Alasti F - Search Results

1

Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus.

Meyer NC, Alasti F, Nishimura CJ, Imanirad P, Kahrizi K, Riazalhosseini Y, Malekpour M, Kochakian N, Jamali P, Van Camp G, Smith RJ, Najmabadi H. Meyer NC, et al. Among authors: alasti f. Am J Med Genet A. 2007 Jul 15;143A(14):1623-9. doi: 10.1002/ajmg.a.31718. Am J Med Genet A. 2007. PMID: 17431902

2

A novel DFNA5 mutation does not cause hearing loss in an Iranian family.

Van Laer L, Meyer NC, Malekpour M, Riazalhosseini Y, Moghannibashi M, Kahrizi K, Vandevelde A, Alasti F, Najmabadi H, Van Camp G, Smith RJH. Van Laer L, et al. Among authors: alasti f. J Hum Genet. 2007;52(6):549-552. doi: 10.1007/s10038-007-0137-2. Epub 2007 Apr 11. J Hum Genet. 2007. PMID: 17427029

3

A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families.

Alasti F, Sanati MH, Behrouzifard AH, Sadeghi A, de Brouwer AP, Kremer H, Smith RJ, Van Camp G. Alasti F, et al. Int J Pediatr Otorhinolaryngol. 2008 Feb;72(2):249-55. doi: 10.1016/j.ijporl.2007.09.023. Epub 2007 Nov 19. Int J Pediatr Otorhinolaryngol. 2008. PMID: 18022253

4

Genome-wide copy number variation analysis of a Branchio-oto-renal syndrome cohort identifies a recombination hotspot and implicates new candidate genes.

Brophy PD, Alasti F, Darbro BW, Clarke J, Nishimura C, Cobb B, Smith RJ, Manak JR. Brophy PD, et al. Among authors: alasti f. Hum Genet. 2013 Dec;132(12):1339-50. doi: 10.1007/s00439-013-1338-8. Epub 2013 Jul 13. Hum Genet. 2013. PMID: 23851940 Free PMC article.

5

A mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian family.

Alasti F, Sadeghi A, Sanati MH, Farhadi M, Stollar E, Somers T, Van Camp G. Alasti F, et al. Am J Hum Genet. 2008 Apr;82(4):982-91. doi: 10.1016/j.ajhg.2008.02.015. Am J Hum Genet. 2008. PMID: 18394579 Free PMC article.

6

Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Deafness, non-syndromic, autosomal recessive.

Alasti F, Peeters N, Wuyts W, Sanati MH, Van Camp G. Alasti F, et al. Hum Genet. 2010 Jan;127(1):116. Hum Genet. 2010. PMID: 20108392 No abstract available.

7

Novel human pathological mutations. Gene symbol: SLC26A4. Disease: deafness, non-syndromic, autosomal recessive.

Alasti F, Peeters N, Wuyts W, Sanati MH, Van Camp G. Alasti F, et al. Hum Genet. 2010 Apr;127(4):471. Hum Genet. 2010. PMID: 21488278 No abstract available.

8

Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11.

Hilgert N, Alasti F, Dieltjens N, Pawlik B, Wollnik B, Uyguner O, Delmaghani S, Weil D, Petit C, Danis E, Yang T, Pandelia E, Petersen MB, Goossens D, Favero JD, Sanati MH, Smith RJ, Van Camp G. Hilgert N, et al. Among authors: alasti f. Clin Genet. 2008 Sep;74(3):223-32. doi: 10.1111/j.1399-0004.2008.01053.x. Epub 2008 Jul 9. Clin Genet. 2008. PMID: 18616530 Free PMC article.

9

Genetics of microtia and associated syndromes.

Alasti F, Van Camp G. Alasti F, et al. J Med Genet. 2009 Jun;46(6):361-9. doi: 10.1136/jmg.2008.062158. Epub 2009 Mar 16. J Med Genet. 2009. PMID: 19293168 Free article. Review.

10

DFNB93, a novel locus for autosomal recessive moderate-to-severe hearing impairment.

Tabatabaiefar MA, Alasti F, Shariati L, Farrokhi E, Fransen E, Nooridaloii MR, Chaleshtori MH, Van Camp G. Tabatabaiefar MA, et al. Among authors: alasti f. Clin Genet. 2011 Jun;79(6):594-8. doi: 10.1111/j.1399-0004.2010.01593.x. Clin Genet. 2011. PMID: 21542834 No abstract available.

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