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Ali Raza, Ph.D.
Ali Raza, Ph.D.
Sindh Institute of Urology and Transplantation, Karachi-Pakistan
Verified email at siut.org - Homepage
Title
Cited by
Cited by
Year
CYP3A5 gene polymorphisms and their impact on dosage and trough concentration of tacrolimus among kidney transplant patients: a systematic review and meta-analysis
KA Rafay, R Ali, S Firasat, A Abid
The Pharmacogenomics Journal 20 (4), 553-562, 2020
532020
The association of urinary interferon-gamma inducible protein-10 (IP10/CXCL10) levels with kidney allograft rejection.
Raza A, Firasat S, Khaliq S, Aziz T, Mubarak M, Naqvi SA, Mehdi SQ, Rizvi SA
Inflamm Res., 2017
272017
Monocyte Chemoattractant Protein-1 (MCP-1/CCL2) Levels and Its Association with Renal Allograft Rejection.
Raza A
Immunol Invest., 2016
192016
HLA class I and II polymorphisms in the Gujjar population from Pakistan
A Raza, S Firasat, S Khaliq, A Abid, SS Shah, SQ Mehdi, A Mohyuddin
Immunological investigations 42 (8), 691-700, 2013
112013
Primary Hyperoxaluria: Comprehensive mutation screening of the disease-causing-genes and spectrum of disease-associated pathogenic variants
Aiysha Abid, Ali Raza, Abdul Rafay Khan,Sadaf Firasat,Saba Shahid,Seema ...
clinical genetic, https://doi.org/10.1111/cge.14240, 2022
6*2022
The effect of chemokine receptor gene polymorphisms (CCR2V64I, CCR5-59029G> A and CCR5Δ32) on renal allograft survival in Pakistani transplant patients
S Firasat, A Raza, A Abid, T Aziz, M Mubarak, SAA Naqvi, SAH Rizvi, ...
Gene 511 (2), 314-319, 2012
62012
HOGA1 gene pathogenic variants in Primary Hyperoxaluria type III: Spectrum of pathogenic sequence variants, and phenotypic association
SK Aiysha Abid, Ali Raza, Tahir Aziz
Human Mutation, 2022
32022
The Prevalence of Pharmacogenomics Variants and Their Clinical Relevance Among the Pakistani Population
AR Khan, SH Shah, S Ajaz, S Firasat, A Abid, A Raza
Evolutionary Bioinformatics 18, 11769343221095834, 2022
12022
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 …
S Firasat, A Raza, AR Khan, A Abid
Molecular Biology Reports 50 (5), 4017-4027, 2023
2023
Genetic Alterations, DNA Methylation, Alloantibodies and Phenotypic Heterogeneity in Type III von Willebrand Disease
SM Muhammad Asif Naveed, Aiysha Abid, Nadir Ali, Yaqoob Hassan, Ali Amar ...
Genes 13 (971), 2022
2022
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