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ANALYSING THE CREDIBILITY OF META-GEOPOLITICAL FRAMEWORK: IMPLICATIONS OF KINDLEBERGER TRAP ON CHINA (POST-BRI)

Margalla papers, 2022-12, Vol.26 (2), p.72-86

2022

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Genomic Epidemiology of Complex, Multispecies, Plasmid-Borne bla KPC Carbapenemase in Enterobacterales in the United Kingdom from 2009 to 2014

Antimicrobial agents and chemotherapy, 2020-04, Vol.64 (5)

2020

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Genomic epidemiology and longitudinal sampling of ward wastewater environments and patients reveals complexity of the transmission dynamics of bla KPC -carbapenemase-producing Enterobacterales in a hospital setting

JAC-antimicrobial resistance, 2024-10, Vol.6 (5), p.dlae140

2024

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Fusion of Watermarking and Steganography for Protecting Image Ownership

Applied computing Journal, 2022-01, p.152-164

2022

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CYP3A5 gene polymorphisms and their impact on dosage and trough concentration of tacrolimus among kidney transplant patients: a systematic review and meta-analysis

The pharmacogenomics journal, 2020-08, Vol.20 (4), p.553-562

2020

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HOGA1 gene pathogenic variants in primary hyperoxaluria type III: Spectrum of pathogenic sequence variants, and phenotypic association

Human mutation, 2022-12, Vol.43 (12), p.1757-1779

2022

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Cadmium modulates intestinal Wnt/β-catenin signaling ensuing intestinal barrier disruption and systemic inflammation

Ecotoxicology and environmental safety, 2024-06, Vol.277, p.116337-116337, Article 116337

2024

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Double-chambered left ventricle: diagnosis by CMR and review of the literature

The Egyptian heart journal, 2023-03, Vol.75 (1), p.15-15, Article 15

2023

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Correction: Double-chambered left ventricle: diagnosis by CMR and review of the literature

The Egyptian heart journal, 2023-03, Vol.75 (1), p.20-20, Article 20

2023

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The prevalence of pharmacogenetic variants of vitamin K epoxide reductase complex subunit 1 gene (rs9923231), cytochrome P450 family 2 subfamily C member 9 gene (rs1799853) and cytochrome P450 family 3 subfamily-A member-5 gene (rs776746) among 13 ethnic groups of Pakistan

Molecular biology reports, 2023-05, Vol.50 (5), p.4017-4027

2023

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The Prevalence of Pharmacogenomics Variants and Their Clinical Relevance Among the Pakistani Population

Evolutionary bioinformatics online, 2022, Vol.18, p.11769343221095834-11769343221095834

2022

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Evaluation of the Early Adolescent Skills for Emotions (EASE) intervention in Lebanon: A randomized controlled trial

Comprehensive psychiatry, 2023-11, Vol.127, p.152424, Article 152424

2023

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Association of vitamin D receptor gene polymorphisms and risk of urolithiasis: results of a genetic epidemiology study and comprehensive meta-analysis

Urolithiasis, 2020-10, Vol.48 (5), p.385-401

2020

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Case report: Aorto-left atrial fistula—A rare complication of native aortic valve endocarditis

The Egyptian heart journal, 2023-07, Vol.75 (1), p.58-58, Article 58

2023

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Osteopontin promoter polymorphisms and risk of urolithiasis: a candidate gene association and meta-analysis study

BMC medical genetics, 2020-08, Vol.21 (1), p.1-172, Article 172

2020

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Genetic Alterations, DNA Methylation, Alloantibodies and Phenotypic Heterogeneity in Type III von Willebrand Disease

Genes, 2022-05, Vol.13 (6), p.971

2022

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Association of specific single nucleotide variants (SNVs) in the promoter and 3′-Untranslated region of Vascular Endothelial growth factor (VEGF) gene with risk and higher tumour grade of head and neck cancers

Oral oncology, 2021-11, Vol.122, p.105519-105519, Article 105519

2021

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Absence of Glutathione S-Transferase Theta 1 Gene Is Significantly Associated With Breast Cancer Susceptibility in Pakistani Population and Poor Overall Survival in Breast Cancer Patients: A Case-Control and Case Series Analysis

Frontiers in oncology, 2021-12, Vol.11, p.678705-678705

2021

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Structural inscrutabilities of Histone (H2BK123) monoubiquitination: A systematic review

International journal of biological macromolecules, 2024-11, Vol.280 (Pt 3), p.135977, Article 135977

2024

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Clinical characteristics and long-term outcome of patients with bioprosthetic mitral valve- Experience from a South Asian country

Journal of clinical imaging science, 2024-07, Vol.14, p.23, Article 23

2024

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Primary hyperoxaluria and genetic linkages: an insight into the disease burden from Pakistan

Urolithiasis, 2022-08, Vol.50 (4), p.439-445

2022

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A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan

Gene, 2012-07, Vol.502 (2), p.133-137

2012

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Comparison of Clinical Outcomes of Calcified and Non-Calcified Coronary Artery Lesion Intervention Under IVUS Guidance

Journal of the College of Physicians and Surgeons--Pakistan, 2023-12, Vol.33 (12), p.1355-1360

2023

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Screening of the LAMB2, WT1, NPHS1 , and NPHS2 Genes in Pediatric Nephrotic Syndrome

Frontiers in genetics, 2018-06, Vol.9, p.214-214

2018

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ANALYSING THE CREDIBILITY OF META-GEOPOLITICAL FRAMEWORK: IMPLICATIONS OF KINDLEBERGER TRAP ON CHINA (POST-BRI)

Carbapenem-resistant Enterobacteriaceae dispersal from sinks is linked to drain position and drainage rates in a laboratory model system

Genomic Epidemiology of Complex, Multispecies, Plasmid-Borne bla KPC Carbapenemase in Enterobacterales in the United Kingdom from 2009 to 2014

Genomic epidemiology and longitudinal sampling of ward wastewater environments and patients reveals complexity of the transmission dynamics of bla KPC -carbapenemase-producing Enterobacterales in a hospital setting

Fusion of Watermarking and Steganography for Protecting Image Ownership

CYP3A5 gene polymorphisms and their impact on dosage and trough concentration of tacrolimus among kidney transplant patients: a systematic review and meta-analysis

HOGA1 gene pathogenic variants in primary hyperoxaluria type III: Spectrum of pathogenic sequence variants, and phenotypic association

Cadmium modulates intestinal Wnt/β-catenin signaling ensuing intestinal barrier disruption and systemic inflammation

Double-chambered left ventricle: diagnosis by CMR and review of the literature

Correction: Double-chambered left ventricle: diagnosis by CMR and review of the literature

The prevalence of pharmacogenetic variants of vitamin K epoxide reductase complex subunit 1 gene (rs9923231), cytochrome P450 family 2 subfamily C member 9 gene (rs1799853) and cytochrome P450 family 3 subfamily-A member-5 gene (rs776746) among 13 ethnic groups of Pakistan

The Prevalence of Pharmacogenomics Variants and Their Clinical Relevance Among the Pakistani Population

Evaluation of the Early Adolescent Skills for Emotions (EASE) intervention in Lebanon: A randomized controlled trial

Association of vitamin D receptor gene polymorphisms and risk of urolithiasis: results of a genetic epidemiology study and comprehensive meta-analysis

Case report: Aorto-left atrial fistula—A rare complication of native aortic valve endocarditis

Osteopontin promoter polymorphisms and risk of urolithiasis: a candidate gene association and meta-analysis study

Genetic Alterations, DNA Methylation, Alloantibodies and Phenotypic Heterogeneity in Type III von Willebrand Disease

Association of specific single nucleotide variants (SNVs) in the promoter and 3′-Untranslated region of Vascular Endothelial growth factor (VEGF) gene with risk and higher tumour grade of head and neck cancers

Absence of Glutathione S-Transferase Theta 1 Gene Is Significantly Associated With Breast Cancer Susceptibility in Pakistani Population and Poor Overall Survival in Breast Cancer Patients: A Case-Control and Case Series Analysis

Structural inscrutabilities of Histone (H2BK123) monoubiquitination: A systematic review

Clinical characteristics and long-term outcome of patients with bioprosthetic mitral valve- Experience from a South Asian country

Primary hyperoxaluria and genetic linkages: an insight into the disease burden from Pakistan

A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan

Comparison of Clinical Outcomes of Calcified and Non-Calcified Coronary Artery Lesion Intervention Under IVUS Guidance

Screening of the LAMB2, WT1, NPHS1 , and NPHS2 Genes in Pediatric Nephrotic Syndrome

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