Shairaz Baksh

1.9k total citations · 1 hit paper
19 papers, 1.6k citations indexed

About

Shairaz Baksh is a scholar working on Molecular Biology, Cell Biology and Oncology. According to data from OpenAlex, Shairaz Baksh has authored 19 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 6 papers in Cell Biology and 4 papers in Oncology. Recurrent topics in Shairaz Baksh's work include Signaling Pathways in Disease (7 papers), Endoplasmic Reticulum Stress and Disease (4 papers) and Biochemical and Molecular Research (4 papers). Shairaz Baksh is often cited by papers focused on Signaling Pathways in Disease (7 papers), Endoplasmic Reticulum Stress and Disease (4 papers) and Biochemical and Molecular Research (4 papers). Shairaz Baksh collaborates with scholars based in Canada, United States and France. Shairaz Baksh's co-authors include Marek Michalak, Steven J. Burakoff, Sebastian Wesselborg, Yi-jin Xiao, Anke Zobywalski, Erwin Bohn, Klaus Schulze‐Osthoff, Ingo B. Autenrieth, Kirsten Lauber and Ralph K. Lindemann and has published in prestigious journals such as Cell, Journal of Biological Chemistry and Molecular Cell.

In The Last Decade

Shairaz Baksh

19 papers receiving 1.5k citations

Hit Papers

Apoptotic Cells Induce Migration of Phagocytes via Caspas... 2003 2026 2010 2018 2003 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
Shairaz Baksh Canada 13 887 669 339 177 158 19 1.6k
Ryutaro Shirakawa Japan 23 673 0.8× 323 0.5× 492 1.5× 167 0.9× 89 0.6× 51 1.5k
Sergio E. Alvarez Argentina 16 1.7k 1.9× 614 0.9× 574 1.7× 280 1.6× 127 0.8× 31 2.2k
Shunsuke Takasuga Japan 20 866 1.0× 317 0.5× 529 1.6× 185 1.0× 154 1.0× 37 1.5k
Paul J. Coffer Netherlands 18 1.4k 1.5× 452 0.7× 232 0.7× 177 1.0× 132 0.8× 27 2.1k
Ralph K. Lindemann Germany 20 1.5k 1.7× 669 1.0× 175 0.5× 195 1.1× 240 1.5× 27 2.2k
Pascal Gélébart Canada 25 1.1k 1.2× 316 0.5× 349 1.0× 77 0.4× 115 0.7× 46 1.7k
Lazaros C. Foukas United Kingdom 18 1.4k 1.6× 347 0.5× 190 0.6× 185 1.0× 107 0.7× 25 2.0k
Marten Jakob Germany 8 846 1.0× 354 0.5× 161 0.5× 153 0.9× 168 1.1× 10 1.2k
K. Yoshino Japan 6 1.5k 1.7× 266 0.4× 239 0.7× 186 1.1× 222 1.4× 7 1.9k
Roberta Mannucci Italy 26 1.3k 1.5× 358 0.5× 147 0.4× 253 1.4× 91 0.6× 38 2.1k

Countries citing papers authored by Shairaz Baksh

Since Specialization
Citations

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

Fields of papers citing papers by Shairaz Baksh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shairaz Baksh

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

All Works

19 of 19 papers shown
1.
Baksh, Shairaz, et al.. (2021). Extractionless nucleic acid detection: a high capacity solution to COVID-19 testing. Diagnostic Microbiology and Infectious Disease. 101(2). 115458–115458. 8 indexed citations
2.
Yang, Ning, Rachel Montpetit, Namrata Patel, et al.. (2019). Non-canonical BAD activity regulates breast cancer cell and tumor growth via 14-3-3 binding and mitochondrial metabolism. Oncogene. 38(18). 3325–3339. 26 indexed citations
3.
Joshi, Harshad, et al.. (2019). A47 INFLAMMTORY MEMORY/IMIPRINTING OF INTESTINAL STEM CELLS DRIVES RELAPSE IN IBD PATIENTS. Journal of the Canadian Association of Gastroenterology. 2(Supplement_2). 94–95. 1 indexed citations
4.
Tan, Chong Teik, Qiling Zhou, Nai Yang Fu, et al.. (2016). MOAP-1 Mediates Fas-Induced Apoptosis in Liver by Facilitating tBid Recruitment to Mitochondria. Cell Reports. 16(1). 174–185. 23 indexed citations
5.
Amith, Schammim Ray, et al.. (2015). Na+/H+ exchange in the tumour microenvironment: does NHE1 drive breast cancer carcinogenesis?. The International Journal of Developmental Biology. 59(7-8-9). 367–377. 34 indexed citations
6.
Glubrecht, Darryl, et al.. (2013). Calcineurin Regulates Nuclear Factor I Dephosphorylation and Activity in Malignant Glioma Cell Lines. Journal of Biological Chemistry. 288(33). 24104–24115. 16 indexed citations
7.
Pyarajan, Saiju, et al.. (2008). Interleukin-3 (IL-3)-induced c-fos Activation Is Modulated by Gab2-Calcineurin Interaction. Journal of Biological Chemistry. 283(35). 23505–23509. 6 indexed citations
8.
Baksh, Shairaz, et al.. (2007). Mitotic regulation of CDK4 by the serine/threonine phosphatase, calcineurin. Biochemical and Biophysical Research Communications. 363(3). 506–512. 1 indexed citations
9.
Lauber, Kirsten, Erwin Bohn, Stefan Kröber, et al.. (2003). Apoptotic Cells Induce Migration of Phagocytes via Caspase-3-Mediated Release of a Lipid Attraction Signal. Cell. 113(6). 717–730. 756 indexed citations breakdown →
10.
Baksh, Shairaz, Hans R. Widlund, Ashley Frazer‐Abel, et al.. (2002). NFATc2-Mediated Repression of Cyclin-Dependent Kinase 4 Expression. Molecular Cell. 10(5). 1071–1081. 146 indexed citations
11.
Tkaczuk, Jean, Edgar L. Milford, Chao‐Lan Yu, et al.. (2001). Intracellular signaling consequences of anti-IL-2Rα blockade by daclizumab. Transplantation Proceedings. 33(1-2). 212–213. 9 indexed citations
12.
Pratt, Joanne C., Vivien Igras, Hiroyuki Maeda, et al.. (2000). Cutting Edge: Gab2 Mediates an Inhibitory Phosphatidylinositol 3′-Kinase Pathway in T Cell Antigen Receptor Signaling. The Journal of Immunology. 165(8). 4158–4163. 55 indexed citations
13.
Baksh, Shairaz, James A. DeCaprio, & Steven J. Burakoff. (2000). Calcineurin regulation of the mammalian G0/G1 checkpoint element, cyclin dependent kinase 4. Oncogene. 19(24). 2820–2827. 49 indexed citations
14.
Baksh, Shairaz & Steven J. Burakoff. (2000). The role of calcineurin in lymphocyte activation. Seminars in Immunology. 12(4). 405–415. 49 indexed citations
15.
Tkaczuk, Jean, Edgar L. Milford, Charles B. Carpenter, et al.. (2000). INTRACELLULAR SIGNALING BY THE INTERMEDIATE-AFFINITY IL-2R CHAINS AFTER TREATMENT WITH DACLIZUMAB.. Transplantation. 69(Supplement). S397–S397. 1 indexed citations
16.
Baksh, Shairaz, Kimberly Burns, Christi Andrin, & Marek Michalak. (1995). Interaction of Calreticulin with Protein Disulfide Isomerase. Journal of Biological Chemistry. 270(52). 31338–31344. 99 indexed citations
17.
Baksh, Shairaz, et al.. (1992). Expression and purification of recombinant and native calreticulin. Protein Expression and Purification. 3(4). 322–331. 31 indexed citations
18.
Michalak, Marek, Shairaz Baksh, & Michał Opas. (1991). Identification and immunolocalization of calreticulin in pancreatic cells: No evidence for “calciosomes”. Experimental Cell Research. 197(1). 91–99. 49 indexed citations
19.
Milner, R E, Shairaz Baksh, Carrie S. Shemanko, et al.. (1991). Calreticulin, and not calsequestrin, is the major calcium binding protein of smooth muscle sarcoplasmic reticulum and liver endoplasmic reticulum.. Journal of Biological Chemistry. 266(11). 7155–7165. 204 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026