Evidence map›Paper›PMID 38661530›Full record

ArticleeLife2024

Disease modeling and pharmacological rescue of autosomal dominant retinitis pigmentosa associated with

Sangeetha Kandoi, Cassandra Martinez, Kevin Xu Chen, Miika Mehine, L Vinod K Reddy, Brian C Mansfield, Jacque L Duncan, Deepak A Lamba

Open access · goldAbstract readCase Reports
In one paragraph

Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
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  8. Human-based complexFrontiers in cell and developmental biology · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 3 countries.

Sangeetha KandoiDepartment of Ophthalmology, University of California, San Francisco, San Francisco, United States.
Cassandra MartinezDepartment of Ophthalmology, University of California, San Francisco, San Francisco, United States.
Kevin Xu ChenEli and Edythe Broad Center of Regeneration Medicine & Stem Cell Research University of California, San Francisco, San Francisco, United States.
Miika MehineBlueprint Genetics, Bethesda, United States.
L Vinod K ReddyDepartment of Ophthalmology, University of California, San Francisco, San Francisco, United States.
Brian C MansfieldSection on Cellular Differentiation, Division of Translational Medicine, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, United States.
Jacque L DuncanDepartment of Ophthalmology, University of California, San Francisco, San Francisco, United States.ORCID https://orcid.org/0000-0002-9593-6412
Deepak A LambaDepartment of Ophthalmology, University of California, San Francisco, San Francisco, United States.ORCID https://orcid.org/0000-0002-2811-307X
National Institutes of Health · USUniversity of California, San Francisco · US

Funding

Rapid-Prototyping and Design CoreP30EY002162 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LAMBA, DEEPAK ASHOK · 1985 to 2024
$16.8M
Developing Cone-Dominant Retinal Disease Models as a Resource for Translational Vision ResearchU24EY029891 · NEI · MEDICAL COLLEGE OF WISCONSIN · PI CARROLL, JOSEPH, DUNCAN, JACQUE LYNNE · 2018 to 2022
$6.6M
Mechanistic analysis and allellic genome editing of iPSC-derived dominant LCA modelR01EY032197 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ULLIAN, ERIK M · 2021 to 2025
$2.5M
NEI NIH HHS EY002162NEI NIH HHS EY029891NEI NIH HHS EY032197NEI NIH HHS P30 EY002162NEI NIH HHS R01 EY032197NEI NIH HHS U24 EY029891
6 · The paper itself

Abstract

Retinitis pigmentosa (RP), a heterogenous group of inherited retinal disorder, causes slow progressive vision loss with no effective treatments available. Mutations in the rhodopsin gene (

Indexed as

DNA Copy Number VariationsRetinitis PigmentosaRhodopsinAgedHumansMaleOrganoidsRhodopsindisease modelinghumaniPSCorganoidsregenerative medicineretinitis pigmentosarhodopsinstem cells

Identifiers

PMID38661530
PMCPMC11045220
OpenAlexW4387869190

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.