Shrimati Shetty

3.6k total citations
155 papers, 2.3k citations indexed

About

Shrimati Shetty is a scholar working on Hematology, Genetics and Molecular Biology. According to data from OpenAlex, Shrimati Shetty has authored 155 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 125 papers in Hematology, 39 papers in Genetics and 21 papers in Molecular Biology. Recurrent topics in Shrimati Shetty's work include Hemophilia Treatment and Research (73 papers), Blood Coagulation and Thrombosis Mechanisms (61 papers) and Platelet Disorders and Treatments (61 papers). Shrimati Shetty is often cited by papers focused on Hemophilia Treatment and Research (73 papers), Blood Coagulation and Thrombosis Mechanisms (61 papers) and Platelet Disorders and Treatments (61 papers). Shrimati Shetty collaborates with scholars based in India, United States and United Kingdom. Shrimati Shetty's co-authors include Kanjaksha Ghosh, D. Mohanty, Dipika Mohanty, Bipin Kulkarni, Kanjaksha Ghosh, Sona Nair, Farah Jijina, Aruna Pawar, Manali Bhave and Anil Pathare and has published in prestigious journals such as The Lancet, Blood and PLoS ONE.

In The Last Decade

Shrimati Shetty

151 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shrimati Shetty India 26 1.5k 400 347 216 211 155 2.3k
André B. Mulder Netherlands 24 792 0.5× 339 0.8× 393 1.1× 257 1.2× 195 0.9× 70 1.9k
Wolfgang Miesbach Germany 27 1.7k 1.1× 371 0.9× 567 1.6× 62 0.3× 332 1.6× 192 3.2k
G. Dolan United Kingdom 27 1.8k 1.2× 533 1.3× 282 0.8× 218 1.0× 157 0.7× 93 2.4k
Yahya Büyükaşık Türkiye 20 818 0.6× 357 0.9× 246 0.7× 113 0.5× 69 0.3× 164 1.6k
Rudolf Pihusch Germany 21 685 0.5× 141 0.4× 253 0.7× 65 0.3× 154 0.7× 43 1.2k
Osman Özcebe Türkiye 21 661 0.5× 266 0.7× 166 0.5× 125 0.6× 76 0.4× 141 1.6k
Elena M. Faioni Italy 22 1.7k 1.1× 451 1.1× 254 0.7× 43 0.2× 737 3.5× 66 2.3k
Enrico Pogliani Italy 25 1.7k 1.2× 1.1k 2.7× 431 1.2× 351 1.6× 509 2.4× 75 2.9k
H. Kronenberg Australia 20 832 0.6× 314 0.8× 285 0.8× 128 0.6× 70 0.3× 125 1.9k
Laszlo Bajzar Canada 27 2.5k 1.7× 516 1.3× 563 1.6× 99 0.5× 559 2.6× 38 3.5k

Countries citing papers authored by Shrimati Shetty

Since Specialization
Citations

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

Fields of papers citing papers by Shrimati Shetty

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shrimati Shetty

This figure shows the co-authorship network connecting the top 25 collaborators of Shrimati Shetty. A scholar is included among the top collaborators of Shrimati Shetty 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 Shrimati Shetty. Shrimati Shetty 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.
Bansal, Shweta, et al.. (2022). Successful Treatment Of Acquired Hemophilia A Using FEIBA Supplemented With Emicizumab. Indian Journal of Hematology and Blood Transfusion. 39(1). 159–160. 1 indexed citations
2.
Shetty, Shrimati, et al.. (2014). Genetic Heterogeneity in a Large Cohort of Indian Type 3 von Willebrand Disease Patients. PLoS ONE. 9(3). e92575–e92575. 13 indexed citations
3.
Ghosh, Kanjaksha, et al.. (2013). Hereditary thrombophilia in cerebral venous thrombosis. Blood Coagulation & Fibrinolysis. 24(5). 540–543. 40 indexed citations
4.
Ghosh, Kanjaksha, et al.. (2013). Elevated Procoagulant Endothelial and Tissue Factor Expressing Microparticles in Women with Recurrent Pregnancy Loss. PLoS ONE. 8(11). e81407–e81407. 31 indexed citations
5.
Ghosh, Kanjaksha, et al.. (2013). Molecular pathology of Bernard–Soulier syndrome in Indian patients. Platelets. 24(7). 571–573. 4 indexed citations
6.
Shetty, Shrimati, et al.. (2011). Pathophysiology of acquired von Willebrand disease: a concise review. European Journal Of Haematology. 87(2). 99–106. 41 indexed citations
7.
Basu, Atanu, et al.. (2011). Dengue virus infection of SK Hep1 cells: inhibition ofin vitroangiogenesis and altered cytomorphology by expressed viral envelope glycoprotein. FEMS Immunology & Medical Microbiology. 62(2). 140–147. 10 indexed citations
8.
Shetty, Shrimati, Manali Bhave, & Kanjaksha Ghosh. (2010). Acquired hemophilia A: Diagnosis, aetiology, clinical spectrum and treatment options. Autoimmunity Reviews. 10(6). 311–316. 72 indexed citations
9.
Shetty, Shrimati, et al.. (2009). Thrombophilia and unexplained pregnancy loss in Indian patients.. PubMed. 21(3). 116–9. 19 indexed citations
10.
Ghosh, Kanjaksha, et al.. (2008). Imaging the interaction between dengue 2 virus and human blood platelets using atomic force and electron microscopy. Journal of Electron Microscopy. 57(3). 113–118. 40 indexed citations
11.
Shetty, Shrimati, Kanjaksha Ghosh, & Farah Jijina. (2006). First-trimester prenatal diagnosis in haemophilia A and B families—10 years experience from a centre in India. Prenatal Diagnosis. 26(11). 1015–1017. 17 indexed citations
12.
Nair, Sona, Kanjaksha Ghosh, Shrimati Shetty, & D. Mohanty. (2005). Mutations in GPIIIa molecule as a cause for Glanzmann thrombasthenia in Indian patients. Journal of Thrombosis and Haemostasis. 3(3). 482–488. 19 indexed citations
13.
Colah, Roshan, Shrimati Shetty, Supriya Phanasgaonkar, et al.. (2004). Prenatal Diagnosis in a Family at Risk for β‐Thalassemia and Hemophilia A: An Uncommon Association. Hemoglobin. 28(4). 343–346. 2 indexed citations
14.
Ghosh, Kanjaksha, Manisha Madkaikar, Farah Jijina, et al.. (2003). Open heart surgery with mitral valve replacement - ordeal of an undiagnosed haemophilia patient.. Clinical & Laboratory Haematology. 25(2). 131–133. 5 indexed citations
15.
Shetty, Shrimati, Kanjaksha Ghosh, & Dipika Mohanty. (2003). Prenatal diagnosis in a haemophilia A family by both factor VIII activity and antigen measurements.. PubMed. 51. 916–8. 3 indexed citations
16.
Ghosh, Kanjaksha, Shrimati Shetty, Sona Nair, et al.. (2002). Spectrum of inherited bleeding disorders from Western India. PubMed. 32(1). 39–47. 16 indexed citations
17.
Shetty, Shrimati, et al.. (2001). Combined factor VIII and IX deficiency in a family. Clinical & Laboratory Haematology. 23(3). 201–204. 7 indexed citations
18.
Ghosh, Kanjaksha, Shrimati Shetty, Manisha Madkaikar, et al.. (2000). Transfusion transmitted diseases in haemophilics from western India.. PubMed. 112. 61–4. 35 indexed citations
19.
Mohanty, Dipika, et al.. (1998). Factor V Leiden gene mutation in young Indian patients with myocardial infarction. Current Science. 74(12). 1078–1080. 5 indexed citations
20.
Todd, Gill, et al.. (1980). WSC volume 28 issue 4 Cover and Front matter. Weed Science. 28(4). f1–f2. 1 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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