Three-dimensional imaging methods for quantitative analysis of facial soft tissues and skeletal morphology in patients with orofacial clefts: a systematic review von Kuijpers, Mette A R, Chiu, Yu-Ting, Nada, Rania M, Carels, Carine E L, Fudalej, Piotr S

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Tooth agenesis patterns in unilateral cleft lip and palate in humans von Bartzela, Theodosia N, Carels, Carine E.L, Bronkhorst, Ewald M, Jagtman, Anne Marie Kuijpers

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Systematic analysis of copy number variants of a large cohort of orofacial cleft patients identifies candidate genes for orofacial clefts von Conte, Federica, Oti, Martin, Dixon, Jill, Carels, Carine E. L., Rubini, Michele, Zhou, Huiqing

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Retinoic acid disrupts osteogenesis in pre-osteoblasts by down-regulating WNT signaling von Roa, Laury A., Bloemen, Marjon, Carels, Carine E.L., Wagener, Frank A.D.T.G., Von den Hoff, Johannes W.

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MSX1 mutations and associated disease phenotypes: genotype-phenotype relations von Liang, Jia, Von den Hoff, Johannes, Lange, Joanna, Ren, Yijin, Bian, Zhuan, Carels, Carine E L

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Retinoic acid effects on in vitro palatal fusion and WNT signaling von Roa Fuentes, Laury Amelia, Bloemen, Marjon, Carels, Carine EL, Wagener, Frank ADTG, Von den Hoff, Johannes W

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Retinoic acid effects on in vitro palatal fusion and WNT signaling von Fuentes, Laury Amelia Roa, Bloemen, Marjoen, Carels, Carine E.L, Wagener, Frank A.D.T.G, Von den Hoff, Johannes W

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Retinoic acid disrupts osteogenesis in pre-osteoblasts by down-regulating WNT signaling von Roa, Laury A, Bloemen, Marjon, Carels, Carine E.L, Wagener, Frank A.D.T.G, Von den Hoff, Johannes W

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A potential osteogenic role for microRNA-181a-5p during palatogenesis von Schoen, Christian, Bloemen, Marjon, Carels, Carine E L, Verhaegh, Gerald W, Van Rheden, Rene, Roa, Laury A, Glennon, Jeffrey C, Von den Hoff, Johannes W

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Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations von Ockeloen, Charlotte W, Willemsen, Marjolein H, de Munnik, Sonja, van Bon, Bregje W M, de Leeuw, Nicole, Verrips, Aad, Kant, Sarina G, Jones, Elizabeth A, Brunner, Han G, van Loon, Rosa L E, Smeets, Eric E J, van Haelst, Mieke M, van Haaften, Gijs, Nordgren, Ann, Malmgren, Helena, Grigelioniene, Giedre, Vermeer, Sascha, Louro, Pedro, Ramos, Lina, Maal, Thomas J J, van Heumen, Celeste C, Yntema, Helger G, Carels, Carine E L, Kleefstra, Tjitske

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Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesis von Ockeloen, Charlotte W., Khandelwal, Kriti D., Dreesen, Karoline, Ludwig, Kerstin U., Sullivan, Robert, van Rooij, Iris A.L.M., Thonissen, Michelle, Swinnen, Steven, Phan, Milien, Conte, Federica, Ishorst, Nina, Gilissen, Christian, Roa Fuentes, Laury, van de Vorst, Maartje, Henkes, Arjen, Steehouwer, Marloes, van Beusekom, Ellen, Bloemen, Marjon, Vankeirsbilck, Bruno, Bergé, Stefaan, Hens, Greet, Schoenaers, Joseph, Vander Poorten, Vincent, Roosenboom, Jasmien, Verdonck, An, Devriendt, Koen, Roeleveldt, Nel, Jhangiani, Shalini N., Vissers, Lisenka E.L.M., Lupski, James R., de Ligt, Joep, Von den Hoff, Johannes W., Pfundt, Rolph, Brunner, Han G., Zhou, Huiqing, Dixon, Jill, Mangold, Elisabeth, van Bokhoven, Hans, Dixon, Michael J., Kleefstra, Tjitske, Hoischen, Alexander, Carels, Carine E.L.

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MicroRNAs in Palatogenesis and Cleft Palate von Schoen, Christian, Aschrafi, Armaz, Thonissen, Michelle, Poelmans, Geert, Von den Hoff, Johannes W, Carels, Carine E L

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Retinoic acid signalling in the development of the epidermis, the limbs and the secondary palate von Mammadova, Aysel, Zhou, Huiqing, Carels, Carine E.L., Von den Hoff, Johannes W.

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Differential microRNA expression in cultured palatal fibroblasts from infants with cleft palate and controls von Schoen, Christian, Glennon, Jeffrey C, Abghari, Shaghayegh, Bloemen, Marjon, Aschrafi, Armaz, Carels, Carine E L, Von den Hoff, Johannes W

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Deletions and loss-of-function variants in TP63 associated with orofacial clefting von Khandelwal, Kriti D, van den Boogaard, Marie-José H, Mehrem, Sarah L, Gebel, Jakob, Fagerberg, Christina, van Beusekom, Ellen, van Binsbergen, Ellen, Topaloglu, Ozan, Steehouwer, Marloes, Gilissen, Christian, Ishorst, Nina, van Rooij, Iris A L M, Roeleveld, Nel, Christensen, Kaare, Schoenaers, Joseph, Bergé, Stefaan, Murray, Jeffrey C, Hens, Greet, Devriendt, Koen, Ludwig, Kerstin U, Mangold, Elisabeth, Hoischen, Alexander, Zhou, Huiqing, Dötsch, Volker, Carels, Carine E L, van Bokhoven, Hans

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Identification of germline mutations in the cancer predisposing gene CDH1 in patients with orofacial clefts von Vogelaar, Ingrid P, Figueiredo, Joana, van Rooij, Iris A L M, Simões-Correia, Joana, van der Post, Rachel S, Melo, Soraia, Seruca, Raquel, Carels, Carine E L, Ligtenberg, Marjolijn J L, Hoogerbrugge, Nicoline

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Variability in dentofacial phenotypes in four families with WNT10A mutations von Vink, Christian P, Ockeloen, Charlotte W, ten Kate, Sietske, Koolen, David A, Ploos van Amstel, Johannes Kristian, Kuijpers-Jagtman, Anne-Marie, van Heumen, Celeste C, Kleefstra, Tjitske, Carels, Carine E L

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AGORA, a data- and biobank for birth defects and childhood cancer von van Rooij, Iris A.L.M., van der Zanden, Loes F.M., Bongers, Ernie M.H.F., Renkema, Kirsten Y., Wijers, Charlotte H.W., Thonissen, Michelle, Dokter, Elisabeth M.J., Marcelis, Carlo L.M., de Blaauw, Ivo, Wijnen, Marc H.W.A., Hoogerbrugge, Peter M., Bokkerink, Jos P.M., Schreuder, Michiel F., Koster-Kamphuis, Linda, Cornelissen, Elisabeth A.M., Kapusta, Livia, van Heijst, Arno F.J., Liem, Kian D., de Gier, Robert P.E., Kuijpers-Jagtman, Anne Marie, Admiraal, Ronald J.C., Bergé, Stefaan J., van der Biezen, Jan Jaap, Verdonck, An, Vander Poorten, Vincent, Hens, Greet, Roosenboom, Jasmien, Lilien, Marc R., de Jong, Tom P., Broens, Paul, Wijnen, Rene, Brooks, Alice, Franke, Barbara, Brunner, Han G., Carels, Carine E.L., Knoers, Nine V.A.M., Feitz, Wout F.J., Roeleveld, Nel

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Deregulated Adhesion Program in Palatal Keratinocytes of Orofacial Cleft Patients von Mammadova, Aysel, Carels, Carine E L, Zhou, Jie, Gilissen, Christian, Helmich, Maria P A C, Bian, Zhuan, Zhou, Huiqing, Von den Hoff, Johannes W

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Identification of a de novo variant in CHUK in a patient with an EEC/AEC syndrome‐like phenotype and hypogammaglobulinemia von Khandelwal, Kriti D., Ockeloen, Charlotte W., Venselaar, Hanka, Boulanger, Cécile, Brichard, Bénédicte, Sokal, Etienne, Pfundt, Rolph, Rinne, Tuula, van Beusekom, Ellen, Bloemen, Marjon, Vriend, Gerrit, Revencu, Nicole, Carels, Carine E. L., van Bokhoven, Hans, Zhou, Huiqing

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