Christine Misquitta

1.5k total citations
17 papers, 936 citations indexed

About

Christine Misquitta is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Physiology. According to data from OpenAlex, Christine Misquitta has authored 17 papers receiving a total of 936 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 7 papers in Cardiology and Cardiovascular Medicine and 4 papers in Physiology. Recurrent topics in Christine Misquitta's work include RNA and protein synthesis mechanisms (10 papers), RNA Research and Splicing (9 papers) and Ion channel regulation and function (5 papers). Christine Misquitta is often cited by papers focused on RNA and protein synthesis mechanisms (10 papers), RNA Research and Splicing (9 papers) and Ion channel regulation and function (5 papers). Christine Misquitta collaborates with scholars based in Canada, United States and Israel. Christine Misquitta's co-authors include Ashok K. Grover, Brendan J. Frey, Qun Pan, Benjamin J. Blencowe, Ofer Shai, Arneet L. Saltzman, Douglas P. Mack, A. K. Grover, Sue E. Samson and Tomas Babak and has published in prestigious journals such as Genes & Development, Molecular Cell and Biochemical Journal.

In The Last Decade

Christine Misquitta

17 papers receiving 923 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christine Misquitta Canada 12 774 108 104 83 51 17 936
Nita Sachan United States 7 552 0.7× 122 1.1× 125 1.2× 53 0.6× 27 0.5× 9 721
Yves Brandenburger United States 13 849 1.1× 175 1.6× 76 0.7× 57 0.7× 78 1.5× 17 1.1k
Erdene Baljinnyam United States 15 595 0.8× 88 0.8× 116 1.1× 77 0.9× 103 2.0× 17 888
Elizabeth M. Sale United Kingdom 11 592 0.8× 142 1.3× 135 1.3× 92 1.1× 79 1.5× 12 803
Seu-Mei Wang Taiwan 17 376 0.5× 106 1.0× 57 0.5× 37 0.4× 97 1.9× 26 599
Hai-Lian Bi China 17 534 0.7× 133 1.2× 95 0.9× 117 1.4× 57 1.1× 27 848
Jerlyn Beltman Germany 10 596 0.8× 92 0.9× 167 1.6× 62 0.7× 57 1.1× 11 815
Debra J. Gawler United Kingdom 17 680 0.9× 103 1.0× 141 1.4× 38 0.5× 161 3.2× 26 868
Jiejia Xu China 16 639 0.8× 81 0.8× 109 1.0× 22 0.3× 34 0.7× 20 741

Countries citing papers authored by Christine Misquitta

Since Specialization
Citations

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

Fields of papers citing papers by Christine Misquitta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christine Misquitta

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

All Works

17 of 17 papers shown
1.
Barash, Yoseph, Joanna Y. Ip, Christine Misquitta, et al.. (2007). Functional coordination of alternative splicing in the mammalian central nervous system. Genome biology. 8(6). R108–R108. 82 indexed citations
2.
Chen, Tao, et al.. (2006). Characterization of SERCA2b Ca2+–Mg2+ ATPase mRNA decay by nuclear proteins. Cell Calcium. 41(6). 581–592. 1 indexed citations
3.
Misquitta, Christine, Tao Chen, & Ashok K. Grover. (2006). Control of protein expression through mRNA stability in calcium signalling. Cell Calcium. 40(4). 329–346. 47 indexed citations
4.
Pan, Qun, Arneet L. Saltzman, Yoon Ki Kim, et al.. (2006). Quantitative microarray profiling provides evidence against widespread coupling of alternative splicing with nonsense-mediated mRNA decay to control gene expression. Genes & Development. 20(2). 153–158. 186 indexed citations
5.
Shai, Ofer, Brendan J. Frey, Quaid Morris, et al.. (2004). Probabilistic Inference of Alternative Splicing Events in Microarray Data. Neural Information Processing Systems. 17. 1241–1248. 2 indexed citations
6.
Pan, Qun, Ofer Shai, Christine Misquitta, et al.. (2004). Revealing Global Regulatory Features of Mammalian Alternative Splicing Using a Quantitative Microarray Platform. Molecular Cell. 16(6). 929–941. 244 indexed citations
7.
Misquitta, Christine, et al.. (2004). Control of SERCA2a Ca2+ pump mRNA stability by nuclear proteins: role of domains in the 3′-untranslated region. Cell Calcium. 37(1). 17–24. 6 indexed citations
8.
Nie, Lin, Islam Ullah Khan, Christine Misquitta, & Ashok K. Grover. (2004). Sarcoplasmic reticulum Ca2+ pump mRNA stability in cardiac and smooth muscle: role of poly A+ tail length. Cell Calcium. 35(5). 479–484. 6 indexed citations
9.
Misquitta, Christine, James Mwanjewe, Lin Nie, & Ashok K. Grover. (2002). Sarcoplasmic reticulum Ca2+ pump mRNA stability in cardiac and smooth muscle: role of the 3′-untranslated region. American Journal of Physiology-Cell Physiology. 283(2). C560–C568. 22 indexed citations
10.
Misquitta, Christine, et al.. (2001). The role of 3′-untranslated region (3′-UTR) mediated mRNA stability in cardiovascular pathophysiology. Molecular and Cellular Biochemistry. 224(1-2). 53–67. 85 indexed citations
11.
Khan, Islam Ullah, Vicky Sandhu, Christine Misquitta, & A. K. Grover. (2000). SERCA pump isoform expression in endothelium of veins and arteries: Every endothelium is not the same. Molecular and Cellular Biochemistry. 203(1-2). 11–15. 25 indexed citations
12.
Misquitta, Christine, Douglas P. Mack, & Ashok K. Grover. (1999). Sarco/endoplasmic reticulum Ca2+(SERCA)-pumps: link to heart beats and calcium waves. Cell Calcium. 25(4). 277–290. 111 indexed citations
13.
Grover, Ashok K., Sue E. Samson, Christine Misquitta, & Adel B. Elmoselhi. (1999). Effects of peroxide on contractility of coronary artery rings of different sizes. Molecular and Cellular Biochemistry. 194(1-2). 159–164. 18 indexed citations
14.
Misquitta, Christine, et al.. (1999). Control of sarcoplasmic/endoplasmic-reticulum Ca2+ pump expression in cardiac and smooth muscle. Biochemical Journal. 338(1). 167–173. 16 indexed citations
15.
Grover, Ashok K., Sue E. Samson, & Christine Misquitta. (1997). Sarco(endo)plasmic reticulum Ca2+ pump isoform SERCA3 is more resistant than SERCA2b to peroxide. American Journal of Physiology-Cell Physiology. 273(2). C420–C425. 57 indexed citations
16.
Misquitta, Christine, Sue E. Samson, & Ashok K. Grover. (1996). Sarcoplasmic reticulum Ca2+-pump density is higher in distal than in proximal segments of porcine left coronary artery. Molecular and Cellular Biochemistry. 158(1). 91–95. 7 indexed citations
17.
Charette, L., Christine Misquitta, Jean‐Frédéric Guay, Denis Riendeau, & Thomas R. Jones. (1995). Involvement of cyclooxygenase 2 (COX-2) in intrinsic tone of isolated guinea pig. Canadian Journal of Physiology and Pharmacology. 73(11). 1561–1567. 21 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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