Riaz M - Search Results

1

The genetic spectrum of familial hypercholesterolemia in Pakistan.

Ahmed W, Whittall R, Riaz M, Ajmal M, Sadeque A, Ayub H, Qamar R, Humphries SE. Ahmed W, et al. Among authors: riaz m. Clin Chim Acta. 2013 Jun 5;421:219-25. doi: 10.1016/j.cca.2013.03.017. Epub 2013 Mar 25. Clin Chim Acta. 2013. PMID: 23535506 Free PMC article.

2

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: riaz m. Gene. 2013 Feb 25;515(2):416-20. doi: 10.1016/j.gene.2012.12.044. Epub 2012 Dec 21. Gene. 2013. PMID: 23266621

3

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: riaz m. Mol Vis. 2013;19:644-53. Epub 2013 Mar 21. Mol Vis. 2013. PMID: 23559858 Free PMC article.

4

Implementation of public health genomics in Pakistan.

Riaz M, Tiller J, Ajmal M, Azam M, Qamar R, Lacaze P. Riaz M, et al. Eur J Hum Genet. 2019 Oct;27(10):1485-1492. doi: 10.1038/s41431-019-0428-z. Epub 2019 May 17. Eur J Hum Genet. 2019. PMID: 31101884 Free PMC article. Review.

5

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: riaz m. PLoS One. 2014 Nov 18;9(11):e112687. doi: 10.1371/journal.pone.0112687. eCollection 2014. PLoS One. 2014. PMID: 25405613 Free PMC article.

6

A nonsense mutation in S-antigen (p.Glu306*) causes Oguchi disease.

Waheed NK, Qavi AH, Malik SN, Maria M, Riaz M, Cremers FP, Azam M, Qamar R. Waheed NK, et al. Among authors: riaz m. Mol Vis. 2012;18:1253-9. Epub 2012 May 12. Mol Vis. 2012. PMID: 22665972 Free PMC article.

7

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: riaz m. Mol Vis. 2011;17:1153-63. Epub 2011 May 4. Mol Vis. 2011. PMID: 21617750 Free PMC article.

8

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: riaz m. PLoS One. 2015 Dec 14;10(12):e0144557. doi: 10.1371/journal.pone.0144557. eCollection 2015. PLoS One. 2015. PMID: 26658948 Free PMC article.

9

Familial Hypercholesterolemia in a Healthy Elderly Population.

Lacaze P, Sebra R, Riaz M, Hooper AJ, Tiller J, Bakshi A, Woods RL, Tonkin AM, Reid CM, Murray AM, Nicholls SJ, Watts GF, Schadt E, McNeil JJ. Lacaze P, et al. Among authors: riaz m. Circ Genom Precis Med. 2020 Aug;13(4):e002938. doi: 10.1161/CIRCGEN.120.002938. Epub 2020 Jun 10. Circ Genom Precis Med. 2020. PMID: 32522009 Free PMC article. No abstract available.

10

Genetic discrimination by Australian insurance companies: a survey of consumer experiences.

Tiller J, Morris S, Rice T, Barter K, Riaz M, Keogh L, Delatycki MB, Otlowski M, Lacaze P. Tiller J, et al. Among authors: riaz m. Eur J Hum Genet. 2020 Jan;28(1):108-113. doi: 10.1038/s41431-019-0426-1. Epub 2019 Jul 8. Eur J Hum Genet. 2020. PMID: 31281182 Free PMC article.

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