Cuno Kuipéri

2.1k total citations
18 papers, 1.7k citations indexed

About

Cuno Kuipéri is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Physiology. According to data from OpenAlex, Cuno Kuipéri has authored 18 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Cardiology and Cardiovascular Medicine, 9 papers in Molecular Biology and 7 papers in Physiology. Recurrent topics in Cuno Kuipéri's work include Alzheimer's disease research and treatments (7 papers), Cardiac electrophysiology and arrhythmias (7 papers) and Ion channel regulation and function (6 papers). Cuno Kuipéri is often cited by papers focused on Alzheimer's disease research and treatments (7 papers), Cardiac electrophysiology and arrhythmias (7 papers) and Ion channel regulation and function (6 papers). Cuno Kuipéri collaborates with scholars based in Belgium, United States and Netherlands. Cuno Kuipéri's co-authors include Ilse Dewachter, Fred Van Leuven, Dieder Moechars, Lucia Dumitrescu‐Ozimek, Gary E. Landreth, M. Kerry O’Banion, Michael T. Heneka, Magdalena Sastre, Thomas Klockgether and Dieter Nuyens and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Neuroscience.

In The Last Decade

Cuno Kuipéri

18 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cuno Kuipéri Belgium 13 936 673 423 330 313 18 1.7k
Kirk Townsend United States 14 782 0.8× 703 1.0× 250 0.6× 312 0.9× 634 2.0× 20 1.9k
Carmela Matrone Italy 24 625 0.7× 668 1.0× 509 1.2× 194 0.6× 185 0.6× 49 1.7k
Darrell Sawmiller United States 19 512 0.5× 435 0.6× 171 0.4× 180 0.5× 131 0.4× 53 1.2k
John Xi Chen United States 17 1.4k 1.5× 1.4k 2.1× 377 0.9× 376 1.1× 257 0.8× 17 2.2k
Yoshio Namba Japan 16 1.3k 1.4× 778 1.2× 349 0.8× 189 0.6× 272 0.9× 28 1.9k
Yi‐Hua Qian China 23 449 0.5× 532 0.8× 213 0.5× 238 0.7× 274 0.9× 54 1.3k
Badreddine Kriem France 17 536 0.6× 506 0.8× 312 0.7× 111 0.3× 141 0.5× 32 1.3k
Nikunj Patel United States 19 800 0.9× 583 0.9× 204 0.5× 210 0.6× 483 1.5× 25 1.5k
Marianne Grant United States 18 1.2k 1.3× 713 1.1× 601 1.4× 297 0.9× 304 1.0× 42 1.9k
Corinne G. Jolivalt United States 24 1.1k 1.2× 462 0.7× 413 1.0× 163 0.5× 265 0.8× 41 1.8k

Countries citing papers authored by Cuno Kuipéri

Since Specialization
Citations

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

Fields of papers citing papers by Cuno Kuipéri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cuno Kuipéri

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

All Works

18 of 18 papers shown
1.
Jacobs, J., Lucas Van Aelst, Jeroen Breckpot, et al.. (2023). Tools to differentiate between Filamin C and Titin truncating variant carriers: value of MRI. European Journal of Human Genetics. 31(11). 1323–1332. 3 indexed citations
2.
Robyns, Tomas, Jeroen Breckpot, Dieter Nuyens, et al.. (2019). Clinical and ECG variables to predict the outcome of genetic testing in hypertrophic cardiomyopathy. European Journal of Medical Genetics. 63(3). 103754–103754. 14 indexed citations
3.
Robyns, Tomas, Dieter Nuyens, Bert Vandenberk, et al.. (2018). Genotype–phenotype relationship and risk stratification in loss‐of‐function SCN5A mutation carriers. Annals of Noninvasive Electrocardiology. 23(5). e12548–e12548. 5 indexed citations
4.
Alaerts, Maaike, Cuno Kuipéri, Anniek Corveleyn, et al.. (2017). Left ventricular non-compaction with Ebstein anomaly attributed to a TPM1 mutation. European Journal of Medical Genetics. 61(1). 8–10. 17 indexed citations
5.
Robyns, Tomas, Rik Willems, Bert Vandenberk, et al.. (2017). Individualized corrected QT interval is superior to QT interval corrected using the Bazett formula in predicting mutation carriage in families with long QT syndrome. Heart Rhythm. 14(3). 376–382. 14 indexed citations
6.
Robyns, Tomas, Cuno Kuipéri, Jeroen Breckpot, et al.. (2017). Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathy. European Journal of Human Genetics. 25(12). 1313–1323. 9 indexed citations
7.
Robyns, Tomas, Cuno Kuipéri, Rik Willems, Anniek Corveleyn, & Dieter Nuyens. (2015). Targeted capture sequencing in a large LQTS family reveals a new pathogenic mutation c.2038delG in KCNH2 initially missed due to allelic dropout. Acta cardiologica. Supplementum. 70(6). 747–749. 2 indexed citations
8.
Gerche, André La, Caroline Robberecht, Cuno Kuipéri, et al.. (2010). Lower than expected desmosomal gene mutation prevalence in endurance athletes with complex ventricular arrhythmias of right ventricular origin. Heart. 96(16). 1268–1274. 134 indexed citations
9.
Gerche, André La, Caroline Robberecht, Cuno Kuipéri, et al.. (2010). Lower than Expected Desmosomal Gene Mutation Prevalence in Endurance Athletes with Complex Ventricular Arrhythmias of Right Ventricular Origin. Heart Lung and Circulation. 19. S231–S231. 5 indexed citations
10.
Rossenbacker, Tom, Els Schollen, Cuno Kuipéri, et al.. (2005). Unconventional intronic splice site mutation in SCN5A associates with cardiac sodium channelopathy. Journal of Medical Genetics. 42(5). e29–e29. 21 indexed citations
11.
Heneka, Michael T., Magdalena Sastre, Lucia Dumitrescu‐Ozimek, et al.. (2005). Acute treatment with the PPARγ agonist pioglitazone and ibuprofen reduces glial inflammation and Aβ1–42 levels in APPV717I transgenic mice. Brain. 128(6). 1442–1453. 479 indexed citations
12.
Rossenbacker, Tom, Huajun Liu, Cuno Kuipéri, et al.. (2004). Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac death. Heart Rhythm. 1(5). 610–615. 55 indexed citations
13.
Etcheberrigaray, René, Ilse Dewachter, Cuno Kuipéri, et al.. (2004). Therapeutic effects of PKC activators in Alzheimer's disease transgenic mice. Proceedings of the National Academy of Sciences. 101(30). 11141–11146. 274 indexed citations
14.
Dewachter, Ilse, Delphine Reversé, Laurence Ris, et al.. (2002). Neuronal Deficiency of Presenilin 1 Inhibits Amyloid Plaque Formation and Corrects Hippocampal Long-Term Potentiation But Not a Cognitive Defect of Amyloid Precursor Protein [V717I] Transgenic Mice. Journal of Neuroscience. 22(9). 3445–3453. 203 indexed citations
15.
Schneider, Ilka, Delphine Reversé, Ilse Dewachter, et al.. (2001). Mutant Presenilins Disturb Neuronal Calcium Homeostasis in the Brain of Transgenic Mice, Decreasing the Threshold for Excitotoxicity and Facilitating Long-term Potentiation. Journal of Biological Chemistry. 276(15). 11539–11544. 115 indexed citations
16.
Dorpe, Jo Van, Ilse Dewachter, Dieter Nuyens, et al.. (2000). Prominent Cerebral Amyloid Angiopathy in Transgenic Mice Overexpressing the London Mutant of Human APP in Neurons. American Journal Of Pathology. 157(4). 1283–1298. 189 indexed citations
17.
Dewachter, Ilse, Jo Van Dorpe, Cuno Kuipéri, et al.. (2000). Aging Increased Amyloid Peptide and Caused Amyloid Plaques in Brain of Old APP/V717I Transgenic Mice by a Different Mechanism than Mutant Presenilin1. Journal of Neuroscience. 20(17). 6452–6458. 91 indexed citations
18.
Moechars, Dieder, et al.. (1998). Aggressive behaviour in transgenic mice expressing APP is alleviated by serotonergic drugs. Neuroreport. 9(16). 3560–3564. 49 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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