2015

ZBTB17 (MIZ1) is important for the cardiac stress response and a novel candidate gene for cardiomyopathy and heart failure.
Buyandelger, B., Mansfield, C., Kostin, S., Choi, O., Roberts, A.M., Ware, J.S., Mazzarotto, F., Pesce, F., Buchan, R., Isaacson, R.L., Vouffo, J., Gunkel, S., Knoell, G., McSweeney, S.J., Wei, H., Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X, Pfeiffer, C., Toliat, M.R., Ilieva, K., Krysztofinska, E., López-Olañeta, M.M., Gómez-Salinero, J.M., Schmidt, A., Ng, K.E., Teucher, N., Chen, J., Teichmann, M., Eilers, M., Haverkamp, W., Regitz-Zagrosek, V., Hasenfuss, G., Braun, T., Pennell, D.J., Gould, I., Barton, P.J.R., Lara-Pezzi, E., Schäfer, S., Hübner, N. ORCID: https://orcid.org/0000-0002-1218-6223, Felkin, L.E., O'Regan, D.P., Petretto, E., Brand, T., Milting, H., Nürnberg, P., Schneider, M.D., Prasad, S. and Knöll, R.
Circulation Cardiovascular Genetics 8 (5): 643-652. October 2015

Malformations of the left ventricle: what comes first: form or function?
Klaassen, S. ORCID: https://orcid.org/0000-0001-5925-9912
Circulation Cardiovascular Genetics 8 (4): 537-540. August 2015

2013

Homozygous founder mutation in desmocollin-2 (DSC2) causes arrhythmogenic cardiomyopathy in the Hutterite population.
Gerull, B. ORCID: https://orcid.org/0000-0002-1363-8826, Kirchner, F., Chong, J.X., Tagoe, J., Chandrasekharan, K., Strohm, O., Waggoner, D., Ober, C. and Duff, H.J.
Circulation Cardiovascular Genetics 6 (4): 327-336. August 2013

2012

Molecular insights into arrhythmogenic right ventricular cardiomyopathy caused by plakophilin-2 missense mutations.
Kirchner, F., Schuetz, A. ORCID: https://orcid.org/0000-0002-0606-2574, Boldt, L.H., Martens, K., Dittmar, G. ORCID: https://orcid.org/0000-0003-3647-8623, Haverkamp, W., Thierfelder, L., Heinemann, U. ORCID: https://orcid.org/0000-0002-8191-3850 and Gerull, B. ORCID: https://orcid.org/0000-0002-1363-8826
Circulation Cardiovascular Genetics 5 (4): 400-411. 1 August 2012

2011

Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype.
Probst, S., Oechslin, E., Schuler, P., Greutmann, M., Boye, P., Knirsch, W., Berger, F., Thierfelder, L., Jenni, R. and Klaassen, S. ORCID: https://orcid.org/0000-0001-5925-9912
Circulation Cardiovascular Genetics 4 (4): 367-374. 1 August 2011

Mutations in the sarcomere protein gene MYH7 in Ebstein's anomaly.
Postma, A.V., van Engelen, K., van de Meerakker, J., Rahman, T., Probst, S., Baars, M.J., Bauer, U., Pickardt, T., Sperling, S.R. ORCID: https://orcid.org/0000-0002-7135-3298, Berger, F., Moorman, A.F., Mulder, B.J., Thierfelder, L., Keavney, B., Goodship, J. and Klaassen, S. ORCID: https://orcid.org/0000-0001-5925-9912
Circulation Cardiovascular Genetics 4 (1): 43-50. February 2011

2009

Association of AHSG gene polymorphisms with fetuin-A plasma levels and cardiovascular diseases in the EPIC-Potsdam study.
Fisher, E., Stefan, N., Saar, K., Drogan, D., Schulze, M.B., Fritsche, A., Joost, H.G., Haering, H.U., Huebner, N. ORCID: https://orcid.org/0000-0002-1218-6223, Boeing, H. and Weikert, C.
Circulation Cardiovascular Genetics 2 (6): 607-613. December 2009