STROKE || Public Health Genomics Knowledge Base (v1.2)

Public Health Genomics Knowledge Base (v1.2)

STROKE

Last Updated: Oct 28, 2016

• The Association Between the Genetic Variants of the NOTCH3 Gene and Ischemic Stroke Risk.
  Yuan Xiaoling, et al. Medical science monitor : international medical journal of experimental and clinical research 2016 10 3910-3914
• Genetics of Sickle Cell-Associated Cardiovascular Disease: An Expert Review with Lessons Learned in Africa.
  Geard Amy et al. Omics : a journal of integrative biology 2016 Oct 20(10) 581-592
• Pediatric Sickle Cell Disease - Past Successes and Future Challenges.
  Meier Emily Riehm et al. Pediatric research 2016 Oct
• Single-Nucleotide Polymorphism rs17611 of Complement Component 5 Shows Association with Ischemic Stroke in Northeast Chinese Population.
  Guo Liang, et al. Genetic testing and molecular biomarkers 2016 10
• No Association Between Single-Nucleotide Polymorphism 56 (SNP56) in Phosphodiesterase 4D (PDE4D) Gene and Susceptibility to Ischemic Stroke: A Meta-Analysis of 15 Studies.
  Zhang Xin-Yong, et al. Medical science monitor : international medical journal of experimental and clinical research 2016 10 3820-3827
• No Association Between SNP56 in PDE4D Gene and Susceptibility to Ischemic Stroke: A Meta-Analysis of 15 Studies.
  Zhang Xin-Yong, et al. Medical science monitor : international medical journal of experimental and clinical research 2016 10 3820-3827
• Polymorphism of the XRCC1 Gene Is Associated with Susceptibility and Short-Term Recovery of Ischemic Stroke.
  He Wei, et al. International journal of environmental research and public health 2016 10 (10)
• World Stroke Day: We Can Prevent Stroke 
• APSH YI-02 THE POLYMORPHISM IN ALDEHYDE DEHYDROGENASE-2 (ALDH2) GENE IS ASSOCIATED WITH MYOCARDIAL INFARCTION AND STROKE IN A CHINESE POPULATION.
  Liu Xin, et al. Journal of hypertension 2016 9 e385
• Circulating Apolipoprotein E Concentration and Cardiovascular Disease Risk: Meta-analysis of Results from Three Studies.
  Sofat Reecha, et al. PLoS medicine 2016 10 (10) e1002146
• OS 05-02 ASSOCIATION OF G-PROTEIN BETA3 SUBUNIT GENE C825T POLYMORPHISM WITH CARDIAC AND CEREBROVASCULAR EVENTS IN CHINESE HYPERTENSIVE PATIENTS.
  Zhu Weiwei, et al. Journal of hypertension 2016 9 e58
• OS 08-03 PHARMACOGENETIC MARKERS OF SURVIVAL.
  Erdman Vera, et al. Journal of hypertension 2016 9 e68
• POA 02-1 GENETIC BASIS OF BLOOD PRESSURE AND HYPERTENSION.
  Dominiczak Anna F, et al. Journal of hypertension 2016 9 e33
• Relationship between Interleukin-6 (-174G/C and -572C/G) Promoter Gene Polymorphisms and Risk of Intracerebral Hemorrhage: A Meta-Analysis.
  Kumar Pradeep, et al. Pulse (Basel, Switzerland) 2016 9 (2-3) 61-68
• Genotypes and phenotypes of protein S deficiency in Thai children with thromboembolism.
  Komwilaisak Patcharee, et al. Pediatric blood & cancer 2016 10

• CDC Information (9)
• CDC-Authored Pub (2)

• Human (15)
• Pathogen (0)

• Human (2562)
• Pathogen (0)

• Human (20)
• Pathogen (0)

• Guidelines (5)
• Tier Table (1)
• Synthesis (10)

• Huamn (43)
• Pathogen (0)

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