Eric M. Brey

6.7k total citations
153 papers, 5.2k citations indexed

About

Eric M. Brey is a scholar working on Biomedical Engineering, Biomaterials and Surgery. According to data from OpenAlex, Eric M. Brey has authored 153 papers receiving a total of 5.2k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Biomedical Engineering, 54 papers in Biomaterials and 46 papers in Surgery. Recurrent topics in Eric M. Brey's work include Electrospun Nanofibers in Biomedical Applications (45 papers), 3D Printing in Biomedical Research (35 papers) and Tissue Engineering and Regenerative Medicine (29 papers). Eric M. Brey is often cited by papers focused on Electrospun Nanofibers in Biomedical Applications (45 papers), 3D Printing in Biomedical Research (35 papers) and Tissue Engineering and Regenerative Medicine (29 papers). Eric M. Brey collaborates with scholars based in United States, Taiwan and Germany. Eric M. Brey's co-authors include Jeffery C. Larson, Ming‐Huei Cheng, Alyssa A. Appel, Yu-Chieh Chiu, Monica L. Moya, Emmanuel C. Opara, Shiri Uriel, Mark A. Anastasio, C. Patrick and Ali Çınar and has published in prestigious journals such as Advanced Materials, PLoS ONE and Biomaterials.

In The Last Decade

Eric M. Brey

152 papers receiving 5.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Eric M. Brey United States	42	2.3k	1.8k	1.6k	1.1k	344	153	5.2k
Felicity R. A. J. Rose United Kingdom	39	2.6k 1.1×	1.6k 0.9×	1.2k 0.8×	875 0.8×	199 0.6×	125	5.1k
Martin Ehrbar Switzerland	41	3.0k 1.3×	1.7k 0.9×	1.2k 0.8×	1.3k 1.3×	566 1.6×	122	5.8k
Jeroen Leijten Netherlands	41	2.5k 1.1×	1.0k 0.6×	1.1k 0.7×	854 0.8×	258 0.8×	120	4.9k
Xiaoming Li China	48	3.8k 1.6×	2.4k 1.4×	1.4k 0.9×	879 0.8×	155 0.5×	194	7.0k
Barbara Pui Chan Hong Kong	38	1.9k 0.8×	1.6k 0.9×	1.9k 1.2×	521 0.5×	139 0.4×	111	5.0k
Yanan Du China	47	3.3k 1.4×	1.4k 0.8×	1.2k 0.7×	1.6k 1.5×	413 1.2×	226	6.8k
Amir M. Ghaemmaghami United Kingdom	41	3.0k 1.3×	1.1k 0.6×	1.1k 0.7×	1.1k 1.0×	274 0.8×	123	6.5k
Jacqueline Alblas Netherlands	41	3.2k 1.4×	957 0.5×	1.2k 0.7×	1.8k 1.7×	337 1.0×	84	6.2k
Thomas H. Barker United States	44	1.6k 0.7×	1.3k 0.7×	1.3k 0.8×	1.8k 1.7×	344 1.0×	114	6.9k
K. Jane Grande‐Allen United States	43	1.4k 0.6×	1.3k 0.7×	1.8k 1.1×	1.0k 1.0×	167 0.5×	179	6.3k

Countries citing papers authored by Eric M. Brey

Since Specialization

Citations

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

Fields of papers citing papers by Eric M. Brey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eric M. Brey. 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 Eric M. Brey. The network helps show where Eric M. Brey may publish in the future.

Co-authorship network of co-authors of Eric M. Brey

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

All Works

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20 of 20 papers shown

Long, Byron L., Chenyue W. Hu, George Britton, et al.. (2022). cytoNet: Spatiotemporal network analysis of cell communities. PLoS Computational Biology. 18(6). e1009846–e1009846. 6 indexed citations

Laas, Kelly, et al.. (2020). Infusing Ethics in Research Groups: A Bottom-Up, Context-Specific Approach.. AEE Journal. 3 indexed citations

Shrestha, Binita, et al.. (2020). Induced Pluripotent Stem Cell-Derived Endothelial Networks Accelerate Vascularization But Not Bone Regeneration. Tissue Engineering Part A. 27(13-14). 940–961. 14 indexed citations

Acosta, Francisca M., et al.. (2020). Diabetic Conditions Confer Metabolic and Structural Modifications to Tissue-Engineered Skeletal Muscle. Tissue Engineering Part A. 27(9-10). 549–560. 4 indexed citations

Acosta, Francisca M., et al.. (2020). A Straightforward Approach to Engineer Vascularized Adipose Tissue Using Microvascular Fragments. Tissue Engineering Part A. 26(15-16). 905–914. 17 indexed citations

Hsiao, Hui‐Yi, Chin‐Yu Yang, Jiawei Liu, Eric M. Brey, & Ming‐Huei Cheng. (2018). Periosteal Osteogenic Capacity Depends on Tissue Source. Tissue Engineering Part A. 24(23-24). 1733–1741. 11 indexed citations

Akar, Banu, Alexander M. Tatara, Alok Sutradhar, et al.. (2018). Large Animal Models of an In Vivo Bioreactor for Engineering Vascularized Bone. Tissue Engineering Part B Reviews. 24(4). 317–325. 21 indexed citations

Akar, Banu, et al.. (2018). Preformed Vascular Networks Survive and Enhance Vascularization in Critical Sized Cranial Defects. Tissue Engineering Part A. 24(21-22). 1603–1615. 28 indexed citations

Appel, Alyssa A., et al.. (2015). Long-Term Function of Alginate-Encapsulated Islets. Tissue Engineering Part B Reviews. 22(1). 34–46. 46 indexed citations

10.

Somo, Sami I., Banu Akar, Elif Seyma Bayrak, et al.. (2015). Pore Interconnectivity Influences Growth Factor-Mediated Vascularization in Sphere-Templated Hydrogels. Tissue Engineering Part C Methods. 21(8). 773–785. 70 indexed citations

11.

Jiang, Bin, et al.. (2012). Fibrin-Loaded Porous Poly(Ethylene Glycol) Hydrogels as Scaffold Materials for Vascularized Tissue Formation. Tissue Engineering Part A. 19(1-2). 224–234. 51 indexed citations

12.

Appel, Alyssa A., Jeffery C. Larson, Sami I. Somo, et al.. (2012). Imaging of Poly(α-hydroxy-ester) Scaffolds with X-ray Phase-Contrast Microcomputed Tomography. Tissue Engineering Part C Methods. 18(11). 859–865. 16 indexed citations

13.

Jiang, Bin, et al.. (2011). PLGA Nanospheres Encapsulated Within Thermo-responsive Hydrogel For Ocular Delivery Of Dexamethasone Sodium Phosphate. Investigative Ophthalmology & Visual Science. 52(14). 467–467. 1 indexed citations

14.

Mehdizadeh, Hamidreza, et al.. (2011). An Agent-Based Model for the Investigation of Neovascularization Within Porous Scaffolds. Tissue Engineering Part A. 17(17-18). 2133–2141. 104 indexed citations

15.

Appel, Alyssa A., Mark A. Anastasio, & Eric M. Brey. (2011). Potential for Imaging Engineered Tissues with X-Ray Phase Contrast. Tissue Engineering Part B Reviews. 17(5). 321–330. 35 indexed citations

16.

Brewster, Luke P., et al.. (2010). FRNK overexpression limits the depth and frequency of vascular smooth muscle cell invasion in a three‐dimensional fibrin matrix. Journal of Cellular Physiology. 225(2). 562–568. 10 indexed citations

17.

Chiu, Yu-Chieh, et al.. (2009). Generation of Porous Poly(Ethylene Glycol) Hydrogels by Salt Leaching. Tissue Engineering Part C Methods. 16(5). 905–912. 90 indexed citations

18.

Mieler, William F., et al.. (2008). Thermo-Responsive Hydrogel Drug Delivery System for the Posterior Segment of the Eye. Investigative Ophthalmology & Visual Science. 49(13). 3873–3873. 2 indexed citations

19.

Papavasiliou, Georgia, et al.. (2008). Three-Dimensional Patterning of Poly(Ethylene Glycol) Hydrogels Through Surface-Initiated Photopolymerization. Tissue Engineering Part C Methods. 14(2). 129–140. 30 indexed citations

20.

Uriel, Shiri, et al.. (2008). Endothelial Cell–Matrix Interactions in Neovascularization. Tissue Engineering Part B Reviews. 14(1). 19–32. 68 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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