1. Age‐related heterogeneity of Burkitt lymphoma: response to Mbulaiteye and Anderson. (9th September 2016) Authors: Poirel, Hélène A.; Vikkula, Miikka Journal: British journal of haematology Issue: Volume 180:Number 1(2018) Page Start: 155 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Angiosarcoma arising from congenital primary lymphedema. Issue 6 (14th September 2018) Authors: Janssens, Pauline; Dekeuleneer, Valérie; Van Damme, An; Brouillard, Pascal; Revencu, Nicole; Clapuyt, Philippe; Ferreira, Ingrid; Ballieux, Fanny; Vikkula, Miikka; Marot, Liliane; Baeck, Marie; Boon, Laurence M. Journal: Pediatric dermatology Issue: Volume 35:Issue 6(2018) Page Start: e382 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Arterial Tortuosity: Novel Implications for an Old Phenotype. Issue 5 (May 2019) Authors: Ciurică, Simina; Lopez-Sublet, Marilucy; Loeys, Bart L.; Radhouani, Ibtissem; Natarajan, Nalin; Vikkula, Miikka; Maas, Angela H.E.M.; Adlam, David; Persu, Alexandre Journal: Hypertension Issue: Volume 73:Issue 5(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Biallelic ANGPT2 loss-of-function causes severe early-onset non-immune hydrops fetalis. Issue 1 (7th December 2021) Authors: Smeland, Marie F.; Brouillard, Pascal; Prescott, Trine; Boon, Laurence M; Hvingel, Bodil; Nordbakken, Cecilie V; Nystad, Mona; Holla, Øystein L.; Vikkula, Miikka Journal: Journal of medical genetics Issue: Volume 60:Issue 1(2023) Page Start: 57 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Cystathionine β-synthase genetic variant rs2124459 is associated with a reduced risk of cleft palate in French and Belgian populations. Issue 12 (17th August 2016) Authors: Goffinet, Laetitia; Oussalah, Abderrahim; Guéant-Rodriguez, Rosa-Maria; Chery, Céline; Basha, Mirta; Avogbe, Patrice Hodonou; Josse, Thomas; Jeannesson, Elise; Rouyer, Pierre; Flayac, Justine; Gerard, Philippe; Le Touze, Anne; Bonin-Goga, Béatrice; Goga, Dominique; Simon, Etienne; Feillet, Franço... Journal: Journal of medical genetics Issue: Volume 53:Issue 12(2016) Page Start: 828 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Disruption of ST5 is associated with mental retardation and multiple congenital anomalies. Issue 2 (19th October 2009) Authors: Göhring, Ina; Tagariello, Andreas; Endele, Sabine; Stolt, Claus C; Ghassibé, Michella; Fisher, Malcolm; Thiel, Christian T; Trautmann, Udo; Vikkula, Miikka; Winterpacht, Andreas; FitzPatrick, David R; Rauch, Anita Journal: Journal of medical genetics Issue: Volume 47:Issue 2(2010) Page Start: 91 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. DNA alteration‐based classification of uveal melanoma gives better prognostic stratification than immune infiltration, which has a neutral effect in high‐risk group. (25th April 2019) Authors: Narasimhaiah, Deepti; Legrand, Catherine; Damotte, Diane; Remark, Romain; Munda, Marco; De Potter, Patrick; Coulie, Pierre G.; Vikkula, Miikka; Godfraind, Catherine Journal: Cancer medicine Issue: Volume 8:Number 6(2019:Jun.) Page Start: 3036 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Enrichment of Rare Variants in Loeys–Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia. Issue 10 (8th September 2020) Authors: Verstraeten, Aline; Perik, Melanie H.A.M.; Baranowska, Anna A.; Meester, Josephina A.N.; Van Den Heuvel, Lotte; Bastianen, Jarl; Kempers, Marlies; Krapels, Ingrid P.C.; Maas, Angela; Rideout, Andrea; Vandersteen, Anthony; Sobey, Glenda; Johnson, Diana; Fransen, Erik; Ghali, Neeti; Webb, Tom; Al-H... Journal: Circulation Issue: Volume 142:Issue 10(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. EPHB4 mutation causes adult and adolescent‐onset primary lymphedema. Issue 12 (7th July 2021) Authors: Greene, Arin K.; Brouillard, Pascal; Sudduth, Christopher L.; Smits, Patrick J.; Konczyk, Dennis J.; Vikkula, Miikka Journal: American journal of medical genetics Issue: Volume 185:Issue 12(2021) Page Start: 3810 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. First International Conference on RASopathies and Neurofibromatoses in Asia: Identification and advances of new therapeutics. Issue 6 (25th March 2019) Authors: Rauen, Katherine A.; Alsaegh, Abeer; Ben‐Shachar, Shay; Berman, Yemima; Blakeley, Jaishri; Cordeiro, Isabel; Elgersma, Ype; Evans, D. Gareth; Fisher, Michael J.; Frayling, Ian M.; George, Joshi; Huson, Susan M.; Kerr, Bronwyn; Khire, Uday; Korf, Bruce; Legius, Eric; Messiaen, Ludwine; van Minkele... Journal: American journal of medical genetics Issue: Volume 179:Issue 6(2019) Page Start: 1091 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗