Rati Devendra

Applications of imaging flow cytometry in the diagnostic assessment of red cell membrane disorders

Tejashree Anil More, Bhavik Dalal, Rati Devendra et al. · Cytometry Part B Clinical Cytometry · 2019 · 26 citations · Full text

Mutation update: Variants of the CYB5R3 gene in recessive congenital methemoglobinemia

Vinod Gupta, Anuja Kulkarni, Prashant Warang et al. · Human Mutation · 2020 · 23 citations

Genetics, Pathology, Molecular Biology +16

Prevalence and spectrum of mutations causing G6PD deficiency in Indian populations

Rati Devendra, Vinodkumar Gupta, Rajasubramaniam Shanmugam et al. · Infection Genetics and Evolution · 2020 · 21 citations

Indian Populations, Allelic Variant, G6pd Deficiency +10

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 Kedar, Rashmi Dongerdiye, Pooja Chilwirwar et al. · The Indian Journal of Pediatrics · 2019 · 20 citations

Genetic Disorder, Genetics, Inherited Metabolic Disease +9

Mechanosensitive Piezo1 ion channel protein (PIEZO1 gene): update and extended mutation analysis of hereditary xerocytosis in India

Tejashree Anil More, Rashmi Dongerdiye, Rati Devendra et al. · Annals of Hematology · 2020 · 14 citations

Extended Mutation Analysis, Hereditary Xerocytosis, Piezo1 Gene +5