Genetic basis of cardiac ion channel diseases - List of publications

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Genetic basis of cardiac ion channel diseases

Koopmann, T.

Publication date

2008

Link to publication

Citation for published version (APA):

Koopmann, T. (2008). Genetic basis of cardiac ion channel diseases.

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GENETICBASIS OFCARDIACIONCHANNELDISEASES

Bezzina CR, Verkerk AO, Busjahn A, Jeron A, Erdmann J, Koopmann TT, Bhuiyan ZA, Wilders R, Mannens MM, Tan HL, Luft FC, Schunkert H, Wilde AA.

A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization.

Cardiovasc Res. 2003;59:27-36.

Smits JP, Koopmann TT, Wilders R, Veldkamp MW, Opthof T, Bhuiyan ZA, Mannens MM, Balser JR, Tan HL, Bezzina CR, Wilde AA (shared first authorship).

A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families.

J Mol Cell Cardiol. 2005;38:969-81.

Coronel R, Casini S, Koopmann TT, Wilms-Schopman FJ, Verkerk AO, de Groot JR, Bhuiyan Z, Bezzina CR, Veldkamp MW, Linnenbank AC, van der Wal AC, Tan HL, Brugada P, Wilde AA, de Bakker JM.

Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational study.

Circulation. 2005;112:2769-77.

Koopmann TT, Alders M, Jongbloed RJ, Guerrero S, Mannens MMAM, Wilde AAM, Bezzina CR. Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by the PCR-based exon-scanning methodologies employed to date.

Heart Rhythm. 2006;3(1):52-5.

Bezzina CR, Shimizu W, Yang P, Koopmann TT, Tanck MWT, Miyamoto Y, Kamakura S, Roden DM, Wilde AAM.

A common sodium channel promoter haplotype in Asian subjects underlies variability in cardiac conduction.

Circulation. 2006;113(3):338-44.

Koopmann TT, Bezzina CR, Wilde AAM.

Voltage-gated sodium channels: Action players with many faces.

Ann Med. 2006;38(7):472-82 (Review).

Koopmann TT, Beekman L, Alders M, Meregalli PG, Mannens MMAM, Moorman AFM, Wilde AAM, Bezzina CR.

Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada Syndrome cohort.

Heart Rhythm. 2007;4(6):752-5.

Yang P, Koopmann TT, Pfeufer A, Jalilzadeh S, Schulze-Bahr E, Kääb S, Wilde AAM, Roden DM, Bezzina CR.

Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activity.

Eur J Hum Genet. 2008;16(3):350-7.

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GENETICBASIS OFCARDIACIONCHANNELDISEASES

Watanabe H, Koopmann TT; Le Scouarnec S, Yang T, Ingram CR, Schott JJ, Demolombe S, Probst V, Anselme F, Escande D, Wiesfeld ACP, Pfeufer A, Kääb S, Wichmann H-E, Hasdemir C, Aizawa Y, Wilde AAM, Roden DM, Bezzina CR (shared first authorship).

Sodium channelβ1-subunit mutations associated with Brugada syndrome and cardiac conduc-tion disease.

J Clin Invest. In press.

Koopmann TT, Postema PG, Bezzina CR, Wilde AAM (shared first authorship). Biophysical properties of cardiac ion channels.

To be published as bookchapter in: Ion Channel Biophysics and Diseases (Research Signpost,