C. Özcelik

2.0k citations

27 papers · 1.4k indexed · h-index 16

Impact in

Cardiology and Cardiovascular Medicine top 2%
- Cardiomyopathy and Myosin Studies
- Cardiovascular Effects of Exercise
- Chemotherapy-induced cardiotoxicity and mitigation
- Cardiac electrophysiology and arrhythmias
Molecular Biology top 10%
- Congenital heart defects research
- Muscle Physiology and Disorders

Papers in ⓘ

Cardiology and Cardiovascular Medicine 17
- Cardiomyopathy and Myosin Studies 13
- Cardiovascular Effects of Exercise 6
- Viral Infections and Immunology Research 3
Epidemiology 8
- Congenital Heart Disease Studies 5

Co-authors: Andreas Perrot (18 shared papers)Bettina Erdmann (5 shared papers)Carmen Birchmeier (2 shared papers)Stefan Britsch (2 shared papers)Alistair N. Garratt (2 shared papers)Bernhard Pilz (2 shared papers)Maximilian Posch (13 shared papers)Kenneth R. Chien (2 shared papers)
Journals: PLoS ONE (3 papers)Current Biology (1 paper)Molecular Genetics and Metabolism (1 paper)Human Molecular Genetics (1 paper)European Journal of Human Genetics (1 paper)
Partner nations: Germany Portugal Spain

In The Last Decade

C. Özcelik

27 papers receiving 1.4k citations

Peers

Countries citing papers authored by C. Özcelik

Since Specialization

Citations

This map shows the geographic impact of C. Özcelik'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 C. Özcelik with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C. Özcelik more than expected).

Fields of papers citing papers by C. Özcelik

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C. Özcelik. 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 C. Özcelik. The network helps show where C. Özcelik may publish in the future.

Co-authors

The 25 scholars most cited alongside C. Özcelik, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with C. Özcelik Line = papers co-authored together C. Özcelik links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 27 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Conditional mutation of the ErbB2 (HER2) receptor in cardiomyocytes leads to dilated cardiomyopathy Proceedings of the National Academy of Sciences ·C. Özcelik, Bettina Erdmann, Bernhard Pilz, Nina Wettschureck, Stefan Britsch, Norbert Hübner, Kenneth R. Chien, Carmen Birchmeier, Alistair N. Garratt	2002	371
2	Mutations in the Human Muscle LIM Protein Gene in Families With Hypertrophic Cardiomyopathy Circulation ·Christian Geier, Andreas Perrot, C. Özcelik, Priska Binner, Damian Counsell, Katrin Hoffmann, Bernhard Pilz, Yvonne Martiniak, Katja Gehmlich, Peter F. M. van der Ven, Dieter O. Fürst, A. Vornwald, Eberhard von Hodenberg, Peter Nürnberg, Thomas Scheffold, Rainer Dietz, Karl Josef Osterziel	2003	163
3	Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy Human Molecular Genetics ·Christian Geier, Katja Gehmlich, Elisabeth Ehler, Sabine Haßfeld, Andreas Perrot, Katrin Hayeß, Nuno Cardim, Katrin Wenzel, Bettina Erdmann, Florian Krackhardt, Maximilian Posch, Angelika Bublak, Herbert Nägele, Thomas Scheffold, Rainer Dietz, Kenneth R. Chien, Simone Spuler, Dieter O. Fürst, Peter Nürnberg, C. Özcelik	2008	118
4	A role of the cryptic gene in the correct establishment of the left–right axis Current Biology ·Ursula Gaio, Axel Schweickert, Anja Fischer, Alistair N. Garratt, Thomas Müller, C. Özcelik, Wolfgang Lankes, Michael Strehle, Stefan Britsch, Martin Blum, Carmen Birchmeier	1999	105
5	A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects Journal of Medical Genetics ·Maximilian Posch, Michael Gramlich, Margaret Sunde, Katharina Schmitt, S. H. Y. Lee, Silke Richter, A.H. Kersten, Andreas Perrot, A. Panek, Iman Al Khatib, Georges Nemer, André Mégarbané, Rainer Dietz, Brigitte Stiller, Felix Berger, Richard P. Harvey, C. Özcelik	2009	98
6	Cardiac Alpha-Myosin (MYH6) Is the Predominant Sarcomeric Disease Gene for Familial Atrial Septal Defects PLoS ONE ·Maximilian Posch, Stephan Waldmüller, Melanie Müller, Thomas Scheffold, David Fournier, Miguel A. Andrade‐Navarro, B. De Geeter, Sophie Guillaumont, Claire Dauphin, Dany Yousseff, Katharina Schmitt, Andreas Perrot, Felix Berger, Roland Hetzer, Patrice Bouvagnet, C. Özcelik	2011	69
7	Dysfunction of dysferlin-deficient hearts Journal of Molecular Medicine ·Katrin Wenzel, Christian Geier, Fatimunnisa Qadri, Norbert Hübner, Herbert Schulz, Bettina Erdmann, Volkmar Groß, David Bauer, Ralf Dechend, Rainer Dietz, Karl Josef Osterziel, Simone Spuler, C. Özcelik	2007	68
8	Genetic deletion of arginine 14 in phospholamban causes dilated cardiomyopathy with attenuated electrocardiographic R amplitudes Heart Rhythm ·Maximilian Posch, Andreas Perrot, Christian Geier, Leif‐Hendrik Boldt, G. Schmidt, H. Lehmkuhl, Roland Hetzer, Rainer Dietz, Matthias Gutberlet, Wilhelm Haverkamp, C. Özcelik	2009	64
9	Molecular genetics of congenital atrial septal defects Clinical Research in Cardiology ·Maximilian Posch, Andreas Perrot, Felix Berger, C. Özcelik	2009	52
10	Mutations in the cardiac transcription factor GATA4 in patients with lone atrial fibrillation European Journal of Medical Genetics ·Maximilian Posch, Leif‐Hendrik Boldt, M. Polotzki, Silke Richter, Sascha Rolf, Andreas Perrot, Rainer Dietz, C. Özcelik, Wilhelm Haverkamp	2010	50
11	A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy Molecular Genetics and Metabolism ·Maximilian Posch, (unknown), (unknown), Christian Geier, Bettina Erdmann, Wolf Mueller, Anette Richter, Volker Ruppert, Sabine Pankuweit, Bernhard Maisch, Andreas Perrot, Jens Buttgereit, Rainer Dietz, Wilhelm Haverkamp, C. Özcelik	2008	46
12	A Matter of the Heart: Myocardial Metastases in Neuroendocrine Tumors Hormone and Metabolic Research ·Henning Jann, T. Wertenbruch, Ulrich F. Pape, C. Özcelik, Timm Denecke, Sydney J. Mehl, Bertram Wiedenmann, Marianne Pavel	2010	40
13	A myomesin mutation associated with hypertrophic cardiomyopathy deteriorates dimerisation properties Biochemical and Biophysical Research Communications ·Romy Siegert, Andreas Perrot, Sandro Keller, Joachim Behlke, Aleksandra Michalewska‐Włudarczyk, Anna Wycisk, Michał Tendera, Ingo Morano, C. Özcelik	2011	34
14	Mutations in NEBL encoding the cardiac Z-disk protein nebulette are associated with various cardiomyopathies Archives of Medical Science ·Andreas Perrot, Pavol Tomašov, Eric Villard, Réka Faludi, Paola Melacini, Janine Lossie, Nadine Lohmann, Pascale Richard, Marzia De Bortoli, Annalisa Angelini, Ákos Varga‐Szemes, Silke Sperling, Tamás Símor, Josef Veselka, C. Özcelik, Philippe Charron	2016	25
15	Evidence for CTLA4 as a susceptibility gene for dilated cardiomyopathy European Journal of Human Genetics ·(unknown), Volker Ruppert, Thomas Meyer, Clarissa Struwe, Jana Petersen, Andreas Perrot, Maximilian Posch, C. Özcelik, Anette Richter, Bernhard Maisch, Sabine Pankuweit	2010	18
16	Correction: Connective Tissue Growth Factor Overexpression in Cardiomyocytes Promotes Cardiac Hypertrophy and Protection against Pressure Overload PLoS ONE ·A. Panek, Maximilian Posch, Natália Alenina, Santhosh Kumar Ghadge, Bettina Erdmann, E. Popova, Andreas Perrot, Christian Geier, Rainer Dietz, Ingo Morano, Michael Bäder, C. Özcelik	2009	15
17	The G-231A Polymorphism in the Endothelin-A Receptor Gene Is Associated With Lower Aortic Pressure in Patients With Dilated Cardiomyopathy American Journal of Hypertension ·Ralph Telgmann, Bassam A. Harb, C. Özcelik, Andreas Perrot, Jacqueline Schönfelder, A Nonnenmacher, Marcus Brand, Klaus Schmidt‐Petersen, Rainer Dietz, Reinhold Kreutz	2006	13
18	Mutations in the EGF-CFC Gene Cryptic Are an Infrequent Cause of Congenital Heart Disease Pediatric Cardiology ·C. Özcelik, Nana Bit‐Avragim, A. Panek, Ursula Gaio, Christian Geier, Peter Lange, Rainer Dietz, Maximilian Posch, Andreas Perrot, Brigitte Stiller	2006	13
19	CCN1 Mutation is Associated with Atrial Septal Defect Pediatric Cardiology ·Andreas Perrot, Katharina Schmitt, Eva-Maria G. Roth, Brigitte Stiller, Maximilian Posch, Edmund Browne, Christian Timmann, Rolf D. Horstmann, Felix Berger, C. Özcelik	2014	13
20	Angiotensin-converting enzyme inhibition, autonomic activity, and hemodynamics in patients with heart failure who perform isometric exercise American Heart Journal ·Roland Willenbrock, C. Özcelik, K. J. Osterziel, Rainer Dietz	1996	8

About C. Özcelik

C. Özcelik is a scholar working on Cardiology and Cardiovascular Medicine, Epidemiology, Molecular Biology, Pulmonary and Respiratory Medicine and Neurology, having authored 27 papers that have together received 1.4k indexed citations. Recurring topics across this work include Cardiomyopathy and Myosin Studies (13 papers), Congenital heart defects research (8 papers), Cardiovascular Effects of Exercise (6 papers), Congenital Heart Disease Studies (5 papers), Tracheal and airway disorders (3 papers), Viral Infections and Immunology Research (3 papers), Connective tissue disorders research (2 papers) and Connective Tissue Growth Factor Research (2 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (793 citations), Molecular Biology (799 citations), Oncology (292 citations), Epidemiology (265 citations) and Aging (9 citations). C. Özcelik has collaborated with scholars based in Germany, Portugal and Spain. Frequent co-authors include Andreas Perrot, Bettina Erdmann, Carmen Birchmeier, Stefan Britsch, Alistair N. Garratt, Bernhard Pilz, Maximilian Posch, Kenneth R. Chien, Norbert Hübner and Rainer Dietz. Their work appears in journals such as PLoS ONE, Current Biology, Molecular Genetics and Metabolism, Human Molecular Genetics and European Journal of Human Genetics.

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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