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Evolution of codon usage in Zika virus genomes is host and vector specific

Emerging microbes & infections, 2016-10, Vol.5 (10), p.e107-14

2016

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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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Landslide dam and subsequent dam-break flood estimation using HEC-RAS model in Northern Pakistan

Natural hazards (Dordrecht), 2013-01, Vol.65 (1), p.241-254

2013

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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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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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Phytochemical Screening and Protective Effects of Prunus persica Seeds Extract on Carbon Tetrachloride-Induced Hepatic Injury in Rats

Current pharmaceutical biotechnology, 2022, Vol.23 (1), p.158

2022

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POLYAR, a new computer program for prediction of poly(A) sites in human sequences

BMC genomics, 2010-11, Vol.11 (1), p.646-646, Article 646

2010

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Biallelic variants in CHST3 cause Spondyloepiphyseal dysplasia with joint dislocations in three Pakistani kindreds

BMC musculoskeletal disorders, 2022-08, Vol.23 (1), p.818-818, Article 818

2022

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

PloS one, 2015-07, Vol.10 (7), p.e0130754

2015

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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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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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Decreased serum PON1 arylesterase activity in familial hypercholesterolemia patients with a mutated LDLR gene

Genetics and molecular biology, 2018-07, Vol.41 (3), p.570-577

2018

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Transethnic analysis of psoriasis susceptibility in South Asians and Europeans enhances fine mapping in the MHC and genome wide

HGG advances, 2022-01, Vol.3 (1), p.100069, Article 100069

2022

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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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Variants in the ASB10 Gene Are Associated with Primary Open Angle Glaucoma

PloS one, 2015-12, Vol.10 (12), p.e0145005-e0145005

2015

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Novel mutation in AAA domain of BCS1L causing Bjornstad syndrome

Journal of human genetics, 2013-12, Vol.58 (12), p.819-821

2013

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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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Mutations in IMPG2, Encoding Interphotoreceptor Matrix Proteoglycan 2, Cause Autosomal-Recessive Retinitis Pigmentosa

American journal of human genetics, 2010-08, Vol.87 (2), p.199-208

2010

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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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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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A canonical splice site mutation in GIPC3 causes sensorineural hearing loss in a large Pakistani family

Journal of human genetics, 2014-12, Vol.59 (12), p.683-686

2014

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The genetic spectrum of familial hypercholesterolemia in Pakistan

Clinica chimica acta, 2013-06, Vol.421, p.219-225

2013

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Evolution of codon usage in Zika virus genomes is host and vector specific

Implementation of public health genomics in Pakistan

Landslide dam and subsequent dam-break flood estimation using HEC-RAS model in Northern Pakistan

Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements

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

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

Phytochemical Screening and Protective Effects of Prunus persica Seeds Extract on Carbon Tetrachloride-Induced Hepatic Injury in Rats

POLYAR, a new computer program for prediction of poly(A) sites in human sequences

Biallelic variants in CHST3 cause Spondyloepiphyseal dysplasia with joint dislocations in three Pakistani kindreds

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

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

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

Decreased serum PON1 arylesterase activity in familial hypercholesterolemia patients with a mutated LDLR gene

Transethnic analysis of psoriasis susceptibility in South Asians and Europeans enhances fine mapping in the MHC and genome wide

Exome sequencing identifies three novel candidate genes implicated in intellectual disability

Variants in the ASB10 Gene Are Associated with Primary Open Angle Glaucoma

Novel mutation in AAA domain of BCS1L causing Bjornstad syndrome

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

Mutations in IMPG2, Encoding Interphotoreceptor Matrix Proteoglycan 2, Cause Autosomal-Recessive Retinitis Pigmentosa

CLRN1 Mutations Cause Nonsyndromic Retinitis Pigmentosa

Inborn errors of metabolism: Historical perspectives to contemporary management

A canonical splice site mutation in GIPC3 causes sensorineural hearing loss in a large Pakistani family

The genetic spectrum of familial hypercholesterolemia in Pakistan

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