Cameron C. Trenor

7.9k total citations · 1 hit paper
71 papers, 4.3k citations indexed

About

Cameron C. Trenor is a scholar working on Surgery, Hematology and Oncology. According to data from OpenAlex, Cameron C. Trenor has authored 71 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Surgery, 24 papers in Hematology and 11 papers in Oncology. Recurrent topics in Cameron C. Trenor's work include Vascular Malformations and Hemangiomas (27 papers), Blood Coagulation and Thrombosis Mechanisms (12 papers) and Venous Thromboembolism Diagnosis and Management (9 papers). Cameron C. Trenor is often cited by papers focused on Vascular Malformations and Hemangiomas (27 papers), Blood Coagulation and Thrombosis Mechanisms (12 papers) and Venous Thromboembolism Diagnosis and Management (9 papers). Cameron C. Trenor collaborates with scholars based in United States, Canada and Italy. Cameron C. Trenor's co-authors include Nancy C. Andrews, Mark D. Fleming, Maureen A. Su, David R. Beier, William F. Dietrich, Dorothee Foernzler, Steven J. Fishman, Gulraiz Chaudry, Ahmad I. Alomari and Cinzia Garuti and has published in prestigious journals such as Journal of Clinical Investigation, Nature Genetics and Genes & Development.

In The Last Decade

Cameron C. Trenor

68 papers receiving 4.2k citations

Hit Papers

Microcytic anaemia mice have a mutation in Nramp2, a cand... 1997 2026 2006 2016 1997 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cameron C. Trenor United States 30 2.1k 1.6k 1.4k 1.3k 623 71 4.3k
Nicola J. Mutch United Kingdom 28 1.6k 0.8× 248 0.2× 1.0k 0.8× 340 0.3× 175 0.3× 67 3.6k
Murray N. Silverstein United States 28 1.5k 0.7× 423 0.3× 1.7k 1.3× 559 0.4× 613 1.0× 66 4.5k
I. Quéré France 41 1.4k 0.7× 150 0.1× 421 0.3× 1.8k 1.4× 763 1.2× 233 5.4k
Martine Aiach France 45 3.8k 1.8× 275 0.2× 1.0k 0.7× 1.2k 0.9× 210 0.3× 212 6.3k
David Launay France 48 451 0.2× 150 0.1× 1000 0.7× 766 0.6× 355 0.6× 321 7.8k
Ariella Zivelin Israel 33 2.9k 1.4× 387 0.2× 1.3k 0.9× 367 0.3× 120 0.2× 85 4.2k
Guillermina Girardi United States 40 1.9k 0.9× 162 0.1× 227 0.2× 372 0.3× 64 0.1× 81 6.4k
Clifford M. Takemoto United States 27 726 0.3× 361 0.2× 238 0.2× 329 0.2× 317 0.5× 78 3.3k
Paolo Bucciarelli Italy 37 2.1k 1.0× 48 0.0× 576 0.4× 633 0.5× 149 0.2× 119 4.1k
Peter J. Margetts Canada 38 283 0.1× 145 0.1× 203 0.1× 1.4k 1.0× 402 0.6× 84 6.0k

Countries citing papers authored by Cameron C. Trenor

Since Specialization
Citations

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

Fields of papers citing papers by Cameron C. Trenor

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cameron C. Trenor. 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 Cameron C. Trenor. The network helps show where Cameron C. Trenor may publish in the future.

Co-authorship network of co-authors of Cameron C. Trenor

This figure shows the co-authorship network connecting the top 25 collaborators of Cameron C. Trenor. A scholar is included among the top collaborators of Cameron C. Trenor 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 Cameron C. Trenor. Cameron C. Trenor 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.
Boccuto, Luigi, et al.. (2020). Childhood Vascular Tumors. Frontiers in Pediatrics. 8. 573023–573023. 7 indexed citations
2.
Taghinia, Amir H., Joseph Upton, Cameron C. Trenor, et al.. (2018). Lymphaticovenous bypass of the thoracic duct for the treatment of chylous leak in central conducting lymphatic anomalies. Journal of Pediatric Surgery. 54(3). 562–568. 29 indexed citations
3.
Oladunjoye, Olubunmi, Cameron C. Trenor, Lynn A. Sleeper, et al.. (2018). An anticoagulation protocol for use after congenital cardiac surgery. Journal of Thoracic and Cardiovascular Surgery. 156(1). 343–352.e4. 11 indexed citations
4.
Emani, Sirisha, et al.. (2017). Platelet testing to guide aspirin dose adjustment in pediatric patients after cardiac surgery. Journal of Thoracic and Cardiovascular Surgery. 154(5). 1723–1730. 16 indexed citations
5.
Bairdain, Sigrid, et al.. (2016). Quality improvement program reduces venous thromboembolism in infants and children with long-gap esophageal atresia (LGEA). Pediatric Surgery International. 32(7). 691–696.
6.
Goyal, Pradeep, Ahmad I. Alomari, Harry P. Kozakewich, et al.. (2016). Imaging features of kaposiform lymphangiomatosis. Pediatric Radiology. 46(9). 1282–1290. 39 indexed citations
7.
Cras, Timothy D. Le, et al.. (2016). Angiopoietins as serum biomarkers for lymphatic anomalies. Angiogenesis. 20(1). 163–173. 50 indexed citations
8.
Uller, Wibke, et al.. (2014). Cutaneovisceral Angiomatosis with Thrombocytopenia without Cutaneous Involvement. The Journal of Pediatrics. 165(4). 876–876.e1. 4 indexed citations
9.
Obeng, Esther A., et al.. (2014). Pediatric Heparin-Induced Thrombocytopenia: Prevalence, Thrombotic Risk, and Application of the 4Ts Scoring System. The Journal of Pediatrics. 166(1). 144–150.e1. 37 indexed citations
10.
Alomari, Ahmad I., Samantha A. Spencer, Ryan W. Arnold, et al.. (2013). Fibro-Adipose Vascular Anomaly. Journal of Pediatric Orthopaedics. 34(1). 109–117. 92 indexed citations
11.
Croteau, Stacy E., Harry P. Kozakewich, Antonio R. Pérez‐Atayde, et al.. (2013). Kaposiform Lymphangiomatosis: A Distinct Aggressive Lymphatic Anomaly. The Journal of Pediatrics. 164(2). 383–388. 109 indexed citations
12.
Emani, Sirisha, David Zurakowski, Christopher W. Baird, et al.. (2013). Hypercoagulability Markers Predict Thrombosis in Single Ventricle Neonates Undergoing Cardiac Surgery. The Annals of Thoracic Surgery. 96(2). 651–656. 29 indexed citations
13.
Barranco, Roger, Patricia E. Burrows, Mary Landrigan‐Ossar, Cameron C. Trenor, & Ahmad I. Alomari. (2012). Gross Hemoglobinuria and Oliguria Are Common Transient Complications of Sclerotherapy for Venous Malformations: Review of 475 Procedures. American Journal of Roentgenology. 199(3). 691–694. 17 indexed citations
14.
Croteau, Stacy E., Marilyn G. Liang, Harry P. Kozakewich, et al.. (2012). Kaposiform Hemangioendothelioma: Atypical Features and Risks of Kasabach-Merritt Phenomenon in 107 Referrals. The Journal of Pediatrics. 162(1). 142–147. 243 indexed citations
15.
Zitomersky, Naamah, Menno Verhave, & Cameron C. Trenor. (2010). Thrombosis and inflammatory bowel disease: A call for improved awareness and prevention. Inflammatory Bowel Diseases. 17(1). 458–470. 78 indexed citations
16.
Shin, Andrew Y., Christopher S. Almond, Rebekah Mannix, et al.. (2006). The Boston Marathon Study: A Novel Approach to Research During Residency. PEDIATRICS. 117(5). 1818–1822. 10 indexed citations
17.
Lim, Jackie E., Ou Jin, Carolyn M. Bennett, et al.. (2005). A mutation in Sec15l1 causes anemia in hemoglobin deficit (hbd) mice. Nature Genetics. 37(11). 1270–1273. 73 indexed citations
18.
Montosi, Giuliana, Adriana Donovan, Antonio Totaro, et al.. (2001). Autosomal-dominant hemochrom-atosis is associated with a mutation in the ferroportin (SLC11A3) gene. Journal of Clinical Investigation. 108(4). 619–623. 391 indexed citations
19.
Montosi, Giuliana, Adriana Donovan, Antonio Totaro, et al.. (2001). Autosomal-dominant hemochrom-atosis is associated with a mutation in the ferroportin (SLC11A3) gene. Journal of Clinical Investigation. 108(4). 619–623. 355 indexed citations
20.
Su, Maureen A., Cameron C. Trenor, Judith C. Fleming, Mark D. Fleming, & Nancy C. Andrews. (1998). The G185R Mutation Disrupts Function of the Iron Transporter Nramp2. Blood. 92(6). 2157–2163. 193 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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