Publications by authors named "Tejashree More"

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Molecular genetics and long-term outcomes of primary distal renal tubular acidosis in Asia.
Sayali Thakare, Anurag Lila, Vaibhav Keskar, Thenral Geetha, Kruteesh Kumar Bs, Tejashree More

Nephrol Dial Transplant· October 2025

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Gardos channelopathies: novel insights into KCNN4 mutations and their clinical impact.
Prashant Warang, Pradnya Dehadrai, Neha Samanpalliwar, Rashmi Dongerdiye, Tejashree Anil More

J Hum Genet· October 2025

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Quantitative assessment of red blood cell surface molecules in hereditary spherocytosis.
Tejashree Anil More, Prabhakar S Kedar

J Clin Pathol· September 2025

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Understanding the genetic architecture and phenotypic landscape of SPTB gene variants causing hereditary spherocytosis in an Indian cohort.
Tejashree Anil More, Prabhakar Kedar

Hum Genet· June 2025

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Hematopoietic Stem Cell Transplant of a Congenital Dyserythropoietic Anemia Type II Patient: A Rare Report from the Indian Population.
Arati Nandan Saptarshi, Kannan Subramaniam, Sandeep Nemani, Tejashree Anil More, Rashmi Dongerdiye

Indian J Hematol Blood Transfus· January 2025

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Congenital Dyserythropoietic Anemia Type II: High Prevalence of c.1385A>G, (p.Tyr462Cys) Mutation in the Indian Population.
Arati Nandan Saptarshi, Tejashree A More, Rashmi Dongerdiye, Prabhakar Kedar

Indian J Pediatr· August 2023

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Development of High-Resolution Melting Curve Analysis for rapid detection of SEC23B gene mutation causing Congenital Dyserythropoietic Anemia type II in Indian population.
Arati Nandan Saptarshi, Rashmi K Dongerdiye, Tejashree Anil More, Prabhakar S Kedar

Ital J Pediatr· July 2023

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Targeted next-generation sequencing identifies eighteen novel mutations expanding the molecular and clinical spectrum of PKLR gene disorders in the Indian population.
Rashmi Dongerdiye, Meghana Bokde, Tejashree Anil More, Arati Saptarshi, Rati Devendra

Ann Hematol· May 2023

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Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum.
Tejashree Anil More, Rati Devendra, Rashmi Dongerdiye, Prashant Warang, Prabhakar Kedar

Mol Genet Genomics· March 2023

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Genotypic analysis of SLC4A1 A858D mutation in Indian population associated with distal renal tubular Acidosis (dRTA) coupled with hemolytic anemia.
Tejashree Anil More, Prabhakar S Kedar

Gene· February 2021

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Applications of imaging flow cytometry in the diagnostic assessment of red cell membrane disorders.
Tejashree Anil More, Bhavik Dalal, Rati Devendra, Prashant Warang, Aruna Shankarkumar

Cytometry B Clin Cytom· May 2020

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Mechanosensitive Piezo1 ion channel protein (PIEZO1 gene): update and extended mutation analysis of hereditary xerocytosis in India.
Tejashree Anil More, Rashmi Dongerdiye, Rati Devendra, Prashant P Warang, Prabhakar S Kedar

Ann Hematol· April 2020

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Antiglycating potential of acesulfame potassium: an artificial sweetener.
Ahmad Ali, Tejashree Anil More, Amaritpal Kaur Hoonjan, Subramanian Sivakami

Appl Physiol Nutr Metab· October 2017

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