Juan Rodríguez‐Soriano

Paracellin-1, a Renal Tight Junction Protein Required for Paracellular Mg ²⁺ Resorption

David B. Simon, Yin Lu, Keith A. Choate et al. · Science · 1999 · 1.1K citations

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

David B. Simon, Ranjit S. Bindra, Traci A. Mansfield et al. · Nature Genetics · 1997 · 863 citations

Channelopathies, Genetic Disorder, Chloride Channel Gene +7

Genetic heterogeneity of Barter's syndrome revealed by mutations in the K+ channel, ROMK

David B. Simon, Fiona E. Karet, Juan Rodríguez‐Soriano et al. · Nature Genetics · 1996 · 820 citations

Mendelian Disorder, Genetic Disorder, Genetics +7

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

Fiona E. Karet, Karin E. Finberg, Raoul D. Nelson et al. · Nature Genetics · 1999 · 681 citations

Renal Function, Molecular Physiology, Biochemistry +8

Mutations in the Tight-Junction Gene Claudin 19 (CLDN19) Are Associated with Renal Magnesium Wasting, Renal Failure, and Severe Ocular Involvement

Martin Konrad, André Schaller, Dominik Seelow et al. · The American Journal of Human Genetics · 2006 · 511 citations · Full text

Urology, Ophthalmology, Medicine +7