Sabika Firasat

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 9

Top Topics

Tyrosine Kinase

Circulating Tumor Cells

Top Venues

Congenital anomalies

Molecular biology reports

This page only lists publications with an associated author ORCID identifier.

Publications

Bushra Gul, Sabika Firasat, Tayyaba Shan, Raeesa Tehreem, Kiran Afshan
Mutational analysis and clinical investigations of medically diagnosed GSD 1a patients from Pakistan. PloS one 18 (11) (2023)
Aleesha Asghar, Sabika Firasat, Kiran Afshan, Shagufta Naz
Association of CDKAL1 gene polymorphism (rs10946398) with gestational diabetes mellitus in Pakistani population. Molecular biology reports (2022)
Afia Iqbal, Shagufta Naz, Haiba Kaul, Saima Sharif, Aysha Khushbakht, Muhammad Asif Naeem, Mehwish Iqtedar, Afshan Kaleem, Sabika Firasat, Farkhanda Manzoor
Mutational analysis in sodium-borate cotransporter SLC4A11 in consanguineous families from Punjab, Pakistan. PloS one 17 (8) (2022)
Raeesa Tehreem, Iris Chen, Mudassar Raza Shah, Yumei Li, Muzammil Ahmad Khan, Kiran Afshan, Rui Chen, Sabika Firasat
Exome Sequencing Identified Molecular Determinants of Retinal Dystrophies in Nine Consanguineous Pakistani Families. Genes 13 (9) (2022)
Raeesa Tehreem, Anam Arooj, Sorath Noorani Siddiqui, Shagufta Naz, Kiran Afshan, Sabika Firasat
Mutation screening of the CYP1B1 gene reveals thirteen novel disease-causing variants in consanguineous Pakistani families causing primary congenital glaucoma. PloS one 17 (9) (2022)
Sabika Firasat, null Dur-E-Shawar, Wajid Ali Khan, Ume Sughra, null Nousheen, Haiba Kaul, Shagufta Naz, Bushra Noreen, Rutaba Gul, Kiran Afshan
SLC4A11 mutations causative of congenital hereditary endothelial dystrophy (CHED) progressing to Harboyan syndrome in consanguineous Pakistani families. Molecular biology reports 48 (11) (2021)
Rutaba Gul, Sabika Firasat, Mulazim Hussain, Kiran Afshan, Dil Nawaz
IDUA gene mutations in mucopolysaccharidosis type-1 patients from two Pakistani inbred families. Congenital anomalies 60 (4) (2019)
Muhammad Shahid, Sabika Firasat, Humayoon Shafique Satti, Tariq Mahmood Satti, Tariq Ghafoor, Imtenan Sharif, Kiran Afshan
Screening of the FANCA gene mutational hotspots in the Pakistani fanconi anemia patients revealed 19 sequence variations. Congenital anomalies 60 (1) (2019)
Rabia Afzal, Sabika Firasat, Haiba Kaul, Bashir Ahmed, Sorath N Siddiqui, Saemah N Zafar, Misbah Shahzadi, Kiran Afshan
Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2. Congenital anomalies 59 (5) (2018)