Steven S. Schreiber

2.8k total citations
53 papers, 2.3k citations indexed

About

Steven S. Schreiber is a scholar working on Molecular Biology, Oncology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Steven S. Schreiber has authored 53 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 13 papers in Oncology and 11 papers in Cellular and Molecular Neuroscience. Recurrent topics in Steven S. Schreiber's work include Cancer-related Molecular Pathways (11 papers), Cell death mechanisms and regulation (10 papers) and Neuroscience and Neuropharmacology Research (9 papers). Steven S. Schreiber is often cited by papers focused on Cancer-related Molecular Pathways (11 papers), Cell death mechanisms and regulation (10 papers) and Neuroscience and Neuropharmacology Research (9 papers). Steven S. Schreiber collaborates with scholars based in United States, Bulgaria and China. Steven S. Schreiber's co-authors include Michel Baudry, Zhiqun Tan, Ning Sun, Georges Tocco, Shahin Sakhi, Mark Fisher, Nam Tran, Kim N. Green, Berislav V. Zloković and Leslie M. Thompson and has published in prestigious journals such as The Lancet, Journal of Neuroscience and Trends in Neurosciences.

In The Last Decade

Steven S. Schreiber

52 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Steven S. Schreiber United States 29 1.1k 683 402 338 288 53 2.3k
Thomas L. Deckwerth United States 16 1.8k 1.6× 813 1.2× 514 1.3× 351 1.0× 269 0.9× 22 3.2k
Suzanne de la Monte United States 26 1.5k 1.3× 535 0.8× 789 2.0× 253 0.7× 443 1.5× 55 3.2k
Ning Sun China 23 670 0.6× 304 0.4× 214 0.5× 250 0.7× 268 0.9× 49 1.5k
Young Soo Ahn South Korea 27 1.3k 1.1× 344 0.5× 327 0.8× 216 0.6× 245 0.9× 60 2.4k
Johan van Beek Switzerland 26 686 0.6× 622 0.9× 394 1.0× 439 1.3× 200 0.7× 40 2.6k
Jeannette M. Dypbukt Sweden 10 1.4k 1.2× 881 1.3× 340 0.8× 281 0.8× 125 0.4× 12 2.4k
Nathalie Cartier France 40 2.7k 2.5× 738 1.1× 1.3k 3.2× 472 1.4× 419 1.5× 87 4.5k
James J. Vornov United States 23 835 0.8× 936 1.4× 254 0.6× 279 0.8× 212 0.7× 39 1.8k
Geoffrey Murdoch United States 25 1.5k 1.4× 711 1.0× 1.1k 2.7× 309 0.9× 189 0.7× 54 3.6k
Paul D. Drew United States 37 1.8k 1.7× 415 0.6× 433 1.1× 1.0k 3.0× 378 1.3× 72 4.0k

Countries citing papers authored by Steven S. Schreiber

Since Specialization
Citations

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

Fields of papers citing papers by Steven S. Schreiber

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Steven S. Schreiber. 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 Steven S. Schreiber. The network helps show where Steven S. Schreiber may publish in the future.

Co-authorship network of co-authors of Steven S. Schreiber

This figure shows the co-authorship network connecting the top 25 collaborators of Steven S. Schreiber. A scholar is included among the top collaborators of Steven S. Schreiber 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 Steven S. Schreiber. Steven S. Schreiber 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.
Fisher, Mark, et al.. (2018). Disseminated Microinfarctions with Cerebral Microbleeds. Journal of Stroke and Cerebrovascular Diseases. 27(6). e95–e97. 2 indexed citations
2.
Tan, Zhiqun, et al.. (2011). Nucleolar stress characterized by downregulation of nucleophosmin: A novel cause of neuronal degeneration. Biochemical and Biophysical Research Communications. 417(1). 514–520. 24 indexed citations
3.
Green, Kim N. & Steven S. Schreiber. (2010). Advances in Our Understanding of the Pathophysiology of Alzheimer’s Disease. 6(1). 28–28. 3 indexed citations
4.
Liu, Bingqian, Suhail Rasool, Zhikuan Yang, et al.. (2009). Amyloid-Peptide Vaccinations Reduce β-Amyloid Plaques but Exacerbate Vascular Deposition and Inflammation in the Retina of Alzheimer’s Transgenic Mice. American Journal Of Pathology. 175(5). 2099–2110. 147 indexed citations
5.
Green, Kim N., Joan S. Steffan, Hilda Martínez‐Coria, et al.. (2008). Nicotinamide Restores Cognition in Alzheimer's Disease Transgenic Mice via a Mechanism Involving Sirtuin Inhibition and Selective Reduction of Thr231-Phosphotau. Journal of Neuroscience. 28(45). 11500–11510. 319 indexed citations
6.
Tan, Zhiqun, Raman Sankar, Don Shin, et al.. (2002). Immunohistochemical study of p53-associated proteins in rat brain following lithium–pilocarpine status epilepticus. Brain Research. 929(1). 129–138. 35 indexed citations
7.
Liu, Wei, et al.. (2001). Kainate excitotoxicity in organotypic hippocampal slice cultures: evidence for multiple apoptotic pathways. Brain Research. 916(1-2). 239–248. 55 indexed citations
8.
Tan, Zhiqun, et al.. (2001). Downregulation of free ubiquitin: a novel mechanism of p53 stabilization and neuronal cell death. Molecular Brain Research. 91(1-2). 179–188. 20 indexed citations
9.
Tan, Zhiqun, et al.. (2001). Increased expression of Fas (CD95/APO-1) in adult rat brain after kainate-induced seizures. Neuroreport. 12(9). 1979–1982. 35 indexed citations
10.
Tan, Zhiqun, Ning Sun, & Steven S. Schreiber. (1998). Immunohistochemical localization of redox factor-1 (Ref-1) in Alzheimerʼs hippocampus. Neuroreport. 9(12). 2749–2752. 57 indexed citations
11.
Tran, Nam, et al.. (1998). Rat Brain Capillary Thrombomodulin. Thrombosis Research. 92(5). 213–219. 5 indexed citations
12.
Tran, Nam, Steven S. Schreiber, & Mark Fisher. (1998). Astrocyte Regulation of Endothelial Tissue Plasminogen Activator in a Blood-Brain Barrier Model. Journal of Cerebral Blood Flow & Metabolism. 18(12). 1316–1324. 39 indexed citations
13.
Sakhi, Shahin, Annadora J. Bruce, Ning Sun, et al.. (1997). Induction of Tumor Suppressor p53 and DNA Fragmentation in Organotypic Hippocampal Cultures Following Excitotoxin Treatment. Experimental Neurology. 145(1). 81–88. 45 indexed citations
14.
Sun, Ning, Annadora J. Bruce, Michel Baudry, & Steven S. Schreiber. (1997). Isolation of the gene encoding lamp-1, a lysosomal membrane protein, by differential screening in an animal model of status epilepticus. Molecular Brain Research. 45(2). 353–355. 3 indexed citations
15.
Schreiber, Steven S., et al.. (1997). Localization of V1a vasopressin receptor mRNA expression in cultured neurons, astroglia, and oligodendroglia of rat cerebral cortex. Molecular Brain Research. 45(1). 138–140. 19 indexed citations
16.
Liu, Wei, et al.. (1996). Increased expression of cyclin D1 in the adult rat brain following kainic acid treatment. Neuroreport. 7(15). 2785–2790. 46 indexed citations
17.
Sakhi, Shahin, Wendy Gilmore, Nam Tran, & Steven S. Schreiber. (1996). p53-deficient mice are protected against adrenalectomy-induced apoptosis. Neuroreport. 8(1). 233–235. 32 indexed citations
18.
Sakhi, Shahin, et al.. (1996). Nuclear accumulation of p53 protein following kainic acid-induced seizures. Neuroreport. 7(2). 493–496. 74 indexed citations
19.
Schreiber, Steven S., Georges Tocco, Imad Najm, et al.. (1992). Absence of c-fos induction in neonatal rat brain after seizures. Neuroscience Letters. 136(1). 31–35. 61 indexed citations
20.
Day, Jonathan, Nicholas J. Laping, Thomas H. McNeill, et al.. (1990). Castration Enhances Expression of Glial Fibrillary Acidic Protein and Sulfated Glycoprotein-2 in the Intact and Lesion-Altered Hippocampus of the Adult Male Rat. Molecular Endocrinology. 4(12). 1995–2002. 103 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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