Kevin T. Booth

Also affiliated with Indiana University – Purdue University Indianapolis

NeuroscienceBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 19 papers. Top paper: “Mini-PCDH15 gene therapy rescues hearing in a mouse model of Usher syndrome type 1F”.

Mini-PCDH15 gene therapy rescues hearing in a mouse model of Usher syndrome type 1F

Nature Communications(2023)10.1038/s41467-023-38038-y

N/A

1.1DataRank · unranked

47 citations

Daniel M. Hathaway, Alex J. Klein, Bifeng Pan, Olga Strelkova, Pedro De‐la‐Torre +10 more

TMPRSS3 expression is limited in spiral ganglion neurons: implication for successful cochlear implantation

Journal of Medical Genetics(2022)10.1136/jmg-2022-108654

N/A

0.769DataRank · unranked

18 citations

Ernesto Cabrera, Brady J. Tucker, Timothy J. Shin, Jasmine V Moawad, Douglas J. Totten +3 more

Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders

EMBO Molecular Medicine(2025)10.1038/s44321-025-00290-8

N/A

0.330DataRank · unranked

8 citations

Marisa W. Friederich, Daniella H. Hock, Jessie R. Zhang, Liana Valin, Jill A. Rosenfeld +35 more

Biallelic Loss-of-Function Variants in BICD1 Are Associated with Peripheral Neuropathy and Hearing Loss

International Journal of Molecular Sciences(2023)10.3390/ijms24108897

N/A

0.104DataRank · unranked

1 citations

Wendy K. Chung, Sergey S. Novoselov, Louis H. Weimer, Alexander M. Rossor, Charles A. LeDuc +9 more

Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss

medRxiv(2021)10.1101/2021.01.27.21250652

N/A

0DataRank · unranked

8 citations

Marina T. DiStefano, Andrea M. Oza, Madeline Y. Hughes, Emma H. Wilcox, Sarah E. Hemphill +18 more

Human cochlear diffusion from the cerebrospinal fluid space with gadolinium contrast

Molecular Therapy(2023)10.1016/j.ymthe.2023.08.001

N/A

0DataRank · unranked

10 citations

Kevin T. Booth, Kristine M. Mosier, Evan C. Cumpston, Cody Whitted, Vanessa Okechuku +3 more

PCDH15 Dual-AAV Gene Therapy for Deafness and Blindness in Usher Syndrome Type 1F

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.11.09.566447

N/A

0DataRank · unranked

7 citations

Daniel M. Hathaway, Eric M. Mulhall, Kevin T. Booth, Mantian Wang, Cole W. Peters +6 more

PCDH15 dual-AAV gene therapy for deafness and blindness in Usher syndrome type 1F models

Journal of Clinical Investigation(2024)10.1172/jci177700

N/A

0DataRank · unranked

24 citations

Daniel M. Hathaway, Eric M. Mulhall, Kevin T. Booth, Mantian Wang, Cole W. Peters +6 more

The auditory midbrain mediates tactile vibration sensing

Cell(2024)10.1016/j.cell.2024.11.014

N/A

0DataRank · unranked

22 citations

Josef Turecek, Michelle M. DeLisle, Ofer Mazor, Gabriel E. Romero, Malvika Dua +7 more

The auditory midbrain mediates tactile vibration sensing

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.03.08.584077

N/A

0DataRank · unranked

2 citations

Josef Turecek, Michelle M. DeLisle, Ofer Mazor, Gabriel E. Romero, Malvika Dua +7 more

De novo and inherited variants in DDX39B cause a novel neurodevelopmental syndrome

Brain(2025)10.1093/brain/awaf035

N/A

0DataRank · unranked

9 citations

Sharayu Jangam, Martin MC Chui, Kayla Treat, Lorenzo Graziani, Alessia Soldano +24 more

Endocochlear potential contributes to hair cell death in TMPRSS3 hearing loss

Journal of Clinical Investigation(2025)10.1172/jci186395

N/A

0DataRank · unranked

6 citations

Yuan-Siao Chen, Stephanie L. Rouse, Xiaohan Wang, Janmaris Marin Fermin, Kevin T. Booth +13 more

ClinGen recuration of hearing loss-associated genes demonstrates significant changes in gene-disease validity over time

Genetics in Medicine(2025)10.1016/j.gim.2025.101392

N/A

0DataRank · unranked

1 citations

Marina T. DiStefano, Andrea M. Oza, Pamela Ajuyah, Ryan Webb, Enyonam Edoh +76 more

Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders

medRxiv(2025)10.1101/2025.07.08.25330848

N/A

0DataRank · unranked

1 citations

Marisa W. Friederich, Daniella H. Hock, Jessie R. Zhang, Liana Valin, Jill A. Rosenfeld +35 more

Insights into the pathophysiology of DFNA10 hearing loss associated with novel EYA4 variants

Scientific Reports(2020)10.1038/s41598-020-63256-5

N/A

0DataRank · unranked

87 citations

Lucía Borreguero, Kevin T. Booth, María Lachgar, P.L.M. Huygen, Manuela Villamar +11 more

Investigation of GSDME results in the identification of the first pathogenic synonymous variants and genotype-phenotype correlations

Human Genetics(2025)10.1007/s00439-025-02782-6

N/A

0DataRank · unranked

0 citations

William D. Walls, Kai Wang, Arthur Duston Odell, Diana L. Kolbe, Kevin T. Booth +3 more

Biallelic mutation of CLRN2 causes non-syndromic hearing loss in humans

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.29.222828

N/A

0DataRank · unranked

3 citations

Neda Mazaheri, Sheng‐Jia Lin, Lucy A Dunbar, Reza Maroofian, Héla Azaiez +19 more

A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

Human Genetics(2021)10.1007/s00439-020-02254-z

N/A

0DataRank · unranked

28 citations

Neda Mazaheri, Sheng‐Jia Lin, Lucy A Dunbar, Reza Maroofian, Héla Azaiez +21 more

A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing

European Journal of Human Genetics(2021)10.1038/s41431-020-00790-w

N/A

0DataRank · unranked

17 citations

Chayada Tangshewinsirikul, Kevin T. Booth, Héla Azaiez, Devorah Yefet, Adina Quint +23 more