Arundhati Sharma

593 total citations
49 papers, 414 citations indexed

About

Arundhati Sharma is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Arundhati Sharma has authored 49 papers receiving a total of 414 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 11 papers in Ophthalmology and 9 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Arundhati Sharma's work include Glaucoma and retinal disorders (8 papers), Corneal surgery and disorders (5 papers) and Retinal Development and Disorders (5 papers). Arundhati Sharma is often cited by papers focused on Glaucoma and retinal disorders (8 papers), Corneal surgery and disorders (5 papers) and Retinal Development and Disorders (5 papers). Arundhati Sharma collaborates with scholars based in India, Australia and United States. Arundhati Sharma's co-authors include Preeti Paliwal, Radhika Tandon, Shweta Birla, Seema Sen, Namrata Sharma, Rasik B. Vajpayee, Punit Kaur, Divya Dube, P. K. Singh and Jeewan S. Titiyal and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neuroscience and Fertility and Sterility.

In The Last Decade

Arundhati Sharma

47 papers receiving 411 citations

Peers

Arundhati Sharma

RNMI

OPHTH

GENET

PHEOH

E Dale United States

Sumita Sethi India

Rocco Plateroti Italy

Si Hyung Lee South Korea

Jacqueline I. Goldstein United States

Naili Ma United States

Anand Rajendran India

Elisabetta Pelo Italy

Yoshimi Nakamura Japan

Dominique Leboeuf Canada

E Dale United States

Arundhati Sharma

118 ×0.7

RNMI

179 ×1.3

OPHTH

150 ×1.3

166 ×2.0

GENET

24 ×0.4

PHEOH

Citations per year, relative to Arundhati Sharma Arundhati Sharma (= 1×) peers E Dale

Countries citing papers authored by Arundhati Sharma

Since Specialization

Citations

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

Fields of papers citing papers by Arundhati Sharma

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arundhati Sharma

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Goyal, Alpesh, Ashish Datt Upadhyay, Devasenathipathy Kandasamy, et al.. (2023). Clinical profile and treatment outcomes among patients with sporadic and multiple endocrine neoplasia syndrome‐related primary hyperparathyroidism. Clinical Endocrinology. 99(5). 449–458. 4 indexed citations

Gupta, Viney, et al.. (2023). A new association of PAX6 variation with Juvenile onset open angle glaucoma. Journal of Human Genetics. 68(5). 355–358. 3 indexed citations

Sharma, Arundhati, et al.. (2022). Assessment of Vitamin D Levels in Relation to Statin Therapy in Elderly Hypertensive Patients with Comorbidities. SHILAP Revista de lepidopterología. 7(4). 88–91. 1 indexed citations

Bagga, Arvind, et al.. (2022). Genetic and clinical profile of patients with hypophosphatemic rickets. European Journal of Medical Genetics. 65(8). 104540–104540. 12 indexed citations

Sharma, Arundhati, et al.. (2022). An Unusual Progression of Membranous Nephropathy. Cureus. 14(10). e30651–e30651.

Sarkar, Siddharth, Renu Singh, Arundhati Sharma, et al.. (2021). Association of Serotonergic Pathway Gene Polymorphisms With Behavioral Parameters in Patients With Opioid Dependence. Cureus. 13(11). e19310–e19310. 3 indexed citations

Bansal, Mayank, Radhika Tandon, Rohit Saxena, et al.. (2020). Ophthalmic genetics practice and research in India: Vision in 2020. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 184(3). 718–727. 3 indexed citations

Gupta, Viney, et al.. (2020). The mutational spectrum of Myocilin gene among familial versus sporadic cases of Juvenile onset open angle glaucoma. Eye. 35(2). 400–408. 17 indexed citations

Nag, Tapas Chandra, et al.. (2019). In ovo Sound Stimulation Mediated Regulation of BDNF in the Auditory Cortex and Hippocampus of Neonatal Chicks. Neuroscience. 408. 293–307. 7 indexed citations

10.

Sharma, Namrata, Prafulla K. Maharana, Tushar Agarwal, et al.. (2019). Multistep Grading System for Evaluation of Chronic Ocular Sequelae in Patients With Stevens-Johnson Syndrome. American Journal of Ophthalmology. 203. 69–77. 20 indexed citations

11.

Selvan, Harathy, Anshul Sharma, Shweta Birla, et al.. (2019). Molecular characterization of a rare phenotype of X-linked retinoschisis with angle-closure glaucoma. Indian Journal of Ophthalmology. 67(7). 1226–1226. 5 indexed citations

12.

Birla, Shweta, Rajesh Khadgawat, Viveka P. Jyotsna, et al.. (2016). Identification of novel GHRHR and GH1 mutations in patients with isolated growth hormone deficiency. Growth Hormone & IGF Research. 29. 50–56. 12 indexed citations

13.

Gupta, Ranjan, Preeti Paliwal, Radhika Tandon, et al.. (2015). Association of ZEB1 and TCF4 rs613872 changes with late onset Fuchs endothelial corneal dystrophy in patients from northern India.. PubMed. 21. 1252–60. 23 indexed citations

14.

Jyotsna, Viveka P., et al.. (2015). Novel MEN 1 gene findings in rare sporadic insulinoma—a case control study. BMC Endocrine Disorders. 15(1). 44–44. 14 indexed citations

15.

Bansal, Virinder Kumar, Arundhati Sharma, Preeti Paliwal, et al.. (2014). Prospective Case–Control Study to Evaluate the Role of Glutathione S Transferases (GSTT1 and GSTM1) Gene Deletion in Breast Carcinoma and Its Prognostic Significance. Indian Journal of Surgery. 77(S3). 1067–1072. 10 indexed citations

16.

Iyer, Venkateswaran K., et al.. (2013). Loss of heterozygosity at 11p13 and 11p15 in Wilms tumor: a study of 22 cases from India. Pediatric Surgery International. 29(3). 223–227. 5 indexed citations

17.

Paliwal, Preeti, Arundhati Sharma, Radhika Tandon, et al.. (2010). TGFBI mutation screening and genotype-phenotype correlation in north Indian patients with corneal dystrophies.. PubMed. 16. 1429–38. 21 indexed citations

18.

Paliwal, Preeti, et al.. (2010). An unusual association of hypospadias with partial deletion of chromosome 1q. Fertility and Sterility. 93(7). 2413.e11–2413.e13. 2 indexed citations

19.

Biswas, Ahitagni, Tarun Puri, Shikha Goyal, et al.. (2009). Spinal Myxopapillary Ependymoma With Down Syndrome: Exploring an Unusual Association. Journal of Pediatric Hematology/Oncology. 32(1). e38–e41. 5 indexed citations

20.

Moorthy, Ganesh S., Sandeep Agarwala, Arundhati Sharma, et al.. (2009). Cytogenetic evaluation of neuroblastoma using fine needle aspiration cultures. Pediatric Surgery International. 25(11). 939–943. 4 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.

Explore authors with similar magnitude of impact