Uma B. Dasgupta

1.6k total citations
39 papers, 1.2k citations indexed

About

Uma B. Dasgupta is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Uma B. Dasgupta has authored 39 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 12 papers in Genetics and 12 papers in Hematology. Recurrent topics in Uma B. Dasgupta's work include Hemoglobinopathies and Related Disorders (10 papers), Iron Metabolism and Disorders (9 papers) and Arsenic contamination and mitigation (7 papers). Uma B. Dasgupta is often cited by papers focused on Hemoglobinopathies and Related Disorders (10 papers), Iron Metabolism and Disorders (9 papers) and Arsenic contamination and mitigation (7 papers). Uma B. Dasgupta collaborates with scholars based in India, United States and Czechia. Uma B. Dasgupta's co-authors include Debendranath Guha Mazumder, WILLIAM C. SUMMERS, William C. Summers, Sarmishtha Chanda, Sarbari Lahiri, Utpal Chaudhuri, Subhankar Das, Nilima Ghosh, Sarmila Chandra and Sunipa Majumdar and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Molecular and Cellular Biology and British Journal of Haematology.

In The Last Decade

Uma B. Dasgupta

38 papers receiving 1.1k citations

Peers

Uma B. Dasgupta

HTM

GENET

HEMAT

Mallika Ghosh United States

Claudie Morzadec France

Dechun Chen China

Bolan Yu China

Alexander R. Bogdan United States

John H. Richburg United States

Shan Fu China

Qingling Wang China

Dan Ma China

Rong Yao China

Mallika Ghosh United States

Uma B. Dasgupta

624 ×1.0

210 ×0.9

179 ×0.9

HTM

45 ×0.3

GENET

24 ×0.2

HEMAT

Citations per year, relative to Uma B. Dasgupta Uma B. Dasgupta (= 1×) peers Mallika Ghosh

Countries citing papers authored by Uma B. Dasgupta

Since Specialization

Citations

This map shows the geographic impact of Uma B. Dasgupta'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 Uma B. Dasgupta with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Uma B. Dasgupta more than expected).

Fields of papers citing papers by Uma B. Dasgupta

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Uma B. Dasgupta. 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 Uma B. Dasgupta. The network helps show where Uma B. Dasgupta may publish in the future.

Co-authorship network of co-authors of Uma B. Dasgupta

This figure shows the co-authorship network connecting the top 25 collaborators of Uma B. Dasgupta. A scholar is included among the top collaborators of Uma B. Dasgupta 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 Uma B. Dasgupta. Uma B. Dasgupta is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Ganguli, Bhaswati, et al.. (2013). GST polymorphic status modifying the arsenic induced clinical manifestations in people of the southern part of West Bengal, India. 3(6). 171–175. 1 indexed citations

Deshpande, Sharvari, et al.. (2012). Genotypic and Allelic Frequencies of IGF1 and IGF2 Genes in Broilers Analysed by Using PCR‐RFLP Techniques. Iranian journal of applied animal science. 2(4). 357–360. 4 indexed citations

Bhattacharya, Gargi, et al.. (2012). hsa-miR-503 Is Downregulated in β Thalassemia Major. Acta Haematologica. 128(3). 187–189. 9 indexed citations

Bhattacharya, Gargi, et al.. (2012). Influence ofBCL11A, HBS1L-MYB, HBBP1Single Nucleotide Polymorphisms and theHBG2 XmnI Polymorphism On Hb F Levels. Hemoglobin. 36(6). 592–599. 17 indexed citations

Ganguli, Bhaswati, et al.. (2011). GlutathioneS-transferase polymorphic status modifies the arsenic induced clinical manifestation in Nadia District of West Bengal, India. Journal of Public Health and Epidemiology. 3(10). 424–428. 1 indexed citations

Mazumder, Debendranath Guha & Uma B. Dasgupta. (2011). Chronic arsenic toxicity: Studies in West Bengal, India. The Kaohsiung Journal of Medical Sciences. 27(9). 360–370. 151 indexed citations

Bhattacharya, Gargi, et al.. (2009). Hb Sallanches [α104(G11)Cys→Tyr, TGC>TAC] Occurs Frequently on the Indian Subcontinent. Hemoglobin. 33(6). 486–491. 3 indexed citations

Mondal, Bama Charan, et al.. (2008). Methylation Status of Promoter-Associated CpG Islands in Primary Acute Myeloid Leukemia. Acta Haematologica. 120(4). 207–210. 1 indexed citations

Bhattacharya, Gargi, et al.. (2008). Polymerase Chain Reaction-Based Search for Two α-Globin Gene Mutations in India. Hemoglobin. 32(5). 485–490. 8 indexed citations

10.

Majumdar, Sunipa, et al.. (2008). Association of cytochrome P450, glutathione S-transferase and N-acetyl transferase 2 gene polymorphisms with incidence of acute myeloid leukemia. European Journal of Cancer Prevention. 17(2). 125–132. 34 indexed citations

11.

Mondal, Bama Charan, et al.. (2006). e19a2 BCR–ABL fusion transcript in typical chronic myeloid leukaemia: a report of two cases: Figure 1. Journal of Clinical Pathology. 59(10). 1102–1103. 17 indexed citations

12.

Chanda, Sarmishtha, Uma B. Dasgupta, Utpal Chaudhuri, et al.. (2005). DNA Hypermethylation of Promoter of Gene p53 and p16 in Arsenic-Exposed People with and without Malignancy. Toxicological Sciences. 89(2). 431–437. 201 indexed citations

13.

Bandyopadhyay, Sanmay, et al.. (2005). Two β‐globin cluster‐linked polymorphic loci in thalassemia patients of variable levels of fetal hemoglobin. European Journal Of Haematology. 75(1). 47–53. 10 indexed citations

14.

Sarkar, Anjali A., et al.. (2005). Co‐inheritance of the Hb Sun Prairie mutation with a point mutation at 5′‐UTR in the eastern Indian population. British Journal of Haematology. 129(2). 282–286. 4 indexed citations

15.

Bandyopadhyay, Aditi, Sanmay Bandyopadhyay, Bama Charan Mondal, et al.. (2004). Profile of β‐thalassemia in eastern India and its prenatal diagnosis. Prenatal Diagnosis. 24(12). 992–996. 15 indexed citations

16.

Karmakar, Parimal, et al.. (2001). Fragile X syndrome in Calcutta, India. Annals of Clinical Biochemistry International Journal of Laboratory Medicine. 38(3). 264–271. 15 indexed citations

17.

Natarajan, A.T., et al.. (2001). Induction of apoptosis by Phenothiazine derivatives in V79 cells. Toxicology Letters. 125(1-3). 19–28. 19 indexed citations

18.

Bandyopadhyay, Sanmay, et al.. (2001). Variable severity of β-thalassemia patients of Eastern India: effect of α-thalassemia and XmnI polymorphism. Clinical and Experimental Medicine. 1(3). 155–159. 17 indexed citations

19.

Dasgupta, Uma B., et al.. (2001). Fragile X syndrome a case report of a family.. PubMed. 44(4). 499–502.

20.

Bandyopadhyay, Aditi, et al.. (1999). Major Beta-Globin Gene Mutations in Eastern India and Their Associated Haplotypes. Human Heredity. 49(4). 232–235. 27 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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