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    • Article de périodique
    Biallelic ANGPT2 loss-of-function causes severe early-onset non-immune hydrops fetalis
    Smeland, Marie F. Brouillard, Pascal[UCL] Prescot, Trine Boon, Laurence M.[UCL] Bodil, Hvingel Nordbakken, Cecilie V. Nystad, Mona Holla, Øystein L. Vikkula, Miikka[UCL] (2023) Journal of medical genetics — Vol. 60, no. 1, p. 57-64 (2023)
    • Article de périodique
    Analysing ambiguities in trypanosomatids taxonomy by barcoding.
    Boucinha, Carolina Caetano, Amanda R Santos, Helena Lc Helaers, Raphaël[UCL] Vikkula, Miikka[UCL] Branquinha, Marta Helena Dos Santos, André Luis Souza Grellier, Philippe Morelli, Karina Alessandra d'Avila-Levy, Claudia Masini (2020) Memorias do Instituto Oswaldo Cruz — Vol. 115, p. e200504 [1-14] (2020)
    • Article de périodique
    Association of localized intravascular coagulopathy with venous malformations
    Dompmartin, Anne[UCL] Acher, Aurélie Thibon, Pascal Tourbach, Sébastien[UCL] Hermans, Cédric[UCL] Deneys, Véronique[UCL] Pocock, Ben[UCL] Lequerrec, Agnès Labbé, Daniel Barrellier, Marie-Thérèse Vanwijck, Romain[UCL] Vikkula, Miikka[UCL] Boon, Laurence M.[UCL] (2008) Archives of Dermatology — Vol. 144, no. 7, p. 873-877 (2008)
    • Chapitre
    Capillary malformation/arteriovenous malformation
    Revencu, Nicole[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2020) Emery and Rimoin’s Principles and Practice in Medical Genetics — [ISBN : 9780128125366]
    • Article de périodique
    Transcriptional drifts associated with environmental changes in endothelial cells
    Afshar, Yalda Ma, Feyiang Quach, Austin Jeong, Anhyo Sunshine, Hannah L Freitas, Vanessa Jami-Alahmadi, Yasaman Helaers, Raphael[UCL] Li, Xinmin Pellegrini, Matteo Wohlschlegel, James A Romanoski, Casey E Vikkula, Miikka[UCL] Iruela-Arispe, M Luisa (2023) eLife — Vol. 12, p. 1-29 (2023)
    • Rapport de recherche
    Direct-to-consumer genetic testing services
    Borry, Pascal Poirel, Hélène[UCL] Baatout, Sarah Blaumeiser, Bettina Cassiman, Jean-Jacques de Thibault de Boesinghe, Léopold Fondu, Michel Godderis, Lode Haufroid, Vincent[UCL] Hulstaert, Frank Kirsch-Volders, Micheline Liebaers, Inge Loeys, Bart Poppe, Bruce Schamps, Geneviève[UCL] Van Larebeke, Nicolas Van Nerom, Anne Van Oyen, Herman Dumoulin, Christine[UCL] Vikkula, Miikka[UCL] (2012)
    • Article de périodique
    EPHB4 Mutation Causes Adult and Adolescent-Onset Primary Lymphedema
    Greene, Arin Brouillard, Pascal[UCL] Sudduth, Christopher Smits, Patrick Konczyk, Dennis Vikkula, Miikka[UCL] (2021) American Journal of Medical Genetics. Part A — Vol. 185, no. 12, p. 3810-3813 (2021)
    • Article de périodique
    Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus.
    Vikkula, Miikka[UCL] Mariman, E C Lui, V C Zhidkova, N I Tiller, G E Goldring, M B van Beersum, S E de Waal Malefijt, M C van den Hoogen, F H Ropers, H H (1995) Cell — Vol. 80, no.3, p. 431-7 (1995)
    • Communication
    Dementia with continuous spike-wave during slow sleep (CSWS): Neuroserpin, a new family group disorder
    Van Rijckevorsel, Germaine[UCL] Godfraind, Catherine[UCL] Raftopoulos, Christian[UCL] Andries, S.[UCL] Coutellier, M.[UCL] Deconinck, N. Ghariani, S.[UCL] Scaravilli, F.[UCL] Vikkula, Miikka[UCL] (2007) 61st Annual Meeting of the American-Epilepsy-Society — Philadelphia (Pa)
    • Article de périodique
    Progressive hyperpigmentation and generalized lentiginosis without associated systemic symptoms: a rare hereditary pigmentation disorder in south-east Germany.
    Zanardo, Livia Stolz, Wilhelm Schmitz, Gerd Kaminski, Wolfgang Vikkula, Miikka[UCL] Landthaler, Michael Vogt, Thomas (2004) Acta dermato-venereologica — Vol. 84, no. 1, p. 57-60 (2004)
    • Article de périodique
    Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase.
    Irrthum, A Alitalo, Kari Karkkainen, M J Devriendt, Koenraad[UCL] Vikkula, Miikka[UCL] (2000) American journal of human genetics — Vol. 67, no. 2, p. 295-301 (2000)
    • Article de périodique
    Genetic causes of vascular malformations.
    Brouillard, Pascal[UCL] Vikkula, Miikka[UCL] (2007) Human molecular genetics — Vol. 16 Spec No. 2, p. R140-9 (2007)
    • Article de périodique
    Sporadic In Utero Generalized Edema Caused by Mutations in the Lymphangiogenic Genes VEGFR3 and FOXC2.
    Ghalamkarpour, Arash Debauche, Christian[UCL] Haan, Eric Van Regemorter, Nicole Sznajer, Yves Thomas, Dominique Revencu, Nicole Gillerot, Yves Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2009) The Journal of pediatrics — Vol. 155, no. 1, p. 90-3 (2009)
    • Chapitre
    SOX18 and the hypotrichosis-lymphedema-telangiectasia syndrome
    Brouillard, Pascal[UCL] Devriendt, Koen Vikkula, Miikka[UCL] (2016) Epstein's Inborn errors of development. The Molecular Basis of Clinical Disorders of Morphogenesis. — [ISBN : 0199934525]
    • Article de périodique
    Expression of Contactin 4 is associated with malignant behavior in pheochromocytomas and paragangliomas.
    Evenepoel, Lucie[UCL] van Nederveen, Francien H Oudijk, Lindsey Papathomas, Thomas G Restuccia, David F Belt, Eric J T de Herder, Wouter W Feelders, Richard A Franssen, Gaston J H Hamoir, Marc[UCL] Maiter, Dominique[UCL] Perren, Aurel Timmers, Henri J L M van Eeden, Susanne Vroonen, Laurent Aydin, Selda[UCL] Robledo, Mercedes Vikkula, Miikka[UCL] de Krijger, Ronald R Dinjens, Winand N M Persu, Alexandre[UCL] Korpershoek, Esther (2018) Journal of Clinical Endocrinology and Metabolism — Vol. 103, no. 1, p. 46-55 (2018)
    • Article de périodique
    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)
    • Article de périodique
    Genetic basis and therapies for Vascular Anomalies.
    Queisser, Angela[UCL] Seront, Emmanuel[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2021) Circulation Research — Vol. x, no.x, p. x (2021)
    • Article de périodique
    Hypotrichosis-lymphedema-telangiectasia syndrome: Report of ileal atresia associated with a SOX18 de novo pathogenic variant and review of the phenotypic spectrum.
    Coulie, Richard[UCL] Niyazov, Dmitriy M Gambello, Michael J Fastré, Elodie[UCL] Brouillard, Pascal[UCL] Vikkula, Miikka[UCL] (2021) American journal of medical genetics. Part A — Vol. 185, no. 7, p. 2153-2159 (2021)
    • Article de périodique
    DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis
    Lorenz-Depiereux, Bettina Bastepe, Murat Benet-Pagès, Anna Amyere, Mustapha[UCL] Wagenstaller, Janine Müller-Barth, Ursula Badenhoop, Klaus Kaiser, Stephanie M. Rittmaster, Roger S. Shlossberg, Alan H. Olivares, José L. Loris, César Ramos, Feliciano J. Glorieux, Francis Vikkula, Miikka[UCL] Jüppner, Harald Strom, Tim M. (2006) Nature Genetics — Vol. 38, no. 11, p. 1248-1250 (2006)
    • Article de périodique
    Theranostic advances in vascular malformations
    Dekeuleneer, Valérie[UCL] Seront, Emmanuel[UCL] Van Damme, An[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2020) The Journal of Investigative Dermatology — Vol. 140, no. 4, p. 756 (2020)
    • Article de périodique
    La génomique en cancérologie expliquée à l’omnipraticien
    Duhoux, François[UCL] Vikkula, Miikka[UCL] (2014) Louvain médical — Vol. 133, no.6, p. 417-421 (Juin-Juillet-Août 2014)
    • Article de périodique
    Etiology and Genetics of Congenital Vascular Lesions
    Queisser, Angela[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2018) Otolaryngologic Clinics of North America — Vol. 51, no. 1, p. 41-53 (2018)
    • Article de périodique
    Incidence of Cellulitis among Children with Primary Lymphedema
    Quéré, Isabelle Nagot, Nicolas Vikkula, Miikka[UCL] (2018) New England Journal of Medicine — Vol. 378, no.21, p. 2047-8
    • Communication
    Glomuvenous malformation ("glomangioma") is a distinct clinicopathologic and genetic entity
    Boon, Laurence M.[UCL] Mulliken, J Enjolras, O Vikkula, Miikka[UCL] (2002) European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics — STRASBOURG (France)
    • Article de périodique
    Micrometric segregation of fluorescent membrane lipids: relevance for endogenous lipids and biogenesis in erythrocytes.
    D'Auria, Ludovic Fenaux, Marisa Aleksandrowicz, Paulina Van Der Smissen, Patrick Chantrain, Christophe Vermylen, Christiane Vikkula, Miikka Courtoy, Pierre J.[UCL] Tyteca, Donatienne[UCL] (2013) Journal of Lipid Research — Vol. 54, no.4, p. 1066-76 (2013)

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