His primary areas of investigation include Internal medicine, Endocrinology, Genetics, Mutation and Blood pressure. His Internal medicine research is multidisciplinary, incorporating elements of Ehlers–Danlos syndrome, Polymorphism and Cardiology. His work in Endocrinology covers topics such as Epithelial sodium channel which are related to areas like Distal convoluted tubule.
His Genetics study combines topics in areas such as Mitral valve and Pathology. His biological study spans a wide range of topics, including Phenotype, Tubulopathy and Genotype. His Blood pressure study combines topics from a wide range of disciplines, such as Case-control study, Genetic epidemiology, Spironolactone, Locus and Hemodynamics.
Xavier Jeunemaitre focuses on Internal medicine, Endocrinology, Genetics, Cardiology and Blood pressure. His Internal medicine research includes elements of Ehlers–Danlos syndrome and Gastroenterology. His research integrates issues of Germline mutation and Genotype in his study of Endocrinology.
The study incorporates disciplines such as Pheochromocytoma and Paraganglioma in addition to Germline mutation. The concepts of his Cardiology study are interwoven with issues in Pulse wave velocity and Fibromuscular dysplasia. Xavier Jeunemaitre has included themes like Mitral valve prolapse and Pathology in his Missense mutation study.
His main research concerns Internal medicine, Ehlers–Danlos syndrome, Cardiology, Fibromuscular dysplasia and Pathology. His Internal medicine study incorporates themes from Gastroenterology and Endocrinology. His Aldosterone and Reabsorption study in the realm of Endocrinology interacts with subjects such as WNK4 and Vascular smooth muscle.
His Ehlers–Danlos syndrome research incorporates elements of Retrospective review, Retrospective cohort study, Natural history and Proband. His research integrates issues of Pulse wave velocity and Arteriovenous fistula in his study of Cardiology. His Pathology research includes themes of ABCC6, Missense mutation, Aneurysm and Mitral valve.
Xavier Jeunemaitre mainly focuses on Internal medicine, Endocrinology, Mitral valve prolapse, Mitral valve and Fibromuscular dysplasia. His Internal medicine study frequently draws connections between related disciplines such as Cardiology. The various areas that Xavier Jeunemaitre examines in his Endocrinology study include WNK1 and WNK Lysine-Deficient Protein Kinase 1.
His study on Mitral valve prolapse also encompasses disciplines like
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Molecular basis of human hypertension: Role of angiotensinogen
Xavier Jeunemaitre;Florent Soubrier;Yuri V. Kotelevtsev;Richard P. Lifton;Richard P. Lifton.
Cell (1992)
Human hypertension caused by mutations in WNK kinases
Frederick H. Wilson;Sandra Disse-Nicodème;Keith A. Choate;Kazuhiko Ishikawa.
Science (2001)
Angiotensin II type 1 receptor gene polymorphisms in human essential hypertension.
Alain Bonnardeaux;Eleanor Davies;Xavier Jeunemaitre;Isabelle Fery.
Hypertension (1994)
The 2017 international classification of the Ehlers-Danlos syndromes
Fransiska Malfait;Clair Francomano;Peter H Byers;John Belmont.
American Journal of Medical Genetics Part C-seminars in Medical Genetics (2017)
Links between dietary salt intake, renal salt handling, blood pressure, and cardiovascular diseases.
Pierre Meneton;Xavier Jeunemaitre;Hugh E. de Wardener;Graham A. Macgregor.
Physiological Reviews (2005)
Genetic Testing in Pheochromocytoma or Functional Paraganglioma
Laurence Amar;Jérôme Bertherat;Eric Baudin;Christiane Ajzenberg.
Journal of Clinical Oncology (2005)
SDHA is a tumor suppressor gene causing paraganglioma
Nelly Burnichon;Jean-Jacques Brière;Rossella Libé;Laure Vescovo.
Human Molecular Genetics (2010)
A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro.
I Inoue;T Nakajima;C S Williams;J Quackenbush.
Journal of Clinical Investigation (1997)
Clinical presentation and penetrance of Pheochromocytoma/ Paraganglioma syndromes.
Diana E. Benn;Anne Paule Gimenez-Roqueplo;Jennifer R. Reilly;Jérôme Bertherat.
The Journal of Clinical Endocrinology and Metabolism (2006)
A molecular variant of angiotensinogen associated with preeclampsia
Ward K;Hata A;Jeunemaitre X;Helin C.
Nature Genetics (1993)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
Université Paris Cité
Inserm
Collège de France
Brigham and Women's Hospital
University of Utah
Université Paris Cité
Université Paris Cité
Fondation Leducq
University of Zurich
Icahn School of Medicine at Mount Sinai
Queen's University Belfast
Bohai University
Genentech
University of Alberta
Kyoto University
Wellcome Sanger Institute
Royal Holloway University of London
Scripps Institution of Oceanography
TU Wien
Copenhagen University Hospital
National Institutes of Health
University of Southern California
The University of Texas MD Anderson Cancer Center
Norwegian University of Science and Technology
University of British Columbia
Carnegie Mellon University