Author details

Full Name

Thomas Scheffold

Affiliation

ORCID

Career Start Year

1987

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
31415634	The association of high-normal international-normalized-ratio (INR) with mortality in patients referred for coronary angiography.	PLoS One	2019
25979592	Targeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathies.	Molecular and Cellular Probes	2015
23853074	A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy.	Eur Heart J	2014
23142374	High-density oligonucleotide-based resequencing assay for mutations causing syndromic and non-syndromic forms of thoracic aortic aneurysms and dissections.	Molecular and Cellular Probes	2013
22139085	Implementation of pharmacotherapy guidelines in heart failure: experience from the German Competence Network Heart Failure.	Clin Res Cardiol	2012
22373485	Economic burden of patients with various etiologies of chronic systolic heart failure analyzed by resource use and costs.	Int J Cardiol	2012
21591574	Metabolic syndrome with or without diabetes contributes to left ventricular diastolic dysfunction.	Acta Cardiologica	2011
21432821	Relation of global longitudinal strain to left ventricular geometry in aortic valve stenosis.		2011
21385355	Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry.	BMC Cardiovascular Disorders	2011
21204960	Cardiovascular autonomic neuropathy contributes to left ventricular diastolic dysfunction in subjects with Type 2 diabetes and impaired glucose tolerance undergoing coronary angiography.	Diabetic Medicine	2011
21248741	Three novel mutations in the ACTA2 gene in German patients with thoracic aortic aneurysms and dissections.	European Journal of Human Genetics	2011
21416189	Contribution of comorbidities to functional impairment is higher in heart failure with preserved than with reduced ejection fraction.	Clin Res Cardiol	2011
21409595	A case of familial hypertrophic cardiomyopathy emphasizes the importance of parallel screening of multiple disease genes.	Clinical Research in Cardiology	2011
20542339	Screening for overt diabetes by oral glucose tolerance test: stratification by fasting blood glucose and patients' age improve practicability of guidelines in cardiological routine.	International Journal of Cardiology	2011
21729325	High sensitive troponin T and heart fatty acid binding protein: novel biomarker in heart failure with normal ejection fraction? A cross-sectional study.	BMC Cardiovasc Disord	2011
21584478	Growth-differentiation factor-15: a novel biomarker in patients with diastolic dysfunction?		2011
21750094	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
22194935	Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defects.	PLoS One	2011
20659321	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.	Cardiovascular Ultrasound	2010
19679361	A network against failing hearts--introducing the German "Competence Network Heart Failure".	Int J Cardiol	2010
20950415	Insulin resistance and glycemic abnormalities are associated with deterioration of left ventricular diastolic function: a cross-sectional study.	Cardiovascular Diabetology	2010
20933357	Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies.	J Am Coll Cardiol	2010
20136522	Gender-based differences in long-term outcome after ST-elevation myocardial infarction in patients treated with percutaneous coronary intervention.	Journal of Women's Health	2010
20102882	Comparison of usefulness of heart-type fatty acid binding protein versus cardiac troponin T for diagnosis of acute myocardial infarction.	American Journal of Cardiology	2010
18614244	The Biomaterialbank of the German Competence Network of Heart Failure (CNHF) is a valuable resource for biomedical and genetic research.	Int J Cardiol	2009
19593942	Increased levels of laminin and collagen type VI may reflect early remodelling in patients with acute myocardial infarction.	Acta Cardiologica	2009
19364889	Supervised training with wireless monitoring of ECG, blood pressure and oxygen-saturation in cardiac patients.	Journal of Telemedicine and Telecare	2009
19198609	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.	Nat Genet	2009
19609047	Increased serum levels of tissue inhibitor of metalloproteinase-1 in patients with acute myocardial infarction.	International Heart Journal	2009
19277455	Newly detected glucose disturbance is associated with a high prevalence of diastolic dysfunction: double risk for the development of heart failure?	Acta Diabetologica	2009
20098572	Soluble P-selectin and matrix metalloproteinase 2 levels are elevated in patients with diastolic dysfunction independent of glucose metabolism disorder or coronary artery disease.		2009
20098571	Deposition of nonsarcomeric alpha-actinin in cardiomyocytes from patients with dilated cardiomyopathy or chronic pressure overload.		2009
19814804	Variation in the human soluble epoxide hydrolase gene and risk of restenosis after percutaneous coronary intervention.	BMC Cardiovascular Disorders	2009
19909503	Elevated plasma levels of TNF-alpha and interleukin-6 in patients with diastolic dysfunction and glucose metabolism disorders.	Cardiovascular Diabetology	2009
18505755	Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.	Human Molecular Genetics	2008
17965946	Congenital coronary artery fistulas in adults: concomitant pathologies and treatment.	International Journal of Cardiovascular Imaging	2008
18258667	Array-based resequencing assay for mutations causing hypertrophic cardiomyopathy.	Clinical Chemistry	2008
18159245	Noncompaction of the ventricular myocardium is associated with a de novo mutation in the beta-myosin heavy chain gene.	PLoS ONE	2007
17418587	Genetic testing in patients with aortic aneurysms/dissections: a novel genotype/phenotype correlation?	European Journal of Cardio-thoracic Surgery	2007
17126131	Systemic stress hormone response in patients undergoing open heart surgery with or without cardiopulmonary bypass.	Annals of Thoracic Surgery	2006
16382379	Plasma levels of NT-pro-BNP in patients with atrial fibrillation before and after electrical cardioversion.		2005
16170688	[Hypertrophic cardiomyopathy].	Herz	2005
14996481	Elevated plasma human urotensin-II-like immunoreactivity in ischemic cardiomyopathy.	International Journal of Cardiology	2004
15085375	Frequency and quantity of the parvovirus B19 genome in endomyocardial biopsies from patients with suspected myocarditis or idiopathic left ventricular dysfunction.		2004
12642359	Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy.	Circulation	2003
12127369	C/T polymorphism of the intercellular adhesion molecule-1 gene (exon 6, codon 469). A risk factor for coronary heart disease and myocardial infarction.	International Journal of Cardiology	2002
12132786	Detection of Helicobacter pylori specific DNA in human atheromatous coronary arteries and its association to prior myocardial infarction and unstable angina.	Digestive and Liver Disease	2002
11515275	[Genetics of dilated cardiomyopathy].		2001
11098555	[New strategies in the treatment of restenosis].		2000
27320521	[New strategies to treat restenosis].		2000