Mitchell J.S. Braam

524 total citations
8 papers, 251 citations indexed

About

Mitchell J.S. Braam is a scholar working on Surgery, Molecular Biology and Immunology. According to data from OpenAlex, Mitchell J.S. Braam has authored 8 papers receiving a total of 251 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Surgery, 4 papers in Molecular Biology and 3 papers in Immunology. Recurrent topics in Mitchell J.S. Braam's work include Immune Cell Function and Interaction (3 papers), Pancreatic function and diabetes (3 papers) and Pluripotent Stem Cells Research (2 papers). Mitchell J.S. Braam is often cited by papers focused on Immune Cell Function and Interaction (3 papers), Pancreatic function and diabetes (3 papers) and Pluripotent Stem Cells Research (2 papers). Mitchell J.S. Braam collaborates with scholars based in Canada, Australia and Japan. Mitchell J.S. Braam's co-authors include Menno J. Oudhoff, Colby Zaph, Frann Antignano, Fábio Rossi, Kelly M. McNagny, C.H. Arrowsmith, Alistair Chenery, Kyle Burrows, Megan K. Levings and David Rattray and has published in prestigious journals such as Journal of Clinical Investigation, The Journal of Experimental Medicine and Endocrine Reviews.

In The Last Decade

Mitchell J.S. Braam

8 papers receiving 249 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mitchell J.S. Braam Canada 7 150 80 52 43 36 8 251
Larissa Hering Switzerland 6 132 0.9× 76 0.9× 28 0.5× 20 0.5× 47 1.3× 10 217
Imme Sakwa Germany 5 116 0.8× 93 1.2× 17 0.3× 68 1.6× 11 0.3× 5 277
Dawn Fernandez United States 7 105 0.7× 75 0.9× 31 0.6× 50 1.2× 11 0.3× 12 216
Sam A. Menzies United Kingdom 5 137 0.9× 40 0.5× 29 0.6× 62 1.4× 36 1.0× 5 196
Bedia Akosman United States 6 119 0.8× 72 0.9× 18 0.3× 39 0.9× 5 0.1× 6 201
Thi Tuyet Mai Nguyen Canada 9 148 1.0× 36 0.5× 10 0.2× 48 1.1× 38 1.1× 14 245
Katherine A. Romer United States 5 200 1.3× 18 0.2× 27 0.5× 15 0.3× 82 2.3× 5 313
Jikun Zha United States 7 188 1.3× 152 1.9× 14 0.3× 11 0.3× 18 0.5× 9 314
Anh Huynh United States 5 225 1.5× 61 0.8× 16 0.3× 18 0.4× 37 1.0× 9 321
Jianli Wu China 9 126 0.8× 36 0.5× 13 0.3× 25 0.6× 44 1.2× 16 390

Countries citing papers authored by Mitchell J.S. Braam

Since Specialization
Citations

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

Fields of papers citing papers by Mitchell J.S. Braam

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mitchell J.S. Braam. 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 Mitchell J.S. Braam. The network helps show where Mitchell J.S. Braam may publish in the future.

Co-authorship network of co-authors of Mitchell J.S. Braam

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

All Works

8 of 8 papers shown
1.
Ellis, Cara E., Majid Mojibian, Shogo Ida, et al.. (2023). Human A2-CAR T Cells Reject HLA-A2+ Human Islets Transplanted Into Mice Without Inducing Graft-versus-host Disease. Transplantation. 107(9). e222–e233. 6 indexed citations
2.
Braam, Mitchell J.S., Jia Zhao, Shogo Ida, et al.. (2023). Protocol development to further differentiate and transition stem cell-derived pancreatic progenitors from a monolayer into endocrine cells in suspension culture. Scientific Reports. 13(1). 8877–8877. 8 indexed citations
3.
Zhao, Jia, et al.. (2023). Differentiation of Human Pluripotent Stem Cells into Insulin-Producing Islet Clusters. Journal of Visualized Experiments. 1 indexed citations
4.
Ramzy, Adam, Mitchell J.S. Braam, Shogo Ida, et al.. (2022). A Century-long Journey From the Discovery of Insulin to the Implantation of Stem Cell–derived Islets. Endocrine Reviews. 44(2). 222–253. 21 indexed citations
5.
Oudhoff, Menno J., Frann Antignano, Alistair Chenery, et al.. (2016). Intestinal Epithelial Cell-Intrinsic Deletion of Setd7 Identifies Role for Developmental Pathways in Immunity to Helminth Infection. PLoS Pathogens. 12(9). e1005876–e1005876. 17 indexed citations
6.
Oudhoff, Menno J., Mitchell J.S. Braam, Spencer A. Freeman, et al.. (2016). SETD7 Controls Intestinal Regeneration and Tumorigenesis by Regulating Wnt/β-Catenin and Hippo/YAP Signaling. Developmental Cell. 37(1). 47–57. 92 indexed citations
7.
Antignano, Frann, Mitchell J.S. Braam, Michael R. Hughes, et al.. (2016). G9a regulates group 2 innate lymphoid cell development by repressing the group 3 innate lymphoid cell program. The Journal of Experimental Medicine. 213(7). 1153–1162. 34 indexed citations
8.
Antignano, Frann, Kyle Burrows, Michael R. Hughes, et al.. (2014). Methyltransferase G9A regulates T cell differentiation during murine intestinal inflammation. Journal of Clinical Investigation. 124(5). 1945–1955. 72 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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