| Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2 M Vikkula, LM Boon, KLC Iii, JT Calvert, AJ Diamonti, B Goumnerov, ... Cell 87 (7), 1181-1190, 1996 | 938 | 1996 |
| Capillary malformation–arteriovenous malformation, a new clinical and genetic disorder caused by RASA1 mutations I Eerola, LM Boon, JB Mulliken, PE Burrows, A Dompmartin, S Watanabe, ... The American Journal of Human Genetics 73 (6), 1240-1249, 2003 | 796 | 2003 |
| Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome TC Pansuriya, R van Eijk, P d'Adamo, MAJH van Ruler, ML Kuijjer, ... Nature genetics 43 (12), 1256-1261, 2011 | 569 | 2011 |
| Infantile hemangiomas: current knowledge, future directions. Proceedings of a research workshop on infantile hemangiomas, April 7-9, 2005, Bethesda, Maryland, USA IJ Frieden, AN Haggstrom, BA Drolet, AJ Mancini, SF Friedlander, L Boon, ... Pediatric dermatology 22 (5), 383-406, 2005 | 529 | 2005 |
| Congenital hemangioma: evidence of accelerated involution LM Boon, O Enjolras, JB Mulliken The Journal of pediatrics 128 (3), 329-335, 1996 | 460 | 1996 |
| Somatic mutations in angiopoietin receptor gene TEK cause solitary and multiple sporadic venous malformations N Limaye, V Wouters, M Uebelhoer, M Tuominen, R Wirkkala, JB Mulliken, ... Nature genetics 41 (1), 118-124, 2009 | 450 | 2009 |
| Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast‐flow vascular anomalies are caused by RASA1 mutations N Revencu, LM Boon, JB Mulliken, O Enjolras, MR Cordisco, PE Burrows, ... Human mutation 29 (7), 959-965, 2008 | 445 | 2008 |
| Rapidly involuting congenital hemangioma: clinical and histopathologic features B Berenguer, JB Mulliken, O Enjolras, LM Boon, M Wassef, P Josset, ... Pediatric and Developmental Pathology 6, 495-510, 2003 | 390 | 2003 |
| Noninvoluting congenital hemangioma: a rare cutaneous vascular anomaly O Enjolras, JB Mulliken, LM Boon, M Wassef, HPW Kozakewich, ... Plastic and reconstructive surgery 107 (7), 1647-1654, 2001 | 386 | 2001 |
| Complications of systemic corticosteroid therapy for problematic hemangioma LM Boon, DM MacDonald, JB Mulliken Plastic and reconstructive surgery 104 (6), 1616-1623, 1999 | 380 | 1999 |
| Glomuvenous malformation (glomangioma) and venous malformation: distinct clinicopathologic and genetic entities LM Boon, JB Mulliken, O Enjolras, M Vikkula Archives of dermatology 140 (8), 971-976, 2004 | 367 | 2004 |
| Genetics of lymphatic anomalies P Brouillard, LM Boon, M Vikkula J Clin Invest 124 (3), 898-904, 2014 | 358 | 2014 |
| Mutations in a novel factor, glomulin, are responsible for glomuvenous malformations (“glomangiomas”) P Brouillard, LM Boon, JB Mulliken, O Enjolras, M Ghassibé, ML Warman, ... The American Journal of Human Genetics 70 (4), 866-874, 2002 | 353 | 2002 |
| Association of localized intravascular coagulopathy with venous malformations A Dompmartin, A Acher, P Thibon, S Tourbach, C Hermans, V Deneys, ... Archives of dermatology 144 (7), 873-877, 2008 | 342 | 2008 |
| Venous malformation: update on aetiopathogenesis, diagnosis and management A Dompmartin, M Vikkula, LM Boon Phlebology 25 (5), 224-235, 2010 | 338 | 2010 |
| Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13. Y Gong, M Vikkula, L Boon, J Liu, P Beighton, R Ramesar, L Peltonen, ... American journal of human genetics 59 (1), 146, 1996 | 325 | 1996 |
| RASA1: variable phenotype with capillary and arteriovenous malformations LM Boon, JB Mulliken, M Vikkula Current opinion in genetics & development 15 (3), 265-269, 2005 | 303 | 2005 |
| Somatic activating PIK3CA mutations cause venous malformation N Limaye, J Kangas, A Mendola, C Godfraind, MJ Schlögel, R Helaers, ... The American Journal of Human Genetics 97 (6), 914-921, 2015 | 288 | 2015 |
| Treatment of infantile haemangiomas: recommendations of a European expert group PH Hoeger, JI Harper, E Baselga, D Bonnet, LM Boon, MCD Atti, ... European journal of pediatrics 174, 855-865, 2015 | 287 | 2015 |
| RASA1 Mutations and Associated Phenotypes in 68 Families with Capillary Malformation–Arteriovenous Malformation N Revencu, LM Boon, A Mendola, MR Cordisco, J Dubois, P Clapuyt, ... Human mutation 34 (12), 1632-1641, 2013 | 276 | 2013 |
Pascal BrouillardPlatform Manager, Institut de Duve, Université catholique de LouvainAdresse e-mail validée de uclouvain.be
