Xavier Jeunemaitre

发表

Hypertension Management : Connection of an Expert System to the Artemis Patient Database

Patrice Degoulet, Olivier Gascuel, Patrick Ferrand, 1986 .

Implementation and assessment of an hypertension expert system

Patrice Degoulet, Olivier Gascuel, J F Boisvieux, 1987 .

Gene polymorphisms of the renin‐angiotensin system in relation to hypertension and parental history of myocardial infarction and stroke: the PEGASE study

Jean Tichet, Pierre-François Plouin, Xavier Jeunemaitre, 1998, Journal of hypertension.

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: phenotype-genotype correlation and outcome in 32 patients with CLDN16 or CLDN19 mutations.

Xavier Jeunemaitre, Pierre Cochat, Marion Vallet, 2012, Clinical journal of the American Society of Nephrology : CJASN.

Mutations in KCNJ5 gene cause hyperaldosteronism.

Maria-Christina Zennaro, Xavier Jeunemaitre, X. Jeunemaître, 2011, Circulation research.

Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor

Emmanuel Messas, Luc Mertens, Dmytro Zerbino, 2017, Front. Physiol..

Blood pressure loci identified with a gene-centric array.

Jean Tichet, Tom R. Gaunt, Jackie A Cooper, 2011, American journal of human genetics.

Corrigendum: Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor

Emmanuel Messas, Luc Mertens, Dmytro Zerbino, 2017, Front. Physiol..

A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism

Thomas J. Jentsch, Maria-Christina Zennaro, Tim M. Strom, 2018, Nature Genetics.

Adrenal Cortex Remodeling and Functional Zona Glomerulosa Hyperplasia in Primary Aldosteronism

Pierre-François Plouin, Arndt Benecke, Maria-Christina Zennaro, 2010, Hypertension.

β-2 Adrenergic Receptor Diplotype Defines a Subset of Salt-Sensitive Hypertension

Nancy J. Brown, Nikheel S. Kolatkar, Benjamin A. Raby, 2006 .

Human Hypertension Caused by Mutations in WNK Kinases

Robert J. Unwin, Murat Gunel, Kazuhiko Ishikawa, 2001, Science.

Correction: Corrigendum: Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels

Véronique Picard, Xavier Jeunemaitre, A. Patapoutian, 2013, Nature Communications.

Molecular basis of human hypertension: Role of angiotensinogen

Steven C. Hunt, Pierre Corvol, Xavier Jeunemaitre, 1992, Cell.

A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism

Thomas J. Jentsch, Maria-Christina Zennaro, Tim M. Strom, 2018, Nature Genetics.