Publications by authors named "Thomas Scheffold"

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The association of high-normal international-normalized-ratio (INR) with mortality in patients referred for coronary angiography.
Graciela E Delgado, Andreas Zirlik, Rudolf Gruber, Thomas Scheffold, Bernhard K Krämer

PLoS One· March 2020

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Targeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathies.
Stephan Waldmüller, Christopher Schroeder, Marc Sturm, Thomas Scheffold, Kerstin Imbrich

Mol Cell Probes· October 2015

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A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy.
Benjamin Meder, Frank Rühle, Tanja Weis, Georg Homuth, Andreas Keller, Thomas Scheffold

Eur Heart J· April 2014

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Relation of global longitudinal strain to left ventricular geometry in aortic valve stenosis.
Wilfried Dinh, Werner Nickl, Jan Smettan, Till Koehler, Lars Bansemir, Thomas Scheffold

Cardiol J· May 2013

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High-density oligonucleotide-based resequencing assay for mutations causing syndromic and non-syndromic forms of thoracic aortic aneurysms and dissections.
Ushanthine Kathiravel, Britta Keyser, Sabine Hoffjan, Judith Kötting, Melanie Müller, Thomas Scheffold

Mol Cell Probes· April 2013

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Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defects.
Maximilian G Posch, Stephan Waldmuller, Melanie Müller, Thomas Scheffold, David Fournier

PLoS One· August 2012

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Economic burden of patients with various etiologies of chronic systolic heart failure analyzed by resource use and costs.
Janine Biermann, Till Neumann, Christiane E Angermann, Raimund Erbel, Bernhard Maisch, Thomas Scheffold

Int J Cardiol· May 2012

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Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure.
Stephan Waldmüller, Jeanette Erdmann, Priska Binner, Götz Gelbrich, Sabine Pankuweit, Thomas Scheffold

Eur J Heart Fail· November 2011

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Contribution of comorbidities to functional impairment is higher in heart failure with preserved than with reduced ejection fraction.
Frank Edelmann, Raoul Stahrenberg, Götz Gelbrich, Kathleen Durstewitz, Christiane E Angermann, Thomas Scheffold

Clin Res Cardiol· September 2011

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Deposition of nonsarcomeric alpha-actinin in cardiomyocytes from patients with dilated cardiomyopathy or chronic pressure overload.
Stefan Hein, Tim Block, René Zimmermann, Sawa Kostin, Thomas Scheffold

Exp Clin Cardiol· July 2011

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Soluble P-selectin and matrix metalloproteinase 2 levels are elevated in patients with diastolic dysfunction independent of glucose metabolism disorder or coronary artery disease.
Reiner Füth, Wilfried Dinh, Werner Nickl, Lars Bansemir, Michael Coll Barroso, Thomas Scheffold

Exp Clin Cardiol· July 2011

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Screening for overt diabetes by oral glucose tolerance test: stratification by fasting blood glucose and patients' age improve practicability of guidelines in cardiological routine.
Kerstin Kempf, Reiner Füth, Wilfried Dinh, Lars Bansemir, Till Köhler, Thomas Scheffold

Int J Cardiol· July 2011

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A case of familial hypertrophic cardiomyopathy emphasizes the importance of parallel screening of multiple disease genes.
Thomas Scheffold, Stephan Waldmüller, Konstantin Borisov

Clin Res Cardiol· July 2011

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Growth-differentiation factor-15: a novel biomarker in patients with diastolic dysfunction?
Wilfried Dinh, Reiner Füth, Mark Lankisch, Georg Hess, Dietmar Zdunek, Thomas Scheffold

Arq Bras Cardiol· July 2011

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High sensitive troponin T and heart fatty acid binding protein: novel biomarker in heart failure with normal ejection fraction? A cross-sectional study.
Wilfried Dinh, Werner Nickl, Reiner Füth, Mark Lankisch, Georg Hess, Thomas Scheffold

BMC Cardiovasc Disord· July 2011

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Three novel mutations in the ACTA2 gene in German patients with thoracic aortic aneurysms and dissections.
Sabine Hoffjan, Stephan Waldmüller, Wulf Blankenfeldt, Judith Kötting, Petra Gehle, Thomas Scheffold

Eur J Hum Genet· May 2011

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Metabolic syndrome with or without diabetes contributes to left ventricular diastolic dysfunction.
Wilfried Dinh, Mark Lankisch, Werner Nickl, Milvia Gies, Daniel Scheyer, Thomas Scheffold

Acta Cardiol· April 2011

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Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry.
Thomas Scheffold, Silke Kullmann, Andreas Huge, Priska Binner, Hermann R Ochs

BMC Cardiovasc Disord· March 2011

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Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies.
Themistocles L Assimes, Hilma Hólm, Sekar Kathiresan, Muredach P Reilly, Gudmar Thorleifsson, Thomas Scheffold

J Am Coll Cardiol· November 2010

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Insulin resistance and glycemic abnormalities are associated with deterioration of left ventricular diastolic function: a cross-sectional study.
Wilfried Dinh, Mark Lankisch, Werner Nickl, Daniel Scheyer, Thomas Scheffold

Cardiovasc Diabetol· October 2010

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Reduced global longitudinal strain in association to increased left ventricular mass in patients with aortic valve stenosis and normal ejection fraction: a hybrid study combining echocardiography and magnetic resonance imaging.
Wilfried Dinh, Werner Nickl, Jan Smettan, Frank Kramer, Thomas Krahn, Thomas Scheffold

Cardiovasc Ultrasound· July 2010

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Gender-based differences in long-term outcome after ST-elevation myocardial infarction in patients treated with percutaneous coronary intervention.
Alexander Bufe, Judith Wolfertz, Wilfried Dinh, Lars Bansemir, Til Koehler, Thomas Scheffold

J Womens Health (Larchmt)· March 2010

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Comparison of usefulness of heart-type fatty acid binding protein versus cardiac troponin T for diagnosis of acute myocardial infarction.
Georg Haltern, Sigune Peiniger, Alexander Bufe, Gebhard Reiss, Hartmut Gülker, Thomas Scheffold

Am J Cardiol· January 2010

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Elevated plasma levels of TNF-alpha and interleukin-6 in patients with diastolic dysfunction and glucose metabolism disorders.
Wilfried Dinh, Reiner Füth, Werner Nickl, Thomas Krahn, Peter Ellinghaus, Thomas Scheffold

Cardiovasc Diabetol· November 2009

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Variation in the human soluble epoxide hydrolase gene and risk of restenosis after percutaneous coronary intervention.
Silke Kullmann, Priska Binner, Kirsten Rackebrandt, Andreas Huge, Georg Haltern, Thomas Scheffold

BMC Cardiovasc Disord· October 2009

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