Prashant P. Warang
Mumbai, MH 400012, India
Last Updated: 09/26/2026
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Found 40 publications
A novel homozygous C15ORF41 variant (c.251T > A; p.Val84Glu) causing congenital dyserythropoietic anemia type Ib in an Indian patient: molecular and structural evidence.
Journal: Molecular biology reports
Published: March 06, 2026
Novel ABCG5 and ABCG8 Variants in Sitosterolemia: Insights Into Haemolysis, Calcium Dysregulation and Therapeutic Challenges.
Journal: Human mutation
Published: February 01, 2026
Gardos channelopathies: novel insights into KCNN4 mutations and their clinical impact.
Journal: Journal of human genetics
Published: April 24, 2025
Isolated Hemolytic Anemia in Phosphoglycerate Kinase 1 Deficiency Associated with a Novel PGK1:c.746 A > G;p.(Asn249Ser) Variant.
Journal: Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion
Published: September 04, 2024
Targeted next-generation sequencing identifies eighteen novel mutations expanding the molecular and clinical spectrum of PKLR gene disorders in the Indian population.
Journal: Annals of hematology
Published: October 13, 2022
Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum.
Journal: Molecular genetics and genomics : MGG
Published: July 06, 2022
Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family.
Journal: BMC medical genomics
Published: January 12, 2021
Erythrocytes as a preferential target of oxidative stress in blood.
Journal: Free radical research
Published: January 11, 2021
Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the HK1 gene causing severe haemolytic anaemia with developmental delay in an Indian family.
Journal: Journal of clinical pathology
Published: August 24, 2020
Prevalence and spectrum of mutations causing G6PD deficiency in Indian populations.
Journal: Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases
Published: June 28, 2020
Mechanosensitive Piezo1 ion channel protein (PIEZO1 gene): update and extended mutation analysis of hereditary xerocytosis in India.
Journal: Annals of hematology
Published: September 26, 2019
Last Updated: 09/26/2026