Rashmi Dongerdiye

Study of pathophysiology and molecular characterization of congenital anemia in India using targeted next-generation sequencing approach

Prabhakar Kedar, Hideo Harigae, Etsuro Ito et al. · International Journal of Hematology · 2019 · 21 citations

Anemia, Molecular Characterization, Medicine +9

Molecular diagnosis of unexplained haemolytic anaemia using targeted next-generation sequencing panel revealed (p.Ala337Thr) novel mutation in GPI gene in two Indian patients

Prabhakar Kedar, Vinod Gupta, Rashmi Dongerdiye et al. · Journal of Clinical Pathology · 2018 · 20 citations

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

Clinical, laboratory, and mutational profile of children with glucose phosphate isomerase deficiency: a single centre report

Abhilasha Sampagar, Manasi Gosavi, Prabhakar Kedar et al. · International Journal of Hematology · 2021 · 11 citations