Ali SH - Search Results

1

Identification of a recurrent insertion mutation in the LDLR gene in a Pakistani family with autosomal dominant hypercholesterolemia.

Ajmal M, Ahmed W, Sadeque A, Ali SH, Bokhari SH, Ahmed N, Qamar R. Ajmal M, et al. Among authors: ali sh. Mol Biol Rep. 2010 Dec;37(8):3869-75. doi: 10.1007/s11033-010-0043-0. Epub 2010 Mar 10. Mol Biol Rep. 2010. PMID: 20217239

2

Association of eNOS and HSP70 gene polymorphisms with glaucoma in Pakistani cohorts.

Ayub H, Khan MI, Micheal S, Akhtar F, Ajmal M, Shafique S, Ali SH, den Hollander AI, Ahmed A, Qamar R. Ayub H, et al. Among authors: ali sh. Mol Vis. 2010 Jan 11;16:18-25. Mol Vis. 2010. PMID: 20069064 Free PMC article.

3

XRCC1 and XPD DNA repair gene polymorphisms: a potential risk factor for glaucoma in the Pakistani population.

Yousaf S, Khan MI, Micheal S, Akhtar F, Ali SH, Riaz M, Ali M, Lall P, Waheed NK, den Hollander AI, Ahmed A, Qamar R. Yousaf S, et al. Among authors: ali m, ali sh. Mol Vis. 2011;17:1153-63. Epub 2011 May 4. Mol Vis. 2011. PMID: 21617750 Free PMC article.

4

Novel mutations in RDH5 cause fundus albipunctatus in two consanguineous Pakistani families.

Ajmal M, Khan MI, Neveling K, Khan YM, Ali SH, Ahmed W, Iqbal MS, Azam M, den Hollander AI, Collin RW, Qamar R, Cremers FP. Ajmal M, et al. Among authors: ali sh. Mol Vis. 2012;18:1558-71. Epub 2012 Jun 13. Mol Vis. 2012. PMID: 22736946 Free PMC article.

5

Association of ANRIL polymorphism (rs1333049:C>G) with myocardial infarction and its pharmacogenomic role in hypercholesterolemia.

Ahmed W, Ali IS, Riaz M, Younas A, Sadeque A, Niazi AK, Niazi SH, Ali SH, Azam M, Qamar R. Ahmed W, et al. Among authors: ali is, ali sh. Gene. 2013 Feb 25;515(2):416-20. doi: 10.1016/j.gene.2012.12.044. Epub 2012 Dec 21. Gene. 2013. PMID: 23266621

6

Exome sequencing identifies a novel and a recurrent BBS1 mutation in Pakistani families with Bardet-Biedl syndrome.

Ajmal M, Khan MI, Neveling K, Tayyab A, Jaffar S, Sadeque A, Ayub H, Abbasi NM, Riaz M, Micheal S, Gilissen C, Ali SH, Azam M, Collin RW, Cremers FP, Qamar R. Ajmal M, et al. Among authors: ali sh. Mol Vis. 2013;19:644-53. Epub 2013 Mar 21. Mol Vis. 2013. PMID: 23559858 Free PMC article.

7

Association of Pro12Ala polymorphism in peroxisome proliferator activated receptor gamma with proliferative diabetic retinopathy.

Tariq K, Malik SB, Ali SH, Maqsood SE, Azam A, Muslim I, Khan MS, Azam M, Waheed NK, Qamar R. Tariq K, et al. Among authors: ali sh. Mol Vis. 2013;19:710-7. Epub 2013 Mar 21. Mol Vis. 2013. PMID: 23559865 Free PMC article.

8

Exome sequencing identifies three novel candidate genes implicated in intellectual disability.

Agha Z, Iqbal Z, Azam M, Ayub H, Vissers LE, Gilissen C, Ali SH, Riaz M, Veltman JA, Pfundt R, van Bokhoven H, Qamar R. Agha Z, et al. Among authors: ali sh. PLoS One. 2014 Nov 18;9(11):e112687. doi: 10.1371/journal.pone.0112687. eCollection 2014. PLoS One. 2014. PMID: 25405613 Free PMC article.

9

Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan.

Maria M, Ajmal M, Azam M, Waheed NK, Siddiqui SN, Mustafa B, Ayub H, Ali L, Ahmad S, Micheal S, Hussain A, Shah ST, Ali SH, Ahmed W, Khan YM, den Hollander AI, Haer-Wigman L, Collin RW, Khan MI, Qamar R, Cremers FP. Maria M, et al. Among authors: ali l, ali sh. PLoS One. 2015 Mar 16;10(3):e0119806. doi: 10.1371/journal.pone.0119806. eCollection 2015. PLoS One. 2015. PMID: 25775262 Free PMC article.

10

Role of ACE and PAI-1 Polymorphisms in the Development and Progression of Diabetic Retinopathy.

Saleem S, Azam A, Maqsood SI, Muslim I, Bashir S, Fazal N, Riaz M, Ali SH, Niazi MK, Ishaq M, Waheed NK, Qamar R, Azam M. Saleem S, et al. Among authors: ali sh. PLoS One. 2015 Dec 14;10(12):e0144557. doi: 10.1371/journal.pone.0144557. eCollection 2015. PLoS One. 2015. PMID: 26658948 Free PMC article.

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