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AddVeterinary clinics of North America. Equine practice
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Genetic Association Analyses Highlight IL6, ALPL, and NAV1 As 3 New Susceptibility Genes Underlying Calcific Aortic Valve Stenosis.Circulation: Genomic and Precision Medicine1 daysaveRefWorksSFX Info
Integration of Large-Scale Genomic Data Sources With Evolutionary History Reveals Novel Genetic Loci for Congenital Heart Disease.Circulation: Genomic and Precision Medicine1 daysaveRefWorksSFX Info
Pathological Overlap of Arrhythmogenic Right Ventricular Cardiomyopathy and Cardiac Sarcoidosis.Circulation: Genomic and Precision Medicine1 daysaveRefWorksSFX Info
Revisiting the Approach to Diagnosis of Arrhythmogenic Cardiomyopathy: Stick to the Arrhythmia Criterion!Circulation: Genomic and Precision Medicine1 daysaveRefWorksSFX Info
Heart Failure in the Era of Precision Medicine: A Scientific Statement From the American Heart Association.Circulation: Genomic and Precision Medicine1 daysaveRefWorksSFX Info
Genetic Mosaicism in Calmodulinopathy.Circulation: Genomic and Precision Medicine29 dayssaveRefWorksSFX Info
Physical Activity, Sedentary Leisure Time, Circulating Metabolic Markers, and Risk of Major Vascular Diseases.Circulation: Genomic and Precision Medicine29 dayssaveRefWorksSFX Info
Biallelic Variants in ASNA1, Encoding a Cytosolic Targeting Factor of Tail-Anchored Proteins, Cause Rapidly Progressive Pediatric Cardiomyopathy.Circulation: Genomic and Precision Medicine29 dayssaveRefWorksSFX Info
LITAF (Lipopolysaccharide-Induced Tumor Necrosis Factor) Regulates Cardiac L-Type Calcium Channels by Modulating NEDD (Neural Precursor Cell Expressed Developmentally Downregulated Protein) 4-1 Ubiquitin Ligase.Circulation: Genomic and Precision Medicine29 dayssaveRefWorksSFX Info
Gut Microbiome and Response to Cardiovascular Drugs.Circulation: Genomic and Precision Medicine29 dayssaveRefWorksSFX Info
Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Desmosomal Variants Are Rarely De Novo: Segregation and Haplotype Analysis of a Multinational Cohort.Circulation: Genomic and Precision Medicine49 dayssaveRefWorksSFX Info
Cardiac [alpha]-Actin (ACTC1) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated Cardiomyopathy.Circulation: Genomic and Precision Medicine49 dayssaveRefWorksSFX Info
Characterization of the CACNA1C-R518C Missense Mutation in the Pathobiology of Long-QT Syndrome Using Human Induced Pluripotent Stem Cell Cardiomyocytes Shows Action Potential Prolongation and L-Type Calcium Channel Perturbation.Circulation: Genomic and Precision Medicine49 dayssaveRefWorksSFX Info
Blood Pressure-Associated Genetic Variants in the Natriuretic Peptide Receptor 1 Gene Modulate Guanylate Cyclase Activity.Circulation: Genomic and Precision Medicine49 dayssaveRefWorksSFX Info
Correction to: Targeted Long-Read RNA Sequencing Demonstrates Transcriptional Diversity Driven by Splice-Site Variation in MYBPC3.Circulation: Genomic and Precision Medicine49 dayssaveRefWorksSFX Info
Correction to: High-Resolution Regulatory Maps Connect Vascular Risk Variants to Disease-Related Pathways.Circulation: Genomic and Precision Medicine49 dayssaveRefWorksSFX Info
Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Desmosomal Variants Are Rarely De Novo: Segregation and Haplotype Analysis of a Multinational Cohort.Circulation: Genomic and Precision Medicine56 dayssaveRefWorksSFX Info
Cardiac [alpha]-Actin (ACTC1) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated Cardiomyopathy.Circulation: Genomic and Precision Medicine56 dayssaveRefWorksSFX Info
Characterization of the CACNA1C-R518C Missense Mutation in the Pathobiology of Long-QT Syndrome Using Human Induced Pluripotent Stem Cell Cardiomyocytes Shows Action Potential Prolongation and L-Type Calcium Channel Perturbation.Circulation: Genomic and Precision Medicine56 dayssaveRefWorksSFX Info
Blood Pressure-Associated Genetic Variants in the Natriuretic Peptide Receptor 1 Gene Modulate Guanylate Cyclase Activity.Circulation: Genomic and Precision Medicine56 dayssaveRefWorksSFX Info
Correction to: Targeted Long-Read RNA Sequencing Demonstrates Transcriptional Diversity Driven by Splice-Site Variation in MYBPC3.Circulation: Genomic and Precision Medicine56 dayssaveRefWorksSFX Info
Correction to: High-Resolution Regulatory Maps Connect Vascular Risk Variants to Disease-Related Pathways.Circulation: Genomic and Precision Medicine56 dayssaveRefWorksSFX Info
Subtype Specificity of Genetic Loci Associated With Stroke in 16 664 Cases and 32 792 Controls.Circulation: Genomic and Precision Medicine91 dayssaveRefWorksSFX Info
Lipidomics, Atrial Conduction, and Body Mass Index: Evidence From Association, Mediation, and Mendelian Randomization Models.Circulation: Genomic and Precision Medicine91 dayssaveRefWorksSFX Info
Use of Twitter to Promote Awareness of Familial Hypercholesterolemia.Circulation: Genomic and Precision Medicine91 dayssaveRefWorksSFX Info
Bi-Allelic Mutations in NUP205 and NUP210 Are Associated With Abnormal Cardiac Left-Right Patterning.Circulation: Genomic and Precision Medicine91 dayssaveRefWorksSFX Info
Letter by Ahamed and Subramanian Regarding Article "Missense Mutations in the FLNC Gene Causing Familial Restrictive Cardiomyopathy".Circulation: Genomic and Precision Medicine91 dayssaveRefWorksSFX Info
Response by Roldan-Sevilla to Letter Regarding Article, "Missense Mutations in the FLNC Gene Causing Familial Restrictive Cardiomyopathy".Circulation: Genomic and Precision Medicine91 dayssaveRefWorksSFX Info
Author: ...Circulation: Genomic and Precision Medicine99 dayssaveRefWorksSFX Info
Validation of Genome-Wide Polygenic Risk Scores for Coronary Artery Disease in French Canadians.Circulation: Genomic and Precision Medicine120 dayssaveRefWorksSFX Info
Using Statistical Modeling to Understand and Predict Pediatric Stem Cell Function.Circulation: Genomic and Precision Medicine120 dayssaveRefWorksSFX Info
Systems Pharmacology Identifies an Arterial Wall Regulatory Gene Network Mediating Coronary Artery Disease Side Effects of Antiretroviral Therapy.Circulation: Genomic and Precision Medicine120 dayssaveRefWorksSFX Info
Clinical Implications of Identifying Pathogenic Variants in Individuals With Thoracic Aortic Dissection.Circulation: Genomic and Precision Medicine120 dayssaveRefWorksSFX Info
Genetic Link Between Arterial Stiffness and Atrial Fibrillation.Circulation: Genomic and Precision Medicine120 dayssaveRefWorksSFX Info
FBN1 Coding Variants and Nonsyndromic Aortic Disease.Circulation: Genomic and Precision Medicine120 dayssaveRefWorksSFX Info
Establishment of Specialized Clinical Cardiovascular Genetics Programs: Recognizing the Need and Meeting Standards: A Scientific Statement From the American Heart Association.Circulation: Genomic and Precision Medicine120 dayssaveRefWorksSFX Info
Correction to: Dyssynchronopathy Can be a Manifestation of Heritable Cardiomyopathy.Circulation: Genomic and Precision Medicine120 dayssaveRefWorksSFX Info
Genome-Wide Association Study-Driven Gene-Set Analyses, Genetic, and Functional Follow-Up Suggest GLIS1 as a Susceptibility Gene for Mitral Valve Prolapse.Circulation: Genomic and Precision Medicine147 dayssaveRefWorksSFX Info
Rare Protein-Truncating Variants in APOB, Lower Low-Density Lipoprotein Cholesterol, and Protection Against Coronary Heart Disease.Circulation: Genomic and Precision Medicine147 dayssaveRefWorksSFX Info
Mortality Risk Associated With Truncating Founder Mutations in Titin.Circulation: Genomic and Precision Medicine147 dayssaveRefWorksSFX Info
Assessment and Validation of a Phenotype-Enhanced Variant Classification Framework to Promote or Demote RYR2 Missense Variants of Uncertain Significance.Circulation: Genomic and Precision Medicine147 dayssaveRefWorksSFX Info
Whole Exome Sequencing Reveals a Large Genetic Heterogeneity and Revisits the Causes of Hypertrophic Cardiomyopathy: Experience of a Multicentric Study of 200 French Patients.Circulation: Genomic and Precision Medicine147 dayssaveRefWorksSFX Info
Dyssynchronopathy Can be a Manifestation of Heritable Cardiomyopathy.Circulation: Genomic and Precision Medicine147 dayssaveRefWorksSFX Info
Targeted Long-Read RNA Sequencing Demonstrates Transcriptional Diversity Driven by Splice-Site Variation in MYBPC3.Circulation: Genomic and Precision Medicine147 dayssaveRefWorksSFX Info
Good Intentions Gone Bad: The Dangers of Sponsored Personalized Genomics.Circulation: Genomic and Precision Medicine147 dayssaveRefWorksSFX Info
Correction to: Variation in Serum PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9), Cardiovascular Disease Risk, and an Investigation of Potential Unanticipated Effects of PCSK9 Inhibition: A Genome-Wide Association Study and Mendelian RandomiCirculation: Genomic and Precision Medicine147 dayssaveRefWorksSFX Info
Subsequent Event Risk in Individuals With Established Coronary Heart Disease: Design and Rationale of the GENIUS-CHD Consortium.Circulation: Genomic and Precision Medicine181 dayssaveRefWorksSFX Info
Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events: A GENIUS-CHD Study of Individual Participant Data.Circulation: Genomic and Precision Medicine181 dayssaveRefWorksSFX Info
Rare Missense Variants in TLN1 Are Associated With Familial and Sporadic Spontaneous Coronary Artery Dissection.Circulation: Genomic and Precision Medicine181 dayssaveRefWorksSFX Info
Circulating Markers of Inflammation Persist in Children and Adults With Giant Aneurysms After Kawasaki Disease.Circulation: Genomic and Precision Medicine181 dayssaveRefWorksSFX Info
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