| 1 | Genetic therapies for cardiomyopathy: survey of attitudes of the patient community for the CureHeart project | 3.0 | 8 | Citations (PDF) |
| 2 | Genome-Wide Analysis of Left Ventricular Maximum Wall Thickness in the UK Biobank Cohort Reveals a Shared Genetic Background With Hypertrophic Cardiomyopathy | 2.9 | 18 | Citations (PDF) |
| 3 | Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease | 13.7 | 15 | Citations (PDF) |
| 4 | Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy | 2.9 | 8 | Citations (PDF) |
| 5 | GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification | 25.2 | 87 | Citations (PDF) |
| 6 | Robust estimates of heritable coronary disease risk in individuals with type 2 diabetes | 3.1 | 8 | Citations (PDF) |
| 7 | Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants | 25.2 | 646 | Citations (PDF) |
| 8 | Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity | 25.2 | 316 | Citations (PDF) |
| 9 | Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability | 13.7 | 134 | Citations (PDF) |
| 10 | The trans-ancestral genomic architecture of glycemic traits | 25.2 | 671 | Citations (PDF) |
| 11 | The power of genetic diversity in genome-wide association studies of lipids | 37.9 | 891 | Citations (PDF) |
| 12 | Identifying small-effect genetic associations overlooked by the conventional fixed-effect model in a large-scale meta-analysis of coronary artery disease | 4.7 | 3 | Citations (PDF) |
| 13 | A key role for the novel coronary artery disease gene JCAD in atherosclerosis via shear stress mechanotransduction | 5.5 | 38 | Citations (PDF) |
| 14 | Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus | 2.9 | 10 | Citations (PDF) |
| 15 | Reevaluation of the South Asian
MYBPC3
Δ25bp
Intronic Deletion in Hypertrophic Cardiomyopathy | 2.9 | 39 | Citations (PDF) |
| 16 | Associations of autozygosity with a broad range of human phenotypes | 13.7 | 118 | Citations (PDF) |
| 17 | Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions | 3.3 | 113 | Citations (PDF) |
| 18 | Genetic variation in CADM2 as a link between psychological traits and obesity | 3.4 | 64 | Citations (PDF) |
| 19 | A multi-ancestry genome-wide study incorporating gene–smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure | 2.9 | 44 | Citations (PDF) |
| 20 | Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids | 25.2 | 134 | Citations (PDF) |
| 21 | Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targets | 3.4 | 46 | Citations (PDF) |
| 22 | A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure | 6.5 | 157 | Citations (PDF) |
| 23 | Neonatal MicroRNA Profile Determines Endothelial Function in Offspring of Hypertensive Pregnancies | 6.6 | 37 | Citations (PDF) |
| 24 | Differential Gene Expression in Macrophages From Human Atherosclerotic Plaques Shows Convergence on Pathways Implicated by Genome-Wide Association Study Risk Variants | 6.0 | 28 | Citations (PDF) |
| 25 | Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits | 25.2 | 1,327 | Citations (PDF) |
| 26 | Mutant Muscle LIM Protein C58G causes cardiomyopathy through protein depletion | 3.8 | 33 | Citations (PDF) |
| 27 | Lack of genetic support for shared aetiology of Coronary Artery Disease and Late-onset Alzheimer’s disease | 3.4 | 19 | Citations (PDF) |
| 28 | Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries | 2.3 | 117 | Citations (PDF) |
| 29 | Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease | 2.3 | 247 | Citations (PDF) |
| 30 | Loss of Cardioprotective Effects at the
ADAMTS7
Locus as a Result of Gene-Smoking Interactions | 18.1 | 60 | Citations (PDF) |
| 31 | A mouse-to-man candidate gene study identifies association of chronic otitis media with the loci TGIF1 and FBXO11 | 3.4 | 24 | Citations (PDF) |
| 32 | Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney | 6.6 | 145 | Citations (PDF) |
| 33 | Association analyses based on false discovery rate implicate new loci for coronary artery disease | 25.2 | 695 | Citations (PDF) |
| 34 | Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis | 8.0 | 408 | Citations (PDF) |
| 35 | Identification of a novel proinsulin-associated SNP and demonstration that proinsulin is unlikely to be a causal factor in subclinical vascular remodelling using Mendelian randomisation | 1.5 | 3 | Citations (PDF) |
| 36 | Identifying systematic heterogeneity patterns in genetic association meta-analysis studies | 3.2 | 22 | Citations (PDF) |
| 37 | Coding Variation in
ANGPTL4,
LPL,
and
SVEP1
and the Risk of Coronary Disease | 34.5 | 487 | Citations (PDF) |
| 38 | A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape | 13.7 | 91 | Citations (PDF) |
| 39 | The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals | 25.2 | 415 | Citations (PDF) |
| 40 | No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis | 3.4 | 31 | Citations (PDF) |
| 41 | Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis | 4.9 | 113 | Citations (PDF) |
| 42 | Causal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization Study | 2.3 | 166 | Citations (PDF) |
| 43 | A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration | 2.9 | 90 | Citations (PDF) |
| 44 | Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWFBlood, 2015, 126, e19-e29 | 4.5 | 77 | Citations (PDF) |
| 45 | The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study | 3.2 | 398 | Citations (PDF) |
| 46 | New genetic loci link adipose and insulin biology to body fat distribution | 37.9 | 1,582 | Citations (PDF) |
| 47 | Genetic studies of body mass index yield new insights for obesity biology | 37.9 | 4,495 | Citations (PDF) |
| 48 | Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility | 13.7 | 191 | Citations (PDF) |
| 49 | A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease | 25.2 | 2,502 | Citations (PDF) |
| 50 | Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans | 2.3 | 71 | Citations (PDF) |
| 51 | Analysis of the Role of Interleukin 6 Receptor Haplotypes in the Regulation of Circulating Levels of Inflammatory Biomarkers and Risk of Coronary Heart Disease | 2.3 | 23 | Citations (PDF) |
| 52 | No Evidence for Genome-Wide Interactions on Plasma Fibrinogen by Smoking, Alcohol Consumption and Body Mass Index: Results from Meta-Analyses of 80,607 Subjects | 2.3 | 9 | Citations (PDF) |
| 53 | Human Genetic Evidence for Involvement of CD137 in Atherosclerosis | 5.6 | 10 | Citations (PDF) |
| 54 | Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population | 3.2 | 392 | Citations (PDF) |
| 55 | Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci | 6.5 | 167 | Citations (PDF) |
| 56 | Association of Low-Frequency and Rare Coding-Sequence Variants with Blood Lipids and Coronary Heart Disease in 56,000 Whites and Blacks | 6.5 | 309 | Citations (PDF) |
| 57 | A Common
LPA
Null Allele Associates With Lower Lipoprotein(a) Levels and Coronary Artery Disease Risk | 6.0 | 58 | Citations (PDF) |
| 58 | Gene-Age Interactions in Blood Pressure Regulation: A Large-Scale Investigation with the CHARGE, Global BPgen, and ICBP Consortia | 6.5 | 126 | Citations (PDF) |
| 59 | Defining the role of common variation in the genomic and biological architecture of adult human height | 25.2 | 1,972 | Citations (PDF) |
| 60 | LPA null mutation genotyping and qPCR analysis refine kringle isoform analysis of Lp(a) levels | 1.5 | 1 | Citations (PDF) |
| 61 | Use of encode data to identify putative functional variants in coronary artery disease GWAS | 1.5 | 0 | Citations (PDF) |
| 62 | Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction | 37.9 | 632 | Citations (PDF) |
| 63 | Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant Statistics | 6.5 | 65 | Citations (PDF) |
| 64 | Re: Rourke et al.: Clinical Spectrum of Presenting Signs and Symptoms of Anterior Urethral Stricture: Detailed Analysis of Single-institutional Cohort (Urology 2012;79:1163-1167) | 1.4 | 0 | Citations (PDF) |
| 65 | Secretory Phospholipase A2-IIA and Cardiovascular Disease | 2.3 | 122 | Citations (PDF) |
| 66 | Association Between the Chromosome 9p21 Locus and Angiographic Coronary Artery Disease Burden | 2.3 | 59 | Citations (PDF) |
| 67 | Re: Elkoushy et al.: Pulsed Fluoroscopy in Ureteroscopy and Percutaneous Nephrolithotomy (Urology 2012;79:1230-1235) | 1.4 | 0 | Citations (PDF) |
| 68 | Re: Hoy et al.: Expanded Use of Dorsal Onlay Augmented Anastomotic Urethroplasty With Buccal Mucosa for Long Segment Bulbar Urethral Strictures: Analysis of Outcomes and Complications (Urology 2013;81:1357-1361) | 1.4 | 1 | Citations (PDF) |
| 69 | Re: Palminteri et al.: Contemporary Urethral Stricture Characteristics in the Developed World (Urology 2013;81:191-197) | 1.4 | 3 | Citations (PDF) |
| 70 | Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits | 3.2 | 421 | Citations (PDF) |
| 71 | Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia | 6.0 | 96 | Citations (PDF) |
| 72 | Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways | 25.2 | 806 | Citations (PDF) |
| 73 | Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke | 25.2 | 408 | Citations (PDF) |
| 74 | Re: Welk et al.: The Augmented Nontransected Anastomotic Urethroplasty for the Treatment of Bulbar Urethral Stricture (Urology 2012;79:917-921) | 1.4 | 0 | Citations (PDF) |
| 75 | Re: Penbegul et al.: Safety and Efficacy of Ultrasound-Guided Percutaneous Nephrolithotomy of Urinary Stone Disease in Children (Urology 2012;79:1015-1019) | 1.4 | 0 | Citations (PDF) |
| 76 | TGFB1 genetic polymorphisms and coronary heart disease risk: a meta-analysis | 1.8 | 34 | Citations (PDF) |
| 77 | A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance | 25.2 | 834 | Citations (PDF) |
| 78 | Large-scale association analysis identifies new risk loci for coronary artery disease | 25.2 | 1,567 | Citations (PDF) |
| 79 | Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk | 37.9 | 2,000 | Citations (PDF) |
| 80 | Genome-Wide Association Identifies Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 Diabetes | 4.2 | 356 | Citations (PDF) |
| 81 | Buccal Mucosal Graft Urethroplasty for Penile Stricture: Only Dorsal or Combined Dorsal and Ventral Graft Placement? | 1.4 | 12 | Citations (PDF) |
| 82 | Variants at the Endocannabinoid Receptor CB1 Gene (CNR1) and Insulin Sensitivity, Type 2 Diabetes, and Coronary Heart Disease | 4.0 | 17 | Citations (PDF) |
| 83 | Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure | 25.2 | 424 | Citations (PDF) |
| 84 | Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index | 25.2 | 2,789 | Citations (PDF) |
| 85 | Common Variants at 10 Genomic Loci Influence Hemoglobin A1C Levels via Glycemic and Nonglycemic Pathways | 4.2 | 426 | Citations (PDF) |
| 86 | New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk | 25.2 | 2,112 | Citations (PDF) |
| 87 | Meatoplasty using double buccal mucosal graft technique | 1.4 | 30 | Citations (PDF) |
| 88 | Genetic Variants Associated with Lp(a) Lipoprotein Level and Coronary Disease | 34.5 | 1,504 | Citations (PDF) |
| 89 | Relationship between CAD Risk Genotype in the Chromosome 9p21 Locus and Gene Expression. Identification of Eight New ANRIL Splice Variants | 2.3 | 155 | Citations (PDF) |
| 90 | Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p | 2.9 | 491 | Citations (PDF) |
| 91 | Adrenal Gland Tumorigenesis after Gonadectomy in Mice Is a Complex Genetic Trait Driven by Epistatic Loci | 2.5 | 47 | Citations (PDF) |
| 92 | eQTL Explorer: integrated mining of combined genetic linkage and expression experiments | 4.7 | 23 | Citations (PDF) |
| 93 | Title is missing! | 1.4 | 7 | Citations (PDF) |
