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Andreas Perrot

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Snigdha Tripathi; Edgar Becker; B Borchert; Bernhard Brenner; Antonio Francino; William J McKenna; Judith Montag; Francisco Navarro-Lopez; Karl Josef Osterziel; Cemil Özcelik; Andreas Perrot; Imke Schultz; Theresia Kraft
Unequal allelic expression of wild-type and mutated β-myosin in familial hypertrophic cardiomyopathy.
Stephan Waldmüller; Wolfgang Zeh; Priska Binner; Wulf Blankenfeldt; Jan Börgel; Turgut Brodherr; Anastassia Dermintzoglou; Jeanette Erdmann; Martin Farr; Christian Geier; Götz Gelbrich; Janine Haremza; Beate Jurmann; Markus Loeffler; Bernhard Maisch; Hendrik Milting; Karl Josef Osterziel; Cemil Özcelik; Sabine Pankuweit; Andreas Perrot; Vera Regitz-Zagrosek; Richard Reinhardt; Steffen Scheer; Thomas Scheffold; Jost Schönberger; Norbert Schulze-Waltrup; Heribert Schunkert; Bernd Timmermann; Rolf Wachter
Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure.
Romy Siegert; Andreas Perrot; Sandro Keller; Joachim Behlke; Aleksandra Michalewska-Włudarczyk; Anna Wycisk; Michal Tendera; Ingo Morano; Cemil Ozcelik
A myomesin mutation associated with hypertrophic cardiomyopathy deteriorates dimerisation properties.

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All Publications

2011: Snigdha Tripathi; Edgar Becker; B Borchert; Bernhard Brenner; Antonio Francino; William J McKenna; Judith Montag; Francisco Navarro-Lopez; Karl Josef Osterziel; Cemil Özcelik; Andreas Perrot; Imke Schultz; Theresia Kraft
Unequal allelic expression of wild-type and mutated β-myosin in familial hypertrophic cardiomyopathy.
Basic research in cardiology 2011;106(6):1041-55.
2011: Stephan Waldmüller; Wolfgang Zeh; Priska Binner; Wulf Blankenfeldt; Jan Börgel; Turgut Brodherr; Anastassia Dermintzoglou; Jeanette Erdmann; Martin Farr; Christian Geier; Götz Gelbrich; Janine Haremza; Beate Jurmann; Markus Loeffler; Bernhard Maisch; Hendrik Milting; Karl Josef Osterziel; Cemil Özcelik; Sabine Pankuweit; Andreas Perrot; Vera Regitz-Zagrosek; Richard Reinhardt; Steffen Scheer; Thomas Scheffold; Jost Schönberger; Norbert Schulze-Waltrup; Heribert Schunkert; Bernd Timmermann; Rolf Wachter
Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure.
European journal of heart failure 2011;13(11):1185-92.
2011: Romy Siegert; Andreas Perrot; Sandro Keller; Joachim Behlke; Aleksandra Michalewska-Włudarczyk; Anna Wycisk; Michal Tendera; Ingo Morano; Cemil Ozcelik
A myomesin mutation associated with hypertrophic cardiomyopathy deteriorates dimerisation properties.
Biochemical and biophysical research communications 2011;405(3):473-9.
2010: Leif-Hendrik Boldt; Maximilian Posch; Andreas Perrot; Michael Polotzki; Sascha Rolf; Abdul S Parwani; Martin Huemer; Alexander Wutzler; Cemil Ozcelik; Wilhelm Haverkamp
Mutational analysis of the PITX2 and NKX2-5 genes in patients with idiopathic atrial fibrillation.
International journal of cardiology 2010;145(2):316-7.
2010: Maximilian Posch; Anna Panek; Andrea Kersten; Santhosh Kumar Ghadge; Christian Geier; Silke Richter; Andreas Perrot; Mudather Gailani; Rainer Dietz; Diana Lüftner; Cemil Ozcelik
Plasma HER2 levels are not associated with cardiac function or hypertrophy in control subjects and heart failure patients.
International journal of cardiology 2010;145(1):105-6.
2010: Maximilian Posch; Leif-Hendrik Boldt; Michael Polotzki; Silke Richter; Sascha Rolf; Andreas Perrot; Rainer Dietz; Cemil Ozcelik; Wilhelm Haverkamp
Mutations in the cardiac transcription factor GATA4 in patients with lone atrial fibrillation.
European journal of medical genetics 2010;53(4):201-3.
2010: Maximilian Posch; Andreas Perrot; Felix Berger; Cemil Ozcelik
Molecular genetics of congenital atrial septal defects.
Clinical research in cardiology : official journal of the German Cardiac Society 2010;99(3):137-47.
2010: Katja Gehmlich; Elisabeth Ehler; Andreas Perrot; Dieter O Fürst; Christian Geier
"MLP: A Stress Sensor Goes Nuclear" by Sylvia Gunkel, Jörg Heineke, Denise Hilfiker-Kleiner, Ralph Knöll, J Mol Cell Cardiol. 2009;47(4):423-5.
Journal of molecular and cellular cardiology 2010;48(2):424-5; author reply 426-7.
2009: B Seebohm; F Matinmehr; J Köhler; Antonio Francino; F Navarro-Lopéz; Andreas Perrot; C Ozcelik; W J McKenna; Bernhard Brenner; Theresia Kraft
Cardiomyopathy mutations reveal variable region of myosin converter as major element of cross-bridge compliance.
Biophysical journal 2009;97(3):806-24.
2009: Maximilian Posch; Andreas Perrot; Christian Geier; Leif-Hendrik Boldt; Gunther Schmidt; Hans B Lehmkuhl; Roland Hetzer; Rainer Dietz; Matthias Gutberlet; Wilhelm Haverkamp; Cemil Ozcelik
Genetic deletion of arginine 14 in phospholamban causes dilated cardiomyopathy with attenuated electrocardiographic R amplitudes.
Heart rhythm : the official journal of the Heart Rhythm Society 2009;6(4):480-6.
2009: Anna N Panek; Maximilian Posch; Natalia Alenina; Santhosh K Ghadge; Bettina Erdmann; Elena Popova; Andreas Perrot; Christian Geier; Rainer Dietz; Rainer Dietz Ingo Morano; Ingo Morano; Michael Bader; Cemil Ozcelik
Connective tissue growth factor overexpression in cardiomyocytes promotes cardiac hypertrophy and protection against pressure overload.
PloS one 2009;4(8):e6743.
2008: Maximilian Posch; Matthias J Posch; Andreas Perrot; Rainer Dietz; Cemil Ozcelik
Variations in DSG2: V56M, V158G and V920G are not pathogenic for arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Nature clinical practice. Cardiovascular medicine 2008;5(12):E1.
2008: Christian Geier; Katja Gehmlich; Elisabeth Ehler; Sabine Hassfeld; Andreas Perrot; Katrin Hayess; nuno cardim; Katrin Wenzel; Bettina Erdmann; Florian Krackhardt; Maximilian Posch; Karl J Osterziel; Angelika Bublak; Herbert Nägele; Thomas Scheffold; Rainer Dietz; Kenneth R Chien; Simone Spuler; Dieter O Fürst; Peter Nürnberg; Cemil Ozcelik
Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.
Human molecular genetics 2008;17(18):2753-65.
2008: Maximilian Posch; Matthias J Posch; Christian Geier; Bettina Erdmann; Wolf Mueller; Anette Richter; Volker Ruppert; Sabine Pankuweit; Bernhard Maisch; Andreas Perrot; Jens Buttgereit; Rainer Dietz; Wilhelm Haverkamp; Cemil Ozcelik
A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy.
Molecular genetics and metabolism 2008;95(1-2):74-80.
2008: Maximilian Posch; Andreas Perrot; Katharina Schmitt; Sebastian Mittelhaus; Eva-Maria Esenwein; Brigitte Stiller; Christian Geier; Rainer Dietz; Reinhard Gessner; Cemil Ozcelik; Felix Berger
Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects.
American journal of medical genetics. Part A 2008;146A(2):251-3.
2007: Christian Geier; Andreas Perrot; Cemil Ozcelik
Letter by Geier et al regarding article, "Hypertrophic cardiomyopathy is predominantly a disease of left ventricular outflow tract obstruction".
Circulation 2007;115(23):e622; author reply e623.
2007: C Michael Gross; Andreas Perrot; Christian Geier; Maximilian Posch; Sabine Hassfeld; Jochen Kramer; Sibylle Schmidt; Wolfgang Derer; Rainer Dietz; Cemil Ozcelik
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.
The Journal of invasive cardiology 2007;19(6):261-4.
2007: Maximilian Posch; Andreas Perrot; Rainer Dietz; Cemil Ozcelik; Sabine Pankuweit; Volker Ruppert; Anette Richter; Bernhard Maisch
Mutations in MYOZ1 as well as MYOZ2 encoding the calsarcins are not associated with idiopathic and familial dilated cardiomyopathy.
Molecular genetics and metabolism 2007;91(2):207-8.
2007: Ralph Telgmann; Bassam A Harb; Cemil Ozcelik; Andreas Perrot; Jacqueline Schönfelder; Andreas Nonnenmacher; Marcus Brand; Klaus Schmidt-Petersen; Rainer Dietz; Reinhold Kreutz; Karl Josef Osterziel; Martin Paul; Stefan-Martin Brand-Herrmann
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 2007;20(1):32-7.
2006: Cemil Ozcelik; Nana Bit-Avragim; Anna Panek; Ursula Gaio; Christian Geier; Peter E Lange; Rainer Dietz; Maximilian Posch; Andreas Perrot; Brigitte Stiller
Mutations in the EGF-CFC gene cryptic are an infrequent cause of congenital heart disease.
Pediatric cardiology 2006;27(6):695-8.
2006: Andreas Perrot; Holger H Sigusch; Herbert Nägele; Janine Genschel; Hans Lehmkuhl; Roland Hetzer; Christian Geier; Veronica Leon Perez; Dirk Reinhard; Rainer Dietz; Karl Josef Osterziel; Hartmut H-J Schmidt
Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: demand for strategies in the management of presymptomatic lamin A/C mutant carriers.
European journal of heart failure 2006;8(5):484-93.
2006: Katrin Wenzel; Miriam Carl; Andreas Perrot; Joanna Zabojszcza; Maziar Assadi; Martin Ebeling; Christian Geier; Peter Robinson; Wolfram Kress; Karl Josef Osterziel; Simone Spuler
Novel sequence variants in dysferlin-deficient muscular dystrophy leading to mRNA decay and possible C2-domain misfolding.
Human mutation 2006;27(6):599-600.
2006: Andreas Perrot; Maximilian Posch; Karl Josef Osterziel
Deletion of Glu at codon 13 in the TCAP gene encoding the Z-disc protein titin-cap/telethonin is a rare non-synonymous polymorphism.
Molecular genetics and metabolism 2006;88(2):199-200.
2005: nuno cardim; Andreas Perrot; Susana Santos; Paulo Morgado; Mário Pádua; Sara Ferreira; Roberto Palma Reis; Carolino Monteiro; Teresa Ferreira; João Martins Correia; Karl Josef Osterziel
Hypertrophic cardiomyopathy in a Portuguese population: mutations in the myosin-binding protein C gene.
Revista portuguesa de cardiologia : orgão oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology 2005;24(12):1463-76.
2005: Andreas Perrot; Zhyldyz Kabaeva; Katrin Wenzel; Karl Josef Osterziel
Gene expression analysis of human tissue from patients with cardiomyopathies: a new tool for guiding therapies in the future?
Journal of cardiac surgery 2005;20(6):S17-9.
2005: Karl Josef Osterziel; Sabine Hassfeld; Christian Geier; Andreas Perrot
[Familial dilated cardiomyopathy].
Herz 2005;30(6):529-34.
2005: Andreas Perrot; Hajo Schmidt-Traub; Bernard Hoffmann; Matthias Prager; Nana Bit-Avragim; Raisa I Rudenko; Dinara A Usupbaeva; Zhyldyz Kabaeva; Bakytbek Imanov; Mirsaid M Mirrakhimov; Rainer Dietz; Anna Wycisk; Michal Tendera; Reinhard Gessner; Karl Josef Osterziel
Prevalence of cardiac beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy.
Journal of molecular medicine (Berlin, Germany) 2005;83(6):468-77.
2005: C Pellnitz; Christian Geier; Andreas Perrot; Rainer Dietz; Karl Josef Osterziel; W Haverkamp
[Sudden cardiac death in familial hypertrophic cardiomyopathy. Identification of high-risk patients].
Deutsche medizinische Wochenschrift (1946) 2005;130(18):1150-4.
2005: Andreas Perrot; Simone Spuler; Christian Geier; Rainer Dietz; Karl Josef Osterziel
[Cardiac manifestations of muscular dystrophies].
Zeitschrift für Kardiologie 2005;94(5):312-20.
2005: Zhyldyz Kabaeva; Andreas Perrot; Bernhard Pilz; Jeanette Schulz-Menger; Friedrich-Wilhelm Mohr; Rainer Dietz; Karl Josef Osterziel
Returning hypertrophy after surgery in a patient with hypertrophic cardiomyopathy caused by a myosin-binding protein C mutation.
International journal of cardiology 2005;100(2):343-5.
2005: Sebastian E Kirschner; Edgar Becker; Massimo Antognozzi; Hans-Peter Kubis; Antonio Francino; Francisco Navarro-López; Nana Bit-Avragim; Andreas Perrot; Mirsaid M Mirrakhimov; Karl Josef Osterziel; William J McKenna; Bernhard Brenner; Theresia Kraft
Hypertrophic cardiomyopathy-related beta-myosin mutations cause highly variable calcium sensitivity with functional imbalances among individual muscle cells.
American journal of physiology. Heart and circulatory physiology 2005;288(3):H1242-51.
2003: Christian Geier; Andreas Perrot; Cemil Ozcelik; Priska Binner; Damian Counsell; Katrin Hoffmann; Bernhard Pilz; Yvonne Martiniak; Katja Gehmlich; Peter F.M. van der Ven; Dieter O Fürst; Arnold Vornwald; Eberhard von Hodenberg; Peter Nürnberg; Thomas Scheffold; Rainer Dietz; Karl Josef Osterziel
Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy.
Circulation 2003;107(10):1390-5.
2003: Michael Bunse; Nana Bit-Avragim; Axel Riefflin; Andreas Perrot; Oliver Schmidt; Friedmar R Kreuz; Rainer Dietz; Wulf-Ingo Jung; Karl Josef Osterziel
Cardiac energetics correlates to myocardial hypertrophy in Friedreich's ataxia.
Annals of neurology 2003;53(1):121-3.
2002: Karl Josef Osterziel; Andreas Perrot
[Molecular basis of heart failure and dilated cardiomyopathy].
Herz 2002;27(8):816-8.
2002: Zhyldyz Kabaeva; Andreas Perrot; Bastian Wolter; Rainer Dietz; nuno cardim; João Martins Correia; Hagen D Schulte; Almaz A Aldashev; Mirsaid M Mirrakhimov; Karl Josef Osterziel
Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy.
European journal of human genetics : EJHG 2002;10(11):741-8.
2002: nuno cardim; Andreas Perrot; Teresa Ferreira; Amadeu Pereira; Karl Josef Osterziel; Roberto Palma Reis; J F Martins Correia
Usefulness of Doppler myocardial imaging for identification of mutation carriers of familial hypertrophic cardiomyopathy.
The American journal of cardiology 2002;90(2):128-32.
2002: Oliver Ritter; Susanne Hack; Kai Schuh; Nicola Röthlein; Andreas Perrot; Karl Josef Osterziel; Hagen D Schulte; Ludwig Neyses
Calcineurin in human heart hypertrophy.
Circulation 2002;105(19):2265-9.
2001: S Herrmann; Klaus Schmidt-Petersen; Jacqueline Pfeifer; Andreas Perrot; Nana Bit-Avragim; C Eichhorn; Rainer Dietz; Reinhold Kreutz; Martin Paul; Karl Josef Osterziel
A polymorphism in the endothelin-A receptor gene predicts survival in patients with idiopathic dilated cardiomyopathy.
European heart journal 2001;22(20):1948-53.
2001: Karl Josef Osterziel; Thomas Scheffold; Andreas Perrot; Rainer Dietz
[Genetics of dilated cardiomyopathy].
Zeitschrift für Kardiologie 2001;90(7):461-9.
2001: B Hoffmann; H Schmidt-Traub; Andreas Perrot; Karl Josef Osterziel; Reinhard Gessner
First mutation in cardiac troponin C, L29Q, in a patient with hypertrophic cardiomyopathy.
Human mutation 2001;17(6):524.
2001: Nana Bit-Avragim; Andreas Perrot; Ludger Schöls; Cornelia Hardt; Friedmar R Kreuz; Christine Zühlke; Stefanie Bubel; Franco Laccone; H P Vogel; Rainer Dietz; Karl Josef Osterziel
The GAA repeat expansion in intron 1 of the frataxin gene is related to the severity of cardiac manifestation in patients with Friedreich's ataxia.
Journal of molecular medicine (Berlin, Germany) 2001;78(11):626-32.