bmc@lumhs.edu.pk (+92)22-9213118
bmc@lumhs.edu.pk (+92)22-9213118

Dr. Shakeel Ahmed Sheikh

Dr. Shakeel Ahmed Sheikh

MBBS; PhD (Molecular Biology)
Associate Professor & Head of Department

Publications

  1. Waryah AM, Narsani AK, Sheikh SA, Shaikh H, Shahani MY. The novel heterozygous thr377arg myoc mutation causes severe juvenile open angle glaucoma in a large pakistani family. Gene. 2013 Oct 10; 528(2):356-9. doi: 10.1016/j.gene.2013.07.016. Epub 2013 Jul 23. Impact Factor 2.498

  2. Sheikh SA, Waryah AM, Narsani AK, Shaikh H, Gilal IA, Shah K, Qasim M, Memon AI, Kewalramani P, Shaikh N. Mutational Spectrum of the Cyp1b1 Gene in Pakistani Patients with Primary Congenital Glaucoma: Novel Variants and Genotype-Phenotype Correlations. Mol Vis.2014 Jul 7;20:991-1001. eCollection 2014. Impact Factor 2.219

  3. Waryah AM, Shahzad M, Shaikh H, Sheikh SA, Channa NA, Hufnagel RB, Makhdoon A, Riazuddin S, Ahmed ZM. A novel CHST3 allele associated with Spondyloepiphyseal dysplasia and hearing loss in Pakistani kindred. 2015; Clin Genet. doi: 10.1111/cge.12694. Impact Factor 3.512

  4. Yousaf S, Shahzad M, Kausar T, Sheikh SA, Tariq N, Shabbir AS, Ali M, Waryah A M, Shaikh RS, Riazuddin S, Ahmed ZM. Identification and clinical characterization of Hermansky–Pudlak syndrome alleles in the Pakistani population. 2015; Pigment Cell & Melanoma Research, 29: 231–235. doi: 10.1111/pcmr.12438. Impact Factor 5.17

  5. Yousaf S, Sheikh SA, Riazuddin S, Waryah AM, Ahmed ZM. INPP5K variant causes autosomal recessive congenital cataract in a Pakistani family. 2017; Clin Genet 93(3): 682-686. Impact Factor 3.512

  6. Waryah YM, Iqbal M, Sheikh SA, Baig MA, Narsani AK, Atif M, Bhinder MA, Ur Rahman A, Memon AI, Pirzado MS, Waryah AM. Two novel variants in CYP1B1 gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients. Int J Ophthalmol. 2019 Jan 18;12(1):8-15. doi: 10.18240/ijo.2019.01.02. eCollection 2019. Impact Factor 1.166

  7. Rashid M, Yousaf S, Sheikh SA, Sajid Z, Shabbir AS, Kausar T, Tariq N, Usman M, Shaikh RS, Ali M, Bukhari SA, Waryah AM, Qasim M, Riazuddin S, Ahmed ZM. Identities and frequencies of variants in CYP1B1 causing primary congenital glaucoma in Pakistan. Mol Vis. 2019, 25:144-154. Impact Factor 2.219

  8. Sheikh SA, Sisk RA, Schiavon CR, Waryah YM, Usmani MA, Steel DH, Sayer JA, Narsani AK, Hufnagel RB, Riazuddin S, Kahn RA, Waryah AM, Ahmed ZM. Homozygous Variant in ARL3 Causes Autosomal Recessive Cone Rod Dystrophy. Invest Ophthalmol Vis Sci. 2019 Nov 1;60(14). Impact Factor 3.81

  9. Kumar G, Sheikh SA, Shahani MY, Ashraf S, Laghari MJ, Memon S, Analysis Of Vitamin-D Intake On Lipid Profile In Patients With Type-Ii Diabetes Mellitus Taking Metformin. JPUMHS;2020;10(03)49-53.

  10. Jarwar P, SheikhSA, Waryah YM , Ujjan IU, Riazuddin S , Waryah AM , Ahmed ZM. Biallelic Variants in EPHA2 Identified in Three Large Inbred Families with Early-Onset Cataract. Int J Mol Sci. 2021 Sep 30;22(19):10655. doi: 10.3390/ijms221910655.

  11. Yousaf S, Tariq N, Sajid Z, Sheikh S.A, Kausar T, Waryah Y.M,  Shaikh R.S, Waryah A.M,  Sethna S,  Riazuddin S,  Ahmed ZM. Delineating the Molecular and Phenotypic Spectrum of the CNGA3-Related Cone Photoreceptor Disorder in Pakistani Families. Genes 2022, 13, 617. https://doi.org/ 10.3390/genes13040617

  12. Khan AS, Memon SH, Sheikh SA, Memon AR, Kumar G, Shahani MY. Evaluation of Trace Elements in Patients with Senile Cataract. Pak Journal of medical and health sciences. 16 (08), August 2022. https://doi.org/10.53350/pjmhs22168500.

  13. Shahani MY, Memon S, Sheikh SA, Bano U, Shaikh P, Memon SG, Shahani SB, Ujjan ID, Narsani AK, Waryah AM. Genetic heterogeneity of primary open-angle glaucoma in Pakistan. Saudi.J.Biol.Sci.30(2023). doi: 10.1016/j.sjbs.2022.103488.Epub 2022 Nov 1. Impact Factor 4.2

Email: shakeel.shaikh@lumhs.edu.pk