| 1 | Title is missing! 2024 | | 5 | Citations (PDF) |
| 2 | <scp>MRAS</scp> in coronary artery disease—Unchartered territory | 2.9 | 2 | Citations (PDF) |
| 3 | MRASin coronary artery disease—Unchartered territory | 2.9 | 0 | Citations (PDF) |
| 4 | Identification of a functional missense variant in the matrix metallopeptidase 10 (MMP10) gene in two families with premature myocardial infarction | 3.4 | 0 | Citations (PDF) |
| 5 | GWAS breakthroughs: mapping the journey from one locus to 393 significant coronary artery disease associations | 5.5 | 19 | Citations (PDF) |
| 6 | Elucidation of the genetic causes of bicuspid aortic valve disease | 5.5 | 44 | Citations (PDF) |
| 7 | Genome-wide association studies of cardiovascular disease | 25.4 | 79 | Citations (PDF) |
| 8 | Homozygous frameshift variant in desmoglein 2 gene causes biventricular arrhythmogenic right ventricular cardiomyopathy | 2.1 | 3 | Citations (PDF) |
| 9 | The DZHK research platform: maximisation of scientific value by enabling access to health data and biological samples collected in cardiovascular clinical studies | 2.8 | 14 | Citations (PDF) |
| 10 | pyHeart4Fish: Chamber-specific heart phenotype quantification of zebrafish in high-content screens | 3.6 | 10 | Citations (PDF) |
| 11 | Female Gene Networks Are Expressed in Myofibroblast-Like Smooth Muscle Cells in Vulnerable Atherosclerotic Plaques | 6.0 | 29 | Citations (PDF) |
| 12 | Genetic insights into resting heart rate and its role in cardiovascular disease | 13.7 | 33 | Citations (PDF) |
| 13 | ADAMTS-7 Modulates Atherosclerotic Plaque Formation by Degradation of TIMP-1 | 13.1 | 48 | Citations (PDF) |
| 14 | Sex differences in the genetic and molecular mechanisms of coronary artery disease | 1.5 | 72 | Citations (PDF) |
| 15 | Autoantibodies against the chemokine receptor 3 predict cardiovascular risk | 2.2 | 23 | Citations (PDF) |
| 16 | Cis-epistasis at the LPA locus and risk of cardiovascular diseases | 5.5 | 27 | Citations (PDF) |
| 17 | Transcriptome-wide association study of coronary artery disease identifies novel susceptibility genes | 7.0 | 47 | Citations (PDF) |
| 18 | Genetically Determined Reproductive Aging and Coronary Heart Disease: A Bidirectional 2-sample Mendelian Randomization | 4.0 | 23 | Citations (PDF) |
| 19 | Wie wichtig ist die Kenntnis des genetischen Populationshintergrundes in der Medizin? Ein humangenetischer Beitrag vor dem Hintergrund der aktuellen Diskussion um die Verwendung des Begriffs „Rasse“ | 0.2 | 0 | Citations (PDF) |
| 20 | Sex matters? Sex matters! | 5.5 | 5 | Citations (PDF) |
| 21 | A novel MAP3K20 mutation causing centronuclear myopathy-6 with fiber-type disproportion in a Pakistani family | 2.0 | 5 | Citations (PDF) |
| 22 | Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants | 25.2 | 693 | Citations (PDF) |
| 23 | Current Developments of Clinical Sequencing and the Clinical Utility of Polygenic Risk Scores in Inflammatory Diseases | 4.9 | 5 | Citations (PDF) |
| 24 | sGC Activity and Regulation of Blood Flow in a Zebrafish Model System | 2.8 | 8 | Citations (PDF) |
| 25 | Unfolding and disentangling coronary vascular disease through genome-wide association studies | 2.2 | 2 | Citations (PDF) |
| 26 | Induced Pluripotent Stem Cells (iPSCs) in Vascular Research: from Two- to Three-Dimensional Organoids | 3.8 | 15 | Citations (PDF) |
| 27 | Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23 | 2.2 | 86 | Citations (PDF) |
| 28 | The CAD risk locus 9p21 increases the risk of vascular calcification in an iPSC-derived VSMC model | 6.6 | 7 | Citations (PDF) |
| 29 | A proteomic atlas of the neointima identifies novel druggable targets for preventive therapy | 2.2 | 23 | Citations (PDF) |
| 30 | Identification of two novel bullous pemphigoid- associated alleles, HLA-DQA1*05:05 and -DRB1*07:01, in Germans | 3.1 | 21 | Citations (PDF) |
| 31 | Effect of Differences in the Microbiome of Cyp17a1-Deficient Mice on Atherosclerotic Background | 4.6 | 5 | Citations (PDF) |
| 32 | The C5a/C5a receptor 1 axis controls tissue neovascularization through CXCL4 release from platelets | 13.7 | 51 | Citations (PDF) |
| 33 | A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family | 2.5 | 10 | Citations (PDF) |
| 34 | Identification of a Functional
PDE5A
Variant at the Chromosome 4q27 Coronary Artery Disease Locus in an Extended Myocardial Infarction Family | 18.0 | 16 | Citations (PDF) |
| 35 | What can we learn from common variants associated with unexpected phenotypes in rare genetic diseases? | 3.1 | 2 | Citations (PDF) |
| 36 | The power of genetic diversity in genome-wide association studies of lipids | 37.9 | 923 | Citations (PDF) |
| 37 | Long-term prevention after myocardial infarction in young patients ≤45 years: the Intensive Prevention Program in the Young (IPP-Y) study | 2.0 | 10 | Citations (PDF) |
| 38 | Polygenic risk scores outperform machine learning methods in predicting coronary artery disease status | 3.1 | 41 | Citations (PDF) |
| 39 | Osteoclast imbalance in primary familial brain calcification: evidence for its role in brain calcification | 8.4 | 4 | Citations (PDF) |
| 40 | Heterozygous
ABCG5
Gene Deficiency and Risk of Coronary Artery Disease | 2.9 | 68 | Citations (PDF) |
| 41 | Studies in Zebrafish Demonstrate That CNNM2 and NT5C2 Are Most Likely the Causal Genes at the Blood Pressure-Associated Locus on Human Chromosome 10q24.32 | 2.4 | 22 | Citations (PDF) |
| 42 | Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus | 2.9 | 10 | Citations (PDF) |
| 43 | Qtlizer: comprehensive QTL annotation of GWAS results | 3.4 | 31 | Citations (PDF) |
| 44 | Mendelian randomization analysis does not support causal associations of birth weight with hypertension risk and blood pressure in adulthood | 5.3 | 12 | Citations (PDF) |
| 45 | CYP17A1 deficient XY mice display susceptibility to atherosclerosis, altered lipidomic profile and atypical sex development | 3.4 | 42 | Citations (PDF) |
| 46 | Evaluating drug targets through human loss-of-function genetic variation | 37.9 | 183 | Citations (PDF) |
| 47 | The mutational constraint spectrum quantified from variation in 141,456 humans | 37.9 | 9,351 | Citations (PDF) |
| 48 | Transcript expression-aware annotation improves rare variant interpretation | 37.9 | 191 | Citations (PDF) |
| 49 | Genomewide Association Study of Severe Covid-19 with Respiratory Failure | 34.5 | 1,834 | Citations (PDF) |
| 50 | White Blood Cells and Blood Pressure | 18.0 | 191 | Citations (PDF) |
| 51 | Dare to Compare. Development of Atherosclerotic Lesions in Human, Mouse, and Zebrafish | 2.4 | 25 | Citations (PDF) |
| 52 | miR-128a Acts as a Regulator in Cardiac Development by Modulating Differentiation of Cardiac Progenitor Cell Populations | 4.4 | 17 | Citations (PDF) |
| 53 | Genetics of educational attainment and coronary risk in Mendelian randomization studies | 2.2 | 7 | Citations (PDF) |
| 54 | Sharing lessons learnt across European cardiovascular research consortia | 6.6 | 1 | Citations (PDF) |
| 55 | A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease | 3.2 | 159 | Citations (PDF) |
| 56 | New technologies for intensive prevention programs after myocardial infarction: rationale and design of the NET-IPP trial | 2.8 | 9 | Citations (PDF) |
| 57 | Population Bias in Polygenic Risk Prediction Models for Coronary Artery Disease | 2.9 | 42 | Citations (PDF) |
| 58 | Associations of autozygosity with a broad range of human phenotypes | 13.7 | 120 | Citations (PDF) |
| 59 | LDL triglycerides, hepatic lipase activity, and coronary artery disease: An epidemiologic and Mendelian randomization study | 1.5 | 45 | Citations (PDF) |
| 60 | CARDIoGRAM celebrates its 10th Anniversary | 2.2 | 5 | Citations (PDF) |
| 61 | Genetically modulated educational attainment and coronary disease risk | 2.2 | 38 | Citations (PDF) |
| 62 | Rare Protein-Truncating Variants in
APOB
, Lower Low-Density Lipoprotein Cholesterol, and Protection Against Coronary Heart Disease | 2.9 | 69 | Citations (PDF) |
| 63 | MicroRNAs and regulation of cardiometabolic phenotypes: novel insights into the complexity of genome-wide association studies loci | 5.5 | 1 | Citations (PDF) |
| 64 | A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A | 3.4 | 20 | Citations (PDF) |
| 65 | Assessing the causal association of glycine with risk of cardio-metabolic diseases | 13.7 | 132 | Citations (PDF) |
| 66 | Association of the coronary artery disease risk gene GUCY1A3 with ischaemic events after coronary intervention | 5.5 | 22 | Citations (PDF) |
| 67 | Polymorphisms in the Mitochondrial Genome Are Associated With Bullous Pemphigoid in Germans | 4.9 | 11 | Citations (PDF) |
| 68 | DNA Sequence Variation in ACVR1C Encoding the Activin Receptor-Like Kinase 7 Influences Body Fat Distribution and Protects Against Type 2 Diabetes | 4.2 | 48 | Citations (PDF) |
| 69 | Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection | 2.3 | 182 | Citations (PDF) |
| 70 | Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targets | 3.4 | 47 | Citations (PDF) |
| 71 | Genome-Wide Association and Functional Studies Identify
SCML4
and
THSD7A
as Novel Susceptibility Genes for Coronary Artery Disease | 6.0 | 44 | Citations (PDF) |
| 72 | Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease | 13.7 | 96 | Citations (PDF) |
| 73 | Etidronate prevents dystrophic cardiac calcification by inhibiting macrophage aggregation | 3.4 | 20 | Citations (PDF) |
| 74 | A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis | 2.9 | 20 | Citations (PDF) |
| 75 | Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide Signaling | 18.0 | 111 | Citations (PDF) |
| 76 | Studies in zebrafish annotate CNNM2 and NT5C2 as the most likely causal genes at the blood pressure locus on chromosome 10Q24.32 | 1.5 | 2 | Citations (PDF) |
| 77 | Association of Genetic Variation at AQP4 Locus with Vascular Depression | 4.2 | 20 | Citations (PDF) |
| 78 | Lp-PLA2, scavenger receptor class B type I gene (SCARB1) rs10846744 variant, and cardiovascular disease | 2.3 | 4 | Citations (PDF) |
| 79 | Genetic Susceptibility Loci for Cardiovascular Disease and Their Impact on Atherosclerotic Plaques | 2.9 | 26 | Citations (PDF) |
| 80 | Druggability of Coronary Artery Disease Risk Loci | 2.9 | 20 | Citations (PDF) |
| 81 | Genome-wide association meta-analysis of coronary artery disease and periodontitis reveals a novel shared risk locus | 3.4 | 49 | Citations (PDF) |
| 82 | Mental Health and Psychosocial Functioning Over the Lifespan of German Patients Undergoing Cardiac Catheterization for Coronary Artery Disease | 2.4 | 4 | Citations (PDF) |
| 83 | Utilization of Mental Health Care, Treatment Patterns, and Course of Psychosocial Functioning in Northern German Coronary Artery Disease Patients with Depressive and/or Anxiety Disorders | 2.4 | 7 | Citations (PDF) |
| 84 | Reversal of Aging‐Induced Increases in Aortic Stiffness by Targeting Cytoskeletal Protein‐Protein Interfaces | 4.0 | 25 | Citations (PDF) |
| 85 | Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci | 3.0 | 76 | Citations (PDF) |
| 86 | CD163+ macrophages promote angiogenesis and vascular permeability accompanied by inflammation in atherosclerosis | 10.6 | 303 | Citations (PDF) |
| 87 | Genome-wide association study in takotsubo syndrome — Preliminary results and future directions | 2.2 | 40 | Citations (PDF) |
| 88 | Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease | 2.3 | 248 | Citations (PDF) |
| 89 | Pyrophosphate Supplementation Prevents Chronic and Acute Calcification in ABCC6-Deficient Mice | 3.4 | 77 | Citations (PDF) |
| 90 | Sex in basic research: concepts in the cardiovascular field | 5.5 | 141 | Citations (PDF) |
| 91 | Functional Characterization of the
GUCY1A3
Coronary Artery Disease Risk Locus | 18.0 | 100 | Citations (PDF) |
| 92 | Loss of Cardioprotective Effects at the
ADAMTS7
Locus as a Result of Gene-Smoking Interactions | 18.0 | 62 | Citations (PDF) |
| 93 | A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis | 2.9 | 109 | Citations (PDF) |
| 94 | Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms | 25.2 | 317 | Citations (PDF) |
| 95 | Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease | 4.0 | 111 | Citations (PDF) |
| 96 | ANGPTL3 Deficiency and Protection Against Coronary Artery Disease | 2.3 | 449 | Citations (PDF) |
| 97 | Additional Candidate Genes for Human Atherosclerotic Disease Identified Through Annotation Based on Chromatin Organization | 3.8 | 22 | Citations (PDF) |
| 98 | PSeudoautosomal region 1 and predisposition to coronary artery disease | 1.5 | 0 | Citations (PDF) |
| 99 | Genetic and functional interaction of the coronary artery disease risk gene ADAMTS7 with LDL-cholesterol | 1.5 | 0 | Citations (PDF) |
| 100 | A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors | 3.4 | 20 | Citations (PDF) |
| 101 | Coronary artery disease associated gene Phactr1 modulates severity of vascular calcification in vitro | 2.1 | 40 | Citations (PDF) |
| 102 | Association analyses based on false discovery rate implicate new loci for coronary artery disease | 25.2 | 699 | Citations (PDF) |
| 103 | [OP.2A.04] EPIGENETIC REGULATION OF HYPERTENSION | 2.1 | 0 | Citations (PDF) |
| 104 | Rheumatoid Arthritis and Coronary Artery Disease: Genetic Analyses Do Not Support a Causal Relation | 2.3 | 9 | Citations (PDF) |
| 105 | Association of NOS3 gene polymorphisms with essential hypertension in Sudanese patients: a case control study | 1.8 | 41 | Citations (PDF) |
| 106 | Genomic correlates of glatiramer acetate adverse cardiovascular effects lead to a novel locus mediating coronary risk | 2.3 | 5 | Citations (PDF) |
| 107 | Common and Rare Genetic Variation in
CCR2
,
CCR5
, or
CX3CR1
and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic Traits | 3.8 | 24 | Citations (PDF) |
| 108 | Coding Variation in
ANGPTL4,
LPL,
and
SVEP1
and the Risk of Coronary Disease | 34.5 | 491 | Citations (PDF) |
| 109 | Cystatin C and Cardiovascular Disease | 2.3 | 138 | Citations (PDF) |
| 110 | Genetic determinants controlling lipid deposits in different wild type strains of zebrafish (Danio rerio) | 1.5 | 0 | Citations (PDF) |
| 111 | Coronary Artery Ectasia Are Frequently Observed in Patients With Bicuspid Aortic Valves With and Without Dilatation of the Ascending Aorta | 4.8 | 24 | Citations (PDF) |
| 112 | The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals | 25.2 | 416 | Citations (PDF) |
| 113 | Proatherosclerotic Effect of the α1-Subunit of Soluble Guanylyl Cyclase by Promoting Smooth Muscle Phenotypic Switching | 3.4 | 22 | Citations (PDF) |
| 114 | No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis | 3.4 | 32 | Citations (PDF) |
| 115 | A genomic approach to therapeutic target validation identifies a glucose-lowering
GLP1R
variant protective for coronary heart disease | 12.5 | 113 | Citations (PDF) |
| 116 | Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals | 6.5 | 91 | Citations (PDF) |
| 117 | Serum microRNA-1233 is a specific biomarker for diagnosing acute pulmonary embolism | 6.4 | 41 | Citations (PDF) |
| 118 | Stimulators of the soluble guanylyl cyclase: promising functional insights from rare coding atherosclerosis-related GUCY1A3 variants | 7.0 | 21 | Citations (PDF) |
| 119 | Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease | 36.3 | 519 | Citations (PDF) |
| 120 | Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function | 13.7 | 507 | Citations (PDF) |
| 121 | Genome-wide association study and targeted metabolomics identifies sex-specific association of CPS1 with coronary artery disease | 13.7 | 133 | Citations (PDF) |
| 122 | Classification of ADAMTS binding sites: The first step toward selective ADAMTS7 inhibitors | 2.1 | 10 | Citations (PDF) |
| 123 | Molecular Variants of Soluble Guanylyl Cyclase Affecting Cardiovascular Risk | 1.7 | 11 | Citations (PDF) |
| 124 | The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study | 3.2 | 402 | Citations (PDF) |
| 125 | Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation | 3.2 | 84 | Citations (PDF) |
| 126 | Identification of a single SNP that affects the LH-beta promoter activity in the Moroccan prolific D'man breed1 | 0.7 | 5 | Citations (PDF) |
| 127 | Systems Genetics Analysis of Genome-Wide Association Study Reveals Novel Associations Between Key Biological Processes and Coronary Artery Disease | 6.0 | 81 | Citations (PDF) |
| 128 | Genetic variants associated with celiac disease and the risk for coronary artery disease | 1.9 | 11 | Citations (PDF) |
| 129 | Dissecting the Roles of MicroRNAs in Coronary Heart Disease via Integrative Genomic Analyses | 6.0 | 58 | Citations (PDF) |
| 130 | Genetic studies of body mass index yield new insights for obesity biology | 37.9 | 4,533 | Citations (PDF) |
| 131 | Psoriasis and Cardiometabolic Traits: Modest Association but Distinct Genetic Architectures | 2.3 | 62 | Citations (PDF) |
| 132 | New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3) | 3.0 | 84 | Citations (PDF) |
| 133 | Shared Genetic Aetiology of Coronary Artery Disease and Atherosclerotic Stroke—2015 | 4.7 | 8 | Citations (PDF) |
| 134 | Genetic variants primarily associated with type 2 diabetes are related to coronary artery disease risk | 1.5 | 28 | Citations (PDF) |
| 135 | Runs of Homozygosity: Association with Coronary Artery Disease and Gene Expression in Monocytes and Macrophages | 6.5 | 44 | Citations (PDF) |
| 136 | Two polymorphisms in the Cx40 promoter are associated with hypertension and left ventricular hypertrophy preferentially in men | 3.1 | 9 | Citations (PDF) |
| 137 | Role of sGC-dependent NO signalling and myocardial infarction risk | 3.7 | 26 | Citations (PDF) |
| 138 | Genetic Evidence for
PLASMINOGEN
as a Shared Genetic Risk Factor of Coronary Artery Disease and Periodontitis | 3.8 | 88 | Citations (PDF) |
| 139 | The impact of low-frequency and rare variants on lipid levels | 25.2 | 348 | Citations (PDF) |
| 140 | ADAMTS-7 Inhibits Re-endothelialization of Injured Arteries and Promotes Vascular Remodeling Through Cleavage of Thrombospondin-1 | 18.0 | 153 | Citations (PDF) |
| 141 | Genetically Determined Height and Coronary Artery Disease | 34.5 | 249 | Citations (PDF) |
| 142 | Circulating Brain‐Derived Neurotrophic Factor Concentrations and the Risk of Cardiovascular Disease in the Community | 4.0 | 134 | Citations (PDF) |
| 143 | Identification of a novel ovine LH-beta promoter region, which dramatically enhances its promoter activity | 1.4 | 0 | Citations (PDF) |
| 144 | Prediction of Causal Candidate Genes in Coronary Artery Disease Loci | 6.0 | 122 | Citations (PDF) |
| 145 | Expression Quantitative Trait Loci Acting Across Multiple Tissues Are Enriched in Inherited Risk for Coronary Artery Disease | 3.8 | 41 | Citations (PDF) |
| 146 | A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease | 25.2 | 2,524 | Citations (PDF) |
| 147 | Genetic analysis for a shared biological basis between migraine and coronary artery disease | 2.8 | 69 | Citations (PDF) |
| 148 | Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction | 3.0 | 82 | Citations (PDF) |
| 149 | Knock-out of nexilin in mice leads to dilated cardiomyopathy and endomyocardial fibroelastosis | 7.0 | 42 | Citations (PDF) |
| 150 | MicroRNA Profile of Nkx2.5 Enhancer Positive Cardiac Progenitor Cells | 0.3 | 0 | Citations (PDF) |
| 151 | Changes in the Concentration of Insulin-Like Growth Factor I and Transforming Growth Factor β1 in Rat Femoral Bone during Growth | 2.8 | 1 | Citations (PDF) |
| 152 | Cigarette smoking reduces DNA methylation levels at multiple genomic loci but the effect is partially reversible upon cessation | 3.0 | 318 | Citations (PDF) |
| 153 | Integrative Genomics Reveals Novel Molecular Pathways and Gene Networks for Coronary Artery Disease | 3.2 | 202 | Citations (PDF) |
| 154 | Coronary Heart Disease-Associated Variation in TCF21 Disrupts a miR-224 Binding Site and miRNA-Mediated Regulation | 3.2 | 115 | Citations (PDF) |
| 155 | Bedeutung moderner Genomstudien für das Herzinfarktrisiko | 0.4 | 2 | Citations (PDF) |
| 156 | Genetische Analysen als Basis einer individualisierten Medizin bei koronarer Herzkrankheit | 0.7 | 2 | Citations (PDF) |
| 157 | DNA methylation and body-mass index: a genome-wide analysis | 62.1 | 754 | Citations (PDF) |
| 158 | Shared Genetic Susceptibility to Ischemic Stroke and Coronary Artery Disease | 5.9 | 333 | Citations (PDF) |
| 159 | How to Include Chromosome X in Your Genome‐Wide Association Study | 3.1 | 111 | Citations (PDF) |
| 160 | Inactivating Mutations in NPC1L1 and Protection from Coronary Heart Disease | 34.5 | 412 | Citations (PDF) |
| 161 | Ultrahigh-resolution, high-speed spectral domain optical coherence phase microscopy | 3.0 | 26 | Citations (PDF) |
| 162 | Genome-Wide Association Study of
l
-Arginine and Dimethylarginines Reveals Novel Metabolic Pathway for Symmetric Dimethylarginine | 3.8 | 59 | Citations (PDF) |
| 163 | Novel Genetic Approach to Investigate the Role of Plasma Secretory Phospholipase A2 (sPLA
2
)-V Isoenzyme in Coronary Heart Disease | 3.8 | 23 | Citations (PDF) |
| 164 | Whole-exome sequencing in an extended family with myocardial infarction unmasks familial hypercholesterolemia | 2.0 | 20 | Citations (PDF) |
| 165 | Defining the role of common variation in the genomic and biological architecture of adult human height | 25.2 | 1,982 | Citations (PDF) |
| 166 | SPG7 Variant Escapes Phosphorylation-Regulated Processing by AFG3L2, Elevates Mitochondrial ROS, and Is Associated with Multiple Clinical Phenotypes | 6.3 | 43 | Citations (PDF) |
| 167 | Loss-of-Function Mutations inAPOC3,Triglycerides, and Coronary Disease | 34.5 | 1,088 | Citations (PDF) |
| 168 | Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction | 37.9 | 635 | Citations (PDF) |
| 169 | Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant Statistics | 6.5 | 65 | Citations (PDF) |
| 170 | Dysfunctional nitric oxide signalling increases risk of myocardial infarction | 37.9 | 263 | Citations (PDF) |
| 171 | Tippfehler im Genom: erbliche Ursachen von Herzerkrankungen | 0.1 | 0 | Citations (PDF) |
| 172 | Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease | 4.7 | 194 | Citations (PDF) |
| 173 | Forty-five years to diagnosis | 0.7 | 10 | Citations (PDF) |
| 174 | Identification of seven loci affecting mean telomere length and their association with disease | 25.2 | 914 | Citations (PDF) |
| 175 | Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture | 25.2 | 659 | Citations (PDF) |
| 176 | Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders | 25.2 | 309 | Citations (PDF) |
| 177 | Genetics of Coronary Artery Disease and Myocardial Infarction - 2013 | 2.9 | 53 | Citations (PDF) |
| 178 | Functional Interaction of Osteogenic Transcription Factors Runx2 and Vdr in Transcriptional Regulation of Opn during Soft Tissue Calcification | 3.4 | 26 | Citations (PDF) |
| 179 | Genetic Predisposition to Higher Blood Pressure Increases Coronary Artery Disease Risk | 6.6 | 74 | Citations (PDF) |
| 180 | Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits | 3.2 | 423 | Citations (PDF) |
| 181 | Genome-Wide Haplotype Analysis of Cis Expression Quantitative Trait Loci in Monocytes | 3.2 | 55 | Citations (PDF) |
| 182 | Multiethnic Meta-Analysis of Genome-Wide Association Studies in >100 000 Subjects Identifies 23 Fibrinogen-Associated Loci but No Strong Evidence of a Causal Association Between Circulating Fibrinogen and Cardiovascular Disease | 18.0 | 142 | Citations (PDF) |
| 183 | Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia | 6.0 | 96 | Citations (PDF) |
| 184 | Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia | 2.9 | 23 | Citations (PDF) |
| 185 | MRas- knock-out mouse: B-cell phenotype and reduced macrophage infiltration in atherosclerotic plaques at the aortic root | 2.2 | 3 | Citations (PDF) |
| 186 | Association of two polymorphisms in the Cx40 promoter with hypertension and leftventricular hypertrophy | 0.6 | 0 | Citations (PDF) |
| 187 | Alterations in the nitric oxide / soluble guanylyl cyclase pathway enhance the risk of myocardial infarction | 0.6 | 0 | Citations (PDF) |
| 188 | Molecular Signatures of Cardiovascular Disease Risk | 3.7 | 5 | Citations (PDF) |
| 189 | The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits | 3.2 | 464 | Citations (PDF) |
| 190 | Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals | 3.2 | 458 | Citations (PDF) |
| 191 | Clinical and Genetic Association of Serum Paraoxonase and Arylesterase Activities With Cardiovascular Risk | 6.0 | 168 | Citations (PDF) |
| 192 | Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate gene | 2.9 | 104 | Citations (PDF) |
| 193 | Common Genetic Variation in the 3′-
BCL11B
Gene Desert Is Associated With Carotid-Femoral Pulse Wave Velocity and Excess Cardiovascular Disease Risk | 3.8 | 97 | Citations (PDF) |
| 194 | Identification of the
BCAR1-CFDP1-TMEM170A
Locus as a Determinant of Carotid Intima-Media Thickness and Coronary Artery Disease Risk | 3.8 | 52 | Citations (PDF) |
| 195 | Erbliche Grundlagen der KHK | 0.0 | 1 | Citations (PDF) |
| 196 | Inheritance of coronary artery disease in men: an analysis of the role of the Y chromosome | 62.1 | 198 | Citations (PDF) |
| 197 | Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies | 62.1 | 791 | Citations (PDF) |
| 198 | Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study | 62.1 | 2,144 | Citations (PDF) |
| 199 | Genome-wide meta-analysis of common variant differences between men and women | 2.9 | 39 | Citations (PDF) |
| 200 | FTO genotype is associated with phenotypic variability of body mass index | 37.9 | 432 | Citations (PDF) |
| 201 | Genetic Markers Enhance Coronary Risk Prediction in Men: The MORGAM Prospective Cohorts | 2.3 | 84 | Citations (PDF) |
| 202 | A Genome-Wide Association Study for Coronary Artery Disease Identifies a Novel Susceptibility Locus in the Major Histocompatibility Complex | 3.8 | 130 | Citations (PDF) |
| 203 | Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease | 25.2 | 325 | Citations (PDF) |
| 204 | Large-scale association analysis identifies new risk loci for coronary artery disease | 25.2 | 1,573 | Citations (PDF) |
| 205 | Comprehensive Exploration of the Effects of miRNA SNPs on Monocyte Gene Expression | 2.3 | 9 | Citations (PDF) |
| 206 | Powerful Identification of Cis-regulatory SNPs in Human Primary Monocytes Using Allele-Specific Gene Expression | 2.3 | 38 | Citations (PDF) |
| 207 | A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy | 2.2 | 345 | Citations (PDF) |
| 208 | Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk | 37.9 | 2,008 | Citations (PDF) |
| 209 | New gene functions in megakaryopoiesis and platelet formation | 37.9 | 428 | Citations (PDF) |
| 210 | Human metabolic individuality in biomedical and pharmaceutical research | 37.9 | 1,000 | Citations (PDF) |
| 211 | Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies | 62.1 | 518 | Citations (PDF) |
| 212 | Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease | 25.2 | 1,836 | Citations (PDF) |
| 213 | Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23 | 2.2 | 136 | Citations (PDF) |
| 214 | A Genome-Wide Association Study Identifies
LIPA
as a Susceptibility Gene for Coronary Artery Disease | 3.8 | 149 | Citations (PDF) |
| 215 | Novel Correlations Between the Genotype and the Phenotype of Hypertrophic and Dilated Cardiomyopathy: Results from the German Competence Network Heart Failure | 7.3 | 79 | Citations (PDF) |
| 216 | Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure | 25.2 | 424 | Citations (PDF) |
| 217 | Integrating Genome-Wide Genetic Variations and Monocyte Expression Data Reveals Trans-Regulated Gene Modules in Humans | 3.2 | 137 | Citations (PDF) |
| 218 | RANTES/CCL5 and Risk for Coronary Events: Results from the MONICA/KORA Augsburg Case-Cohort, Athero-Express and CARDIoGRAM Studies | 2.3 | 47 | Citations (PDF) |
| 219 | Biological, clinical and population relevance of 95 loci for blood lipids | 37.9 | 3,470 | Citations (PDF) |
| 220 | A trans-acting locus regulates an anti-viral expression network and type 1 diabetes risk | 37.9 | 283 | Citations (PDF) |
| 221 | Hundreds of variants clustered in genomic loci and biological pathways affect human height | 37.9 | 1,887 | Citations (PDF) |
| 222 | Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index | 25.2 | 2,795 | Citations (PDF) |
| 223 | Identifizierung von Risikogenen für den Herzinfarkt durch genomweite Assoziationsstudien | 0.8 | 1 | Citations (PDF) |
| 224 | Common Variants at 10 Genomic Loci Influence Hemoglobin A1C Levels via Glycemic and Nonglycemic Pathways | 4.2 | 427 | Citations (PDF) |
| 225 | Genetics of myocardial infarction: a progress report | 2.2 | 94 | Citations (PDF) |
| 226 | Genetic Association Study Identifies HSPB7 as a Risk Gene for Idiopathic Dilated Cardiomyopathy | 3.2 | 121 | Citations (PDF) |
| 227 | Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control Studies | 2.3 | 87 | Citations (PDF) |
| 228 | Genetic Regulation of Serum Phytosterol Levels and Risk of Coronary Artery Disease | 3.8 | 153 | Citations (PDF) |
| 229 | 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 | 1.5 | 149 | Citations (PDF) |
| 230 | Myeloid CD34+CD13+ Precursor Cells Transdifferentiate into Chondrocyte-Like Cells in Atherosclerotic Intimal Calcification | 3.4 | 35 | Citations (PDF) |
| 231 | Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study | 3.8 | 170 | Citations (PDF) |
| 232 | Genetic risk stratification in patients undergoing coronary artery bypass graft (CABG) surgery: relative allele frequencies of leading SNPs associated with CAD/MI | 0.3 | 0 | Citations (PDF) |
| 233 | Genetic Variants Associated With Cardiac Structure and Function | 16.5 | 215 | Citations (PDF) |
| 234 | Genetic Loci Associated With C-Reactive Protein Levels and Risk of Coronary Heart Disease | 16.5 | 586 | Citations (PDF) |
| 235 | A Genome-Wide Association Study Reveals Variants in ARL15 that Influence Adiponectin Levels | 3.2 | 156 | Citations (PDF) |
| 236 | Genetic Determinants of Circulating Sphingolipid Concentrations in European Populations | 3.2 | 204 | Citations (PDF) |
| 237 | Genetik des Herzinfarktes. Der lange Weg von der positiven Familienanamnese zum Gen | 0.2 | 0 | Citations (PDF) |
| 238 | The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts | 3.1 | 79 | Citations (PDF) |
| 239 | Genetic basis of myocardial infarction: Novel insights from genome-wide association studies | 1.7 | 2 | Citations (PDF) |
| 240 | New susceptibility locus for coronary artery disease on chromosome 3q22.3 | 25.2 | 449 | Citations (PDF) |
| 241 | Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease | 25.2 | 449 | Citations (PDF) |
| 242 | A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium | 25.2 | 509 | Citations (PDF) |
| 243 | Nexilin mutations destabilize cardiac Z-disks and lead to dilated cardiomyopathy | 33.0 | 206 | Citations (PDF) |
| 244 | Polymorphisms in the promoter region of the dimethylarginine dimethylaminohydrolase 2 gene are associated with prevalence of hypertension | 9.1 | 30 | Citations (PDF) |
| 245 | Lack of Association Between a Common Polymorphism Near the INSIG2 Gene and BMI, Myocardial Infarction, and Cardiovascular Risk Factors | 4.0 | 12 | Citations (PDF) |
| 246 | Macrophage cholesterol efflux correlates with lipoprotein subclass distribution and risk of obstructive coronary artery disease in patients undergoing coronary angiography | 3.8 | 32 | Citations (PDF) |
| 247 | A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and functionBlood, 2009, 113, 3831-3837 | 4.8 | 120 | Citations (PDF) |
| 248 | Common Polymorphisms Influencing Serum Uric Acid Levels Contribute to Susceptibility to Gout, but Not to Coronary Artery Disease | 2.3 | 99 | Citations (PDF) |
| 249 | Systematic pathway-analysis of kinesin protein family (KIF) using genome-wide SNP data in patients with myocardial infarction: Genetic variation in KIFC3 gene associates with myocardial infarction | 0.3 | 0 | Citations (PDF) |
| 250 | Common polymorphisms in the cannabinoid CB2 receptor gene (CNR2) are not associated with myocardial infarction and cardiovascular risk factors | 4.4 | 6 | Citations (PDF) |
| 251 | Die Herzinsuffizienz als komplexe genetische Erkrankung | 0.4 | 3 | Citations (PDF) |
| 252 | Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction | 3.7 | 8 | Citations (PDF) |
| 253 | 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 | 3.7 | 90 | Citations (PDF) |
| 254 | Coronary Artery Disease–Associated Locus on Chromosome 9p21 and Early Markers of Atherosclerosis | 6.0 | 81 | Citations (PDF) |
| 255 | SNPtoGO: characterizing SNPs by enriched GO terms | 4.7 | 28 | Citations (PDF) |
| 256 | An Alternative Splice Variant in Abcc6, the Gene Causing Dystrophic Calcification, Leads to Protein Deficiency in C3H/He Mice | 2.2 | 59 | Citations (PDF) |
| 257 | Characterization of the GNAQ promoter and association of increased Gq expression with cardiac hypertrophy in humans | 2.2 | 36 | Citations (PDF) |
| 258 | Lack of Association Between the
MEF2A
Gene and Myocardial Infarction | 18.0 | 45 | Citations (PDF) |
| 259 | Repeated Replication and a Prospective Meta-Analysis of the Association Between Chromosome 9p21.3 and Coronary Artery Disease | 18.0 | 364 | Citations (PDF) |
| 260 | Association between PPARα gene polymorphisms and myocardial infarction | 6.2 | 18 | Citations (PDF) |
| 261 | Genetic variation in the arachidonate 5-lipoxygenase-activating protein (ALOX5AP) is associated with myocardial infarction in the German population | 6.2 | 33 | Citations (PDF) |
| 262 | Association of Common Polymorphisms in GLUT9 Gene with Gout but Not with Coronary Artery Disease in a Large Case-Control Study | 2.3 | 77 | Citations (PDF) |
| 263 | 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 | 2.3 | 154 | Citations (PDF) |
| 264 | Ultrafine mapping of Dyscalc1 to an 80-kb chromosomal segment on chromosome 7 in mice susceptible for dystrophic calcification | 2.4 | 26 | Citations (PDF) |
| 265 | Genomewide Association Analysis of Coronary Artery Disease | 34.5 | 1,955 | Citations (PDF) |
| 266 | Familial aggregation of left main coronary artery disease and future risk of coronary events in asymptomatic siblings of affected patients | 2.2 | 52 | Citations (PDF) |
| 267 | Epistatic interaction between haplotypes of the ghrelin ligand and receptor genes influence susceptibility to myocardial infarction and coronary artery disease | 2.9 | 36 | Citations (PDF) |
| 268 | The common Y402H variant in complement factor H gene is not associated with susceptibility to myocardial infarction and its related risk factors | 6.2 | 24 | Citations (PDF) |
| 269 | Association between arterial pressure and coronary artery calcification | 2.1 | 26 | Citations (PDF) |
| 270 | Impact of Diabetes on QT Dynamicity in Patients With and Without Myocardial Infarction: The KORA Family Heart Study | 1.1 | 5 | Citations (PDF) |
| 271 | Robust association of the APOE ?4 allele with premature myocardial infarction especially in patients without hypercholesterolaemia: the Aachen study | 3.0 | 15 | Citations (PDF) |
| 272 | Lymphotoxin-α and galectin-2 SNPs are not associated with myocardial infarction in two different German populations | 3.7 | 25 | Citations (PDF) |
| 273 | A locus on chromosome 10 influences C-reactive protein levels in two independent populations | 2.9 | 9 | Citations (PDF) |
| 274 | Genetik der koronaren Herzkrankheit und des Herzinfarkts | 0.2 | 0 | Citations (PDF) |
| 275 | Novel missense mutations (p.T596M and p.P1797H) in NOTCH1 in patients with bicuspid aortic valve | 2.1 | 219 | Citations (PDF) |
| 276 | No association of the CYP3A5*1 allele with blood pressure and left ventricular mass and geometry: the KORA/MONICA Augsburg echocardiographic substudy | 6.2 | 12 | Citations (PDF) |
| 277 | Association of a functional polymorphism in the CYP4A11 gene with systolic blood pressure in survivors of myocardial infarction | 2.1 | 43 | Citations (PDF) |
| 278 | Arterial calcification in mice after freeze-thaw injury | 1.5 | 13 | Citations (PDF) |
| 279 | Genetic Factors for Overweight and CAD | 0.7 | 10 | Citations (PDF) |
| 280 | Association of low-grade urinary albumin excretion with left ventricular hypertrophy in the general population | 0.8 | 76 | Citations (PDF) |
| 281 | Association of the Ghrelin Receptor Gene Region With Left Ventricular Hypertrophy in the General Population | 6.6 | 27 | Citations (PDF) |
| 282 | Genetics and heritability of coronary artery disease and myocardial infarction | 2.8 | 135 | Citations (PDF) |
| 283 | Hypertrophe Kardiomyopathie | 0.7 | 16 | Citations (PDF) |
| 284 | Intronic ANG II type 2 receptor gene polymorphism 1675 G/A modulates receptor protein expression but not mRNA splicing | 2.4 | 36 | Citations (PDF) |
| 285 | Ahnak is critical for cardiac Ca(v)1.2 calcium channel function and its β‐adrenergic regulation | 0.6 | 73 | Citations (PDF) |
| 286 | Association of the T8590C Polymorphism of
CYP4A11
With Hypertension in the MONICA Augsburg Echocardiographic Substudy | 6.6 | 81 | Citations (PDF) |
| 287 | Distinct Heritable Patterns of Angiographic Coronary Artery Disease in Families With Myocardial Infarction | 18.0 | 165 | Citations (PDF) |
| 288 | Association of angiotensin-converting enzyme 2 (ACE2) gene polymorphisms with parameters of left ventricular hypertrophy in men | 3.7 | 99 | Citations (PDF) |
| 289 | The assertion that a G21V mutation in AGTR2 causes mental retardation is not supported by other studies | 2.9 | 11 | Citations (PDF) |
| 290 | KCNJ11 polymorphisms and sudden cardiac death in patients with acute myocardial infarction | 3.8 | 28 | Citations (PDF) |
| 291 | No association of interleukin-6 gene polymorphism (−174 G/C) with myocardial infarction or traditional cardiovascular risk factors | 2.2 | 72 | Citations (PDF) |
| 292 | Lack of association of a 9 bp insertion/deletion polymorphism within the bradykinin 2 receptor gene with myocardial infarction | 6.2 | 12 | Citations (PDF) |
| 293 | Mutation spectrum in a large cohort of unrelated consecutive patients with hypertrophic cardiomyopathy | 2.1 | 214 | Citations (PDF) |
| 294 | Angiotensin converting enzyme gene polymorphism and myocardial infarction a large association and linkage study | 2.6 | 19 | Citations (PDF) |
| 295 | A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization | 5.5 | 160 | Citations (PDF) |
| 296 | Well kept secrets of the genome | 2.2 | 1 | Citations (PDF) |
| 297 | Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutations Prediction of clinical status—is molecular genetics a new tool for the management of hypertrophic cardiomyopathy in clinical practice? | 5.5 | 2 | Citations (PDF) |
| 298 | 1291 The QTc interval duration is correlated to KCNQ1 polymorphisms in a population based MONICA survey | 2.2 | 0 | Citations (PDF) |
| 299 | P3419 Fine-mapping on chromosome 1p31.1 in a family with Ebsteins anomaly and atrioventricular canal | 2.2 | 0 | Citations (PDF) |
| 300 | Relation of the G Protein β
3
-Subunit Polymorphism With Left Ventricle Structure and Function | 6.6 | 19 | Citations (PDF) |
| 301 | Angiotensin II type 2 receptor gene polymorphism and cardiovascular phenotypes: the GLAECO and GLAOLD studies | 7.3 | 37 | Citations (PDF) |
| 302 | Novel mutations in sarcomeric protein genes in dilated cardiomyopathy | 2.1 | 145 | Citations (PDF) |
| 303 | Genetische Einflüsse beim Herzinfarkt | 0.7 | 1 | Citations (PDF) |
| 304 | Effect of the angiotensin II type 2-receptor gene (+1675 G/A) on left ventricular structure in humans | 2.3 | 87 | Citations (PDF) |
| 305 | Aldosterone synthase (CYP11B2) −344 C/T polymorphism is associated with left ventricular structure in human arterial hypertension | 2.3 | 51 | Citations (PDF) |
| 306 | Spectrum of clinical phenotypes and gene variants in cardiac myosin-binding protein C mutation carriers with hypertrophic cardiomyopathy | 2.3 | 130 | Citations (PDF) |
| 307 | Bradykinin B2BKR receptor polymorphism and left-ventricular growth response | 62.1 | 106 | Citations (PDF) |
| 308 | Lack of association between polymorphisms of angiotensin II receptor genes and response to short-term angiotensin II infusion | 2.1 | 13 | Citations (PDF) |
| 309 | Functional gene testing of the Glu298Asp polymorphism of the endothelial NO synthase | 2.1 | 69 | Citations (PDF) |
| 310 | Evaluation of three polymorphisms in the promoter region of the angiotensin II type I receptor gene | 2.1 | 39 | Citations (PDF) |
| 311 | Investigation of the human serotonin 6 (5-HT6) receptor gene in bipolar affective disorder and schizophrenia 2000, 96, 217-221 | | 64 | Citations (PDF) |
| 312 | Morphology-related effects on gene expression and protein accumulation of the yeast Arxula adeninivorans LS3 | 2.4 | 43 | Citations (PDF) |
| 313 | Characterization of polymorphisms in the promoter of the human angiotensin II subtype 1 (AT1) receptor gene | 1.1 | 36 | Citations (PDF) |
| 314 | Expression of ACE mRNA in the human atrial myocardium is not dependent on left ventricular function, ACE inhibitor therapy, or the ACE I/D genotype | 3.7 | 10 | Citations (PDF) |
| 315 | Age-associated changes in the stimulatory effect of transforming growth factor beta on human osteogenic colony formation | 4.7 | 32 | Citations (PDF) |
| 316 | Screening the human bradykinin B2 receptor gene in patients with cardiovascular diseases: Identification of a functional mutation in the promoter and a new coding variant (T21M) | 0.5 | 22 | Citations (PDF) |
| 317 | Effects of Estrogen on the Concentration of Insulin-like Growth Factor-I in Rat Bone Matrix | 3.4 | 8 | Citations (PDF) |
| 318 | Cloning and Characterization of the 5′-Flanking Region of the Human Cardiotrophin-1 Gene | 2.1 | 11 | Citations (PDF) |
| 319 | Assignment of the human serotonin 1F receptor gene (HTR1F) to the short arm of chromosome 3 (3p13-p14.1) | 2.9 | 5 | Citations (PDF) |
| 320 | Human 5-HT5AReceptor Gene: Systematic Screening for DNA Sequence Variation and Linkage Mapping on Chromosome 7q34–q36 Using a Polymorphism in the 5′ Untranslated Region | 2.1 | 22 | Citations (PDF) |
| 321 | 5-HT2A receptor and bipolar affective disorder: association studies in affected patients | 1.9 | 54 | Citations (PDF) |
| 322 | Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: Identification of two naturally occurring receptor variants and association analysis in schizophrenia | 2.9 | 197 | Citations (PDF) |
| 323 | Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophrenia 1996, 67, 225-228 | | 17 | Citations (PDF) |
| 324 | Systematic screening for mutations in the promoter and the coding region of the 5-HT1A gene | 0.5 | 62 | Citations (PDF) |
| 325 | Binding properties of the naturally occurring human 5-HT1A receptor variant with the Ile28Val substitution in the extracellular domain | 2.6 | 14 | Citations (PDF) |
| 326 | Lack of genetically determined structural variants of the human serotonin-1E (5-HT1E) receptor protein points to its evolutionary conservation | 2.6 | 23 | Citations (PDF) |
| 327 | Genetic variation of the 5-HT2A receptor and response to clozapine | 62.1 | 111 | Citations (PDF) |
| 328 | Detection of four polymorphic sites in the human dopamine D1 receptor gene (DRD1) | 2.9 | 62 | Citations (PDF) |
| 329 | Identification of Genetic Variation in the Human Serotonin 1Dβ Receptor Gene | 2.1 | 65 | Citations (PDF) |
| 330 | Dinucleotide repeat polymorphism at the D18S99 locus | 2.9 | 0 | Citations (PDF) |
| 331 | Dinucleotide repeat polymorphism at the D18S365 locus | 2.9 | 0 | Citations (PDF) |
| 332 | Differential Regulation of Plasminogen Activator and Plasminogen Activator Inhibitor by Osteotropic Factors in Primary Cultures of Mature Osteoblasts and Osteoblast Precursors* | 2.5 | 81 | Citations (PDF) |
| 333 | Genetic Causes of Myocardial Infarction | 0.1 | 30 | Citations (PDF) |
| 334 | A decade of genome-wide association studies for coronary artery disease: the challenges ahead | 5.5 | 256 | Citations (PDF) |
| 335 | Title is missing! 0 | | 1 | Citations (PDF) |
