Physician
Cardiology
Dr. Klaus Lindpaintner, MD
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Klaus Lindpaintner, MD works in the field of Cardiology. Klaus Lindpaintner has written publications. He has 99 publications published with PubMed. The lastest publication is: 'Acute myocardial necrosis during administration of amsacrine.'
Publications
- A prospective study of TaqIB polymorphism in the gene coding for cholesteryl ester transfer protein and risk of myocardial infarction in middle-aged men.
- Efficacy of SSH PCR in isolating differentially expressed genes.
- Pharmacogenetics and the future of medical practice.
- The impact of pharmacogenetics and pharmacogenomics on drug discovery.
- The importance of being modest--reflections on the pharmacogenetics of abacavir.
- Pharmacogenetic analysis of adverse drug effect reveals genetic variant for susceptibility to liver toxicity.
- Alanine for proline substitution in the peroxisome proliferator-activated receptor gamma-2 (PPARG2) gene and the risk of incident myocardial infarction.
- Pharmacogenetics and pharmacogenomics in drug discovery and development: an overview.
- Statistical methods for analyzing microarray feature data with replications.
- IL-1 cluster genes and occurrence of post-percutaneous transluminal coronary angioplasty restenosis: a prospective, angiography-based evaluation.
- Polymorphism in the P-selectin and interleukin-4 genes as determinants of stroke: a population-based, prospective genetic analysis.
- TP53 haplotype-based analysis and incidence of post-angioplasty restenosis.
- Absence of association between polymorphisms in the hemostatic factor pathway genes and carotid intimal medial thickness: the Framingham Heart Study.
- Ethnic differences in the linkage disequilibrium and distribution of single-nucleotide polymorphisms in 35 candidate genes for cardiovascular diseases.
- Genotypes and haplotypes predisposing to myocardial infarction: a multilocus case-control study.
- Genome sequence of the Brown Norway rat yields insights into mammalian evolution.
- Threonine for alanine substitution in the eotaxin (CCL11) gene and the risk of incident myocardial infarction.
- A method for gene expression analysis by oligonucleotide arrays from minute biological materials.
- Pharmacogenetics: ethical problems and solutions.
- C-reactive protein gene polymorphisms and the incidence of post-angioplasty restenosis.
- Risk of coronary artery disease associated with polymorphism of the cytochrome P450 epoxygenase CYP2J2.
- Case-control association study of the close homologue of L1 (CHL1) gene and schizophrenia in the Chinese population.
- An expectation-maximization-likelihood-ratio test for handling missing data: application in experimental crosses.
- Effect of hepatic lipase -514C->T polymorphism and its interactions with apolipoprotein C3 -482C->T and apolipoprotein E exon 4 polymorphisms on the risk of nephropath...
- Pharmacogenetics and pharmacogenomics.
- Molecular genetics of pseudoxanthoma elasticum: type and frequency of mutations in ABCC6.
- Association between the brain-derived neurotrophic factor (BDNF) gene and schizophrenia in the Chinese population.
- Homocysteine, 5,10-methylenetetrahydrofolate reductase 677C>T polymorphism, nutrient intake, and incident cardiovascular disease in 24,968 initially healthy women.
- C-reactive protein gene variation and type 2 diabetes mellitus: a case-control study.
- Intercellular adhesion molecule 1 (ICAM1) Lys56Met and Gly241Arg gene variants, plasma-soluble ICAM1 concentrations, and risk of incident cardiovascular events in 23,0...
- Soluble epoxide hydrolase is a susceptibility factor for heart failure in a rat model of human disease.
- Association of four DNA polymorphisms with acute rejection after kidney transplantation.
- A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.
- Association study on the mitochondrial gene NDUFV2 and bipolar disorder in the Chinese Han population.
- The functional variant rs1048990 in PSMA6 is associated with susceptibility to myocardial infarction in a Chinese population.
- First evidence of association between G72 and bipolar disorder in the Chinese Han population.
- TAQIB and I405V polymorphisms of CETP are moderately associated with obesity risk in the Chinese adult population.
- Association study on the NAPG gene and bipolar disorder in the Chinese Han population.
- Association of two CETP polymorphisms with HDL levels in the Chinese obese population.
- The 1425G/A SNP in PRKCH is associated with ischemic stroke and cerebral hemorrhage in a Chinese population.
- The Val/Met functional polymorphism in COMT confers susceptibility to bipolar disorder: evidence from an association study and a meta-analysis.
- Association study between RGS4 and bipolar disorder in the Chinese Han population.
- Voluntary exploratory data submissions to the US FDA and the EMA: experience and impact.
- Positive association between GRIN2B gene and bipolar disorder in the Chinese Han Population.
- The common rs9939609 variant of the fat mass and obesity-associated gene is associated with obesity risk in children and adolescents of Beijing, China.
- A1166C genetic variation of the angiotensin II type I receptor gene and susceptibility to coronary heart disease: collaborative of 53 studies with 20,435 cases and 23,...
- Biomarkers: call on industry to share.
- From genomic databases to translation: a call to action.
- RapidChek SELECT Salmonella enteritidis test system for the detection of Salmonella enteritidis in poultry house drag swabs, shell egg pools, and chicken carcass rinsa...
- Impact of immunization technology and assay application on antibody performance--a systematic comparative evaluation.
- Localization of a gene for peripheral arterial occlusive disease to chromosome 1p31.
- Localization of a susceptibility gene for common forms of stroke to 5q12.
- A genome-wide search for genes affecting circulating fibrinogen levels in the Framingham Heart Study.
- Case-control association study of Disrupted-in-Schizophrenia-1 (DISC1) gene and schizophrenia in the Chinese population.
- Polymorphism in the beta2-adrenergic receptor and lipoprotein lipase genes as risk determinants for idiopathic venous thromboembolism: a multilocus, population-based, ...
- Pseudoxanthoma elasticum: evaluation of diagnostic criteria based on molecular data.
- Association of lipoprotein lipase S447X, apolipoprotein E exon 4, and apoC3 -455T>C polymorphisms on the susceptibility to diabetic nephropathy.
- [Relationship between alpha-ENaC gene Thr663Ala polymorphism and ischemic stroke].
- [Pharmacogenetics: forerunner for individualized medicine].
- Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem disease.
- Multi-locus candidate gene polymorphisms and risk of myocardial infarction: a population-based, prospective genetic analysis.
- Proteomic analysis of the cerebrospinal fluid of patients with schizophrenia.
- Preservation of gene expression ratios among multiple complex cDNAs after PCR amplification: application to differential gene expression studies.
- Lipid metabolism and occurrence of post-percutaneous transluminal coronary angioplasty restenosis: role of cholesteryl ester transfer protein and paraoxonase/arylester...
- Lack of association between the SOST gene and bone mineral density in perimenopausal women: analysis of five polymorphisms.
- A prospective evaluation of the angiotensin-converting enzyme D/I polymorphism and left ventricular remodeling in the ''Healing and Early Afterload Reducing Therapy'' ...
- Pharmacogenetics and the future of medical practice: conceptual considerations.
- Non-random chromosomal distribution of SSLPs: systematic assessment using a novel genetic linkage map between two closely related rat strains.
- Genetic linkage analysis in hypertension: principles and practice.
- Left ventricular remodeling after myocardial infarction: does the cardiac renin-angiotensin system play a role?
- Incremental reductions of positive charge within the S4 region of a voltage-gated K+ channel result in corresponding decreases in gating charge.
- Genetic variation in hypertensive and 'control' strains. What are we controlling for anyway?
- Tissue renin-angiotensin systems and their modulation: the heart as a paradigm for new aspects of converting enzyme inhibition.
- Genetic mapping of a gene causing hypertension in the stroke-prone spontaneously hypertensive rat.
- Chromosomal mapping of two genetic loci associated with blood-pressure regulation in hereditary hypertensive rats.
- The cardiac renin-angiotensin system: a synopsis of current experimental and clinical data.
- Genetic basis of hypertension. The renin-angiotensin paradigm.
- Structural alterations of the renin gene in stroke-prone spontaneously hypertensive rats: examination of genotype-phenotype correlations.
- The cardiac renin-angiotensin system. An appraisal of present experimental and clinical evidence.
- Transgenic rats: new animal models in hypertension research. Invited lecture.
- Molecular biology, endocrinology, and pharmacology of the cardiac renin-angiotensin system.
- Cardiac angiotensinogen and its local activation in the isolated perfused beating heart.
- Role of myocardial hypertrophy in trophic stimulation of indices of sympathetic cardiac innervation.
- DNA fingerprinting of spontaneously hypertensive and Wistar-Kyoto rats: implications for hypertension research.
- Cardiac renin-angiotensin system.
- Aspects of molecular biology and biochemistry of the cardiac renin-angiotensin system.
- The tissue renin-angiotensin system: a target for angiotensin-converting enzyme inhibitors.
- Role of beta 1-adrenoceptors in hypertensive cardiac hypertrophy.
- Effects of chronic progressive myocardial hypertrophy on indexes of cardiac autonomic innervation.
- Role of sodium in hypertensive cardiac hypertrophy.
- Tissue renin-angiotensin systems: focus on the heart.
- Endogenous tissue renin-angiotensin systems. From molecular biology to therapy.
- Tissue renin-angiotensin systems aspects of molecular biology and pharmacology.
- Tissue-specific regulation of gene expression for renin and angiotensinogen.
- Intracardiac generation of angiotensin and its physiologic role.
- Segmental necrotising enterocolitis: pathological and clinical features of 22 cases in Bangladesh.
- Acute ischemia as a contributing factor in torsade de pointes: treatment by coronary artery bypass grafting.
- Acute myocardial necrosis during administration of amsacrine.
Doctors Specialties
- Cardiology
Accepted Insurances
- First Health (Coventry Health Care) PPO
- MultiPlan PPO
- PHCS Network PPO
Education
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University of Iowa Hospitals and Clinics -
Leopold Franzen University Innsbruck Faculty of Medicine
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