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Subtype Specificity of Genetic Loci Associated With Stroke in 16 664 Cases and 32 792 Controls.Circulation: Genomic and Precision Medicine31 dayssaveRefWorksSFX Info
Lipidomics, Atrial Conduction, and Body Mass Index: Evidence From Association, Mediation, and Mendelian Randomization Models.Circulation: Genomic and Precision Medicine31 dayssaveRefWorksSFX Info
Use of Twitter to Promote Awareness of Familial Hypercholesterolemia.Circulation: Genomic and Precision Medicine31 dayssaveRefWorksSFX Info
Bi-Allelic Mutations in NUP205 and NUP210 Are Associated With Abnormal Cardiac Left-Right Patterning.Circulation: Genomic and Precision Medicine31 dayssaveRefWorksSFX Info
Letter by Ahamed and Subramanian Regarding Article "Missense Mutations in the FLNC Gene Causing Familial Restrictive Cardiomyopathy".Circulation: Genomic and Precision Medicine31 dayssaveRefWorksSFX Info
Response by Roldan-Sevilla to Letter Regarding Article, "Missense Mutations in the FLNC Gene Causing Familial Restrictive Cardiomyopathy".Circulation: Genomic and Precision Medicine31 dayssaveRefWorksSFX Info
Author: ...Circulation: Genomic and Precision Medicine39 dayssaveRefWorksSFX Info
Validation of Genome-Wide Polygenic Risk Scores for Coronary Artery Disease in French Canadians.Circulation: Genomic and Precision Medicine60 dayssaveRefWorksSFX Info
Using Statistical Modeling to Understand and Predict Pediatric Stem Cell Function.Circulation: Genomic and Precision Medicine60 dayssaveRefWorksSFX Info
Systems Pharmacology Identifies an Arterial Wall Regulatory Gene Network Mediating Coronary Artery Disease Side Effects of Antiretroviral Therapy.Circulation: Genomic and Precision Medicine60 dayssaveRefWorksSFX Info
Clinical Implications of Identifying Pathogenic Variants in Individuals With Thoracic Aortic Dissection.Circulation: Genomic and Precision Medicine60 dayssaveRefWorksSFX Info
Genetic Link Between Arterial Stiffness and Atrial Fibrillation.Circulation: Genomic and Precision Medicine60 dayssaveRefWorksSFX Info
FBN1 Coding Variants and Nonsyndromic Aortic Disease.Circulation: Genomic and Precision Medicine60 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 Medicine60 dayssaveRefWorksSFX Info
Correction to: Dyssynchronopathy Can be a Manifestation of Heritable Cardiomyopathy.Circulation: Genomic and Precision Medicine60 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 Medicine87 dayssaveRefWorksSFX Info
Rare Protein-Truncating Variants in APOB, Lower Low-Density Lipoprotein Cholesterol, and Protection Against Coronary Heart Disease.Circulation: Genomic and Precision Medicine87 dayssaveRefWorksSFX Info
Mortality Risk Associated With Truncating Founder Mutations in Titin.Circulation: Genomic and Precision Medicine87 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 Medicine87 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 Medicine87 dayssaveRefWorksSFX Info
Dyssynchronopathy Can be a Manifestation of Heritable Cardiomyopathy.Circulation: Genomic and Precision Medicine87 dayssaveRefWorksSFX Info
Targeted Long-Read RNA Sequencing Demonstrates Transcriptional Diversity Driven by Splice-Site Variation in MYBPC3.Circulation: Genomic and Precision Medicine87 dayssaveRefWorksSFX Info
Good Intentions Gone Bad: The Dangers of Sponsored Personalized Genomics.Circulation: Genomic and Precision Medicine87 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 Medicine87 dayssaveRefWorksSFX Info
Subsequent Event Risk in Individuals With Established Coronary Heart Disease: Design and Rationale of the GENIUS-CHD Consortium.Circulation: Genomic and Precision Medicine121 dayssaveRefWorksSFX Info
Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events: A GENIUS-CHD Study of Individual Participant Data.Circulation: Genomic and Precision Medicine121 dayssaveRefWorksSFX Info
Rare Missense Variants in TLN1 Are Associated With Familial and Sporadic Spontaneous Coronary Artery Dissection.Circulation: Genomic and Precision Medicine121 dayssaveRefWorksSFX Info
Circulating Markers of Inflammation Persist in Children and Adults With Giant Aneurysms After Kawasaki Disease.Circulation: Genomic and Precision Medicine121 dayssaveRefWorksSFX Info
HeartBioPortal: An Internet-of-Omics for Human Cardiovascular Disease Data.Circulation: Genomic and Precision Medicine121 dayssaveRefWorksSFX Info
Subsequent Event Risk in Individuals With Established Coronary Heart Disease: Design and Rationale of the GENIUS-CHD Consortium.Circulation: Genomic and Precision Medicine123 dayssaveRefWorksSFX Info
Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events: A GENIUS-CHD Study of Individual Participant Data.Circulation: Genomic and Precision Medicine123 dayssaveRefWorksSFX Info
Rare Missense Variants in TLN1 Are Associated With Familial and Sporadic Spontaneous Coronary Artery Dissection.Circulation: Genomic and Precision Medicine123 dayssaveRefWorksSFX Info
Circulating Markers of Inflammation Persist in Children and Adults With Giant Aneurysms After Kawasaki Disease.Circulation: Genomic and Precision Medicine123 dayssaveRefWorksSFX Info
HeartBioPortal: An Internet-of-Omics for Human Cardiovascular Disease Data.Circulation: Genomic and Precision Medicine123 dayssaveRefWorksSFX Info
High-Resolution Regulatory Maps Connect Vascular Risk Variants to Disease-Related Pathways.Circulation: Genomic and Precision Medicine151 dayssaveRefWorksSFX Info
Accuracy of Clinical Diagnostic Criteria for Patients With Vascular Ehlers-Danlos Syndrome in a Tertiary Referral Centre.Circulation: Genomic and Precision Medicine151 dayssaveRefWorksSFX Info
Thyroid Function and Dysfunction in Relation to 16 Cardiovascular Diseases: A Mendelian Randomization Study.Circulation: Genomic and Precision Medicine151 dayssaveRefWorksSFX Info
Resting Heart Rate and Cardiovascular Disease: Mendelian Randomization Analysis.Circulation: Genomic and Precision Medicine151 dayssaveRefWorksSFX Info
Phenotypic Characterization of Individuals With Variants in Cardiovascular Genes in the Absence of a Primary Cardiovascular Indication for Testing.Circulation: Genomic and Precision Medicine151 dayssaveRefWorksSFX Info
Delayed Diagnosis of Danon Disease in Patients Presenting With Isolated Cardiomyopathy.Circulation: Genomic and Precision Medicine151 dayssaveRefWorksSFX Info
Missense Mutations in the FLNC Gene Causing Familial Restrictive Cardiomyopathy: Growing Evidence.Circulation: Genomic and Precision Medicine151 dayssaveRefWorksSFX Info
Letter by Cheung et al Regarding Article, "Concealed Arrhythmogenic Right Ventricular Cardiomyopathy in Sudden Unexplained Cardiac Death Events".Circulation: Genomic and Precision Medicine151 dayssaveRefWorksSFX Info
Response by Ingles and Semsarian to Letter Regarding Article, "Concealed Arrhythmogenic Right Ventricular Cardiomyopathy in Sudden Unexplained Cardiac Death Events".Circulation: Genomic and Precision Medicine151 dayssaveRefWorksSFX Info
Correction to: Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy.Circulation: Genomic and Precision Medicine151 dayssaveRefWorksSFX Info
Medical Misinformation: Vet the Message!Circulation: Genomic and Precision Medicine167 dayssaveRefWorksSFX Info
Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes.Circulation: Genomic and Precision Medicine167 dayssaveRefWorksSFX Info
International Triadin Knockout Syndrome Registry: The Clinical Phenotype and Treatment Outcomes of Patients With Triadin Knockout Syndrome.Circulation: Genomic and Precision Medicine167 dayssaveRefWorksSFX Info
Integrative Functional Annotation of 52 Genetic Loci Influencing Myocardial Mass Identifies Candidate Regulatory Variants and Target Genes.Circulation: Genomic and Precision Medicine167 dayssaveRefWorksSFX Info
Interleukin-6 Receptor Signaling and Abdominal Aortic Aneurysm Growth Rates.Circulation: Genomic and Precision Medicine167 dayssaveRefWorksSFX Info
Common Genetic Variation in Relation to Brachial Vascular Dimensions and Flow-Mediated Vasodilation.Circulation: Genomic and Precision Medicine167 dayssaveRefWorksSFX Info
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