Aiysha Abid
6PUBLICATIONS
3CO-AUTHORS
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Publications (6)
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|Feb 28, 2023
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.Sadaf Firasat, Ali Raza, Abdul Rafay Khan
|Oct 19, 2022
HOGA1 gene pathogenic variants in primary hyperoxaluria type III: Spectrum of pathogenic sequence variants, and phenotypic association.Aiysha Abid, Ali Raza, Tahir Aziz
|Oct 03, 2022
Primary hyperoxaluria: Comprehensive mutation screening of the disease causing genes and spectrum of disease-associated pathogenic variants.Aiysha Abid, Ali Raza, Abdul Rafay Khan
|Jun 24, 2022
Genetic Alterations, DNA Methylation, Alloantibodies and Phenotypic Heterogeneity in Type III von Willebrand Disease.Muhammad Asif Naveed, Aiysha Abid, Nadir Ali
|Jan 07, 2020
CYP3A5 gene polymorphisms and their impact on dosage and trough concentration of tacrolimus among kidney transplant patients: a systematic review and meta-analysis.Abdul Rafay Khan, Ali Raza, Sadaf Firasat
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