Brownstein Z - Search Results

1

High-throughput sequencing to decipher the genetic heterogeneity of deafness.

Brownstein Z, Bhonker Y, Avraham KB. Brownstein Z, et al. Genome Biol. 2012 May 29;13(5):245. doi: 10.1186/gb-2012-13-5-245. Genome Biol. 2012. PMID: 22647651 Free PMC article. Review.

2

A novel SLC26A4 (PDS) deafness mutation retained in the endoplasmic reticulum.

Brownstein ZN, Dror AA, Gilony D, Migirov L, Hirschberg K, Avraham KB. Brownstein ZN, et al. Arch Otolaryngol Head Neck Surg. 2008 Apr;134(4):403-7. doi: 10.1001/archotol.134.4.403. Arch Otolaryngol Head Neck Surg. 2008. PMID: 18427006

3

Deafness genes in Israel: implications for diagnostics in the clinic.

Brownstein Z, Avraham KB. Brownstein Z, et al. Pediatr Res. 2009 Aug;66(2):128-34. doi: 10.1203/PDR.0b013e3181aabd7f. Pediatr Res. 2009. PMID: 19390476 Review.

4

Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern families.

Brownstein Z, Friedman LM, Shahin H, Oron-Karni V, Kol N, Abu Rayyan A, Parzefall T, Lev D, Shalev S, Frydman M, Davidov B, Shohat M, Rahile M, Lieberman S, Levy-Lahad E, Lee MK, Shomron N, King MC, Walsh T, Kanaan M, Avraham KB. Brownstein Z, et al. Genome Biol. 2011 Sep 14;12(9):R89. doi: 10.1186/gb-2011-12-9-r89. Genome Biol. 2011. PMID: 21917145 Free PMC article.

5

Integration of human and mouse genetics reveals pendrin function in hearing and deafness.

Dror AA, Brownstein Z, Avraham KB. Dror AA, et al. Among authors: brownstein z. Cell Physiol Biochem. 2011;28(3):535-44. doi: 10.1159/000335163. Epub 2011 Nov 18. Cell Physiol Biochem. 2011. PMID: 22116368 Free PMC article. Review.

6

Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencing.

Brownstein Z, Abu-Rayyan A, Karfunkel-Doron D, Sirigu S, Davidov B, Shohat M, Frydman M, Houdusse A, Kanaan M, Avraham KB. Brownstein Z, et al. Eur J Hum Genet. 2014 Jun;22(6):768-75. doi: 10.1038/ejhg.2013.232. Epub 2013 Oct 9. Eur J Hum Genet. 2014. PMID: 24105371 Free PMC article.

7

PNPT1, MYO15A, PTPRQ, and SLC12A2-associated genetic and phenotypic heterogeneity among hearing impaired assortative mating families in Southern India.

Vanniya S P, Chandru J, Jeffrey JM, Rabinowitz T, Brownstein Z, Krishnamoorthy M, Avraham KB, Cheng L, Shomron N, Srisailapathy CRS. Vanniya S P, et al. Among authors: brownstein z. Ann Hum Genet. 2022 Jan;86(1):1-13. doi: 10.1111/ahg.12442. Epub 2021 Aug 9. Ann Hum Genet. 2022. PMID: 34374074

8

[INNOVATIONS IN RESEARCH OF HEREDITARY DEAFNESS].

Ben-Dov T, Brownstein Z, Nageris B, Avraham KB. Ben-Dov T, et al. Among authors: brownstein z. Harefuah. 2020 Feb;159(1):117-122. Harefuah. 2020. PMID: 32048492 Review. Hebrew.

9

The R245X mutation of PCDH15 in Ashkenazi Jewish children diagnosed with nonsyndromic hearing loss foreshadows retinitis pigmentosa.

Brownstein Z, Ben-Yosef T, Dagan O, Frydman M, Abeliovich D, Sagi M, Abraham FA, Taitelbaum-Swead R, Shohat M, Hildesheimer M, Friedman TB, Avraham KB. Brownstein Z, et al. Pediatr Res. 2004 Jun;55(6):995-1000. doi: 10.1203/01.PDR.0000125258.58267.56. Epub 2004 Mar 17. Pediatr Res. 2004. PMID: 15028842

10

Chromosomal mapping and phenotypic characterization of hereditary otosclerosis linked to the OTSC4 locus.

Brownstein Z, Goldfarb A, Levi H, Frydman M, Avraham KB. Brownstein Z, et al. Arch Otolaryngol Head Neck Surg. 2006 Apr;132(4):416-24. doi: 10.1001/archotol.132.4.416. Arch Otolaryngol Head Neck Surg. 2006. PMID: 16618911

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