Publications by authors named "Rati Devendra"

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Molecularly confirmed para-Bombay (Ah) secretor phenotype with FUT1 c.328G>A and FUT2 c.357C>T mutations: first case report from India.
Thamizhsurabi Arivazhagan, Tejaswi Chada, Srinivasarao Chunchu, Monali Lokhande, Rati Devendra

Blood Transfus· November 2025

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Weak or partial D: Importance of molecular characterization of D variants.
Akshaya Tomar, Rati Devendra, Disha Parchure, Swati Kulkarni

Transfus Apher Sci· April 2025

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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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Successful management of Methemoglobinemia and G6PD deficiency in a patient posted for surgical excision of branchial cyst.
V J Arun, Anuradha Deorukhkar, Aboobacker Mohamed Rafi, Deepak Charles, Rati Devendra

Asian J Transfus Sci· May 2022

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Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the gene causing severe haemolytic anaemia with developmental delay in an Indian family.
Rashmi Dongerdiye, Sujatha Jagadeesh, Beena Suresh, Aruna Rajendran, Rati Devendra

J Clin Pathol· October 2021

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Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family.
Rashmi Dongerdiye, Abhilasha Sampagar, Rati Devendra, Prashant Warang, Prabhakar Kedar

BMC Med Genomics· July 2021

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Prevalence and spectrum of mutations causing G6PD deficiency in Indian populations.
Rati Devendra, Vinodkumar Gupta, Rajasubramaniam Shanmugam, M P S S Singh, Purushottam Patel

Infect Genet Evol· December 2020

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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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Mutation update: Variants of the CYB5R3 gene in recessive congenital methemoglobinemia.
Vinod Gupta, Anuja Kulkarni, Prashant Warang, Rati Devendra, Ashish Chiddarwar

Hum Mutat· April 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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G6PD A- is the major cause of G6PD deficiency among the Siddis of Karnataka, India.
Rati Devendra, Vinod Gupta, Somashekhar S Biradar, Pradeep Bhat, Shantharam Hegde

Ann Hum Biol· February 2020

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Glucose Phosphate Isomerase Deficiency: High Prevalence of p.Arg347His Mutation in Indian Population Associated with Severe Hereditary Non-Spherocytic Hemolytic Anemia Coupled with Neurological Dysfunction.
Prabhakar S Kedar, Rashmi Dongerdiye, Pooja Chilwirwar, Vinod Gupta, Ashish Chiddarwar, Rati Devendra

Indian J Pediatr· August 2019

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Red cell adenylate kinase deficiency in India: identification of two novel missense mutations (c.71A>G and c.413G>A).
Rashmi Dongerdiye, Pranoti Kamat, Punit Jain, Prashant Warang, Rati Devendra

J Clin Pathol· June 2019

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Congenital dyserythropoietic anemia type II mimicking hereditary spherocytosis in Indian patient with SEC23B-Y462C mutations.
Prabhakar Kedar, Vaishali Parmar, Rati Devendra, Vinod Gupta, Prashant Warang

Ann Hematol· December 2017

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Does novel P5'N-1 mutation in combination with G6PD Asahi in an Indian male contribute to Budd Chiari Syndrome?
Prashant Warang, Rati Devendra, Ashish Chiddarwar, Vinod Gupta, Darshana Mirgal

Blood Cells Mol Dis· July 2017

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Do UGT1A1 and HMOX1 gene promoter polymorphisms increase the risk of hyperbilirubinemia and gallstones in patients with hereditary spherocytosis?
Prashant Warang, Rati Devendra, Selma D'Silva, Ashish Chiddarwar, Prabhakar Kedar

Ann Hematol· January 2015

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Primaquine-induced severe methemoglobinemia developed during treatment of Plasmodium vivax malarial infection in an Indian family associated with a novel mutation (p.Agr57Trp) in the CYB5R3 gene.
Prabhakar Kedar, Prashant Warang, Subhaprakash Sanyal, Rati Devendra, Kanjaksha Ghosh

Clin Chim Acta· November 2014

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