C. Özcelik - Concepedia

Author

C. Özcelik

Also Known As

C OZCELIK, C Özcelik, C. Ozcelik, C. Özcelik, Cemil Ozcelik, Cemil Özcelik, Cemil Özcelik, Maximilian G Posch, Rainer Dietz, Özcelik Cemil

Publications

1.9K

Citations

H-Index

Concepts

All Affiliations

Charité - Universitätsmedizin Berlin Max Delbrück Center Deutsches Herzzentrum der Charité Deutsches Herzzentrum München Berlin Heart (Germany)

CÖ

About

C. Özcelik is an author at Charité - Universitätsmedizin Berlin specializing in medicine, cardiology, and cardiovascular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	552
2	Molecular Genetics	3	3	266
3	Pathology	3	3	133
4	Molecular Biology	2	2	106
5	Natural Sciences	1	1	65

C. Özcelik

Publications

1.5K

Citations

H-Index

Page 1

	Year	Citations
Conditional mutation of the ErbB2 (HER2) receptor in cardiomyocytes leads to dilated cardiomyopathy C. Özcelik, Bettina Erdmann, Bernhard Pilz, Proceedings of the National Academy of Sciences	2002	469
Mutations in the Human Muscle LIM Protein Gene in Families With Hypertrophic Cardiomyopathy Christian Geier, Andreas Perrot, C. Özcelik, Circulation	2003	249
A role of the cryptic gene in the correct establishment of the left–right axis Ursula Gaio, Axel Schweickert, Anja Fischer, Current Biology Developmental BiologyDevelopmental GeneticsGeneticsGene StructureGenetic Mechanism	1999	133
A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects Maximilian Posch, Michael Gramlich, Margaret Sunde, Journal of Medical Genetics	2009	131
Cardiac Alpha-Myosin (MYH6) Is the Predominant Sarcomeric Disease Gene for Familial Atrial Septal Defects Maximilian Posch, Stephan Waldmüller, Melanie Müller, PLoS ONE Cardiac MuscleCardiomyopathyHeart FailureMedicineGenetics	2011	92
Genetic deletion of arginine 14 in phospholamban causes dilated cardiomyopathy with attenuated electrocardiographic R amplitudes Maximilian Posch, Andreas Perrot, Christian Geier, Heart Rhythm Cardiac MuscleCardiomyopathyHeart FailureArginine 14Cardiovascular Disease	2009	90
Dysfunction of dysferlin-deficient hearts Katrin Wenzel, Christian Geier, Fatimunnisa Qadri, Journal of Molecular Medicine CardiomyopathyHeart FailureStructural Heart DiseaseCardiovascular DiseasePhysiology	2007	90
Mutations in the cardiac transcription factor GATA4 in patients with lone atrial fibrillation Maximilian Posch, Leif‐Hendrik Boldt, M. Polotzki, European Journal of Medical Genetics CardiomyopathyNatural SciencesGeneticsMolecular BiologyLone Atrial Fibrillation	2010	65
A Matter of the Heart: Myocardial Metastases in Neuroendocrine Tumors Henning Jann, T. Wertenbruch, Ulrich F. Pape, Hormone and Metabolic Research	2010	50
A myomesin mutation associated with hypertrophic cardiomyopathy deteriorates dimerisation properties Romy Siegert, Andreas Perrot, Sandro Keller, Biochemical and Biophysical Research Communications Cardiac MuscleCardiomyopathyMendelian DisorderGeneticsMolecular Biology	2011	41

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