Article

Clinical genetics and outcome of left ventricular non-compaction cardiomyopathy.
Sedaghat-Hamedani, F., Haas, J., Zhu, F., Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Kayvanpour, E., Liss, M. ORCID: https://orcid.org/0000-0002-0585-7850, Lai, A., Frese, K., Pribe-Wolferts, R., Amr, A., Li, D.T., Samani, O.S., Carstensen, A., Bordalo, D.M., Müller, M., Fischer, C., Shao, J., Wang, J., Nie, M., Yuan, L., Haßfeld, S., Schwartz, C., Zhou, M., Zhou, Z., Shu, Y., Wang, M., Huang, K., Zeng, Q., Cheng, L., Fehlmann, T., Ehlermann, P., Keller, A., Dieterich, C. ORCID: https://orcid.org/0000-0001-9468-6311, Streckfuß-Bömeke, K., Liao, Y., Gotthardt, M. ORCID: https://orcid.org/0000-0003-1788-3172, Katus, H.A. and Meder, B.
European Heart Journal 38 (46): 3449-3460. 7 December 2017

199th ENMC international workshop: FHL1 related myopathies, June 7-9, 2013, Naarden, The Netherlands.
Bertrand, A.T., Boennemann, C.G. and Bonne, G.
Neuromuscular Disorders 24 (5): 453-462. May 2014

Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure.
Waldmueller, S., Erdmann, J., Binner, P., Gelbrich, G., Pankuweit, S., Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Timmermann, B., Haremza, J., Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X, Scheer, S., Wachter, R., Schulze-Waltrup, N., Dermintzoglou, A., Schoenberger, J., Zeh, W., Jurmann, B., Brodherr, T., Boergel, J., Farr, M., Milting, H., Blankenfeldt, W., Reinhardt, R., Oezcelik, C., Osterziel, K.J., Loeffler, M., Maisch, B., Regitz-Zagrosek, V., Schunkert, H. and Scheffold, T.
European Journal of Heart Failure 13 (11): 1185-1192. November 2011

Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation.
Knoblauch, H., Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Adams, S., Budde, B., Rudolph, A., Zacharias, U., Schulz-Menger, J. ORCID: https://orcid.org/0000-0003-3100-1092, Spuler, A., Yaou, R.B., Nuernberg, P., Voit, T., Bonne, G. and Spuler, S. ORCID: https://orcid.org/0000-0002-0155-1117
Annals of Neurology 67 (1): 136-140. January 2010

Connective tissue growth factor overexpression in cardiomyocytes promotes cardiac hypertrophy and protection against pressure overload.
Panek, A.N., Posch, M.G., Alenina, N. ORCID: https://orcid.org/0000-0002-6071-5433, Ghadge, S.K. ORCID: https://orcid.org/0000-0002-5541-5663, Erdmann, B., Popova, E. ORCID: https://orcid.org/0000-0002-3043-9650, Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X, Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Dietz, R., Morano, I. ORCID: https://orcid.org/0000-0001-7315-2222, Bader, M. ORCID: https://orcid.org/0000-0003-4780-4164 and Oezcelik, C.
PLoS ONE 4 (8): e6743. 25 August 2009

Genetic deletion of arginine 14 in phospholamban causes dilated cardiomyopathy with attenuated electrocardiographic R amplitudes.
Posch, M.G., Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X, Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Boldt, L.H., Schmidt, G., Lehmkuhl, H.B., Hetzer, R., Dietz, R., Gutberlet, M., Haverkamp, W. and Oezcelik, C.
Heart Rhythm 6 (4): 480-486. April 2009

Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.
Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Gehmlich, K. ORCID: https://orcid.org/0000-0003-4019-1844, Ehler, E., Hassfeld, S., Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X, Hayess, K., Cardim, N., Wenzel, K., Erdmann, B., Krackhardt, F., Posch, M.G., Bublak, A., Naegele, H., Scheffold, T., Dietz, R., Chien, K.R., Spuler, S. ORCID: https://orcid.org/0000-0002-0155-1117, Fuerst, D.O., Nuernberg, P. and Oezcelik, C.
Human Molecular Genetics 17 (18): 2753-2765. 15 September 2008

A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy.
Posch, M.G., Posch, M.J., Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Erdmann, B., Mueller, W., Richter, A., Ruppert, V., Pankuweit, S., Maisch, B., Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X, Buttgereit, J., Dietz, R., Haverkamp, W. and Oezcelik, C.
Molecular Genetics and Metabolism 95 (1-2): 74-80. September 2008

Sequence analysis of myozenin 2 in 438 European patients with familial hypertrophic cardiomyopathy.
Posch, M.G., Thiemann, L., Tomasov, P., Veselka, J., Cardim, N., Garcia-Castro, M., Coto, E., Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X, Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Dietz, R., Haverkamp, W. and Oezcelik, C.
Medical Science Monitor 14 (7): CR372-CR374. 1 July 2008

A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy.
Fokstuen, S., Lyle, R., Munoz, A., Gehrig, C., Lerch, R., Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X, Osterziel, K.J., Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Beghetti, M., Mach, F., Sztajzel, J., Sigwart, U., Antonarakis, S.E. and Blouin, J.L.
Human Mutation 29 (6): 879-885. June 2008

Mitochondrial transcription factors TFA, TFB1 and TFB2: A search for DNA variants/haplotypes and the risk of cardiac hypertrophy.
Alonso-Montes, C., Castro, M.G., Reguero, J.R., Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X, Oezcelik, C., Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Posch, M.G., Moris, C., Alvarez, V., Ruiz-Ortega, M. and Coto, E.
Disease Markers 25 (3): 131-139. 2008

Dysfunction of dysferlin-deficient hearts.
Wenzel, K., Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Qadri, F. ORCID: https://orcid.org/0000-0002-8500-489X, Huebner, N. ORCID: https://orcid.org/0000-0002-1218-6223, Schulz, H. ORCID: https://orcid.org/0000-0002-0226-964X, Erdmann, B., Gross, V., Bauer, D., Dechend, R. ORCID: https://orcid.org/0000-0001-6636-3080, Dietz, R., Osterziel, K.J., Spuler, S. ORCID: https://orcid.org/0000-0002-0155-1117 and Oezcelik, C.
Journal of Molecular Medicine 85 (11): 1203-1214. November 2007

Recurrent in-stent restenosis is not associated with the angiotensin-converting enzyme D/I, angiotensinogen Thr174Met and Met235Thr, and the angiotensin-II receptor 1 A1166C polymorphism.
Gross, C.M., Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X, Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Posch, M.G., Hassfeld, S., Kramer, J., Schmidt, S., Derer, W., Dietz, R. and Oezcelik, C.
Journal of Invasive Cardiology 19 (6): 261-264. 1 June 2007

Mutations in the EGF-CFC gene Cryptic are an infrequent cause of congenital heart disease.
Oezcelik, C., Bit-Avragim, N. ORCID: https://orcid.org/0000-0003-4606-1899, Panek, A., Gaio, U., Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Lange, P.E., Dietz, R., Posch, M.G., Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X and Stiller, B.
Pediatric Cardiology 27 (6): 695-698. December 2006

Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: Demand for strategies in the management of presymptomatic lamin A/C mutant carriers.
Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X, Sigusch, H.H., Naegele, H., Genschel, J., Lehmkuhl, H., Hetzer, R., Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Perez, L.V., Reinhard, D., Dietz, R., Osterziel, K.J. and Schmidt, H.H.
European Journal of Heart Failure 8 (5): 484-493. August 2006

Constitutive upregulations of titin-based signalling proteins in KY deficient muscles.
Beatham, J., Gehmlich, K. ORCID: https://orcid.org/0000-0003-4019-1844, van der Ven, P.F.M., Sarparanta, J., Williams, D., Underhill, P., Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Fuerst, D.O., Udd, B. and Blanco, G.
Neuromuscular Disorders 16 (7): 437-445. July 2006

Novel sequence variants in dysferlin-deficient muscular dystrophy leading to mRNA decay and possible C2-domain misfolding.
Wenzel, K., Carl, M., Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X, Zabojszcza, J. ORCID: https://orcid.org/0000-0001-8810-0492, Assadi, M., Ebeling, M., Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Robinson, P.N., Kress, W., Osterziel, K.J. and Spuler, S. ORCID: https://orcid.org/0000-0002-0155-1117
Human Mutation 27 : 599-600. June 2006

Familiaere dilatative Kardiomyopathie [Familial dilated cardiomyopathy].
Osterziel, K.J., Hassfeld, S., Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187 and Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X
Herz 30 : 529-534. 1 September 2005

Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy.
Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X, Ozcelik, C., Binner, P., Counsell, D., Hoffmann, K., Pilz, B., Martiniak, Y., Gehmlich, K. ORCID: https://orcid.org/0000-0003-4019-1844, van der Ven, P.F.M., Furst, D.O., Vornwald, A., von Hodenberg, E., Nuernberg, P., Scheffold, T., Dietz, R. and Osterziel, K.J.
Circulation 107 (10): 1390-1395. 18 March 2003

Distribution and transport of cholesterol in Caenorhabditis elegans.
Matyash, V., Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Henske, A., Mukherjee, S., Hirsh, D., Thiele, C., Grant, B., Maxfield, F.R. and Kurzchalia, T.V.
Molecular Biology of the Cell 12 (6): 1725-1736. June 2001

Review

Back to square one: what do we know about the functions of muscle LIM protein in the heart?
Gehmlich, K. ORCID: https://orcid.org/0000-0003-4019-1844, Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Milting, H., Fuerst, D. and Ehler, E.
Journal of Muscle Research and Cell Motility 29 (6-8): 155-158. December 2008

Der ploetzliche Herztod bei familiaerer hypertropher Kardiomyopathie. Identifizierung von Hochrisikopatienten [Sudden cardiac death in familial hypertrophic cardiomyopathy. Identification of high-risk patients].
Pellnitz, C., Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X, Dietz, R., Osterziel, K.J. and Haverkamp, W.
Deutsche Medizinische Wochenschrift 130 : 1150-1154. 1 January 2005

Kardiale Manifestationen bei Muskeldystrophien [Cardiac manifestations of muscular dystrophies].
Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X, Spuler, S. ORCID: https://orcid.org/0000-0002-0155-1117, Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Dietz, R. and Osterziel, K.J.
Zeitschrift fuer Kardiologie 94 : 312-320. 1 January 2005

Letter

Guiding the molecular diagnosis of hypertrophic cardiomyopathy.
Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Schulze-Bahr, E. and Bonne, G.
Journal of Thoracic and Cardiovascular Surgery 143 (5): 1234. May 2012

Plasma HER2 levels are not associated with cardiac function or hypertrophy in control subjects and heart failure patients.
Posch, M.G., Panek, A., Kersten, A., Ghadge, S.K. ORCID: https://orcid.org/0000-0002-5541-5663, Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Richter, S., Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X, Gailani, M., Dietz, R., Lueftner, D. and Oezcelik, C.
International Journal of Cardiology 145 (1): 105-106. 5 November 2010

"MLP: A Stress Sensor Goes Nuclear" By Sylvia Gunkel, Joerg Heineke, Denise Hilfiker-Kleiner, Ralph Knoell, J Mol Cell Cardiol. 2009;47(4):423-5.
Gehmlich, K. ORCID: https://orcid.org/0000-0003-4019-1844, Ehler, E., Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X, Fuerst, D.O. and Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187
Journal of Molecular and Cellular Cardiology 48 (2): 424-425. February 2010

Hypertrophic cardiomyopathy - a matter of genes.
Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Elgeti, T. and Ozcelik, C.
Canadian Journal of Anaesthesia 55 (5): 309-311. May 2008

Subacute coronary stent thrombosis in cancer patients.
Gross, C.M., Posch, M.G., Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Olthoff, H., Kraemer, J., Dechend, R. ORCID: https://orcid.org/0000-0001-6636-3080, Dietz, R. and Oezcelik, C.
Journal of the American College of Cardiology 51 (12): 1232-1233. 25 March 2008

Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects.
Posch, M.G., Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X, Schmitt, K., Mittelhaus, S., Esenwein, E.M., Stiller, B., Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Dietz, R., Gessner, R., Oezcelik, C. and Berger, F.
American Journal of Medical Genetics A 146 (2): 251-253. 15 January 2008

Letter by Geier et al regarding article, "Hypertrophic cardiomyopathy is predominantly a disease of left ventricular outflow tract obstruction".
Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Perrot, A. ORCID: https://orcid.org/0000-0002-8800-342X and Oezcelik, C.
Circulation 115 (23): e622. 12 June 2007

Insulin-like growth factor-binding proteins 2 and 3 are independent predictors of a poor prognosis in patients with dilated cardiomyopathy.
Hassfeld, S., Eichhorn, C., Stehr, K., Naegele, H., Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Steeg, M., Ranke, M.B., Oezcelik, C. and Osterziel, K.J.
Heart 93 (3): 359-360. 1 March 2007

A new LMNA mutation causing limb girdle muscular dystrophy 1B.
Spuler, S. ORCID: https://orcid.org/0000-0002-0155-1117, Geier, C. ORCID: https://orcid.org/0000-0001-5281-8187, Osterziel, K.J., Gutberlet, M., Genschel, J., Lehmann, T.N., Zinn-Justin, S., Gilquin, B. and Schmidt, H.
Journal of Neurology 252 (5): 621-623. May 2005