Evidence map›Paper›PMID 37144477›Full record

ReviewMolecular medicine reports2023

CRISPR‑based diagnostic approaches: Implications for rapid management of future pandemics (Review).

Mohd Shariq, Mohammad Firoz Khan, Reshmi Raj, Nuzhat Ahsan, Rinky Singh, Pramod Kumar

Open access · hybridAbstract readReview
In one paragraph

Review in Molecular medicine reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

  1. Understanding the Psychological Impacts of Shielding From COVID-19 for Immunocompromised Individuals.Health expectations : an international journal of public participation in health care and health policy · 2026
    Article
  2. Review
  3. Review
  4. Article
  5. Ultrasensitive CRISPR/Cas12a-Based System for Detection ofCurrent issues in molecular biology · 2025
    Article
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

6 authors.

Mohd ShariqBiophotonics Group, Quant Lase Imaging Laboratory, Quant Lase Lab LLC, Abu Dhabi, United Arab Emirates.
Mohammad Firoz KhanBiophotonics Group, Quant Lase Imaging Laboratory, Quant Lase Lab LLC, Abu Dhabi, United Arab Emirates.
Reshmi RajBiophotonics Group, Quant Lase Imaging Laboratory, Quant Lase Lab LLC, Abu Dhabi, United Arab Emirates.
Nuzhat AhsanBiophotonics Group, Quant Lase Imaging Laboratory, Quant Lase Lab LLC, Abu Dhabi, United Arab Emirates.
Rinky SinghBiophotonics Group, Quant Lase Imaging Laboratory, Quant Lase Lab LLC, Abu Dhabi, United Arab Emirates.
Pramod KumarBiophotonics Group, Quant Lase Imaging Laboratory, Quant Lase Lab LLC, Abu Dhabi, United Arab Emirates.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sudden viral outbreaks have increased in the early part of the 21st century, such as those of severe acute respiratory syndrome coronavirus (SARS‑CoV), Middle East respiratory syndrome corona virus, and SARS‑CoV‑2, owing to increased human access to wildlife habitats. Therefore, the likelihood of zoonotic transmission of human‑associated viruses has increased. The emergence of severe acute respiratory syndrome coronavirus 2 in China and its spread worldwide within months have highlighted the need to be ready with advanced diagnostic and antiviral approaches to treat newly emerging diseases with minimal harm to human health. The gold‑standard molecular diagnostic approaches currently used are time‑consuming, require trained personnel and sophisticated equipment, and therefore cannot be used as point‑of‑care devices for widespread monitoring and surveillance. Clustered regularly interspaced short palindromic repeats (CRISPR)‑associated (Cas) systems are widespread and have been reported in bacteria, archaea and bacteriophages. CRISPR‑Cas systems are organized into CRISPR arrays and adjacent Cas proteins. The detection and in‑depth biochemical characterization of class 2 type V and VI CRISPR‑Cas systems and orthologous proteins such as Cas12 and Cas13 have led to the development of CRISPR‑based diagnostic approaches, which have been used to detect viral diseases and distinguish between serotypes and subtypes. CRISPR‑based diagnostic approaches detect human single nucleotide polymorphisms in samples from patients with cancer and are used as antiviral agents to detect and destroy viruses that contain RNA as a genome. CRISPR‑based diagnostic approaches are likely to improve disease detection methods in the 21st century owing to their ease of development, low cost, reduced turnaround time, multiplexing and ease of deployment. The present review discusses the biochemical properties of Cas12 and Cas13 orthologs in viral disease detection and other applications. The present review expands the scope of CRISPR‑based diagnostic approaches to detect diseases and fight viruses as antivirals.

Indexed as

COVID-19BacteriaCOVID-19 TestingCRISPR-Cas SystemsHumansPandemicsSARS-CoV-2collateral activityCRISPRCRISPR‑associated systemsCRISPR RNAdiagnosticsfluorescence‑quencherpoint‑of‑care devicesreportersensitivityspecificity

Identifiers

PMID37144477
PMCPMC10196884
OpenAlexW4367842666

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.