Search

Pages

1. • Journal article

   • 

   Routine use of gene panel testing in hereditary breast cancer should be performed with caution

   van Marcke, Cédric[UCL] De Leener, Anne[UCL] Berlière, Martine[UCL] Vikkula, Miikka[UCL] Duhoux, François[UCL] (2017) CRC Critical Reviews in Oncology - Hematology — Vol. x, no.x, p. x (2017)
2. • Journal article

   • 

   Vascular pathologies. Angiogenomics: towards a genetic nosology and understanding of vascular anomalies

   Vikkula, Miikka[UCL] (2007) European Journal of Human Genetics — Vol. 15, no. 8, p. 821-822 (2007)
3. • Journal article

   • 

   Molecular identification of aspartate N-acetyltransferase and its mutation in hypoacetylaspartia

   Wiame, Elsa[UCL] Tyteca, Donatienne[UCL] Pierrot, Nathalie[UCL] Collard, François[UCL] Amyere, Mustapha[UCL] Noël, Gaëtane[UCL] Desmedt, Jonathan[UCL] Nassogne, Marie-Cécile[UCL] Vikkula, Miikka[UCL] Octave, Jean-Noël[UCL] Vincent, Marie-Françoise[UCL] Courtoy, Pierre J.[UCL] Boltshauser, Eugen Van Schaftingen, Emile[UCL] (2010) Biochemical Journal — Vol. 425, no. 1, p. 127-136 (2010)
4. • Journal article

   • 

   Progressive AV-block and anomalous venous return among cardiac anomalies associated with two novel missense mutations in the CSX/NKX2-5 gene.

   Gutierrez-Roelens, Ilse[UCL] Sluysmans, Thierry[UCL] Gewillig, Marc Devriendt, Koen Vikkula, Miikka[UCL] (2002) Human Mutation — Vol. 20, no. 1, p. 75-81 (2002)
5. • Journal article

   • 

   Rare presentation of familial paraganglioma without evidence of mutation in the SDH, RET and VHL genes: towards further genetic heterogeneity.

   Persu, Alexandre[UCL] Amyere, Mustapha[UCL] Gutierrez-Roelens, Ilse[UCL] Rustin, Pierre Sempoux, Christine[UCL] Lecouvet, Frédéric[UCL] Van Beers, Bernard[UCL] Horsmans, Yves[UCL] De Plaen, Jean-François[UCL] Hamoir, Marc[UCL] Vikkula, Miikka[UCL] (2009) Journal of Hypertension — Vol. 27, no. 1, p. 76-82 (2009)
6. • Journal article

   • 

   Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome

   Ferreira de Lima, Renata Hoper, Sarah Ghassibé, Michella[UCL] Cooper, Margaret Rorick, Nicholas Kondo, Shinji Katz, Lori Marazita, Mary Compton, John Bale, Sherri Hehr, Ute Dixon, Michael Daack-Hirsch, Sandra Boute, Odile Bayet, Bénédicte[UCL] Revencu, Nicole[UCL] Dumoulin, Christine[UCL] Vikkula, Miikka[UCL] Richieri-Costa, Antônio Moretti-Ferreira, Danilo Murray, Jeffrey Schutte, Brian (2009) Genetics in Medicine — Vol. 11, no. 4, p. 241-247 (2009)
7. • Dissertation

   • 

   Molecular genetics of vascular anomalies

   Vikkula, Miikka[UCL] (2000)
8. • Journal article

   • 

   Vascular anomalies

   Vikkula, Miikka[UCL] (2007) Experimental Dermatology — Vol. 16, no.10, p. 877-879 (2007)
9. • Journal article

   • 

   FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish.

   Ghassibé, Michella[UCL] Desmyter, Laurence Langenberg, Tobias Claes, Filip Boute, Odile Bayet, Bénédicte[UCL] Pellerin, Philippe Hermans, Karlien Backx, Liesbeth Mansilla, Maria Adela Imoehl, Sandra Nowak, Stefanie Ludwig, Kerstin U Baluardo, Carlotta Ferrian, Melissa Mossey, Peter A Noethen, Markus Dewerchin, Mieke François, Geneviève Revencu, Nicole Vanwijck, Romain Hecht, Jacqueline Mangold, Elisabeth Murray, Jeffrey Rubini, Michele Vermeesch, Joris R Poirel, Hélène[UCL] Carmeliet, Peter Vikkula, Miikka (2011) American Journal of Human Genetics — Vol. 88, no. 2, p. 150-161 (2011)
10. • Journal article

    • 

    CDKN2A, CDKN2B and p14ARF are frequently and differentially methylated in ependymal tumours.

    Rousseau, Emmanuel[UCL] Ruchoux, M-M Scaravilli, F. Chapon, F Vinchon, M De Smet, Charles[UCL] Godfraind, Catherine[UCL] Vikkula, Miikka[UCL] (2003) Neuropathology and applied neurobiology — Vol. 29, no. 6, p. 574-83 (2003)
11. • Journal article

    • 

    5q14.3 neurocutaneous syndrome: a novel continguous gene syndrome caused by simultaneous deletion of RASA1 and MEF2C.

    Carr, Christopher W Zimmerman, Holly H Martin, Christa Lese Vikkula, Miikka Byrd, Adam C Abdul-Rahman, Omar A (2011) American Journal of Medical Genetics. Part A — Vol. 155A, no.7, p. 1640-5 (2011)
12. • Journal article

    • 

    The putative glucose 6-phosphate translocase gene is mutated in essentially all cases of glycogen storage disease type I non-a.

    Veiga da Cunha, Maria[UCL] Gerin, Isabelle[UCL] Chen, Yuan-Tsong Lee, Philip J Leonard, James V Maire, Irène Wendel, Udo Vikkula, Miikka[UCL] Van Schaftingen, Emile[UCL] (1999) European journal of human genetics — Vol. 7, no. 6, p. 717-23 (1999)
13. • Journal article

    • 

    Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population.

    Ghassibé, Michella[UCL] Bayet, Benedicte Revencu, Nicole Dumoulin, Christine[UCL] Gillerot, Yves Vanwijck, Romain[UCL] Vikkula, Miikka[UCL] (2005) European journal of human genetics : EJHG — Vol. 13, no. 11, p. 1239-42 (2005)
14. • Journal article

    • 

    Cerebral cavernous malformation: new molecular and clinical insights.

    Revencu, Nicole[UCL] Vikkula, Miikka[UCL] (2006) Journal of Medical Genetics — Vol. 43, no. 9, p. 716-721 (2006)
15. • Journal article

    • 

    A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?

    Gutierrez-Roelens, Ilse[UCL] De Roy, Lucas[UCL] Ovaert, Caroline[UCL] Sluysmans, Thierry[UCL] Devriendt, Koen Brunner, Han G Vikkula, Miikka[UCL] (2006) European Journal of Human Genetics — Vol. 14, no. 12, p. 1313-1316 (2006)
16. • Journal article

    • 

    L'identification des facteurs impliqués dans l'angiogenèse par l'etude des anomalies vasculaires.

    Vikkula, Miikka[UCL] (2005) Bulletin et mémoires de l'Académie royale de médecine de Belgique — Vol. 160, no. 10-12, p. 435-43; discussion 443-4 (2005)
17. • BookChapter

    • 

    An update on the Molecular Basis of Vascular Malformations

    Vikkula, Miikka[UCL] (2002) Benigne Gefäßfehl- und Neubildungen der Haut (Benign vascular malformations and tumors) — [ISBN : 3-89412-502-0]
18. • Journal article

    • 

    Tumour necrosis and microvascular proliferation are associated with 9p deletion and CDKN2A alterations in 1p/19q-deleted oligodendrogliomas.

    Godfraind, Catherine[UCL] Rousseau, Emmanuel[UCL] Ruchoux, M-M Scaravilli, F. Vikkula, Miikka[UCL] (2003) Neuropathology and applied neurobiology — Vol. 29, no. 5, p. 462-471 (2003)
19. • Journal article

    • 

    Alpha-cardiac actin mutations produce atrial septal defects.

    Matsson, Hans Eason, Jacqueline Bookwalter, Carol S Klar, Joakim Gustavsson, Peter Sunnegårdh, Jan Enell, Henrik Jonzon, Anders Vikkula, Miikka[UCL] Gutierrez-Roelens, Ilse[UCL] Granados-Riveron, Javier Pope, Mark Bu'Lock, Frances Cox, Jane Robinson, Thelma E Song, Feifei Brook, David J Marston, Steven Trybus, Kathleen M Dahl, Niklas (2008) Human molecular genetics — Vol. 17, no. 2, p. 256-65 (2008)
20. • Journal article

    • 

    Pathogénie et génétique des anomalies vasculaires.

    Vikkula, Miikka[UCL] (2006) Annales de Chirurgie Plastique Esthetique — Vol. 51, no. 4-5, p. 282-286 (2006)
21. • Journal article

    • 

    Vascular malformations: localized defects in vascular morphogenesis.

    Brouillard, Pascal[UCL] Vikkula, Miikka[UCL] (2003) Clinical genetics — Vol. 63, no. 5, p. 340-351 (2003)
22. • Journal article

    • 

    Gene symbol IRF6. Disease: Van der Woude syndrome and popliteal pterygium.

    Ghassibé, Michella[UCL] Revencu, Nicole[UCL] Bayet, Bénédicte[UCL] Gillerot, Y.[UCL] Vanwijck, Romain[UCL] Dumoulin, Christine[UCL] Vikkula, Miikka[UCL] (2003) Human genetics — Vol. 113, no. 6, p. 556-558 (2003)
23. • Journal article

    • 

    Hydrops fetalis: an unusual prenatal presentation of hereditary congenital lymphedema.

    Daniel-Spiegel, Etty Ghalamkarpour, Arash[UCL] Spiegel, Ronen Weiner, Ehud Vikkula, Miikka[UCL] Shalev, Eliezer Shalev, Stavit Alon (2005) Prenatal Diagnosis — Vol. 25, no. 11, p. 1015-1018 (2005)
24. • Journal article

    • 

    Localization of candidate regions for a novel gene for Kartagener syndrome.

    Gutierrez-Roelens, Ilse[UCL] Sluysmans, Thierry[UCL] Jorissen, Mark Amyere, Mustapha[UCL] Vikkula, Miikka[UCL] (2006) European Journal of Human Genetics — Vol. 14, no. 7, p. 809-815 (2006)
25. • Journal article

    • 

    Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas

    Persu, Alexandre[UCL] Yao, Li Schiavi, Francesca Cascon, Alberto Qin, Yuejuan Inglada-Pérez, Lucia King, Elizabeth E Toledo, Rodrigo A Ercolino, Tonino Rapizzi, Elena Ricketts, Christopher J Mori, Luigi Giacchè, Mara Mendola, Antonella[UCL] Taschin, Elisa Boaretto, Francesca Loli, Paola Iacobone, Maurizio Rossi, Gian-Paolo Biondi, Bernadette Lima-Junior, José Viana Kater, Claudio E Bex, Marie Vikkula, Miikka[UCL] Grossman, Ashley B Gruber, Stephen B (2010) JAMA : the journal of the American Medical Association — Vol. 304, no.23, p. 2611-9 (2010)

Pages