Thomas B. Friedman
Impact in
- Sensory Systems top 0.01%
- Hearing, Cochlea, Tinnitus, Genetics
- Neurology top 0.2%
- Vestibular and auditory disorders
Papers in
- Sensory Systems 116
- Hearing, Cochlea, Tinnitus, Genetics 114
-
- RNA regulation and disease 22
- Connexins and lens biology 20
- RNA and protein synthesis mechanisms 15
- Muscle Physiology and Disorders 13
- Congenital heart defects research 12
- Co-authors
- Inna A. Belyantseva (45 shared papers)Andrew J. Griffith (33 shared papers)Robert J. Morell (50 shared papers)Zubair M. Ahmed (45 shared papers)Sheikh Riazuddin (44 shared papers)Saima Riazuddin (42 shared papers)Edward R. Wilcox (21 shared papers)Gregory I. Frolenkov (14 shared papers)
- Journals
- Human Genetics (13 papers)The American Journal of Human Genetics (11 papers)Science (8 papers)Journal of Medical Genetics (7 papers)Human Mutation (7 papers)
- Partner nations
- United StatesPakistanUnited Kingdom
In The Last Decade
Thomas B. Friedman
187 papers receiving 10.5k citations
Peers
Comparison fields: 5 of 185
- Sensory Systems 6.5k
- Neurology 2.2k
- Otorhinolaryngology 789
- Molecular Biology 5.7k
- Endocrine and Autonomic Systems 472
Countries citing papers authored by Thomas B. Friedman
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
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-authors
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.
All Works
Showing the 20 most-cited of 192 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1998 | 447 | |
| 2 | 2001 | 374 | |
| 3 | 1998 | 358 | |
| 4 | 1998 | 356 | |
| 5 | 2001 | 341 | |
| 6 | 2005 | 293 | |
| 7 | 1998 | 280 | |
| 8 | 2006 | 235 | |
| 9 | 2006 | 228 | |
| 10 | 2002 | 225 | |
| 11 | 2003 | 202 | |
| 12 | 2003 | 182 | |
| 13 | 1995 | 177 | |
| 14 | 2004 | 174 | |
| 15 | 2004 | 171 | |
| 16 | 2003 | 163 | |
| 17 | 2010 | 158 | |
| 18 | 2007 | 158 | |
| 19 | 2010 | 156 | |
| 20 | 2000 | 152 |
About Thomas B. Friedman
Thomas B. Friedman is a scholar working on Sensory Systems, Molecular Biology, Neurology, Cell Biology and Cognitive Neuroscience, having authored 192 papers that have together received 10.9k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (114 papers), Vestibular and auditory disorders (31 papers), RNA regulation and disease (22 papers), Connexins and lens biology (20 papers), Hearing Loss and Rehabilitation (16 papers), RNA and protein synthesis mechanisms (15 papers), Muscle Physiology and Disorders (13 papers) and Congenital heart defects research (12 papers). The work is most often cited by research in Sensory Systems (6.5k citations), Neurology (2.2k citations), Otorhinolaryngology (789 citations), Molecular Biology (5.7k citations) and Endocrine and Autonomic Systems (472 citations). Thomas B. Friedman has collaborated with scholars based in United States, Pakistan and United Kingdom. Frequent co-authors include Inna A. Belyantseva, Andrew J. Griffith, Robert J. Morell, Zubair M. Ahmed, Sheikh Riazuddin, Saima Riazuddin, Edward R. Wilcox, Gregory I. Frolenkov, Erich T. Boger and James H. Asher. Their work appears in journals such as Human Genetics, The American Journal of Human Genetics, Science, Journal of Medical 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.