Elevated Lp(a) Levels Correlate with Severe and Multiple Coronary Artery Stenotic Lesions von Al Hageh, Cynthia, Chacar, Stephanie, Ghassibe-Sabbagh, Michella, Platt, Daniel E, Henschel, Andreas, Hamdan, Hamdan, Gauguier, Dominique, El Murr, Yara, Alefishat, Eman, Chammas, Elie, O'Sullivan, Siobhán, Abchee, Antoine, Nader, Moni, Zalloua, Pierre A

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Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene von Ghassibé, M, Revencu, N, Bayet, B, Gillerot, Y, Vanwijck, R, Verellen-Dumoulin, C, Vikkula, M

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Four common glomulin mutations cause two thirds of glomuvenous malformations (“familial glomangiomas”): evidence for a founder effect von Brouillard, P, Ghassibé, M, Penington, A, Boon, L M, Dompmartin, A, Temple, I K, Cordisco, M, Adams, D, Piette, F, Harper, J I, Syed, S, Boralevi, F, Taïeb, A, Danda, S, Baselga, E, Enjolras, O, Mulliken, J B, Vikkula, M

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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 syn... von de Lima, Renata L L Ferreira, Hoper, Sarah A, Ghassibe, Michella, Cooper, Margaret E, Rorick, Nicholas K, Kondo, Shinji, Katz, Lori, Marazita, Mary L, Compton, John, Bale, Sherri, Hehr, Ute, Dixon, Michael J, Daack-Hirsch, Sandra, Boute, Odile, Bayet, Bénédicte, Revencu, Nicole, Verellen-Dumoulin, Christine, Vikkula, Miikka, Richieri-Costa, Antônio, Moretti-Ferreira, Danilo, Murray, Jeffrey C, Schutte, Brian C

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Mutations in a Novel Factor, Glomulin, Are Responsible for Glomuvenous Malformations (“Glomangiomas”) von Brouillard, Pascal, Boon, Laurence M., Mulliken, John B., Enjolras, Odile, Ghassibé, Michella, Warman, Matthew L., Tan, O.T., Olsen, Bjorn R., Vikkula, Miikka

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Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population von Ghassibé, Michella, Bayet, Benedicte, Revencu, Nicole, Verellen-Dumoulin, Christine, Gillerot, Yves, Vanwijck, Romain, Vikkula, Miikka

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Orofacial clefting: update on the role of genetics von Ghassibe, M, Bayet, B, Revencu, N, Desmyter, L, Verellen-Dumoulin, C, Gillerot, Y, Deggouj, N, Vanwijck, R, Vikkula, M

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Disruption of ST5 is associated with mental retardation and multiple congenital anomalies von 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

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Gene symbol: IRF6. Disease: Van der Woude syndrome von Ghassibe, M, Revencu, N, Bayet, B, Gillerot, Y, Vanwijck, R, Verellen-Dumoulin, C, Vikkula, M

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Gene symbol: IRF6. Disease: Van der Woude syndrome von Ghassibe, M, Revencu, N, Bayet, B, Gillerot, Y, Vanwijck, R, Verellen-Dumoulin, C, Vikkula, M

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Gene symbol: IRF6. Disease: Van der Woude syndrome von Ghassibe, M, Revencu, N, Bayet, B, Gillerot, Y, Vanwijck, R, Verellen-Dumoulin, C, Vikkula, M

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Gene symbol: IRF6. Disease: Van der Woude syndrome von Ghassibe, M, Revencu, N, Bayet, B, Gillerot, Y, Vanwijck, R, Verellen-Dumoulin, C, Vikkula, M

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Gene symbol: IRF6. Disease: Van der Woude syndrome von Ghassibe, M, Revencu, N, Bayet, B, Gillerot, Y, Vanwijck, R, Verellen-Dumoulin, C, Vikkula, M

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IRF6 screening of syndromic and a priori non-syndromic cleft lip and palatet patients: Identification of a new type of minor VWS sign von Desmyter, L, Ghassibe, M, Revencu, N, Boute, O, Lees, M, François, G, Verellen-Dumoulin, C, Sznajer, Y, Moncla, A, Benateau, H, Claes, K, Devriendt, Koenraad, Mathieu, M, Van Maldergem, L, Addor, M.C, Drouin-Garraud, V, Mortier, G, Bouma, M, Dieux-Coeslier, A, Genevieve, D, Goldenberg, A, Gozu, A, Makrythanasis, P, McEntagart, M, Sanchez, A, Vilain, C, Vermeer, S, Connell, F, Verheij, J, Manouvrier, S, Pierquin, G, Odent, S, Holder-Espinasse, M, Vincent-Delorme, C, Gillerot, Y, Vanwijck, R, Bayet, B, Vikkula, M

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“I try the one that they say is good.” - factors influencing choice of health care provider and pathways to diabetes care for Syrian refugees in Lebanon von Haderer, F, Venables, E, van Olmen, J, Orcutt, M, Ghassibe-Sabbagh, M, van den Boogaard, W

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Disruption of ST5 is associated with mental-retardation and multiple congenital anomalies von Göhring, I, Tagariello, A, Endele, S, Stolt, C C, Ghassibé, M, Fisher, M, Thiel, C T, Trautmann, U, Vikkula, M, Winterpacht, A, FitzPatrick, D R, Rauch, A

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A novel mutation in the MSX2 homeobox gene of a family with foramina parietalia permagna, headache and vascular anomaly von GHASSIBE, Michella, BERNIER, Vincent, BOON, Laurence M, VIKKULA, Miikka

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Gene symbol IRF6. Disease: Van der Woude syndrome and popliteal pterygium von Ghassibe, Michella, Revencu, N, Bayet, B, Gillerot, Y, Vanwijck, R, Verellen-Dumoulin, C, Vikkula, M

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IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS Sign von Desmyter, L, Ghassibe, M, Revencu, N, Boute, O, Lees, M, Francois, G, Verellen-Dumoulin, C, Sznajer, Y, Moncla, A, Benateau, H, Claes, K, Devriendt, K, Mathieu, M, Van Maldergem, Lionel, Addor, M. C, Drouin-Garraud, V, Mortier, G, Bouma, M, Dieux-Coeslier, A, Genevieve, D, Goldenberg, A, Gozu, A, Makrythanasis, P, McEntagart, U, Sanchez, A, Vilain, C, Vermeer, S, Connell, F, Verheij, J, Manouvrier, S, Pierquin, Geneviève, Odent, S, Holder-Espinasse, M, Vincent-Delorme, C, Gillerot, Y, Vanwijck, R, Bayet, B, Vikkula, M

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NOVEL GLOMULIN MUTATIONS, WHICH ALTER VASCULAR SMOOTH MUSCLE CELL DIFFERENTIATION AND RESULT IN GLOMUVENOUS MALFORMATIONS, REVEAL STRONG FOUNDER EFFECT FOR TWO OF THE MUTATIONS von Brouillard, Pascal, Ghassibé, Michella, Pennington, Anthony, Boon, Laurence M, Dompmartin, Anne, Temple, Karen, Cordisco, Maria, Adams, Denise, Piette, Frédéric, Harper, John, Labrèze, Christine, Danda, Sumita, Enjolras, Odile, Mulliken, John B, Vikkula, Miikka

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