Heart disease || Public Health Genomics Knowledge Base (v1.0)

Public Health Genomics Knowledge Base (v1.0)








Last Updated: May 07, 2016

• The interleukin 6 c.-174 CC genotype is a predictor for new cardiovascular events in patients with coronary heart disease within three years follow-up.
  Reichert Stefan, et al. Cytokine 2016 4 136-138
• Fetal bradycardia without fetal distress: case presentation and review of the literature.
  Webster R D et al. Obstetrics and gynecology 1977 Jul 50(1 Suppl) 50s-52s
• Familial hypercholesterolaemia reduces the quality of life of patients not reaching treatment targets.
  Mortensen Gitte Lee et al. Danish medical journal 2016 May 63(5)
• A Biobank for Long-term and Sustainable Research in the Field of Congenital Heart Disease in Germany.
  Pickardt Thomas et al. Genomics, proteomics & bioinformatics 2016 Apr
• Association study of inflammatory genes with rheumatic heart disease in North Indian population: A multi-analytical approach.
  Gupta Usha, et al. Immunology letters 2016 4 53-62
• 3'UTR SNPs and Haplotypes in the GATA4 Gene Contribute to the Genetic Risk of Congenital Heart Disease.
  Pulignani Silvia, et al. Revista espanola de cardiologia (English ed.) 2016 4
• Effect of SORT1, APOB and APOE polymorphisms on LDL-C and coronary heart disease in Pakistani subjects and their comparison with Northwick Park Heart Study II.
  Shahid Saleem Ullah, et al. Lipids in health and disease 2016 0 (1) 83
• Cardiovascular Risk Factors and Ischemic Heart Disease: Is the Confluence of Risk Factors Greater than the Parts? A Genetic Approach.
  Elosua Roberto et al. Circulation. Cardiovascular genetics 2016 Apr
• Identifying familial hypercholesterolemia in acute coronary syndrome.
  Gencer Baris et al. Current opinion in lipidology 2016 Apr
• Brain natriuretic peptide and insulin resistance in older adults.
  Kim F, et al. Diabetic medicine : a journal of the British Diabetic Association 2016 4
• Chromosome 9p21 and ABCA1 Genetic Variants and Their Interactions on Coronary Heart Disease and Ischemic Stroke in a Chinese Han Population.
  Cao Xiao-Li, et al. International journal of molecular sciences 2016 0 (4)
• [GENES ALLELE STATUS OF ANGIOTENSINCONVERTING ENZYME (I/D) AND END OTHELIAL NITRIC OXIDE SYNTHASE (894 G > T) IN PATIENTS WITH ACUTE CORONARY SYNDROME].
  Sydorchuk L P, et al. Likars'ka sprava / Ministerstvo okhorony zdorov'ia Ukrai?ny 0 0 (5-6) 24-34
• Sex-Specific Genetic Variants are Associated With Coronary Endothelial Dysfunction.
  Yoshino Satoshi, et al. Journal of the American Heart Association 2016 0 (4)
• Nutrigenomics, the Microbiome, and Gene-Environment Interactions: New Directions in Cardiovascular Disease Research, Prevention, and Treatment A Scientific Statement From the American Heart Association
  JF Ferguson et al, AHA Scientific Statement, Circulation, Cardiovascular Genetics, April 2016
• Cardiovascular Risk Factors and Ischemic Heart Disease: Is the Confluence of Risk Factors Greater than the Parts? A Genetic Approach 
  R Elusua et al, Circulation: Cardiovascular Genetics, April 2016
• [Desaturases of fatty acids (FADS) and their physiological and clinical implication].
  Žák Aleš, et al. Casopi?s le?kar?u? c?esky?ch 2016 0 (2) 15-21
• Cracking the connection between genes and diet could lead to future heart disease treatments,
  American Heart Association News, April 19, 2016
• Reassessing Risk Factors in Pediatric Patients With Pacemakers Implanted for Atrioventricular Block: The Impact of Nonsustained Ventricular Tachycardia.
  Niu Mary C, et al. Journal of cardiovascular electrophysiology 2016 4 (4) 471-9
• MnSOD and GPx1 polymorphism relationship with coronary heart disease risk and severity.
  Souiden Yosra, et al. Biological research 2016 0 (1) 22
• MADD-FOLH1 Polymorphisms and Their Haplotypes with Serum Lipid Levels and the Risk of Coronary Heart Disease and Ischemic Stroke in a Chinese Han Population.
  Wu Dong-Feng, et al. Nutrients 2016 0 (4)
• The FoxO3 gene and cause-specific mortality.
  Willcox Bradley J, et al. Aging cell 2016 4
• Plasma levels of vitamin K and the risk of ischemic heart disease: a Mendelian randomization study.
  Schooling C Mary, et al. Journal of thrombosis and haemostasis : JTH 2016 4
• Efficacy of clinical diagnostic criteria for familial hypercholesterolemia genetic testing in Poland.
  Mickiewicz Agnieszka, et al. Atherosclerosis 2016 3 52-58
• Detection and putative effect of GATA4 gene variants in patients with congenital cardiac septal defects.
  Al-Azzouny M A, et al. Cellular and molecular biology (Noisy-le-Grand, France) 2016 0 (3) 10-4
• Association of a Family History of Coronary Heart Disease With Initiation of Statin Therapy in Individuals at Intermediate Risk
  Safarova MS, et al. JAMA Cardiol. April 13, 2016
• De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects.
  Priest James R, et al. PLoS genetics 2016 4 (4) e1005963
• Associations of NKX2-5 Genetic Polymorphisms with the Risk of Congenital Heart Disease: A Meta-analysis.
  Xie Xiaochuan, et al. Pediatric cardiology 2016 3
• [Genes for Fibrogenesis in the Determination of Susceptibility to Myocardial Infarction].
  Goncharova I A, et al. Molekuliarnaia biologiia 0 0 (1) 94-105
• Treatment Gaps in Adults with Heterozygous Familial Hypercholesterolemia in the United States: Data from the CASCADE-FH Registry.
  deGoma Emil M et al. Circulation. Cardiovascular genetics 2016 Mar
• A twist on the genetic link between Alzheimer’s and heart disease,
  by Julie Corliss, Harvard Health Blog, March 25, 2016

• CDC Information (17)
• CDC-Authored Pub (11)

• Human (0)
• Pathogen (1)

• Human (7085)
• Pathogen (0)

• Human (113)
• Pathogen (0)

• Guidelines (10)
• Tier Table (8)
• Synthesis (29)

• Implementation (109)

Relevant Resources

• Cancer Genomics and Epidemiology Navigator (CGEN)
• Genetics and Genomics Competencies Center (G2C2)
• NIH Genetic Testing Registry
• NIH MedGen Database
• Online Mendelian Inheritance in Man (OMIM)
• PharmGKB