Christina Bark

2.0k total citations
39 papers, 1.6k citations indexed

About

Christina Bark is a scholar working on Molecular Biology, Cell Biology and Surgery. According to data from OpenAlex, Christina Bark has authored 39 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 26 papers in Cell Biology and 13 papers in Surgery. Recurrent topics in Christina Bark's work include Cellular transport and secretion (25 papers), Pancreatic function and diabetes (13 papers) and RNA Research and Splicing (11 papers). Christina Bark is often cited by papers focused on Cellular transport and secretion (25 papers), Pancreatic function and diabetes (13 papers) and RNA Research and Splicing (11 papers). Christina Bark collaborates with scholars based in Sweden, United States and Japan. Christina Bark's co-authors include Michael C. Wilson, Per‐Olof Berggren, Klaus M. Hahn, Andrey E. Ryabinin, M C Wilson, Jan Zabielski, Marieangela C. Wilson, Ulf Pettersson, Björn Meister and Slavena A. Mandic and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Christina Bark

39 papers receiving 1.5k citations

Peers

Christina Bark

CMN

SURGE

GENET

Detlev Grabs Canada

Johnny K. Ngsee Canada

Francisco Gracia‐Navarro Spain

Guido Hermey Germany

Joachim Kremerskothen Germany

Sergey V. Voronov United States

Lambert Edelmann United States

A Zanini Italy

Friso R. Postma Netherlands

Judith A. Kowalchyk United States

Detlev Grabs Canada

Christina Bark

1.5k ×1.4

1.4k ×2.0

607 ×1.5

CMN

209 ×0.9

SURGE

71 ×0.4

GENET

Citations per year, relative to Christina Bark Christina Bark (= 1×) peers Detlev Grabs

Countries citing papers authored by Christina Bark

Since Specialization

Citations

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

Fields of papers citing papers by Christina Bark

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christina Bark

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

All Works

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20 of 20 papers shown

Zurawski, Zack, et al.. (2019). Disabling Gβγ-SNAP-25 interaction in gene-targeted mice results in enhancement of long-term potentiation at Schaffer collateral-CA1 synapses in the hippocampus. Neuroreport. 30(10). 695–699. 3 indexed citations

Gopaul, Katisha R., et al.. (2019). SNAP-25 isoforms differentially regulate synaptic transmission and long-term synaptic plasticity at central synapses. Scientific Reports. 9(1). 6403–6403. 44 indexed citations

Bark, Christina, et al.. (2018). SNAP-25 Puts SNAREs at Center Stage in Metabolic Disease. Neuroscience. 420. 86–96. 10 indexed citations

Bombek, Lidija Križančić, Marko Gosak, Ismael Valladolid‐Acebes, et al.. (2017). SNAP-25b-deficiency increases insulin secretion and changes spatiotemporal profile of Ca2+oscillations in β cell networks. Scientific Reports. 7(1). 7744–7744. 30 indexed citations

Valladolid‐Acebes, Ismael, Kerstin Brismar, Tibor Harkany, et al.. (2015). Replacing SNAP-25b with SNAP-25a expression results in metabolic disease. Proceedings of the National Academy of Sciences. 112(31). E4326–35. 27 indexed citations

Mandic, Slavena A., et al.. (2011). Munc18-1 and Munc18-2 Proteins Modulate β-Cell Ca2+ Sensitivity and Kinetics of Insulin Exocytosis Differently. Journal of Biological Chemistry. 286(32). 28026–28040. 26 indexed citations

Bark, Christina. (2009). SNAP‐25 and Gene‐targeted Mouse Mutants. Annals of the New York Academy of Sciences. 1152(1). 145–153. 7 indexed citations

Johansson, Jenny U., Jesper Ericsson, Juliette Janson, et al.. (2008). An Ancient Duplication of Exon 5 in the Snap25 Gene Is Required for Complex Neuronal Development/Function. PLoS Genetics. 4(11). e1000278–e1000278. 70 indexed citations

Lu, Ming, Lars Forsberg, Anders Höög, et al.. (2008). Heterogeneous expression of SNARE proteins SNAP-23, SNAP-25, Syntaxin1 and VAMP in human parathyroid tissue. Molecular and Cellular Endocrinology. 287(1-2). 72–80. 11 indexed citations

10.

Meister, Björn, et al.. (2005). DARPP-32 and inhibitor-1 are expressed in pancreatic β-cells. Biochemical and Biophysical Research Communications. 329(2). 673–677. 9 indexed citations

11.

Johansson, Jenny U., Haruhiro Higashida, Björn Meister, et al.. (2005). Cyclin-dependent kinase 5 activators p35 and p39 facilitate formation of functional synapses. Molecular Brain Research. 138(2). 215–227. 15 indexed citations

12.

Johansson, Jenny U., Jesper Gromada, Slavena A. Mandic, et al.. (2004). Cyclin-dependent Kinase 5 Associated with p39 Promotes Munc18-1 Phosphorylation and Ca2+-dependent Exocytosis. Journal of Biological Chemistry. 279(28). 29534–29541. 56 indexed citations

13.

Bark, Christina, Frederick P. Bellinger, Ashutosh Kaushal, et al.. (2004). Developmentally Regulated Switch in Alternatively Spliced SNAP-25 Isoforms Alters Facilitation of Synaptic Transmission. Journal of Neuroscience. 24(40). 8796–8805. 75 indexed citations

14.

Zhang, Wei, et al.. (2004). Mint1, a Munc-18-interacting protein, is expressed in insulin-secreting β-cells. Biochemical and Biophysical Research Communications. 320(3). 717–721. 16 indexed citations

15.

Bäckström, Anders, et al.. (1998). Molecular cloning and characterisation of a mouse gene encoding an isoform of the neuronal cyclin-dependent kinase 5 (CDK5) activator. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1398(3). 371–376. 9 indexed citations

16.

Jacobsson, Gunilla, Fredrik Piehl, Christina Bark, Xu Zhang, & Björn Meister. (1996). Differential subcellular localization of SNAP-25a and SNAP-25b RNA transcripts in spinal motoneurons and plasticity in expression after nerve injury. Molecular Brain Research. 37(1-2). 49–62. 21 indexed citations

17.

Bark, Christina & Michael C. Wilson. (1994). Human cDNA clones encoding two different isoforms of the nerve terminal protein SNAP-25. Gene. 139(2). 291–292. 126 indexed citations

18.

Bark, Christina. (1993). Structure of the Chicken Gene for SNAP-25 Reveals Duplicated Exons Encoding Distinct Isoforms of the Protein. Journal of Molecular Biology. 233(1). 67–76. 108 indexed citations

19.

Bark, Christina & Ulf Pettersson. (1989). Nucleotide sequence and organization of full length human U4 RNA pseudogenes. Gene. 80(2). 385–389. 3 indexed citations

20.

Westin, Gunnar, et al.. (1984). Clustered genes for human U2 RNA.. Proceedings of the National Academy of Sciences. 81(12). 3811–3815. 69 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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