Azam M - Search Results

1

Implementation of public health genomics in Pakistan.

Riaz M, Tiller J, Ajmal M, Azam M, Qamar R, Lacaze P. Riaz M, et al. Among authors: azam m. 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.

2

A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family.

Azam M, Collin RW, Khan MI, Shah ST, Qureshi N, Ajmal M, den Hollander AI, Qamar R, Cremers FP. Azam M, et al. Mol Vis. 2009 Sep 5;15:1788-93. Mol Vis. 2009. PMID: 19753316 Free PMC article.

3

A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa.

Azam M, Khan MI, Gal A, Hussain A, Shah ST, Khan MS, Sadeque A, Bokhari H, Collin RW, Orth U, van Genderen MM, den Hollander AI, Cremers FP, Qamar R. Azam M, et al. Mol Vis. 2009 Dec 3;15:2526-34. Mol Vis. 2009. PMID: 19960070 Free PMC article.

4

Novel CNGA3 and CNGB3 mutations in two Pakistani families with achromatopsia.

Azam M, Collin RW, Shah ST, Shah AA, Khan MI, Hussain A, Sadeque A, Strom TM, Thiadens AA, Roosing S, den Hollander AI, Cremers FP, Qamar R. Azam M, et al. Mol Vis. 2010 Apr 29;16:774-81. Mol Vis. 2010. PMID: 20454696 Free PMC article.

5

Role of tissue plasminogen activator and plasminogen activator inhibitor polymorphism in myocardial infarction.

Ahmed W, Malik M, Saeed I, Khan AA, Sadeque A, Kaleem U, Ahmed N, Ajmal M, Azam M, Qamar R. Ahmed W, et al. Among authors: azam m. Mol Biol Rep. 2011 Apr;38(4):2541-8. doi: 10.1007/s11033-010-0392-8. Epub 2010 Nov 17. Mol Biol Rep. 2011. PMID: 21082259

6

Missense mutations at homologous positions in the fourth and fifth laminin A G-like domains of eyes shut homolog cause autosomal recessive retinitis pigmentosa.

Khan MI, Collin RW, Arimadyo K, Micheal S, Azam M, Qureshi N, Faradz SM, den Hollander AI, Qamar R, Cremers FP. Khan MI, et al. Among authors: azam m. Mol Vis. 2010 Dec 15;16:2753-9. Mol Vis. 2010. PMID: 21179430 Free PMC article.

7

CLRN1 mutations cause nonsyndromic retinitis pigmentosa.

Khan MI, Kersten FF, Azam M, Collin RW, Hussain A, Shah ST, Keunen JE, Kremer H, Cremers FP, Qamar R, den Hollander AI. Khan MI, et al. Among authors: azam m. Ophthalmology. 2011 Jul;118(7):1444-8. doi: 10.1016/j.ophtha.2010.10.047. Epub 2011 Feb 18. Ophthalmology. 2011. PMID: 21310491

8

A novel pathogenic nonsense triple-nucleotide mutation in the low-density lipoprotein receptor gene and its clinical correlation with familial hypercholesterolemia.

Ajmal M, Ahmed W, Akhtar N, Sadeque A, Khalid A, Benish Ali SH, Ahmed N, Azam M, Qamar R. Ajmal M, et al. Among authors: azam m. Genet Test Mol Biomarkers. 2011 Sep;15(9):601-6. doi: 10.1089/gtmb.2010.0184. Epub 2011 Apr 3. Genet Test Mol Biomarkers. 2011. PMID: 21457052

9

Identification of novel mutations in Pakistani families with autosomal recessive retinitis pigmentosa.

Azam M, Collin RW, Malik A, Khan MI, Shah ST, Shah AA, Hussain A, Sadeque A, Arimadyo K, Ajmal M, Azam A, Qureshi N, Bokhari H, Strom TM, Cremers FP, Qamar R, den Hollander AI. Azam M, et al. Among authors: azam a. Arch Ophthalmol. 2011 Oct;129(10):1377-8. doi: 10.1001/archophthalmol.2011.290. Arch Ophthalmol. 2011. PMID: 21987686 No abstract available.

10

Novel and recurrent LDLR gene mutations in Pakistani hypercholesterolemia patients.

Ahmed W, Ajmal M, Sadeque A, Whittall RA, Rafiq S, Putt W, Khawaja A, Imtiaz F, Ahmed N, Azam M, Humphries SE, Qamar R. Ahmed W, et al. Among authors: azam m. Mol Biol Rep. 2012 Jul;39(7):7365-72. doi: 10.1007/s11033-012-1568-1. Epub 2012 Feb 7. Mol Biol Rep. 2012. PMID: 22311046

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

884 results

Search Page