Endophenotypes, heritability, and underlying complexity in hypertension

American Journal of Hypertension

Volumn 23, Issue 8, 2010, Pages 819-

  Williams, Scott M ^a  

^a VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANGIOTENSINOGEN;

BLOOD PRESSURE; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETIC VARIABILITY; HERITABILITY; HUMAN; HYPERTENSION; NOTE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; SINGLE NUCLEOTIDE POLYMORPHISM; BLOOD; GENETICS;

ANGIOTENSINOGEN; BLOOD PRESSURE; HUMANS; HYPERTENSION; PHENOTYPE;

EID: 77955767155     PISSN: 08957061     EISSN: None     Source Type: Journal    
DOI: 10.1038/ajh.2010.101     Document Type: Note

References (4)

1. Watkins WS, Rohrwasser A, Peiffer A, Leppert MF, Lalouel J-M, Jorde LB. AGT genetic variation, plasma AGT, and blood pressure: an analysis of the Utah Genetic Reference Project pedigrees. Am J Hypertens 2010; 23:917-923.
2. Moore JH, Williams SM. New strategies for identifying gene-gene interactions in hypertension. Ann Med 2002; 34:88-95.
3. Williams SM, Haines JL, Moore JH. The use of animal models in the study of complex disease: all else is never equal or why do so many human studies fail to replicate animal findings? Bioessays 2004; 26:170-179.
4. Clark AG. The role of haplotypes in candidate gene studies. Genet Epidemiol 2004; 27:321-333.