Evidence map›Paper›PMID 42194996›Full record

ArticleGenes2026

Expanding the Genetic Landscape of Congenital Stationary Night Blindness Through the Analysis of Consanguineous Pakistani Families.

Razia Parveen, Muhammad Iqbal, Shahbaz Khan, Abdur Rashid, Helen Nabiryo Frederiksen, Sergey Oreshkov, Ghulam Mustafa, Muhammad Asif Naeem, Hafiz Muhammad Azhar Baig, Muhammad Ansar

Abstract read
In one paragraph

Article in Genes, 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

10 authors.

Razia ParveenDepartment of Biochemistry and Molecular Biology, Institute of Biochemistry, Biotechnology and Bioinformatics, The Islamia University of Bahawalpur, Bahawalpur 63100, Pakistan.
Muhammad IqbalDepartment of Biotechnology, Institute of Biochemistry, Biotechnology and Bioinformatics, The Islamia University of Bahawalpur, Bahawalpur 63100, Pakistan.
Shahbaz KhanDepartment of Biochemistry and Molecular Biology, Institute of Biochemistry, Biotechnology and Bioinformatics, The Islamia University of Bahawalpur, Bahawalpur 63100, Pakistan.
Abdur RashidDepartment of Ophthalmology, University of Lausanne, Jules Gonin Eye Hospital, Fondation Asile des Aveugles, 1004 Lausanne, Switzerland.
Helen Nabiryo FrederiksenDepartment of Ophthalmology, University of Lausanne, Jules Gonin Eye Hospital, Fondation Asile des Aveugles, 1004 Lausanne, Switzerland.ORCID 0009-0001-8686-4461
Sergey OreshkovDepartment of Ophthalmology, University of Lausanne, Jules Gonin Eye Hospital, Fondation Asile des Aveugles, 1004 Lausanne, Switzerland.
Ghulam MustafaDepartment of Biotechnology, Institute of Biochemistry, Biotechnology and Bioinformatics, The Islamia University of Bahawalpur, Bahawalpur 63100, Pakistan.
Muhammad Asif NaeemCentre for Applied Molecular Biology, University of the Punjab, Lahore 53700, Pakistan.
Hafiz Muhammad Azhar BaigJacobs Retina Center, Shiley Eye Institute, University of California San Diego, La Jolla, CA 92039, USA.ORCID 0000-0002-9370-1716
Muhammad AnsarDepartment of Ophthalmology, University of Lausanne, Jules Gonin Eye Hospital, Fondation Asile des Aveugles, 1004 Lausanne, Switzerland.

Funding

Swiss National Science Foundation 320030_212959
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Eye Diseases, HereditaryGenetic Diseases, X-LinkedMyopiaNight BlindnessChildConsanguinityExome SequencingFemaleG-Protein-Coupled Receptor Kinase 1HumansMaleMutationPakistanPedigreeSouth Asian PeopleTRPM Cation ChannelsG-Protein-Coupled Receptor Kinase 1TRPM Cation ChannelsconsanguinityCSNBexome sequencingGPR179GRK1SAGSLC24A1TRPM1

Identifiers

PMID42194996
PMCPMC13205639

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.