Friedman RA - Search Results

1

GRM7 variants confer susceptibility to age-related hearing impairment.

Friedman RA, Van Laer L, Huentelman MJ, Sheth SS, Van Eyken E, Corneveaux JJ, Tembe WD, Halperin RF, Thorburn AQ, Thys S, Bonneux S, Fransen E, Huyghe J, Pyykkö I, Cremers CW, Kremer H, Dhooge I, Stephens D, Orzan E, Pfister M, Bille M, Parving A, Sorri M, Van de Heyning PH, Makmura L, Ohmen JD, Linthicum FH Jr, Fayad JN, Pearson JV, Craig DW, Stephan DA, Van Camp G. Friedman RA, et al. Hum Mol Genet. 2009 Feb 15;18(4):785-96. doi: 10.1093/hmg/ddn402. Epub 2008 Dec 1. Hum Mol Genet. 2009. PMID: 19047183 Free PMC article.

2

Prognostic factors for hearing preservation in vestibular schwannoma surgery.

Brackmann DE, Owens RM, Friedman RA, Hitselberger WE, De la Cruz A, House JW, Nelson RA, Luxford WM, Slattery WH 3rd, Fayad JN. Brackmann DE, et al. Among authors: friedman ra. Am J Otol. 2000 May;21(3):417-24. doi: 10.1016/s0196-0709(00)80054-x. Am J Otol. 2000. PMID: 10821558 Review.

3

Early proactive management of vestibular schwannomas in neurofibromatosis type 2.

Brackmann DE, Fayad JN, Slattery WH 3rd, Friedman RA, Day JD, Hitselberger WE, Owens RM. Brackmann DE, et al. Among authors: friedman ra. Neurosurgery. 2001 Aug;49(2):274-80; discussion 280-3. doi: 10.1097/00006123-200108000-00007. Neurosurgery. 2001. PMID: 11504103

4

Eya1 acts upstream of Tbx1, Neurogenin 1, NeuroD and the neurotrophins BDNF and NT-3 during inner ear development.

Friedman RA, Makmura L, Biesiada E, Wang X, Keithley EM. Friedman RA, et al. Mech Dev. 2005 May;122(5):625-34. doi: 10.1016/j.mod.2004.12.011. Epub 2005 Jan 8. Mech Dev. 2005. PMID: 15817220 Free article.

5

Identification of two major loci that suppress hearing loss and cochlear dysmorphogenesis in Eya1bor/bor mice.

Niu H, Makmura L, Shen T, Sheth SS, Blair K, Friedman RA. Niu H, et al. Among authors: friedman ra. Genomics. 2006 Sep;88(3):302-8. doi: 10.1016/j.ygeno.2006.01.005. Epub 2006 Feb 20. Genomics. 2006. PMID: 16488112 Free article.

6

Mapping of genetic modifiers of Eya1 ( bor/bor ) in CAST/EiJ and BALB/cJ that suppress cochlear aplasia and associated deafness.

Niu H, Li X, Makmura L, Friedman RA. Niu H, et al. Among authors: friedman ra. Mamm Genome. 2008 Sep;19(9):634-9. doi: 10.1007/s00335-008-9145-6. Epub 2008 Oct 4. Mamm Genome. 2008. PMID: 18836772

7

Amino acid 572 in TMC1: hot spot or critical functional residue for dominant mutations causing hearing impairment.

Hilgert N, Monahan K, Kurima K, Li C, Friedman RA, Griffith AJ, Van Camp G. Hilgert N, et al. Among authors: friedman ra. J Hum Genet. 2009 Mar;54(3):188-90. doi: 10.1038/jhg.2009.1. Epub 2009 Jan 30. J Hum Genet. 2009. PMID: 19180119 Free PMC article.

8

Genome-wide screening for genetic loci associated with noise-induced hearing loss.

White CH, Ohmen JD, Sheth S, Zebboudj AF, McHugh RK, Hoffman LF, Lusis AJ, Davis RC, Friedman RA. White CH, et al. Among authors: friedman ra. Mamm Genome. 2009 Apr;20(4):207-13. doi: 10.1007/s00335-009-9178-5. Epub 2009 Apr 1. Mamm Genome. 2009. PMID: 19337678 Free PMC article.

9

Evolution in the management of facial nerve schwannoma.

Wilkinson EP, Hoa M, Slattery WH 3rd, Fayad JN, Friedman RA, Schwartz MS, Brackmann DE. Wilkinson EP, et al. Among authors: friedman ra. Laryngoscope. 2011 Oct;121(10):2065-74. doi: 10.1002/lary.22141. Epub 2011 Sep 6. Laryngoscope. 2011. PMID: 21898431

10

Hearing preservation with the middle cranial fossa approach for neurofibromatosis type 2.

Friedman RA, Goddard JC, Wilkinson EP, Schwartz MS, Slattery WH 3rd, Fayad JN, Brackmann DE. Friedman RA, et al. Otol Neurotol. 2011 Dec;32(9):1530-7. doi: 10.1097/MAO.0b013e3182355855. Otol Neurotol. 2011. PMID: 21986931

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