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Dr Prabhakar Kedar
Dr Prabhakar Kedar
Scientist E, ICMR National Institute of Immunohematology
Verified email at icmr.gov.in
Title
Cited by
Cited by
Year
Experience with eosin‐5′‐maleimide as a diagnostic tool for red cell membrane cytoskeleton disorders
PS Kedar, RB Colah, S Kulkarni, K Ghosh, D Mohanty
Clinical & Laboratory Haematology 25 (6), 373-376, 2003
1042003
Flow cytometric osmotic fragility—an effective screening approach for red cell membranopathies
P Warang, M Gupta, P Kedar, K Ghosh, R Colah
Cytometry Part B: Clinical Cytometry 80 (3), 186-190, 2011
632011
Molecular and clinical heterogeneity in pyruvate kinase deficiency in India
P Warang, P Kedar, K Ghosh, R Colah
Blood Cells, Molecules, and Diseases 51 (3), 133-137, 2013
412013
Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis
AK Stewart, PS Kedar, BE Shmukler, DH Vandorpe, A Hsu, B Glader, ...
American Journal of Physiology-Cell Physiology 300 (5), C1034-C1046, 2011
412011
Proteomic investigation on the pyk-F gene knockout Escherichia coli for aromatic amino acid production
P Kedar, R Colah, K Shimizu
Enzyme and microbial technology 41 (4), 455-465, 2007
372007
Clinical spectrum and molecular basis of recessive congenital methemoglobinemia in India
PP Warang, PS Kedar, C Shanmukaiah, K Ghosh, RB Colah
Clinical Genetics 87 (1), 62-67, 2015
312015
Hemolytic anemia and distal renal tubular acidosis in two Indian patients homozygous for SLC4A1/AE1 mutation A858D
BE Shmukler, PS Kedar, P Warang, M Desai, M Madkaikar, K Ghosh, ...
American journal of hematology 85 (10), 824, 2010
312010
Applications of imaging flow cytometry in the diagnostic assessment of red cell membrane disorders
TA More, B Dalal, R Devendra, P Warang, A Shankarkumar, P Kedar
Cytometry Part B: Clinical Cytometry 98 (3), 238-249, 2020
232020
Study of pathophysiology and molecular characterization of congenital anemia in India using targeted next-generation sequencing approach
PS Kedar, H Harigae, E Ito, H Muramatsu, S Kojima, Y Okuno, T Fujiwara, ...
International Journal of Hematology 110, 618-626, 2019
212019
Spectrum of novel mutations in the human PKLR gene in pyruvate kinase‐deficient Indian patients with heterogeneous clinical phenotypes
P Kedar, T Hamada, P Warang, A Nadkarni, K Shimizu, H Fujji, K Ghosh, ...
Clinical genetics 75 (2), 157-162, 2009
212009
Red cell pyruvate kinase deficiency in neonatal jaundice cases in India
PS Kedar, P Warang, RB Colah, D Mohanty
The Indian Journal of Pediatrics 73, 985-988, 2006
212006
Mutation update: Variants of the CYB5R3 gene in recessive congenital methemoglobinemia
V Gupta, A Kulkarni, P Warang, R Devendra, A Chiddarwar, P Kedar
Human Mutation 41 (4), 737-748, 2020
202020
A novel R198H mutation in the glucose-6-phosphate dehydrogenase gene in the tribal groups of the Nilgiris in Southern India
R Chalvam, PS Kedar, RB Colah, K Ghosh, MB Mukherjee
Journal of human genetics 53 (2), 181-184, 2008
202008
Novel mutation (R192C) in CYB5R3 gene causing NADH-cytochrome b5 reductase deficiency in eight Indian patients associated with autosomal recessive congenital methemoglobinemia …
PS Kedar, V Gupta, P Warang, A Chiddarwar, M Madkaikar
Hematology 23 (8), 567-573, 2018
182018
Congenital methemoglobinemia caused by Hb‐MRatnagiri (β‐63CAT→TAT, His→Tyr) in an Indian family
PS Kedar, AH Nadkarni, S Phanasgoankar, M Madkaikar, K Ghosh, ...
American journal of hematology 79 (2), 168-170, 2005
182005
Prevalence and spectrum of mutations causing G6PD deficiency in Indian populations
R Devendra, V Gupta, R Shanmugam, M Singh, P Patel, N Valecha, ...
Infection, Genetics and Evolution 86, 104597, 2020
172020
Molecular diagnosis of unexplained haemolytic anaemia using targeted next-generation sequencing panel revealed (p. Ala337Thr) novel mutation in GPI gene in two Indian patients
PS Kedar, V Gupta, R Dongerdiye, A Chiddarwar, P Warang, ...
Journal of Clinical Pathology 72 (1), 81-85, 2019
152019
Hereditary non-spherocytic hemolytic anemia and severe glucose phosphate isomerase deficiency in an Indian patient homozygous for the L487F mutation in the human GPI gene
P Warang, P Kedar, K Ghosh, RB Colah
International journal of hematology 96 (2), 263-267, 2012
152012
Severe mental retardation and recessive congenital methemoglobinemia in three Indian patients: Compound heterozygous for NADH‐cytochrome b5 reductase gene mutations
PS Kedar, P Warang, K Ghosh, RB Colah
American journal of hematology 86 (3), 327-329, 2011
152011
Congenital methemoglobinemia due to NADH-methemoglobin reductase deficiency in three Indian families.
PS Kedar, RB Colah, K Ghosh, D Mohanty
Haematologia 32 (4), 543-549, 2002
152002
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