Evidence map›Paper›PMID 40858907›Full record

ArticleNature genetics2025

Author Correction: Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.

Saima Riazuddin, Inna A Belyantseva, Arnaud P J Giese, Kwanghyuk Lee, Artur A Indzhykulian, Sri Pratima Nandamuri, Rizwan Yousaf, Ghanshyam P Sinha, Sue Lee, David Terrell and 21 more

Abstract readPublished Erratum
PubMed Publisher
In one paragraph

Article in Nature genetics, 2025. 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

5 · Who and what money

Authors and funding

31 authors.

Saima RiazuddinDivision of Pediatric Otolaryngology/Head & Neck Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Inna A BelyantsevaLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, Rockville, Maryland, USA.
Arnaud P J GieseDivision of Pediatric Otolaryngology/Head & Neck Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Kwanghyuk LeeDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Artur A IndzhykulianDepartment of Physiology, University of Kentucky, Lexington, Kentucky, USA.
Sri Pratima NandamuriDepartment of Biological Sciences, McMicken College of Arts and Sciences, University of Cincinnati, Cincinnati, Ohio, USA.
Rizwan YousafDivision of Pediatric Otolaryngology/Head & Neck Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Ghanshyam P SinhaDepartment of Physiology, University of Kentucky, Lexington, Kentucky, USA.
Sue LeeLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, Rockville, Maryland, USA.
David TerrellDivision of Pediatric Ophthalmology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Rashmi S HegdeDivision of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Rana A AliNational Center for Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.
Saima AnwarNational Center for Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.
Paula B Andrade-ElizondoDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Asli SirmaciDepartment of Human Genetics, Miller School of Medicine, University of Miami, Miami, Florida, USA.
Leslie V PariseDepartment of Biochemistry & Biophysics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Sulman BasitDepartment of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.
Abdul WaliInstitute of Biotechnology, Baluchistan University of Information Technology, Quetta, Pakistan.
Muhammad AyubInstitute of Biochemistry, University of Baluchistan, Quetta, Pakistan.
Muhammad AnsarDepartment of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.
Wasim AhmadDepartment of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.
Shaheen N KhanNational Center for Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.
Javed AkramAllama Iqbal Medical College, Lahore, Pakistan.
Mustafa TekinDepartment of Human Genetics, Miller School of Medicine, University of Miami, Miami, Florida, USA.
Sheikh RiazuddinAllama Iqbal Medical College, Lahore, Pakistan.
Tiffany CookDivision of Pediatric Ophthalmology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Elke K BuschbeckDepartment of Biological Sciences, McMicken College of Arts and Sciences, University of Cincinnati, Cincinnati, Ohio, USA.
Gregory I FrolenkovDepartment of Physiology, University of Kentucky, Lexington, Kentucky, USA.
Suzanne M LealDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Thomas B FriedmanLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, Rockville, Maryland, USA.
Zubair M AhmedDivision of Pediatric Otolaryngology/Head & Neck Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA. zubair.ahmed@cchmc.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID40858907

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.