RickAFriedmanMDPhD

PubMed

• 140 citations
  GRM7 variants confer susceptibility to age-related hearing impairment
  Rick A. Friedman, Lut Van Laer, Matthew J. Huentelman, Sonal S. Sheth, Els Van Eyken
  Human Molecular Genetics. 2009-02-15
• 1108 citations
  TGFbeta2 knockout mice have multiple developmental defects that are non-overlapping with other TGFbeta knockout phenotypes
  L P Sanford, Ilona Ormsby, A C Gittenberger-de Groot, H Sariola, Rick A. Friedman
  Development. 1997-07-01
• 109 citations
  Hybrid mouse diversity panel: a panel of inbred mouse strains suitable for analysis of complex genetic traits.
  Anatole Ghazalpour, Christoph Rau, Charles R. Farber, Brian J. Bennett, Luz D. Orozco
  Mammalian Genome. 2012-08-15

Journal Articles

• 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  
  Ho MK, Li X, Wang J, Ohmen JD, Friedman RA, Audiol Neurotol Extra, 1/1/2014
• Total ossiculoplasty: short-and long-term results using a titanium prosthesis with footplate shoe  
  Fayad JN, Ursick J, Brackmann DE, Friedman RA, Otol Neurotol, 1/1/2014
• Evaluation of the increased use of partial resection of large vestibular schwanommas: facial nerve outcomes and recurrence/growth rates  
  Schwartz MS, Kari E, strickland BM, Berliner K, Brackmann DE, House JW, Friedman RA, Otol Neurotol, 10/1/2013
• Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Menière's disease  
  Gazquez I, Moreno A, Requena T, Ohmen J, Santos-Perez S, Aran I, Soto-Varela A, Perez-Garrigues H, Lpez-Nevot A, Batuecas A, Friedman RA, Lopez-Nevot MA, Lopez-Escamez JA, Eur Arch Otorhinolaryngol, 3/1/2013
• Genome-wide association analysis of age-related hearing loss in the mouse: A meta-analysis  
  Jeffrey Ohmen, Eun Yong Kang, Xin Li, Jong Wha Joo, Farhad Hormozdiari, Qing Yin Zheng, Richard Davis, Aldons J. Lusis, Eleazar Eskin, and Rick Friedman, JARO, 1/1/2013
• Imaging case of the month: Fibrous dysplasia causing superior canal dehiscence  
  Goddard JC, Go JL, Friedman RA, Otol Neurotol, 1/1/2013
• Surgical Management of Endolymphatic Sac Tumors  
  Friedman, RA.; Hoa, Michael; Brackmann, Derald E, Journal of Neurological Surgery Part B: Skull Base, 1/1/2012
• Genome-wide Screening for Genetic Loci Associated with Noise-Induced Hearing Loss  
  White, C.H., Ohmen, J.D., Sheth, S., Zebboudj, A., McHugh, R.K., Hoffman, L.F., Lusis, A.J., Davis, R.C., Friedman, RA, Mammalian Genome, 1/1/2009
• Mapping of genetic modifiers of Eya1bor/bor in CAst/EiJ and BALB/cJ that suppress cochlear aplasia and associated deafness  
  Niu H, Li Xin, Makmura L, Friedman RA, Mammalian Genome, 1/1/2008
• Identification of two major loci that suppress hearing loss and cochlear dysmorphogenesis in Eya1(bor/bor) mice  
  Niu H, Makmura L, Shen T, Sheth SS, Blair K, Friedman RA, Genomics, 9/1/2006
• Neurotologic Skull Base surgery in pediatric patients  
  Cunningham, Calhoun D. III; Friedman, Rick A.; Brackmann, Derald E.; Hitselberger, William E.; Lin, Harrison W, Otology and Neurotology, 3/1/2005
• Evolution of the management of petroclival meningioma  
  Shen T, Friedman RA, Brackmann DE, Slattery WE, Hitselberger WE, Schwartz M, Otol Neurotol, 5/1/2004
• Long-term hearing preservation after middle fossa removal of vestibular schwannoma  
  Friedman RA, Kesser B, Brackmann DE, Fisher LM, Slattery WH, Hitselberger WE, Otolaryngoly Head Neck Surg, 12/1/2003
• A natural allele of NxF1/TAP suppresses retroviral insertional mutations  
  Floyd JA, Gold DA, Concepcion D, Poon th, Wand X, Keithley E, Chen D, Ward EJ, Chinn SB, Friedman RA, Yu H, Moriwaki K, Shiroishi T, Hamilton BA, Nat Genet, 11/1/2003
• Hereditary Hearing Loss  
  Li XC, Friedman RA, the Otolaryngologic Clinics of North America, 4/1/2002
• Hearing preservation in patients with sudden hearing loss and vestibular schwannoma  
  Friedman RA, Kesser B, Brackmann DE, Hitselberger WE, Otol Head Neck Surg, 1/1/2001
• the middle cranial fossa approach to vestibular schwannomas  
  Friedman RA, Brackmann DE, Operative Techniques in Neurosurgery, 1/1/2001
• Prognostic factors for hearing preservation in middle fossa acoustic tumor surgery  
  Brackmann DE, Owens R, Friedman RA, Slattery WH, Hitselberger WE, House JW, Luxford WM, DelaCruz A, Nelson RA, Fayad J, Am J Otol, 1/1/2000
• Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) gene  
  Sue CM, Tanji K, Hadjigeorgiou G, Andreu AL, Nishino I, Krishna S, Bruno C, Hirano M, Shanske S, Bonilla E, Fischel-Ghodsian N, DiMauro S, Friedman RA, Neurology, 6/10/1999
• Maternally Inherited Non-syndromic Hearing Loss  
  Friedman RA, Bykhovskaya Y, Sue CM, DiMauro S, Bradley R, Fallis R, Paradies N, Pensak ML, Smith RJ, Groden J, Li XC, Fischel-Ghodsian N, Am J Med Genet, 6/1/1999
• Transcochlear Approach  
  Friedman RA, Brackmann DE, Operative Techniques in Neurosurgery, 5/1/1999
• Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome  
  Johnson, KR; Cook, SA; Erway, LC; Matthews, AN; Sanford, LP; Paradies, NE; Friedman, RA, Human Molecular Genetics, 4/1/1999
• An analysis of a large postlingually deaf family with hereditary non-syndromic profound hearing loss  
  Angeli SI, Naranjo c, Friedman RA, Naranjo A, Henríquez O, Fischel-Ghodsian N, Chiossone E, Acta Otolaryngol (stockh), 3/1/1999
• Trigeminal schwannomas: the role of the neurotologist in their multi-disciplinary management  
  Friedman RA, Pensak ML, Osterhus DR, Tew JM, Jr., van Loveren HR, Otol Head Neck Surg, 1/1/1999
• Trigeminal Neuroma: Imaging case of the month  
  Osterhaus DR, Van Loveren HR, Friedman RA, Am J Otol, 1/1/1999
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