Multi-Center Genetic Study of Hypertension

Article Properties
Abstract
Journal Categories
Medicine
Internal medicine
Specialties of internal medicine
Diseases of the blood and blood-forming organs
Medicine
Internal medicine
Specialties of internal medicine
Diseases of the circulatory (Cardiovascular) system
Medicine
Internal medicine
Specialties of internal medicine
Diseases of the respiratory system
Medicine
Medicine (General)
Description

Can genetics unlock the secrets of hypertension across diverse populations? This multi-center study examines the genetics of blood pressure levels and hypertension in African American, Mexican American, Asian, and non-Hispanic white populations. The Family Blood Pressure Program (FBPP) utilized complementary approaches to efficiently leverage the unique characteristics of each population and the expertise of the investigators. Core study components were unified into a single cohesive program, including standardized clinic and laboratory protocols, coordinated laboratories, genome-wide marker typing, and a pooled data set containing phenotype and genotype information from over 11,000 individuals. This comprehensive approach allows for direct comparison of results across networks. The FBPP aims to identify genetic factors contributing to hypertension and blood pressure regulation. By pooling data and standardizing methods, the program seeks to advance our understanding of the complex genetic architecture underlying hypertension, potentially leading to more targeted prevention and treatment strategies.

Published in Hypertension, this genetic study directly addresses the journal's core focus on the causes and mechanisms of high blood pressure. By examining diverse populations and utilizing standardized protocols, the research aligns with the journal's commitment to advancing our understanding of hypertension and developing effective prevention and treatment strategies. The study's emphasis on genetics complements other research published in the journal exploring various aspects of cardiovascular health.

Refrences
Citations
Citations Analysis
The first research to cite this article was titled A BDNF Coding Variant is Associated with the NEO Personality Inventory Domain Neuroticism, a Risk Factor for Depression and was published in 2002. The most recent citation comes from a 2023 study titled A BDNF Coding Variant is Associated with the NEO Personality Inventory Domain Neuroticism, a Risk Factor for Depression . This article reached its peak citation in 2009 , with 20 citations.It has been cited in 64 different journals, 21% of which are open access. Among related journals, the Journal of Hypertension cited this research the most, with 8 citations. The chart below illustrates the annual citation trends for this article.
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