Waryah AM - Search Results

1

Disease-associated variants of Gap Junction Beta 2 protein (GJB2) in the deaf population of Southern Punjab of Pakistan.

Kausar N, Haque A, Masoud MS, Nahid N, Ashfaq UA, Waryah AM, Bhatti R, Qasim M. Kausar N, et al. Among authors: waryah am. PLoS One. 2021 Oct 25;16(10):e0259083. doi: 10.1371/journal.pone.0259083. eCollection 2021. PLoS One. 2021. PMID: 34695157 Free PMC article.

2

Mutational spectrum of the CYP1B1 gene in Pakistani patients with primary congenital glaucoma: novel variants and genotype-phenotype correlations.

Sheikh SA, Waryah AM, Narsani AK, Shaikh H, Gilal IA, Shah K, Qasim M, Memon AI, Kewalramani P, Shaikh N. Sheikh SA, et al. Among authors: waryah am. Mol Vis. 2014 Jul 7;20:991-1001. eCollection 2014. Mol Vis. 2014. PMID: 25018621 Free PMC article.

3

Genetic Testing of Non-familial Deaf Patients for CIB2 and GJB2 Mutations: Phenotype and Genetic Counselling.

Shaikh H, Waryah AM, Narsani AK, Iqbal M, Shahzad M, Waryah YM, Shaikh N, Mahmood A. Shaikh H, et al. Among authors: waryah ym, waryah am. Biochem Genet. 2017 Dec;55(5-6):410-420. doi: 10.1007/s10528-017-9828-3. Epub 2017 Oct 31. Biochem Genet. 2017. PMID: 29086887 Clinical Trial.

4

Identities and frequencies of variants in CYP1B1 causing primary congenital glaucoma in Pakistan.

Rashid M, Yousaf S, Sheikh SA, Sajid Z, Shabbir AS, Kausar T, Tariq N, Usman M, Shaikh RS, Ali M, Bukhari SA, Waryah AM, Qasim M, Riazuddin S, Ahmed ZM. Rashid M, et al. Among authors: waryah am. Mol Vis. 2019 Feb 22;25:144-154. eCollection 2019. Mol Vis. 2019. PMID: 30820150 Free PMC article.

5

Consanguinity: A blessing or menace at population level?

Bhinder MA, Sadia H, Mahmood N, Qasim M, Hussain Z, Rashid MM, Zahoor MY, Bhatti R, Shehzad W, Waryah AM, Jahan S. Bhinder MA, et al. Among authors: waryah am. Ann Hum Genet. 2019 Jul;83(4):214-219. doi: 10.1111/ahg.12308. Epub 2019 Mar 19. Ann Hum Genet. 2019. PMID: 30891741 Review.

6

Genetic Causes of Oculocutaneous Albinism in Pakistani Population.

Sajid Z, Yousaf S, Waryah YM, Mughal TA, Kausar T, Shahzad M, Rao AR, Abbasi AA, Shaikh RS, Waryah AM, Riazuddin S, Ahmed ZM. Sajid Z, et al. Among authors: waryah ym, waryah am. Genes (Basel). 2021 Mar 28;12(4):492. doi: 10.3390/genes12040492. Genes (Basel). 2021. PMID: 33800529 Free PMC article.

7

Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.

Shabbir MI, Ahmed ZM, Khan SY, Riazuddin S, Waryah AM, Khan SN, Camps RD, Ghosh M, Kabra M, Belyantseva IA, Friedman TB, Riazuddin S. Shabbir MI, et al. Among authors: waryah am. J Med Genet. 2006 Aug;43(8):634-40. doi: 10.1136/jmg.2005.039834. Epub 2006 Feb 3. J Med Genet. 2006. PMID: 16459341 Free PMC article.

8

DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15.

Waryah AM, Rehman A, Ahmed ZM, Bashir ZH, Khan SY, Zafar AU, Riazuddin S, Friedman TB, Riazuddin S. Waryah AM, et al. Clin Genet. 2009 Sep;76(3):270-5. doi: 10.1111/j.1399-0004.2009.01209.x. Epub 2009 Jul 23. Clin Genet. 2009. PMID: 19650862

9

Molecular and clinical studies of X-linked deafness among Pakistani families.

Waryah AM, Ahmed ZM, Bhinder MA, Choo DI, Sisk RA, Shahzad M, Khan SN, Friedman TB, Riazuddin S, Riazuddin S. Waryah AM, et al. J Hum Genet. 2011 Jul;56(7):534-40. doi: 10.1038/jhg.2011.55. Epub 2011 Jun 2. J Hum Genet. 2011. PMID: 21633365 Free PMC article.

10

The novel heterozygous Thr377Arg MYOC mutation causes severe Juvenile Open Angle Glaucoma in a large Pakistani family.

Waryah AM, Narsani AK, Sheikh SA, Shaikh H, Shahani MY. Waryah AM, et al. Gene. 2013 Oct 10;528(2):356-9. doi: 10.1016/j.gene.2013.07.016. Epub 2013 Jul 23. Gene. 2013. PMID: 23886590

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