Author

Tehmina Nafees Sonia Khan

Observed names: Khan Tehmina Nafees Sonia, Tehmina Nafees, Tehmina Nafees Khan, Tehmina S. Nafees, Tehmina nafees sonia Khan

Institution: IMU University

Observed institutions: National Institute Of Blood Disease and Bone Marrow Transplantation, IMU University

ORCID: 0000-0001-6033-7375

Observed ORCID: 0000-0001-6033-7375

OpenAlex ID: A5032321418

Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population

2017 · Arshi Naz, Arijit Biswas, et al. · Thrombosis Journal · 24

Usefulness of convalescent plasma transfusion for the treatment of severely ill COVID-19 patients in Pakistan

2021 · Tehmina Nafees Sonia Khan, Samina Naz Mukry, et al. · BMC Infectious Diseases · 14

Performance Assessment of First-Generation Anti-SARS-CoV-2 Serological Assays

2020 · Mehjabeen Imam, Shabnum Khawaja, et al. · medRxiv · 2

Hemostatic and thrombotic parameters in acure leukemia- A comparison of pre and post remission induction phase

2022 · Tehmina Nafees Sonia Khan, Tariq Masood, et al. · Liaquat Medical Research Journal · 1

Correction to: Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population

2019 · Arshi Naz, Arijit Biswas, et al. · Thrombosis Journal · 1

Establishment of diagnostic facilities for autosomal recessive bleeding disorders in Pakistan

2018 · Arshi Naz, Humayun Patel, et al. · Blood Advances · 1

Exploring factor XIII genetic diversity: a familial approach to inheritance and variation

2025 · Arshi Naz, Sana Zameer, et al. · Thrombosis Journal

Analysis of pattern of ABO Blood groups in pediatric diabetic patients – An observational study

2022 · Nimra Javed, Shazia Yasin, et al. · Liaquat Medical Research Journal

An identified spectrum of mutations in alpha gene of congenital afibrinogenemia patients

2018 · Tehmina nafees sonia Khan · The Japanese Society of Hematology

Identification of novel mutations and molecular modelling of novel missense mutations in Pakistani patients of congenital afibrinogenemia

2016 · Khan Tehmina Nafees Sonia, Arshi Naz, et al. · 日本人類遺伝学会大会プログラム・抄録集

Identification of Molecular Defects in ITGA2B and ITGB3 Genes and Phenotypic Correlation in Pakistani Patients with Glanzmann Thrombasthenia

2015 · Yonus Jamal, Shariq Ahmed, et al. · Blood

Identification of Novel Mutations with Molecular Modelling of Missense Mutations of Congenital Afibrinogenemia Patients in Pakistan

2015 · Tehmina nafees sonia Khan, Arshi Naz, et al. · Blood

Characterization of Phenotypic Expression of Inherited Fibrinogen Coagulopathy in Pakistani Index Patients

2015 · Arshi Naz, Tehmina nafees sonia Khan, et al. · Blood

Works count: 13

Citation count: 43

H-index: 2

I10-index: 2