Patrick Linsel-Nitschke

Author PubWeight™ 60.89‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet 2009 12.19
2 Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease. Circulation 2008 5.20
3 New susceptibility locus for coronary artery disease on chromosome 3q22.3. Nat Genet 2009 5.12
4 Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. Nat Genet 2009 4.63
5 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 2.17
6 A PEST sequence in ABCA1 regulates degradation by calpain protease and stabilization of ABCA1 by apoA-I. J Clin Invest 2003 1.75
7 ATP-binding cassette transporter A7 enhances phagocytosis of apoptotic cells and associated ERK signaling in macrophages. J Cell Biol 2006 1.63
8 An alternative splice variant in Abcc6, the gene causing dystrophic calcification, leads to protein deficiency in C3H/He mice. J Biol Chem 2008 1.51
9 Association between degenerative aortic valve disease and long-term exposure to cardiovascular risk factors: results of the longitudinal population-based KORA/MONICA survey. Eur Heart J 2009 1.51
10 Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy. PLoS Genet 2010 1.37
11 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. J Mol Med (Berl) 2008 1.35
12 ATP-binding cassette transporter A7 (ABCA7) binds apolipoprotein A-I and mediates cellular phospholipid but not cholesterol efflux. J Biol Chem 2003 1.26
13 Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23. Eur Heart J 2010 1.25
14 Genetic regulation of serum phytosterol levels and risk of coronary artery disease. Circ Cardiovasc Genet 2010 1.23
15 Lack of association between the MEF2A gene and myocardial infarction. Circulation 2007 1.07
16 Expression and role of cubilin in the internalization of nutrients during the peri-implantation development of the rodent embryo. Biol Reprod 2004 0.99
17 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. Atherosclerosis 2009 0.94
18 Association of a functional polymorphism in the CYP4A11 gene with systolic blood pressure in survivors of myocardial infarction. J Hypertens 2006 0.93
19 Lack of association between a common polymorphism near the INSIG2 gene and BMI, myocardial infarction, and cardiovascular risk factors. Obesity (Silver Spring) 2009 0.91
20 Genetic causes of myocardial infarction: new insights from genome-wide association studies. Dtsch Arztebl Int 2010 0.90
21 Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction. J Mol Med (Berl) 2008 0.84
22 Physicians' perception of guideline-recommended low-density lipoprotein target values: characteristics of misclassified patients. Eur Heart J 2010 0.83