Arupa Ganguly

10.8k total citations · 2 hit papers
144 papers, 6.5k citations indexed

About

Arupa Ganguly is a scholar working on Molecular Biology, Ophthalmology and Oncology. According to data from OpenAlex, Arupa Ganguly has authored 144 papers receiving a total of 6.5k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Molecular Biology, 41 papers in Ophthalmology and 40 papers in Oncology. Recurrent topics in Arupa Ganguly's work include Ocular Oncology and Treatments (41 papers), Hyperglycemia and glycemic control in critically ill and hospitalized patients (27 papers) and Cutaneous Melanoma Detection and Management (19 papers). Arupa Ganguly is often cited by papers focused on Ocular Oncology and Treatments (41 papers), Hyperglycemia and glycemic control in critically ill and hospitalized patients (27 papers) and Cutaneous Melanoma Detection and Management (19 papers). Arupa Ganguly collaborates with scholars based in United States, United Kingdom and Canada. Arupa Ganguly's co-authors include Darwin J. Prockop, Carol L. Shields, Matthew J. Rock, Charles A. Stanley, Courtney MacMullen, Show‐Ling Shyng, Jennifer Richards‐Yutz, Tapan Ganguly, Lynn Godmilow and Kathryn G. Ewens and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Arupa Ganguly

141 papers receiving 6.4k citations

Hit Papers

Conformation-sensitive ge... 1993 2026 2004 2015 1993 1997 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Arupa Ganguly United States 48 2.5k 1.6k 1.3k 1.2k 1.1k 144 6.5k
Carole Perruzzi United States 27 4.8k 1.9× 547 0.3× 1.3k 1.0× 204 0.2× 711 0.6× 31 7.9k
Peter M. Sadow United States 41 1.1k 0.4× 670 0.4× 1.3k 1.0× 2.4k 1.9× 116 0.1× 221 5.3k
Jaume Mora Spain 36 3.1k 1.2× 344 0.2× 1.2k 0.9× 200 0.2× 354 0.3× 216 5.5k
Robert Bookstein United States 35 4.3k 1.7× 1.7k 1.1× 3.8k 2.9× 116 0.1× 1.7k 1.5× 52 7.9k
Annelies de Klein Netherlands 52 5.2k 2.0× 1.3k 0.8× 1.9k 1.5× 81 0.1× 1.9k 1.7× 219 11.5k
Jan P. Dumanski Sweden 43 3.6k 1.4× 2.0k 1.3× 1.0k 0.8× 199 0.2× 87 0.1× 146 7.4k
Gary D. Shipley United States 32 3.2k 1.2× 476 0.3× 1.5k 1.1× 393 0.3× 107 0.1× 48 5.8k
Deborah J. Marsh Australia 43 4.2k 1.7× 1.3k 0.8× 1.8k 1.4× 1.4k 1.1× 39 0.0× 130 7.4k
Michael L. Robinson United States 37 3.9k 1.5× 899 0.6× 985 0.8× 88 0.1× 549 0.5× 107 5.5k
Paul J. Goodfellow United States 51 5.1k 2.0× 2.2k 1.4× 2.8k 2.1× 1.2k 1.0× 64 0.1× 222 11.1k

Countries citing papers authored by Arupa Ganguly

Since Specialization
Citations

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

Fields of papers citing papers by Arupa Ganguly

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arupa Ganguly

This figure shows the co-authorship network connecting the top 25 collaborators of Arupa Ganguly. A scholar is included among the top collaborators of Arupa Ganguly 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 Arupa Ganguly. Arupa Ganguly 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.
Boodhansingh, Kara E., et al.. (2025). Congenital Hyperinsulinism and Long QT Syndrome Attributable to a Variant in KCNE1. Hormone Research in Paediatrics. 1–15.
2.
Stålhammar, Gustav, Sarah E. Coupland, Kathryn G. Ewens, et al.. (2023). Improved Staging of Ciliary Body and Choroidal Melanomas Based on Estimation of Tumor Volume and Competing Risk Analyses. Ophthalmology. 131(4). 478–491. 14 indexed citations
3.
Surrey, Lea F., Abhay Srinivasan, Dong Li, et al.. (2023). Microcystic lymphatic malformations in Turner syndrome are due to somatic mosaicism of PIK3CA. American Journal of Medical Genetics Part A. 194(1). 64–69. 1 indexed citations
4.
Jung, Eun Mi, Greta R. Bunin, Arupa Ganguly, Rebecca Johnson, & Logan G. Spector. (2023). The association between maternal nutrient intake during pregnancy and the risk of sporadic unilateral retinoblastoma among offspring. Cancer Epidemiology. 85. 102376–102376. 1 indexed citations
5.
Mayro, Eileen L., et al.. (2021). Outcomes of The Cancer Genome Atlas (TCGA) Classification in Uveal Melanoma by Patient Age in 1001 Eyes. Investigative Ophthalmology & Visual Science. 62(8). 40–40. 1 indexed citations
7.
Koutlas, Ioannis G., Ana Sueli Rodrigues Cavalcante, Mohammed Al Kindi, et al.. (2020). Orofacial overgrowth with peripheral nerve enlargement and perineuriomatous pseudo-onion bulb proliferations is part of the PIK3CA-related overgrowth spectrum. SHILAP Revista de lepidopterología. 1(1). 100009–100009. 6 indexed citations
8.
Kalish, Jennifer M., Kara E. Boodhansingh, Tricia Bhatti, et al.. (2015). Congenital hyperinsulinism in children with paternal 11p uniparental isodisomy and Beckwith–Wiedemann syndrome. Journal of Medical Genetics. 53(1). 53–61. 64 indexed citations
9.
Shields, Carol L., Aparna Ramasubramanian, Arupa Ganguly, Diwakar Mohan, & Jerry A. Shields. (2011). CYTOGENETIC TESTING OF IRIS MELANOMA USING FINE NEEDLE ASPIRATION BIOPSY IN 17 PATIENTS. Retina. 31(3). 574–580. 15 indexed citations
10.
Magge, Sheela N., Show‐Ling Shyng, Courtney MacMullen, et al.. (2004). Familial Leucine-Sensitive Hypoglycemia of Infancy Due to a Dominant Mutation of the β-Cell Sulfonylurea Receptor. The Journal of Clinical Endocrinology & Metabolism. 89(9). 4450–4456. 45 indexed citations
11.
Citron, Michael, Lynn Godmilow, Tapan Ganguly, & Arupa Ganguly. (2002). High throughput mutation screening of the factor VIII gene (F8C) in hemophilia A: 37 novel mutations and genotype-phenotype correlation. Human Mutation. 20(4). 267–274. 37 indexed citations
12.
Blackwood, M. Anne, Robin Holmes, Marie Synnestvedt, et al.. (2002). Multiple primary melanoma revisited. Cancer. 94(8). 2248–2255. 53 indexed citations
13.
Hsu, Betty Y.L., Vito Iacobazzi, Zhili Wang, et al.. (2001). Aberrant mRNA Splicing Associated with Coding Region Mutations in Children with Carnitine-Acylcarnitine Translocase Deficiency. Molecular Genetics and Metabolism. 74(1-2). 248–255. 31 indexed citations
14.
Lonlay, Pascale de, Chantal Benelli, Françoise Fouque, et al.. (2001). Hyperinsulinism and Hyperammonemia Syndrome: Report of Twelve Unrelated Patients. Pediatric Research. 50(3). 353–357. 55 indexed citations
15.
Kuivaniemi, Helena, et al.. (1998). Fibulin-2 exhibits high degree of variability, but no structural changes concordant with abdominal aortic aneurysms. European Journal of Human Genetics. 6(6). 642–646. 6 indexed citations
16.
Ganguly, Arupa, et al.. (1997). Genetic Testing for Breast Cancer Susceptibility: Frequency of BRCA1 and BRCA2 Mutations. Genetic Testing. 1(2). 85–90. 21 indexed citations
17.
Williams, Charlene J., Arupa Ganguly, Eileen L. Considine, et al.. (1996). A−2→G transition at the 3′ acceptor splice site of IVS17 characterizes the COL2A1 gene mutation in the original stickler syndrome kindred. American Journal of Medical Genetics. 63(3). 461–467. 69 indexed citations
18.
Williams, Charlene J., Matthew J. Rock, Eileen L. Considine, et al.. (1995). Three new point mutations in type II procollagen (COL2A1) and identification of a fourth family with the COL2A1 Arg519→Cys base substitution using conformation sensitive gel electrophoresis. Human Molecular Genetics. 4(2). 309–312. 59 indexed citations
20.
Fertala, Andrzej, Aleksander L. Sieroń, Yoshio Hojima, Arupa Ganguly, & Darwin J. Prockop. (1994). Self-assembly into fibrils of collagen II by enzymic cleavage of recombinant procollagen II. Lag period, critical concentration, and morphology of fibrils differ from collagen I. Journal of Biological Chemistry. 269(15). 11584–11589. 41 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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