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Role of Nitric Oxide in the Cardiovascular and Renal Systems

International journal of molecular sciences, 2018-09, Vol.19 (9), p.2605

2018

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Implementation of public health genomics in Pakistan

European journal of human genetics : EJHG, 2019-10, Vol.27 (10), p.1485-1492

2019

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Expression profiling of extracellular matrix related genes in patients with strabismus

Clinical & experimental ophthalmology, 2023-08, Vol.51 (6), p.646-649

2023

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CBS mutations and MTFHR SNPs causative of hyperhomocysteinemia in Pakistani children

Molecular biology reports, 2018-06, Vol.45 (3), p.353-360

2018

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Exome Sequencing Identifies a Biallelic GALNS Variant (p.Asp233Asn) Causing Mucopolysaccharidosis Type IVA in a Pakistani Consanguineous Family

Genes, 2022-09, Vol.13 (10), p.1743

2022

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Molecular Mechanisms of Complement System Proteins and Matrix Metalloproteinases in the Pathogenesis of Age-Related Macular Degeneration

Current molecular medicine, 2019-01, Vol.19 (10), p.705-718

2019

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Association of IGF1 and VEGFA polymorphisms with diabetic retinopathy in Pakistani population

Acta diabetologica, 2020-02, Vol.57 (2), p.237-245

2020

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Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families

PloS one, 2014-06, Vol.9 (6), p.e100146

2014

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Genetic Association of Butyrylcholinesterase with Major Depressive Disorder

Biochemical genetics, 2022-04, Vol.60 (2), p.720-737

2022

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Interaction between nitric oxide and renal α1-adrenoreceptors mediated vasoconstriction in rats with left ventricular hypertrophyin Wistar Kyoto rats

PloS one, 2018-02, Vol.13 (2), p.e0189386

2018

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Role of ACE and PAI-1 Polymorphisms in the Development and Progression of Diabetic Retinopathy

PloS one, 2015-12, Vol.10 (12), p.e0144557

2015

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Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan

PloS one, 2015-03, Vol.10 (3), p.e0119806-e0119806

2015

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Association of rs10490924 in ARMS2/HTRA1 with age‐related macular degeneration in the Pakistani population

Annals of human genetics, 2019-07, Vol.83 (4), p.285-290

2019

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Up Regulation of cystathione γ lyase and Hydrogen Sulphide in the Myocardium Inhibits the Progression of Isoproterenol-Caffeine Induced Left Ventricular Hypertrophy in Wistar Kyoto Rats

PloS one, 2016-03, Vol.11 (3), p.e0150137

2016

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Rare Variants Residing in Novel Cis-Acting Element in Visual System Homeobox 1 and Their Contribution in the Pathogenesis of Keratoconus

Applied sciences, 2023-04, Vol.13 (8), p.4888

2023

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Exome sequencing identifies three novel candidate genes implicated in intellectual disability

PloS one, 2014-11, Vol.9 (11), p.e112687-e112687

2014

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A 3′ untranslated region polymorphism rs2304277 in the DNA repair pathway gene OGG1 is a novel risk modulator for urothelial bladder carcinoma

Annals of human genetics, 2018-03, Vol.82 (2), p.74-87

2018

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Cystathione gamma lyase/Hydrogen Sulphide Pathway Up Regulation Enhances the Responsiveness of α1A and α1B-Adrenoreceptors in the Kidney of Rats with Left Ventricular Hypertrophy

PloS one, 2016-05, Vol.11 (5), p.e0154995-e0154995

2016

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Inborn errors of metabolism: Historical perspectives to contemporary management

Clinica chimica acta, 2024-08, Vol.562, p.119883, Article 119883

2024

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CLRN1 Mutations Cause Nonsyndromic Retinitis Pigmentosa

Ophthalmology (Rochester, Minn.), 2011-07, Vol.118 (7), p.1444-1448

2011

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Prevalence of human T-lymphotropic virus 1/2 in Nigeria’s capital territory and meta-analysis of Nigerian studies

SAGE open medicine, 2019, Vol.7, p.2050312119843706-2050312119843706

2019

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The molecular basis of retinal dystrophies in pakistan

Genes, 2014-03, Vol.5 (1), p.176-195

2014

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Compound heterozygous mutations p.Q1530X and 6103delG in COL7A1 causing recessive dystrophic epidermolysis bullosa in a Pakistani family

Journal of dermatology, 2012-05, Vol.39 (5), p.472-474

2012

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Role of Nitric Oxide in the Cardiovascular and Renal Systems

Implementation of public health genomics in Pakistan

Expression profiling of extracellular matrix related genes in patients with strabismus

CBS mutations and MTFHR SNPs causative of hyperhomocysteinemia in Pakistani children

Exome Sequencing Identifies a Biallelic GALNS Variant (p.Asp233Asn) Causing Mucopolysaccharidosis Type IVA in a Pakistani Consanguineous Family

Molecular Mechanisms of Complement System Proteins and Matrix Metalloproteinases in the Pathogenesis of Age-Related Macular Degeneration

Association of IGF1 and VEGFA polymorphisms with diabetic retinopathy in Pakistani population

Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families

Genetic Association of Butyrylcholinesterase with Major Depressive Disorder

Interaction between nitric oxide and renal α1-adrenoreceptors mediated vasoconstriction in rats with left ventricular hypertrophyin Wistar Kyoto rats

Role of ACE and PAI-1 Polymorphisms in the Development and Progression of Diabetic Retinopathy

Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan

Association of rs10490924 in ARMS2/HTRA1 with age‐related macular degeneration in the Pakistani population

Up Regulation of cystathione γ lyase and Hydrogen Sulphide in the Myocardium Inhibits the Progression of Isoproterenol-Caffeine Induced Left Ventricular Hypertrophy in Wistar Kyoto Rats

Rare Variants Residing in Novel Cis-Acting Element in Visual System Homeobox 1 and Their Contribution in the Pathogenesis of Keratoconus

Exome sequencing identifies three novel candidate genes implicated in intellectual disability

A 3′ untranslated region polymorphism rs2304277 in the DNA repair pathway gene OGG1 is a novel risk modulator for urothelial bladder carcinoma

Undiagnosed diseases: Needs and opportunities in 20 countries participating in the Undiagnosed Diseases Network International

Cystathione gamma lyase/Hydrogen Sulphide Pathway Up Regulation Enhances the Responsiveness of α1A and α1B-Adrenoreceptors in the Kidney of Rats with Left Ventricular Hypertrophy

Inborn errors of metabolism: Historical perspectives to contemporary management

CLRN1 Mutations Cause Nonsyndromic Retinitis Pigmentosa

Prevalence of human T-lymphotropic virus 1/2 in Nigeria’s capital territory and meta-analysis of Nigerian studies

Unmet needs in countries participating in the undiagnosed diseases network international: an international survey considering national health care and economic indicators

The molecular basis of retinal dystrophies in pakistan

Compound heterozygous mutations p.Q1530X and 6103delG in COL7A1 causing recessive dystrophic epidermolysis bullosa in a Pakistani family

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