Prabhakar S Kedar (Prabhakar Kedar)

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 20

Top Venues

Molecular genetics and genomics : MGG

Annals of hematology

Journal of clinical pathology

Indian journal of pediatrics

National Institute of Immunohaematology

Kyushu Institute of Technology (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

National Institute of Immunohaematology Apr 21 1992 - Mar 31 2018

India

Assistant Director -Scientist d :: Hematogenetics

Education History

Kyushu Institute of Technology Apr 01 2003 - Mar 31 2007

Japan

PHD

Publications

Rashmi Dongerdiye, Prabhakar S Kedar, Arati Saptarshi, Abhilasha A Sampagar, Chandrakala Shanmukhaiah, Sangeeta Mudaliar, Purva Kanvinde, Mahesh S Desai, Manisha Rajan Madkaikar
Non-syndromic congenital sideroblastic anaemia; phenotype, and genotype of 15 Indian patients. Annals of hematology (2024)
Tejashree Anil More, Rati Devendra, Rashmi Dongerdiye, Prashant Warang, Prabhakar S Kedar
Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum. Molecular genetics and genomics : MGG 298 (2) (2023)
Tejashree Anil More, Rati Devendra, Rashmi Dongerdiye, Prashant Warang, Prabhakar S Kedar
Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum. Molecular genetics and genomics : MGG 298 (2) (2023)
Rashmi Dongerdiye, Meghana Bokde, Tejashree Anil More, Arati Saptarshi, Rati Devendra, Ashish S Chiddarwar, Prashant Warang, Prabhakar S Kedar
Targeted next-generation sequencing identifies eighteen novel mutations expanding the molecular and clinical spectrum of PKLR gene disorders in the Indian population. Annals of hematology (2023)
Tejashree Anil More, Rati Devendra, Rashmi Dongerdiye, Prashant Warang, Prabhakar S Kedar
Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum. Molecular genetics and genomics : MGG 298 (2) (2023)
Tejashree Anil More, Rati Devendra, Rashmi Dongerdiye, Prashant Warang, Prabhakar S Kedar
Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum. Molecular genetics and genomics : MGG 298 (2) (2023)
Tejashree Anil More, Rati Devendra, Rashmi Dongerdiye, Prashant Warang, Prabhakar S Kedar
Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum. Molecular genetics and genomics : MGG (2023)
Arati Nandan Saptarshi, Rashmi K Dongerdiye, Tejashree Anil More, Prabhakar S Kedar
Development of High-Resolution Melting Curve Analysis for rapid detection of SEC23B gene mutation causing Congenital Dyserythropoietic Anemia type II in Indian population. Italian journal of pediatrics 49 (1) (2023)
Arati Nandan Saptarshi, Tejashree A More, Rashmi Dongerdiye, Prabhakar S Kedar
Congenital Dyserythropoietic Anemia Type II: High Prevalence of c.1385A>G, (p.Tyr462Cys) Mutation in the Indian Population. Indian journal of pediatrics (2023)
Prabhakar S Kedar, Rashmi Dongerdiye, Shanmukhaiah Chandrakala, Umair Ahmed Bargir, Manisha Rajan Madkaikar
Targeted next-generation sequencing revealed a novel homozygous mutation in the LRBA gene causes severe haemolysis associated with Inborn Errors of Immunity in an Indian family. Hematology (Amsterdam, Netherlands) 27 (1) (2022)
Anuradha Deorukhkar, Anuja Kulkarni, Prabhakar S Kedar
Three novel mutations in CYB5R3 gene causing NADH-cytochrome b5 reductase enzyme deficiency leads to recessive congenital methaemoglobinemia. Molecular biology reports 49 (3) (2022)
Rashmi Dongerdiye, Abhilasha Sampagar, Rati Devendra, Prashant Warang, Prabhakar S Kedar
Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family. BMC medical genomics 14 (1) (2021)
Vinod Gupta, Anuja Kulkarni, Prashant Warang, Rati Devendra, Ashish Chiddarwar, Prabhakar S Kedar
Mutation update: Variants of the CYB5R3 gene in recessive congenital methemoglobinemia. Human mutation 41 (4) (2020)
Tejashree Anil More, Rashmi Dongerdiye, Rati Devendra, Prashant P Warang, Prabhakar S Kedar
Mechanosensitive Piezo1 ion channel protein (PIEZO1 gene): update and extended mutation analysis of hereditary xerocytosis in India. Annals of hematology 99 (4) (2020)
Rashmi Dongerdiye, Sujatha Jagadeesh, Beena Suresh, Aruna Rajendran, Rati Devendra, Prashant Warang, Prabhakar S Kedar
Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the HK1 gene causing severe haemolytic anaemia with developmental delay in an Indian family. Journal of clinical pathology 74 (10) (2020)
Tejashree Anil More, Bhavik Dalal, Rati Devendra, Prashant Warang, Aruna Shankarkumar, Prabhakar S Kedar
Applications of imaging flow cytometry in the diagnostic assessment of red cell membrane disorders. Cytometry. Part B, Clinical cytometry 98 (3) (2019)
Prabhakar S Kedar, Rashmi Dongerdiye, Pooja Chilwirwar, Vinod Gupta, Ashish Chiddarwar, Rati Devendra, Prashant Warang, Harsha Prasada, Abhilasha Sampagar, Sunil Bhat, S Chandrakala, Manisha Madkaikar
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. Indian journal of pediatrics 86 (8) (2019)
Rashmi Dongerdiye, Pranoti Kamat, Punit Jain, Prashant Warang, Rati Devendra, Nilesh Wasekar, Ratna Sharma, Ketaki Mhaskar, Manisha R Madkaikar, Mamta V Manglani, Prabhakar S Kedar
Red cell adenylate kinase deficiency in India: identification of two novel missense mutations (c.71A>G and c.413G>A). Journal of clinical pathology 72 (6) (2019)
Prabhakar S Kedar, Hideo Harigae, Etsuro Ito, Hideki Muramatsu, Seiji Kojima, Yusuke Okuno, Tohru Fujiwara, Rashmi Dongerdiye, Prashant P Warang, Manisha R Madkaikar
Study of pathophysiology and molecular characterization of congenital anemia in India using targeted next-generation sequencing approach. International journal of hematology 110 (5) (2019)
Prabhakar S Kedar, Vinod Gupta, Rashmi Dongerdiye, Ashish Chiddarwar, Prashant Warang, Manisha R Madkaikar
Molecular diagnosis of unexplained haemolytic anaemia using targeted next-generation sequencing panel revealed (p.Ala337Thr) novel mutation in GPI gene in two Indian patients. Journal of clinical pathology 72 (1) (2018)

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Publication Activity (10 Years)

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Prabhakar S Kedar (Prabhakar Kedar)