Thomas B. Friedman

Also affiliated with National Institute on Deafness and Other Communication Disorders

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

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 42 papers. Top paper: “Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F”.

Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F

The American Journal of Human Genetics(2001)10.1086/321277

N/A

0.905DataRank · unranked

417 citations

Saima Riazuddin, Steve L. Bernstein, Zahoor Ahmed, Shaheen Khan, Andrew J. Griffith +5 more

Myosins and Hearing

Advances in experimental medicine and biology(2020)10.1007/978-3-030-38062-5_13

N/A

0.561DataRank · unranked

41 citations

Inna A. Belyantseva, Gregory I. Frolenkov, Thomas B. Friedman

Atypical and ultra-rare Usher syndrome: a review

Ophthalmic Genetics(2020)10.1080/13816810.2020.1747090

N/A

0.538DataRank · unranked

35 citations

Robert B. Hufnagel, Thomas B. Friedman, Amy Turriff, Carmen C. Brewer, Christopher Zalewski +6 more

Variants of LRP2 , encoding a multifunctional cell‐surface endocytic receptor, associated with hearing loss and retinal dystrophy

Clinical Genetics(2023)10.1111/cge.14312

N/A

0.477DataRank · unranked

23 citations

Rizwan Yousaf, Shoujun Gu, Sayaka Inagaki, Amy Turriff, Keith Pelstring +22 more

Variants of human CLDN9 cause mild to profound hearing loss

Human Mutation(2021)10.1002/humu.24260

N/A

0.476DataRank · unranked

6 citations

Christophe Philippe, Inna A. Belyantseva, Yoko Nakano, Cristina Fenollar‐Ferrer, Risa Tona +19 more

Proposed therapy, developed in a Pcdh15-deficient mouse, for progressive loss of vision in human Usher syndrome

eLife(2021)10.7554/elife.67361

N/A

0.457DataRank · unranked

20 citations

Wadih M Zein, Sehar Riaz, Arnaud PJ Giese, Julie M Schultz, Todd Duncan +8 more

Myosin-driven Nucleation of Actin Filaments Drives Stereocilia Development Critical for Hearing

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.07.09.451618

N/A

0.385DataRank · unranked

12 citations

Fangfang Jiang, Carlos Aguilar, Melanie Barzik, Rui Gong, Arik Shams +16 more

Taperin bundles F-actin at stereocilia pivot points enabling optimal lifelong mechanosensitivity

The Journal of Cell Biology(2025)10.1083/jcb.202408026

N/A

0.312DataRank · unranked

7 citations

C S C Liu, Abigail K. Dragich, Takushi Miyoshi, Sayaka Inagaki, Ayesha Imtiaz +35 more

Interaction between the TBC1D24 TLDc domain and the KIBRA C2 domain is disrupted by two epilepsy-associated TBC1D24 missense variants

Journal of Biological Chemistry(2024)10.1016/j.jbc.2024.107725

N/A

0.167DataRank · unranked

2 citations

Sayaka Inagaki, Yasuko Ishibashi, Rabia Faridi, Rizwan Yousaf, Isabelle Roux +6 more

Biallelic variants in DAP3 result in reduced assembly of the mitoribosomal small subunit with altered intrinsic and extrinsic apoptosis and a Perrault syndrome-spectrum phenotype

medRxiv(2024)10.1101/2024.08.19.24312079

N/A

0.165DataRank · unranked

2 citations

Robert Kopajtich, Leigh Demain, Alessandro Rea, Huw B. Thomas, Manuel Schiff +35 more

Single-molecule fluorescence microscopy reveals regulatory mechanisms of MYO7A-driven cargo transport in stereocilia of live inner ear hair cells

Nature Communications(2025)10.1038/s41467-025-63102-0

N/A

0.104DataRank · unranked

1 citations

Harshad D. Vishwasrao, Inna A. Belyantseva, Junko Miyoshi, Mrudhula Sajeevadathan, Yasuko Ishibashi +5 more

Semi-automated single-molecule microscopy screening of fast-dissociating specific antibodies directly from hybridoma cultures

Cell Reports(2021)10.1016/j.celrep.2021.108708

N/A

0DataRank · unranked

22 citations

Qianli Zhang, Takafumi Miyake, Shin Watanabe, Hiroe Ohnishi, Jiji Chen +9 more

Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria

European Journal of Human Genetics(2021)10.1038/s41431-021-00984-w

N/A

0DataRank · unranked

16 citations

Rabia Faridi, Parna Chattaraj, Rizwan Yousaf, Risa Tona, Samuel Okorie +10 more

Fast-dissociating but highly specific antibodies are novel tools in biology, especially useful for multiplex super-resolution microscopy

STAR Protocols(2021)10.1016/j.xpro.2021.100967

N/A

0DataRank · unranked

3 citations

Thomas B. Friedman, Naoki Watanabe, Takushi Miyoshi

TRIOBP promotes bidirectional radial stiffness gradients within the organ of Corti

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.06.28.450090

N/A

0DataRank · unranked

0 citations

Inna A. Belyantseva, Rizwan Yousaf, Risa Tona, Shadan Hadi, Elizabeth Wilson +5 more

ANKRD24 organizes TRIOBP to reinforce stereocilia insertion points

The Journal of Cell Biology(2022)10.1083/jcb.202109134

N/A

0DataRank · unranked

20 citations

Chang Liu, Inna A. Belyantseva, Michael Bateschell, Rachel A. Dumont, Jennifer Goldsmith +13 more

Unbalanced bidirectional radial stiffness gradients within the organ of Corti promoted by TRIOBP

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2115190119

N/A

0DataRank · unranked

11 citations

Inna A. Belyantseva, Rizwan Yousaf, Risa Tona, Shadan Hadi, Sayaka Inagaki +6 more

Late‐onset hearing loss case associated with a heterozygous truncating variant of DIAPH1

Clinical Genetics(2022)10.1111/cge.14115

N/A

0DataRank · unranked

5 citations

Takushi Miyoshi, Taimur Chaudhry, Thomas B. Friedman, Byung Yoon Choi, Takehiko Ueyama +1 more

Dual-AAV vector-mediated expression of MYO7A improves vestibular function in a mouse model of Usher syndrome 1B

Molecular Therapy — Methods & Clinical Development(2023)10.1016/j.omtm.2023.08.012

N/A

0DataRank · unranked

22 citations

M’hamed Grati, Kevin Isgrig, Moaz Sinan, Kaitlyn R. Calabro, Jianliang Zhu +9 more

Combined AAV-mediated gene replacement therapy improves auditory function in a mouse model of human DFNB42 deafness

Molecular Therapy(2023)10.1016/j.ymthe.2023.07.014

N/A

0DataRank · unranked

12 citations

Alexander X. Cartagena‐Rivera, Hong Jun Wang, M’hamed Grati, Katharine Fernandez, Thomas B. Friedman +3 more

Deafness DFNB110 associated with a human MAP3K1 recessive variant recapitulates hearing loss of Map3k1 kinase deficient mice

Research Square(2023)10.21203/rs.3.rs-3310464/v1

N/A

0DataRank · unranked

0 citations

Rizwan Yousaf, Sayaka Inagaki, Rafal T. Olszewski, Shoujun Gu, Robert J. Morell +9 more

Bi-allelic variants in DAP3 result in reduced assembly of the mitoribosomal small subunit with altered apoptosis and a Perrault-syndrome-spectrum phenotype

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.11.007

N/A

0DataRank · unranked

7 citations

Robert Kopajtich, Leigh Demain, Alessandro Rea, Huw B. Thomas, Manuel Schiff +34 more

Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome

Clinical Genetics(2024)10.1111/cge.14514

N/A

0DataRank · unranked

6 citations

Pamela Stratton, Noemi Salmeri, Robert J. Morell, Asma Ali Khan, Muhammad A. Usmani +4 more

SLC26A4-AP-2 mu2 interaction regulates SLC26A4 plasma membrane abundance in the endolymphatic sac

Science Advances(2024)10.1126/sciadv.adm8663

N/A

0DataRank · unranked

3 citations

Cristina Fenollar‐Ferrer, Kevin Isgrig, Ya-Xian Wang, Kerstin Valente, Juleh Eide +9 more

Deafness DFNB128 Associated with a Recessive Variant of Human MAP3K1 Recapitulates Hearing Loss of Map3k1-Deficient Mice

Genes(2024)10.3390/genes15070845

N/A

0DataRank · unranked

2 citations

Rizwan Yousaf, Sayaka Inagaki, Rafal T. Olszewski, Shoujun Gu, Robert J. Morell +9 more

Live-cell single-molecule fluorescence microscopy for protruding organelles reveals regulatory mechanisms of MYO7A-driven cargo transport in stereocilia of inner ear hair cells

Research Square(2024)10.21203/rs.3.rs-4369958/v1

N/A

0DataRank · unranked

0 citations

Harshad D. Vishwasrao, Inna A. Belyantseva, Mrudhula Sajeevadathan, Yasuko Ishibashi, Samuel Mawuli Adadey +4 more

Myosin-based nucleation of actin filaments contributes to stereocilia development critical for hearing

Nature Communications(2025)10.1038/s41467-025-55898-8

N/A

0DataRank · unranked

11 citations

Fangfang Jiang, Carlos Aguilar, Melanie Barzik, Rui Gong, Ghazaleh Behnammanesh +19 more

Issue Information

Human Mutation(2018)10.1002/humu.23568

N/A

0DataRank · unranked

0 citations

R. Donald Harvey, Tracy Dudding‐Byth, Liliana Catherine Patiño, Isabelle Beau, Adrien Morel +135 more

MSRB3 antioxidant activity is necessary for inner ear cuticular plate structure and hair bundle integrity

Disease Models & Mechanisms(2025)10.1242/dmm.052194

N/A

0DataRank · unranked

1 citations

Élodie M. Richard, Byung Cheon Lee, Gavin P. Riordan, Inna A. Belyantseva, Bruno Manta +4 more

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

Nature Genetics(2025)10.1038/s41588-025-02332-w

N/A

0DataRank · unranked

1 citations

Inna A. Belyantseva, Arnaud P. J. Giese, Kwanghyuk Lee, Artur A. Indzhykulian, Sri Pratima Nandamuri +26 more

A truncated CDC14A retains catalytic structure and phosphatase activity preserving male fertility but causes nonsyndromic deafness

Journal of Biological Chemistry(2025)10.1016/j.jbc.2025.110982

N/A

0DataRank · unranked

0 citations

Gina Jackisch, Inna A. Belyantseva, Muhammad Imran, Sadaf Naz, Céleste Sèle +6 more

AAV-mediated inner ear gene delivery triggers mild host immune responses in the mammalian inner ear

Molecular Therapy — Methods & Clinical Development(2025)10.1016/j.omtm.2025.101456

N/A

0DataRank · unranked

3 citations

Jianliang Zhu, Gwladys Gernoux, Yunkai Yu, Michelle J. Suh, Kevin Isgrig +8 more

Exosomes mediate sensory hair cell protection in the inner ear

Journal of Clinical Investigation(2020)10.1172/jci128867

N/A

0DataRank · unranked

108 citations

Lindsey May, Melanie Barzik, Nora C. Welsh, Shimon P. Francis, Tucker Costain +8 more

Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness

Genes(2020)10.3390/genes11101122

N/A

0DataRank · unranked

20 citations

Iván A. López, Cristina Fenollar‐Ferrer, Rabia Faridi, Claudio Anselmi, Asma Ali Khan +10 more

The ATPase mechanism of myosin 15, the molecular motor mutated in DFNB3 human deafness

Journal of Biological Chemistry(2020)10.1074/jbc.ra120.014903

N/A

0DataRank · unranked

17 citations

Yasuharu Takagi, Arik Shams, Sarah M. Heissler, Thomas B. Friedman, James R. Sellers +2 more

Myosin 18Aα targets the guanine nucleotide exchange factor β‐Pix to the dendritic spines of cerebellar Purkinje neurons and promotes spine maturation

The FASEB Journal(2020)10.1096/fj.202001449r

N/A

0DataRank · unranked

9 citations

Melanie Barzik, Ikuko Fujiwara, Kirsten Remmert, Ya‐Xian Wang, Ronald S. Petralia +3 more

Vestibular phenotype‐genotype correlation in a cohort of 90 patients with Usher syndrome

Clinical Genetics(2020)10.1111/cge.13868

N/A

0DataRank · unranked

37 citations

Rabia Faridi, Kelly King, Christopher Zalewski, Rizwan Yousaf, Julie M. Schultz +9 more

Noncoding Microdeletion in Mouse Hgf Disrupts Neural Crest Migration into the Stria Vascularis, Reduces the Endocochlear Potential, and Suggests the Neuropathology for Human Nonsyndromic Deafness DFNB39

Journal of Neuroscience(2020)10.1523/jneurosci.2278-19.2020

N/A

0DataRank · unranked

34 citations

Rafal T. Olszewski, Risa Tona, Samuel Leitess, Talah Wafa, Ian Taukulis +13 more

The ATPase mechanism of myosin 15, the molecular motor mutated in DFNB3 human deafness

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.17.155424

N/A

0DataRank · unranked

1 citations

Yasuharu Takagi, Arik Shams, Sarah M. Heissler, Thomas B. Friedman, James R. Sellers +2 more

New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder

Human Genetics(2021)10.1007/s00439-021-02319-7

N/A

0DataRank · unranked

52 citations

Alessandro Rea, Cristina Fenollar‐Ferrer, Raymond T. O’Keefe, Shoujun Gu, Zunaira Munir +7 more

Actin at stereocilia tips is regulated by mechanotransduction and ADF/cofilin

Current Biology(2021)10.1016/j.cub.2020.12.006

N/A

0DataRank · unranked

36 citations

Chun-Yu Tung, Xiayi Liao, Inna A. Belyantseva, Pallabi Roy, Oisorjo Chakraborty +10 more

Human deafness-associated variants alter the dynamics of key molecules in hair cell stereocilia F-actin cores

Human Genetics(2021)10.1007/s00439-021-02304-0

N/A

0DataRank · unranked

19 citations

Inna A. Belyantseva, Shin‐ichiro Kitajiri, Hiroki Miyajima, Shin‐ya Nishio, Shin‐ichi Usami +6 more