TB Friedman

566 total citations
9 papers, 407 citations indexed

About

TB Friedman is a scholar working on Sensory Systems, Neurology and Molecular Biology. According to data from OpenAlex, TB Friedman has authored 9 papers receiving a total of 407 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Sensory Systems, 4 papers in Neurology and 3 papers in Molecular Biology. Recurrent topics in TB Friedman's work include Hearing, Cochlea, Tinnitus, Genetics (7 papers), Vestibular and auditory disorders (4 papers) and Ear Surgery and Otitis Media (3 papers). TB Friedman is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (7 papers), Vestibular and auditory disorders (4 papers) and Ear Surgery and Otitis Media (3 papers). TB Friedman collaborates with scholars based in United States, Pakistan and Spain. TB Friedman's co-authors include AJ Griffith, Saima Riazuddin, Tomoko Makishima, Tayyab Husnaın, J. Amos, Lindsay A. Farrer, Peter Beighton, Mohsin Shahzad, Sheikh Riazuddin and Ryan P. McNamara and has published in prestigious journals such as Clinical Genetics, Oral Diseases and PubMed.

In The Last Decade

TB Friedman

9 papers receiving 397 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
TB Friedman United States	9	260	238	110	81	49	9	407
Valerie A. Street United States	11	211 0.8×	334 1.4×	109 1.0×	88 1.1×	46 0.9×	14	570
Xuezhong Liu United States	11	350 1.3×	461 1.9×	87 0.8×	107 1.3×	77 1.6×	14	659
Sigrid Wayne United States	11	364 1.4×	344 1.4×	115 1.0×	36 0.4×	55 1.1×	19	543
Theru A. Sivakumaran United States	7	218 0.8×	188 0.8×	65 0.6×	93 1.1×	59 1.2×	12	441
Kris Flothmann Belgium	8	233 0.9×	237 1.0×	90 0.8×	113 1.4×	68 1.4×	8	409
Steve D.M. Brown United Kingdom	7	316 1.2×	354 1.5×	106 1.0×	34 0.4×	68 1.4×	8	522
Meghan C. Drummond United States	8	271 1.0×	242 1.0×	72 0.7×	36 0.4×	48 1.0×	10	409
Julie M. Schultz United States	10	321 1.2×	284 1.2×	122 1.1×	41 0.5×	39 0.8×	12	470
Steven J. H. Bom Netherlands	12	268 1.0×	125 0.5×	172 1.6×	51 0.6×	41 0.8×	20	392
Xiuhong Pang China	13	203 0.8×	185 0.8×	71 0.6×	47 0.6×	38 0.8×	25	323

Countries citing papers authored by TB Friedman

Since Specialization

Citations

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

Fields of papers citing papers by TB Friedman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of TB Friedman

This figure shows the co-authorship network connecting the top 25 collaborators of TB Friedman. A scholar is included among the top collaborators of TB Friedman 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 TB Friedman. TB Friedman 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:

9 of 9 papers shown

1.

Friedman, TB, et al.. (2016). Unresolved questions regarding human hereditary deafness. Oral Diseases. 23(5). 551–558. 21 indexed citations

2.

Riazuddin, Saima, et al.. (2009). Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan. Clinical Genetics. 75(3). 237–243. 79 indexed citations

3.

Waryah, Ali Muhammad, et al.. (2009). DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2‐q15. Clinical Genetics. 76(3). 270–275. 11 indexed citations

4.

Riazuddin, Saima, et al.. (2008). USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22‐23. Clinical Genetics. 75(1). 86–91. 31 indexed citations

5.

Peters, Linda, et al.. (2008). A locus for autosomal dominant progressive non‐syndromic hearing loss, DFNA27, is on chromosome 4q12‐13.1. Clinical Genetics. 73(4). 367–372. 14 indexed citations

6.

Makishima, Tomoko, et al.. (2007). A novel mutation at the DFNA36 hearing loss locus reveals a critical function and potential genotype–phenotype correlation for amino acid‐572 of TMC1. Clinical Genetics. 71(2). 148–152. 42 indexed citations

7.

McNamara, Ryan P., Tomoko Makishima, Tayyab Husnaın, et al.. (2007). Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan. Clinical Genetics. 72(6). 546–550. 55 indexed citations

8.

Labay, Valentina, Gema Garrido, Anne C. Madeo, et al.. (2007). Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA^Ser(UCN) in sensorineural hearing loss. Clinical Genetics. 73(1). 50–54. 11 indexed citations

9.

Farrer, Lindsay A., et al.. (1992). Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium.. PubMed. 50(5). 902–13. 143 indexed citations

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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