Donate Help Contact The AHA Sign In Home
American Heart Association
Hypertension
Search: search_blue_button Advanced Search
Hypertension. 2002;39:3-9
doi: 10.1161/hy1201.100415
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrowPubmed/NCBI databases
Medline Plus Health Information
*High Blood Pressure
Related Collections
Right arrow Genetics of cardiovascular disease
Right arrow Hypertension - basic studies

(Hypertension. 2002;39:3.)
© 2002 American Heart Association, Inc.


Scientific Contributions

Multi-Center Genetic Study of Hypertension

The Family Blood Pressure Program (FBPP)

The FBPP Investigators

For names of investigators and network affiliations, please see the Appendix.

Correspondence to Eric Boerwinkle, PhD, Human Genetics Center, 1200 Herman Pressler, Houston, TX 77030. E-mail eric.boerwinkle{at}uth.tmc.edu

The Family Blood Pressure Program (FBPP) consists of 4 independently established multicenter networks of investigators who have complementary approaches to the genetics of blood pressure levels and hypertension. The program has recruited participants from the African American, Mexican American, Asian, and non-Hispanic white populations. Each network utilized study designs, laboratory measurements, and analytic methods that made efficient use of the unique characteristics of their populations and the investigators’ expertise. The individual networks subsequently unified core study components into a single cohesive program. The unified FBPP includes (1) standardized clinic and laboratory protocols for core variables to facilitate direct comparison of results among networks, (2) coordination among laboratories to avoid unnecessary duplication of effort, (3) utilization of a single laboratory for genome-wide marker typing, and (4) a pooled data set containing phenotype and genotype information from >11 000 individuals.


Key Words: blood pressure • genetics • sibling pairs • linkage mapping




This article has been cited by other articles:


Home page
HypertensionHome page
P.-a. B. Shih and D. T. O'Connor
Hereditary Determinants of Human Hypertension: Strategies in the Setting of Genetic Complexity
Hypertension, June 1, 2008; 51(6): 1456 - 1464.
[Full Text] [PDF]


Home page
StrokeHome page
R. Sherva, M. B. Miller, J. S. Pankow, S. C. Hunt, E. Boerwinkle, T. H. Mosley, A. B. Weder, J. D. Curb, A. Luke, A. C. Morrison, et al.
A Whole-Genome Scan for Stroke or Myocardial Infarction in Family Blood Pressure Program Families
Stroke, April 1, 2008; 39(4): 1115 - 1120.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
A. A. Ellington, A. R. Malik, G. G. Klee, S. T. Turner, A. D. Rule, T. H. Mosley Jr, and I. J. Kullo
Association of Plasma Resistin With Glomerular Filtration Rate and Albuminuria in Hypertensive Adults
Hypertension, October 1, 2007; 50(4): 708 - 714.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
G. Wen, J. Wessel, W. Zhou, G. B. Ehret, F. Rao, M. Stridsberg, S. K. Mahata, P. M. Gent, M. Das, R. S. Cooper, et al.
An ancestral variant of Secretogranin II confers regulation by PHOX2 transcription factors and association with hypertension
Hum. Mol. Genet., July 15, 2007; 16(14): 1752 - 1764.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
G. L. Schwartz, K. R. Bailey, T. Mosley, D. S. Knopman, C. R. Jack Jr, V. J. Canzanello, and S. T. Turner
Association of Ambulatory Blood Pressure With Ischemic Brain Injury
Hypertension, June 1, 2007; 49(6): 1228 - 1234.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
D. M. Hallman, E. Boerwinkle, V. H. Gonzalez, B. E. K. Klein, R. Klein, and C. L. Hanis
A Genome-Wide Linkage Scan for Diabetic Retinopathy Susceptibility Genes in Mexican Americans With Type 2 Diabetes From Starr County, Texas
Diabetes, April 1, 2007; 56(4): 1167 - 1173.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Public HealthHome page
P. A. Marshall, C. A. Adebamowo, A. A. Adeyemo, T. O. Ogundiran, M. Vekich, T. Strenski, J. Zhou, T. E. Prewitt, R. S. Cooper, and C. N. Rotimi
Voluntary Participation and Informed Consent to International Genetic Research
Am J Public Health, November 1, 2006; 96(11): 1989 - 1995.
[Abstract] [Full Text] [PDF]


Home page
J. Am. Soc. Nephrol.Home page
S. T. Turner, S. L.R. Kardia, T. H. Mosley, A. D. Rule, E. Boerwinkle, and M. de Andrade
Influence of Genomic Loci on Measures of Chronic Kidney Disease in Hypertensive Sibships
J. Am. Soc. Nephrol., July 1, 2006; 17(7): 2048 - 2055.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
I. J. Kullo, K. Ding, E. Boerwinkle, S. T. Turner, T. H. Mosley Jr, S. L.R. Kardia, and M. de Andrade
Novel Genomic Loci Influencing Plasma Homocysteine Levels
Stroke, July 1, 2006; 37(7): 1703 - 1709.
[Abstract] [Full Text] [PDF]


Home page
J. Lipid Res.Home page
J. H. Stengard, S. L. R. Kardia, S. C. Hamon, R. Frikke-Schmidt, A. Tybjaerg-Hansen, V. Salomaa, E. Boerwinkle, and C. F. Sing
Contribution of regulatory and structural variations in APOE to predicting dyslipidemia
J. Lipid Res., February 1, 2006; 47(2): 318 - 328.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
S. J. Bielinski, A. I. Lynch, M. B. Miller, A. Weder, R. Cooper, A. Oberman, Y.-D. I. Chen, S. T. Turner, M. Fornage, M. Province, et al.
Genome-Wide Linkage Analysis for Loci Affecting Pulse Pressure: The Family Blood Pressure Program
Hypertension, December 1, 2005; 46(6): 1286 - 1293.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
A. T. Kraja, D. C. Rao, A. B. Weder, R. Cooper, J. D. Curb, C. L. Hanis, S. T. Turner, M. de Andrade, C. A. Hsiung, T. Quertermous, et al.
Two Major QTLs and Several Others Relate to Factors of Metabolic Syndrome in the Family Blood Pressure Program
Hypertension, October 1, 2005; 46(4): 751 - 757.
[Abstract] [Full Text] [PDF]


Home page
Diabetes CareHome page
D. M. Hallman, J. C. Huber Jr., V. H. Gonzalez, B. E.K. Klein, R. Klein, and C. L. Hanis
Familial Aggregation of Severity of Diabetic Retinopathy in Mexican Americans From Starr County, Texas
Diabetes Care, May 1, 2005; 28(5): 1163 - 1168.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
P. An, B. I. Freedman, C. L. Hanis, Y.-D. I. Chen, A. B. Weder, N. J. Schork, E. Boerwinkle, M. A. Province, C. A. Hsiung, X. Wu, et al.
Genome-wide Linkage Scans for Fasting Glucose, Insulin, and Insulin Resistance in the National Heart, Lung, and Blood Institute Family Blood Pressure Program: Evidence of Linkages to Chromosome 7q36 and 19q13 From Meta-Analysis
Diabetes, March 1, 2005; 54(3): 909 - 914.
[Abstract] [Full Text] [PDF]


Home page
Arch Intern MedHome page
J. G. O'Meara, S. L. R. Kardia, J. J. Armon, C. A. Brown, E. Boerwinkle, and S. T. Turner
Ethnic and Sex Differences in the Prevalence, Treatment, and Control of Dyslipidemia Among Hypertensive Adults in the GENOA Study
Arch Intern Med, June 28, 2004; 164(12): 1313 - 1318.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
K. E. North, K. M. Rose, I. B. Borecki, A. Oberman, S. C. Hunt, M. B. Miller, J. Blangero, L. Almasy, and J. S. Pankow
Evidence for a Gene on Chromosome 13 Influencing Postural Systolic Blood Pressure Change and Body Mass Index
Hypertension, April 1, 2004; 43(4): 780 - 784.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
S. T. Turner, C. R. Jack, M. Fornage, T. H. Mosley, E. Boerwinkle, and M. de Andrade
Heritability of Leukoaraiosis in Hypertensive Sibships
Hypertension, February 1, 2004; 43(2): 483 - 487.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
R. A. Barkley, A. Chakravarti, R. S. Cooper, R. C. Ellison, S. C. Hunt, M. A. Province, S. T. Turner, A. B. Weder, E. Boerwinkle, and on behalf of the Family Blood Pressure Program
Positional Identification of Hypertension Susceptibility Genes on Chromosome 2
Hypertension, February 1, 2004; 43(2): 477 - 482.
[Abstract] [Full Text] [PDF]


Home page
Vasc MedHome page
I. J Kullo, K. R Bailey, S. L. Kardia, T. H Mosley Jr, E. Boerwinkle, and S. T Turner
Ethnic differences in peripheral arterial disease in the NHLBI Genetic Epidemiology Network of Arteriopathy (GENOA) study
Vascular Medicine, November 1, 2003; 8(4): 237 - 242.
[Abstract] [PDF]


Home page
J. Lipid Res.Home page
R. A. Barkley, A. C. Brown, C. L. Hanis, S. L. Kardia, S. T. Turner, and E. Boerwinkle
Lack of genetic linkage evidence for a trans-acting factor having a large effect on plasma lipoprotein[a] levels in African Americans
J. Lipid Res., July 1, 2003; 44(7): 1301 - 1305.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
A. C. Morrison, A. Brown, S. L.R. Kardia, S. T. Turner, and E. Boerwinkle
Evaluating the Context-Dependent Effect of Family History of Stroke in a Genome Scan for Hypertension
Stroke, May 1, 2003; 34(5): 1170 - 1175.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
A. B. Weder, M. C. Delgado, X. Zhu, L. Gleiberman, D. Kan, and A. Chakravarti
Erythrocyte Sodium-Lithium Countertransport and Blood Pressure: A Genome-Wide Linkage Study
Hypertension, March 1, 2003; 41(3): 842 - 846.
[Abstract] [Full Text] [PDF]


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
L. A. Lange, E. M. Lange, L. F. Bielak, C. D. Langefeld, S. L. Kardia, P. Royston, S. T. Turner, P. F. Sheedy II, E. Boerwinkle, and P. A. Peyser
Autosomal Genome-Wide Scan for Coronary Artery Calcification Loci in Sibships at High Risk for Hypertension
Arterioscler. Thromb. Vasc. Biol., March 1, 2002; 22(3): 418 - 423.
[Abstract] [Full Text] [PDF]