| 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 | 290 | 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 | 277 | 2013 |
| Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas L Yao, F Schiavi, A Cascon, Y Qin, L Inglada-Pérez, EE King, RA Toledo, ... Jama 304 (23), 2611-2619, 2010 | 235 | 2010 |
| 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 | 230 | 2015 |
| 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 | 192 | 2017 |
| Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathy P Ostergaard, MA Simpson, A Mendola, P Vasudevan, FC Connell, ... The American Journal of Human Genetics 90 (2), 356-362, 2012 | 182 | 2012 |
| Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema A Mendola, MJ Schlögel, A Ghalamkarpour, A Irrthum, HL Nguyen, ... Molecular syndromology 4 (6), 257-266, 2013 | 108 | 2013 |
| 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 | 106 | 2013 |
| 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 | 60 | 2017 |
| Evaluation of clinical manifestations in patients with severe lymphedema with and without CCBE1 mutations M Alders, A Mendola, L Adès, L Al Gazali, C Bellini, B Dallapiccola, ... Molecular syndromology 4 (3), 107-113, 2013 | 57 | 2013 |
| 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 | 51 | 2020 |
| No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome MJ Schlögel, A Mendola, E Fastré, P Vasudevan, K Devriendt, ... Orphanet Journal of Rare Diseases 10, 1-11, 2015 | 19 | 2015 |
| STK39 and WNK1 are potential hypertension susceptibility genes in the BELHYPGEN cohort A Persu, L Evenepoel, Y Jin, A Mendola, G Ngueta, WY Yang, D Gruson, ... Medicine 95 (15), e2968, 2016 | 18* | 2016 |
| Prevalence and spectrum of SDHx mutations in pheochromocytoma and paraganglioma in patients from Belgium: an update A Persu, N Lannoy, D Maiter, A Mendola, P Montigny, P Oriot, W Vinck, ... Hormone and metabolic research 44 (05), 349-353, 2012 | 14 | 2012 |
| Preclinical evaluation of the association of the cyclin-dependent kinase 4/6 inhibitor, ribociclib, and cetuximab in squamous cell carcinoma of the head and neck G van Caloen, S Schmitz, C Van Marcke, X Caignet, A Mendola, ... Cancers 13 (6), 1251, 2021 | 8 | 2021 |
| Tumor-agnostic plasma assay for circulating tumor DNA detects minimal residual disease and predicts outcome in locally advanced squamous cell carcinoma of the head and neck N Honoré, C van Marcke, R Galot, R Helaers, J Ambroise, A van Maanen, ... Annals of Oncology 34 (12), 1175-1186, 2023 | 4 | 2023 |
| Pyr dit Ruys, S.; Roger, PP; Vertommen, D.; Machiels, J.-P. Preclinical Evaluation of the Association of the Cyclin-Dependent Kinase 4/6 Inhibitor, Ribociclib, and Cetuximab in … G Van Caloen, S Schmitz, C van Marcke, X Caignet, A Mendola s Note: MDPI stays neutral with regard to jurisdictional claims in published …, 2021 | 1 | 2021 |
| Liquid biopsy for mutational profiling of locoregional recurrent and/or metastatic squamous cell carcinoma of the head and neck R Galot, CVM de Lummen, R Helaers, A Mendola, RM Goebbels, ... Annals of Oncology 30, v468-v469, 2019 | 1 | 2019 |
| Isolated bilateral transverse agenesis of the distal segments of the lower limbs at the level of the knee joint in a human fetus AB Christiaens, PML Deprez, M Amyere, A Mendola, P Bernard, Y Gillerot, ... American Journal of Medical Genetics Part A 170 (2), 523-530, 2016 | 1 | 2016 |
| No locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome MJ Schlögel, A Mendola, E Fastré, K Devriendt, T de Ravel de l'Argentière, ... European Journal of Human Genetics 22, 123-123, 2014 | 1 | 2014 |
