Prashant Warang

589 total citations
31 papers, 345 citations indexed

About

Prashant Warang is a scholar working on Pediatrics, Perinatology and Child Health, Physiology and Genetics. According to data from OpenAlex, Prashant Warang has authored 31 papers receiving a total of 345 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Pediatrics, Perinatology and Child Health, 22 papers in Physiology and 13 papers in Genetics. Recurrent topics in Prashant Warang's work include Erythrocyte Function and Pathophysiology (22 papers), Neonatal Health and Biochemistry (20 papers) and Hemoglobinopathies and Related Disorders (13 papers). Prashant Warang is often cited by papers focused on Erythrocyte Function and Pathophysiology (22 papers), Neonatal Health and Biochemistry (20 papers) and Hemoglobinopathies and Related Disorders (13 papers). Prashant Warang collaborates with scholars based in India, Japan and Italy. Prashant Warang's co-authors include Prabhakar Kedar, Roshan Colah, Kanjaksha Ghosh, Manisha Madkaikar, Malay B. Mukherjee, Takujiro Homma, Junichi Fujii, Anita Nadkarni, Sho Kobayashi and Maya Gupta and has published in prestigious journals such as SHILAP Revista de lepidopterología, British Journal of Haematology and Journal of Clinical Pathology.

In The Last Decade

Prashant Warang

31 papers receiving 338 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Prashant Warang India 12 195 156 113 108 87 31 345
Alkmini T. Anastasiadi Greece 12 192 1.0× 56 0.4× 89 0.8× 74 0.7× 51 0.6× 26 328
Ainoon Othman Malaysia 9 100 0.5× 137 0.9× 66 0.6× 51 0.5× 69 0.8× 22 287
Ernest Beutler United States 12 134 0.7× 69 0.4× 264 2.3× 310 2.9× 39 0.4× 13 550
W. Schr�ter Germany 9 166 0.9× 98 0.6× 50 0.4× 77 0.7× 42 0.5× 31 361
A Karaklis Greece 10 150 0.8× 127 0.8× 251 2.2× 228 2.1× 48 0.6× 18 423
Jean D. Ross United States 9 81 0.4× 123 0.8× 77 0.7× 79 0.7× 82 0.9× 14 329
Binal N. Shah United States 11 43 0.2× 34 0.2× 166 1.5× 156 1.4× 30 0.3× 36 413
Stephanie van Straaten Netherlands 7 113 0.6× 35 0.2× 83 0.7× 80 0.7× 18 0.2× 9 229
Edis Belini Brazil 10 70 0.4× 31 0.2× 246 2.2× 181 1.7× 15 0.2× 22 330
G. W. L�hr Germany 10 187 1.0× 109 0.7× 63 0.6× 55 0.5× 21 0.2× 17 325

Countries citing papers authored by Prashant Warang

Since Specialization
Citations

This map shows the geographic impact of Prashant Warang's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Prashant Warang with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Prashant Warang more than expected).

Fields of papers citing papers by Prashant Warang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Prashant Warang. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Prashant Warang. The network helps show where Prashant Warang may publish in the future.

Co-authorship network of co-authors of Prashant Warang

This figure shows the co-authorship network connecting the top 25 collaborators of Prashant Warang. A scholar is included among the top collaborators of Prashant Warang based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Prashant Warang. Prashant Warang is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Warang, Prashant, et al.. (2022). Role of Oxidative Stress and the Protective Effect of Fermented Papaya Preparation in Sickle Cell Disease. Hemoglobin. 46(4). 260–264. 1 indexed citations
2.
Fujii, Junichi, Takujiro Homma, Sho Kobayashi, et al.. (2021). Erythrocytes as a preferential target of oxidative stress in blood. Free Radical Research. 55(8). 781–799. 48 indexed citations
3.
Singh, Monika, Neena Valecha, Neelima Mishra, et al.. (2020). Prevalence and spectrum of mutations causing G6PD deficiency in Indian populations. Infection Genetics and Evolution. 86. 104597–104597. 13 indexed citations
4.
Warang, Prashant, et al.. (2018). Potential involvement of ubiquitin‐proteasome system dysfunction associated with oxidative stress in the pathogenesis of sickle cell disease. British Journal of Haematology. 182(4). 559–566. 17 indexed citations
5.
6.
Warang, Prashant, et al.. (2018). A Novel G6PD p. Gly 321 Val Mutation Causing Severe Hemolysis in an Indian Infant. Indian Journal of Hematology and Blood Transfusion. 35(2). 399–401. 3 indexed citations
7.
8.
Kedar, Prabhakar, Anand Desai, Prashant Warang, & Roshan Colah. (2016). A microplate reader-based method to quantify NADH-cytochrome b5 reductase activity for diagnosis of recessive congenital methaemoglobinemia. Hematology. 22(4). 252–257. 5 indexed citations
9.
Warang, Prashant, et al.. (2015). A novel nine base deletion mutation in NADH-cytochrome b5 reductase gene in an Indian family with recessive congenital methemoglobinemia-type-II. SHILAP Revista de lepidopterología. 5. 44–47. 5 indexed citations
10.
Warang, Prashant, Prabhakar Kedar, Kanjaksha Ghosh, & Roshan Colah. (2013). Molecular and clinical heterogeneity in pyruvate kinase deficiency in India. Blood Cells Molecules and Diseases. 51(3). 133–137. 24 indexed citations
11.
Warang, Prashant, Prabhakar Kedar, Rakhee Kar, Kanjaksha Ghosh, & Roshan Colah. (2012). New missense homozygous mutation (Q270Ter) in the pyrimidine 5′ nucleotidase type I-related gene in two Indian families with hereditary non-spherocytic hemolytic anemia. Annals of Hematology. 92(5). 715–717. 2 indexed citations
12.
Warang, Prashant, Prabhakar Kedar, Kanjaksha Ghosh, & Roshan Colah. (2012). 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. International Journal of Hematology. 96(2). 263–267. 13 indexed citations
13.
Warang, Prashant, Maya Gupta, Prabhakar Kedar, Kanjaksha Ghosh, & Roshan Colah. (2011). Flow cytometric osmotic fragility—An effective screening approach for red cell membranopathies. Cytometry Part B Clinical Cytometry. 80B(3). 186–190. 34 indexed citations
14.
Warang, Prashant, Prabhakar Kedar, Krishna Ghosh, & Roshan Colah. (2011). A new simple approach for the determination of pyrimidine 5′‐nucleotidase activity in human erythrocytes using an ELISA reader. International Journal of Laboratory Hematology. 34(3). 232–236. 3 indexed citations
15.
Nair, Sona, et al.. (2010). Five α globin chain variants identified during screening for haemoglobinopathies. European Journal of Clinical Investigation. 40(3). 226–232. 9 indexed citations
16.
Kedar, Prabhakar, Prashant Warang, Kanjaksha Ghosh, & Roshan Colah. (2010). Severe mental retardation and recessive congenital methemoglobinemia in three Indian patients: Compound heterozygous for NADH‐cytochrome b5 reductase gene mutations. American Journal of Hematology. 86(3). 327–329. 10 indexed citations
17.
Kedar, Prabhakar, Prashant Warang, Anita Nadkarni, et al.. (2009). Spectrum of novel mutations in the human PKLR gene in pyruvate kinase‐deficient Indian patients with heterogeneous clinical phenotypes. Clinical Genetics. 75(2). 157–162. 16 indexed citations
18.
Kedar, Prabhakar, Prashant Warang, Anita Nadkarni, Roshan Colah, & Kanjaksha Ghosh. (2007). A novel G143D mutation in the NADH-cytochrome b5 reductase gene in an Indian patient with type I recessive hereditary methemoglobinemia. Blood Cells Molecules and Diseases. 40(3). 323–327. 8 indexed citations
19.
Gupta, Neerja, Paola Bianchi, Elisa Fermo, et al.. (2006). Prenatal diagnosis for a novel homozygous mutation in PKLR gene in an Indian family. Prenatal Diagnosis. 27(2). 117–118. 9 indexed citations
20.
Kedar, Prabhakar, Prashant Warang, Roshan Colah, & Dipika Mohanty. (2006). Red cell pyruvate kinase deficiency in neonatal jaundice cases in India. The Indian Journal of Pediatrics. 73(11). 985–988. 10 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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