Sadaf Firasat

Karachi, SD, Pakistan

Last Updated: 09/26/2026

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Found 14 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

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

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

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

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

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

Journal: The pharmacogenomics journal

Published: April 10, 2019

"Like sugar in milk": reconstructing the genetic history of the Parsi population.

"Like sugar in milk": reconstructing the genetic history of the Parsi population.

Journal: Genome biology

Published: February 01, 2017

Monocyte Chemoattractant Protein-1 (MCP-1/CCL2) Levels and Its Association with Renal Allograft Rejection.

Monocyte Chemoattractant Protein-1 (MCP-1/CCL2) Levels and Its Association with Renal Allograft Rejection.

Journal: Immunological investigations

Published: December 15, 2016

The association of urinary interferon-gamma inducible protein-10 (IP10/CXCL10) levels with kidney allograft rejection.

The association of urinary interferon-gamma inducible protein-10 (IP10/CXCL10) levels with kidney allograft rejection.

Journal: Inflammation research : official journal of the European Histamine Research Society ... [et al.]

Published: May 21, 2016

Unique molecular alteration patterns in von Hippel-Lindau (VHL) gene in a cohort of sporadic renal cell carcinoma patients from Pakistan.

Unique molecular alteration patterns in von Hippel-Lindau (VHL) gene in a cohort of sporadic renal cell carcinoma patients from Pakistan.

Journal: Mutation research

Published: November 30, 2013

Showing 1-12 of 14

Last Updated: 09/26/2026