Hameed A - Search Results

1

Application of Short Tandem Repeat markers in diagnosis of chromosomal aneuploidies and forensic DNA investigation in Pakistan.

Chishti HM, Ansar M, Ajmal M, Hameed A. Chishti HM, et al. Among authors: hameed a. Gene. 2014 Sep 15;548(2):217-22. doi: 10.1016/j.gene.2014.07.035. Epub 2014 Jul 15. Gene. 2014. PMID: 25034657

2

Inability of the most commonly used forensic genetic markers to distinguish between samples belonging to different ethnicities of Pakistan with diverse genetic background.

Chishti HM, Manica A, Ansar M, Eriksson A, Ajmal M, Hameed A. Chishti HM, et al. Among authors: hameed a. Forensic Sci Int Genet. 2016 May;22:e7-e8. doi: 10.1016/j.fsigen.2016.01.006. Epub 2016 Jan 21. Forensic Sci Int Genet. 2016. PMID: 26846676 No abstract available.

3

Genetic association analysis of serotonin transporter polymorphism (5-HTTLPR) with type 2 diabetes patients of Pakistani population.

Hameed A, Ajmal M, Nasir M, Ismail M. Hameed A, et al. Diabetes Res Clin Pract. 2015 Apr;108(1):67-71. doi: 10.1016/j.diabres.2015.01.009. Epub 2015 Jan 20. Diabetes Res Clin Pract. 2015. PMID: 25680681

4

Molecular analysis of lipoid proteinosis: identification of a novel nonsense mutation in the ECM1 gene in a Pakistani family.

Nasir M, Latif A, Ajmal M, Qamar R, Naeem M, Hameed A. Nasir M, et al. Among authors: hameed a. Diagn Pathol. 2011 Jul 26;6:69. doi: 10.1186/1746-1596-6-69. Diagn Pathol. 2011. PMID: 21791056 Free PMC article.

5

Whole exome sequencing for handedness in a large and highly consanguineous family.

Kavaklioglu T, Ajmal M, Hameed A, Francks C. Kavaklioglu T, et al. Among authors: hameed a. Neuropsychologia. 2016 Dec;93(Pt B):342-349. doi: 10.1016/j.neuropsychologia.2015.11.010. Epub 2015 Nov 12. Neuropsychologia. 2016. PMID: 26581626

6

In silico analysis of a disease-causing mutation in PCDH15 gene in a consanguineous Pakistani family with Usher phenotype.

Saleha S, Ajmal M, Jamil M, Nasir M, Hameed A. Saleha S, et al. Among authors: hameed a. Int J Ophthalmol. 2016 May 18;9(5):662-8. doi: 10.18240/ijo.2016.05.04. eCollection 2016. Int J Ophthalmol. 2016. PMID: 27275418 Free PMC article.

7

Bioinformatics evaluation of NPHS2 deletion mutation associated with congenital nephrotic syndrome in a consanguineous Pakistani family.

Hameed A, Mir A, Nasir M, Ajmal M. Hameed A, et al. Clin Genet. 2015 Jun;87(6):599-601. doi: 10.1111/cge.12486. Epub 2014 Nov 11. Clin Genet. 2015. PMID: 25143137 No abstract available.

8

Novel human pathological mutations. Gene symbol: ECM1. Disease: Lipoid Proteinosis.

Hameed A, Nasir M, Ajmal M, Latif L. Hameed A, et al. Hum Genet. 2009 Aug;126(2):336. Hum Genet. 2009. PMID: 19694009 No abstract available.

9

P53 (Pro72Arg) polymorphism associated with the risk of oral squamous cell carcinoma in gutka, niswar and manpuri addicted patients of Pakistan.

Saleem S, Azhar A, Hameed A, Khan MA, Abbasi ZA, Qureshi NR, Ajmal M. Saleem S, et al. Among authors: hameed a. Oral Oncol. 2013 Aug;49(8):818-23. doi: 10.1016/j.oraloncology.2013.04.004. Epub 2013 May 14. Oral Oncol. 2013. PMID: 23683469

10

A novel homozygous 62-bp insertion in ECM1 causes lipoid proteinosis in a multigeneration Pakistani family.

Nasir M, Latif A, Ajmal M, Ismail M, Hameed A. Nasir M, et al. Among authors: hameed a. Br J Dermatol. 2009 Sep;161(3):688-90. doi: 10.1111/j.1365-2133.2009.09275.x. Epub 2009 Jun 9. Br J Dermatol. 2009. PMID: 19519837 No abstract available.

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