P. Binner

发表

Noncompaction of the Ventricular Myocardium Is Associated with a De Novo Mutation in the β-Myosin Heavy Chain Gene

R. Goody, P. Nürnberg, W. Blankenfeldt, 2007, PloS one.

MHC class I antigen processing pathway defects, ras mutations and disease stage in colorectal carcinoma

B. Seliger, S. Störkel, S. Ferrone, 2004, International journal of cancer.

High-density oligonucleotide-based resequencing assay for mutations causing syndromic and non-syndromic forms of thoracic aortic aneurysms and dissections.

M. Bonin, B. Keyser, M. Stuhrmann, 2013, Molecular and cellular probes.

FH ALERT: A feasibility study of a novel approach to identify patients with familial hypercholesterolemia

W. März, S. Schwab, B. Krämer, 2020 .

Variation in the human soluble epoxide hydrolase gene and risk of restenosis after percutaneous coronary intervention

R. Füth, H. Bestehorn, S. Kullmann, 2009, BMC cardiovascular disorders.

' s response to reviews Title : Variation in the human soluble epoxide hydrolase gene and risk of restenosis after percutaneous coronary intervention

H. Bestehorn, S. Kullmann, G. Haltern, 2009 .

Mutations in the Human Muscle LIM Protein Gene in Families With Hypertrophic Cardiomyopathy

R. Dietz, D. Fürst, P. Nürnberg, 2003, Circulation.

Severe hypertriglyceridemia in a patient heterozygous for a lipoprotein lipase gene allele with two novel missense variants

W. März, E. Steinhagen-Thiessen, I. Demuth, 2015, European Journal of Human Genetics.

FH ALERT: efficacy of a novel approach to identify patients with familial hypercholesterolemia

W. März, B. Krämer, K. Ray, 2021, Scientific Reports.

Clinical characterization and mutation spectrum of German patients with familial hypercholesterolemia.

W. März, U. Laufs, M. Kleber, 2016, Atherosclerosis.

Array-Based Resequencing Assay for Mutations Causing Hypertrophic Cardiomyopathy

S. Poths, M. Bonin, T. Scheffold, 2008, Clinical chemistry.

Three novel mutations in the ACTA2 gene in German patients with thoracic aortic aneurysms and dissections

W. Blankenfeldt, J. Epplen, P. Gehle, 2011, European Journal of Human Genetics.

Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry

H. Heuer, M. Stoll, W. Schöls, 2011, BMC cardiovascular disorders.

Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure

Steffen Scheer, Jeanette Erdmann, Heribert Schunkert, 2011, European journal of heart failure.

Variation in the human soluble epoxide hydrolase gene and risk of restenosis after percutaneous coronary intervention

R. Füth, H. Bestehorn, S. Kullmann, 2009, BMC cardiovascular disorders.

Clinical characterization and mutation spectrum of patients with hypertriglyceridemia in a German outpatient clinic.

M. Kleber, I. Demuth, U. Kassner, 2024, Journal of lipid research.