JC Reed

6.9k total citations · 4 hit papers
31 papers, 6.0k citations indexed

About

JC Reed is a scholar working on Molecular Biology, Oncology and Pathology and Forensic Medicine. According to data from OpenAlex, JC Reed has authored 31 papers receiving a total of 6.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 11 papers in Oncology and 7 papers in Pathology and Forensic Medicine. Recurrent topics in JC Reed's work include Cell death mechanisms and regulation (8 papers), Lymphoma Diagnosis and Treatment (6 papers) and Chronic Lymphocytic Leukemia Research (5 papers). JC Reed is often cited by papers focused on Cell death mechanisms and regulation (8 papers), Lymphoma Diagnosis and Treatment (6 papers) and Chronic Lymphocytic Leukemia Research (5 papers). JC Reed collaborates with scholars based in United States, France and Italy. JC Reed's co-authors include Toshiyuki Miyashita, Stanisław Krajewski, Antonella Aiello, D Delia, M Hanada, Edward A. Stadtmauer, Krzysztof Reiss, Piero Anversa, G Olivetti and Wei Cheng and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Neuroscience and The Journal of Cell Biology.

In The Last Decade

JC Reed

31 papers receiving 5.8k citations

Hit Papers

Bcl-2 and the regulation of programmed cell death 1993 2026 2004 2015 1994 1996 1993 1993 500 1000 1.5k 2.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
JC Reed United States 20 4.0k 1.7k 1.0k 854 630 31 6.0k
Luisa Lanfrancone Italy 38 4.9k 1.2× 1.6k 1.0× 1.2k 1.2× 392 0.5× 813 1.3× 95 7.8k
Gregory Hollis United States 36 2.7k 0.7× 1.0k 0.6× 996 1.0× 501 0.6× 369 0.6× 101 5.1k
W. Stratford May United States 38 4.5k 1.1× 1.4k 0.8× 998 1.0× 405 0.5× 660 1.0× 78 6.4k
Elizabeth Yang United States 18 5.7k 1.4× 1.6k 0.9× 1.2k 1.2× 579 0.7× 774 1.2× 25 7.2k
Natalie Roy Canada 10 3.8k 1.0× 1.1k 0.6× 924 0.9× 409 0.5× 706 1.1× 13 5.0k
Lars Rönnstrand Sweden 54 5.9k 1.5× 2.0k 1.2× 2.0k 1.9× 399 0.5× 957 1.5× 173 10.2k
Jeffrey I. Kreisberg United States 42 3.2k 0.8× 852 0.5× 368 0.4× 520 0.6× 694 1.1× 103 5.9k
Vassiliki Poulaki United States 39 5.1k 1.3× 1.8k 1.1× 864 0.8× 383 0.4× 931 1.5× 55 8.2k
Agostino Tafuri Italy 36 4.3k 1.1× 1.7k 1.0× 2.3k 2.2× 508 0.6× 787 1.2× 160 8.3k
Giuseppe Viglietto Italy 48 5.4k 1.4× 2.3k 1.4× 687 0.7× 591 0.7× 1.6k 2.5× 150 8.2k

Countries citing papers authored by JC Reed

Since Specialization
Citations

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

Fields of papers citing papers by JC Reed

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of JC Reed

This figure shows the co-authorship network connecting the top 25 collaborators of JC Reed. A scholar is included among the top collaborators of JC Reed 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 JC Reed. JC Reed 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.
Chua, Chu Chang, Jinping Gao, Xingshun Xu, et al.. (2008). Over-expression of a modified bifunctional apoptosis regulator protects against cardiac injury and doxorubicin-induced cardiotoxicity in transgenic mice. Cardiovascular Research. 81(1). 20–27. 18 indexed citations
2.
Sekiya, Masuo, et al.. (1996). Interleukin-2 (IL-2) upregulates BAG-1 gene expression through serine- rich region within IL-2 receptor beta c chain. Blood. 88(11). 4118–4123. 31 indexed citations
3.
Adachi, M, Masuo Sekiya, Toshihiko Torigoe, et al.. (1996). Interleukin-2 (IL-2) upregulates BAG-1 gene expression through serine- rich region within IL-2 receptor beta c chain. Blood. 88(11). 4118–4123. 27 indexed citations
4.
Orlofsky, Amos, et al.. (1996). A1, a Bcl-2 family member, prolongs cell survival and permits myeloid differentiation. Blood. 87(3). 983–992. 133 indexed citations
5.
Kajstura, Jan, Wei Cheng, Krzysztof Reiss, et al.. (1996). Apoptotic and necrotic myocyte cell deaths are independent contributing variables of infarct size in rats.. PubMed. 74(1). 86–107. 866 indexed citations breakdown →
6.
Gillardon, Frank, Marco Zimmermann, Eugen Uhlmann, et al.. (1996). Antisense oligodeoxynucleotides to bax mRNA promote survival of rat sympathetic neurons in culture. Journal of Neuroscience Research. 43(6). 726–734. 3 indexed citations
7.
Arber, Nadir, et al.. (1995). Differences in epithelial apoptosis and apoptosis-related gene expression between the rat small and large intestine. Gastroenterology. 108(4). A741–A741. 4 indexed citations
8.
Selvakumaran, Muthu, Toshiyuki Miyashita, Hong‐Gang Wang, et al.. (1994). Immediate early up-regulation of bax expression by p53 but not TGF beta 1: a paradigm for distinct apoptotic pathways.. PubMed. 9(6). 1791–8. 425 indexed citations
9.
Torigoe, Toshihiko, et al.. (1994). Bcl-2 inhibits T-cell-mediated cytolysis of a leukemia cell line.. PubMed. 54(18). 4851–4. 35 indexed citations
10.
Reed, JC. (1994). Bcl-2 and the regulation of programmed cell death. The Journal of Cell Biology. 124(1). 1–6. 2065 indexed citations breakdown →
11.
Selvakumaran, Muthu, JC Reed, Dan A. Liebermann, & B Hoffman. (1994). Progression of the myeloid differentiation program is dominant to transforming growth factor-beta 1-induced apoptosis in M1 myeloid leukemic cells. Blood. 84(4). 1036–1042. 5 indexed citations
12.
Taichman, Russell S., Isabel Mérida, Toshihiko Torigoe, Glen N. Gaulton, & JC Reed. (1993). Evidence that protein tyrosine kinase p56-Lck regulates the activity of phosphatidylinositol-3'-kinase in interleukin-2-dependent T-cells.. Journal of Biological Chemistry. 268(27). 20031–20036. 47 indexed citations
13.
Miyashita, Toshiyuki & JC Reed. (1993). Bcl-2 oncoprotein blocks chemotherapy-induced apoptosis in a human leukemia cell line. Blood. 81(1). 151–157. 763 indexed citations breakdown →
14.
Hanada, M, D Delia, Antonella Aiello, Edward A. Stadtmauer, & JC Reed. (1993). bcl-2 gene hypomethylation and high-level expression in B-cell chronic lymphocytic leukemia. Blood. 82(6). 1820–1828. 46 indexed citations
15.
Hanada, M, D Delia, Antonella Aiello, Edward A. Stadtmauer, & JC Reed. (1993). bcl-2 gene hypomethylation and high-level expression in B-cell chronic lymphocytic leukemia. Blood. 82(6). 1820–1828. 533 indexed citations breakdown →
16.
Reed, JC, Shigeki Tanaka, & Michael Cuddy. (1992). Cell cycle analysis of p26-BCL-2 protein levels in proliferating lymphoma and leukemia cell lines.. PubMed. 52(10). 2802–5. 19 indexed citations
17.
Louie, DC, et al.. (1992). Frequent incidence of somatic mutations in translocated BCL2 oncogenes of non-Hodgkin's lymphomas. Blood. 79(1). 229–237. 83 indexed citations
19.
Louie, DC, et al.. (1992). Frequent incidence of somatic mutations in translocated BCL2 oncogenes of non-Hodgkin's lymphomas. Blood. 79(1). 229–237. 4 indexed citations
20.
Reed, JC, et al.. (1978). Legionnaires' disease. American Journal of Roentgenology. 131(5). 892–894. 2 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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