Sandra Disse-Nicodème

Author

Also Known As

Disse-Nicodeme, S, S Disse-Nicodème, S. Disse-Nicodème, Sandra Disse-Nicodeme, Sandra Disse-Nicodème, Sandra Disse-Nicodème, Sandra Disse‐Nicodeme

Publications

Citations

H-Index

Concepts

All Affiliations

Inserm Collège de France Hôpital Européen Georges-Pompidou Centre Hospitalier Universitaire Amiens-Picardie Université de Limoges

About

Sandra Disse-Nicodème is an author at Inserm specializing in medicine, hypertension, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	413
2	Public Health	1	1	36
3	Biostatistics	1	1	36
4	Cell Biology	1	1	194
5	Genetic Medicine	1	1	36

Sandra Disse-Nicodème

Publications

Citations

H-Index

Page 1

	Year	Citations
Human Hypertension Caused by Mutations in WNK Kinases Frederick H. Wilson, Sandra Disse-Nicodème, Keith A. Choate, Science	2001	1.5K
Multiple Promoters in the WNK1 Gene: One Controls Expression of a Kidney-Specific Kinase-Defective Isoform Céline Delaloy, Jingyu Lu, Anne-Marie Houot, Molecular and Cellular Biology HypertensionGeneticsNovel ExonRenal FunctionSignaling Pathway	2003	194
A New Locus on Chromosome 12p13.3 for Pseudohypoaldosteronism Type II, an Autosomal Dominant Form of Hypertension Sandra Disse-Nicodème, Jean‐Michel Achard, Isabelle Desitter, The American Journal of Human Genetics HypertensionPseudohypoaldosteronism Type IiGeneticsChromosome 12P13.3New Locus	2000	112
Phenotypic And Genetic Heterogeneity Of Familial Hyperkalaemic Hypertension (Gordon Syndrome) Jean‐Michel Achard, Sandra Disse-Nicodème, Béatrice Fiquet‐Kempf, Clinical and Experimental Pharmacology and Physiology	2001	86
Familial hyperkalemic hypertension: phenotypic analysis in a large family with the WNK1 deletion mutation Jean‐Michel Achard, David G. Warnock, Sandra Disse-Nicodème, The American Journal of Medicine HypertensionGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic Epidemiology	2003	58
Genetic heterogeneity of familial hyperkalaemic hypertension Sandra Disse-Nicodème, Isabelle Desitter, Béatrice Fiquet‐Kempf, Journal of Hypertension HypertensionGeneticsGenetic EpidemiologyHuman PolymorphismGenetic Linkage	2001	36
Familial hyperkalemic hypertension (Gordon syndrome): evidence for phenotypic variability in a study of 7 families. Sandra Disse-Nicodème, Achard Jm, Julie F. N. Potier, PubMed HypertensionGordon SyndromeGenetic DisorderGeneticsGenetic Epidemiology	2001	13

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