Rick A. Friedman - Concepedia

Author

Rick A. Friedman

Also Known As

R A Friedman, R Friedman, R. A. Friedman, R. Friedman, Rick A Friedman, Rick A. Friedman, Rick Adam Friedman, Rick Friedman

Publications

2.6K

Citations

H-Index

Concepts

All Affiliations

House Clinic University of Southern California University of California San Diego University of California, Los Angeles National Institute on Deafness and Other Communication Disorders

About

Rick A. Friedman is an author at House Clinic specializing in hearing loss, medicine, and audiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	444
2	Arts	8	8	434
3	Health Sciences	3	3	200
4	Public Health	2	2	188
5	Natural Sciences	1	1	16

Rick A. Friedman

Publications

Citations

H-Index

Page 1

	Year	Citations
Balance and Hearing Deficits in Mice with a Null Mutation in the Gene Encoding Plasma Membrane Ca2+-ATPase Isoform 2 Peter Kozel, Rick A. Friedman, Lawrence C. Erway, Journal of Biological Chemistry	1998	304
GRM7 variants confer susceptibility to age-related hearing impairment Rick A. Friedman, Lut Van Laer, Matthew J. Huentelman, Human Molecular Genetics	2008	208
Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA <sup>Ser(UCN)</sup> gene Carolyn M. Sue, Kurenai Tanji, George Hadjigeorgiou, Neurology	1999	162
Intratympanic Steroid Injection for Treatment of Idiopathic Sudden Hearing Loss William H. Slattery, Laurel M. Fisher, Zarina Iqbal, Otolaryngology	2005	141
Ruffling membrane, stress fiber, cell spreading and proliferation abnormalities in human Schwannoma cells Patricia D. Pelton, Larry S. Sherman, Tilat A. Rizvi, Oncogene Stress FiberCell SpreadingCell InteractionVestibular SchwannomaHuman Schwannoma Cells	1998	127
Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment Erik Fransén, Sarah Bonneux, Jason J. Corneveaux, European Journal of Human Genetics Genome-wide Association StudyPolygenic CharacterGeneticsGenetic EpidemiologyAudiology	2014	102
Inner Ear and Kidney Anomalies Caused by IAP Insertion in an Intron of the Eya1 Gene in a Mouse Model of BOR Syndrome Keith R. Johnson, Susan A. Cook, Lawrence C. Erway, Human Molecular Genetics	1999	89
FoxO1-dependent induction of acute myeloid leukemia by osteoblasts in mice Aruna Kode, Ioanna Mosialou, Sridharan Manavalan, Leukemia Hematological MalignancyAcute Myeloid LeukemiaMalignant Blood DisorderHematologyMyeloid Neoplasia	2015	87
Genome-Wide Association Study Identifies Nox3 as a Critical Gene for Susceptibility to Noise-Induced Hearing Loss Joel Lavinsky, Amanda L. Crow, Calvin Pan, PLoS Genetics GeneticsGenetic EpidemiologyUnited StatesGenome-wide Association StudyNoise	2015	86
GRM7 variants associated with age-related hearing loss based on auditory perception Dina L. Newman, Laurel M. Fisher, Jeffrey D. Ohmen, Hearing Research Auditory ProcessingAge-related Hearing LossHealth SciencesAudiologyAuditory Physiology	2012	82

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