PubRank

P S Andersen

Author PubWeight™ 40.78‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Chronic inflammation: importance of NOD2 and NALP3 in interleukin-1beta generation. Clin Exp Immunol 2007 2.12
2 Rapid detection, differentiation and typing of methicillin-resistant Staphylococcus aureus harbouring either mecA or the new mecA homologue mecA(LGA251). Clin Microbiol Infect 2012 2.08
3 CACNA1C (rs1006737) is associated with schizophrenia. Mol Psychiatry 2010 1.93
4 A novel missense mutation, Leu390Val, in the cardiac beta-myosin heavy chain associated with pronounced septal hypertrophy in two families with hypertrophic cardiomyopathy. Scand Cardiovasc J 2000 1.41
5 Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations. J Med Genet 2001 1.33
6 Cloning and occurrence of czrC, a gene conferring cadmium and zinc resistance in methicillin-resistant Staphylococcus aureus CC398 isolates. Antimicrob Agents Chemother 2010 1.24
7 Multiple transcriptional control of the Lactococcus lactis trp operon. J Bacteriol 1998 1.24
8 Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes. Heart 2008 1.17
9 Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome. Clin Chem 2001 1.17
10 The B form of dihydroorotate dehydrogenase from Lactococcus lactis consists of two different subunits, encoded by the pyrDb and pyrK genes, and contains FMN, FAD, and [FeS] redox centers. J Biol Chem 1996 1.16
11 National prevalence of respiratory allergic disorders. Respir Med 2004 1.05
12 Two genes encoding uracil phosphoribosyltransferase are present in Bacillus subtilis. J Bacteriol 1995 1.05
13 Nucleotide metabolism in Lactococcus lactis: salvage pathways of exogenous pyrimidines. J Bacteriol 1994 1.02
14 Efficient method for constructing comprehensive murine Fab antibody libraries displayed on phage. Nucleic Acids Res 1993 1.02
15 Clinical and genetic characteristics of alpha cardiac actin gene mutations in hypertrophic cardiomyopathy. J Med Genet 2004 0.92
16 Recent developments in high-throughput mutation screening. Pharmacogenomics 2001 0.89
17 A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome. Clin Chim Acta 1999 0.87
18 The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age. Am J Cardiol 2001 0.87
19 Mapping the energy of superantigen Staphylococcus enterotoxin C3 recognition of an alpha/beta T cell receptor using alanine scanning mutagenesis. J Exp Med 2000 0.86
20 Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene. Eur J Hum Genet 1999 0.86
21 High-throughput single-strand conformation polymorphism analysis by automated capillary electrophoresis: robust multiplex analysis and pattern-based identification of allelic variants. Hum Mutat 1999 0.86
22 Shared fine specificity between T-cell receptors and an antibody recognizing a peptide/major histocompatibility class I complex. Proc Natl Acad Sci U S A 1996 0.85
23 Development and application of linkage analysis in genetic diagnosis of familial hypertrophic cardiomyopathy. J Med Genet 2001 0.84
24 Effects of a 17q21 chromosome gene variant, tobacco smoke and furred pets on infant wheeze. Genes Immun 2011 0.84
25 Apo E in multiple sclerosis and optic neuritis: the apo E-epsilon4 allele is associated with progression of multiple sclerosis. Mult Scler 2005 0.82
26 Phage-display libraries of murine and human antibody Fab fragments. Mol Biotechnol 1996 0.82
27 Comparison of the effects of fish oil and olive oil on blood lipids and aortic atherosclerosis in Watanabe heritable hyperlipidaemic rabbits. Br J Nutr 1998 0.82
28 Living & learning with allergy: a European perception study on respiratory allergic disorders. Respir Med 2004 0.82
29 Predictors of coronary in-stent restenosis: importance of angiotensin-converting enzyme gene polymorphism and treatment with angiotensin-converting enzyme inhibitors. J Am Coll Cardiol 2001 0.81
30 Phage display used for gene cloning of human recombinant antibody against the erythrocyte surface antigen, rhesus D. J Immunol Methods 1995 0.81
31 Human β-defensin-2 as a marker for disease severity and skin barrier properties in atopic dermatitis. Br J Dermatol 2013 0.81
32 Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2. Clin Genet 2000 0.81
33 High throughput mutation screening by automated capillary electrophoresis. Comb Chem High Throughput Screen 2000 0.79
34 Phage-display libraries of murine and human antibody Fab fragments. Methods Mol Biol 1995 0.79
35 Modeling the interactions of a peptide-major histocompatibility class I ligand with its receptors. I. Recognition by two alpha beta T cell receptors. J Comput Aided Mol Des 2000 0.79
36 Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndrome. J Cardiovasc Electrophysiol 1998 0.78
37 Familial hypertrophic cardiomyopathy associated with a novel missense mutation affecting the ATP-binding region of the cardiac beta-myosin heavy chain. J Mol Cell Cardiol 1999 0.77
38 Modeling the interactions of a peptide-major histocompatibility class I ligand with its receptors. II. Cross-reaction between a monoclonal antibody and two alpha beta T cell receptors. J Comput Aided Mol Des 2000 0.77
39 T-cell receptor downregulation by ceramide-induced caspase activation and cleavage of the zeta chain. Scand J Immunol 2001 0.77
40 Infliximab dependency in children with Crohn's disease. Aliment Pharmacol Ther 2009 0.76
41 Automated mutation screening using dideoxy fingerprinting and capillary array electrophoresis. Hum Mutat 2001 0.76
42 Measuring protein interactions by optical biosensors. Curr Protoc Protein Sci 2001 0.76
43 Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 gene. Clin Genet 1999 0.75