Prasad S - Search Results

1

Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31.

Greinwald JH Jr, Wayne S, Chen AH, Scott DA, Zbar RI, Kraft ML, Prasad S, Ramesh A, Coucke P, Srisailapathy CR, Lovett M, Van Camp G, Smith RJ. Greinwald JH Jr, et al. Among authors: prasad s. Am J Med Genet. 1998 Jun 30;78(2):107-13. Am J Med Genet. 1998. PMID: 9674898

2

Pendred syndrome and DFNB4-mutation screening of SLC26A4 by denaturing high-performance liquid chromatography and the identification of eleven novel mutations.

Prasad S, Kölln KA, Cucci RA, Trembath RC, Van Camp G, Smith RJ. Prasad S, et al. Am J Med Genet A. 2004 Jan 1;124A(1):1-9. doi: 10.1002/ajmg.a.20272. Am J Med Genet A. 2004. PMID: 14679580

3

Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.

Wayne S, Robertson NG, DeClau F, Chen N, Verhoeven K, Prasad S, Tranebjärg L, Morton CC, Ryan AF, Van Camp G, Smith RJ. Wayne S, et al. Among authors: prasad s. Hum Mol Genet. 2001 Feb 1;10(3):195-200. doi: 10.1093/hmg/10.3.195. Hum Mol Genet. 2001. PMID: 11159937

4

Presymptomatic diagnosis of nonsyndromic hearing loss by genotyping.

Chen AH, Mueller RF, Prasad SD, Greinwald JH Jr, Manaligod J, Muilenburg AC, Verhoeven K, Van Camp G, Smith RJ. Chen AH, et al. Among authors: prasad sd. Arch Otolaryngol Head Neck Surg. 1998 Jan;124(1):20-4. doi: 10.1001/archotol.124.1.20. Arch Otolaryngol Head Neck Surg. 1998. PMID: 9440775 Review.

5

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13).

McGuirt WT, Prasad SD, Griffith AJ, Kunst HP, Green GE, Shpargel KB, Runge C, Huybrechts C, Mueller RF, Lynch E, King MC, Brunner HG, Cremers CW, Takanosu M, Li SW, Arita M, Mayne R, Prockop DJ, Van Camp G, Smith RJ. McGuirt WT, et al. Among authors: prasad sd. Nat Genet. 1999 Dec;23(4):413-9. doi: 10.1038/70516. Nat Genet. 1999. PMID: 10581026

6

Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment.

Verhoeven K, Fagerheim T, Prasad S, Wayne S, De Clau F, Balemans W, Verstreken M, Schatteman I, Solem B, Van de Heyning P, Tranebjärg L, Smith RJ, Van Camp G. Verhoeven K, et al. Among authors: prasad s. Hum Genet. 2000 Jul;107(1):7-11. doi: 10.1007/s004390000319. Hum Genet. 2000. PMID: 10982027

7

Genetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA).

Prasad S, Cucci RA, Green GE, Smith RJ. Prasad S, et al. Hum Mutat. 2000 Dec;16(6):502-8. doi: 10.1002/1098-1004(200012)16:6<502::AID-HUMU7>3.0.CO;2-4. Hum Mutat. 2000. PMID: 11102979

8

A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment.

Van Laer L, Coucke P, Mueller RF, Caethoven G, Flothmann K, Prasad SD, Chamberlin GP, Houseman M, Taylor GR, Van de Heyning CM, Fransen E, Rowland J, Cucci RA, Smith RJ, Van Camp G. Van Laer L, et al. Among authors: prasad sd. J Med Genet. 2001 Aug;38(8):515-8. doi: 10.1136/jmg.38.8.515. J Med Genet. 2001. PMID: 11483639 Free PMC article.

9

Genotype-phenotype correlations for SLC26A4-related deafness.

Azaiez H, Yang T, Prasad S, Sorensen JL, Nishimura CJ, Kimberling WJ, Smith RJ. Azaiez H, et al. Among authors: prasad s. Hum Genet. 2007 Dec;122(5):451-7. doi: 10.1007/s00439-007-0415-2. Epub 2007 Aug 10. Hum Genet. 2007. PMID: 17690912 Free PMC article.

10

The M34T allele variant of connexin 26.

Cucci RA, Prasad S, Kelley PM, Green GE, Storm K, Willocx S, Cohn ES, Van Camp G, Smith RJ. Cucci RA, et al. Among authors: prasad s. Genet Test. 2000;4(4):335-44. doi: 10.1089/109065700750065063. Genet Test. 2000. PMID: 11216656

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