The Japanese Society of Hypertension guidelines for the management of hypertension (JSH 2019)

S Umemura, H Arima, S Arima, K Asayama… - Hypertension …, 2019‏ - nature.com
The Japanese Society of Hypertension (JSH) revised the Guidelines for the Management of
Hypertension 2014 (JSH 2014), and published the JSH 2019. In the development of the JSH …

Animal models of hypertension: a scientific statement from the American Heart Association

LO Lerman, TW Kurtz, RM Touyz, DH Ellison… - …, 2019‏ - ahajournals.org
Hypertension is the most common chronic disease in the world, yet the precise cause of
elevated blood pressure often cannot be determined. Animal models have been useful for …

Genomics of hypertension: the road to precision medicine

S Padmanabhan, AF Dominiczak - Nature Reviews Cardiology, 2021‏ - nature.com
The known genetic architecture of blood pressure now comprises> 30 genes, with rare
variants resulting in monogenic forms of hypertension or hypotension and> 1,477 common …

Salt sensitivity of blood pressure: a scientific statement from the American Heart Association

F Elijovich, MH Weinberger, CAM Anderson… - …, 2016‏ - ahajournals.org
Hypertension is available at http://hyper. ahajournals. org DOI: 10.1161/HYP.
0000000000000047 e8 Hypertension September 2016 distributed trait. Therefore, defining …

Evolving importance of kidney disease: from subspecialty to global health burden

KU Eckardt, J Coresh, O Devuyst, RJ Johnson… - The Lancet, 2013‏ - thelancet.com
In the past decade, kidney disease diagnosed with objective measures of kidney damage
and function has been recognised as a major public health burden. The population …

[HTML][HTML] Gitelman syndrome: consensus and guidance from a kidney disease: improving global outcomes (KDIGO) controversies conference

A Blanchard, D Bockenhauer, D Bolignano, LA Calo… - Kidney international, 2017‏ - Elsevier
Gitelman syndrome (GS) is a rare, salt-losing tubulopathy characterized by hypokalemic
metabolic alkalosis with hypomagnesemia and hypocalciuria. The disease is recessively …

Searching for missing heritability: designing rare variant association studies

O Zuk, SF Schaffner, K Samocha, R Do… - Proceedings of the …, 2014‏ - pnas.org
Genetic studies have revealed thousands of loci predisposing to hundreds of human
diseases and traits, revealing important biological pathways and defining novel therapeutic …

Initial impact of the sequencing of the human genome

ES Lander - Nature, 2011‏ - nature.com
The sequence of the human genome has dramatically accelerated biomedical research.
Here I explore its impact, in the decade since its publication, on our understanding of the …

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

M Choi, UI Scholl, W Ji, T Liu, IR Tikhonova… - Proceedings of the …, 2009‏ - pnas.org
Protein coding genes constitute only approximately 1% of the human genome but harbor
85% of the mutations with large effects on disease-related traits. Therefore, efficient …

The genetics of quantitative traits: challenges and prospects

TFC Mackay, EA Stone, JF Ayroles - Nature Reviews Genetics, 2009‏ - nature.com
A major challenge in current biology is to understand the genetic basis of variation for
quantitative traits. We review the principles of quantitative trait locus map** and …