Tamara T. Koopmann

3.7k total citations
21 papers, 1.6k citations indexed

About

Tamara T. Koopmann is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Tamara T. Koopmann has authored 21 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Cardiology and Cardiovascular Medicine, 15 papers in Molecular Biology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Tamara T. Koopmann's work include Cardiac electrophysiology and arrhythmias (16 papers), Ion channel regulation and function (14 papers) and Cardiovascular Effects of Exercise (5 papers). Tamara T. Koopmann is often cited by papers focused on Cardiac electrophysiology and arrhythmias (16 papers), Ion channel regulation and function (14 papers) and Cardiovascular Effects of Exercise (5 papers). Tamara T. Koopmann collaborates with scholars based in Netherlands, United States and France. Tamara T. Koopmann's co-authors include Connie R. Bezzina, Arthur A.M. Wilde, Marieke W. Veldkamp, Michael W.T. Tanck, Dan M. Roden, Marcel M. A. M. Mannens, Hanno L. Tan, Zahurul A. Bhuiyan, Jean‐Jacques Schott and Vincent Probst and has published in prestigious journals such as Circulation, Journal of Clinical Investigation and Circulation Research.

In The Last Decade

Tamara T. Koopmann

20 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tamara T. Koopmann Netherlands	15	1.4k	1.1k	181	74	38	21	1.6k
Riyaz A. Kaba United Kingdom	16	774 0.5×	674 0.6×	58 0.3×	30 0.4×	9 0.2×	50	1.2k
Priscila Y. Sato United States	12	534 0.4×	546 0.5×	121 0.7×	19 0.3×	4 0.1×	22	917
Tina S. Fong United States	6	395 0.3×	459 0.4×	100 0.6×	13 0.2×	16 0.4×	7	654
Jeffrey R. Winterfield United States	11	422 0.3×	260 0.2×	62 0.3×	50 0.7×	7 0.2×	47	697
Véronique Fressart France	18	879 0.6×	637 0.6×	130 0.7×	46 0.6×	2 0.1×	47	1.0k
D. Bendixen Denmark	14	399 0.3×	514 0.5×	110 0.6×	52 0.7×	13 0.3×	19	674
Julien Barc France	14	843 0.6×	662 0.6×	110 0.6×	46 0.6×	4 0.1×	29	977
Federica Dagradi Italy	18	910 0.6×	629 0.6×	89 0.5×	25 0.3×	14 0.4×	38	1.1k
Joel Temple United States	9	381 0.3×	297 0.3×	62 0.3×	44 0.6×	5 0.1×	19	495
Marcia Blair United States	19	579 0.4×	319 0.3×	182 1.0×	158 2.1×	28 0.7×	34	969

Countries citing papers authored by Tamara T. Koopmann

Since Specialization

Citations

This map shows the geographic impact of Tamara T. Koopmann'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 Tamara T. Koopmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tamara T. Koopmann more than expected).

Fields of papers citing papers by Tamara T. Koopmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tamara T. Koopmann. 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 Tamara T. Koopmann. The network helps show where Tamara T. Koopmann may publish in the future.

Co-authorship network of co-authors of Tamara T. Koopmann

This figure shows the co-authorship network connecting the top 25 collaborators of Tamara T. Koopmann. A scholar is included among the top collaborators of Tamara T. Koopmann 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 Tamara T. Koopmann. Tamara T. Koopmann 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

Ruivenkamp, Claudia, et al.. (2024). A Deep Intronic Splice Variant in COL1A1 Causing Osteogenesis Imperfecta Type II. American Journal of Medical Genetics Part A. 197(5). e63972–e63972.

Haak, Monique C., P. N. Adama van Scheltema, Cacha Peeters‐Scholte, et al.. (2019). From diagnostic yield to clinical impact: a pilot study on the implementation of prenatal exome sequencing in routine care. Genetics in Medicine. 21(10). 2303–2310. 39 indexed citations

Chatterjee, Diptendu, Meena Fatah, Deniz Akdiş, et al.. (2018). An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesis. European Heart Journal. 39(44). 3932–3944. 102 indexed citations

Chatterjee, Diptendu, Meena Fatah, Danna Spears, et al.. (2017). 2889A novel serum biomarker identifying Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC). European Heart Journal. 38(suppl_1). 2 indexed citations

Rafiq, Muhammad, Tamara T. Koopmann, Laura Zahavich, Meena Fatah, & Robert M. Hamilton. (2017). An Inherited Arrhythmia Syndrome with Long QT, Sudden Death and Depolarization Disorder Due to an In-Frame Deletion in Exon 16 of the CACNA1C Gene. 4(1). 2 indexed citations

Xiao, Ling, Tamara T. Koopmann, Balázs Ördög, et al.. (2013). Unique Cardiac Purkinje Fiber Transient Outward Current β-Subunit Composition. Circulation Research. 112(10). 1310–1322. 60 indexed citations

Postema, Pieter G., Imke Christiaans, Nynke Hofman, et al.. (2011). Founder mutations in the Netherlands: familial idiopathic ventricular fibrillation and DPP6. Netherlands Heart Journal. 19(6). 290–296. 30 indexed citations

Koopmann, Tamara T., Arie O. Verkerk, Connie R. Bezzina, Jacques M.T. de Bakker, & Arthur A.M. Wilde. (2011). The Chemical Compound PTC124 Does Not Affect Cellular Electrophysiology of Cardiac Ventricular Myocytes. Cardiovascular Drugs and Therapy. 26(1). 41–45. 7 indexed citations

Marsman, Roos F., Abdennasser Bardai, Alex V. Postma, et al.. (2011). A Complex Double Deletion in LMNA Underlies Progressive Cardiac Conduction Disease, Atrial Arrhythmias, and Sudden Death. Circulation Cardiovascular Genetics. 4(3). 280–287. 17 indexed citations

10.

Alders, Mariëlle, Tamara T. Koopmann, Imke Christiaans, et al.. (2009). Haplotype-Sharing Analysis Implicates Chromosome 7q36 Harboring DPP6 in Familial Idiopathic Ventricular Fibrillation. The American Journal of Human Genetics. 84(4). 468–476. 101 indexed citations

11.

Watanabe, Hiroshi, Tamara T. Koopmann, Solena Le Scouarnec, et al.. (2008). Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans. Journal of Clinical Investigation. 118(6). 2260–8. 317 indexed citations

12.

Meregalli, Paola G., Hanno L. Tan, Vincent Probst, et al.. (2008). Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies. Heart Rhythm. 6(3). 341–348. 154 indexed citations

13.

Koopmann, Tamara T., Leander Beekman, Mariëlle Alders, et al.. (2007). Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohort. Heart Rhythm. 4(6). 752–755. 36 indexed citations

14.

Yang, Ping, Tamara T. Koopmann, Arne Pfeufer, et al.. (2007). Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activity. European Journal of Human Genetics. 16(3). 350–357. 24 indexed citations

15.

Watanabe, Hiroshi, Tamara T. Koopmann, Jean‐Jacques Schott, et al.. (2007). Mutations in an alternately processed sodium channel beta-1 subunit associated with Brugada syndrome and cardiac conduction defect. Data Archiving and Networked Services (DANS). 116(16). 55–55. 3 indexed citations

16.

Koopmann, Tamara T., Connie R. Bezzina, & Arthur A.M. Wilde. (2006). Voltage‐gated sodium channels: Action players with many faces. Annals of Medicine. 38(7). 472–482. 29 indexed citations

17.

Koopmann, Tamara T., Mariëlle Alders, Roselie Jongbloed, et al.. (2006). Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies. Heart Rhythm. 3(1). 52–55. 49 indexed citations

18.

Bezzina, Connie R., Wataru Shimizu, Ping Yang, et al.. (2006). Common Sodium Channel Promoter Haplotype in Asian Subjects Underlies Variability in Cardiac Conduction. Circulation. 113(3). 338–344. 161 indexed citations

19.

SMITS, J, Tamara T. Koopmann, Ronald Wilders, et al.. (2005). A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families. Journal of Molecular and Cellular Cardiology. 38(6). 969–981. 158 indexed citations

20.

Coronel, Ruben, Simona Casini, Tamara T. Koopmann, et al.. (2005). Right Ventricular Fibrosis and Conduction Delay in a Patient With Clinical Signs of Brugada Syndrome. Circulation. 112(18). 2769–2777. 327 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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