Miikka Vikkula

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Laurence M BoonProfessor, Coord. Vasc Anom Ctr, Clin. univ. St Luc, Univ cathol LouvainPatvirtintas el. paštas uclouvain.be
Pascal BrouillardPlatform Manager, Institut de Duve, Université catholique de LouvainPatvirtintas el. paštas uclouvain.be
nicole revencuCentre de Génétique Humaine, Cliniques universitaires Saint-Luc, Université catholique de LouvainPatvirtintas el. paštas uclouvain.be
Anne DompmartinMédecin Dermatologue CHU CaenPatvirtintas el. paštas chu-caen.fr
Mustapha AmyereDocteur, Université catholique de Louvain, BelgiquePatvirtintas el. paštas uclouvain.be
Raphaël HelaersBioinformatician, de Duve Institute, Université catholique de LouvainPatvirtintas el. paštas uclouvain.be
Michella GhassibeAssistant Professor in Human Genetics, Lebanese American UniversityPatvirtintas el. paštas lau.edu.lb
Alexandre IrrthumBreast International Group - aisblPatvirtintas el. paštas bigagainstbc.org
philippe clapuytProfesseur clinique, Université de LouvainPatvirtintas el. paštas uclouvain.be
Hélène A. Poirel (Antoine-Poirel)Professor, Centre for Human Genetics, Clin. univ. st-Luc, Université catholique de LouvainPatvirtintas el. paštas uclouvain.be
Francois P DuhouxCliniques universitaires Saint-Luc, Université catholique de LouvainPatvirtintas el. paštas uclouvain.be
Emile Van Schaftingende Duve Institute, Université catholique de LouvainPatvirtintas el. paštas uclouvain.be
Matthieu J. SchlögelPh.D. Student, de Duve Institute, Universite catholique de Louvain, BelgiumPatvirtintas el. paštas uclouvain.be
Melanie UebelhoerHuman Molecular Genetics, de Duve Institute, Université catholique de LouvainPatvirtintas el. paštas uclouvain.be
Julie SobletPhD Student, de Duve Institute, Université catholique de Louvain, BrusselsPatvirtintas el. paštas uclouvain.be
Joyce BischoffBoston Children's Hospital, Harvard Medical SchoolPatvirtintas el. paštas childrens.harvard.edu

Stebėti

Miikka Vikkula

Professor of Human Genetics, de Duve Institute, UCLouvain

Patvirtintas el. paštas uclouvain.be - Pagrindinis puslapis

Genetics & Pathophysiology Vascular anomalies Lymphedema Cleft Lip and Palate Models & (Pre)


Pavadinimas Rūšiuoti pagal šaltinius Rūšiuoti pagal metus Rūšiuoti pagal pavadinimą	Cituota Cituota	Metai
LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development Y Gong, RB Slee, N Fukai, G Rawadi, S Roman-Roman, AM Reginato, ... Cell 107 (4), 513-523, 2001	2714	2001
Vascular anomalies classification: recommendations from the International Society for the Study of Vascular Anomalies M Wassef, F Blei, D Adams, A Alomari, E Baselga, A Berenstein, ... Pediatrics 136 (1), e203-e214, 2015	1400	2015
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	971	2009
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	971	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	845	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	599	2011
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	571	2006
Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase A Irrthum, MJ Karkkainen, K Devriendt, K Alitalo, M Vikkula The American Journal of Human Genetics 67 (2), 295-301, 2000	525	2000
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	495	2009
Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia A Irrthum, K Devriendt, D Chitayat, G Matthijs, C Glade, PM Steijlen, ... The American Journal of Human Genetics 72 (6), 1470-1478, 2003	495	2003
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	463	2008
Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus M Vikkula, ECM Madman, VCH Lui, NI Zhidkova, GE Tiller, MB Goldring, ... Cell 80 (3), 431-437, 1995	448	1995
Suppressed NFAT-dependent VEGFR1 expression and constitutive VEGFR2 signaling in infantile hemangioma M Jinnin, D Medici, L Park, N Limaye, Y Liu, E Boscolo, J Bischoff, ... Nature medicine 14 (11), 1236-1246, 2008	446	2008
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	382	2004
Genetics of lymphatic anomalies P Brouillard, L Boon, M Vikkula The Journal of clinical investigation 124 (3), 898-904, 2014	374	2014
Venous malformation: update on aetiopathogenesis, diagnosis and management A Dompmartin, M Vikkula, LM Boon Phlebology 25 (5), 224-235, 2010	365	2010
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	365	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	355	2008
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	332	1996
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	322	2015

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