Aiysha Abid

Karachi, SD, Pakistan

Last Updated: 09/26/2026

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Found 28 publications

Publisher Correction: Clinical burden, genetic heterogeneity, and diagnostic implications in primary hyperoxaluria type 2.

Publisher Correction: Clinical burden, genetic heterogeneity, and diagnostic implications in primary hyperoxaluria type 2.

Journal: Pediatric nephrology (Berlin, Germany)

Published: March 16, 2026

Clinical burden, genetic heterogeneity, and diagnostic implications in primary hyperoxaluria type 2.

Clinical burden, genetic heterogeneity, and diagnostic implications in primary hyperoxaluria type 2.

Journal: Pediatric nephrology (Berlin, Germany)

Published: November 06, 2025

Rare and heterogeneous manifestations of leucocyte adhesion deficiency type 1: report of two cases with diagnostic dilemmas and novel ITGB2 mutation.

Rare and heterogeneous manifestations of leucocyte adhesion deficiency type 1: report of two cases with diagnostic dilemmas and novel ITGB2 mutation.

Journal: Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology

Published: August 05, 2022

Primary hyperoxaluria: Comprehensive mutation screening of the disease causing genes and spectrum of disease-associated pathogenic variants.

Primary hyperoxaluria: Comprehensive mutation screening of the disease causing genes and spectrum of disease-associated pathogenic variants.

Journal: Clinical genetics

Published: July 19, 2022

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

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

Journal: Human mutation

Published: July 08, 2022

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 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.

Journal: Molecular biology reports

Published: June 04, 2022

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

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

Journal: Genes

Published: April 23, 2022

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

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

Journal: Urolithiasis

Published: March 15, 2022

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

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

Journal: Evolutionary bioinformatics online

Published: October 16, 2021

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.

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.

Journal: Oral oncology

Published: May 05, 2021

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.

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.

Journal: Frontiers in oncology

Published: March 10, 2021

Possible ethnic associations in primary hyperoxaluria type-III-associated HOGA1 sequence variants.

Possible ethnic associations in primary hyperoxaluria type-III-associated HOGA1 sequence variants.

Journal: Molecular biology reports

Published: December 22, 2020

Showing 1-12 of 28

Last Updated: 09/26/2026