| Chromosome instability is common in human cleavage-stage embryos E Vanneste, T Voet, C Le Caignec, M Ampe, P Konings, C Melotte, ... Nature medicine 15 (5), 577, 2009 | 946 | 2009 |
| DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis B Lorenz-Depiereux, M Bastepe, A Benet-Pagès, M Amyere, ... Nature genetics 38 (11), 1248-1250, 2006 | 555 | 2006 |
| Constitutive macropinocytosis in oncogene-transformed fibroblasts depends on sequential permanent activation of phosphoinositide 3-kinase and phospholipase C M Amyere, B Payrastre, U Krause, PVD Smissen, A Veithen, PJ Courtoy Molecular biology of the cell 11 (10), 3453-3467, 2000 | 262 | 2000 |
| Germline loss-of-function mutations in EPHB4 cause a second form of capillary malformation-arteriovenous malformation (CM-AVM2) deregulating RAS-MAPK signaling M Amyere, N Revencu, R Helaers, E Pairet, E Baselga, M Cordisco, ... Circulation 136 (11), 1037-1048, 2017 | 238 | 2017 |
| Origin, originality, functions, subversions and molecular signalling of macropinocytosis M Amyere, M Mettlen, P Van Der Smissen, A Platek, B Payrastre, ... International journal of medical microbiology 291 (6-7), 487-494, 2001 | 233 | 2001 |
| TMEM165 deficiency causes a congenital disorder of glycosylation F Foulquier, M Amyere, J Jaeken, R Zeevaert, E Schollen, V Race, ... The American Journal of Human Genetics 91 (1), 15-26, 2012 | 210 | 2012 |
| Molecular identification of aspartate N-acetyltransferase and its mutation in hypoacetylaspartia E Wiame, D Tyteca, N Pierrot, F Collard, M Amyere, G Noel, J Desmedt, ... Biochemical Journal 425 (1), 127-139, 2010 | 155 | 2010 |
| Src triggers circular ruffling and macropinocytosis at the apical surface of polarized MDCK cells M Mettlen, A Platek, P Van Der Smissen, S Carpentier, M Amyere, ... Traffic 7 (5), 589-603, 2006 | 88 | 2006 |
| Somatic uniparental isodisomy explains multifocality of glomuvenous malformations M Amyere, V Aerts, P Brouillard, BAS McIntyre, FP Duhoux, M Wassef, ... The American Journal of Human Genetics 92 (2), 188-196, 2013 | 84 | 2013 |
| KITLG mutations cause familial progressive hyper-and hypopigmentation M Amyere, T Vogt, J Hoo, F Brandrup, A Bygum, L Boon, M Vikkula Journal of investigative dermatology 131 (6), 1234-1239, 2011 | 66 | 2011 |
| Vascular anomalies caused by abnormal signaling within endothelial cells: targets for novel therapies HL Nguyen, LM Boon, M Vikkula Seminars in interventional radiology 34 (03), 233-238, 2017 | 58 | 2017 |
| Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16 I Balikova, K Martens, C Melotte, M Amyere, S Van Vooren, Y Moreau, ... The American Journal of Human Genetics 82 (1), 181-187, 2008 | 52 | 2008 |
| Regulation of macropinocytosis in v-Src-transformed fibroblasts: cyclic AMP selectively promotes regurgitation of macropinosomes A Veithen, M Amyere, PVD Smissen, P Cupers, PJ Courtoy Journal of cell science 111 (16), 2329-2335, 1998 | 39 | 1998 |
| v-Src accelerates spontaneous motility via phosphoinositide 3-kinase, phospholipase C and phospholipase D, but abrogates chemotaxis in Rat-1 and MDCK cells A Platek, M Mettlen, I Camby, R Kiss, M Amyere, PJ Courtoy Journal of cell science 117 (20), 4849-4861, 2004 | 24 | 2004 |
| Giant cell tumor occurring in familial Paget's disease of bone: report of clinical characteristics and linkage analysis of a large pedigree F Gianfrancesco, D Rendina, D Merlotti, T Esposito, M Amyere, ... Journal of Bone and Mineral Research 28 (2), 341-350, 2013 | 21 | 2013 |
| Common somatic alterations identified in maffucci syndrome by molecular karyotyping M Amyere, A Dompmartin, V Wouters, O Enjolras, I Kaitila, PL Docquier, ... Molecular syndromology 5 (6), 259-267, 2014 | 19 | 2014 |
| Localization of candidate regions for a novel gene for Kartagener syndrome I Gutierrez-Roelens, T Sluysmans, M Jorissen, M Amyere, M Vikkula European journal of human genetics 14 (7), 809-815, 2006 | 12 | 2006 |
| Identification of candidate regions for a novel Usher syndrome type II locus IB Rebeh, Z Benzina, H Dhouib, I Hadjamor, M Amyere, L Ayadi, K Turki, ... Molecular vision 14, 1719, 2008 | 11 | 2008 |
| Genetics of arteriovenous malformations M Amyere, LM Boon, M Vikkula Brain arteriovenous malformations: pathogenesis, epidemiology, diagnosis …, 2017 | 2 | 2017 |
| Rare presentation of familial paraganglioma without evidence of mutation in the SDH, RET and VHL genes: towards further genetic heterogeneity A Persu, M Amyere, I Gutierrez-Roelens, P Rustin, C Sempoux, ... Journal of hypertension 27 (1), 76-82, 2009 | 2 | 2009 |
pierre courtoyprofesseur biologie cellulaire Louvain Bruxelles Verified email at uclouvain.be
