Thomas B. Friedman

17.1k citations

181 papers · 9.8k indexed · h-index 57

Impact in

Sensory Systems top 0.01%
- Hearing, Cochlea, Tinnitus, Genetics
Neurology top 0.2%
- Vestibular and auditory disorders

Papers in

Sensory Systems 110
- Hearing, Cochlea, Tinnitus, Genetics 108
Neurology 39
- Vestibular and auditory disorders 33

Co-authors: Inna A. Belyantseva Robert J. Morell Andrew J. Griffith Zubair M. Ahmed Sheikh Riazuddin Saima Riazuddin Edward R. Wilcox Gregory I. Frolenkov
Journals: Human Genetics (13 papers)The American Journal of Human Genetics (11 papers)Science (8 papers)Human Molecular Genetics (7 papers)Human Mutation (7 papers)
Partner nations: United States Pakistan United Kingdom

In The Last Decade

Thomas B. Friedman

180 papers receiving 9.6k citations

Peers

Countries citing papers authored by Thomas B. Friedman

Since Specialization

Citations

This map shows the geographic impact of Thomas B. Friedman'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 Thomas B. Friedman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thomas B. Friedman more than expected).

Fields of papers citing papers by Thomas B. Friedman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas B. Friedman. 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 Thomas B. Friedman. The network helps show where Thomas B. Friedman may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Thomas B. Friedman, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Thomas B. Friedman Line = papers co-authored together Thomas B. Friedman links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome Clinical Genetics ·Rabia Faridi, Pamela Stratton, Noemi Salmeri, Robert J. Morell, Asma Ali Khan, C. Mayorga, William G. Newman, Sheikh Riazuddin, Thomas B. Friedman	2024	4
2	Late‐onset hearing loss case associated with a heterozygous truncating variant of DIAPH1 Clinical Genetics ·Bong Jik Kim, Takushi Miyoshi, João Nuno Maia e Silva, Thomas B. Friedman, Byung Yoon Choi, Takehiko Ueyama	2022	2
3	ANKRD24 organizes TRIOBP to reinforce stereocilia insertion points The Journal of Cell Biology ·Jocelyn F. Krey, Chang Liu, Inna A. Belyantseva, 丁玉英, Rachel A. Dumont, Andrew D. Sens, Paroma Chatterjee, Caitlin Corner, Lev M. Fedorov, Sarah Foster, Jin‐Kyung Kim, Alfred L. Nuttall, Sherri M. Jones, Dongseok Choi, Thomas B. Friedman, Anthony J. Ricci, Bo Zhao, Peter G. Gillespie	2022	11
4	Fast-dissociating but highly specific antibodies are novel tools in biology, especially useful for multiplex super-resolution microscopy STAR Protocols ·Takushi Miyoshi, Thomas B. Friedman, Naoki Watanabe	2021	3
5	New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder Human Genetics ·Rabia Faridi, Jim Bologna, Cristina Fenollar‐Ferrer, Raymond T. O’Keefe, Shoujun Gu, Rakshit Patial, Asma Ali Khan, Sheikh Riazuddin, Michael Hoa, Sadaf Naz, William G. Newman, Thomas B. Friedman	2021	28
6	Vestibular phenotype‐genotype correlation in a cohort of 90 patients with Usher syndrome Clinical Genetics ·P Peltonen, Rabia Faridi, Kelly King, Christopher Zalewski, Rizwan Yousaf, Julie M. Schultz, Robert J. Morell, Julie Muskett, Amy Turriff, Ekaterini Tsilou, Andrew J. Griffith, Thomas B. Friedman, Wadih M. Zein, Carmen C. Brewer	2020	24
7	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 ·Robert J. Morell, Rafal T. Olszewski, Risa Tona, RAVLEEN KAUR, P Peltonen, Wiggins Bryan, Julie M. Schultz, 冯克永, سارا مهرابیپور, de A. Lorm, Connor Hill, Thomas L. Saunders, Matthew F. Starost, Tracy S. Fitzgerald, Elizabeth Wilson, Takahiro Ohyama, Thomas B. Friedman, Michael Hoa	2020	23
8	The ATPase mechanism of myosin 15, the molecular motor mutated in DFNB3 human deafness Journal of Biological Chemistry ·Fangfang Jiang, Yasuharu Takagi, Julie Jarnigan, Sarah M. Heissler, Thomas B. Friedman, James R. Sellers, Jonathan E. Bird	2020	11
9	Growth factor and receptor malfunctions associated with human genetic deafness Clinical Genetics ·Sadaf Naz, Thomas B. Friedman	2019	5
10	Bipolar filaments of human nonmuscle myosin 2-A and 2-B have distinct motile and mechanical properties eLife ·Luca Melli, Neil Billington, Sara A. Sun, Jonathan E. Bird, Attila Nagy, Thomas B. Friedman, Yasuharu Takagi, James R. Sellers	2018	51
11	Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange‐Nielsen Syndrome and Romano‐Ward Syndrome Human Mutation ·Rabia Faridi, Risa Tona, Alessandra Brofferio, Michael Hoa, Rafal T. Olszewski, Isabelle Schrauwen, Muhammad Zaman Khan Assir, B. Fobel, Asma Ali Khan, Atteeq U. Rehman, Carmen C. Brewer, 王永纯, Suzanne M. Leal, Sheikh Riazuddin, Steven E. Boyden, Thomas B. Friedman	2018	27
12	Mutations in Grxcr1 Are The Basis for Inner Ear Dysfunction in the Pirouette Mouse The American Journal of Human Genetics ·Hana M. Odeh, Kristina L. Hunker, Inna A. Belyantseva, Héla Azaiez, Matthew R. Avenarius, Lili Zheng, Linda Peters, Leona H. Gagnon, Nobuko Hagiwara, Michael J. Skynner, Murray H. Brilliant, Nicholas D. Allen, Saima Riazuddin, Kenneth R. Johnson, Yehoash Raphael, Hossein Najmabadi, Thomas B. Friedman, James R. Bartles, Richard J. Smith, David C. Kohrman	2010	40
13	Mutations of theRDXgene cause nonsyndromic hearing loss at theDFNB24locus Human Mutation ·Shahid Y. Khan, Zubair M. Ahmed, Dave Mannes, Shin‐ichiro Kitajiri, Paul Agbo, Cheng Xu, Masaki Morotomi, Arabandi Ramesh, T. I. Liaudat, Shaheen N. Khan, Richard J. Smith, Saima Riazuddin, Thomas B. Friedman, Sheikh Riazuddin	2007	60
14	Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2–q13.3 Human Genetics ·Shahid Y. Khan, Saima Riazuddin, Muhammad Tariq, Saima Anwar, Dave Mannes, Sheikh Riazuddin, Shaheen N. Khan, Tayyab Husnaın, Zubair M. Ahmed, Thomas B. Friedman	2006	20
15	Tricellulin Is a Tight-Junction Protein Necessary for Hearing The American Journal of Human Genetics ·Saima Riazuddin, Zubair M. Ahmed, Alan S. Fanning, Ayala Lagziel, Shin‐ichiro Kitajiri, Khushnooda Ramzan, Shaheen N. Khan, Parna Chattaraj, Penelope L. Friedman, James M. Anderson, Inna A. Belyantseva, Andrew Forge, Sheikh Riazuddin, Thomas B. Friedman	2006	205
16	Mutations in TRIOBP, Which Encodes a Putative Cytoskeletal-Organizing Protein, Are Associated with Nonsyndromic Recessive Deafness The American Journal of Human Genetics ·Saima Riazuddin, Shaheen N. Khan, Zubair M. Ahmed, Manju Ghosh, Kyle Caution, EWelman, Madhulika Kabra, Ahmad Usman Zafar, Kevin Chen, Sadaf Naz, Anthony Antonellis, William J. Pavan, Eric D. Green, Edward R. Wilcox, Penelope L. Friedman, Robert J. Morell, Sheikh Riazuddin, Thomas B. Friedman	2005	76
17	Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle Proceedings of the National Academy of Sciences ·Inna A. Belyantseva, Erich T. Boger, Thomas B. Friedman	2003	184
18	Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37 The American Journal of Human Genetics ·Zubair M. Ahmed, Robert J. Morell, Saima Riazuddin, Andrea Gropman, Shahzad Shaukat, J.R. Dewey, Saidi Mohiddin, Lameh Fananapazir, Rafael C. Caruso, Tayyab Husnaın, Shaheen N. Khan, Sheikh Riazuddin, Andrew J. Griffith, Thomas B. Friedman, Edward R. Wilcox	2003	151
19	Apparent Digenic Inheritance of Waardenburg Syndrome Type 2 (WS2) and Autosomal Recessive Ocular Albinism (AROA) Human Molecular Genetics ·Robert J. Morell, Richard A. Spritz, A. Tricot, John W. Pierpont, Wei Guo, Thomas B. Friedman, James H. Asher	1997	68
20	The faint band/interband region 28C2 to 28C4-5(−) of the Drosophila melanogaster salivary gland polytene chromosomes is rich in transcripts Molecular and General Genetics MGG ·Thomas B. Friedman, Kelly N. Owens, Jean B. Burnett, V. G. C. Ongaratto, Lori L. Wallrath	1991	8

About Thomas B. Friedman

Thomas B. Friedman is a scholar working on Sensory Systems, Neurology, Otorhinolaryngology, Molecular Biology and Cell Biology, having authored 181 papers that have together received 9.8k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (108 papers), Vestibular and auditory disorders (33 papers), Connexins and lens biology (21 papers), RNA regulation and disease (20 papers), Hearing Loss and Rehabilitation (18 papers), RNA and protein synthesis mechanisms (16 papers), Ear Surgery and Otitis Media (13 papers) and Muscle Physiology and Disorders (12 papers). The work is most often cited by research in Sensory Systems (5.9k citations), Neurology (2.4k citations), Otorhinolaryngology (933 citations), Molecular Biology (5.7k citations) and Endocrine and Autonomic Systems (481 citations). Thomas B. Friedman has collaborated with scholars based in United States, Pakistan and United Kingdom. Frequent co-authors include Inna A. Belyantseva, Robert J. Morell, Andrew J. Griffith, Zubair M. Ahmed, Sheikh Riazuddin, Saima Riazuddin, Edward R. Wilcox, Gregory I. Frolenkov, Erich T. Boger and James R. Sellers. Their work appears in journals such as Human Genetics, The American Journal of Human Genetics, Science, Human Molecular Genetics and Human Mutation.

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.

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