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Ali Muhammad Waryah

Liaquat University of Medical and Health Sciences

30

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564

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Disease-associated variants of Gap Junction Beta 2 protein (GJB2) in the deaf population of Southern Punjab of Pakistan.

2021 PLOS ONE
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Mutational analysis of CYP1B1 (rs56010818) variant in primary open angle glaucoma (POAG) affected patients of Pakistan

2021 Saudi Journal of Biological Sciences
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Biallelic Variants in EPHA2 Identified in Three Large Inbred Families with Early-Onset Cataract

2021 International Journal of Molecular Sciences
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Genetic Causes of Oculocutaneous Albinism in Pakistani Population.

2021 Genes
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P.arg102ser is a common Pde6? mutation causing autosomal recessive retinitis pigmentosa in Pakistani families

2020 Journal of Pakistan Medical Association
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Two novel variants in CYP1B1 gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients

2019 International Journal of Ophthalmology
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Identities and frequencies of variants in CYP1B1 causing primary congenital glaucoma in Pakistan

2019 Molecular Vision
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MTHFR and F5 genetic variations have association with preeclampsia in Pakistani patients: a case control study

2019 BMC Medical Genetics
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Homozygous variant in ARL3 causes autosomal recessive cone rod dystrophy

2019 Investigative Ophthalmology & Visual Science
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Consanguinity: A blessing or menace at population level?

2019 Annals of Human Genetics
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Citations (9)