Evidence map›Paper›PMID 37239392›Full record

ArticleGenes2023

Rajech Sharkia, Sahil Jain, Muhammad Mahajnah, Clair Habib, Abdussalam Azem, Wasif Al-Shareef, Abdelnaser Zalan

Open access · goldAbstract read
In one paragraph

Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

4 citing papers in PubMed, 10 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

7 authors at 5 institutions in 1 country.

Rajech SharkiaUnit of Human Biology and Genetics, Triangle Regional Research and Development Center, Kfar Qari 30075, Israel.ORCID 0000-0002-0483-3443
Sahil JainDepartment of Biochemistry and Molecular Biology, Faculty of Life Sciences, Tel Aviv University, Tel Aviv 69978, Israel.
Muhammad MahajnahThe Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa 31096, Israel.
Clair HabibGenetics Institute, Rambam Health Care Campus, Haifa 31096, Israel.
Abdussalam AzemDepartment of Biochemistry and Molecular Biology, Faculty of Life Sciences, Tel Aviv University, Tel Aviv 69978, Israel.
Wasif Al-ShareefUnit of Human Biology and Genetics, Triangle Regional Research and Development Center, Kfar Qari 30075, Israel.
Abdelnaser ZalanUnit of Human Biology and Genetics, Triangle Regional Research and Development Center, Kfar Qari 30075, Israel.ORCID 0000-0003-4776-0675
Tel Aviv University · ILTriangle Research and Development Center · ILBeit Berl College · ILRambam Health Care Campus · ILTechnion – Israel Institute of Technology · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peptidyl-tRNA hydrolase 2 (PTRH2) is an evolutionarily highly conserved mitochondrial protein. The biallelic mutations in the

Indexed as

Carboxylic Ester HydrolasesCerebellar AtaxiaMitochondrial ProteinsNervous System MalformationsAtaxiaCerebellumCodon, NonsenseDevelopmental DisabilitiesHumansMutationCarboxylic Ester HydrolasesCodon, NonsenseMitochondrial ProteinsPTH2 protein, humanautosomal recessive disorderbioinformatics analysisclinical featuresIMNEPDPTRH2 genePTRH2 variantsrare genetic diseases

Identifiers

PMID37239392
PMCPMC10217894
OpenAlexW4367627669

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.