P. Linsel-Nitschke

发表

Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease

Benjamin J. Wright, I. König, A. Ziegler, 2009, Nature Genetics.

ATP-binding Cassette Transporter A7 (ABCA7) Binds Apolipoprotein A-I and Mediates Cellular Phospholipid but Not Cholesterol Efflux*

P. Linsel-Nitschke, A. Tall, N. Wang, 2003, Journal of Biological Chemistry.

New susceptibility locus for coronary artery disease on chromosome 3q22.3

Daniel F. Schwarz, Benjamin J. Wright, A. Peters, 2009, Nature Genetics.

Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23.

C. Gieger, A. Peters, C. Loley, 2011, European heart journal.

Repeated Replication and a Prospective Meta-Analysis of the Association Between Chromosome 9 p 21 . 3 and Coronary Artery Disease

Ludwig A Hothorn, Nilesh J Samani, Andreas Ziegler, 2008 .

Correction: Lifelong Reduction of LDL-Cholesterol Related to a Common Variant in the LDL-Receptor Gene Decreases the Risk of Coronary Artery Disease—A Mendelian Randomisation Study

C. Gieger, F. Kronenberg, A. Peters, 2008, PLoS ONE.

An Alternative Splice Variant in Abcc6, the Gene Causing Dystrophic Calcification, Leads to Protein Deficiency in C3H/He Mice*

J. Erdmann, H. Schunkert, P. Linsel-Nitschke, 2008, Journal of Biological Chemistry.

Physicians' perception of guideline-recommended low-density lipoprotein target values: characteristics of misclassified patients.

W. Lieb, H. Schunkert, P. Linsel-Nitschke, 2010, European heart journal.

A PEST sequence in ABCA 1 regulates degradation by calpain protease and stabilization of ABCA 1 by apoA-I

P. Linsel-Nitschke, A. Tall, Wengen Chen, 2018 .

A PEST sequence in ABCA1 regulates degradation by calpain protease and stabilization of ABCA1 by apoA-I.

P. Linsel-Nitschke, A. Tall, Wengen Chen, 2003, The Journal of clinical investigation.

Potential role of ABCA7 in cellular lipid efflux to apoA-I Published, JLR Papers in Press, November 1, 2004. DOI 10.1194/jlr.M400247-JLR200

P. Linsel-Nitschke, A. Tall, Jing Shan, 2005, Journal of Lipid Research.

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

Alberto Piazza, William Matthai, Flora Peyvandi, 2009, Nature Genetics.

Lack of Association Between the MEF2A Gene and Myocardial Infarction Genetics

I. König, A. Ziegler, J. Erdmann, 2008 .

Lack of Association Between the MEF 2 A Gene and Myocardial Infarction

I. König, A. Ziegler, J. Erdmann, 2007 .

Genetic Regulation of Serum Phytosterol Levels and Risk of Coronary Artery Disease

C. Gieger, I. König, N. Samani, 2010, Circulation. Cardiovascular genetics.

Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease.

C. Gieger, F. Kronenberg, A. Peters, 2010, Atherosclerosis.

Genetic Association Study Identifies HSPB7 as a Risk Gene for Idiopathic Dilated Cardiomyopathy

I. König, L. Fauchier, V. Regitz-Zagrosek, 2010, PLoS genetics.

Abstract 1879: Genetic Variation at Chromosome 1p13.3 Affects Sortilin mRNA Expression, Cellular LDL Uptake and Serum LDL Levels Which Translates to the Risk of Coronary Artery Disease

C. Gieger, F. Kronenberg, A. Peters, 2009 .

Lifelong Reduction of LDL-Cholesterol Related to a Common Variant in the LDL-Receptor Gene Decreases the Risk of Coronary Artery Disease—A Mendelian Randomisation Study

C. Gieger, F. Kronenberg, A. Peters, 2008, PloS one.

Edinburgh Research Explorer Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

Tom R. Gaunt, Andrew D. Johnson, Nicholette D. Palmer, 2022 .

Expression and Role of Cubilin in the Internalization of Nutrients During the Peri-Implantation Development of the Rodent Embryo1

P. Linsel-Nitschke, P. Verroust, F. Illien, 2005, Biology of reproduction.

Lack of Association Between the Trp 719 Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control

Alexander F. Wilson, A. F. Wilson, D. Absher, 2017 .

Protein-6 and Coronary Artery Disease in 19 Case-Control Studies Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like

Alexander F. Wilson, A. F. Wilson, D. Absher, 2012 .

Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies.

Alexander F. Wilson, A. F. Wilson, Benjamin J. Wright, 2010, Journal of the American College of Cardiology.

P Lack of Association Between the Trp 719 Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control Studies

Alexander F. Wilson, A. F. Wilson, D. Absher, 2010 .

ATP-binding cassette transporter A7 enhances phagocytosis of apoptotic cells and associated ERK signaling in macrophages

P. Linsel-Nitschke, A. Tall, W. Janssen, 2006, The Journal of cell biology.

Lack of Association Between a Common Polymorphism Near the INSIG2 Gene and BMI, Myocardial Infarction, and Cardiovascular Risk Factors

S. Wiedmann, J. Erdmann, C. Hengstenberg, 2009, Obesity.

The novel genetic variant predisposing to coronary artery disease in the region of the PSRC1 and CELSR2 genes on chromosome 1 associates with serum cholesterol

Paul R. Burton, Andreas Ziegler, Nilesh J. Samani, 2008, Journal of Molecular Medicine.

Association between degenerative aortic valve disease and long-term exposure to cardiovascular risk factors: results of the longitudinal population-based KORA/MONICA survey.

H. Hense, W. Lieb, H. Schunkert, 2009, European heart journal.

HDL as a target in the treatment of atherosclerotic cardiovascular disease

P. Linsel-Nitschke, A. Tall, 2005, Nature Reviews Drug Discovery.

HDL as a target in the treatment of atherosclerotic cardiovascular disease

P. Linsel-Nitschke, A. Tall, 2005, Nature Reviews Drug Discovery.

Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10 p 11 . 23

C. Gieger, A. Peters, C. Loley, 2010 .

Association of the single nucleotide polymorphism rs599839 in the vicinity of the sortilin 1 gene with LDL and triglyceride metabolism, coronary heart disease and myocardial infarction. The Ludwigshafen Risk and Cardiovascular Health Study.

P. Linsel-Nitschke, P. Bugert, W. März, 2010, Atherosclerosis.

Macrophage cholesterol efflux correlates with lipoprotein subclass distribution and risk of obstructive coronary artery disease in patients undergoing coronary angiography

H. Kalbitzer, J. Erdmann, W. Lieb, 2009, Lipids in Health and Disease.

Association of a functional polymorphism in the CYP4A11 gene with systolic blood pressure in survivors of myocardial infarction

I. König, A. Ziegler, H. Hense, 2006, Journal of hypertension.

Genetic variation in the arachidonate 5-lipoxygenase-activating protein (ALOX5AP) is associated with myocardial infarction in the German population.

I. König, A. Ziegler, J. Erdmann, 2008, Clinical science.

Lack of Association Between the MEF2A Gene and Myocardial Infarction

I. König, A. Ziegler, J. Erdmann, 2008, Circulation.

Genetic causes of myocardial infarction: new insights from genome-wide association studies.

J. Erdmann, H. Schunkert, P. Linsel-Nitschke, 2010, Deutsches Arzteblatt international.

Genetic Causes of Myocardial Infarction

J. Erdmann, H. Schunkert, P. Linsel-Nitschke, 2010 .

Repeated Replication and a Prospective Meta-Analysis of the Association Between Chromosome 9p21.3 and Coronary Artery Disease

Daniel F. Schwarz, P. Deloukas, I. König, 2008, Circulation.

Chromosome 9p21 and coronary risk--the mystery continues.

H. Schunkert, P. Linsel-Nitschke, 2011, Atherosclerosis.

Sorting out cholesterol and coronary artery disease.

N. Samani, H. Schunkert, P. Linsel-Nitschke, 2010, The New England journal of medicine.

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

Tom R. Gaunt, Nicholette D. Palmer, Y. J. Kim, 2016, Nature Communications.