Articles with public access mandates - Xavier JEUNEMAITRELearn more
Not available anywhere: 11
KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron
H Louis-Dit-Picard, J Barc, D Trujillano, S Miserey-Lenkei, N Bouatia-Naji, ...
Nature genetics 44 (4), 456-460, 2012
Mandates: National Institute of Health and Medical Research, France, Government of Spain
A decade (2001–2010) of genetic testing for pheochromocytoma and paraganglioma
A Buffet, A Venisse, V Nau, I Roncellin, V Boccio, N Le Pottier, ...
Hormone and Metabolic Research 44 (05), 359-366, 2012
Mandates: National Institute of Health and Medical Research, France
Exome sequencing in seven families and gene-based association studies indicate genetic heterogeneity and suggest possible candidates for fibromuscular dysplasia
SR Kiando, C Barlassina, D Cusi, P Galan, M Lathrop, PF Plouin, ...
Journal of hypertension 33 (9), 1802-1810, 2015
Mandates: Government of Italy
Pathogenesis of pseudohypoaldosteronism type 2 by WNK1 mutations
S Bergaya, E Vidal-Petiot, X Jeunemaitre, J Hadchouel
Current Opinion in Nephrology and Hypertension 21 (1), 39-45, 2012
Mandates: National Institute of Health and Medical Research, France
Bilateral idiopathic adrenal hyperplasia: genetics and beyond
MC Zennaro, F Fernandes-Rosa, S Boulkroun, X Jeunemaitre
Hormone and Metabolic research 47 (13), 947-952, 2015
Mandates: National Institute of Health and Medical Research, France
Classical Ehlers‐Danlos syndrome with a propensity to arterial events: A new report on a French family with a COL1A1 p.(Arg312Cys) variant
S Adham, S Dupuis‐Girod, E Charpentier, JM Mazzella, X Jeunemaitre, ...
Clinical Genetics 97 (2), 357-361, 2020
Mandates: National Institute of Health and Medical Research, France
Natural history and surgical management of colonic perforations in vascular Ehlers-Danlos syndrome: a retrospective review
S Adham, FM Zinzindohoué, X Jeunemaitre, M Frank
Diseases of the Colon & Rectum 62 (7), 859-866, 2019
Mandates: National Institute of Health and Medical Research, France
Arterial stiffening with ultrafast ultrasound imaging gives new insight into arterial phenotype of vascular Ehlers-Danlos mouse models
G Goudot, C Papadacci, B Dizier, V Baudrie, I Ferreira, C Boisson-Vidal, ...
Ultraschall in der Medizin-European Journal of Ultrasound 40 (06), 734-742, 2019
Mandates: Agence Nationale de la Recherche
Regulation of ion transport by microRNAs
E Elvira-Matelot, X Jeunemaitre, J Hadchouel
Current Opinion in Nephrology and Hypertension 20 (5), 541-546, 2011
Mandates: National Institute of Health and Medical Research, France
Genes of the Renin-Angiotensin System and the Genetics of Human Hypertension
X Jeunemaitre, RP Lifton
Cellular and Molecular Biology of the Renin-Angiotensin System, 537-555, 2018
Mandates: American Heart Association
Renin-Angiotensin System
AV Haas, R Baudrand, RM Easly, GR Murray, RM Touyz, LH Pojoga, ...
Mandates: US National Institutes of Health, British Heart Foundation
Available somewhere: 104
SDHA is a tumor suppressor gene causing paraganglioma
N Burnichon, JJ Brière, R Libé, L Vescovo, J Rivière, F Tissier, E Jouanno, ...
Human molecular genetics 19 (15), 3011-3020, 2010
Mandates: US National Institutes of Health
Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension
F Beuschlein, S Boulkroun, A Osswald, T Wieland, HN Nielsen, ...
Nature genetics 45 (4), 440-444, 2013
Mandates: German Research Foundation, Danish Council for Independent Research …
The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas
N Burnichon, V Rohmer, L Amar, P Herman, S Leboulleux, V Darrouzet, ...
The Journal of Clinical Endocrinology & Metabolism 94 (8), 2817-2827, 2009
Mandates: National Institute of Health and Medical Research, France
First international consensus on the diagnosis and management of fibromuscular dysplasia
HL Gornik, A Persu, D Adlam, LS Aparicio, M Azizi, M Boulanger, ...
Vascular Medicine 24 (2), 164-189, 2019
Mandates: British Heart Foundation, Doris Duke Charitable Foundation
Mitral valve disease—morphology and mechanisms
RA Levine, AA Hagége, DP Judge, M Padala, JP Dal-Bianco, E Aikawa, ...
Nature reviews cardiology 12 (12), 689-710, 2015
Mandates: US National Institutes of Health, Fonds de recherche du Québec - Santé …
Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels
J Albuisson, SE Murthy, M Bandell, B Coste, H Louis-dit-Picard, J Mathur, ...
Nature communications 4 (1), 1884, 2013
Mandates: US National Institutes of Health, National Institute of Health and Medical …
Prevalence, Clinical, and Molecular Correlates of KCNJ5 Mutations in Primary Aldosteronism
S Boulkroun, F Beuschlein, GP Rossi, JF Golib-Dzib, E Fischer, L Amar, ...
Hypertension 59 (3), 592-598, 2012
Mandates: German Research Foundation, National Institute of Health and Medical …
Genetic spectrum and clinical correlates of somatic mutations in aldosterone-producing adenoma
FL Fernandes-Rosa, TA Williams, A Riester, O Steichen, F Beuschlein, ...
Hypertension 64 (2), 354-361, 2014
Mandates: German Research Foundation, National Institute of Health and Medical …
Spectrum of mutations in Gitelman syndrome
R Vargas-Poussou, K Dahan, D Kahila, A Venisse, E Riveira-Munoz, ...
Journal of the American Society of Nephrology 22 (4), 693-703, 2011
Mandates: National Institute of Health and Medical Research, France
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