellular Reprogramming during HIV-1 Entry
inferredcites →https://doi.org/10.1016/j.virol.2013.08.031openalex-snapshot
Expression of non-structural-1A binding protein in lung epithelial cells is modulated by miRNA-548an on exposure to influenza A virus
inferredcites →https://doi.org/10.1017/thg.2020.85openalex-snapshot
Self-Reported Symptoms of COVID-19, Including Symptoms Most Predictive of SARS-CoV-2 Infection, Are Heritable
inferredcites →https://doi.org/10.1038/nature24277openalex-snapshot
Genetic effects on gene expression across human tissues
inferredcites →https://doi.org/10.1038/ng.3679openalex-snapshot
Reference-based phasing using the Haplotype Reference Consortium panel
inferredcites →https://doi.org/10.1038/ng.608openalex-snapshot
Common SNPs explain a large proportion of the heritability for human height
inferredcites →https://doi.org/10.1038/nrg2322openalex-snapshot
Heritability in the genomics era — concepts and misconceptions
inferredcites →https://doi.org/10.1038/s41431-020-0636-6openalex-snapshot
The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic
inferredcites →https://doi.org/10.1038/s41562-020-00944-2openalex-snapshot
Population-scale longitudinal mapping of COVID-19 symptoms, behaviour and testing
inferredcites →https://doi.org/10.1038/s41577-020-0348-8openalex-snapshot
Considering how biological sex impacts immune responses and COVID-19 outcomes
inferredcites →https://doi.org/10.1038/s41586-020-2265-1openalex-snapshot
Whole-genome sequencing of a sporadic primary immunodeficiency cohort
inferredcites →https://doi.org/10.1056/nejmoa2020283openalex-snapshot
Genomewide Association Study of Severe Covid-19 with Respiratory Failure
inferredcites →https://doi.org/10.1073/pnas.1818012115openalex-snapshot
Structural–functional interactions of NS1-BP protein with the splicing and mRNA export machineries for viral and host gene expression
inferredcites →https://doi.org/10.1093/bioinformatics/btq340openalex-snapshot
METAL: fast and efficient meta-analysis of genomewide association scans
inferredcites →https://doi.org/10.1093/bioinformatics/btx299openalex-snapshot
FlashPCA2: principal component analysis of Biobank-scale genotype datasets
inferredcites →https://doi.org/10.1136/bmj.m2870openalex-snapshot
Covid-19: Male disadvantage highlights the importance of sex disaggregated data
inferredcites →https://doi.org/10.1534/g3.119.400448openalex-snapshot
A Prospective Analysis of Genetic Variants Associated with Human Lifespan
inferredcites →https://doi.org/10.15585/mmwr.mm6924e2openalex-snapshot
Coronavirus Disease 2019 Case Surveillance — United States, January 22–May 30, 2020
inferredcites →https://doi.org/10.3389/fimmu.2018.02249openalex-snapshot
Immunoglobulin Light Chain Gene Rearrangements, Receptor Editing and the Development of a Self-Tolerant Antibody Repertoire
inferredcites →https://doi.org/10.4049/jimmunol.1601896openalex-snapshot
Sex-Based Differences in Susceptibility to Severe Acute Respiratory Syndrome Coronavirus Infection

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1002/cyto.a.24662openalex-snapshot
Mass versus personalized medicine against COVID ‐19 in the “system sciences” era
inferred← citeshttps://doi.org/10.1002/jmv.27849openalex-snapshot
Individual genetic variability mainly of Proinflammatory cytokines, cytokine receptors, and toll‐like receptors dictates pathophysiology of COVID‐19 disease
inferred← citeshttps://doi.org/10.1002/path.5664openalex-snapshot
Advancing drug discovery using the power of the human genome
inferred← citeshttps://doi.org/10.1002/rmv.2466openalex-snapshot
Host genetic determinants of COVID‐19 susceptibility and severity: A systematic review and meta‐analysis
inferred← citeshttps://doi.org/10.1007/978-3-031-28012-2_6openalex-snapshot
Genetic Associations with Coronavirus Susceptibility and Disease Severity
inferred← citeshttps://doi.org/10.1007/s00709-022-01754-1openalex-snapshot
ABO blood groups and the risk of SARS-CoV-2 infection
inferred← citeshttps://doi.org/10.1007/s10528-024-10669-wopenalex-snapshot
Role of the Neanderthal Genome in Genetic Susceptibility to COVID-19: 3p21.31 Locus in the Spotlight
inferred← citeshttps://doi.org/10.1007/s10875-021-01071-xopenalex-snapshot
MHC Haplotyping of SARS-CoV-2 Patients: HLA Subtypes Are Not Associated with the Presence and Severity of COVID-19 in the Israeli Population
inferred← citeshttps://doi.org/10.1016/b978-0-323-91794-0.00009-3openalex-snapshot
Omics approaches in COVID-19: An overview
inferred← citeshttps://doi.org/10.1016/j.cub.2021.05.067openalex-snapshot
An ancient viral epidemic involving host coronavirus interacting genes more than 20,000 years ago in East Asia
inferred← citeshttps://doi.org/10.1016/j.ebiom.2021.103629openalex-snapshot
Host genetic factors determining COVID-19 susceptibility and severity
inferred← citeshttps://doi.org/10.1016/j.ebiom.2021.103695openalex-snapshot
Genome-wide association study of hospitalized COVID-19 patients in the United Arab Emirates
inferred← citeshttps://doi.org/10.1016/j.epidem.2021.100446openalex-snapshot
Modelling suggests ABO histo-incompatibility may substantially reduce SARS-CoV-2 transmission
inferred← citeshttps://doi.org/10.1016/j.ijid.2021.09.070openalex-snapshot
Clinical Characteristics of Patients with Coronavirus Disease (COVID-19): Preliminary Baseline Report of Japan COVID-19 Task Force, a Nationwide Consortium to Investigate Host Genetics of COVID-19
inferred← citeshttps://doi.org/10.1016/j.ijid.2022.06.030openalex-snapshot
Host genetic loci LZTFL1 and CCL2 associated with SARS-CoV-2 infection and severity of COVID-19
inferred← citeshttps://doi.org/10.1016/j.isci.2023.107629openalex-snapshot
A GWAS in the pandemic epicenter highlights the severe COVID-19 risk locus introgressed by Neanderthals
inferred← citeshttps://doi.org/10.1038/s41431-022-01089-8openalex-snapshot
Coronavirus Host Genetics South Africa (COHG-SA) database—a variant database for gene regions associated with SARS-CoV-2 outcomes
inferred← citeshttps://doi.org/10.1038/s41467-021-24824-zopenalex-snapshot
Integrative genomic analyses identify susceptibility genes underlying COVID-19 hospitalization
inferred← citeshttps://doi.org/10.1038/s41467-021-26888-3openalex-snapshot
COVID-19 genetic risk variants are associated with expression of multiple genes in diverse immune cell types
inferred← citeshttps://doi.org/10.1038/s41576-022-00478-5openalex-snapshot
The human genetic epidemiology of COVID-19
inferred← citeshttps://doi.org/10.1038/s41586-021-03767-xopenalex-snapshot
Mapping the human genetic architecture of COVID-19
inferred← citeshttps://doi.org/10.1038/s41586-022-05163-5openalex-snapshot
DOCK2 is involved in the host genetics and biology of severe COVID-19
inferred← citeshttps://doi.org/10.1038/s41588-021-01006-7openalex-snapshot
Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease
inferred← citeshttps://doi.org/10.1038/s41588-022-01042-xopenalex-snapshot
Expanded COVID-19 phenotype definitions reveal distinct patterns of genetic association and protective effects
inferred← citeshttps://doi.org/10.1038/s41598-024-65732-8openalex-snapshot
The association of rs17713054 with Neanderthal origin at 3p21.31 locus with the severity of COVID-19 in Iranian patients
inferred← citeshttps://doi.org/10.1038/s42003-023-04805-2openalex-snapshot
Genome-wide cross-trait analysis and Mendelian randomization reveal a shared genetic etiology and causality between COVID-19 and venous thromboembolism
inferred← citeshttps://doi.org/10.1080/02664763.2022.2064975openalex-snapshot
Classification and severity progression measure of COVID-19 patients using pairs of multi-omic factors
inferred← citeshttps://doi.org/10.1093/hmg/ddab125openalex-snapshot
Integrative genomics analysis reveals a 21q22.11 locus contributing risk to COVID-19
inferred← citeshttps://doi.org/10.1097/id9.0000000000000115openalex-snapshot
Genetic Basis for Mucormycosis Progression in COVID-19 Patients: From Susceptibility to Severity
inferred← citeshttps://doi.org/10.1101/2020.11.16.385401openalex-snapshot
An ancient viral epidemic involving host coronavirus interacting genes more than 20,000 years ago in East Asia
inferred← citeshttps://doi.org/10.1101/2020.12.07.20245308openalex-snapshot
Integrative analyses identify susceptibility genes underlying COVID-19 hospitalization
inferred← citeshttps://doi.org/10.1101/2021.03.10.21252820openalex-snapshot
Mapping the human genetic architecture of COVID-19 by worldwide meta-analysis
inferred← citeshttps://doi.org/10.1101/2021.12.06.21267386openalex-snapshot
Factors influencing COVID-19 Infection in older individuals: History of Alcohol Use Disorder, Major Depressive illness, genetic variation and current use of alcohol
inferred← citeshttps://doi.org/10.1101/2022.03.28.22273040openalex-snapshot
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative
inferred← citeshttps://doi.org/10.1101/2022.05.21.22275413openalex-snapshot
Shared genetic etiology and causality between COVID-19 and venous thromboembolism: evidence from genome-wide cross trait analysis and bi-directional Mendelian randomization study
inferred← citeshttps://doi.org/10.1101/2022.06.08.495202openalex-snapshot
Better together against genetic effect heterogeneity: a sex-combined interaction analysis of testosterone levels in the UK Biobank data
inferred← citeshttps://doi.org/10.1101/2022.06.23.22276797openalex-snapshot
Genetic risk factors associated with SARS-CoV-2 susceptibility in multiethnic populations
inferred← citeshttps://doi.org/10.1111/tan.14574openalex-snapshot
Minimal observed impact of HLA genotype on hospitalization and severity of SARS‐CoV ‐2 infection
inferred← citeshttps://doi.org/10.1126/science.adk5081openalex-snapshot
From North Asia to South America: Tracing the longest human migration through genomic sequencing
inferred← citeshttps://doi.org/10.1128/mbio.01454-22openalex-snapshot
A Multitrait Locus Regulates Sarbecovirus Pathogenesis
inferred← citeshttps://doi.org/10.1134/s1022795425700012openalex-snapshot
The Human Genome and COVID-19
inferred← citeshttps://doi.org/10.1136/bmjopen-2021-049657openalex-snapshot
COVID-19 susceptibility and severity risks in a cross-sectional survey of over 500 000 US adults
inferred← citeshttps://doi.org/10.1371/journal.pgen.1010367openalex-snapshot
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative
inferred← citeshttps://doi.org/10.1371/journal.pgen.1011221openalex-snapshot
Better together against genetic heterogeneity: A sex-combined joint main and interaction analysis of 290 quantitative traits in the UK Biobank
inferred← citeshttps://doi.org/10.1371/journal.pone.0269017openalex-snapshot
Assessing the added value of linking electronic health records to improve the prediction of self-reported COVID-19 testing and diagnosis
inferred← citeshttps://doi.org/10.1371/journal.pone.0276700openalex-snapshot
Ancestral origins are associated with SARS-CoV-2 susceptibility and protection in a Florida patient population
inferred← citeshttps://doi.org/10.1556/650.2025.33280openalex-snapshot
A SARS-CoV-2-fertőzés iránti fogékonyság és a súlyos COVID–19 hátterében álló genetikai tényezők
inferred← citeshttps://doi.org/10.17816/gc624810openalex-snapshot
Exome-wide association study for replication of rare variants affecting the severity of COVID-19 in the Russian population
inferred← citeshttps://doi.org/10.2174/1381612828666220518102440openalex-snapshot
Docosahexaenoic Acid Ester of Phloridzin Reduces Inflammation and Insulin Resistance via AMPK
inferred← citeshttps://doi.org/10.2174/1381612828666220519150821openalex-snapshot
Immunopathogenesis and Immunogenetic Variants in COVID-19
inferred← citeshttps://doi.org/10.2217/fvl-2021-0090openalex-snapshot
Association Between Blood Groups and COVID-19 Outcome in Iranian Patients
inferred← citeshttps://doi.org/10.3103/s0891416823020088openalex-snapshot
LZTFL1 rs17713054 Polymorphism as an Indicator Allele for COVID-19 Severity
inferred← citeshttps://doi.org/10.32352/0367-3057.3.21.03openalex-snapshot
Biosocial portrait of a patient with COVID-19
inferred← citeshttps://doi.org/10.33137/juls.v15i1.36956openalex-snapshot
Inconsistent trends regarding the association between ABO blood groups and susceptibility to SARS-CoV-2 infections
inferred← citeshttps://doi.org/10.3389/fgene.2022.928466openalex-snapshot
COVID-19 in pediatrics: Genetic susceptibility
inferred← citeshttps://doi.org/10.3389/fgene.2024.1434681openalex-snapshot
GWAS-significant loci and severe COVID-19: analysis of associations, link with thromboinflammation syndrome, gene-gene, and gene-environmental interactions
inferred← citeshttps://doi.org/10.3389/fimmu.2022.902837openalex-snapshot
Exposing and Overcoming Limitations of Clinical Laboratory Tests in COVID-19 by Adding Immunological Parameters; A Retrospective Cohort Analysis and Pilot Study
inferred← citeshttps://doi.org/10.3389/fmed.2021.759648openalex-snapshot
Allelic Variants Within the ABO Blood Group Phenotype Confer Protection Against Critical COVID-19 Hospital Presentation
inferred← citeshttps://doi.org/10.3390/biomed2010007openalex-snapshot
Interoperability of COVID-19 Clinical Phenotype Data with Host and Viral Genetics Data
inferred← citeshttps://doi.org/10.3390/healthcare10020349openalex-snapshot
Informed Consent and Protection of Personal Data in Genetic Research on COVID-19
inferred← citeshttps://doi.org/10.3390/ijms25147674openalex-snapshot
Genomic Landscape of Susceptibility to Severe COVID-19 in the Slovenian Population
inferred← citeshttps://doi.org/10.3390/jpm11060475openalex-snapshot
Implementing Personalized Medicine in COVID-19 in Andalusia: An Opportunity to Transform the Healthcare System
inferred← citeshttps://doi.org/10.3390/jpm11121318openalex-snapshot
Genomic Characterization of Host Factors Related to SARS-CoV-2 Infection in People with Dementia and Control Populations: The GR@ACE/DEGESCO Study
inferred← citeshttps://doi.org/10.3390/jpm13010123openalex-snapshot
Host Genetic Variants Linked to COVID-19 Neurological Complications and Susceptibility in Young Adults—A Preliminary Analysis
inferred← citeshttps://doi.org/10.3390/life11090921openalex-snapshot
Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent
inferred← citeshttps://doi.org/10.3390/life12091300openalex-snapshot
Exome-Wide Association Study Reveals Host Genetic Variants Likely Associated with the Severity of COVID-19 in Patients of European Ancestry
inferred← citeshttps://doi.org/10.3390/v13020160openalex-snapshot
ABO Blood Types and COVID-19: Spurious, Anecdotal, or Truly Important Relationships? A Reasoned Review of Available Data
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.