Dominique Chauveau - Concepedia

Author

Dominique Chauveau

Also Known As

Chauveau Dominique, Chauveau, D., D Chauveau, D. Chauveau, DOMINIQUE CHAUVEAU, Dominique Chauveau, Kai-Uwe Eckardt, Lionet Arnaud, Luc Frimat, Nassim Kamar

314

Publications

9.5K

Citations

H-Index

131

Concepts

All Affiliations

Inserm Hôpital Rangueil Assistance Publique – Hôpitaux de Paris Hôpital Necker-Enfants Malades Sorbonne Université

About

Dominique Chauveau is an author at Inserm specializing in medicine, nephrology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	34	55	4.7K
2	Public Health	8	8	500
3	Cell Biology	3	3	445
4	Allergy	2	2	56
5	Natural Sciences	1	1	164

Dominique Chauveau

102

Publications

7.7K

Citations

H-Index

Page 1

	Year	Citations
Pancreatic involvement in von Hippel–Lindau disease Pascal Hammel, Valérie Vilgrain, Benoı̂t Terris, Gastroenterology Pancreatic InvolvementPancreatic Fluid CollectionHistopathologyGastroenterologyPathology	2000	422
Clinical Spectrum Associated with Hepatocyte Nuclear Factor-1β Mutations Christine Bellanné‐Chantelot, Dominique Chauveau, Jean–François Gautier, Annals of Internal Medicine	2004	351
Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management—A KDIGO consensus report Kai‐Uwe Eckardt, Seth L. Alper, Corinne Antignac, Kidney International Glomerular DiseaseGlomerulonephritisUrologyRenal DiseaseMedicine	2015	345
Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease Sandro Rossetti, Vickie Kubly, Mark Consugar, Kidney International UrologyGene DosageGenetic DisorderCyst InitiationGenetics	2009	289
Large Genomic Rearrangements in the Hepatocyte Nuclear Factor-1β (<i>TCF2</i>) Gene Are the Most Frequent Cause of Maturity-Onset Diabetes of the Young Type 5 Christine Bellanné‐Chantelot, Séverine Clauin, Dominique Chauveau, Diabetes GeneticsPathologyMolecular GeneticsTcf2 RearrangementsDisease Gene Identification	2005	270
Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current Karin Jurkat‐Rott, Nenad Mitrović, Chao Hang, Proceedings of the National Academy of Sciences	2000	265
Renal replacement therapy for autosomal dominant polycystic kidney disease (ADPKD) in Europe: prevalence and survival--an analysis of data from the ERA-EDTA Registry Edwin M. Spithoven, Anneke Kramer, Esther Meijer, Nephrology Dialysis Transplantation	2014	232
A Cluster of Mutations in the UMOD Gene Causes Familial Juvenile Hyperuricemic Nephropathy with Abnormal Expression of Uromodulin Karin Dahan, Olivier Devuyst, Michèle Smaers, Journal of the American Society of Nephrology	2003	220
Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype Sandro Rossetti, Dominique Chauveau, Vickie Kubly, The Lancet Mutation PositionVascular PhenotypeGenetic DisorderMedicineGenetics	2003	218
Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood Stanislas Faguer, Stéphane Decramer, Nicolas Chassaing, Kidney International Glomerular DiseaseGlomerulonephritisRenal FunctionRenal DiseaseMedicine	2011	211

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