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Article

ZBTB17 (MIZ1) is important for the cardiac stress response and a novel candidate gene for cardiomyopathy and heart failure.
Buyandelger, B. and Mansfield, C. and Kostin, S. and Choi, O. and Roberts, A.M. and Ware, J.S. and Mazzarotto, F. and Pesce, F. and Buchan, R. and Isaacson, R.L. and Vouffo, J. and Gunkel, S. and Knoell, G. and McSweeney, S.J. and Wei, H. and Perrot, A. and Pfeiffer, C. and Toliat, M.R. and Ilieva, K. and Krysztofinska, E. and López-Olañeta, M.M. and Gómez-Salinero, J.M. and Schmidt, A. and Ng, K.E. and Teucher, N. and Chen, J. and Teichmann, M. and Eilers, M. and Haverkamp, W. and Regitz-Zagrosek, V. and Hasenfuss, G. and Braun, T. and Pennell, D.J. and Gould, I. and Barton, P.J.R. and Lara-Pezzi, E. and Schäfer, S. and Hübner, N. and Felkin, L.E. and O'Regan, D.P. and Petretto, E. and Brand, T. and Milting, H. and Nürnberg, P. and Schneider, M.D. and Prasad, S. and Knöll, R.
Circulation Cardiovascular Genetics 8 (5): 643-652. October 2015

Homozygous founder mutation in desmocollin-2 (DSC2) causes arrhythmogenic cardiomyopathy in the Hutterite population.
Gerull, B. and Kirchner, F. and Chong, J.X. and Tagoe, J. and Chandrasekharan, K. and Strohm, O. and Waggoner, D. and Ober, C. and Duff, H.J.
Circulation Cardiovascular Genetics 6 (4): 327-336. August 2013

Molecular insights into arrhythmogenic right ventricular cardiomyopathy caused by plakophilin-2 missense mutations.
Kirchner, F. and Schuetz, A. and Boldt, L.H. and Martens, K. and Dittmar, G. and Haverkamp, W. and Thierfelder, L. and Heinemann, U. and Gerull, B.
Circulation Cardiovascular Genetics 5 (4): 400-411. 1 August 2012

Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype.
Probst, S. and Oechslin, E. and Schuler, P. and Greutmann, M. and Boye, P. and Knirsch, W. and Berger, F. and Thierfelder, L. and Jenni, R. and Klaassen, S.
Circulation Cardiovascular Genetics 4 (4): 367-374. 1 August 2011

Mutations in the sarcomere protein gene MYH7 in Ebstein's anomaly.
Postma, A.V. and van Engelen, K. and van de Meerakker, J. and Rahman, T. and Probst, S. and Baars, M.J. and Bauer, U. and Pickardt, T. and Sperling, S.R. and Berger, F. and Moorman, A.F. and Mulder, B.J. and Thierfelder, L. and Keavney, B. and Goodship, J. and Klaassen, S.
Circulation Cardiovascular Genetics 4 (1): 43-50. February 2011

Association of AHSG gene polymorphisms with fetuin-A plasma levels and cardiovascular diseases in the EPIC-Potsdam study.
Fisher, E. and Stefan, N. and Saar, K. and Drogan, D. and Schulze, M.B. and Fritsche, A. and Joost, H.G. and Haering, H.U. and Huebner, N. and Boeing, H. and Weikert, C.
Circulation Cardiovascular Genetics 2 (6): 607-613. December 2009

Editorial

Malformations of the left ventricle: what comes first: form or function?
Klaassen, S.
Circulation Cardiovascular Genetics 8 (4): 537-540. August 2015