| Molecular basis of human hypertension: role of angiotensinogen X Jeunemaitre, F Soubrier, YV Kotelevtsev, RP Lifton, CS Williams, ... Cell 71 (1), 169-180, 1992 | 2585 | 1992 |
| Human hypertension caused by mutations in WNK kinases FH Wilson, S Disse-Nicodeme, KA Choate, K Ishikawa, ... Science 293 (5532), 1107-1112, 2001 | 1648 | 2001 |
| The 2017 international classification of the Ehlers–Danlos syndromes F Malfait, C Francomano, P Byers, J Belmont, B Berglund, J Black, ... American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2017 | 1606 | 2017 |
| Angiotensin II type 1 receptor gene polymorphisms in human essential hypertension. A Bonnardeaux, E Davies, X Jeunemaitre, I Fery, A Charru, E Clauser, ... Hypertension 24 (1), 63-69, 1994 | 1222 | 1994 |
| Links between dietary salt intake, renal salt handling, blood pressure, and cardiovascular diseases P Meneton, X Jeunemaitre, HE de Wardener, GA Macgregor Physiological reviews, 2005 | 997 | 2005 |
| Genetic testing in pheochromocytoma or functional paraganglioma L Amar, J Bertherat, E Baudin, C Ajzenberg, B Bressac-de Paillerets, ... Journal of Clinical Oncology 23 (34), 8812-8818, 2005 | 782 | 2005 |
| 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 | 765 | 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, CS Williams, J Quackenbush, R Puryear, M Powers, ... The Journal of clinical investigation 99 (7), 1786-1797, 1997 | 730 | 1997 |
| Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes DE Benn, AP Gimenez-Roqueplo, JR Reilly, J Bertherat, J Burgess, ... The Journal of Clinical Endocrinology & Metabolism 91 (3), 827-836, 2006 | 706 | 2006 |
| Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus L Zhu, R Vranckx, PK Van Kien, A Lalande, N Boisset, F Mathieu, ... Nature genetics 38 (3), 343-349, 2006 | 692 | 2006 |
| Mutations in the SDHB Gene Are Associated with Extra-adrenal and/or Malignant Phaeochromocytomas AP Gimenez-Roqueplo, J Favier, P Rustin, C Rieubland, M Crespin, ... Cancer research 63 (17), 5615-5621, 2003 | 663 | 2003 |
| A molecular variant of angiotensinogen associated with preeclampsia K Ward, A Hata, X Jeunemaitre, C Helin, L Nelson, C Namikawa, ... Nature genetics 4 (1), 59-61, 1993 | 653 | 1993 |
| Absence of linkage between the angiotensin converting enzyme locus and human essential hypertension X Jeunemaitre, RP Lifton, SC Hunt, RR Williams, JM Lalouel Nature genetics 1 (1), 72-75, 1992 | 571 | 1992 |
| 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 | 566 | 2013 |
| Succinate dehydrogenase B gene mutations predict survival in patients with malignant pheochromocytomas or paragangliomas L Amar, E Baudin, N Burnichon, S Peyrard, S Silvera, J Bertherat, ... The Journal of Clinical Endocrinology & Metabolism 92 (10), 3822-3828, 2007 | 501 | 2007 |
| Contribution of genetic polymorphism in the renin-angiotensin system to the development of renal complications in insulin-dependent diabetes: Genetique de la Nephropathie … M Marre, X Jeunemaitre, Y Gallois, M Rodier, G Chatellier, C Sert, ... The Journal of clinical investigation 99 (7), 1585-1595, 1997 | 452 | 1997 |
| The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia … AP Gimenez-Roqueplo, J Favier, P Rustin, JJ Mourad, PF Plouin, ... The American Journal of Human Genetics 69 (6), 1186-1197, 2001 | 431 | 2001 |
| 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 | 424 | 2009 |
| Haplotypes of angiotensinogen in essential hypertension X Jeunemaitre, I Inoue, C Williams, A Charru, J Tichet, M Powers, ... The American Journal of Human Genetics 60 (6), 1448-1460, 1997 | 417 | 1997 |
| Effect of celiprolol on prevention of cardiovascular events in vascular Ehlers-Danlos syndrome: a prospective randomised, open, blinded-endpoints trial KT Ong, J Perdu, J De Backer, E Bozec, P Collignon, J Emmerich, ... The Lancet 376 (9751), 1476-1484, 2010 | 385 | 2010 |
