Marit Bakke

1.7k total citations
48 papers, 1.4k citations indexed

About

Marit Bakke is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Marit Bakke has authored 48 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 26 papers in Genetics and 10 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Marit Bakke's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (16 papers), Estrogen and related hormone effects (13 papers) and Sexual Differentiation and Disorders (12 papers). Marit Bakke is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (16 papers), Estrogen and related hormone effects (13 papers) and Sexual Differentiation and Disorders (12 papers). Marit Bakke collaborates with scholars based in Norway, United States and Sweden. Marit Bakke's co-authors include Johan Lund, Erling A. Høivik, Keith L. Parker, Aurélia E. Lewis, Liping Zhao, Neil A. Hanley, Gunnar Mellgren, Lisa J. Cushman, Albert F. Parlow and Sally A. Camper and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Marit Bakke

45 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marit Bakke Norway 21 752 747 301 209 145 48 1.4k
Caroline J. Speed Australia 17 655 0.9× 669 0.9× 172 0.6× 161 0.8× 69 0.5× 22 1.5k
Mariko Shirota Japan 14 526 0.7× 351 0.5× 573 1.9× 258 1.2× 78 0.5× 51 1.5k
Susan M. Aronica United States 16 802 1.1× 1.1k 1.4× 368 1.2× 228 1.1× 217 1.5× 25 1.9k
Jeffrey C. Webster United States 12 394 0.5× 451 0.6× 352 1.2× 117 0.6× 64 0.4× 14 1.2k
Kenji Ohe Japan 21 669 0.9× 309 0.4× 196 0.7× 80 0.4× 71 0.5× 74 1.3k
Mohamad Zubair Japan 16 660 0.9× 597 0.8× 235 0.8× 122 0.6× 34 0.2× 19 1.0k
Yoshikatsu Uematsu Japan 9 622 0.8× 434 0.6× 210 0.7× 379 1.8× 48 0.3× 10 1.7k
Michelle L. Brinkmeier United States 21 916 1.2× 488 0.7× 676 2.2× 97 0.5× 60 0.4× 44 1.5k
Marie‐Laure Kottler France 25 835 1.1× 780 1.0× 296 1.0× 564 2.7× 62 0.4× 56 1.8k
Tim Wintermantel Germany 15 439 0.6× 419 0.6× 223 0.7× 436 2.1× 89 0.6× 20 1.2k

Countries citing papers authored by Marit Bakke

Since Specialization
Citations

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

Fields of papers citing papers by Marit Bakke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marit Bakke

This figure shows the co-authorship network connecting the top 25 collaborators of Marit Bakke. A scholar is included among the top collaborators of Marit Bakke 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 Marit Bakke. Marit Bakke 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.
Pedersen, Line, Reidun Aesöy, Haruna Muwonge, et al.. (2019). Mice depleted for Exchange Proteins Directly Activated by cAMP (Epac) exhibit irregular liver regeneration in response to partial hepatectomy. Scientific Reports. 9(1). 13789–13789. 6 indexed citations
2.
Gandasi, Nikhil R., Muhmmad Omar‐Hmeadi, Marit Bakke, et al.. (2019). Fusion Pore Regulation by EPAC2/cAMP Controls Cargo Release during Insulin Exocytosis. Biophysical Journal. 116(3). 314a–314a.
3.
Gandasi, Nikhil R., Muhmmad Omar‐Hmeadi, Marit Bakke, et al.. (2019). Fusion pore regulation by cAMP/Epac2 controls cargo release during insulin exocytosis. eLife. 8. 38 indexed citations
4.
Aesöy, Reidun, Haruna Muwonge, Reidun Kristin Kopperud, et al.. (2018). Deletion of exchange proteins directly activated by cAMP (Epac) causes defects in hippocampal signaling in female mice. PLoS ONE. 13(7). e0200935–e0200935. 11 indexed citations
5.
Kopperud, Reidun, Erling A. Høivik, Reidun Aesöy, et al.. (2016). Long-term consumption of an obesogenic high fat diet prior to ischemia-reperfusion mediates cardioprotection via Epac1-dependent signaling. Nutrition & Metabolism. 13(1). 87–87. 18 indexed citations
6.
Lewis, Aurélia E., Reidun Aesöy, & Marit Bakke. (2016). Role of EPAC in cAMP-Mediated Actions in Adrenocortical Cells. Frontiers in Endocrinology. 7. 63–63. 15 indexed citations
7.
Hellesen, Alexander, et al.. (2015). Peripheral Blood Cells from Patients with Autoimmune Addison's Disease Poorly Respond to Interferons In Vitro , Despite Elevated Serum Levels of Interferon-Inducible Chemokines. Journal of Interferon & Cytokine Research. 35(10). 759–770. 16 indexed citations
8.
Aesöy, Reidun, Katarina Gradin, Erling A. Høivik, et al.. (2014). Regulation of CDKN2B expression by interaction of Arnt with Miz-1 - a basis for functional integration between the HIF and Myc gene regulatory pathways. Molecular Cancer. 13(1). 54–54. 9 indexed citations
9.
Sharma, Yogita, Chandra Sekhar Reddy Chilamakuri, Marit Bakke, & Boris Lenhard. (2014). Computational Characterization of Modes of Transcriptional Regulation of Nuclear Receptor Genes. PLoS ONE. 9(2). e88880–e88880. 5 indexed citations
10.
Høivik, Erling A., et al.. (2013). DNA Methylation of Alternative Promoters Directs Tissue Specific Expression of Epac2 Isoforms. PLoS ONE. 8(7). e67925–e67925. 46 indexed citations
11.
12.
Zhao, Liping, Marit Bakke, Neil A. Hanley, et al.. (2004). Tissue-specific knockouts of steroidogenic factor 1. Molecular and Cellular Endocrinology. 215(1-2). 89–94. 49 indexed citations
13.
Hoang, Tuyen, et al.. (2004). cAMP-dependent Protein Kinase Regulates Ubiquitin-Proteasome-mediated Degradation and Subcellular Localization of the Nuclear Receptor Coactivator GRIP1. Journal of Biological Chemistry. 279(47). 49120–49130. 62 indexed citations
14.
Stallings, Nancy R., Neil A. Hanley, Gregor Majdič, et al.. (2002). DEVELOPMENT OF A TRANSGENIC GREEN FLUORESCENT PROTEIN LINEAGE MARKER FOR STEROIDOGENIC FACTOR 1. Endocrine Research. 28(4). 497–504. 23 indexed citations
15.
Stallings, Nancy R., Neil A. Hanley, Gregor Majdič, et al.. (2002). Development of a Transgenic Green Fluorescent Protein Lineage Marker for Steroidogenic Factor 1. Molecular Endocrinology. 16(10). 2360–2370. 56 indexed citations
16.
Bakke, Marit, Liping Zhao, & Keith L. Parker. (2001). Approaches to define the role of SF-1 at different levels of the hypothalamic-pituitary-steroidogenic organ axis. Molecular and Cellular Endocrinology. 179(1-2). 33–37. 17 indexed citations
17.
Bakke, Marit, Liping Zhao, Neil A. Hanley, & Keith L. Parker. (2001). SF-1: a critical mediator of steroidogenesis. Molecular and Cellular Endocrinology. 171(1-2). 5–7. 46 indexed citations
18.
Zhao, Liping, Marit Bakke, & Keith L. Parker. (2001). Pituitary-specific knockout of steroidogenic factor 1. Molecular and Cellular Endocrinology. 185(1-2). 27–32. 59 indexed citations
19.
Bakke, Marit, Liping Zhao, Neil A. Hanley, & Keith L. Parker. (2000). Approaches to Define the Role of SF-1 at Different Levels of the Hypothalamic-Pituitary-Steroidogenic Organ Axis. Endocrine Research. 26(4). 1067–1073. 7 indexed citations
20.

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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