Venkatraman Bhat

784 total citations
74 papers, 468 citations indexed

About

Venkatraman Bhat is a scholar working on Surgery, Pulmonary and Respiratory Medicine and Epidemiology. According to data from OpenAlex, Venkatraman Bhat has authored 74 papers receiving a total of 468 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Surgery, 24 papers in Pulmonary and Respiratory Medicine and 16 papers in Epidemiology. Recurrent topics in Venkatraman Bhat's work include Congenital Heart Disease Studies (9 papers), RNA modifications and cancer (4 papers) and Tumors and Oncological Cases (4 papers). Venkatraman Bhat is often cited by papers focused on Congenital Heart Disease Studies (9 papers), RNA modifications and cancer (4 papers) and Tumors and Oncological Cases (4 papers). Venkatraman Bhat collaborates with scholars based in India, Qatar and United States. Venkatraman Bhat's co-authors include Paul C. Salins, Siddaramappa J. Patil, Ashok Parchani, Ashwin Dalal, Aneek Das Bhowmik, Moni Abraham Kuriakose, Sofia Rahman, Jyoti Matalia, Ammar C. Al‐Rikabi and Vivek Shetty and has published in prestigious journals such as SHILAP Revista de lepidopterología, BMJ Open and Journal of Oral and Maxillofacial Surgery.

In The Last Decade

Venkatraman Bhat

69 papers receiving 454 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Venkatraman Bhat India 12 196 106 100 69 60 74 468
Özgür Öztekin Türkiye 18 234 1.2× 108 1.0× 63 0.6× 77 1.1× 82 1.4× 66 747
Ümit Belet Türkiye 15 197 1.0× 195 1.8× 89 0.9× 45 0.7× 70 1.2× 51 619
Amparo Castellote Spain 14 232 1.2× 105 1.0× 76 0.8× 67 1.0× 87 1.4× 30 540
Oliver Rompel Germany 12 156 0.8× 194 1.8× 86 0.9× 109 1.6× 70 1.2× 49 576
Nanda Venkatanarasimha Singapore 13 335 1.7× 160 1.5× 107 1.1× 47 0.7× 56 0.9× 60 622
N Khandelwal India 14 217 1.1× 77 0.7× 70 0.7× 52 0.8× 105 1.8× 46 546
Alok A. Bhatt United States 14 336 1.7× 98 0.9× 82 0.8× 33 0.5× 84 1.4× 88 661
Ralf‐Bodo Tröbs Germany 13 369 1.9× 91 0.9× 66 0.7× 97 1.4× 43 0.7× 86 618
Çetin Çelenk Türkiye 15 136 0.7× 269 2.5× 99 1.0× 32 0.5× 55 0.9× 41 573
Gerhard Schoen Germany 12 135 0.7× 106 1.0× 119 1.2× 72 1.0× 16 0.3× 28 485

Countries citing papers authored by Venkatraman Bhat

Since Specialization
Citations

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

Fields of papers citing papers by Venkatraman Bhat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Venkatraman Bhat

This figure shows the co-authorship network connecting the top 25 collaborators of Venkatraman Bhat. A scholar is included among the top collaborators of Venkatraman Bhat 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 Venkatraman Bhat. Venkatraman Bhat 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.
Dalal, Ashwin, et al.. (2023). Familial monoallelic CYP26B1 truncating variant causes a syndromic craniosynostosis due to haploinsufficiency ?. European Journal of Medical Genetics. 66(7). 104772–104772. 1 indexed citations
2.
Aggarwal, Shagun, et al.. (2022). Fetal presentation of chondrodysplasia with joint dislocations, GPAPP type, caused by novel biallelic IMPAD1 variants. American Journal of Medical Genetics Part A. 188(4). 1287–1292.
3.
Bhat, Venkatraman, et al.. (2022). Late Onset Subacute Profound Biotinidase Deficiency Caused by a Novel Homozygous Variant c.466-3T>G in the BTD Gene. The Indian Journal of Pediatrics. 89(6). 594–596. 2 indexed citations
4.
5.
Patil, Siddaramappa J., et al.. (2020). Bosley–Salih–Alorainy syndrome in patients from India. American Journal of Medical Genetics Part A. 182(11). 2699–2703. 2 indexed citations
6.
Bhat, Venkatraman, et al.. (2020). Hyperbaric Oxygen Therapy in the Management of Zygomatic Bone Osteomyelitis. Journal of Maxillofacial and Oral Surgery. 20(3). 414–417. 2 indexed citations
7.
Pillai, Vijay, Vikram D. Kekatpure, Nirav Trivedi, et al.. (2019). Prognostic determinants of locally advanced buccal mucosa cancer: Do we need to relook the current staging criteria?. Oral Oncology. 95. 43–51. 30 indexed citations
8.
Patil, Siddaramappa J., et al.. (2018). Autosomal recessive otofaciocervical syndrome type 2 with novel homozygous small insertion in PAX1 gene. American Journal of Medical Genetics Part A. 176(5). 1200–1206. 21 indexed citations
9.
Bhowmik, Aneek Das, et al.. (2018). Novel splice-site variant of UCHL1 in an Indian family with autosomal recessive spastic paraplegia-79. Journal of Human Genetics. 63(8). 927–933. 17 indexed citations
10.
Bhat, Venkatraman. (2017). Quantification of Liver Fat with mDIXON Magnetic Resonance Imaging, Comparison with the Computed Tomography and the Biopsy. JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH. 11(7). TC06–TC10. 22 indexed citations
11.
Bhat, Venkatraman, et al.. (2017). Main pulmonary artery trifurcation in association with persistent right common pulmonary vein: a piece of embryological puzzle. Quantitative Imaging in Medicine and Surgery. 7(3). 380–382. 1 indexed citations
12.
Bhat, Venkatraman, et al.. (2016). Air Leak into the Soft Tissues During the Puffed Cheek CT Evaluation of Oral Cavity: Diagnosis and Implication of a Rare Phenomenon. Journal of Maxillofacial and Oral Surgery. 16(3). 374–376. 1 indexed citations
13.
Bhat, Venkatraman. (2016). Illustrated Imaging Essay on Congenital Heart Diseases: Multimodality Approach Part III: Cyanotic Heart Diseases and Complex Congenital Anomalies. JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH. 10(7). TE01–10. 6 indexed citations
14.
Bhat, Venkatraman, et al.. (2015). Tracheal quadrifurcation associated with congenital heart disease. Pediatric Radiology. 45(8). 1236–1238. 2 indexed citations
15.
Patil, Siddaramappa J., et al.. (2015). Familial 7q11.23 duplication with variable phenotype. American Journal of Medical Genetics Part A. 167(11). 2727–2730. 7 indexed citations
16.
Bhat, Venkatraman, et al.. (2013). Anterior mediastinal teratoma presenting with pseudo-aneurysms of aorta. European Heart Journal - Cardiovascular Imaging. 15(2). 227–227. 1 indexed citations
17.
Patil, Siddaramappa J., et al.. (2012). Confirmation of the Zechi‐Ceide syndrome. American Journal of Medical Genetics Part A. 158A(6). 1467–1471. 1 indexed citations
18.
19.
Bhat, Venkatraman, et al.. (2008). Meandering vessels: A sign of arterial tortuosity on plain chest radiography. Heart Views. 9(1). 24. 3 indexed citations
20.
Bhat, Venkatraman, et al.. (1998). Abdominal tuberculosis in Qatar: a clinico-radiological study.. PubMed. 2(7). 563–8. 5 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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