Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing by Hoebel, A.K., Drichel, D., van de Vorst, M., Böhmer, A.C., Sivalingam, S., Ishorst, N., Klamt, J., Gölz, L., Alblas, M., Maaser, A., Keppler, K., Zink, A.M., Dixon, M.J., Dixon, J., Hemprich, A., Kruse, T., Graf, I., Dunsche, A., Schmidt, G., Daratsianos, N., Nowak, S., Aldhorae, K.A., Nöthen, M.M., Knapp, M., Thiele, H., Gilissen, C., Reutter, H., Hoischen, A., Mangold, E., Ludwig, K.U.

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Comprehensive review of the duplication 3q syndrome and report of a patient with Currarino syndrome and de novo duplication 3q26.32‐q27.2 by Dworschak, G.C., Crétolle, C., Hilger, A., Engels, H., Korsch, E., Reutter, H., Ludwig, M.

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Epispadias and the associated embryopathies: genetic and developmental basis by Suzuki, K., Matsumaru, D., Matsushita, S., Murashima, A., Ludwig, M., Reutter, H., Yamada, G.

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Brain Abnormalities in Patients with Germline Variants in H3F3 : Novel Imaging Findings and Neurologic Symptoms Beyond Somatic Variants and Brain Tumors by Alves, C A P F, Sherbini, O, D'Arco, F, Steel, D, Kurian, M A, Radio, F C, Ferrero, G B, Carli, D, Tartaglia, M, Balci, T B, Powell-Hamilton, N N, Schrier Vergano, S A, Reutter, H, Hoefele, J, Günthner, R, Roeder, E R, Littlejohn, R O, Lessel, D, Lüttgen, S, Kentros, C, Anyane-Yeboa, K, Catarino, C B, Mercimek-Andrews, S, Denecke, J, Lyons, M J, Klopstock, T, Bhoj, E J, Bryant, L, Vanderver, A

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VATER/VACTERL Association: Evidence for the Role of Genetic Factors by Reutter, H., Ludwig, M.

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Strong Association of Variants around FOXE1 and Orofacial Clefting by Ludwig, K.U., Böhmer, A.C., Rubini, M., Mossey, P.A., Herms, S., Nowak, S., Reutter, H., Alblas, M.A., Lippke, B., Barth, S., Paredes-Zenteno, M., Muñoz-Jimenez, S.G., Ortiz-Lopez, R., Kreusch, T., Hemprich, A., Martini, M., Braumann, B., Jäger, A., Pötzsch, B., Molloy, A., Peterlin, B., Hoffmann, P., Nöthen, M.M., Rojas-Martinez, A., Knapp, M., Steegers-Theunissen, R.P., Mangold, E.

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Mutations in CRLF1 cause familial achalasia by Busch, A., Žarković, M., Lowe, C., Jankofsky, M., Ganschow, R., Buers, I., Kurth, I., Reutter, H., Rutsch, F., Hübner, C.A.

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Comparison of environmental risk factors for esophageal atresia, anorectal malformations, and the combined phenotype in 263 German families by Zwink, N., Choinitzki, V., Baudisch, F., Hölscher, A., Boemers, T. M., Turial, S., Kurz, R., Heydweiller, A., Keppler, K., Müller, A., Bagci, S., Pauly, M., Brokmeier, U., Leutner, A., Degenhardt, P., Schmiedeke, E., Märzheuser, S., Grasshoff‐Derr, S., Holland‐Cunz, S., Palta, M., Schäfer, M., Ure, B. M., Lacher, M., Nöthen, M. M., Schumacher, J., Jenetzky, E., Reutter, H.

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1403 Does Amnioticfluid Play a Nutritive Role Before Birth? a Retrospective Analysis of Newborninfants with Upper and Lower Gastrointestinal Atresia by Zillhardt, H, Korczyk, J, Heydweiller, A, Reutter, H, Müller, A, Bartmann, P, Bagci, S

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Practice of dilatation after surgical correction in anorectal malformations by Jenetzky, Ekkehart, Reckin, S., Schmiedeke, E., Schmidt, D., Schwarzer, N., Grasshoff-Derr, S., Zwink, N., Bartels, E., Rißmann, A., Leonhardt, J., Weih, S., Obermayr, F., Rädecke, J., Palta, M., Kosch, F., Götz, G., Hofbauer, A., Schäfer, M., Reutter, H., Holland-Cunz, S., Märzheuser, S.

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Microdeletions Including FMR1 in Three Female Patients with Intellectual Disability - Further Delineation of the Phenotype and Expression Studies by Zink, A.M., Wohlleber, E., Engels, H., Rødningen, O.K., Ravn, K., Heilmann, S., Rehnitz, J., Katzorke, N., Kraus, C., Blichfeldt, S., Hoffmann, P., Reutter, H., Brockschmidt, F.F., Kreiß-Nachtsheim, M., Vogt, P.H., Prescott, T.E., Tümer, Z., Lee, J.A.

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WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish by Baranowska Körberg, Izabella, Hofmeister, Wolfgang, Markljung, Ellen, Cao, Jia, Nilsson, Daniel, Ludwig, Michael, Draaken, Markus, Holmdahl, Gundela, Barker, Gillian, Reutter, Heiko, Vukojević, Vladana, Clementson Kockum, Christina, Lundin, Johanna, Lindstrand, Anna, Nordenskjöld, Agneta

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The impact of perioperative care on complications and short term outcome in ARM type rectovestibular fistula: An ARM-Net consortium study by van der Steeg, H.J.J., van Rooij, I.A.L.M., Iacobelli, B.D., Sloots, C.E.J., Leva, E., Broens, P., Fascetti Leon, F., Makedonsky, I., Schmiedeke, E., García Vázquez, A., Midrio, P., Lisi, G., Amerstorfer, E., Miserez, M., Fanjul, M., Ludwiczek, J., Stenström, P., Giuliani, S., van der Steeg, A.F.W., de Blaauw, I.

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Evaluation of sexual function in females with exstrophy-epispadias-complex: A survey of the multicenter German CURE-Net by Ebert, Anne-Karoline, Lange, Theresa, Reutter, Heiko, Jenetzky, Ekkehart, Stein, Raimund, Boemers, Thomas M, Hirsch, Karin, Rösch, Wolfgang H, Zwink, Nadine

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ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development by Zhang, Rong, Knapp, Michael, Suzuki, Kentaro, Kajioka, Daiki, Schmidt, Johanna M., Winkler, Jonas, Yilmaz, Öznur, Pleschka, Michael, Cao, Jia, Kockum, Christina Clementson, Barker, Gillian, Holmdahl, Gundela, Beaman, Glenda, Keene, David, Woolf, Adrian S., Cervellione, Raimondo M., Cheng, Wei, Wilkins, Simon, Gearhart, John P., Sirchia, Fabio, Di Grazia, Massimo, Ebert, Anne-Karolin, Rösch, Wolfgang, Ellinger, Jörg, Jenetzky, Ekkehart, Zwink, Nadine, Feitz, Wout F., Marcelis, Carlo, Schumacher, Johannes, Martinón-Torres, Federico, Hibberd, Martin Lloyd, Khor, Chiea Chuen, Heilmann-Heimbach, Stefanie, Barth, Sandra, Boyadjiev, Simeon A., Brusco, Alfredo, Ludwig, Michael, Newman, William, Nordenskjöld, Agneta, Yamada, Gen, Odermatt, Benjamin, Reutter, Heiko

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Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated cla... by Reutter, Heiko, Draaken, Markus, Pennimpede, Tracie, Wittler, Lars, Brockschmidt, Felix F, Ebert, Anne-Karolin, Bartels, Enrika, Rösch, Wolfgang, Boemers, Thomas M, Hirsch, Karin, Schmiedeke, Eberhard, Meesters, Christian, Becker, Tim, Stein, Raimund, Utsch, Boris, Mangold, Elisabeth, Nordenskjöld, Agneta, Barker, Gillian, Kockum, Christina Clementsson, Zwink, Nadine, Holmdahl, Gundula, Läckgren, Göran, Jenetzky, Ekkehart, Feitz, Wouter F J, Marcelis, Carlo, Wijers, Charlotte H W, Van Rooij, Iris A L M, Gearhart, John P, Herrmann, Bernhard G, Ludwig, Michael, Boyadjiev, Simeon A, Nöthen, Markus M, Mattheisen, Manuel

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Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region by Draaken, Markus, Baudisch, Friederike, Timmermann, Bernd, Kuhl, Heiner, Kerick, Martin, Proske, Judith, Wittler, Lars, Pennimpede, Tracie, Ebert, Anne-Karoline, Rösch, Wolfgang, Stein, Raimund, Bartels, Enrika, von Lowtzow, Catharina, Boemers, Thomas M., Herms, Stefan, Gearhart, John P., Lakshmanan, Yegappan, Kockum, Christina Clementsson, Holmdahl, Gundela, Läckgren, Göran, Nordenskjöld, Agnetha, Boyadjiev, Simeon A., Herrmann, Bernhard G., Nöthen, Markus M., Ludwig, Michael, Reutter, Heiko

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SLC20A1 Is Involved in Urinary Tract and Urorectal Development by Rieke, Johanna Magdalena, Zhang, Rong, Braun, Doreen, Yilmaz, Öznur, Japp, Anna S, Lopes, Filipa M, Pleschka, Michael, Hilger, Alina C, Schneider, Sophia, Newman, William G, Beaman, Glenda M, Nordenskjöld, Agneta, Ebert, Anne-Karoline, Promm, Martin, Rösch, Wolfgang H, Stein, Raimund, Hirsch, Karin, Schäfer, Frank-Mattias, Schmiedeke, Eberhard, Boemers, Thomas M, Lacher, Martin, Kluth, Dietrich, Gosemann, Jan-Hendrik, Anderberg, Magnus, Barker, Gillian, Holmdahl, Gundela, Läckgren, Göran, Keene, David, Cervellione, Raimondo M, Giorgio, Elisa, Di Grazia, Massimo, Feitz, Wouter F J, Marcelis, Carlo L M, Van Rooij, Iris A L M, Bökenkamp, Arend, Beckers, Goedele M A, Keegan, Catherine E, Sharma, Amit, Dakal, Tikam Chand, Wittler, Lars, Grote, Phillip, Zwink, Nadine, Jenetzky, Ekkehart, Brusco, Alfredo, Thiele, Holger, Ludwig, Michael, Schweizer, Ulrich, Woolf, Adrian S, Odermatt, Benjamin, Reutter, Heiko

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A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy by Mingardo, Enrico, Beaman, Glenda, Grote, Philip, Nordenskjöld, Agneta, Newman, William, Woolf, Adrian S., Eckstein, Markus, Hilger, Alina C., Dworschak, Gabriel C., Rösch, Wolfgang, Ebert, Anne-Karolin, Stein, Raimund, Brusco, Alfredo, Di Grazia, Massimo, Tamer, Ali, Torres, Federico M., Hernandez, Jose L., Erben, Philipp, Maj, Carlo, Olmos, Jose M., Riancho, Jose A., Valero, Carmen, Hostettler, Isabel C., Houlden, Henry, Werring, David J., Schumacher, Johannes, Gehlen, Jan, Giel, Ann-Sophie, Buerfent, Benedikt C., Arkani, Samara, Åkesson, Elisabeth, Rotstein, Emilia, Ludwig, Michael, Holmdahl, Gundela, Giorgio, Elisa, Berettini, Alfredo, Keene, David, Cervellione, Raimondo M., Younsi, Nina, Ortlieb, Melissa, Oswald, Josef, Haid, Bernhard, Promm, Martin, Neissner, Claudia, Hirsch, Karin, Stehr, Maximilian, Schäfer, Frank-Mattias, Schmiedeke, Eberhard, Boemers, Thomas M., van Rooij, Iris A. L. M., Feitz, Wouter F. J., Marcelis, Carlo L. M., Lacher, Martin, Nelson, Jana, Ure, Benno, Fortmann, Caroline, Gale, Daniel P., Chan, Melanie M. Y., Ludwig, Kerstin U., Nöthen, Markus M., Heilmann, Stefanie, Zwink, Nadine, Jenetzky, Ekkehart, Odermatt, Benjamin, Knapp, Michael, Reutter, Heiko

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First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B by Gehlen, Jan, Giel, Ann-Sophie, Köllges, Ricarda, Haas, Stephan L., Zhang, Rong, Trcka, Jiri, Sungur, Ayse Ö., Renziehausen, Florian, Bornholdt, Dorothea, Jung, Daphne, Hoyer, Paul D., Nordenskjöld, Agneta, Tibboel, Dick, Vlot, John, Spaander, Manon C.W., Smigiel, Robert, Patkowski, Dariusz, Roeleveld, Nel, van Rooij, Iris ALM, de Blaauw, Ivo, Hölscher, Alice, Pauly, Marcus, Leutner, Andreas, Fuchs, Joerg, Niethammer, Joel, Melissari, Maria-Theodora, Jenetzky, Ekkehart, Zwink, Nadine, Thiele, Holger, Hilger, Alina Christine, Hess, Timo, Trautmann, Jessica, Marks, Matthias, Baumgarten, Martin, Bläss, Gaby, Landén, Mikael, Fundin, Bengt, Bulik, Cynthia M., Pennimpede, Tracie, Ludwig, Michael, Ludwig, Kerstin U., Mangold, Elisabeth, Heilmann-Heimbach, Stefanie, Moebus, Susanne, Herrmann, Bernhard G., Alsabeah, Kristina, Burgos, Carmen M., Lilja, Helene E., Azodi, Sahar, Stenström, Pernilla, Arnbjörnsson, Einar, Frybova, Barbora, Lebensztejn, Dariusz M., Debek, Wojciech, Kolodziejczyk, Elwira, Kozera, Katarzyna, Kierkus, Jaroslaw, Kaliciński, Piotr, Stefanowicz, Marek, Socha-Banasiak, Anna, Kolejwa, Michal, Piaseczna-Piotrowska, Anna, Czkwianianc, Elzbieta, Nöthen, Markus M., Grote, Phillip, Rygl, Michal, Reinshagen, Konrad, Spychalski, Nicole, Ludwikowski, Barbara, Hubertus, Jochen, Heydweiller, Andreas, Ure, Benno, Muensterer, Oliver J., Aubert, Ophelia, Gosemann, Jan-Hendrik, Lacher, Martin, Degenhardt, Petra, Boemers, Thomas M., Mokrowiecka, Anna, Małecka-Panas, Ewa, Wöhr, Markus, Knapp, Michael, Seitz, Guido, de Klein, Annelies, Oracz, Grzegorz, Brosens, Erwin, Reutter, Heiko, Schumacher, Johannes

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