Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract von Hwang, Daw-Yang, Dworschak, Gabriel C., Kohl, Stefan, Saisawat, Pawaree, Vivante, Asaf, Hilger, Alina C., Reutter, Heiko M., Soliman, Neveen A., Bogdanovic, Radovan, Kehinde, Elijah O., Tasic, Velibor, Hildebrandt, Friedhelm

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Currarino syndrome: a comprehensive genetic review of a rare congenital disorder von Dworschak, Gabriel C., Reutter, Heiko M., Ludwig, Michael

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Circulating microRNAs are associated with Pulmonary Hypertension and Development of Chronic Lung Disease in Congenital Diaphragmatic Hernia von Herrera-Rivero, Marisol, Zhang, Rong, Heilmann-Heimbach, Stefanie, Mueller, Andreas, Bagci, Soyhan, Dresbach, Till, Schröder, Lukas, Holdenrieder, Stefan, Reutter, Heiko M., Kipfmueller, Florian

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EU’s rural development policy at the regional level—Are expenditures for natural capital linked with territorial needs? von Zasada, I., Weltin, M., Reutter, M., Verburg, P.H., Piorr, A.

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Mutations of the SLIT2–ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract von Hwang, Daw-Yang, Kohl, Stefan, Fan, Xueping, Vivante, Asaf, Chan, Stefanie, Dworschak, Gabriel C., Schulz, Julian, van Eerde, Albertien M., Hilger, Alina C., Gee, Heon Yung, Pennimpede, Tracie, Herrmann, Bernhard G., van de Hoek, Glenn, Renkema, Kirsten Y., Schell, Christoph, Huber, Tobias B., Reutter, Heiko M., Soliman, Neveen A., Stajic, Natasa, Bogdanovic, Radovan, Kehinde, Elijah O., Lifton, Richard P., Tasic, Velibor, Lu, Weining, Hildebrandt, Friedhelm

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PKD1L1 Is Involved in Congenital Chylothorax von Whitchurch, Jonathan B, Schneider, Sophia, Hilger, Alina C, Köllges, Ricarda, Stegmann, Jil D, Waffenschmidt, Lea, Dyer, Laura, Thiele, Holger, Dhabhai, Bhanupriya, Dakal, Tikam Chand, Müller, Andreas, Norris, Dominic P, Reutter, Heiko M

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A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies von van de Putte, Romy, Dworschak, Gabriel C., Brosens, Erwin, Reutter, Heiko M., Marcelis, Carlo L. M., Acuna-Hidalgo, Rocio, Kurtas, Nehir E., Steehouwer, Marloes, Dunwoodie, Sally L., Schmiedeke, Eberhard, Maerzheuser, Stefanie, Schwarzer, Nicole, Brooks, Alice S., de Klein, Annelies, Sloots, Cornelius E. J., Tibboel, Dick, Brisighelli, Giulia, Morandi, Anna, Bedeschi, Maria F., Bates, Michael D., Levitt, Marc A., Pena, Alberto, de Blaauw, Ivo, Roeleveld, Nel, Brunner, Han G., van Rooij, Iris A. L. M., Hoischen, Alexander

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Treatment Strategies and Outcome of the Exstrophy-Epispadias Complex in Germany: Data From the German CURE-Net von Ebert, Anne-Karoline, Zwink, Nadine, Reutter, Heiko M., Jenetzky, Ekkehart, Stein, Raimund, Hoelscher, Alice C., Lacher, Martin, Fortmann, Caroline, Obermayr, Florian, Fisch, Margit, Mortazawi, Kiarasch, Schmiedeke, Eberhard, Promm, Martin, Hirsch, Karin, Schaefer, Frank-Mattias, Roesch, Wolfgang H.

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Loss of Function of GALNT2 Lowers High-Density Lipoproteins in Humans, Nonhuman Primates, and Rodents von Khetarpal, Sumeet A., Schjoldager, Katrine T., Christoffersen, Christina, Raghavan, Avanthi, Edmondson, Andrew C., Reutter, Heiko M., Ahmed, Bouhouche, Ouazzani, Reda, Peloso, Gina M., Vitali, Cecilia, Zhao, Wei, Somasundara, Amritha Varshini Hanasoge, Millar, John S., Park, YoSon, Fernando, Gayani, Livanov, Valentin, Choi, Seungbum, Noé, Eric, Patel, Pritesh, Ho, Siew Peng, Kirchgessner, Todd G., Wandall, Hans H., Hansen, Lars, Bennett, Eric P., Vakhrushev, Sergey Y., Saleheen, Danish, Kathiresan, Sekar, Brown, Christopher D., Abou Jamra, Rami, LeGuern, Eric, Clausen, Henrik, Rader, Daniel J.

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Mapping the NPHP-JBTS-MKS Protein Network Reveals Ciliopathy Disease Genes and Pathways von Sang, Liyun, Miller, Julie J., Corbit, Kevin C., Giles, Rachel H., Brauer, Matthew J., Otto, Edgar A., Baye, Lisa M., Wen, Xiaohui, Scales, Suzie J., Kwong, Mandy, Huntzicker, Erik G., Sfakianos, Mindan K., Sandoval, Wendy, Bazan, J. Fernando, Kulkarni, Priya, Garcia-Gonzalo, Francesc R., Seol, Allen D., O'Toole, John F., Held, Susanne, Reutter, Heiko M., Lane, William S., Rafiq, Muhammad Arshad, Noor, Abdul, Ansar, Muhammad, Devi, Akella Radha Rama, Sheffield, Val C., Slusarski, Diane C., Vincent, John B., Doherty, Daniel A., Hildebrandt, Friedhelm, Reiter, Jeremy F., Jackson, Peter K.

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Mild Recessive Mutations in Six Fraser Syndrome-Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract von KOHL, Stefan, HWANG, Daw-Yang, TASIC, Velibor, HILDEBRANDT, Friedhelm, DWORSCHAK, Gabriel C, HILGER, Alina C, SAISAWAT, Pawaree, VIVANTE, Asaf, STAJIC, Natasa, BOGDANOVIC, Radovan, REUTTER, Heiko M, KEHINDE, Elijah O

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Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association von Saisawat, Pawaree, Kohl, Stefan, Hilger, Alina C., Hwang, Daw-Yang, Yung Gee, Heon, Dworschak, Gabriel C., Tasic, Velibor, Pennimpede, Tracie, Natarajan, Sivakumar, Sperry, Ethan, Matassa, Danilo S., Stajić, Nataša, Bogdanovic, Radovan, de Blaauw, Ivo, Marcelis, Carlo L.M., Wijers, Charlotte H.W., Bartels, Enrika, Schmiedeke, Eberhard, Schmidt, Dominik, Märzheuser, Stefanie, Grasshoff-Derr, Sabine, Holland-Cunz, Stefan, Ludwig, Michael, Nöthen, Markus M., Draaken, Markus, Brosens, Erwin, Heij, Hugo, Tibboel, Dick, Herrmann, Bernhard G., Solomon, Benjamin D., de Klein, Annelies, van Rooij, Iris A.L.M., Esposito, Franca, Reutter, Heiko M., Hildebrandt, Friedhelm

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Successful ECMO therapy in a child with COVID‐19‐associated ARDS and acute lymphoblastic leukemia von Ebach, Fabian, Hainmann, Ina, Eis‐Hübinger, Anna M., Escherisch, Gabriele, Dilloo, Dagmar, Reutter, Heiko M., Müller, Andreas

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How to improve the conservation of species-rich grasslands with result-oriented payment schemes? von Kaiser, T., Reutter, M., Matzdorf, B.

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Gender‐associated differences in the psychosocial and developmental outcome in patients affected with the bladder exstrophy‐epispadias complex von LEE, CELINE, REUTTER, HEIKO M., GRÄßER, MELANIE F., FISCH, MARGIT, NOEKER, MEINOLF

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The Role of De Novo Variants in Formation of Human Anorectal Malformations von Dworschak, Gabriel C., van Rooij, Iris A. L. M., Reutter, Heiko M.

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Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tract von Kohl, Stefan, Chen, Jing, Vivante, Asaf, Hwang, Daw-Yang, Shril, Shirlee, Dworschak, Gabriel C, Van Der Ven, Amelie, Sanna-Cherchi, Simone, Bauer, Stuart B, Lee, Richard S, Soliman, Neveen A, Kehinde, Elijah O, Reutter, Heiko M, Tasic, Velibor, Hildebrandt, Friedhelm

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Scimitar syndrome in a case with VACTERL association von Fritz, Christian J., Reutter, Heiko M., Herberg, Ulrike

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More than fetal urine: enteral uptake of amniotic fluid as a major predictor for fetal growth during late gestation von Bagci, Soyhan, Brosens, Erwin, Tibboel, Dick, De Klein, Annelies, Ijsselstijn, Hanneke, Wijers, Charlotte H. W., Roeleveld, Nel, de Blaauw, Ivo, Broens, Paul M., van Rooij, Iris A. L. M., Hölscher, Alice, Boemers, Thomas M., Pauly, Marcus, Münsterer, Oliver J., Schmiedeke, Eberhard, Schäfer, Mattias, Ure, Benno E., Lacher, Martin, Choinitzki, Vera, Schumacher, Johannes, Zwink, Nadine, Jenetzky, Ekkehart, Katzer, David, Arand, Joerg, Bartmann, Peter, Reutter, Heiko M.

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"Nutrient Inputs to the Laurentian Great Lakes by Source and Watershed Estimated Using SPARROW Watershed Models" by Dale M. Robertson and David A. Saad von Peter Richards, R., Alameddine, Ibrahim, David Allan, J., Baker, David B., Bosch, Nathan S., Confesor, Remegio, DePinto, Joseph V., Dolan, David M., Reutter, Jeffrey M., Scavia, Donald

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