Tamara T. Koopmann

3.7k citations

21 papers · 1.6k indexed · h-index 15

Cardiology and Cardiovascular Medicine top 1%
Molecular Biology top 10%
Cellular and Molecular Neuroscience top 10%
Genetics
Pediatrics, Perinatology and Child Health

Co-authors: 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
Topics: Cardiac electrophysiology and arrhythmias (16 papers)Ion channel regulation and function (14 papers)Cardiovascular Effects of Exercise (5 papers)
Cited by: Cardiology and Cardiovascular Medicine Molecular Biology Cellular and Molecular Neuroscience
Journals: Circulation Journal of Clinical Investigation Circulation Research
Partner nations: Netherlands United States France

In The Last Decade

Tamara T. Koopmann

20 papers receiving 1.6k citations

Peers

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

#	Work	Indexed citations
1	A Deep Intronic Splice Variant in COL1A1 Causing Osteogenesis Imperfecta Type II 2024 ·American Journal of Medical Genetics Part A ·(unknown),Claudia Ruivenkamp,Tamara T. Koopmann,Gijs W.E. Santen,Peter G. J. Nikkels,Karin van der Tuin	0
2	From diagnostic yield to clinical impact: a pilot study on the implementation of prenatal exome sequencing in routine care 2019 ·Genetics in Medicine ·(unknown),Monique C. Haak,P. N. Adama van Scheltema,Cacha Peeters‐Scholte,Tamara T. Koopmann,Esther Nibbeling,Emmelien Aten,Nicolette S. den Hollander,Claudia Ruivenkamp,Mariëtte J.V. Hoffer,Gijs W.E. Santen	39
3	An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesis 2018 ·European Heart Journal ·Diptendu Chatterjee,Meena Fatah,Deniz Akdiş,Danna Spears,Tamara T. Koopmann,Kirti Mittal,Muhammad Rafiq,B.M. Cattanach,Qili Zhao,Jeff S. Healey,Michael J. Ackerman,J. Martijn Bos,Yu Sun,Jason T. Maynes,Corinna Brunckhorst,Argelia Medeiros‐Domingo,Fırat Duru,Ardan M. Saguner,Robert M. Hamilton	102
4	2889A novel serum biomarker identifying Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) 2017 ·European Heart Journal ·Diptendu Chatterjee,Meena Fatah,(unknown),Danna Spears,Tamara T. Koopmann,Kirti Mittal,Corinna Brunckhorst,(unknown),Ardan M. Saguner,(unknown)	2
5	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 2017 ·Muhammad Rafiq,Tamara T. Koopmann,Laura Zahavich,Meena Fatah,Robert M. Hamilton	2
6	Unique Cardiac Purkinje Fiber Transient Outward Current β-Subunit Composition 2013 ·Circulation Research ·Ling Xiao,Tamara T. Koopmann,Balázs Ördög,Pieter G. Postema,Arie O. Verkerk,Vivek Iyer,Kevin J. Sampson,Gerard J.J. Boink,Maya Mamarbachi,András Varró,Luc Jordaens,Jan Res,Robert S. Kass,Arthur A. Wilde,Connie R. Bezzina,Stanley Nattel	60
7	Founder mutations in the Netherlands: familial idiopathic ventricular fibrillation and DPP6 2011 ·Netherlands Heart Journal ·Pieter G. Postema,Imke Christiaans,Nynke Hofman,Mariëlle Alders,Tamara T. Koopmann,Connie R. Bezzina,Peter Loh,Katja Zeppenfeld,Paul G.A. Volders,Arthur A.M. Wilde	30
8	The Chemical Compound PTC124 Does Not Affect Cellular Electrophysiology of Cardiac Ventricular Myocytes 2011 ·Cardiovascular Drugs and Therapy ·Tamara T. Koopmann,Arie O. Verkerk,Connie R. Bezzina,Jacques M.T. de Bakker,Arthur A.M. Wilde	7
9	A Complex Double Deletion in LMNA Underlies Progressive Cardiac Conduction Disease, Atrial Arrhythmias, and Sudden Death 2011 ·Circulation Cardiovascular Genetics ·Roos F. Marsman,Abdennasser Bardai,Alex V. Postma,Jan C.J.,Tamara T. Koopmann,Leander Beekman,Allard C. van der Wal,Yigal M. Pinto,Ronald H. Lekanne Deprez,Arthur A.M. Wilde,Luc Jordaens,Connie R. Bezzina	17
10	Haplotype-Sharing Analysis Implicates Chromosome 7q36 Harboring DPP6 in Familial Idiopathic Ventricular Fibrillation 2009 ·The American Journal of Human Genetics ·Mariëlle Alders,Tamara T. Koopmann,Imke Christiaans,Pieter G. Postema,Leander Beekman,Michael W.T. Tanck,Katja Zeppenfeld,Peter Loh,Karel T. Koch,Sophie Demolombe,Marcel M. A. M. Mannens,Connie R. Bezzina,Arthur A.M. Wilde	101
11	Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans 2008 ·Journal of Clinical Investigation ·Hiroshi Watanabe,Tamara T. Koopmann,Solena Le Scouarnec,Tao Yang,(unknown),Jean‐Jacques Schott,Sophie Demolombe,Vincent Probst,Frédéric Anselme,Denis Escande,Ans C.P. Wiesfeld,Arne Pfeufer,Stefan Kääb,Hans Wichmann,Can Hasdemir,Yoshifusa Aizawa,Arthur A.M. Wilde,Dan M. Roden,Connie R. Bezzina	317
12	Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies 2008 ·Heart Rhythm ·Paola G. Meregalli,Hanno L. Tan,Vincent Probst,Tamara T. Koopmann,Michael W.T. Tanck,Zahurul A. Bhuiyan,Frédéric Sacher,Florence Kyndt,Jean‐Jacques Schott,Juliette Albuisson,Philippe Mabo,Connie R. Bezzina,Hervé Le Marec,Arthur A.M. Wilde	154
13	Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohort 2007 ·Heart Rhythm ·Tamara T. Koopmann,Leander Beekman,Mariëlle Alders,Paola G. Meregalli,Marcel M. A. M. Mannens,Antoon F.M. Moorman,Arthur A.M. Wilde,Connie R. Bezzina	36
14	Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activity 2007 ·European Journal of Human Genetics ·Ping Yang,Tamara T. Koopmann,Arne Pfeufer,Shapour Jalilzadeh,Eric Schulze‐Bahr,Stefan Kääb,Arthur A.M. Wilde,Dan M. Roden,Connie R. Bezzina	24
15	Mutations in an alternately processed sodium channel beta-1 subunit associated with Brugada syndrome and cardiac conduction defect 2007 ·Data Archiving and Networked Services (DANS) ·Hiroshi Watanabe,Tamara T. Koopmann,Jean‐Jacques Schott,Tao Yang,(unknown),(unknown),Sophie Demolombe,Denis Escande,Ans C.P. Wiesfeld,Arne Pfeufer,Yoshifusa Aizawa,Arthur A.M. Wilde,Dan M. Roden,Connie R. Bezzina	3
16	Voltage‐gated sodium channels: Action players with many faces 2006 ·Annals of Medicine ·Tamara T. Koopmann,Connie R. Bezzina,Arthur A.M. Wilde	29
17	Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies 2006 ·Heart Rhythm ·Tamara T. Koopmann,Mariëlle Alders,Roselie Jongbloed,(unknown),Marcel M. A. M. Mannens,Arthur A.M. Wilde,Connie R. Bezzina	49
18	Common Sodium Channel Promoter Haplotype in Asian Subjects Underlies Variability in Cardiac Conduction 2006 ·Circulation ·Connie R. Bezzina,Wataru Shimizu,Ping Yang,Tamara T. Koopmann,Michael W.T. Tanck,Yoshihiro Miyamoto,Shiro Kamakura,Dan M. Roden,Arthur A.M. Wilde	161
19	A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families 2005 ·Journal of Molecular and Cellular Cardiology ·J SMITS,Tamara T. Koopmann,Ronald Wilders,Marieke W. Veldkamp,T. Opthof,Zahir A. Bhuiyan,Marcel M. A. M. Mannens,Jeffrey R. Balser,H H Tan,Connie R. Bezzina	158
20	Right Ventricular Fibrosis and Conduction Delay in a Patient With Clinical Signs of Brugada Syndrome 2005 ·Circulation ·Ruben Coronel,Simona Casini,Tamara T. Koopmann,Francien J. G. Wilms-Schopman,Arie O. Verkerk,Joris R. de Groot,Zahurul A. Bhuiyan,Connie R. Bezzina,Marieke W. Veldkamp,André C. Linnenbank,Allard C. van der Wal,Hanno L. Tan,Pedro Brugada,Arthur A.M. Wilde,Jacques M.T. de Bakker	327

About Tamara T. Koopmann

Tamara T. Koopmann is a scholar working on Cardiology and Cardiovascular Medicine, Orthopedics and Sports Medicine and Molecular Biology, having authored 21 papers that have together received 1.6k indexed citations. Recurring topics across this work include Cardiac electrophysiology and arrhythmias (16 papers), Ion channel regulation and function (14 papers) and Cardiovascular Effects of Exercise (5 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (1.4k citations), Molecular Biology (1.1k citations) and Cellular and Molecular Neuroscience (181 citations). Tamara T. Koopmann has collaborated with scholars based in Netherlands, United States and France. Frequent 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. Their work appears in journals such as Circulation, Journal of Clinical Investigation and Circulation Research.

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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