Evidence map›Paper›PMID 35571054›Full record

ArticleFrontiers in genetics2022

SARS-CoV-2 Susceptibility and

Nirmal Vadgama, Alexander Kreymerman, Jackie Campbell, Olga Shamardina, Christiane Brugger, Genomics England Research Consortium, Alexandra M Deaconescu, Richard T Lee, Christopher J Penkett, Casey A Gifford and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.7field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 27 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 6 institutions in 2 countries.

Nirmal VadgamaDepartment of Cardiothoracic Surgery and Cardiovascular Institute, Stanford University, Palo Alto, CA, United States.
Alexander KreymermanCardiovascular Institute and Department of Medicine, Stanford University, Palo Alto, CA, United States.
Jackie CampbellDivision of Life Sciences, Waterside Campus, University Drive, University of Northampton, Northampton, United Kingdom.
Olga ShamardinaNIHR BioResource, Cambridge Biomedical Campus, University of Cambridge, Cambridge, United Kingdom.
Christiane BruggerDepartment of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, RI, United States.
Genomics England Research ConsortiumGenomics England, London, United Kingdom.
Alexandra M DeaconescuDepartment of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, RI, United States.
Richard T LeeDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, United States.
Christopher J PenkettNIHR BioResource, Cambridge Biomedical Campus, University of Cambridge, Cambridge, United Kingdom.
Casey A GiffordDepartment of Pediatrics, Division of Cardiology, Stanford School of Medicine, Department of Genetics, Stanford School of Medicine, BASE Initiative, Betty Irene Moore Children's Heart Center, Lucile Packard Children's Hospital, Palo Alto, CA, United States.
Mark MercolaCardiovascular Institute and Department of Medicine, Stanford University, Palo Alto, CA, United States.
Jamal NasirDivision of Life Sciences, Waterside Campus, University Drive, University of Northampton, Northampton, United Kingdom.
Ioannis KarakikesDepartment of Cardiothoracic Surgery and Cardiovascular Institute, Stanford University, Palo Alto, CA, United States.
Harvard University · USLucile Packard Children's Hospital · USBrown University · USCardiovascular Institute of the South · USUniversity of Cambridge · GBUniversity of Northampton · GB

Funding

MECHANISMS AND MACROMOLECULAR INTERACTIONS UNDERLYING CELLULAR RESPONSES TO STRESS SIGNALSR35GM144124 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI Alexandra M. Deaconescu · 2022 to 2026
$2.0M
Mechanisms for Stress-Induced Transcriptional Reprogramming via Anti-AdaptorsR01GM121975 · NIGMS · BROWN UNIVERSITY · PI DEACONESCU, ALEXANDRA M. · 2017 to 2021
$1.7M
The role of mitochondrial DNA mutations in chemotherapy induced cardiomyopathyF32HL154644 · NHLBI · STANFORD UNIVERSITY · PI KREYMERMAN, ALEXANDER · 2020 to 2023
$237k
NHLBI NIH HHS F32 HL154644NIGMS NIH HHS R01 GM121975NIGMS NIH HHS R35 GM144124
6 · The paper itself

Abstract

There is considerable variability in the susceptibility and progression for COVID-19 and it appears to be strongly correlated with age, gender, ethnicity and pre-existing health conditions. However, to our knowledge, cohort studies of COVID-19 in clinically vulnerable groups are lacking. Host genetics has also emerged as a major risk factor for COVID-19, and variation in the ACE2 receptor, which facilitates entry of the SARS-CoV-2 virus into the cell, has become a major focus of attention. Thus, we interrogated an ethnically diverse cohort of National Health Service (NHS) patients in the United Kingdom (United Kingdom) to assess the association between variants in the

Indexed as

ACE2COVID-19eQTLsgeneticsSARS-CoV-2variants

Identifiers

PMID35571054
PMCPMC9091502
OpenAlexW4225824189

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.