The molecular basis of blood pressure variation

Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities

(2012) Lynn M. Boyden et al.   NATURE

Hypertension with or without adrenal hyperplasia due to different inherited mutations in the potassium channel KCNJ5

(2012) U. I. Scholl et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Disruption of Na + ,HCO 3 − Cotransporter NBCn1 (slc4a7) Inhibits NO-Mediated Vasorelaxation, Smooth Muscle Ca 2+ Sensitivity, and Hypertension Development in Mice

(2011) Ebbe Boedtkjer et al.   CIRCULATION

Role of renal medullary oxidative and/or carbonyl stress in salt-sensitive hypertension and diabetes

(2011) Takefumi Mori et al.   CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY

Linkage Analysis in the Next-Generation Sequencing Era

(2011) Joan E. Bailey-Wilson et al.   HUMAN HEREDITY

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

(2011) Georg B. Ehret et al.   NATURE

Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians

(2011) Norihiro Kato et al.   NATURE GENETICS

Under pressure: the search for the essential mechanisms of hypertension

(2011) Thomas M Coffman   NATURE MEDICINE

Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects

(2011) Hannsjörg W. Seyberth et al.   PEDIATRIC NEPHROLOGY

Genetic testing in renal disease

(2011) Detlef Bockenhauer et al.   PEDIATRIC NEPHROLOGY

K+ Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension

(2011) M. Choi et al.   SCIENCE

Inherited renal tubular dysgenesis may not be universally fatal

(2010) Ruth Schreiber et al.   PEDIATRIC NEPHROLOGY

KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function

(2010) M. Reichold et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Renin–angiotensin system in kidney development: renal tubular dysgenesis

(2009) Marie Claire Gubler et al.   KIDNEY INTERNATIONAL

Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure

(2009) Christopher Newton-Cheh et al.   NATURE GENETICS

Genome-wide association study identifies eight loci associated with blood pressure

(2009) Christopher Newton-Cheh et al.   NATURE GENETICS

Genome-wide association study of blood pressure and hypertension

(2009) Daniel Levy et al.   NATURE GENETICS

Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10

(2009) U. I. Scholl et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A Novel Form of Human Mendelian Hypertension Featuring Nonglucocorticoid-Remediable Aldosteronism

(2008) David S. Geller et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Rare independent mutations in renal salt handling genes contribute to blood pressure variation

(2008) Weizhen Ji et al.   NATURE GENETICS

Inversion Region for Hypertension and Brachydactyly on Chromosome 12p Features Multiple Splicing and Noncoding RNA

(2007) Sylvia Bähring et al.   HYPERTENSION