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Acute Management of Ventricular Arrhythmia in Patients With Suspected Inherited Heart Rhythm Disorders Z Laskman et al, JACC Electrophysiology, March 2019
Establishing a familial hypercholesterolaemia register - The first year. Tilney Myra et al. Atherosclerosis. Supplements 2019 Mar 3624-27 Similar articles in PubMed
Lessons from exome sequencing in prenatally diagnosed heart defects: a basis for prenatal testing. Westphal Dominik S et al. Clinical genetics 2019 Mar Similar articles in PubMed
Investigating the association between familial hypercholesterolemia and perceived depression. Chang Nien-Tzu et al. Atherosclerosis. Supplements 2019 Mar 3631-36 Similar articles in PubMed
Shared mechanisms between coronary heart disease and depression: findings from a large UK general population-based cohort. Khandaker Golam M et al. Molecular psychiatry 2019 Mar Similar articles in PubMed
Clinicopathological features and clinical efficacy of crizotinib in Chinese patients with ROS1 -positive non-small cell lung cancer. Zhu You-Cai et al. Oncology letters 2019 Mar 17(3) 3466-3474 Similar articles in PubMed
Variable expression and penetrance in Portuguese families with Familial Hypercholesterolemia with mild phenotype. Gaspar I M et al. Atherosclerosis. Supplements 2019 Mar 3628-30 Similar articles in PubMed
Applying Data Science methods and tools to unveil healthcare use of lung cancer patients in a teaching hospital in Spain. Cruz-Bermúdez J L et al. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2019 Mar Similar articles in PubMed
A Machine Learning Based Model for Out of Hospital Cardiac Arrest Outcome Classification and Sensitivity Analysis. Harford Samuel et al. Resuscitation 2019 Mar Similar articles in PubMed
Use of whole exome sequencing in the NICU: Case of an extremely low birth weight infant with syndromic features. Kuehne Benjamin et al. Molecular and cellular probes 2019 Mar Similar articles in PubMed
Predicting deterioration of ventricular function in patients with repaired tetralogy of Fallot using machine learning. Samad Manar D et al. European heart journal cardiovascular Imaging 2018 19(7) 730-738 Similar articles in PubMed
The phenotypic spectrum of proximal 6q deletions based on a large cohort derived from social media and literature reports. Engwerda Aafke et al. European journal of human genetics : EJHG 2018 26(10) 1478-1489 Similar articles in PubMed
Genetic testing for inherited heart diseases: longitudinal impact on health-related quality of life. Ingles Jodie et al. Genetics in medicine : official journal of the American College of Medical Genetics 2012 14(8) 749-752 Similar articles in PubMed
Value of Measuring Lipoprotein(a) During Cascade Testing for Familial Hypercholesterolemia. Ellis Katrina L et al. Journal of the American College of Cardiology 2019 Mar 73(9) 1029-1039 Similar articles in PubMed
Large next-generation sequencing gene panels in genetic heart disease: challenges in clinical practice. Christiaans I et al. Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation 2019 Mar Similar articles in PubMed
Large next-generation sequencing gene panels in genetic heart disease: yield of pathogenic variants and variants of unknown significance. van Lint F H M et al. Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation 2019 Mar Similar articles in PubMed
Association of genetically predicted testosterone with thromboembolism, heart failure, and myocardial infarction: mendelian randomisation study in UK Biobank. Luo Shan et al. BMJ (Clinical research ed.) 2019 Mar 364l476 Similar articles in PubMed
EVALUATION OF TREATMENT EFFICACY IN PATIENTS WITH NON-ALCOHOLIC-STEATOHEPATITIS AND HETEROZYGOTIC FAMILIAL HYPERCHOLESTEROLEMIA. Yakimenko ? et al. Georgian medical news 2019 Jan (286) 67-72 Similar articles in PubMed
Premarital Screening and Genetic Counseling Program: Studies from an Endogamous Population. Bener Abdulbari et al. International journal of applied & basic medical research 9(1) 20-26 Similar articles in PubMed
Mutational profile of Brazilian lung adenocarcinoma unveils association of EGFR mutations with high Asian ancestry and independent prognostic role of KRAS mutations. Leal Letícia Ferro et al. Scientific reports 2019 Mar 9(1) 3209 Similar articles in PubMed
Genetic interpretation and clinical translation of minor genes related to Brugada syndrome. Campuzano Oscar et al. Human mutation 2019 Feb Similar articles in PubMed
Determinants of In-Hospital Mortality After Percutaneous Coronary Intervention: A Machine Learning Approach. Al'Aref Subhi J et al. Journal of the American Heart Association 2019 Mar 8(5) e011160 Similar articles in PubMed
A Rare Cause of Cardiac Arrest in the Era of Genetic Testing. Schleien Charles et al. Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies 2019 Mar 20(3) 297-298 Similar articles in PubMed
ASSOCIATION OF POLYGENIC RISK SCORES WITH PREMATURE CORONARY HEART DISEASE: A COMPARATIVE STUDY O Dikilitas et al, JACC, March 2019
Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations. Regalado Ellen S et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 20(10) 1206-1215 Similar articles in PubMed
[Pulmonary arterial hypertension as leading manifestation of methylmalonic aciduria: clinical characteristics and gene testing in 15 cases]. Liu X Q et al. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2017 49(5) 768-777 Similar articles in PubMed
Comparative aspects of the care of familial hypercholesterolemia in the "Ten Countries Study". Pang Jing et al. Journal of clinical lipidology 2019 Jan Similar articles in PubMed
The spectrum of genetic variants and phenotypic features of Southeast Asian patients with Noonan syndrome. Koh Ai-Ling et al. Molecular genetics & genomic medicine 2019 Feb e581 Similar articles in PubMed
The clinical and molecular diversity of homozygous familial hypercholesterolemia in children: Results from the GeneTics of clinical homozygous hypercholesterolemia (GoTCHA) study. Luirink Ilse K et al. Journal of clinical lipidology 2018 Dec Similar articles in PubMed
Evaluating a custom-designed aid to improve communication of genetic results in families with hypertrophic cardiomyopathy: study protocol for a randomised controlled trial. Burns Charlotte et al. BMJ open 2019 Feb 9(1) e026627 Similar articles in PubMed
A Genetic Risk Score for Atrial Fibrillation Predicts the Response to Catheter Ablation. Choe Won Seok et al. Korean circulation journal 2018 Dec Similar articles in PubMed
CYP2C19 Genotype-Guided Antiplatelet Therapy and 30-Day Outcomes After Percutaneous Coronary Intervention. Williams Alexis K et al. Circulation. Genomic and precision medicine 2019 Feb 12(2) e002441 Similar articles in PubMed
Impact of NBS for VLCAD deficiency on genetic, enzymatic and clinical outcomes. Bleeker Jeannette C et al. Journal of inherited metabolic disease 2019 Feb Similar articles in PubMed
Genetic basis and outcome in a nationwide study of Finnish patients with hypertrophic cardiomyopathy. Jääskeläinen Pertti et al. ESC heart failure 2019 Feb Similar articles in PubMed
Genetic testing for familial hypercholesterolemia: Impact on diagnosis, treatment and cardiovascular risk. Lee Seohyuk et al. European journal of preventive cardiology 2019 Feb 2047487319829746 Similar articles in PubMed
Prevalence of pathogenic and likely pathogenic variants in the RASopathy genes in patients who have had panel testing for cardiomyopathy. Aljeaid Deema et al. American journal of medical genetics. Part A 2019 Feb Similar articles in PubMed
Heart failure in patients with arrhythmogenic right ventricular cardiomyopathy: Genetic characteristics. Vischer Annina S et al. International journal of cardiology 2019 Jan Similar articles in PubMed
Application of quality indicators to data from the National Network of Congenital Anomalies of Argentina. Groisman Boris et al. Birth defects research 2019 Feb Similar articles in PubMed
From patient-specific induced pluripotent stem cells to clinical translation in long QT syndrome Type 2. Schwartz Peter J et al. European heart journal 2019 Feb Similar articles in PubMed
How to identify familial premature myocardial infarction: comparing approaches to identify familial hypercholesterolemia. Beheshti Sabina et al. The Journal of clinical endocrinology and metabolism 2019 Feb Similar articles in PubMed
How to identify familial premature myocardial infarction: comparing approaches to identify familial hypercholesterolemia. Beheshti Sabina et al. The Journal of clinical endocrinology and metabolism 2019 Feb Similar articles in PubMed
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis. Bandres-Ciga Sara et al. Annals of neurology 2019 Feb Similar articles in PubMed
An African-specific haplotype in MRGPRX4 is associated with menthol cigarette smoking. Kozlitina Julia et al. PLoS genetics 2019 Feb 15(2) e1007916 Similar articles in PubMed
Genetic Tools for Coronary Risk Assessment in Type 2 Diabetes: A Cohort Study From the ACCORD Clinical Trial. Morieri Mario Luca et al. Diabetes care 2018 Nov 41(11) 2404-2413 Similar articles in PubMed
Screening of familial hypercholesterolemia among patients in age under 40 years old exposed by duplex scanning of carotid arteries, by the local registry data. Gaisenok O V et al. Terapevticheskii arkhiv 2018 Sep 90(9) 37-41 Similar articles in PubMed
Possible roles of genetic variations in chemotherapy related cardiotoxicity in pediatric acute lymphoblastic leukemia and osteosarcoma. Sági Judit C et al. BMC cancer 2018 Jul 18(1) 704 Similar articles in PubMed
The Edinburgh CT and genetic diagnostic criteria for lobar intracerebral haemorrhage associated with cerebral amyloid angiopathy: model development and diagnostic test accuracy study. Rodrigues Mark A et al. The Lancet. Neurology 2018 17(3) 232-240 Similar articles in PubMed
Effect of lipid-lowering treatment in cardiovascular disease prevalence in familial hypercholesterolemia S Perez-Calahorra et al., Atherosclerosis, February 2019
Impact of Age on the Efficacy and Safety of Alirocumab in Patients with Heterozygous Familial Hypercholesterolemia. Ginsberg Henry N et al. Cardiovascular drugs and therapy 2019 Feb Similar articles in PubMed
Association Between ABCB1 Polymorphisms and Outcomes of Clopidogrel Treatment in Patients With Minor Stroke or Transient Ischemic Attack- Secondary Analysis of a Randomized Clinical Trial Y Pan et al, JAMA Neurology, February 11, 2019
Adults with familial hypercholesterolaemia have healthier dietary and lifestyle habits compared with their non-affected relatives: the SAFEHEART study. Arroyo-Olivares Raquel et al. Public health nutrition 2019 Feb 1-11 Similar articles in PubMed
Genetic Diagnostic Testing for Inherited Cardiomyopathies: Considerations for Offering Multi-Gene Tests in a Health Care Setting. Daoud Hussein et al. The Journal of molecular diagnostics : JMD 2019 Feb Similar articles in PubMed
Actions in Support of Newborn Screening for Critical Congenital Heart Disease — United States, 2011–2018 CDC MMWR, February 7, 2019
Misclassification of VLCAD carriers due to variable confirmatory testing after a positive NBS result. Atkins Anne E et al. Journal of community genetics 2019 Feb Similar articles in PubMed
Hospitalizations with hereditary hemorrhagic telangiectasia and pulmonary hypertension in the United States from 2000 to 2014. Harder Eileen M et al. Respiratory medicine 2019 Feb 14726-30 Similar articles in PubMed
Screening of common genetic variants in the APOB gene related to familial hypercholesterolemia in a Saudi population: A case-control study. Batais Mohammed Ali et al. Medicine 2019 Jan 98(4) e14247 Similar articles in PubMed
Contemporary characteristics and outcomes of adults with familial dilated cardiomyopathy listed for heart transplantation. Khayata Mohamed et al. World journal of cardiology 2019 Jan 11(1) 38-46 Similar articles in PubMed
Universal Electrocardiographic Screening for Long QT Syndrome in Hospitalized Neonates. Kaemingk Bethany D et al. American journal of perinatology 2019 Feb Similar articles in PubMed
Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study. Lord Jenny et al. Lancet (London, England) 2019 Jan Similar articles in PubMed
Body composition and atrial fibrillation: a Mendelian randomization study. Tikkanen Emmi et al. European heart journal 2019 Feb Similar articles in PubMed
Mendelian Randomization Analysis of Hemoglobin A 1c as a Risk Factor for Coronary Artery Disease. Leong Aaron et al. Diabetes care 2019 Jan Similar articles in PubMed
Lifelong genetically lowered sclerostin and risk of cardiovascular disease. J Bovjin et al, BIORxIV, February 1, 2019
Targeted next-generation sequencing in Slovak cardiomyopathy patients. Nagyova E et al. Bratislavske lekarske listy 2019 120(1) 46-51 Similar articles in PubMed
A validated PROM in genetic counselling: the psychometric properties of the Dutch version of the Genetic Counselling Outcome Scale. Voorwinden Jan S et al. European journal of human genetics : EJHG 2019 Jan Similar articles in PubMed
Attitudes of clinicians toward cardiac surgery and trisomy 18. Kaulfus Meagan E et al. Journal of genetic counseling 2019 Jan Similar articles in PubMed
Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy. Walsh Roddy et al. Genome medicine 2019 Jan 11(1) 5 Similar articles in PubMed
Risk of cardiovascular disease in women with BRCA1 and BRCA2 mutations. Powell C Bethan et al. Gynecologic oncology 2018 151(3) 489-493 Similar articles in PubMed
The Prevalence and Clinical Features of Fabry Disease in Hemodialysis Patients: Russian Nationwide Fabry Dialysis Screening Program. Moiseev Sergey et al. Nephron 2019 Jan 1-7 Similar articles in PubMed
Prevalence of familial hypercholesterolemia in patients with premature myocardial infarction. Cui Yuxia et al. Clinical cardiology 2019 Jan Similar articles in PubMed
Life-threatening arrhythmic presentation in patients with arrhythmogenic cardiomyopathy before and after entering the genomic era; a two-decade experience from a large volume center. Rootwelt-Norberg Christine et al. International journal of cardiology 2018 Dec Similar articles in PubMed
Parental hypercholesterolemia and family medical history as predictors of hypercholesterolemia in their children. Robledo Jorge A et al. Archivos argentinos de pediatria 2019 117(1) 41-47 Similar articles in PubMed
The Usefulness of Muscle Biopsy in Initial Diagnostic Evaluation of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes. Baek Min Seong et al. Yonsei medical journal 2019 Jan 60(1) 98-105 Similar articles in PubMed
The Clinical Utility of a Precision Medicine Blood Test Incorporating Age, Sex, and Gene Expression for Evaluating Women with Stable Symptoms Suggestive of Obstructive Coronary Artery Disease: Analysis from the PRESET Registry. Gul Burcu et al. Journal of women's health (2002) 2019 Jan Similar articles in PubMed
Expediting Comprehensive Molecular Analysis to Optimize Initial Treatment of Lung Cancer Patients with Minimal Smoking History. Dagogo-Jack Ibiayi et al. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2019 Jan Similar articles in PubMed
Assessment of the Relationship Between Genetic Determinants of Thyroid Function and Atrial Fibrillation A Mendelian Randomization Study C Ellervik et al, JAMA Cardiology, January 23, 2019
Cost-effectiveness analysis of pharmacogenomics-guided clopidogrel treatment in Spanish patients undergoing percutaneous coronary intervention. Fragoulakis Vasilios et al. The pharmacogenomics journal 2019 Jan Similar articles in PubMed
Genetic risk score (GRS) constructed from polymorphisms in the PON1, IL-6, ITGB3, and ALDH2 genes is associated with the risk of coronary artery disease in Pakistani subjects. Shabana N A et al. Lipids in health and disease 2018 Sep 17(1) 224 Similar articles in PubMed
The clinical and genetic spectrum of catecholaminergic polymorphic ventricular tachycardia: findings from an international multicentre registry. Roston Thomas M et al. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2018 20(3) 541-547 Similar articles in PubMed
A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers. Mosley Jonathan D et al. Nature communications 2018 9(1) 3522 Similar articles in PubMed
Validation of a clinical pharmacogenetic model to predict methotrexate nonresponse in rheumatoid arthritis patients. Eektimmerman Frank et al. Pharmacogenomics 2019 Jan Similar articles in PubMed
Alpha 1-antitrypsin deficiency in patients with chronic obstructive pulmonary disease patients: is systematic screening necessary? da Costa Cláudia Henrique et al. BMC research notes 2019 Jan 12(1) 10 Similar articles in PubMed
Place-Based Inequity in Smoking Prevalence in the Largest Cities in the United States EC Leas et al, JAMA Internal Medicine, January 2019
Prognostic Impact of Genetic Polymorphism in Mineralocorticoid Receptor and Comorbidity With Hypertension in Androgen-Deprivation Therapy. Shiota Masaki et al. Frontiers in oncology 2018 8635 Similar articles in PubMed
Healthy Lifestyle Factors Associated With Lower Risk of Colorectal Cancer Irrespective of Genetic Risk. Carr Prudence R et al. Gastroenterology 2018 155(6) 1805-1815.e5 Similar articles in PubMed
Effects of Genetic Variants Associated with Familial Hypercholesterolemia on Low-Density Lipoprotein-Cholesterol Levels and Cardiovascular Outcomes in the Million Veteran Program Y San et al. Circulation Genomics Prec Medicine, December 2018
Follow-up of fatty acid β-oxidation disorders in expanded newborn screening era. Janeiro Patrícia et al. European journal of pediatrics 2019 Jan Similar articles in PubMed
Familial hypercholesterolemia and young patients' thoughts on own condition and treatment. Urke Eli Bjørnøy et al. Patient education and counseling 2018 Dec Similar articles in PubMed
Metabolic Syndrome Prediction Using Machine Learning Models with Genetic and Clinical Information from a Nonobese Healthy Population. Choe Eun Kyung et al. Genomics & informatics 2018 Dec 16(4) e31 Similar articles in PubMed
GEN-O-MA project: an Italian network studying clinical course and pathogenic pathways of moyamoya disease-study protocol and preliminary results. Bersano Anna et al. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2019 Jan Similar articles in PubMed
Impact of genetic testing on low-density lipoprotein cholesterol in patients with familial hypercholesterolemia (GenTLe-FH): a randomised waiting list controlled open-label study protocol. Nomura Akihiro et al. BMJ open 2018 Dec 8(12) e023636 Similar articles in PubMed
Uptake and radiological findings of screening cerebral magnetic resonance scans in patients with hereditary haemorrhagic telangiectasia. Fatania Gavin et al. Intractable & rare diseases research 2018 Nov 7(4) 236-244 Similar articles in PubMed
Hypertension genetic risk score is associated with burden of coronary heart disease among patients referred for coronary angiography. Lukács Krogager Maria et al. PloS one 2018 13(12) e0208645 Similar articles in PubMed
Fetal congenital heart disease: Associated anomalies, identification of genetic anomalies by single-nucleotide polymorphism array analysis, and postnatal outcome. Cai Meiying et al. Medicine 2018 Dec 97(50) e13617 Similar articles in PubMed
Association between genetic polymorphisms of CYP2C9 and VKORC1 and safety and efficacy of warfarin: Results of a 5 years audit. Biswas Mansij et al. Indian heart journal 2018 Dec 70 Suppl 3S13-S19 Similar articles in PubMed
Impact of pharmacogenetics on statin-induced myopathy in South-Indian subjects. Ramakumari Nuthalapati et al. Indian heart journal 2018 Dec 70 Suppl 3S120-S125 Similar articles in PubMed
Predicting Patient Response to the Antiarrhythmic Mexiletine Based on Genetic Variation: Personalized Medicine for Long QT Syndrome. Zhu Wandi et al. Circulation research 2018 Dec Similar articles in PubMed
Genetic variations in familial hypercholesterolemia and cascade screening in East Asians. Chan Melody Lok-Yi et al. Molecular genetics & genomic medicine 2018 Dec Similar articles in PubMed
Blood-Based Biomarkers for Predicting the Risk for Five-Year Incident Coronary Heart Disease in the Framingham Heart Study via Machine Learning. Dogan Meeshanthini V et al. Genes 2018 Dec 9(12) Similar articles in PubMed
Prevalence of Noonan spectrum disorders in a pediatric population with valvar pulmonary stenosis. Anderson Kailyn et al. Congenital heart disease 2018 Dec Similar articles in PubMed
Clinical and genetic profile of congenital long QT syndrome in Hong Kong: a 20-year experience in paediatrics. Kwok S Y et al. Hong Kong medical journal = Xianggang yi xue za zhi 2018 Dec Similar articles in PubMed