1. 6C.05: STK39 AND WNK1 ARE POTENTIAL HYPERTENSION SUSCEPTIBILITY GENES IN THE BELHYPGEN COHORT. (June 2015) Authors: Persu, A.; Evenepoel, L.; Jin, Y.; Mendola, A.; Staessen, J.A.; Vikkula, M. Journal: Journal of hypertension Issue: Volume 33(2015)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 9B.09: IDENTIFICATION OF MARKERS PREDICTIVE FOR MALIGNANT BEHAVIOR OF PHEOCHROMOCYTOMAS AND PARAGANGLIOMAS. (June 2015) Authors: Evenepoel, L.; Van Nederveen, F.H.; Oudijk, L.; Papathomas, T.G.; Restuccia, D.F.; Belt, E.J.T.; Franssen, G.J.H.; Feelders, R.A.; Van Eeden, S.; Timmers, H.; De Herder, W.W.; Aydin, S.; Vikkula, M.; De Krijger, R.R.; Dinjens, W.N.M.; Persu, A.; Korpershoek, E. Journal: Journal of hypertension Issue: Volume 33(2015)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. [OP.6B.03] KIF1B AND NF1 ARE THE MOST FREQUENTLY MUTATED GENES IN PARAGANGLIOMAS AND PHEOCHROMOCYTOMAS TUMOURS FROM A BELGIAN MULTICENTRIC COHORT. (September 2017) Authors: Evenepoel, L.; Helaers, R.; Vroonen, L.; Aydin, S.; Hamoir, M.; Maiter, D.; Vikkula, M.; Persu, A. Journal: Journal of hypertension Issue: Volume 35(2017)Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Five int22h homologous copies at the Xq28 locus identified in intron22 inversion type 3 of the Factor VIII gene. (January 2016) Authors: Lannoy, N.; Ravoet, M.; Grisart, B.; Fretigny, M.; Vikkula, M.; Hermans, C. Journal: Thrombosis research Issue: Volume 137(2016) Page Start: 224 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Five int22h homologous copies at the Xq28 locus identified in intron22 inversion type 3 of the Factor VIII gene. (January 2016) Authors: Lannoy, N.; Ravoet, M.; Grisart, B.; Fretigny, M.; Vikkula, M.; Hermans, C. Journal: Thrombosis research Issue: Volume 137(2016) Page Start: 224 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Hypotrichosis‐lymphedema‐telangiectasia‐renal defect associated with a truncating mutation in the SOX18 gene. (16th April 2014) Authors: Moalem, S.; Brouillard, P.; Kuypers, D.; Legius, E.; Harvey, E.; Taylor, G.; Francois, M.; Vikkula, M.; Chitayat, D. Journal: Clinical genetics Issue: Volume 87:Number 4(2015:Apr.) Page Start: 378 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Overrepresentation of missense mutations in mild hemophilia A patients from Belgium: founder effect or independent occurrence?. Issue 6 (June 2015) Authors: Lannoy, N.; Lambert, C.; Vikkula, M.; Hermans, C. Journal: Thrombosis research Issue: Volume 135:Issue 6(2015) Page Start: 1057 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Prevalence of pathogenic variants and variants of unknown significance in patients at high risk of breast cancer: A systematic review and meta-analysis of gene-panel data. (December 2018) Authors: van Marcke, C.; Collard, A.; Vikkula, M.; Duhoux, F.P. Journal: Critical reviews in oncology/hematology Issue: Volume 132(2018) Page Start: 138 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Splice‐site mutations in VEGFC cause loss of function and Nonne‐Milroy‐like primary lymphedema. Issue 1 (15th March 2018) Authors: Fastré, E.; Lanteigne, L‐E.; Helaers, R.; Giacalone, G.; Revencu, N.; Dionyssiou, D.; Demiri, E.; Brouillard, P.; Vikkula, M. Journal: Clinical genetics Issue: Volume 94:Issue 1(2018) Page Start: 179 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Tandem inversion duplication within F8 Intron 1 associated with mild haemophilia A. (11th May 2015) Authors: Lannoy, N.; Bandelier, C.; Grisart, B.; Reginster, M.; Ronge‐Collard, E.; Vikkula, M.; Hermans, C. Journal: Haemophilia Issue: Volume 21:Number 4(2015:Jul.) Page Start: 516 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗