Manjula Sritharan

1.0k total citations
44 papers, 788 citations indexed

About

Manjula Sritharan is a scholar working on Infectious Diseases, Parasitology and Epidemiology. According to data from OpenAlex, Manjula Sritharan has authored 44 papers receiving a total of 788 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Infectious Diseases, 16 papers in Parasitology and 14 papers in Epidemiology. Recurrent topics in Manjula Sritharan's work include Leptospirosis research and findings (15 papers), Tuberculosis Research and Epidemiology (14 papers) and Mycobacterium research and diagnosis (14 papers). Manjula Sritharan is often cited by papers focused on Leptospirosis research and findings (15 papers), Tuberculosis Research and Epidemiology (14 papers) and Mycobacterium research and diagnosis (14 papers). Manjula Sritharan collaborates with scholars based in India, United Kingdom and United States. Manjula Sritharan's co-authors include Kiranmayi Vemuri, Colin Ratledge, P. Sridhar, Prasad Dandawate, Subhash Padhyé, Sridhar Velineni, Satya Deo Pandey, Swapna Asuthkar, E. M. Khan and Friedrich Altmann and has published in prestigious journals such as The EMBO Journal, Biochemical Journal and Journal of Bacteriology.

In The Last Decade

Manjula Sritharan

43 papers receiving 770 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Manjula Sritharan India 17 351 193 186 172 165 44 788
Patricia Torres United States 5 391 1.1× 231 1.2× 354 1.9× 99 0.6× 341 2.1× 8 1.0k
D.I. Edwards United Kingdom 5 186 0.5× 114 0.6× 207 1.1× 65 0.4× 90 0.5× 8 712
Wilfried Moreira Singapore 12 157 0.4× 196 1.0× 250 1.3× 37 0.2× 129 0.8× 16 571
Jorge Castro‐Garza Mexico 15 295 0.8× 206 1.1× 146 0.8× 71 0.4× 120 0.7× 47 648
Matthias Stehr Germany 19 201 0.6× 226 1.2× 445 2.4× 39 0.2× 41 0.2× 29 863
Mary Ann DeGroote United States 10 382 1.1× 308 1.6× 232 1.2× 17 0.1× 91 0.6× 13 706
Mack Kuo United States 9 398 1.1× 198 1.0× 434 2.3× 44 0.3× 362 2.2× 11 901
Santiago Ramón‐García Spain 16 564 1.6× 451 2.3× 393 2.1× 27 0.2× 115 0.7× 31 1.0k
Ellen Z. Baum United States 19 127 0.4× 211 1.1× 501 2.7× 23 0.1× 203 1.2× 26 997
Pornwaratt Niyomrattanakit Singapore 16 809 2.3× 410 2.1× 677 3.6× 22 0.1× 195 1.2× 20 1.5k

Countries citing papers authored by Manjula Sritharan

Since Specialization
Citations

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

Fields of papers citing papers by Manjula Sritharan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Manjula Sritharan. 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 Manjula Sritharan. The network helps show where Manjula Sritharan may publish in the future.

Co-authorship network of co-authors of Manjula Sritharan

This figure shows the co-authorship network connecting the top 25 collaborators of Manjula Sritharan. A scholar is included among the top collaborators of Manjula Sritharan 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 Manjula Sritharan. Manjula Sritharan 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.
Eapen, Charu, et al.. (2024). Urinary leptospiral sphingomyelinases as diagnostic markers of leptospirosis in dengue patients co-infected with leptospirosis. Diagnostic Microbiology and Infectious Disease. 111(3). 116647–116647.
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Sritharan, Manjula, et al.. (2020). Organophosphate hydrolase interacts with ferric-enterobactin and promotes iron uptake in association with TonB-dependent transport system. Biochemical Journal. 477(15). 2821–2840. 2 indexed citations
4.
Eapen, Charu, et al.. (2018). Pathogen-specific leptospiral proteins in urine of patients with febrile illness aids in differential diagnosis of leptospirosis from dengue. European Journal of Clinical Microbiology & Infectious Diseases. 37(3). 423–433. 14 indexed citations
5.
Yaseen, Imtiyaz, et al.. (2017). Histone methyltransferase SUV 39H1 participates in host defense by methylating mycobacterial histone‐like protein HupB. The EMBO Journal. 37(2). 183–200. 25 indexed citations
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Pandey, Satya Deo, et al.. (2014). Iron-Regulated Protein HupB of Mycobacterium tuberculosis Positively Regulates Siderophore Biosynthesis and Is Essential for Growth in Macrophages. Journal of Bacteriology. 196(10). 1853–1865. 54 indexed citations
8.
Jain, Sreepat, et al.. (2012). Serum iron profile and ELISA-based detection of antibodies against the iron-regulated protein HupB of Mycobacterium tuberculosis in TB patients and household contacts in Hyderabad (Andhra Pradesh), India. Transactions of the Royal Society of Tropical Medicine and Hygiene. 107(1). 43–50. 11 indexed citations
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Vemuri, Kiranmayi, et al.. (2012). Synthesis and in vitro anticancer and antitubercular activity of diarylpyrazole ligated dihydropyrimidines possessing lipophilic carbamoyl group. Bioorganic & Medicinal Chemistry Letters. 22(8). 2708–2711. 93 indexed citations
11.
Velineni, Sridhar, Sundru Manjulata Devi, Niyaz Ahmed, & Manjula Sritharan. (2008). Diagnostic potential of an iron-regulated hemin-binding protein HbpA that is widely conserved in Leptospira interrogans. Infection Genetics and Evolution. 8(6). 772–776. 8 indexed citations
12.
Sritharan, Manjula, Sridhar Velineni, Swapna Asuthkar, Umabala Pamidimukkala, & V Lakshmi. (2007). Serological evaluation of leptospirosis in Hyderabad, Andhra Pradesh: A retrospective hospital-based study. Indian Journal of Medical Microbiology. 25(1). 24–24. 17 indexed citations
13.
Sritharan, Manjula, Sridhar Velineni, & Swapna Asuthkar. (2006). Iron limitation and expression of immunoreactive outer membrane proteins inLeptospira interrogansserovar icterohaemorrhagiae strain lai. Indian Journal of Medical Microbiology. 24(4). 339–339. 3 indexed citations
14.
Sritharan, Manjula & Venkataraman Sritharan. (2000). Polymerase chain reaction in the diagnosis of tuberculosis. Indian Journal of Clinical Biochemistry. 15(S1). 200–216. 8 indexed citations
15.
Devaraj, S., et al.. (2000). Isolation, PCR based identification, and sensitivity pattern of environmental mycobacteria from leprosy and tuberculosis patients. Indian Journal of Clinical Biochemistry. 15(2). 94–103. 1 indexed citations
16.
Kamatchiammal, S., et al.. (2000). Direct diagnosis ofMycobacterium tuberculosis in blood samples of HIV infected patients by polymerase chain reaction. Indian Journal of Clinical Biochemistry. 15(2). 76–82. 1 indexed citations
17.
Rao, Vivek & Manjula Sritharan. (1999). Identification of a LDL-receptor in the lymphatic filarial parasiteWuchereria bancrofti. Indian Journal of Clinical Biochemistry. 14(2). 213–219. 1 indexed citations
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Sritharan, Manjula & Colin Ratledge. (1989). Co-ordinated expression of the components of iron transport (mycobactin, exochelin and envelope proteins) inMycobacterium neoaurum. FEMS Microbiology Letters. 60(2). 183–185. 16 indexed citations
20.
Hall, Richard M., Manjula Sritharan, A. J. M. MESSENGER, & Colin Ratledge. (1987). Iron Transport in Mycobacterium smegmatis: Occurrence of Iron-regulated Envelope Proteins as Potential Receptors for Iron Uptake. Microbiology. 133(8). 2107–2114. 37 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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