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Vinod Gupta

Mutation update: Variants of the CYB5R3 gene in recessive congenital methemoglobinemia
2020 · Vinod Gupta, Anuja Kulkarni, et al. · Human Mutation · 26
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Novel mutation (R192C) in CYB5R3 gene causing NADH-cytochrome b5 reductase deficiency in eight Indian patients associated with autosomal recessive congenital methemoglobinemia type-I
2018 · Prabhakar S. Kedar, Vinod Gupta, et al. · Hematology · 22
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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
2019 · Prabhakar S. Kedar, Rashmi Dongerdiye, et al. · The Indian Journal of Pediatrics · 18
Molecular diagnosis of unexplained haemolytic anaemia using targeted next-generation sequencing panel revealed (p.Ala337Thr) novel mutation in GPI gene in two Indian patients
2018 · Prabhakar S Kedar, Vinod Gupta, et al. · Journal of Clinical Pathology · 18
G6PD A- is the major cause of G6PD deficiency among the Siddis of Karnataka, India
2019 · Rati Devendra, Vinod Gupta, et al. · Annals of Human Biology · 11
Congenital dyserythropoietic anemia type II mimicking hereditary spherocytosis in Indian patient with SEC23B-Y462C mutations
2017 · Prabhakar Kedar, Vaishali Parmar, et al. · Annals of Hematology · 8
Identification of a novel S184F mutation causing glucose-6-phosphate-dehydrogenase deficiency in a tribal family of Madhya Pradesh, Central India
2017 · R Devendra, R Shanmugam, et al. · Meta Gene · 4
A Novel G6PD p. Gly 321 Val Mutation Causing Severe Hemolysis in an Indian Infant
2018 · R. Devendra, P. Warang, et al. · Indian Journal of Hematology and Blood Transfusion · 3
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Two Novel C-Terminal Frame shift Mutations in the CYB5R3 Gene Lead to Global Growth and Developmental Delay Associated with Recessive Congenital Methemoglobinemia Type II
2018 · Vinod Gupta · Journal of Medical Science And clinical Research · 2
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Does novel P5′N-1 mutation in combination with G6PD Asahi in an Indian male contribute to Budd Chiari Syndrome?
2017 · Prashant Warang, Rati Devendra, et al. · Blood Cells Molecules and Diseases · 2
Works count: 11
Citation count: 114
H-index: 6
I10-index: 5
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