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Rick Adam Friedman

Observed names: A Friedman, Rick, Friedman, Rick A., R Friedman, R. A. Friedman, R. Friedman, Rick A Friedman, Rick A. Friedman, Rick Friedman
Observed institutions: University of Southern California, Cedars-Sinai Medical Center, Translational Genomics Research Institute, Universidade Federal do Rio Grande do Sul, House Clinic, University of California, Los Angeles, UC San Diego Health System, University of California San Diego, Vall d'Hebron Hospital Universitari, University of California San Diego Medical Center, University of Cincinnati, Columbia University
ORCID: 0000-0002-5490-8562
Observed ORCIDs: 0000-0002-5490-8562, 0000-0001-8921-4459
OpenAlex ID: A5111987614
Balance and Hearing Deficits in Mice with a Null Mutation in the Gene Encoding Plasma Membrane Ca2+-ATPase Isoform 2
1998 · Peter J. Kozel, Rick A. Friedman, et al. · Journal of Biological Chemistry · 306
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GRM7 variants confer susceptibility to age-related hearing impairment
2008 · Rick A. Friedman, Lut Van Laer, et al. · Human Molecular Genetics · 209
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Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA Ser(UCN) gene
1999 · C.M. Sue, K. Tanji, et al. · Neurology · 165
Hybrid mouse diversity panel: a panel of inbred mouse strains suitable for analysis of complex genetic traits
2012 · Anatole Ghazalpour, Christoph D. Rau, et al. · Mammalian Genome · 144
Intratympanic Steroid Injection for Treatment of Idiopathic Sudden Hearing Loss
2005 · William H. Slattery, Laurel M. Fisher, et al. · Otolaryngology · 142
Ruffling membrane, stress fiber, cell spreading and proliferation abnormalities in human Schwannoma cells
1998 · Patricia D Pelton, Larry S Sherman, et al. · Oncogene · 128
Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment
2014 · Erik Fransen, Sarah Bonneux, et al. · European Journal of Human Genetics · 100
Inner Ear and Kidney Anomalies Caused by IAP Insertion in an Intron of the Eya1 Gene in a Mouse Model of BOR Syndrome
1999 · K. R. Johnson, S. A. Cook, et al. · Human Molecular Genetics · 88
GRM7 variants associated with age-related hearing loss based on auditory perception
2012 · Dina L. Newman, Laurel M. Fisher, et al. · Hearing Research · 85
Genome-Wide Association Study Identifies Nox3 as a Critical Gene for Susceptibility to Noise-Induced Hearing Loss
2015 · Joel Lavinsky, Amanda L. Crow, et al. · PLoS Genetics · 80
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The Development of Antibiotic Resistant Organisms with the Use of Ototopical Medications
2004 · Peter C. Weber, Peter S. Roland, et al. · Otolaryngology · 72
Advances in understanding of presbycusis
2019 · Kareem O. Tawfik, Kristin Klepper, et al. · Journal of Neuroscience Research · 68
Ototoxicity of Ototopical Antibiotic Drops in Humans
2004 · Greg Matz, Leonard Rybak, et al. · Otolaryngology · 61
Genetic Evidence for an Ethnic Diversity in the Susceptibility to Ménière’s Disease
2013 · Jeffrey Douglass Ohmen, Cory H. White, et al. · Otology & Neurotology · 54
Maternally inherited nonsyndromic hearing loss
1999 · Rick A. Friedman, Yelena Bykhovskaya, et al. · American Journal of Medical Genetics · 51
De novo variants in GREB1L are associated with non-syndromic inner ear malformations and deafness
2018 · Isabelle Schrauwen, Elina Kari, et al. · Human Genetics · 45
Animal Ototoxicity of Topical Antibiotics and the Relevance to Clinical Treatment of Human Subjects
2004 · Peter S. Roland, Leonard Rybak, et al. · Otolaryngology · 44
Mutations of MAP1B encoding a microtubule-associated phosphoprotein cause sensorineural hearing loss
2020 · Limei Cui, Jing Zheng, et al. · JCI Insight · 41
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Prognostic implications of and audiometric evidence for hearing fluctuation in M eniere's disease
2015 · Michael Hoa, Rick A. Friedman, et al. · The Laryngoscope · 40
Molecular Analysis of the Pou3F4 Gene in Patients with Clinical and Radiographic Evidence of X-Linked Mixed Deafness with Perilymphatic Gusher
1997 · Yelena Bykhovskaya, David F. Wilson, et al. · Annals of Otology Rhinology & Laryngology · 39
A natural allele of Nxf1 suppresses retrovirus insertional mutations
2003 · Jennifer A Floyd, David A Gold, et al. · Nature Genetics · 38
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Genome-Wide Association Study for Age-Related Hearing Loss (AHL) in the Mouse: A Meta-Analysis
2014 · Jeffrey Ohmen, Eun Yong Kang, et al. · Journal of the Association for Research in Otolaryngology · 34
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Eya1 acts upstream of Tbx1, Neurogenin 1, NeuroD and the neurotrophins BDNF and NT-3 during inner ear development
2005 · Rick A. Friedman, Linna Makmura, et al. · Mechanisms of Development · 34
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Large-scale phenotyping of noise-induced hearing loss in 100 strains of mice
2015 · Anthony Myint, Cory H. White, et al. · Hearing Research · 31
Oral Steroid Treatment for Hearing Improvement in Ménière’s Disease and Endolymphatic Hydrops
2012 · Laurel M. Fisher, M. Jennifer Derebery, et al. · Otology & Neurotology · 31
Works count: 74
Citation count: 2,562
H-index: 28
I10-index: 45
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