Ahmed W - 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: ahmed n, ahmed w. 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

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: ahmed n, ahmed w. 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

3

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: ahmed n. 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

4

Identification of recurrent and novel mutations in TULP1 in Pakistani families with early-onset retinitis pigmentosa.

Ajmal M, Khan MI, Micheal S, Ahmed W, Shah A, Venselaar H, Bokhari H, Azam A, Waheed NK, Collin RW, den Hollander AI, Qamar R, Cremers FP. Ajmal M, et al. Among authors: ahmed w. Mol Vis. 2012;18:1226-37. Epub 2012 May 10. Mol Vis. 2012. PMID: 22665969 Free PMC article.

5

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: ahmed w. Mol Vis. 2012;18:1558-71. Epub 2012 Jun 13. Mol Vis. 2012. PMID: 22736946 Free PMC article.

6

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. 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.

7

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: ahmed n. 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

8

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

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: ahmed w. 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

Clinical Utility of a Coronary Heart Disease Risk Prediction Gene Score in UK Healthy Middle Aged Men and in the Pakistani Population.

Beaney KE, Cooper JA, Ullah Shahid S, Ahmed W, Qamar R, Drenos F, Crockard MA, Humphries SE. Beaney KE, et al. Among authors: ahmed w. PLoS One. 2015 Jul 2;10(7):e0130754. doi: 10.1371/journal.pone.0130754. eCollection 2015. PLoS One. 2015. PMID: 26133560 Free PMC article.

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