Kevin T. Booth

3.8k total citations · 1 hit paper
42 papers, 1.3k citations indexed

About

Kevin T. Booth is a scholar working on Sensory Systems, Molecular Biology and Neurology. According to data from OpenAlex, Kevin T. Booth has authored 42 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Sensory Systems, 24 papers in Molecular Biology and 7 papers in Neurology. Recurrent topics in Kevin T. Booth's work include Hearing, Cochlea, Tinnitus, Genetics (28 papers), Vestibular and auditory disorders (7 papers) and Ear Surgery and Otitis Media (6 papers). Kevin T. Booth is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (28 papers), Vestibular and auditory disorders (7 papers) and Ear Surgery and Otitis Media (6 papers). Kevin T. Booth collaborates with scholars based in United States, Iran and Japan. Kevin T. Booth's co-authors include Héla Azaiez, Richard J. Smith, Carla Nishimura, E. Ann Black-Ziegelbein, Christina Sloan-Heggen, A. Eliot Shearer, Diana L. Kolbe, Seiji B. Shibata, Donghong Wang and Paul T. Ranum and has published in prestigious journals such as Cell, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Kevin T. Booth

38 papers receiving 1.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss

2016 379 citations Christina Sloan-Heggen, A. Eliot Shearer et al. Human Genetics profile →

Peers

Countries citing papers authored by Kevin T. Booth

Since Specialization

Citations

This map shows the geographic impact of Kevin T. Booth's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Kevin T. Booth with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kevin T. Booth more than expected).

Fields of papers citing papers by Kevin T. Booth

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kevin T. Booth. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Kevin T. Booth. The network helps show where Kevin T. Booth may publish in the future.

Co-authorship network of co-authors of Kevin T. Booth

This figure shows the co-authorship network connecting the top 25 collaborators of Kevin T. Booth. A scholar is included among the top collaborators of Kevin T. Booth based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Kevin T. Booth. Kevin T. Booth is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Endocochlear potential contributes to hair cell death in TMPRSS3 hearing loss 2025 ·Journal of Clinical Investigation ·A. Eliot Shearer, (unknown), (unknown), Xiaohan Wang, (unknown), Kevin T. Booth, (unknown), (unknown), Jinan Li, Hae‐Young Kim, Michael Hoa, Rafal T. Olszewski, Jieping Lei, (unknown), Douglas J. Totten, Bo Zhao, Jeffrey R. Holt, Rick F. Nelson	1
2	PCDH15 dual-AAV gene therapy for deafness and blindness in Usher syndrome type 1F models 2024 ·Journal of Clinical Investigation ·Maryna V. Ivanchenko, (unknown), Eric M. Mulhall, Kevin T. Booth, Mantian Wang, Cole W. Peters, (unknown), (unknown), Yaqiao Li, Bence György, David P. Corey	11
3	A Novel Candidate Gene MACF1 is Associated with Autosomal Dominant Non-syndromic Hearing Loss in an Iranian Family 2024 ·Archives of Iranian Medicine ·Niloofar Bazazzadegan, Mojgan Babanejad, (unknown), Sanaz Arzhangi, Kimia Kahrizi, Kevin T. Booth, Hossein Najmabadi	0
4	ZMIZ1 :: ABL1 Fusion: An Uncommon Molecular Event With Clinical Implications in Pediatric Cancer 2024 ·Archives of Pathology & Laboratory Medicine ·Kevin T. Booth, Rachael Schulte, (unknown), Hongyu Gao, (unknown), Yunlong Liu, Shalini C. Reshmi, Gail H. Vance	1
5	The auditory midbrain mediates tactile vibration sensing 2024 ·Cell ·Erica L. Huey, Josef Turecek, Michelle M. DeLisle, Ofer Mazor, (unknown), (unknown), (unknown), (unknown), Kevin T. Booth, Lisa V. Goodrich, David P. Corey, David D. Ginty	5
6	Biochemical and molecular confirmation of alkaptonuria in a Sumatran orangutan (Pongo abelii) 2023 ·Molecular Genetics and Metabolism ·(unknown), Kevin T. Booth, (unknown), (unknown), (unknown), (unknown), Marcus J. Miller	1
7	Mini-PCDH15 gene therapy rescues hearing in a mouse model of Usher syndrome type 1F 2023 ·Nature Communications ·Maryna V. Ivanchenko, (unknown), (unknown), Bifeng Pan, Olga Strelkova, Pedro De‐la‐Torre, Xudong Wu, Cole W. Peters, Eric M. Mulhall, Kevin T. Booth, (unknown), (unknown), Marcos Sotomayor, Artur A. Indzhykulian, David P. Corey	23
8	Genetic etiology of hearing loss in Iran 2022 ·Human Genetics ·Mojgan Babanejad, Maryam Beheshtian, (unknown), Marzieh Mohseni, Kevin T. Booth, Kimia Kahrizi, Hossein Najmabadi	14
9	DVPred: a disease-specific prediction tool for variant pathogenicity classification for hearing loss 2022 ·Human Genetics ·Fengxiao Bu, Mingjun Zhong, Qinyi Chen, Yumei Wang, (unknown), Qian Zhang, (unknown), Kevin T. Booth, Héla Azaiez, Yu Lu, Jing Cheng, Richard J. Smith, Huijun Yuan	10
10	Identification of Novel and Recurrent Variants in MYO15A in Ashkenazi Jewish Patients With Autosomal Recessive Nonsyndromic Hearing Loss 2021 ·Frontiers in Genetics ·Kevin T. Booth, Yoel Hirsch, (unknown), Josef Ekstein, (unknown), (unknown), (unknown), David P. Corey	0
11	Insights into the pathophysiology of DFNA10 hearing loss associated with novel EYA4 variants 2020 ·Scientific Reports ·Matías Morin, (unknown), Kevin T. Booth, (unknown), P.L.M. Huygen, Manuela Villamar, Fernando Mayo, Luis C. Barrio, (unknown), Carmelo Morales‐Angulo, Ignacio del Castillo, (unknown), Dolores Tellerı́a, Richard J. Smith, Héla Azaiez, Miguel A. Moreno‐Pelayo	66
12	Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing loss 2020 ·Human Genetics ·Kevin T. Booth, (unknown), (unknown), (unknown), Mureed Hussain, Kathy Frees, (unknown), Carla Nishimura, Mohsin Shahzad, Richard J. Smith, Zubair M. Ahmed, Héla Azaiez, Saima Riazuddin	16
13	Defective Tmprss3-Associated Hair Cell Degeneration in Inner Ear Organoids 2019 ·Stem Cell Reports ·Pei-Ciao Tang, (unknown), Jing Nie, Jiyoon Lee, Adam Roth, Kevin T. Booth, Karl R. Koehler, Eri Hashino, Rick F. Nelson	55
14	Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37 2018 ·Genetics in Medicine ·Kevin T. Booth, James W. Askew, Zohreh Talebizadeh, P.L.M. Huygen, James D. Eudy, Judith B. Kenyon, Denise M. Hoover, Michael S. Hildebrand, Katherine R. Smith, Melanie Bahlo, William J. Kimberling, Richard J. Smith, Héla Azaiez, Shelley D. Smith	38
15	Variants in CIB2 cause DFNB48 and not USH1J 2017 ·Clinical Genetics ·Kevin T. Booth, Kimia Kahrizi, (unknown), (unknown), Güney Bademci, Sanaz Arzhangi, Davood Zare‐Abdollahi, Duygu Duman, A. Amraoui, Mustafa Tekin, Hossein Najmabadi, Héla Azaiez, Richard J. Smith	44
16	Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss breakdown → 2016 ·Human Genetics ·Christina Sloan-Heggen, (unknown), A. Eliot Shearer, Diana L. Kolbe, Carla Nishimura, Kathy L. Frees, (unknown), Seiji B. Shibata, Kevin T. Booth, Colleen A. Campbell, Paul T. Ranum, Amy E. Weaver, E. Ann Black-Ziegelbein, Donghong Wang, Héla Azaiez, Richard J. Smith	379
17	PDZD7 and hearing loss: More than just a modifier 2015 ·American Journal of Medical Genetics Part A ·Kevin T. Booth, Héla Azaiez, Kimia Kahrizi, Allen C. Simpson, (unknown), Christina M. Sloan, Nicole C. Meyer, Mojgan Babanejad, (unknown), Sanaz Arzhangi, Michael J. Schnieders, Hossein Najmabadi, Richard J. Smith	46
18	HOMER2, a Stereociliary Scaffolding Protein, Is Essential for Normal Hearing in Humans and Mice 2015 ·PLoS Genetics ·Héla Azaiez, Amanda R. Decker-Farrell, Kevin T. Booth, Allen C. Simpson, A. Eliot Shearer, P.L.M. Huygen, Fengxiao Bu, Michael S. Hildebrand, Paul T. Ranum, Seiji B. Shibata, (unknown), Yuzhou Zhang, William J. Kimberling, Robert A. Cornell, Richard J. Smith	40
19	Hearing Loss Caused by a P2RX2 Mutation Identified in a MELAS Family With a Coexisting Mitochondrial 3243AG Mutation 2015 ·Annals of Otology Rhinology & Laryngology ·Hideaki Moteki, Héla Azaiez, Kevin T. Booth, Mitsuru Hattori, Ai Sato, Yoshihiko Sato, Mitsuo Motobayashi, Christina M. Sloan, Diana L. Kolbe, A. Eliot Shearer, Richard J. Smith, Shin‐ichi Usami	17
20	Healthcare Screening in Police Custody: Insights and Innovations 2013 ·Research Explorer (The University of Manchester) ·Heather Noga, Iain McKinnon, (unknown), Kevin T. Booth	1

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact