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  1. Korsch, Leonie Annina [Author] ; Boemers, Thomas Michael [Other]

    Symptomatik, Diagnostik und Therapie der kongenitalen tracheoösophagealen H-Fistel (Typ IV nach Vogt) in Abgrenzung zur sekundären tracheoösophagealen H-Fistel nach unvollständiger Korrektur einer Ösophagusatresie (Typ IIIa oder c nach Vogt) sowie einem Fistelrezidiv

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    Köln: Universitäts- und Stadtbibliothek Köln, 2022

  2. Korsch, Leonie Annina [Author] ; Boemers, Thomas Michael [Other]

    Symptomatik, Diagnostik und Therapie der kongenitalen tracheoösophagealen H-Fistel (Typ IV nach Vogt) in Abgrenzung zur sekundären tracheoösophagealen H-Fistel nach unvollständiger Korrektur einer Ösophagusatresie (Typ IIIa oder c nach Vogt) sowie einem Fistelrezidiv

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    Köln: Universitäts- und Stadtbibliothek Köln, 2022

  3. Mingardo, Enrico [Author]; Beaman, Glenda [Author]; Grote, Philip [Author]; Nordenskjöld, Agneta [Author]; Newman, William [Author]; Woolf, Adrian S. [Author]; Eckstein, Markus [Author]; Hilger, Alina C. [Author]; Dworschak, Gabriel C. [Author]; Rösch, Wolfgang [Author]; Ebert, Anne-Karolin [Author]; Stein, Raimund [Author]; Brusco, Alfredo [Author]; Di Grazia, Massimo [Author]; Tamer, Ali [Author]; Torres, Federico M. [Author]; Hernandez, Jose L. [Author]; Erben, Philipp [Author]; Maj, Carlo [Author]; Olmos, Jose M. [Author]; Riancho, Jose A. [Author]; Valero, Carmen [Author]; Hostettler, Isabel C. [Author]; Houlden, Henry [Author]; [...]

    A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy

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    09 November 2022

    Published in: Communications biology ; 5(2022) vom: Nov., Artikel-ID 1203, Seite 1-11

  4. Reutter, Heiko; Betz, Regina C.; Ludwig, Michael; Boemers, Thomas M.

    MTHFR 677 TT genotype in a mother and her child with Down syndrome, atrioventricular canal and exstrophy of the bladder: implications of a mutual genetic risk factor?

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    Springer Science and Business Media LLC, 2006

    Published in: European Journal of Pediatrics, 165 (2006) 8, Seite 566-568

  5. Mallmann, Michael R.; Reutter, Heiko; Müller, Andreas; Boemers, Thomas M.; Geipel, Annegret; Berg, Christoph; Gembruch, Ulrich

    Prenatal Diagnosis of Covered Cloacal Exstrophy

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    S. Karger AG, 2014

    Published in: Fetal Diagnosis and Therapy, 36 (2014) 4, Seite 333-336

  6. Reutter, Heiko; Thauvin-Robinet, Christel; Boemers, Thomas M.; Rösch, Wolfgang H.; Ludwig, Michael

    Bladder exstrophy–epispadias complex: Investigation of suppressor of variegation, enhancer of zeste and Trithorax (SET) as a candidate gene in a large cohort of patients

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    Informa UK Limited, 2006

    Published in: Scandinavian Journal of Urology and Nephrology, 40 (2006) 3, Seite 221-224

  7. Reutter, Heiko; Bökenkamp, Arend; Ebert, Anne-Karolin; Rösch, Wolfgang; Boemers, Thomas M.; Nöthen, Markus M.; Ludwig, Michael

    Possible association of Down syndrome and exstrophy–epispadias complex: report of two new cases and review of the literature

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    Springer Science and Business Media LLC, 2009

    Published in: European Journal of Pediatrics, 168 (2009) 7, Seite 881-883

  8. Mallmann, Michael R.; Mack-Detlefsen, Birte; Reutter, Heiko; Pohle, Rebecca; Gottschalk, Ingo; Geipel, Annegret; Berg, Christoph; Boemers, Thomas M.; Gembruch, Ulrich

    Isolated bladder exstrophy in prenatal diagnosis

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    Springer Science and Business Media LLC, 2019

    Published in: Archives of Gynecology and Obstetrics, 300 (2019) 2, Seite 355-363

  9. Reutter, Heiko; Becker, Tim; Ludwig, Michael; Schäfer, Niklas; Detlefsen, Birte; Beaudoin, Sylvie; Fisch, Margit; Ebert, Anne‐Karoline; Rösch, Wolfgang; Nöthen, Markus M.; Boemers, Thomas M.; Betz, Regina C.

    Family‐based association study of the MTHFR polymorphism C677T in the bladder‐exstrophy‐epispadias‐complex

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    Wiley, 2006

    Published in: American Journal of Medical Genetics Part A, 140A (2006) 22, Seite 2506-2509

  10. Laschat, Michael; Choinitzki, Vera; Zwink, Nadine; Jenetzky, Ekkehart; Münsterer, Oliver; Kurz, Ralf; Pauly, Marcus; Brokmeier, Ulrike; Leutner, Andreas; Ure, Benno; Lacher, Martin; Schumacher, Johannes; Reutter, Heiko; Boemers, Thomas; Hölscher, Alice

    Quality of Life after Surgical Treatment for Esophageal Atresia: Long-Term Outcome of 154 Patients

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    Georg Thieme Verlag KG, 2017

    Published in: European Journal of Pediatric Surgery, 27 (2017) 5, Seite 443-448

  11. DRAAKEN, MARKUS; PRINS, WIEBKE; ZEIDLER, CLAUDIA; HILGER, ALINA; MUGHAL, SADAF S.; LATUS, JEANETTE; BOEMERS, THOMAS M.; SCHMIDT, DOMINIK; SCHMIEDEKE, EBERHARD; SPYCHALSKI, NICOLE; BARTELS, ENRIKA; NÖTHEN, MARKUS M.; REUTTER, HEIKO; LUDWIG, MICHAEL

    Involvement of the WNT and FGF signaling pathways in non-isolated anorectal malformations: Sequencing analysis of WNT3A, WNT5A, WNT11, DACT1, FGF10, FGFR2 and the T gene

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    Spandidos Publications, 2012

    Published in: International Journal of Molecular Medicine, 30 (2012) 6, Seite 1459-1464

  12. Draaken, Markus; Knapp, Michael; Pennimpede, Tracie; Schmidt, Johanna M.; Ebert, Anne-Karolin; Rösch, Wolfgang; Stein, Raimund; Utsch, Boris; Hirsch, Karin; Boemers, Thomas M.; Mangold, Elisabeth; Heilmann, Stefanie; Ludwig, Kerstin U.; Jenetzky, Ekkehart; Zwink, Nadine; Moebus, Susanne; Herrmann, Bernhard G.; Mattheisen, Manuel; Nöthen, Markus M.; Ludwig, Michael; Reutter, Heiko

    Genome-wide Association Study and Meta-Analysis Identify ISL1 as Genome-wide Significant Susceptibility Gene for Bladder Exstrophy

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    Public Library of Science (PLoS), 2015

    Published in: PLOS Genetics, 11 (2015) 3, Seite e1005024

  13. Zhang, Rong; Marsch, Florian; Kause, Franziska; Degenhardt, Franziska; Schmiedeke, Eeberhard; Märzheuser, Stefanie; Hoppe, Bernd; Bachour, Haitham; Boemers, Thomas M.; Schäfer, Matthias; Spychalski, Nicole; Neser, Jörg; Leonhardt, Johannes; Kosch, Ferdinand; Ure, Benno; Gómez, Barbara; Lacher, Martin; Deffaa, Oliver J.; Palta, Markus; Wittekindt, Boris; Kleine, Katharina; Schmedding, Andrea; Grasshoff‐Derr, Sabine; Ven, Amelie van der; [...]

    Array‐based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL‐like patients identifies disease‐causing copy number variations

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    Wiley, 2017

    Published in: Birth Defects Research, 109 (2017) 13, Seite 1063-1069

  14. von Lowtzow, Catharina; Hofmann, Andrea; Zhang, Rong; Marsch, Florian; Ebert, Anne-Karoline; Rösch, Wolfgang; Stein, Raimund; Boemers, Thomas M.; Hirsch, Karin; Marcelis, Carlo; Feitz, Wouter F. J.; Brusco, Alfredo; Migone, Nicola; Di Grazia, Massimo; Moebus, Susanne; Nöthen, Markus M.; Reutter, Heiko; Ludwig, Michael; Draaken, Markus

    CNV analysis in 169 patients with bladder exstrophy-epispadias complex

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    Springer Science and Business Media LLC, 2016

    Published in: BMC Medical Genetics, 17 (2016) 1

  15. 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.; [...]

    Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region

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    Wiley, 2014

    Published in: Birth Defects Research Part A: Clinical and Molecular Teratology, 100 (2014) 6, Seite 512-517

  16. Zeidler, Claudia; Woelfle, Joachim; Draaken, Markus; Mughal, Sadaf S.; Große, Greta; Hilger, Alina C.; Dworschak, Gabriel C.; Boemers, Thomas M.; Jenetzky, Ekkehart; Zwink, Nadine; Lacher, Martin; Schmidt, Dominik; Schmiedeke, Eberhard; Grasshoff‐Derr, Sabine; Märzheuser, Stefanie; Holland‐Cunz, Stefan; Schäfer, Mattias; Bartels, Enrika; Keppler, Kathleen; Palta, Markus; Leonhardt, Johannes; Kujath, Christina; Rißmann, Anke; Nöthen, Markus M.; [...]

    Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies

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    Wiley, 2014

    Published in: Birth Defects Research Part A: Clinical and Molecular Teratology, 100 (2014) 10, Seite 750-759