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Heiko Reutter

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TOP 3
Gabriel C Dworschak; Alina Hilger; Mark Born; Markus Draaken; Heiko Reutter; Michael Ludwig
An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome.
Nadine Zwink; Thomas M Boemers; Hermann Brenner; Karin Hirsch; Ekkehart Jenetzky; Florian Obermayr; Sabrina Reckin; Peter Reifferscheid; Heiko Reutter; Wolfgang H Rösch; Dominik Schmidt; Eberhard Schmiedeke; Raimund Stein; Anne-Karoline Ebert
Assisted reproductive techniques and risk of exstrophy-epispadias complex: a german case-control study.
Markus Draaken; Anne-Karoline Ebert; Bernhard G Herrmann; Per Hoffmann; Enrika Bartels; Thomas M Boemers; Susanne Moebus; Sadaf S Mughal; Markus M Nöthen; Tracie Pennimpede; Heiko Reutter; Wolfgang Rösch; Dominik Schmidt; Eberhard Schmiedeke; Raimund Stein; Lars Wittler; Stefanie Wolter; Michael Ludwig
Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12.

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All Publications

2013: Gabriel C Dworschak; Alina Hilger; Mark Born; Markus Draaken; Heiko Reutter; Michael Ludwig
An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome.
International journal of molecular medicine 2013;32(1):174-8.
2013: Nadine Zwink; Thomas M Boemers; Hermann Brenner; Karin Hirsch; Ekkehart Jenetzky; Florian Obermayr; Sabrina Reckin; Peter Reifferscheid; Heiko Reutter; Wolfgang H Rösch; Dominik Schmidt; Eberhard Schmiedeke; Raimund Stein; Anne-Karoline Ebert
Assisted reproductive techniques and risk of exstrophy-epispadias complex: a german case-control study.
The Journal of urology 2013;189(4):1524-9.
2013: Markus Draaken; Anne-Karoline Ebert; Bernhard G Herrmann; Per Hoffmann; Enrika Bartels; Thomas M Boemers; Susanne Moebus; Sadaf S Mughal; Markus M Nöthen; Tracie Pennimpede; Heiko Reutter; Wolfgang Rösch; Dominik Schmidt; Eberhard Schmiedeke; Raimund Stein; Lars Wittler; Stefanie Wolter; Michael Ludwig
Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12.
Birth defects research. Part A, Clinical and molecular teratology 2013;97(3):133-9.
2013: Heiko Reutter; Michael Ludwig
VATER/VACTERL Association: Evidence for the Role of Genetic Factors.
Molecular syndromology 2013;4(1-2):16-9.
2013: S M Pasternack; M Refke; Heiko Reutter; V Tasic; Regina C Betz; D Böckenhauer; M Born; C Conrad; M Draaken; Michael Ludwig
A premature termination mutation in a patient with Lowe syndrome without congenital cataracts: dropping the "O" in OCRL.
Klinische Pädiatrie 2013;225(1):29-33.
2012: Benjamin D Solomon; Dick Tibboel; Kelly A Bear; Annelies de Klein; Virginia E Kimonis; Heiko Reutter; Daryl A Scott; Charles Shaw-Smith; Philip F Giampietro
Clinical geneticists' views of VACTERL/VATER association.
American journal of medical genetics. Part A 2012;158A(12):3087-100.
2012: Markus Draaken; Alina Hilger; Jeanette Latus; Enrika Bartels; Thomas M Boemers; Sadaf S Mughal; Markus M Nöthen; Wiebke Prins; Heiko Reutter; Dominik Schmidt; Eberhard Schmiedeke; Nicole Spychalski; Claudia Zeidler; Michael Ludwig
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.
International journal of molecular medicine 2012;30(6):1459-64.
2012: A Ebert; C Neissner; Heiko Reutter; WH Rösch
[Transition of adolescents with the exstrophy-epispadias complex to adult medicine: influence of long-term outcome results on management].
Klinische Pädiatrie 2012;224(7):455-60.
2012: Entessar Nasser; Markus M Nöthen; Stefanie Nowak; Bernd Pötzsch; Rudolf H Reich; Heiko Reutter; Daniela C Tradowsky; Philipp Wahle; Sandra Barth; Jessica Becker; Anne C Boehmer; Bert Braumann; Heide Fier; Nadine Fricker; Alexander Hemprich; Ruth Herberz; Per Hoffmann; Michael Knapp; Franz-Josef Kramer; Thomas Kreusch; Christoph Lange; Carola Lauster; Elisabeth Mangold; Kerstin U Ludwig
Resequencing of VAX1 in patients with nonsyndromic cleft lip with or without cleft palate.
Birth defects research. Part A, Clinical and molecular teratology 2012;94(11):925-33.
2012: Ekkehart Jenetzky; F Kosch; J Leonhardt; E Bartels; G Götz; S Grasshoff-Derr; A Hofbauer; Stefan Holland-Cunz; F Obermayr; M Palta; J Rädecke; S Reckin; Heiko Reutter; A Rissmann; M Schäfer; D Schmidt; E Schmiedeke; N Schwarzer; S Weih; N Zwink; S Märzheuser
Practice of dilatation after surgical correction in anorectal malformations.
Pediatric surgery international 2012;28(11):1095-9.
2012: Elisabeth Mangold; Sergio G Muñoz-Jiménez; Markus M Nöthen; Stefanie Nowak; Rocío Ortiz-López; Mario Paredes-Zenteno; Heiko Reutter; Abelardo Arizpe-Cantú; Stefan Herms; Michael Knapp; Franz-Josef Kramer; Rafael B R León-Cachón; Kerstin U Ludwig; Thomas F Wienker; Óscar Chacón-Camacho; Augusto Rojas-Martínez
Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate.
European journal of oral sciences 2012;120(5):373-7.
2012: A Ebert; Sabine Kliesch; Claudia Neissner; Heiko Reutter; WH Rösch
Testicular tumors in patients with exstrophy-epispadias complex.
The Journal of urology 2012;188(4):1300-5.
2012: Enrika Bartels; Peter Bartmann; Friederike Baudisch; Christoph Berg; Markus Draaken; Gabriel C Dworschak; Annegret Geipel; Ulrich Gembruch; Alina C Hilger; Per Hoffmann; Michael Ludwig; Carlo M Marcelis; Manuel Mattheisen; Nicole W Mora; Andreas Müller; Markus M Nöthen; Daniel E Pineda-Alvarez; Jochen Ritgen; Eberhard Schmiedeke; Anna C Schulz; Benjamin D Solomon; Rüdiger Stressig; Iris A L M van Rooij; Charlotte H W Wijers; Soyhan Bagci; Heiko Reutter
VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis.
Clinical dysmorphology 2012;21(4):191-5.
2012: Anna Carina Schulz; Rüdiger Stressig; Jochen Ritgen; Soyhan Bagci; Peter Bartmann; Christoph Berg; Annegret Geipel; Ulrich Gembruch; Andreas Müller; Heiko Reutter
A classic twin study of isolated gastroschisis.
Fetal and pediatric pathology 2012;31(5):324-30.
2012: Lars Wittler; Markus Draaken; Anne-Karoline Ebert; Alina Hilger; Markus M Nöthen; Tracie Pennimpede; Judith Proske; Heiko Reutter; Wolfgang Rösch; Raimund Stein; Michael Ludwig
Murine expression and mutation analyses of the prostate androgen-regulated mucin-like protein 1 (Parm1) gene, a candidate for human epispadias.
Gene 2012;506(2):392-5.
2012: Eberhard Schmiedeke; Nicole Schwarzer; Nadine Zwink; Enrika Bartels; Sabine Grasshoff-Derr; Stefan Holland-Cunz; Stuart Hosie; Karsten Jablonka; Christian Lorenz; Stefanie Maerzheuser; Heiko Reutter; Dominik Schmidt; Ekkehart Jenetzky
Unexpected results of a nationwide, treatment-independent assessment of fecal incontinence in patients with anorectal anomalies.
Pediatric surgery international 2012;28(8):825-30.
2012: Enrika Bartels; Sabine Grasshoff-Derr; Stefan Holland-Cunz; Stuart Hosie; Ekkehart Jenetzky; Christina Kujath; Johannes Leonhardt; Michael Ludwig; Stefanie Märzheuser; Markus M Nöthen; Markus Palta; Heiko Reutter; Anke Rissmann; Mattias Schäfer; Dominik Schmidt; Eberhard Schmiedeke; Benjamin D Solomon; Sandra Weih; Nadine Zwink
Inheritance of the VATER/VACTERL association.
Pediatric surgery international 2012;28(7):681-5.
2012: Alina Hilger; Per Hoffmann; Enrika Bartels; Markus Draaken; Gabriel Dworschak; Sadaf S Mughal; Markus M Nöthen; Heiko Reutter; Charlotte Schramm; Michael Ludwig
Familial occurrence of the VATER/VACTERL association.
Pediatric surgery international 2012;28(7):725-9.
2012: Bregje W M van Bon; Joris Veltman; Nienke Wieskamp; Han G Brunner; Bert B A de Vries; Petra de Vries; Hartmut Engels; Metin Eser; Christian Gilissen; Dorothy K Grange; Raoul C M Hennekam; Bertrand Isidor; Hulya Kayserili; Martine Le Merrer; Eva Morava; John R Ostergaard; Heiko Reutter; Stephen P Robertson; Marloes Steehouwer; Konstantinos Tsiakas; Alexander Hoischen
Cantú syndrome is caused by mutations in ABCC9.
American journal of human genetics 2012;90(6):1094-101.
2012: Hartmut Engels; Raoul C M Hennekam; Alexander Hoischen; Martina Kreiss-Nachtsheim; Christian Kubisch; Jennifer A Lee; Barbara Leube; Kerstin U Ludwig; Sabine Rudnik-Schöneborn; Herdit M Schüler; Gesa Schwanitz; Ruthild G Weber; Eva Wohlleber; Alexander M Zink; Antje Brockschmidt; Matthias Drechsler; Heiko Reutter
A phenotype map for 14q32.3 terminal deletions.
American journal of medical genetics. Part A 2012;158A(4):695-706.
2012: Anna Carina Schulz; Johannes Schumacher; Rüdiger Stressig; Jochen Ritgen; Eberhard Schmiedeke; Haitham Bachour; Soyhan Bagci; Enrika Bartels; Peter Bartmann; Christoph Berg; Markus Draaken; Annegret Geipel; Ulrich Gembruch; Andreas Heydweiller; Michael Ludwig; Manuel Mattheisen; Andreas Müller; Markus M Nöthen; Heiko Reutter
Nine new twin pairs with esophageal atresia: a review of the literature and performance of a twin study of the disorder.
Birth defects research. Part A, Clinical and molecular teratology 2012;94(3):182-6.
2012: Nadine Zwink; Helen Ameis; Enrika Bartels; Hermann Brenner; Sabine Grasshoff-Derr; Stefan Holland-Cunz; Stuart Hosie; Ekkehart Jenetzky; Christina Kujath; Stefanie Märzheuser; Florian Obermayr; Peter Reifferscheid; Heiko Reutter; Anke Rissmann; Dominik Schmidt; Eberhard Schmiedeke; Nicole Schwarzer; Sandra Weih
Assisted reproductive techniques and the risk of anorectal malformations: a German case-control study.
Orphanet journal of rare diseases 2012;7():65.
2012: A L Berner; E Engels; A Müller; S Bağci; P Bartmann; R G Weber; E Wohlleber; Heiko Reutter
Familial translocation t(6;20)(p21;p13) resulting in partial trisomy 6p and partial monosomy 20p: report of a new case and review of the literature.
Cytogenetic and genome research 2012;136(4):308-13.
2012: Heiko Reutter; Sabrina Spengler; Soyhan Bagci; Peter Bartmann; Christoph Berg; Thomas Eggermann; Annegret Geipel; Ulrich Gembruch; Andreas Müller; Sabine Rudnik-Schöneborn
Primary pulmonary hypertension, congenital heart defect, central nervous system malformations, hypo- and aplastic toes: another case of Yunis-Varón syndrome or report of a new entity.
European journal of medical genetics 2012;55(1):27-31.
2011: Stefanie Weber; Duncan T Wilcox; Janine Altmüller; Rolf Beetz; Markus Draaken; Peter Frommolt; Neil A Hanley; Peter F Hoyer; Rachel Jennings; Martin Konrad; Michael Ludwig; Sevgi Mir; William G Newman; Peter Nürnberg; Parisa Ranjzad; Heiko Reutter; Franz Schaefer; Karl Peter Schlingmann; Betül Sozeri; Helen M Stuart; Uwe Thiel; Holger Thiele; Mohammad Reza Toliat; Adrian S Woolf
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome.
American journal of human genetics 2011;89(5):668-74.
2011: Heiko Reutter; Sebastian Rogenhofer; Wolfgang H Rösch; Annette Schröder; Raimund Stein; Boris Utsch; Hannes Vogt; Nadine Zwink; Enrika Bartels; Goedele M A Beckers; Thomas M Boemers; Arend Bökenkamp; Simeon Boyd; Birte Detlefsen; Markus Draaken; Anne-Karoline Ebert; Lisa Gambhir; John P Gearhart; Rita Gobet; Enrique Jaureguizar; Abdol-Mohammad Kajbafzadeh; Yegappan Lakshmanan; Michael Ludwig; Martin Müller; Markus M Nöthen; Ekkehart Jenetzky
Phenotype severity in the bladder exstrophy-epispadias complex: analysis of genetic and nongenetic contributing factors in 441 families from North America and Europe.
The Journal of pediatrics 2011;159(5):825-831.e1.
2011: Stefanie Maerzheuser; Heiko Reutter; Enrika Bartels; Gabriel Goetz; Sabine Grasshoff-Derr; Stefan Holland-Cunz; Stuart Hosie; Ekkehart Jenetzky; Eberhard Schmiedeke; Nicole Schwarzer; Nicole Spychalski; Nadine Zwink; Dominik Schmidt
German network for congenital uro-rectal malformations: first evaluation and interpretation of postoperative urological complications in anorectal malformations.
Pediatric surgery international 2011;27(10):1085-9.
2011: Meinolf Noeker; Heiko Reutter; Dominik Schmidt; Eberhard Schmiedeke; Muriel Schmitz; Nadine Zwink; Ekkehart Jenetzky
Medical predictors of psychological anxieties in VATER patients.
Pediatric surgery international 2011;27(10):1079-83.
2011: A Ebert; Andreas Falkert; Andrea Hofstädter; Heiko Reutter; WH Rösch
Pregnancy management in women within the bladder-exstrophy-epispadias complex (BEEC) after continent urinary diversion.
Archives of gynecology and obstetrics 2011;284(4):1043-6.
2011: Lihong Qi; Kun Chen; David J Hur; Garima Yagnik; Yegappan Lakshmanan; Lori E Kotch; Gerald H Ashrafi; Francisco Martinez-Murillo; Jeanne Kowalski; Cyrill Naydenov; Lars Wittler; John P Gearhart; Markus Draaken; Heiko Reutter; Michael Ludwig; Simeon Boyd
Genome-wide expression profiling of urinary bladder implicates desmosomal and cytoskeletal dysregulation in the bladder exstrophy-epispadias complex.
International journal of molecular medicine 2011;27(6):755-65.
2011: Charlotte Schramm; Gabriel Tewes; Stefanie Märzheuser; Markus M Nöthen; Lutz Priebe; Heiko Reutter; Eberhard Schmiedeke; Stefan Aretz; Enrika Bartels; Markus Draaken; Sabine Grasshoff-Derr; Per Hoffmann; Stefan Holland-Cunz; Stuart Hosie; Martina Kreiss-Nachtsheim; Michael Ludwig
Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literature.
European journal of pediatrics 2011;170(6):741-6.
2011: Charlotte Schramm; Markus Draaken; Enrika Bartels; Thomas M Boemers; Eberhard Schmiedeke; Sabine Grasshoff-Derr; Stefanie Märzheuser; Stuart Hosie; Stefan Holland-Cunz; Friederike Baudisch; Lutz Priebe; Per Hoffmann; Alexander M Zink; Hartmut Engels; Felix F Brockschmidt; Stefan Aretz; Markus M Nöthen; Michael Ludwig; Heiko Reutter
De novo duplication of 18p11.21-18q12.1 in a female with anorectal malformation.
American journal of medical genetics. Part A 2011;155A(2):445-9.
2011: E Bartels; F Baudisch; M Draaken; B Kazmierczak; Michael Ludwig; Markus M Nöthen; E Schmiedeke; C Schramm; S Spranger; Heiko Reutter
De novo partial trisomy 18p and partial monosomy 18q in a patient with anorectal malformation.
Cytogenetic and genome research 2011;134(3):243-8.
2011: Nilma Almeida de Assis; Stefanie Nowak; Kerstin U Ludwig; Heiko Reutter; Jennifer Vollmer; Stefanie Heilmann; Nadine Kluck; Carola Lauster; Bert Braumann; Rudolf H Reich; Alexander Hemprich; Michael Knapp; Thomas F Wienker; Franz-Josef Kramer; Per Hoffmann; Markus M Nöthen; Elisabeth Mangold
SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in Central European patients.
International journal of pediatric otorhinolaryngology 2011;75(1):49-52.
2011: Charlotte Schramm; Markus Draaken; Enrika Bartels; Thomas M Boemers; Stefan Aretz; Felix F Brockschmidt; Markus M Nöthen; Michael Ludwig; Heiko Reutter
De novo microduplication at 22q11.21 in a patient with VACTERL association.
European journal of medical genetics 2011;54(1):9-13.
2010: Bonnie J Ching; Lars Wittler; Judith Proske; Garima Yagnik; Lihong Qi; Markus Draaken; Heiko Reutter; John P Gearhart; Michael Ludwig; Simeon Boyd
p63 (TP73L) a key player in embryonic urogenital development with significant dysregulation in human bladder exstrophy tissue.
International journal of molecular medicine 2010;26(6):861-7.
2010: Heiko Reutter; Franz Rüschendorf; Manuel Mattheisen; Markus Draaken; Enrika Bartels; Norbert Hübner; Per Hoffmann; Seyedmedhi Payabvash; Kathrin Saar; Markus M Nöthen; Abdol-Mohammad Kajbafzadeh; Michael Ludwig
Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family.
Birth defects research. Part A, Clinical and molecular teratology 2010;88(9):757-61.
2010: Markus Draaken; Judith Proske; Charlotte Schramm; Lars Wittler; Enrika Bartels; Markus M Nöthen; Heiko Reutter; Michael Ludwig
Embryonic expression of the cysteine rich protein 61 (CYR61) gene: A candidate for the development of human epispadias.
Birth defects research. Part A, Clinical and molecular teratology 2010;88(7):546-50.
2010: Augusto Rojas-Martinez; Heiko Reutter; Oscar Chacon-Camacho; Rafael B R Leon-Cachon; Sergio G Munoz-Jimenez; Stefanie Nowak; Jessica Becker; Ruth Herberz; Kerstin U Ludwig; Mario Paredes-Zenteno; Abelardo Arizpe-Cantú; Susanne Raeder; Stefan Herms; Rocio Ortiz-Lopez; Michael Knapp; Per Hoffmann; Markus M Nöthen; Elisabeth Mangold
Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population: Evidence for IRF6 and variants at 8q24 and 10q25.
Birth defects research. Part A, Clinical and molecular teratology 2010;88(7):535-7.
2010: Markus Draaken; Heiko Reutter; Charlotte Schramm; Enrika Bartels; Thomas M Boemers; Anne-Karoline Ebert; Wolfgang Rösch; Annette Schröder; Raimund Stein; Susanne Moebus; Dietlinde Stienen; Per Hoffmann; Markus M Nöthen; Michael Ludwig
Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy.
European journal of medical genetics 2010;53(2):55-60.
2010: Soyhan Bağci; Andreas Müller; Axel Franz; Andreas Heydweiller; Christoph Berg; Markus M Nöthen; Peter Bartmann; Heiko Reutter
Intestinal atresia, encephalocele, and cardiac malformations in infants with 47,XXX: Expansion of the phenotypic spectrum and a review of the literature.
Fetal diagnosis and therapy 2010;27(2):113-7.
2009: Stefanie Birnbaum; Kerstin U Ludwig; Heiko Reutter; Stefan Herms; Nilma A de Assis; Amalia Diaz-Lacava; Sandra Barth; Carola Lauster; Gül Schmidt; Martin Scheer; Mitra Saffar; Markus Martini; Rudolf H Reich; Franziska Schiefke; Alexander Hemprich; Simone Pötzsch; Bernd Pötzsch; Thomas F Wienker; Per Hoffmann; Michael Knapp; Franz-Josef Kramer; Markus M Nöthen; Elisabeth Mangold
IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate.
European journal of oral sciences 2009;117(6):766-9.
2009: Elisabeth Mangold; Heiko Reutter; Stefanie Birnbaum; Maja Walier; Manuel Mattheisen; Henning Henschke; Carola Lauster; Gül Schmidt; Franziska Schiefke; Rudolf H Reich; Martin Scheer; Alexander Hemprich; Markus Martini; Bert Braumann; Michael Krimmel; Charlotte Opitz; Jan-Hendrik Lenz; Franz-Josef Kramer; Thomas F Wienker; Markus M Nöthen; Amalia Diaz-Lacava
Genome-wide linkage scan of nonsyndromic orofacial clefting in 91 families of central European origin.
American journal of medical genetics. Part A 2009;149A(12):2680-94.
2009: Heiko Reutter; Stefanie Birnbaum; Meinhard Mende; Nilma Almeida de Assis; Per Hoffmann; Amalia Diaz Lacava; Stefan Herms; Bert Braumann; Martin Scheer; Carola Lauster; Gül Schmidt; Franziska Schiefke; Anton Dunsche; Markus Martini; Michael Knapp; Franz-Josef Kramer; Markus M Nöthen; Elisabeth Mangold
Transforming growth factor-beta receptor type 1 (TGFBR1) is not associated with non-syndromic cleft lip with or without cleft palate in patients of Central European descent.
International journal of pediatric otorhinolaryngology 2009;73(10):1334-8.
2009: Heiko Reutter; Arend Bökenkamp; Anne-Karolin Ebert; Wolfgang Rösch; Thomas M Boemers; Markus M Nöthen; Michael Ludwig
Possible association of Down syndrome and exstrophy-epispadias complex: report of two new cases and review of the literature.
European journal of pediatrics 2009;168(7):881-3.
2009: Michael Ludwig; Bonnie Ching; Heiko Reutter; Simeon Boyd
Bladder exstrophy-epispadias complex.
Birth defects research. Part A, Clinical and molecular teratology 2009;85(6):509-22.
2009: Stefanie Birnbaum; Heiko Reutter; Meinhard Mende; Nilma A de Assis; Amalia Diaz-Lacava; Stefan Herms; Martin Scheer; Carola Lauster; Bert Braumann; Gül Schmidt; Markus Martini; Alexander Hemprich; Simone Pötzsch; Michael Knapp; Markus M Nöthen; Franz-Josef Kramer; Elisabeth Mangold
Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate.
European journal of oral sciences 2009;117(2):200-3.
2009: Michael Ludwig; Franz Rüschendorf; Kathrin Saar; Norbert Hübner; Lothar Siekmann; Simeon Boyd; Heiko Reutter
Genome-wide linkage scan for bladder exstrophy-epispadias complex.
Birth defects research. Part A, Clinical and molecular teratology 2009;85(2):174-8.
2008: Victoria Krüger; Mercedeh Khoshvaghti; Heiko Reutter; Hannes Vogt; Thomas M Boemers; Michael Ludwig
Investigation of FGF10 as a candidate gene in patients with anorectal malformations and exstrophy of the cloaca.
Pediatric surgery international 2008;24(8):893-7.
2008: Lisa Gambhir; Heiko Reutter; Michael Ludwig
Successful assisted reproduction in adult males with bladder extrophy-epispadias complex.
European journal of obstetrics, gynecology, and reproductive biology 2008;139(2):259-60.
2008: Lisa Gambhir; Tobias Höller; M Müller; G Schott; Hannes Vogt; B Detlefsen; A-K Ebert; Margit Fisch; S Beaudoin; R Stein; Simeon Boyd; John P Gearhart; Wolfgang Rösch; Boris Utsch; Thomas M Boemers; Heiko Reutter; Michael Ludwig
Epidemiological survey of 214 families with bladder exstrophy-epispadias complex.
The Journal of urology 2008;179(4):1539-43.
2008: Stefanie Birnbaum; Heiko Reutter; Carola Lauster; Martin Scheer; Gül Schmidt; Mitra Saffar; Markus Martini; Alexander Hemprich; Henning Henschke; Franz-Josef Kramer; Elisabeth Mangold
Mutation screening in the IRF6-gene in patients with apparently nonsyndromic orofacial clefts and a positive family history suggestive of autosomal-dominant inheritance.
American journal of medical genetics. Part A 2008;146A(6):787-90.
2008: Heiko Reutter; Stefanie Birnbaum; Meinhard Mende; Carola Lauster; Gül Schmidt; Henning Henschke; Mitra Saffar; Markus Martini; Roland Lauster; Franziska Schiefke; Rudolf H Reich; Bert Braumann; Martin Scheer; Michael Knapp; Markus M Nöthen; Franz-Josef Kramer; Elisabeth Mangold
TGFB3 displays parent-of-origin effects among central Europeans with nonsyndromic cleft lip and palate.
Journal of human genetics 2008;53(7):656-61.
2007: Boris Utsch; Colleen D McCabe; Kenneth Galbraith; Ricardo Gonzalez; Mark Born; Jörg Dötsch; Michael Ludwig; Heiko Reutter; Jeffrey W Innis
Molecular characterization of HOXA13 polyalanine expansion proteins in hand-foot-genital syndrome.
American journal of medical genetics. Part A 2007;143A(24):3161-8.
2007: Heiko Reutter; Lihong Qi; John P Gearhart; Thomas M Boemers; Anne-Karoline Ebert; Wolfgang Rösch; Michael Ludwig; Simeon Boyd
Concordance analyses of twins with bladder exstrophy-epispadias complex suggest genetic etiology.
American journal of medical genetics. Part A 2007;143A(22):2751-6.
2007: Heiko Reutter; Alexander Hoischen; Michael Ludwig; Raimund Stein; Bernhard Radlwimmer; Hartmut Engels; Katja P Wolffenbuttel; Ruthild G Weber
Genome-wide analysis for micro-aberrations in familial exstrophy of the bladder using array-based comparative genomic hybridization.
BJU international 2007;100(3):646-50.
2007: Stefanie Birnbaum; Heiko Reutter; Meinhard Mende; Amalia Díaz-Lacava; Henning Henschke; Stefaan Bergé; Bert Braumann; Carola Lauster; Alexander Hemprich; Matthias Wenghoefer; Mitra Saffar; Rudolf H Reich; Martin Scheer; Michael Knapp; Franz-Josef Kramer; Elisabeth Mangold
A family-based association study in Central Europeans: no evidence for the cystathionine beta-synthase c.844ins68 gene variant as a risk factor for non-syndromic cleft lip and palate.
American journal of medical genetics. Part A 2007;143(2):205-7.
2006: Heiko Reutter; Tim Becker; Michael Ludwig; Nico Schäfer; Birte Detlefsen; Sylvie Beaudoin; Margit Fisch; Anne-Karoline Ebert; Wolfgang Rösch; Markus M Nöthen; Thomas M Boemers; Regina C Betz
Family-based association study of the MTHFR polymorphism C677T in the bladder-exstrophy-epispadias-complex.
American journal of medical genetics. Part A 2006;140(22):2506-9.
2006: Boris Utsch; Analisa Difeo; Annegret Kujat; Stephanie M Karle; Volker Schuster; Harald Lenk; Ulla Jacobs; Martin Müller; Jörg Dötsch; Wolfgang Rascher; Heiko Reutter; John A Martignetti; Michael Ludwig; Ralf-Bodo Tröbs
Bladder exstrophy and Epstein type congenital macrothrombocytopenia: evidence for a common cause?
American journal of medical genetics. Part A 2006;140(20):2251-3.
2006: Heiko Reutter; Regina C Betz; Michael Ludwig; Thomas M Boemers
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?
European journal of pediatrics 2006;165(8):566-8.
2006: Mark Born; Heiko Reutter
[Duplication of the alimentary tract with ectopic gastric mucosa as cause of lower abdominal pain].
Zeitschrift für Gastroenterologie 2006;44(5):391-4.
2006: Celine Lee; Heiko Reutter; Melanie F Grässer; Margit Fisch; Meinolf Noeker
Gender-associated differences in the psychosocial and developmental outcome in patients affected with the bladder exstrophy-epispadias complex.
BJU international 2006;97(2):349-53.
2006: Heiko Reutter; Christel Thauvin-Robinet; Thomas M Boemers; Wolfgang Rösch; Michael Ludwig
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.
Scandinavian journal of urology and nephrology 2006;40(3):221-4.
2005: Michael Ludwig; Boris Utsch; Heiko Reutter
[Genetic and molecular biological aspects of the bladder exstrophy-epispadias complex (BEEC)].
Der Urologe. Ausg. A 2005;44(9):1037-8, 1040-4.
2005: Heiko Reutter; C Lee; M F Grässer; Meinolf Noeker
[Subjective developmental outcome in bladder exstrophy and epispadias. A pilot study].
Der Urologe. Ausg. A 2005;44(1):57-63.
2003: Heiko Reutter; Ellen Shapiro; Jeffrey R Gruen
Seven new cases of familial isolated bladder exstrophy and epispadias complex (BEEC) and review of the literature.
American journal of medical genetics. Part A 2003;120A(2):215-21.
2002: Hartmut Engels; Kristin Bosse; Antje Ehrbrecht; Susanne Zahn; Alexander Hoischen; Peter Propping; Lutz Bindl; Heiko Reutter
Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations.
American journal of medical genetics 2002;111(2):205-9.
2001: Jung Ahn; Tae-Woong Won; A Zia; Heiko Reutter; Deborah E Kaplan; R Sparks; Jeffrey R Gruen
Peaks of linkage are localized by a BAC/PAC contig of the 6p reading disability locus.
Genomics 2001;78(1-2):19-29.