C. Özcelik

2.0k total citations
27 papers, 1.4k citations indexed

About

C. Özcelik is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Epidemiology. According to data from OpenAlex, C. Özcelik has authored 27 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Cardiology and Cardiovascular Medicine, 13 papers in Molecular Biology and 8 papers in Epidemiology. Recurrent topics in C. Özcelik's work include Cardiomyopathy and Myosin Studies (13 papers), Congenital heart defects research (8 papers) and Cardiovascular Effects of Exercise (6 papers). C. Özcelik is often cited by papers focused on Cardiomyopathy and Myosin Studies (13 papers), Congenital heart defects research (8 papers) and Cardiovascular Effects of Exercise (6 papers). C. Özcelik collaborates with scholars based in Germany, Portugal and Spain. C. Özcelik's co-authors include Andreas Perrot, Bettina Erdmann, Bernhard Pilz, Alistair N. Garratt, Stefan Britsch, Carmen Birchmeier, Maximilian Posch, Kenneth R. Chien, Norbert Hübner and Rainer Dietz and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Circulation and PLoS ONE.

In The Last Decade

C. Özcelik

27 papers receiving 1.4k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
C. Özcelik Germany 16 799 793 292 265 142 27 1.4k
Milena B. Furtado Australia 20 973 1.2× 504 0.6× 134 0.5× 186 0.7× 97 0.7× 30 1.4k
Giulia Mearini Germany 23 943 1.2× 1.1k 1.4× 95 0.3× 193 0.7× 24 0.2× 39 1.6k
Heesuk Zang United States 8 649 0.8× 155 0.2× 159 0.5× 93 0.4× 64 0.5× 8 934
Wolfgang M. Franz Germany 18 855 1.1× 840 1.1× 38 0.1× 59 0.2× 54 0.4× 34 1.4k
Yonghao Gui China 19 609 0.8× 143 0.2× 47 0.2× 116 0.4× 59 0.4× 43 924
Salma M. Wakil Saudi Arabia 19 517 0.6× 135 0.2× 61 0.2× 293 1.1× 60 0.4× 67 1.2k
Jeffrey D. Gamez United States 13 848 1.1× 50 0.1× 265 0.9× 120 0.5× 81 0.6× 22 1.2k
Danielle E.W. Clout Netherlands 10 1.2k 1.5× 567 0.7× 24 0.1× 207 0.8× 70 0.5× 13 1.4k
Katja Gehmlich United Kingdom 22 732 0.9× 1.1k 1.4× 44 0.2× 89 0.3× 20 0.1× 55 1.5k
James M. Dunn Canada 14 749 0.9× 93 0.1× 470 1.6× 57 0.2× 94 0.7× 29 1.3k

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-authorship network of co-authors of C. Özcelik

This figure shows the co-authorship network connecting the top 25 collaborators of C. Özcelik. A scholar is included among the top collaborators of C. Özcelik based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with C. Özcelik. C. Özcelik is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Perrot, Andreas, et al.. (2020). Identification of a novel titin-cap/telethonin mutation in a Portuguese family with hypertrophic cardiomyopathy. Revista Portuguesa de Cardiologia. 39(6). 317–327. 5 indexed citations
2.
Perrot, Andreas, Pavol Tomašov, Eric Villard, et al.. (2016). Mutations in NEBL encoding the cardiac Z-disk protein nebulette are associated with various cardiomyopathies. Archives of Medical Science. 2(2). 263–278. 25 indexed citations
3.
Montag, Judith, Imke Schulte, Francisco Navarro‐López, et al.. (2012). MYH7-Mutation Associated Allelic Imbalance in Familial Hypertrophic Cardiomyopathy: Molecular Mechanisms and Correlation with Disease Prognosis. Biophysical Journal. 102(3). 613a–613a. 1 indexed citations
4.
Marjaneh, Mahdi Moradi, Edwin P. Kirk, Maximilian Posch, et al.. (2011). Investigation of Association between PFO Complicated by Cryptogenic Stroke and a Common Variant of the Cardiac Transcription Factor GATA4. PLoS ONE. 6(6). e20711–e20711. 4 indexed citations
5.
Posch, Maximilian, Stephan Waldmüller, Melanie Müller, et al.. (2011). Cardiac Alpha-Myosin (MYH6) Is the Predominant Sarcomeric Disease Gene for Familial Atrial Septal Defects. PLoS ONE. 6(12). e28872–e28872. 69 indexed citations
6.
Perrot, Andreas, Sandro Keller, Joachim Behlke, et al.. (2011). A myomesin mutation associated with hypertrophic cardiomyopathy deteriorates dimerisation properties. Biochemical and Biophysical Research Communications. 405(3). 473–479. 34 indexed citations
7.
Posch, Maximilian, Leif‐Hendrik Boldt, Silke Richter, et al.. (2010). Mutations in the cardiac transcription factor GATA4 in patients with lone atrial fibrillation. European Journal of Medical Genetics. 53(4). 201–203. 50 indexed citations
8.
Ruppert, Volker, Thomas Meyer, Andreas Perrot, et al.. (2010). Evidence for CTLA4 as a susceptibility gene for dilated cardiomyopathy. European Journal of Human Genetics. 18(6). 694–699. 18 indexed citations
9.
Jann, Henning, Ulrich F. Pape, C. Özcelik, et al.. (2010). A Matter of the Heart: Myocardial Metastases in Neuroendocrine Tumors. Hormone and Metabolic Research. 42(13). 967–976. 40 indexed citations
10.
Panek, A., Maximilian Posch, Natália Alenina, et al.. (2009). Correction: Connective Tissue Growth Factor Overexpression in Cardiomyocytes Promotes Cardiac Hypertrophy and Protection against Pressure Overload. PLoS ONE. 4(9). 15 indexed citations
11.
Posch, Maximilian, Andreas Perrot, Felix Berger, & C. Özcelik. (2009). Molecular genetics of congenital atrial septal defects. Clinical Research in Cardiology. 99(3). 137–147. 52 indexed citations
12.
Posch, Maximilian, Michael Gramlich, Margaret Sunde, et al.. (2009). A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects. Journal of Medical Genetics. 47(4). 230–235. 98 indexed citations
13.
Posch, Maximilian, Andreas Perrot, Christian Geier, et al.. (2009). Genetic deletion of arginine 14 in phospholamban causes dilated cardiomyopathy with attenuated electrocardiographic R amplitudes. Heart Rhythm. 6(4). 480–486. 64 indexed citations
14.
Geier, Christian, Katja Gehmlich, Elisabeth Ehler, et al.. (2008). Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy. Human Molecular Genetics. 17(18). 2753–2765. 118 indexed citations
15.
Posch, Maximilian, Christian Geier, Bettina Erdmann, et al.. (2008). A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy. Molecular Genetics and Metabolism. 95(1-2). 74–80. 46 indexed citations
16.
Wenzel, Katrin, Christian Geier, Fatimunnisa Qadri, et al.. (2007). Dysfunction of dysferlin-deficient hearts. Journal of Molecular Medicine. 85(11). 1203–1214. 68 indexed citations
17.
Telgmann, Ralph, C. Özcelik, Andreas Perrot, et al.. (2006). 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. 20(1). 32–37. 13 indexed citations
18.
Özcelik, C., Nana Bit‐Avragim, A. Panek, et al.. (2006). Mutations in the EGF-CFC Gene Cryptic Are an Infrequent Cause of Congenital Heart Disease. Pediatric Cardiology. 27(6). 695–698. 13 indexed citations
19.
Geier, Christian, Andreas Perrot, C. Özcelik, et al.. (2003). Mutations in the Human Muscle LIM Protein Gene in Families With Hypertrophic Cardiomyopathy. Circulation. 107(10). 1390–1395. 163 indexed citations
20.
Schweickert, Axel, Anja Fischer, Alistair N. Garratt, et al.. (1999). A role of the cryptic gene in the correct establishment of the left–right axis. Current Biology. 9(22). 1339–1342. 105 indexed citations

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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