Shariq Ahmed

Karachi, SD 75300, Pakistan

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 19 publications

Glanzmann Thrombasthenia in Pakistani Patients: Identification of 7 Novel Pathogenic Variants in the Fibrinogen Receptor αIIbβ3.

Glanzmann Thrombasthenia in Pakistani Patients: Identification of 7 Novel Pathogenic Variants in the Fibrinogen Receptor αIIbβ3.

Journal: Cells

Published: November 15, 2022

Sequencing of SARS-CoV-2 in local transmission cases through Oxford Nanopore MinION platform from Karachi Pakistan.

Sequencing of SARS-CoV-2 in local transmission cases through Oxford Nanopore MinION platform from Karachi Pakistan.

Journal: Journal of infection in developing countries

Published: February 12, 2021

von Willebrand factor propeptide missense variants affect anterograde transport to Golgi resulting in ER retention.

von Willebrand factor propeptide missense variants affect anterograde transport to Golgi resulting in ER retention.

Journal: Human mutation

Published: September 23, 2020

Novel Genetic Variations in Acute Myeloid Leukemia in Pakistani Population.

Novel Genetic Variations in Acute Myeloid Leukemia in Pakistani Population.

Journal: Frontiers in genetics

Published: October 25, 2019

Frequency of Alpha Thalassaemia in homozygous Beta Thalassaemia paediatric patients and its clinical impact at a blood disease centre in Karachi, Pakistan.

Frequency of Alpha Thalassaemia in homozygous Beta Thalassaemia paediatric patients and its clinical impact at a blood disease centre in Karachi, Pakistan.

Journal: JPMA. The Journal of the Pakistan Medical Association

Published: July 17, 2019

Characterization of the mutation spectrum in a Pakistani cohort of type 3 von Willebrand disease.

Characterization of the mutation spectrum in a Pakistani cohort of type 3 von Willebrand disease.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: May 10, 2019

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

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

Journal: Thrombosis journal

Published: March 06, 2019

A Novel Nonsense Mutation in FERMT3 Causes LAD-III in a Pakistani Family.

A Novel Nonsense Mutation in FERMT3 Causes LAD-III in a Pakistani Family.

Journal: Frontiers in genetics

Published: December 07, 2018

Establishment of diagnostic facilities for autosomal recessive bleeding disorders in Pakistan.

Establishment of diagnostic facilities for autosomal recessive bleeding disorders in Pakistan.

Journal: Blood advances

Published: December 04, 2018

Managing thalassemia in the developing world: an evidence-based approach for prevention, transfusion independency, and curative treatment with hematopoietic stem cell transplantation.

Managing thalassemia in the developing world: an evidence-based approach for prevention, transfusion independency, and curative treatment with hematopoietic stem cell transplantation.

Journal: Blood advances

Published: December 04, 2018

Homozygous CALR Mutation in Primary Myelofibrosis and Its Effect on Disease Phenotype: A Case Report and Review of the Literature.

Homozygous CALR Mutation in Primary Myelofibrosis and Its Effect on Disease Phenotype: A Case Report and Review of the Literature.

Journal: Case reports in hematology

Published: September 14, 2018

Association of Thrombomodulin Gene Polymorphism (C1418T) With Coronary Artery Disease in Pakistani Population.

Association of Thrombomodulin Gene Polymorphism (C1418T) With Coronary Artery Disease in Pakistani Population.

Journal: Pakistan journal of medical sciences

Published: July 24, 2018

Showing 1-12 of 19

Last Updated: 09/26/2026