Rick A. Friedman

2.6k total citations
53 papers, 1.7k citations indexed

About

Rick A. Friedman is a scholar working on Sensory Systems, Neurology and Cognitive Neuroscience. According to data from OpenAlex, Rick A. Friedman has authored 53 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Sensory Systems, 13 papers in Neurology and 12 papers in Cognitive Neuroscience. Recurrent topics in Rick A. Friedman's work include Hearing, Cochlea, Tinnitus, Genetics (40 papers), Vestibular and auditory disorders (13 papers) and Hearing Loss and Rehabilitation (12 papers). Rick A. Friedman is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (40 papers), Vestibular and auditory disorders (13 papers) and Hearing Loss and Rehabilitation (12 papers). Rick A. Friedman collaborates with scholars based in United States, Brazil and China. Rick A. Friedman's co-authors include Laurel M. Fisher, Lawrence C. Erway, Jeffrey D. Ohmen, William H. Slattery, Nancy Liu, Zarina Iqbal, Marian L. Miller, John Duffy, Lynne H. Liu and Tara M. Riddle and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and Neurology.

In The Last Decade

Rick A. Friedman

52 papers receiving 1.7k citations

Peers

Rick A. Friedman

NEURO

OTORH

Tatsuo Matsunaga Japan

Ronna Hertzano United States

Shiming Yang China

Anil K. Lalwani United States

Hashem Shahin Palestinian Territory

Huawei Li China

Hubert Löwenheim Germany

Markus Pfister Germany

Kazuo Oshima Japan

Kunihiro Fukushima Japan

Tatsuo Matsunaga Japan

Rick A. Friedman

1.1k ×1.2

760 ×1.1

446 ×1.0

NEURO

319 ×1.4

268 ×1.2

OTORH

Citations per year, relative to Rick A. Friedman Rick A. Friedman (= 1×) peers Tatsuo Matsunaga

Countries citing papers authored by Rick A. Friedman

Since Specialization

Citations

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

Fields of papers citing papers by Rick A. Friedman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rick A. Friedman

This figure shows the co-authorship network connecting the top 25 collaborators of Rick A. Friedman. A scholar is included among the top collaborators of Rick A. 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 Rick A. Friedman. Rick A. Friedman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Fisch, Kathleen M., Sara Brin Rosenthal, Adam Mark, et al.. (2024). The genomic landscape of Ménière's disease: a path to endolymphatic hydrops. BMC Genomics. 25(1). 646–646. 5 indexed citations

Novotny, Mark, Yuzuru Ninoyu, Eric Y. Du, et al.. (2023). Cochlear transcriptome analysis of an outbred mouse population (CFW). Frontiers in Cellular Neuroscience. 17. 1256619–1256619. 5 indexed citations

Currais, António, et al.. (2023). Attenuation of Age-Related Hearing Impairment in Senescence-Accelerated Mouse Prone 8 (SAMP8) Mice Treated with Fatty Acid Synthase Inhibitor CMS121. Journal of Molecular Neuroscience. 73(4-5). 307–315. 6 indexed citations

Du, Eric Y., et al.. (2022). Genetics of noise-induced hearing loss in the mouse model. Hearing Research. 425. 108505–108505. 7 indexed citations

Ninoyu, Yuzuru, Cayla M. Miller, Leonardo R. Andrade, et al.. (2022). Cochlear ribbon synapse maturation requires Nlgn1 and Nlgn3. iScience. 25(8). 104803–104803. 7 indexed citations

Du, Eric Y., et al.. (2022). Large-scale phenotyping and characterization of age-related hearing loss in outbred CFW mice. Hearing Research. 424. 108605–108605. 4 indexed citations

Lavinsky, Joel, et al.. (2021). Large-scale phenotyping of ABR P1-N1 amplitudes before and after exposure to noise in 69 strains of mice. Mammalian Genome. 32(6). 427–434. 2 indexed citations

Lavinsky, Joel, et al.. (2021). Noise Exposure and Distortion Product Otoacoustic Emission Suprathreshold Amplitudes: A Genome-Wide Association Study. Audiology and Neurotology. 26(6). 445–453. 3 indexed citations

Schrauwen, Isabelle, Elina Kari, Lorida Llaci, et al.. (2018). De novo variants in GREB1L are associated with non-syndromic inner ear malformations and deafness. Human Genetics. 137(6-7). 459–470. 28 indexed citations

10.

Kode, Aruna, Ioanna Mosialou, Chozhavendan Rathinam, et al.. (2015). FoxO1-dependent induction of acute myeloid leukemia by osteoblasts in mice. Leukemia. 30(1). 1–13. 73 indexed citations

11.

Lavinsky, Joel, Calvin Pan, Ksenia A. Aaron, et al.. (2015). Genome-Wide Association Study Identifies Nox3 as a Critical Gene for Susceptibility to Noise-Induced Hearing Loss. PLoS Genetics. 11(4). e1005094–e1005094. 62 indexed citations

12.

White, Cory, et al.. (2015). Large-scale phenotyping of noise-induced hearing loss in 100 strains of mice. Hearing Research. 332. 113–120. 22 indexed citations

13.

Ohmen, Jeffrey D., et al.. (2014). FVB/NJ Mice Demonstrate a Youthful Sensitivity to Noise-Induced Hearing Loss and Provide a Useful Genetic Model for the Study of Neural Hearing Loss. PubMed. 4(1). 1–11. 10 indexed citations

14.

Hilgert, Nele, et al.. (2009). Amino acid 572 in TMC1: hot spot or critical functional residue for dominant mutations causing hearing impairment. Journal of Human Genetics. 54(3). 188–190. 12 indexed citations

15.

White, Cory, Jeffrey D. Ohmen, Sonal S. Sheth, et al.. (2009). Genome-wide screening for genetic loci associated with noise-induced hearing loss. Mammalian Genome. 20(4). 207–213. 25 indexed citations

16.

Friedman, Rick A., et al.. (2006). Genetics of hearing loss: Allelism and modifier genes produce a phenotypic continuum. The Anatomical Record Part A Discoveries in Molecular Cellular and Evolutionary Biology. 288A(4). 370–381. 24 indexed citations

17.

Gold, David, Tiffany Poon, Xiaobo Wang, et al.. (2003). A natural allele of Nxf1 suppresses retrovirus insertional mutations. Nature Genetics. 35(3). 221–228. 32 indexed citations

18.

Friedman, Rick A., et al.. (2002). Nonsyndromic hereditary hearing loss. Otolaryngologic Clinics of North America. 35(2). 275–285. 13 indexed citations

19.

Johnson, Keith R., Susan A. Cook, Lawrence C. Erway, et al.. (1999). Inner Ear and Kidney Anomalies Caused by IAP Insertion in an Intron of the Eya1 Gene in a Mouse Model of BOR Syndrome. Human Molecular Genetics. 8(4). 645–653. 71 indexed citations

20.

Friedman, Rick A., Yelena Bykhovskaya, Carolyn M. Sue, et al.. (1999). Maternally inherited nonsyndromic hearing loss. American Journal of Medical Genetics. 84(4). 369–372. 37 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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