Evidence map›Paper›PMID 37554178›Full record

ArticleGenes & diseases2023

A novel variant of GALC in a familial case of Krabbe disease: Insights from structural bioinformatics and molecular dynamics simulation.

Ikram Ullah, Muhammad Waqas, Muhammad Ilyas, Sobia Ahsan Halim, Akmal Ahmad, Natalia Dominik, Wahid Ullah, Muhammad Abbas, Muhammad Aamir, SYNaPS Study Group and 5 more

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Article in Genes & diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Ikram UllahCentre for Omic Sciences, Islamia College University Peshawar, Peshawar, Khyber Pakhtunkhwa 25120, Pakistan.
Muhammad WaqasDepartment of Biotechnology and Genetic Engineering, Hazara University, Mansehra, Dhodial 21120, Pakistan.
Muhammad IlyasCentre for Omic Sciences, Islamia College University Peshawar, Peshawar, Khyber Pakhtunkhwa 25120, Pakistan.
Sobia Ahsan HalimNatural and Medical Sciences Research Center, University of Nizwa, Nizwa 616, Sultanate of Oman.
Akmal AhmadDepartment of Biotechnology and Genetic Engineering, Hazara University, Mansehra, Dhodial 21120, Pakistan.
Natalia DominikDepartment of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London WC1N 3BG, United Kingdom.
Wahid UllahCentre for Omic Sciences, Islamia College University Peshawar, Peshawar, Khyber Pakhtunkhwa 25120, Pakistan.
Muhammad AbbasCentre for Omic Sciences, Islamia College University Peshawar, Peshawar, Khyber Pakhtunkhwa 25120, Pakistan.
Muhammad AamirCentre for Omic Sciences, Islamia College University Peshawar, Peshawar, Khyber Pakhtunkhwa 25120, Pakistan.
SYNaPS Study Group
Queen Square Genomics
Henry HouldenDepartment of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London WC1N 3BG, United Kingdom.
Stephanie EfthymiouDepartment of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London WC1N 3BG, United Kingdom.
Ajmal KhanNatural and Medical Sciences Research Center, University of Nizwa, Nizwa 616, Sultanate of Oman.
Ahmed Al-HarrasiNatural and Medical Sciences Research Center, University of Nizwa, Nizwa 616, Sultanate of Oman.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID37554178
PMCPMC10404946

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Registered trials

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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.