Evidence map›Paper›PMID 42852362›Full record

ArticleThe Yale journal of biology and medicine2026

Novel Splice Site Variant in

Syeda Farwa Naqvi, Esra Yıldız Bölükbaşı, Muhammad Touseef, Sulman Basit, Nafees Ahmad, Aslıhan Tolun, Sajid Malik

Abstract read
In one paragraph

Article in The Yale journal of biology and medicine, 2026. 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

7 authors.

Syeda Farwa NaqviHuman Genetics Program, Department of Zoology, Faculty of Biological Sciences Quaid-i-Azam University, Islamabad, Pakistan.
Esra Yıldız BölükbaşıDepartment of Molecular Biology and Genetics Boğaziçi University, Istanbul, Türkiye.
Muhammad TouseefMirpur University of Science and Technology, Mirpur, Pakistan.
Sulman BasitDepartment of Basic Medical Sciences, Centre for Genetics and Inherited Diseases Taibah University Madinah, Kingdom of Saudi Arabia.
Nafees AhmadInstitute of Biomedical and Genetic Engineering.
Aslıhan TolunFaculty of Science and Letters Istanbul Technical University, Istanbul, Türkiye.ORCID https://orcid.org/0000-0002-0328-6046
Sajid MalikHuman Genetics Program, Department of Zoology, Faculty of Biological Sciences Quaid-i-Azam University, Islamabad, Pakistan.ORCID https://orcid.org/0000-0001-5563-9053

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Periventricular heterotopia (PH) is a rare developmental cause of intellectual disability (ID). One form is autosomal recessive PH with microcephaly (ARPHM), characterized by developmental delay and learning difficulties, with onset in infancy, plus recurrent seizures that onset in mid-adolescence. It is caused by biallelic variants in

Indexed as

Guanine Nucleotide Exchange FactorsPeriventricular Nodular HeterotopiaRNA Splice SitesAdultFemaleHomozygoteHumansIntellectual DisabilityMalePedigreePhenotypePolymorphism, Single NucleotideYoung AdultARFGEF2 protein, humanGuanine Nucleotide Exchange FactorsRNA Splice Sitesabsent pubertal onsetARFGEF2contracture deformitydevelopmental delaydystoniaflat feetgenome sequencingintellectual disabilityperiventricular heterotopia

Identifiers

PMID42852362
PMCPMC13648096

What OpenQuestion holds

Textmetadata
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.