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Precision Health Database


Genomics & Health Impact Scan Database|Search|PHGKB

Last data update: Jan 27, 2023. (Total: 52315 Documents since 2012)
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Topic: Hypertrophic Cardiomyopathy: Current Treatment and Future Options.
Sebastian Sneha Annie et al. Current problems in cardiology 2022 101552
Hypertrophic Cardiomyopathy (HCM) and Family Health History of Sudden Death
CDC, December 2022
Genetic screening of relatives of decedents experiencing sudden unexpected death: medical examiner's office referrals to a multi-disciplinary cardiogenetics program.
Siskind Tamar et al. Journal of community genetics 2022
Polygenic Risk Score Predicts Sudden Death in Patients With Coronary Disease and Preserved Systolic Function.
Sandhu Roopinder K et al. Journal of the American College of Cardiology 2022 80(9) 873-883
Hematological, Biochemical Properties, and Clinical Correlates of Hemoglobin S Variant Disorder: A New Insight Into Sickle Cell Trait.
Khaled Safaa A A et al. Journal of hematology 2022 11(3) 92-108
Signal-to-Noise Analysis Can Inform the Likelihood That Incidentally Identified Variants in Sarcomeric Genes Are Associated with Pediatric Cardiomyopathy.
Kurzlechner Leonie M et al. Journal of personalized medicine 2022 12(5)
Arrhythmias as Presentation of Genetic Cardiomyopathy.
Lukas Laws J et al. Circulation research 2022 130(11) 1698-1722
KCNH2 p.Gly262AlafsTer98: A New Threatening Variant Associated with Long QT Syndrome in a Spanish Cohort.
Lorca Rebeca et al. Life (Basel, Switzerland) 2022 12(4)
Genetic Determinants of Sudden Unexpected Death in Pediatrics.
Koh Hyun Yong et al. Genetics in medicine : official journal of the American College of Medical Genetics 2022 24(4) 839-850
Left Cardiac Sympathetic Denervation for Long QT Syndrome: 50 Years' Experience Provides Guidance for Management.
Dusi Veronica et al. JACC. Clinical electrophysiology 2022 8(3) 281-294
Family Screening After Sudden Death in a Population-Based Study of Children.
Kannankeril Prince J et al. Pediatrics 2022
Racial Disparities in Ion Channelopathies and Inherited Cardiovascular Diseases Associated With Sudden Cardiac Death
M Chahine et al, May 2022
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Barc Julien et al. Nature genetics 2022
Sudden Death in Diabetic Ketoacidosis Complicated by Sickle Cell Trait.
Dau Georgia E et al. The American journal of forensic medicine and pathology 2022
Variant interpretation in molecular autopsy: a useful dilemma.
Scheiper-Welling Stefanie et al. International journal of legal medicine 2022
De novo mutations in childhood cases of sudden unexplained death that disrupt intracellular Ca regulation.
Halvorsen Matthew et al. Proceedings of the National Academy of Sciences of the United States of America 2021 118(52)
Molecular Autopsy of Sudden Cardiac Death in the Genomics Era.
Castiglione Vincenzo et al. Diagnostics (Basel, Switzerland) 2021 11(8)
Disease Expression and Outcomes in Black and White Adults With Hypertrophic Cardiomyopathy.
Arabadjian Milla E et al. Journal of the American Heart Association 2021 e019978
A college student’s near fatal collapse uncovered a frightening family legacy
SG Boodman, Washington Post, August 23, 2021
Genomic Autopsy of Sudden Deaths in Young Individuals.
Webster Gregory et al. JAMA cardiology 2021
Genomic Autopsy of Sudden Deaths in Young Individuals
G Webster et al, JAMA Cardiology, August 13, 2021
Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot.
Reuter Miriam S et al. Circulation. Genomic and precision medicine 2021
Return-to-Play for Athletes With Long QT Syndrome or Genetic Heart Diseases Predisposing to Sudden Death.
Tobert Kathryn E et al. Journal of the American College of Cardiology 2021
The Added Value of Coronary Calcium Score in Predicting Cardiovascular Events in Familial Hypercholesterolemia.
Gallo Antonio et al. JACC. Cardiovascular imaging 2021
Phenotype and progression among patients with dilated cardiomyopathy and RBM20 mutations.
Robles-Mezcua Ainhoa et al. European journal of medical genetics 2021 64(9) 104278
Sudden Death in the Young: Information for the Primary Care Provider.
Erickson Christopher C et al. Pediatrics 2021
Genetics and genomics of arrhythmic risk: current and future strategies to prevent sudden cardiac death.
Scrocco Chiara et al. Nature reviews. Cardiology 2021
Genetic Variants Associated With Unexplained Sudden Cardiac Death in Adult White and African American Individuals
L Guo et al, JAMA Cardiology, June 2, 2021
Diagnostic Yield of Genetic Testing in Sudden Cardiac Death with Autopsy Findings of Uncertain Significance.
Iglesias Mercedes et al. Journal of clinical medicine 2021 10(9)
Clinical and genetic characteristics and course of congenital long QT syndrome in children: A nine-year single-center experience.
Ergül Yakup et al. Anatolian journal of cardiology 2021 25(4) 250-257
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