Xosé M. Lens - Concepedia

Concepedia

Author

Xosé M. Lens

Complejo Hospitalario Universitario de Santiago

Also Known As

Winfried März, X M Lens, X. Lens, X.M. Lens, XOSE M. LENS, Xose Lens, Xose M. Lens, Xose Manuel Lens, Xosé M Lens, Xosé M. Lens

38

Publications

1.3K

Citations

15

H-Index

42

Concepts

All Affiliations

Complejo Hospitalario Universitario de Santiago Complexo Hospitalario Universitario A Coruña Johns Hopkins University Albert Einstein College of Medicine UCLouvain

XM

About

Xosé M. Lens is an author at Complejo Hospitalario Universitario de Santiago specializing in medicine, pathology, and urology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	12	638
2	Public Health	1	1	109
3	Endocrinology	1	1	11
4	Hepatology	1	1	11
5	Immunology	1	1	11

Xosé M. Lens

×

17

Publications

1.3K

Citations

15

H-Index

	Year	Citations
Renal Failure in Multiple Myeloma Joan Bladé, Patricia Fernández‐Llama, Francesc Bosch, Archives of Internal Medicine	1998	381
Mutations in theCOL4A4 and COL4A3 Genes Cause Familial Benign Hematuria Célia Bádenas, Manuel Praga, Bárbara Tazón‐Vega, Journal of the American Society of Nephrology	2002	125
Comparison between siblings and twins supports a role for modifier genes in ADPKD Alexandre Persu, M. Duyme, Yves Pirson, Kidney International Genetic AnalysisDevelopmental BiologyGenetic DisorderGeneticsGenetic Epidemiology	2004	109
Aberrant Splicing in the PKD2 Gene as a Cause of Polycystic Kidney Disease David M. Reynolds, Tomohito Hayashi, Yiqiang Cai, Journal of the American Society of Nephrology Aberrant SplicingGeneticsRenal PathologyPathologyMolecular Genetics	1999	107
Evaluating the clinical utility of a molecular genetic test for polycystic kidney disease Miguel A. García-González, Jeffrey G. Jones, Susan K. Allen, Molecular Genetics and Metabolism Genetic TestingUrologyClinical UtilityGeneticsChronic Kidney Disease	2007	92
Long-term anti-proteinuric effect of Losartan in renal transplant recipients treated for hypertension Jesús Calviño, Xosé M. Lens, Rafael Romero, Nephrology Dialysis Transplantation	2000	70
Homozygosity for uromodulin disorders: FJHN and MCKD-type 2 Wânia Rezende-Lima, Kleber Simônio Parreira, Miguel A. García-González, Kidney International Uromodulin DisordersMendelian DisorderGenetic DisorderGeneticsInherited Metabolic Disease	2004	65
Autosomal recessive Alport’s syndrome and benign familial hematuria are collagen type IV diseases Bárbara Tazón Vega, Célia Bádenas, Elisabet Ars, American Journal of Kidney Diseases UrologyMendelian DisorderGenetic DisorderPathologyMedicine	2003	56
A Novel Pattern of Mutation in Uromodulin Disorders: Autosomal Dominant Medullary Cystic Kidney Disease Type 2, Familial Juvenile Hyperuricemic Nephropathy, and Autosomal Dominant Glomerulocystic Kidney Disease Xosé M. Lens, Julio Fernandez-Banet, Patricia Outeda, American Journal of Kidney Diseases Glomerular DiseaseGlomerulonephritisUromodulin DisordersUrologyRenal Disease	2005	49
Novel stop and frameshifting mutations in the autosomal dominant polycystic kidney disease 2 (PKD2) gene Miguel Viribay, Tomohito Hayashi, Dolores Tellerı́a, Human Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsRenal Pathology	1997	48

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