Tejashree A. More - 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

Gardos channelopathies: novel insights into KCNN4 mutations and their clinical impact.

Journal: Journal of human genetics

Published: April 24, 2025

Molecular genetics and long-term outcomes of primary distal renal tubular acidosis in Asia.

Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association

Published: February 01, 2025

Quantitative assessment of red blood cell surface molecules in hereditary spherocytosis.

Journal: Journal of clinical pathology

Published: January 15, 2025

Understanding the genetic architecture and phenotypic landscape of SPTB gene variants causing hereditary spherocytosis in an Indian cohort.

Journal: Human genetics

Published: January 09, 2025

Hematopoietic Stem Cell Transplant of a Congenital Dyserythropoietic Anemia Type II Patient: A Rare Report from the Indian Population.

Journal: Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Published: March 20, 2024

Congenital Dyserythropoietic Anemia Type II: High Prevalence of c.1385A>G, (p.Tyr462Cys) Mutation in the Indian Population.

Journal: Indian journal of pediatrics

Published: April 13, 2023

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

Development of High-Resolution Melting Curve Analysis for rapid detection of SEC23B gene mutation causing Congenital Dyserythropoietic Anemia type II in Indian population.

Journal: Italian journal of pediatrics

Published: July 01, 2022

Genotypic analysis of SLC4A1 A858D mutation in Indian population associated with distal renal tubular Acidosis (dRTA) coupled with hemolytic anemia.

Journal: Gene

Published: August 18, 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