Britta Keyser

832 total citations
25 papers, 620 citations indexed

About

Britta Keyser is a scholar working on Genetics, Cardiology and Cardiovascular Medicine and Molecular Biology. According to data from OpenAlex, Britta Keyser has authored 25 papers receiving a total of 620 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 12 papers in Cardiology and Cardiovascular Medicine and 9 papers in Molecular Biology. Recurrent topics in Britta Keyser's work include Connective tissue disorders research (12 papers), Cardiac Valve Diseases and Treatments (8 papers) and Aortic Disease and Treatment Approaches (7 papers). Britta Keyser is often cited by papers focused on Connective tissue disorders research (12 papers), Cardiac Valve Diseases and Treatments (8 papers) and Aortic Disease and Treatment Approaches (7 papers). Britta Keyser collaborates with scholars based in Germany, United States and Netherlands. Britta Keyser's co-authors include Kurt Ullrich, Chris Mühlhausen, Thomas Braulke, Yskert Von Kodolitsch, Sara Sheikhzadeh, Peter N. Robinson, Meike Rybczynski, David M. Koeller, Stefan Blankenberg and Thomas S. Mir and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Journal of Virology.

In The Last Decade

Britta Keyser

25 papers receiving 613 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Britta Keyser Germany 17 268 259 207 180 136 25 620
Esther Vamos Belgium 15 286 1.1× 23 0.1× 179 0.9× 90 0.5× 54 0.4× 21 533
Sofía Gouveia Spain 11 152 0.6× 59 0.2× 114 0.6× 38 0.2× 37 0.3× 37 361
Alice Goldenberg France 9 382 1.4× 15 0.1× 87 0.4× 35 0.2× 117 0.9× 12 527
М. С. Назаренко Russia 11 215 0.8× 66 0.3× 56 0.3× 57 0.3× 5 0.0× 88 381
Pik To Cheung Hong Kong 9 391 1.5× 54 0.2× 175 0.8× 8 0.0× 10 0.1× 9 679
María Soledad Fernández‐García Spain 7 232 0.9× 12 0.0× 30 0.1× 63 0.3× 72 0.5× 11 438
Torben A. Kruse Denmark 9 326 1.2× 282 1.1× 100 0.5× 15 0.1× 10 0.1× 27 623
J P Harpey France 9 232 0.9× 16 0.1× 45 0.2× 33 0.2× 98 0.7× 21 442
Makoto Hase Japan 8 321 1.2× 49 0.2× 56 0.3× 30 0.2× 11 0.1× 8 481
Sabrina Biardel Canada 9 360 1.3× 93 0.4× 13 0.1× 481 2.7× 15 0.1× 16 754

Countries citing papers authored by Britta Keyser

Since Specialization
Citations

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

Fields of papers citing papers by Britta Keyser

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Britta Keyser

This figure shows the co-authorship network connecting the top 25 collaborators of Britta Keyser. A scholar is included among the top collaborators of Britta Keyser 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 Britta Keyser. Britta Keyser 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.
Montag, Judith, Julia Beck, Britta Keyser, et al.. (2019). P1617Contractile imbalance as trigger for HCM pathogenesis: evidence from mutations in different sarcomeric proteins. European Heart Journal. 40(Supplement_1). 1 indexed citations
2.
Montag, Judith, Julia Beck, Britta Keyser, et al.. (2018). Burst-Like Transcription of Mutant and Wildtype MYH7-Alleles as Possible Origin of Cell-to-Cell Contractile Imbalance in Hypertrophic Cardiomyopathy. Frontiers in Physiology. 9. 359–359. 30 indexed citations
3.
Montag, Judith, Britta Keyser, Cristobal G. dos Remedios, et al.. (2017). Intrinsic MYH7 expression regulation contributes to tissue level allelic imbalance in hypertrophic cardiomyopathy. Journal of Muscle Research and Cell Motility. 38(3-4). 291–302. 18 indexed citations
4.
Backer, Julie De, Kerstin Kutsche, Laura Muiño Mosquera, et al.. (2016). Mitral valve prolapse syndrome and MASS phenotype: Stability of aortic dilatation but progression of mitral valve prolapse. IJC Heart & Vasculature. 10. 39–46. 9 indexed citations
5.
Arslan‐Kirchner, Mine, Eloisa Arbustini, Cathérine Boileau, et al.. (2015). Clinical utility gene card for: Hereditary thoracic aortic aneurysm and dissection including next-generation sequencing-based approaches. European Journal of Human Genetics. 24(1). 146–150. 17 indexed citations
6.
Derda, Anselm A., Sabrina Thum, Johan M. Lorenzen, et al.. (2015). Blood-based microRNA signatures differentiate various forms of cardiac hypertrophy. International Journal of Cardiology. 196. 115–122. 81 indexed citations
7.
Wellbrock, Jasmin, Sara Sheikhzadeh, Leticia Oliveira‐Ferrer, et al.. (2014). Overexpression of Gremlin-1 in Patients with Loeys-Dietz Syndrome: Implications on Pathophysiology and Early Disease Detection. PLoS ONE. 9(8). e104742–e104742. 12 indexed citations
8.
Sheikhzadeh, Sara, Julie De Backer, Meike Rybczynski, et al.. (2014). The main pulmonary artery in adults: a controlled multicenter study with assessment of echocardiographic reference values, and the frequency of dilatation and aneurysm in Marfan syndrome. Orphanet Journal of Rare Diseases. 9(1). 203–203. 27 indexed citations
9.
Adsay, Volkan, Sara Sheikhzadeh, Britta Keyser, et al.. (2013). Observational Cohort Study of Ventricular Arrhythmia in Adults with Marfan Syndrome Caused by FBN1 Mutations. PLoS ONE. 8(12). e81281–e81281. 44 indexed citations
10.
Keyser, Britta, Sara Sheikhzadeh, Christian Detter, et al.. (2012). FBN1 gene mutation characteristics and clinical features for the prediction of mitral valve disease progression. International Journal of Cardiology. 168(2). 953–959. 15 indexed citations
11.
Sheikhzadeh, Sara, Martin Kusch, Meike Rybczynski, et al.. (2012). A simple clinical model to estimate the probability of Marfan syndrome. QJM. 105(6). 527–535. 18 indexed citations
12.
Keyser, Britta, Sabine Hoffjan, Melanie Müller, et al.. (2012). High-density oligonucleotide-based resequencing assay for mutations causing syndromic and non-syndromic forms of thoracic aortic aneurysms and dissections. Molecular and Cellular Probes. 27(2). 103–108. 9 indexed citations
13.
Singh, Krishna K., et al.. (2012). TGFBR3 variation is not a common cause of Marfan-like syndrome and Loeys-Dietz-like syndrome. Journal of Negative Results in BioMedicine. 11(1). 9–9. 9 indexed citations
14.
Keyser, Britta, et al.. (2011). Glutaric Aciduria Type 1 Metabolites Impair the Succinate Transport from Astrocytic to Neuronal Cells. Journal of Biological Chemistry. 286(20). 17777–17784. 59 indexed citations
15.
Sheikhzadeh, Sara, Britta Keyser, Manfred Stuhrmann, et al.. (2011). Analysis of phenotype and genotype information for the diagnosis of Marfan syndrome. Clinical Genetics. 82(3). 240–247. 38 indexed citations
16.
Keyser, Britta, et al.. (2011). Herpes Simplex Virus Immediate-Early Protein ICP0 Is Targeted by SIAH-1 for Proteasomal Degradation. Journal of Virology. 85(15). 7644–7657. 24 indexed citations
17.
Sheikhzadeh, Sara, Meike Rybczynski, Mine Arslan‐Kirchner, et al.. (2010). Dural ectasia in individuals with Marfan-like features but exclusion of mutations in the genes FBN1, TGFBR1 and TGFBR2. Clinical Genetics. 79(6). 568–574. 16 indexed citations
18.
Keyser, Britta, Markus Glatzel, Zoltán Lukács, et al.. (2008). Transport and distribution of 3-hydroxyglutaric acid before and during induced encephalopathic crises in a mouse model of glutaric aciduria type 1. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1782(6). 385–390. 27 indexed citations
19.
Keyser, Britta, Chris Mühlhausen, Achim Dickmanns, et al.. (2008). Disease-causing missense mutations affect enzymatic activity, stability and oligomerization of glutaryl-CoA dehydrogenase (GCDH). Human Molecular Genetics. 17(24). 3854–3863. 33 indexed citations
20.
Keyser, Britta, Birgitta C. Burckhardt, Hermann Koepsell, et al.. (2007). 3-Hydroxyglutaric acid is transported via the sodium-dependent dicarboxylate transporter NaDC3. Journal of Molecular Medicine. 85(7). 763–770. 34 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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