Juan Rodríguez‐Soriano

Author

Also Known As

J RODRIGUEZ-SORIANO, J Rodriguez-Soriano, J Rodriguez‐Soriano, J Rodríguez-Soriano, J Rodríguez-soriano, J. RODRIGUEZ‐SORIANO, J. Rodriguez-Soriano, J. Rodriguez‐Soriano, J. Rodríguez-Soriano, J. Rodríguez‐Soriano

106

Publications

6.7K

Citations

H-Index

Concepts

All Affiliations

Hospital de Cruces Yale University Howard Hughes Medical Institute King Faisal Specialist Hospital & Research Centre Universidad de Deusto

About

Juan Rodríguez‐Soriano is an author at Hospital de Cruces specializing in medicine, nephrology, and chronic kidney disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	34	4.3K
2	Health Sciences	5	5	143
3	Allergy	2	2	114
4	Education	1	1	15
5	Public Health	1	1	99

Juan Rodríguez‐Soriano

Publications

Citations

H-Index

Page 1

	Year	Citations
Paracellin-1, a Renal Tight Junction Protein Required for Paracellular Mg <sup>2+</sup> Resorption David B. Simon, Yin Lu, Keith A. Choate, Science	1999	1.1K
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III David B. Simon, Ranjit S. Bindra, Traci A. Mansfield, Nature Genetics ChannelopathiesGenetic DisorderChloride Channel GeneGeneticsPathogenesis	1997	863
Genetic heterogeneity of Barter's syndrome revealed by mutations in the K+ channel, ROMK David B. Simon, Fiona E. Karet, Juan Rodríguez‐Soriano, Nature Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyK+ Channel	1996	820
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, Nature Genetics Renal FunctionMolecular PhysiologyBiochemistrySodium HomeostasisPhysiology	1999	681
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, The American Journal of Human Genetics UrologyOphthalmologyMedicineGeneticsRenal Failure	2006	511
Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I David S. Geller, Juan Rodríguez‐Soriano, Alfredo V. Boado, Nature Genetics GeneticsPhysiologyPrimary AldosteronismMineralocorticoid Receptor BiologyMedicine	1998	425
Transient pseudohypoaldosteronism secondary to obstructive uropathy in infancy Juan Rodríguez‐Soriano, Alfredo Vallo, Roberto Oliveros, The Journal of Pediatrics UrologyMedicinePediatricsPrimary AldosteronismAdrenal Disease	1983	135
Autosomal Dominant Pseudohypoaldosteronism Type 1 David S. Geller, Junhui Zhang, Maria‐Christina Zennaro, Journal of the American Society of Nephrology UrologyGenetic DisorderMedicineGeneticsPhysiology	2006	131
Enteropathy related to fish, rice, and chicken. Juan Carlos Vitoria, Camarero Salcés C, A Sojo, PubMed NutritionGastroenterologyPathologyDigestive TractPrecision Dairy	1982	99
Renal handling of water and sodium in infancy and childhood: A study using clearance methods during hypotonic saline diuresis Juan Rodríguez‐Soriano, Alfredo Vallo, Gonzalo Castillo, Kidney International Electrolyte DisorderUrologyRenal HandlingHypotonic Saline DiuresisRenal Function	1981	97

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