Qasim M - Search Results

1

Targeted next generation sequencing reveals a novel intragenic deletion of the TPO gene in a family with intellectual disability.

Iqbal Z, Neveling K, Razzaq A, Shahzad M, Zahoor MY, Qasim M, Gilissen C, Wieskamp N, Kwint MP, Gijsen S, de Brouwer AP, Veltman JA, Riazuddin S, van Bokhoven H. Iqbal Z, et al. Among authors: qasim m. Arch Med Res. 2012 May;43(4):312-6. doi: 10.1016/j.arcmed.2012.01.011. Epub 2012 Mar 3. Arch Med Res. 2012. PMID: 22387573

2

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: qasim m. 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.

3

Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome.

Ahmed ZM, Riazuddin S, Aye S, Ali RA, Venselaar H, Anwar S, Belyantseva PP, Qasim M, Riazuddin S, Friedman TB. Ahmed ZM, et al. Among authors: qasim m. Hum Genet. 2008 Oct;124(3):215-23. doi: 10.1007/s00439-008-0543-3. Epub 2008 Aug 22. Hum Genet. 2008. PMID: 18719945 Free PMC article.

4

Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes.

Schultz JM, Bhatti R, Madeo AC, Turriff A, Muskett JA, Zalewski CK, King KA, Ahmed ZM, Riazuddin S, Ahmad N, Hussain Z, Qasim M, Kahn SN, Meltzer MR, Liu XZ, Munisamy M, Ghosh M, Rehm HL, Tsilou ET, Griffith AJ, Zein WM, Brewer CC, Riazuddin S, Friedman TB. Schultz JM, et al. Among authors: qasim m. J Med Genet. 2011 Nov;48(11):767-75. doi: 10.1136/jmedgenet-2011-100262. Epub 2011 Sep 22. J Med Genet. 2011. PMID: 21940737

5

SE33 locus as a reliable genetic marker for forensic DNA analysis systems.

Bhinder MA, Zahoor MY, Sadia H, Qasim M, Perveen R, Anjum GM, Iqbal M, Ullah N, Shehzad W, Tariq M, Waryah AM. Bhinder MA, et al. Among authors: qasim m. Turk J Med Sci. 2018 Jun 14;48(3):611-614. doi: 10.3906/sag-1801-21. Turk J Med Sci. 2018. PMID: 29916220 Free article.

6

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: qasim m. Mol Vis. 2014 Jul 7;20:991-1001. eCollection 2014. Mol Vis. 2014. PMID: 25018621 Free PMC article.

7

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: qasim m. Mol Vis. 2019 Feb 22;25:144-154. eCollection 2019. Mol Vis. 2019. PMID: 30820150 Free PMC article.

8

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: qasim m. PLoS One. 2021 Oct 25;16(10):e0259083. doi: 10.1371/journal.pone.0259083. eCollection 2021. PLoS One. 2021. PMID: 34695157 Free PMC article.

9

Computational screening of phytochemicals against survivin protein: A potent target for cancer.

Hussain G, Ashfaq UA, Rahman M, Masoud MS, Nahid N, Bhinder MA, Aslam N, Yousaf N, Ahmed U, Qasim M. Hussain G, et al. Among authors: qasim m. Pak J Pharm Sci. 2019 May;32(3 (Supplementary)):1145-1154. Pak J Pharm Sci. 2019. PMID: 31303583

10

Inhibition of HCV 3a genotype entry through host CD81 and HCV E2 antibodies.

Ashfaq UA, Qasim M, Yousaf MZ, Awan MT, Jahan S. Ashfaq UA, et al. Among authors: qasim m. J Transl Med. 2011 Nov 10;9:194. doi: 10.1186/1479-5876-9-194. J Transl Med. 2011. PMID: 22074322 Free PMC article.

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