Evidence map›Paper›PMID 42818558›Full record

ArticlebioRxiv : the preprint server for biology2026

A comparative single-cell transcriptomic atlas for diverse populations of vertebrate hair cells.

Mahashweta Basu, Nesrine Benkafadar, Beatrice Milon, Carlo Colantuoni, Brian R Herb, Amanda Ciani Berlingeri, Ivan A Cruz, Joshua Orvis, Emilia Luca, Mitsuo P Sato and 23 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

33 authors.

Mahashweta BasuInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD.
Nesrine BenkafadarDepartment of Otolaryngology - Head & Neck Surgery. Stanford University, Palo Alto, CA.ORCID 0000-0002-7390-7688
Beatrice MilonSection on Omics and Translational Science of Hearing, Neurotology Branch, National Institute on Deafness and Other Communication Disorders, Intramural Research Program, Bethesda, MD.
Carlo ColantuoniInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD.
Brian R HerbInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD.
Amanda Ciani BerlingeriDepartment of Otolaryngology Head & Neck Surgery, University of Washington, Seattle, WA.
Ivan A CruzDepartment of Otolaryngology Head & Neck Surgery, University of Washington, Seattle, WA.
Joshua OrvisInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD.
Emilia LucaDepartment of Biological Sciences, Sunnybrook Research Institute, Toronto, CA.
Mitsuo P SatoDepartment of Otolaryngology - Head & Neck Surgery. Stanford University, Palo Alto, CA.
Dunia Abdul-AzizDepartment of Otolaryngology, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, MA.
Meghan DewanSection on Omics and Translational Science of Hearing, Neurotology Branch, National Institute on Deafness and Other Communication Disorders, Intramural Research Program, Bethesda, MD.
Kathleen GwilliamSection on Omics and Translational Science of Hearing, Neurotology Branch, National Institute on Deafness and Other Communication Disorders, Intramural Research Program, Bethesda, MD.
Gabriella ManillaSection on Omics and Translational Science of Hearing, Neurotology Branch, National Institute on Deafness and Other Communication Disorders, Intramural Research Program, Bethesda, MD.
Christopher ShultsSection on Omics and Translational Science of Hearing, Neurotology Branch, National Institute on Deafness and Other Communication Disorders, Intramural Research Program, Bethesda, MD.
R Shaun AdkinsInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD.
Yang SongInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD.
Anup MahurkarInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD.
John V BrigandeOregon Hearing Research Center, Oregon Health & Science University, Portland, OR.
Alain DabdoubDepartment of Biological Sciences, Sunnybrook Research Institute, Toronto, CA.ORCID 0000-0002-4259-2425
Albert EdgeDepartment of Otolaryngology, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, MA.ORCID 0000-0001-8641-755X
Andrew K GrovesDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0002-0784-7998
Ksenia GnedevaDepartment of Otolaryngology - Head and Neck Surgery and Stem Cell Biology & Regenerative Medicine, University of Southern California, Los Angeles, CA.ORCID 0000-0002-3870-9256
Stefan HellerDepartment of Otolaryngology - Head & Neck Surgery. Stanford University, Palo Alto, CA.ORCID 0000-0002-0490-4440
Ronna HertzanoInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD.
Tatjana PiotrowskiStowers Institute for Medical Research, Kansas City, MO.ORCID 0000-0001-8098-2574
David W RaibleDepartment of Otolaryngology Head & Neck Surgery, University of Washington, Seattle, WA.ORCID 0000-0002-5342-5841
Yehoash RaphaelDepartment of Otolaryngology-Head and Neck Surgery, University of Michigan, Ann Arbor, MI.
Jennifer StoneDepartment of Otolaryngology Head & Neck Surgery, University of Washington, Seattle, WA.ORCID 0000-0002-6742-0590
Litao TaoDepartment of Biomedical Sciences, Creighton University, Omaha, NE.
Mark E WarcholDepartment of Anatomy and Neurobiology, Washington University School of Medicine, St. Louis, MO.
Seth A AmentInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD.ORCID 0000-0001-6443-7509
Lisa V GoodrichDepartment of Neurobiology, Harvard Medical School, Boston, MA.ORCID 0000-0002-3331-8600

Funding

Understanding the progression of hearing loss in an endolymphatic hydrops modelP20GM139762 · NIGMS · CREIGHTON UNIVERSITY · PI Hui Hong · 2021 to 2026
$16.1M
Multi-Omic and Functional Analyses for Hearing Preservation and RestorationZIADC000094 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI HERTZANO, RONNA · 2023 to 2025
$10.3M
MECHANISMS OF SENSORY REGENERATIONR01DC006283 · NIDCD · WASHINGTON UNIVERSITY · PI WARCHOL, MARK · 2004 to 2025
$6.8M
Enhancing Atoh1 function in hair cell regenerationR01DC014832 · NIDCD · WASHINGTON UNIVERSITY · PI Gabriel Corfas, Andrew K Groves · 2016 to 2026
$6.7M
Regenerative pathways in the avian cochleaR01DC019619 · NIDCD · STANFORD UNIVERSITY · PI Stefan Heller · 2022 to 2026
$3.2M
Determination of Hair Cell Fate from Postnatal Cochlear Supporting CellsR01DC020322 · NIDCD · MASSACHUSETTS EYE AND EAR INFIRMARY · PI Albert Edge · 2022 to 2026
$3.1M
Zebrafish Sensory Hair Cell RegenerationR01DC015488 · NIDCD · STOWERS INSTITUTE FOR MEDICAL RESEARCH · PI Tatjana Piotrowski · 2017 to 2026
$2.9M
The gEAR portal - Advancing Data Sharing, Analysis and Discovery for Hearing and Balance ResearchU01DC019370 · NIDCD · UNIVERSITY OF MARYLAND BALTIMORE · PI MAHURKAR, ANUP · 2023 to 2025
$1.8M
Hippo-mediated control of growth and regeneration in the inner ear sensory organsR01DC020268 · NIDCD · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Ksenia Gnedeva · 2023 to 2026
$1.5M
Avian-inspired Regenerative Therapies for Hearing LossR21DC021755 · NIDCD · STANFORD UNIVERSITY · PI Nesrine Benkafadar · 2024 to 2026
$579k
Dissecting the sensory hair cell nucleus: Development of a novel method for investigating chromatin interactions (Tn5-Capture) in small cell numbersR21DC020773 · NIDCD · CREIGHTON UNIVERSITY · PI TAO, LITAO · 2023 to 2024
$364k
Intramural NIH HHS ZIA DC000094NIDCD NIH HHS R01 DC006283NIDCD NIH HHS R01 DC014832NIDCD NIH HHS R01 DC015488NIDCD NIH HHS R01 DC019619NIDCD NIH HHS R01 DC020268NIDCD NIH HHS R01 DC020322NIDCD NIH HHS R21 DC020773NIDCD NIH HHS R21 DC021755NIDCD NIH HHS U01 DC019370NIGMS NIH HHS P20 GM139762
6 · The paper itself

Abstract

Mechanosensitive hair cells vary widely in morphology and regenerative capacity across vertebrate organs and species. To investigate their underlying transcriptomic diversity, we integrated human, mouse, chicken, and zebrafish single-cell and single-nucleus RNA sequencing datasets and assembled a cross-species atlas of hair cells spanning organs, developmental stages, and species. Analysis of 29 hair cell populations, encompassing the major cochlear, vestibular, and lateral-line hair cell types, identified approximately 5,000 genes enriched in at least one hair cell population compared to supporting cells from the same organs. Unsupervised clustering of these hair cell-enriched (HCE) genes defined species-, organ-, and hair cell state-associated cohorts as well as broadly conserved hair cell-enriched programs. Using an AUC-based scoring framework, we further defined 884 pan hair cell-enriched (pan-HCE) genes with elevated expression in most developing and/or mature hair cell populations, including genes implicated in deafness, mechanotransduction, and synaptic transmission, along with genes not previously linked to hair cell function. Independent analysis of developing hair cells using the same metrics stratified pan-HCE genes based on when they are first enriched and identified an additional 97 genes that are transiently enriched. We used the pan- and developing HCE gene sets to assess transcriptional similarity between baseline hair cell states and hair cells produced during avian hair cell regeneration and in mouse cochlear organoids, as well as hair cell-like populations produced by fibroblast reprogramming. HCE gene sets with different developmental dynamics identified young

Identifiers

PMID42818558
PMCPMC13622526

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