Priya Hariharan
Mumbai, MH, India
Last Updated: 09/26/2026
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Found 21 publications
Diagnostic accuracy of HemoTypeSC for detecting sickle cell disease in newborns: A multicentric study.
Journal: The Indian journal of medical research
Published: January 20, 2025
When a synonymous mutation breaks the silence in a thalassaemia patient.
Journal: British journal of haematology
Published: May 16, 2023
Rapid molecular identification of a rare β-globin gene deletion & its clinical implication.
Journal: The Indian journal of medical research
Published: September 20, 2022
Dynamic interplay of microRNA in diseases and therapeutic.
Journal: Clinical genetics
Published: July 21, 2022
Role of microRNA in hydroxyurea mediated HbF induction in sickle cell anaemia patients.
Journal: Scientific reports
Published: May 31, 2022
Diagnostic challenges posed by a rare unstable hemoglobin variant Hb Southampton [HBB: c.320T → C] with pyrimidine 5' nucleotidase deficiency and the response to HU therapy.
Journal: Blood cells, molecules & diseases
Published: February 15, 2022
The Changing Trends in Prenatal Diagnosis of Hemoglobinopathies in India: The Quest of a Single Center to Reduce the Burden of Disease over Three Decades.
Journal: Hemoglobin
Published: April 08, 2021
Significance of genetic modifiers of hemoglobinopathies leading towards precision medicine.
Journal: Scientific reports
Published: February 28, 2021
Hb Yaizu: A rare beta-globin chain variant posing diagnostic dilemma in high-performance liquid chromatography.
Journal: Indian journal of pathology & microbiology
Published: November 06, 2020
Insight of fetal to adult hemoglobin switch: Genetic modulators and therapeutic targets.
Journal: Blood reviews
Published: August 19, 2020
Last Updated: 09/26/2026