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 | 104 | 2003 |
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 | 63 | 2011 |
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 | 41 | 2013 |
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 | 41 | 2011 |
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 | 37 | 2007 |
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 | 31 | 2015 |
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 | 31 | 2010 |
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 | 24 | 2020 |
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 | 23 | 2019 |
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 | 22 | 2009 |
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 | 22 | 2006 |
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 | 20 | 2020 |
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 | 20 | 2008 |
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 | 18 | 2018 |
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 | 18 | 2005 |
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 | 17 | 2020 |
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 | 16 | 2019 |
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 | 16 | 2012 |
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 | 15 | 2011 |
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 | 15 | 2002 |