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Limaye, Nisha
Limaye, Nisha
Verified email at uclouvain.be
Title
Cited by
Cited by
Year
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
5692011
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
4502009
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
4272008
Association of extensive polymorphisms in the SLAM/CD2 gene cluster with murine lupus
AE Wandstrat, C Nguyen, N Limaye, AY Chan, S Subramanian, XH Tian, ...
Immunity 21 (6), 769-780, 2004
3222004
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
2882015
Rapamycin improves TIE2-mutated venous malformation in murine model and human subjects
E Boscolo, N Limaye, L Huang, KT Kang, J Soblet, M Uebelhoer, ...
The Journal of clinical investigation 125 (9), 3491-3504, 2015
2282015
Blue rubber bleb nevus (BRBN) syndrome is caused by somatic TEK (TIE2) mutations
J Soblet, J Kangas, M Nätynki, A Mendola, R Helaers, M Uebelhoer, ...
Journal of Investigative Dermatology 137 (1), 207-216, 2017
1902017
Hereditary cutaneomucosal venous malformations are caused by TIE2 mutations with widely variable hyper-phosphorylating effects
V Wouters, N Limaye, M Uebelhoer, A Irrthum, LM Boon, JB Mulliken, ...
European Journal of Human Genetics 18 (4), 414-420, 2010
1742010
Variable somatic TIE2 mutations in half of sporadic venous malformations
J Soblet, N Limaye, M Uebelhoer, LM Boon, M Vikkula
Molecular syndromology 4 (4), 179-183, 2013
1702013
From germline towards somatic mutations in the pathophysiology of vascular anomalies
N Limaye, LM Boon, M Vikkula
Human molecular genetics 18 (R1), R65-R74, 2009
1302009
Venous malformation-causative TIE2 mutations mediate an AKT-dependent decrease in PDGFB
M Uebelhoer, M Nätynki, J Kangas, A Mendola, HL Nguyen, J Soblet, ...
Human molecular genetics 22 (17), 3438-3448, 2013
1052013
Classification of vascular anomalies: an update
JE Steiner, BA Drolet
Seminars in Interventional Radiology 34 (03), 225-232, 2017
982017
Common and specific effects of TIE2 mutations causing venous malformations
M Nätynki, J Kangas, I Miinalainen, R Sormunen, R Pietilä, J Soblet, ...
Human molecular genetics 24 (22), 6374-6389, 2015
942015
PDGFRB gain-of-function mutations in sporadic infantile myofibromatosis
FA Arts, R Sciot, B Brichard, M Renard, A de Rocca Serra, G Dachy, ...
Human molecular genetics 26 (10), 1801-1810, 2017
862017
Susceptibility genes in the pathogenesis of murine lupus
C Nguyen, N Limaye, EK Wakeland
Arthritis Research 4 (Suppl 3), S255-63, 2002
822002
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
582017
Liquid biopsy for mutational profiling of locoregional recurrent and/or metastatic head and neck squamous cell carcinoma
R Galot, C van Marcke, R Helaers, A Mendola, RM Goebbels, X Caignet, ...
Oral oncology 104, 104631, 2020
512020
B cell–intrinsic CD84 and Ly108 maintain germinal center B cell tolerance
EB Wong, C Soni, AY Chan, PP Domeier, S Shwetank, T Abraham, ...
The Journal of Immunology 194 (9), 4130-4143, 2015
502015
Association of PDGFRB mutations with pediatric myofibroma and myofibromatosis
G Dachy, RR De Krijger, S Fraitag, I Théate, B Brichard, SB Hoffman, ...
JAMA dermatology 155 (8), 946-950, 2019
482019
Advances in the medical management of vascular anomalies
KW Ricci
Seminars in interventional radiology 34 (03), 239-249, 2017
422017
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