HRS Bibliography
C
Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31. European Journal of Human Genetics. 2019;27(2):269-277. doi:10.1038/s41431-018-0277-1.
Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals. Human Molecular Genetics. 2015;24(12):3582-3594. doi:10.1093/hmg/ddv097.
G
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. Am J Hum Genet. 2013;93(3):545-54. doi:10.1016/j.ajhg.2013.07.010.
http://www.ncbi.nlm.nih.gov/pubmed/23972371?dopt=Abstract
M
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci. Nat Genet. 2016;48(10):1162-70. doi:10.1038/ng.3660.
N
New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals. Circulation: Cardiovascular Genetics. 2017;10(5):e001778. doi:10.1161/CIRCGENETICS.117.001778.
P
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nat Genet. 2018;50(1):26-41. doi:10.1038/s41588-017-0011-x.
http://www.ncbi.nlm.nih.gov/pubmed/29273807?dopt=Abstract
R
Rare and low-frequency coding variants alter human adult height. Nature. 2017;542(7640):186-190. doi:10.1038/nature21039.
http://www.ncbi.nlm.nih.gov/pubmed/28146470?dopt=Abstract
Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure. PLoS Genetics. 2017;13(3):e1006678. doi:10.1371/journal.pgen.1006678.
S
Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. PLoS Genetics. 2017;13(5):e1006728. doi:10.1371/journal.pgen.1006728.