Hereditary Determinants of Human Hypertension

This publication has 67 references indexed in Scilit:

• Angiotensin-converting enzyme gene polymorphism predicts the time-course of blood pressure response to angiotensin converting enzyme inhibition in the AASK trial
  Journal Of Hypertension, 2007
• Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes
  BMC Medical Genetics, 2007
• Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness
  BMC Medical Genetics, 2007
• Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular risk
  Journal of Clinical Investigation, 2007
• Human microRNA-155 on Chromosome 21 Differentially Interacts with Its Polymorphic Target in the AGTR1 3′ Untranslated Region: A Mechanism for Functional Single-Nucleotide Polymorphisms Related to Phenotypes
  American Journal of Human Genetics, 2007
• An ancestral variant of Secretogranin II confers regulation by PHOX2 transcription factors and association with hypertension
  Human Molecular Genetics, 2007
• Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
  Nature, 2007
• An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP)
  Human Genetics, 2007
• Multiple Genes for Essential-Hypertension Susceptibility on Chromosome 1q
  American Journal of Human Genetics, 2007
• Contributions of the sympathetic nervous system, glutathione, body mass and gender to blood pressure increase with normal aging: influence of heredity
  Journal of Human Hypertension, 2005