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Research to Prevent Blindness

Research Database

University of Cincinnati Research, funded by RPB from 2010-2014 matching Career Development Award to Ahmed, Zubair M / PhD

First 10 Citations, Sorted by Month and Year

There are 12 matching Citations in our database. Please use the filters at left to narrow your search.

June, 2014
Planned preterm delivery and treatment of retinal neovascularization in norrie disease.

Sisk RA, Hufnagel RB, Bandi S, Polzin WJ, Ahmed ZM

Ophthalmology. 2014 Jun;121(6):1312-3

University of Cincinnati - Career Development Award - Ahmed, Zubair M / PhD

Keywords: Retina/Retinal Diseases, Other: Neovascularization, Other: Norrie Disease

September, 2013
Genetic analysis through OtoSeq of pakistani families segregating prelingual hearing loss.

Shahzad M, Sivakumaran TA, Qaiser TA, Schultz JM, Hussain Z, Flanagan M, Bhinder MA, Kissell D, Greinwald JH,Jr, Khan SN, Friedman TB, Zhang K, Riazuddin S, Riazuddin S, Ahmed ZM

Otolaryngol Head Neck Surg. 2013 Sep;149(3):478-87

University of Cincinnati - Career Development Award - Ahmed, Zubair M / PhD

Keywords: Gene Research/Therapy, Other: Usher Syndrome, Other: Deafness, Other: MY07A

April, 2013
Genetic studies of TYRP1 and SLC45A2 in pakistani patients with nonsyndromic oculocutaneous albinism.

Kausar T, Jaworek TJ, Tariq N, Sadia S, Ali M, Shaikh RS, Ahmed ZM

J Invest Dermatol. 2013 Apr;133(4):1099-102

University of Cincinnati - Career Development Award - Ahmed, Zubair M / PhD

Keywords: Gene Research/Therapy, Other: Oculocutaneous Albinism, Other: TYRP1, Other: SLC45A2

January, 2013
OCA5, a novel locus for non-syndromic oculocutaneous albinism, maps to chromosome 4q24.

Kausar T, Bhatti M, Ali M, Shaikh R, Ahmed Z

Clin Genet. 2013;84(1):91-3

University of Cincinnati - Career Development Award - Ahmed, Zubair M / PhD

Keywords: Gene Research/Therapy, Other: Blindness, Other: Oculocutaneous Albinism, Other: OCA

November, 2012
Alterations of the CIB2 calcium- and integrin-binding protein cause usher syndrome type 1J and nonsyndromic deafness DFNB48.

Riazuddin S, Belyantseva IA, Giese AP, Lee K, Indzhykulian AA, Nandamuri SP, Yousaf R, Sinha GP, Lee S, Terrell D, Hegde RS, Ali RA, Anwar S, Andrade-Elizondo PB, Sirmaci A, Parise LV, Basit S, Wali A, Ayub M, Ansar M, Ahmad W, Khan SN, Akram J, Tekin M, Riazuddin S, Cook T, Buschbeck EK, Frolenkov GI, Leal SM, Friedman TB, Ahmed ZM

Nat Genet. 2012 Nov;44(11):1265-71

University of Cincinnati - Career Development Award - Ahmed, Zubair M / PhD

Keywords: Gene Research/Therapy, Retina/Retinal Diseases (Usher Syndrome), Other: Deafness

October, 2012
USH1K, a novel locus for type I usher syndrome, maps to chromosome 10p11.21-q21.1.

Jaworek TJ, Bhatti R, Latief N, Khan SN, Riazuddin S, Ahmed ZM

J Hum Genet. 2012 Oct;57(10):633-7

University of Cincinnati - Career Development Award - Ahmed, Zubair M / PhD

Keywords: Gene Research/Therapy, Retina/Retinal Diseases (Usher Syndrome), Other: Deafness

May, 2012
DFNB86, a novel autosomal recessive non-syndromic deafness locus on chromosome 16p13.3.

Ali RA, Rehman AU, Khan SN, Husnain T, Riazuddin S, Friedman TB, Ahmed ZM, Riazuddin S

Clin Genet. 2012 May;81(5):498-500

University of Cincinnati - Career Development Award - Ahmed, Zubair M / PhD

Keywords: Gene Research/Therapy, Retina/Retinal Diseases (Usher Syndrome), Other: Deafness

July, 2011
Molecular and clinical studies of X-linked deafness among pakistani families.

Waryah AM, Ahmed ZM, Binder MA, Choo DI, Sisk RA, Shahzad M, Khan SN, Friedman TB, Riazuddin S, Riazuddin S

J Hum Genet. 2011 Jul;56(7):534-40

University of Cincinnati - Career Development Award - Ahmed, Zubair M / PhD

Keyword: Genetics

January, 2011
Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74.

Ahmed ZM, Yousaf R, Lee BC, Khan SN, Lee S, Lee K, Husnain T, Rehman AU, Bonneux S, Ansar M, Ahmad W, Leal SM, Gladyshev VN, Belyantseva IA, Van Camp G, Riazuddin S, Friedman TB, Riazuddin S

Am J Hum Genet. 2011 Jan 7;88(1):19-29

University of Cincinnati - Career Development Award - Ahmed, Zubair M / PhD

Keyword: Genetics

January, 2010
A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness.

Riazuddin SA, Shahzadi A, Zeitz C, Ahmed ZM, Ayyagari R, Chavali VR, Ponferrada VG, Audo I, Michiels C, Lancelot ME, Nasir IA, Zafar AU, Khan SN, Husnain T, Jiao X, MacDonald IM, Riazuddin S, Sieving PA, Katsanis N, Hejtmancik JF

Am J Hum Genet 2010;87(4):523-531

University of Cincinnati - Career Development Award - Ahmed, Zubair M / PhD

Keywords: Genetics, Retina/Retinal Diseases

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