Prashant Chittiboina

3.4k total citations
103 papers, 1.6k citations indexed

About

Prashant Chittiboina is a scholar working on Endocrinology, Diabetes and Metabolism, Surgery and Neurology. According to data from OpenAlex, Prashant Chittiboina has authored 103 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Endocrinology, Diabetes and Metabolism, 33 papers in Surgery and 33 papers in Neurology. Recurrent topics in Prashant Chittiboina's work include Pituitary Gland Disorders and Treatments (38 papers), Adrenal and Paraganglionic Tumors (18 papers) and Cancer, Hypoxia, and Metabolism (16 papers). Prashant Chittiboina is often cited by papers focused on Pituitary Gland Disorders and Treatments (38 papers), Adrenal and Paraganglionic Tumors (18 papers) and Cancer, Hypoxia, and Metabolism (16 papers). Prashant Chittiboina collaborates with scholars based in United States, China and Greece. Prashant Chittiboina's co-authors include Russell R. Lonser, Anil Nanda, Constantine A. Stratakis, Maya Lodish, Gloria Caldito, John D. Heiss, David Connor, Zhengping Zhuang, Grégoire P. Chatain and Fábio R. Faucz and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Immunology and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Prashant Chittiboina

94 papers receiving 1.5k citations

Peers

Prashant Chittiboina
Todd C. Hankinson United States
Pankaj K. Agarwalla United States
Jo Haraoka Japan
Hiroyoshi Akutsu Japan
Carmelo Anile Italy
Angelika Gutenberg Germany
Kyung-Jae Park South Korea
Jeroen C. Jansen Netherlands
Filippo Gagliardi Italy
Sanda Alexandrescu United States
Todd C. Hankinson United States
Prashant Chittiboina
Citations per year, relative to Prashant Chittiboina Prashant Chittiboina (= 1×) peers Todd C. Hankinson

Countries citing papers authored by Prashant Chittiboina

Since Specialization
Citations

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

Fields of papers citing papers by Prashant Chittiboina

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Prashant Chittiboina

This figure shows the co-authorship network connecting the top 25 collaborators of Prashant Chittiboina. A scholar is included among the top collaborators of Prashant Chittiboina 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 Prashant Chittiboina. Prashant Chittiboina 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.
Zainab, Rida, Justin Lack, Morgan Similuk, et al.. (2025). Genetic evaluation of pediatric pituitary adenomas and USP8-related genotype-phenotype correlations in Cushing’s disease. Pituitary. 28(5). 92–92.
2.
Vocke, Cathy D., C. Ricketts, Alexandra Lebensohn, et al.. (2025). Multigenerational VHL family characterized by pathogenic germline ELOC variant: Response to belzutifan. Urologic Oncology Seminars and Original Investigations. 44(2). 120.e21–120.e27.
3.
Oliver, Jeremie D., Fábio R. Faucz, Charalampos S. Floudas, et al.. (2024). Spatial Transcriptomic Analysis of Pituitary Corticotroph Tumors. Journal of the Endocrine Society. 8(6). bvae064–bvae064. 2 indexed citations
4.
5.
Hogan, Elizabeth, David T. Asuzu, Tianxia Wu, et al.. (2023). Diurnal Range and Intra-patient Variability of ACTH Is Restored With Remission in Cushing's Disease. The Journal of Clinical Endocrinology & Metabolism. 108(11). 2812–2820. 3 indexed citations
6.
Chittiboina, Prashant, David T. Asuzu, Panagiotis Mastorakos, et al.. (2023). Proteostasis Modulation in Germline Missense von Hippel Lindau Disease. Clinical Cancer Research. 29(12). 2199–2209. 2 indexed citations
7.
Asuzu, David T., et al.. (2023). Cortisol and ACTH Measurements at Extubation From Pituitary Surgery Predicts Hypothalamic-Pituitary-Adrenal Axis Function. Journal of the Endocrine Society. 7(4). bvad025–bvad025. 2 indexed citations
8.
Pankratz, Nathan, John Lane, Fábio R. Faucz, et al.. (2023). OR2802 A Novel CABLES1 Missense Variant Associated With Cushing's Disease Disrupts Protein Structure And Stability. Journal of the Endocrine Society. 7(Supplement_1).
9.
Hernández‐Ramírez, Laura C., Nathan Pankratz, John Lane, et al.. (2022). Genetic drivers of Cushing’s disease: Frequency and associated phenotypes. Genetics in Medicine. 24(12). 2516–2525. 9 indexed citations
10.
Chittiboina, Prashant, et al.. (2020). Robotic assisted resection of an obturator nerve neurofibroma in the right iliac fossa. SHILAP Revista de lepidopterología. 7. 100038–100038. 2 indexed citations
11.
Pankratz, Nathan, John Lane, Fábio R. Faucz, et al.. (2020). Germline CDKN1B Loss-of-Function Variants Cause Pediatric Cushing’s Disease With or Without an MEN4 Phenotype. The Journal of Clinical Endocrinology & Metabolism. 105(6). 1983–2005. 32 indexed citations
12.
Belyavskaya, Elena, Margaret F. Keil, Prashant Chittiboina, et al.. (2018). Postoperative Diabetes Insipidus and Hyponatremia in Children after Transsphenoidal Surgery for Adrenocorticotropin Hormone and Growth Hormone Secreting Adenomas. The Journal of Pediatrics. 195. 169–174.e1. 10 indexed citations
13.
Keil, Margaret F., Laura C. Hernández‐Ramírez, Amit Tirosh, et al.. (2018). Children with MEN1 gene mutations may present first (and at a young age) with Cushing disease. Clinical Endocrinology. 89(4). 437–443. 17 indexed citations
14.
Lu, Jie, Grégoire P. Chatain, Xiang Wang, et al.. (2017). Histone Deacetylase Inhibitor SAHA Is a Promising Treatment of Cushing Disease. The Journal of Clinical Endocrinology & Metabolism. 102(8). 2825–2835. 49 indexed citations
15.
Solomon, Beth, et al.. (2017). Natural History of Speech and Swallowing Function in Neurofibromatosis 2 Includes Hypoglossal Dysfunction. Journal of Neurological Surgery Part B Skull Base. 78(S 01). S1–S156.
16.
Feldman, Michael J., Saman Sizdahkhani, Nancy A. Edwards, et al.. (2016). Loss of Quiescence in von Hippel-Lindau Hemangioblastomas is Associated with Erythropoietin Signaling. Scientific Reports. 6(1). 35486–35486. 6 indexed citations
17.
Chittiboina, Prashant & Russell R. Lonser. (2015). Von Hippel–Lindau disease. Handbook of clinical neurology. 132. 139–156. 126 indexed citations
18.
Feng, Jie, Yonggang Wu, Chuzhong Li, et al.. (2014). Identification of a subtype-specific ENC1 gene related to invasiveness in human pituitary null cell adenoma and oncocytomas. Journal of Neuro-Oncology. 119(2). 307–315. 20 indexed citations
19.
Chittiboina, Prashant, et al.. (2012). Metastatic Prostate Mass to the Intradural Foramen Magnum Region: A Case Report. SHILAP Revista de lepidopterología. 73(1). 9–13. 2 indexed citations
20.
Sonig, Ashish, et al.. (2012). Is posttraumatic cerebrospinal fluid fistula a predictor of posttraumatic meningitis? A US Nationwide Inpatient Sample database study. Neurosurgical FOCUS. 32(6). E4–E4. 14 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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