Heiko Martin Reutter (Heiko Reutter, Heiko M Reutter)

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 54

Top Venues

Children (Basel, Switzerland)

European journal of human genetics : EJHG

Genes

Cells

University of Bonn

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Bonn Oct 01 2012

Germany

Senior Researcher and Consultant :: Institute of Human Genetics and Department of Neonatology

Publications

Jonathan B Whitchurch, Sophia Schneider, Alina C Hilger, Ricarda Köllges, Jil D Stegmann, Lea Waffenschmidt, Laura Dyer, Holger Thiele, Bhanupriya Dhabhai, Tikam Chand Dakal, Andreas Müller, Dominic P Norris, Heiko Martin Reutter
PKD1L1 Is Involved in Congenital Chylothorax. Cells 13 (2) (2024)
Jil D Stegmann, Jeshurun C Kalanithy, Gabriel C Dworschak, Nina Ishorst, Enrico Mingardo, Filipa M Lopes, Yee Mang Ho, Phillip Grote, Tobias T Lindenberg, Öznur Yilmaz, Khadija Channab, Steve Seltzsam, Shirlee Shril, Friedhelm Hildebrandt, Felix Boschann, André Heinen, Angad Jolly, Katherine Myers, Kim McBride, Mir Reza Bekheirnia, Nasim Bekheirnia, Marcello Scala, Manuela Morleo, Vincenzo Nigro, Annalaura Torella, null null, Michele Pinelli, Valeria Capra, Andrea Accogli, Silvia Maitz, Alice Spano, Rory J Olson, Eric W Klee, Brendan C Lanpher, Se Song Jang, Jong-Hee Chae, Philipp Steinbauer, Dietmar Rieder, Andreas R Janecke, Julia Vodopiutz, Ida Vogel, Jenny Blechingberg, Jennifer L Cohen, Kacie Riley, Victoria Klee, Laurence E Walsh, Matthias Begemann, Miriam Elbracht, Eggermann Thomas, Arzu Stoppe, Kyra Stuurman, Marjon van Slegtenhorst, Tahsin Stefan Barakat, Maureen S Mulhern, Tristan T Sands, Cheryl Cytrynbaum, Rosanna Weksberg, Federica Isidori, Tommaso Pippucci, Giulia Severi, Francesca Montanari, Michael C Kruer, Somayeh Bakhtiari, Hossein Darvish, Heiko Martin Reutter, Gregor Hagelueken, Matthias Geyer, Adrian S Woolf, Jennifer E Posey, James R. Lupski, Benjamin Odermatt, Alina C Hilger
Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies. NPJ genomic medicine 9 (1) (2024)
Jonathan B Whitchurch, Sophia Schneider, Alina C Hilger, Ricarda Köllges, Jil D Stegmann, Lea Waffenschmidt, Laura Dyer, Holger Thiele, Bhanupriya Dhabhai, Tikam Chand Dakal, Andreas Müller, Dominic P Norris, Heiko Martin Reutter
PKD1L1 Is Involved in Congenital Chylothorax. Cells 13 (2) (2024)
Maria Carla Borroto, Coralie Michaud, Chloé Hudon, Pankaj B Agrawal, Katherine Agre, Carolyn D Applegate, Alan H Beggs, Hans T Bjornsson, Bert Callewaert, Mei-Jan Chen, Cynthia Curry, Orrin Devinsky, Tracy Dudding-Byth, Kelly Fagan, Candice R Finnila, Ralitza Gavrilova, Casie A Genetti, Susan M Hiatt, Friedhelm Hildebrandt, Monica Hsiung Wojcik, Tjitske Kleefstra, Caroline M Kolvenbach, Bruce R Korf, Paul S Kruszka, Hong Li, Jessica Litwin, Julien Marcadier, Konrad Platzer, Patrick R Blackburn, Margot R F Reijnders, Heiko Martin Reutter, Ina Schanze, Joseph T Shieh, Cathy A Stevens, Zaheer Valivullah, Marie-José H van den Boogaard, Eric W Klee, Philippe M Campeau
A Genotype/Phenotype Study of KDM5B -Associated Disorders Suggests a Pathogenic Effect of Dominantly Inherited Missense Variants. Genes 15 (8) (2024)
Jonathan B Whitchurch, Sophia Schneider, Alina C Hilger, Ricarda Köllges, Jil D Stegmann, Lea Waffenschmidt, Laura Dyer, Holger Thiele, Bhanupriya Dhabhai, Tikam Chand Dakal, Andreas Müller, Dominic P Norris, Heiko Martin Reutter
PKD1L1 Is Involved in Congenital Chylothorax. Cells 13 (2) (2024)
Jonathan B Whitchurch, Sophia Schneider, Alina C Hilger, Ricarda Köllges, Jil D Stegmann, Lea Waffenschmidt, Laura Dyer, Holger Thiele, Bhanupriya Dhabhai, Tikam Chand Dakal, Andreas Müller, Dominic P Norris, Heiko Martin Reutter
PKD1L1 Is Involved in Congenital Chylothorax. Cells 13 (2) (2024)
Michael Karl Baumgartner, Anna-Lena Behr, Anne Christina Garbe, Christoph Quatember, Heiko Martin Reutter, Joachim Woelfle, Fabian Benedikt Fahlbusch, Gregor Hanslik
Diving into the Digital Landscape: Assessing the Quality of Online Information on Neonatal Jaundice for Parents. Children (Basel, Switzerland) 11 (7) (2024)
Judit H Schultewolter, Anke Rissmann, Dietrich von Schweinitz, Michael Christoph Frühwald, Claudia Blattmann, Lars Fischer, Björn Sönke Lange, Rüdiger Wessalowski, Birgit Fröhlich, Wolfgang Behnisch, Irene Schmid, Harald Reinhard, Matthias Dürken, Patrick Hundsdörfer, Martin Heimbrodt, Christian Vokuhl, Stefan Schönberger, Dominik T Schneider, Guido Seitz, Leendert Looijenga, Ulrich Göbel, Rüdiger von Kries, Heiko Martin Reutter, Gabriele Calaminus
Non-Syndromic and Syndromic Defects in Children with Extracranial Germ Cell Tumors: Data of 2610 Children Registered with the German MAKEI 96/MAHO 98 Registry Compared to the General Population. Cancers 16 (11) (2024)
Jil D Stegmann, Jeshurun C Kalanithy, Gabriel C Dworschak, Nina Ishorst, Enrico Mingardo, Filipa M Lopes, Yee Mang Ho, Phillip Grote, Tobias T Lindenberg, Öznur Yilmaz, Khadija Channab, Steve Seltzsam, Shirlee Shril, Friedhelm Hildebrandt, Felix Boschann, André Heinen, Angad Jolly, Katherine Myers, Kim McBride, Mir Reza Bekheirnia, Nasim Bekheirnia, Marcello Scala, Manuela Morleo, Vincenzo Nigro, Annalaura Torella, null null, Michele Pinelli, Valeria Capra, Andrea Accogli, Silvia Maitz, Alice Spano, Rory J Olson, Eric W Klee, Brendan C Lanpher, Se Song Jang, Jong-Hee Chae, Philipp Steinbauer, Dietmar Rieder, Andreas R Janecke, Julia Vodopiutz, Ida Vogel, Jenny Blechingberg, Jennifer L Cohen, Kacie Riley, Victoria Klee, Laurence E Walsh, Matthias Begemann, Miriam Elbracht, Eggermann Thomas, Arzu Stoppe, Kyra Stuurman, Marjon van Slegtenhorst, Tahsin Stefan Barakat, Maureen S Mulhern, Tristan T Sands, Cheryl Cytrynbaum, Rosanna Weksberg, Federica Isidori, Tommaso Pippucci, Giulia Severi, Francesca Montanari, Michael C Kruer, Somayeh Bakhtiari, Hossein Darvish, Heiko Martin Reutter, Gregor Hagelueken, Matthias Geyer, Adrian S Woolf, Jennifer E Posey, James R. Lupski, Benjamin Odermatt, Alina C Hilger
Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies. NPJ genomic medicine 9 (1) (2024)
Jil D Stegmann, Jeshurun C Kalanithy, Gabriel C Dworschak, Nina Ishorst, Enrico Mingardo, Filipa M Lopes, Yee Mang Ho, Phillip Grote, Tobias T Lindenberg, Öznur Yilmaz, Khadija Channab, Steve Seltzsam, Shirlee Shril, Friedhelm Hildebrandt, Felix Boschann, André Heinen, Angad Jolly, Katherine Myers, Kim McBride, Mir Reza Bekheirnia, Nasim Bekheirnia, Marcello Scala, Manuela Morleo, Vincenzo Nigro, Annalaura Torella, null null, Michele Pinelli, Valeria Capra, Andrea Accogli, Silvia Maitz, Alice Spano, Rory J Olson, Eric W Klee, Brendan C Lanpher, Se Song Jang, Jong-Hee Chae, Philipp Steinbauer, Dietmar Rieder, Andreas R Janecke, Julia Vodopiutz, Ida Vogel, Jenny Blechingberg, Jennifer L Cohen, Kacie Riley, Victoria Klee, Laurence E Walsh, Matthias Begemann, Miriam Elbracht, Eggermann Thomas, Arzu Stoppe, Kyra Stuurman, Marjon van Slegtenhorst, Tahsin Stefan Barakat, Maureen S Mulhern, Tristan T Sands, Cheryl Cytrynbaum, Rosanna Weksberg, Federica Isidori, Tommaso Pippucci, Giulia Severi, Francesca Montanari, Michael C Kruer, Somayeh Bakhtiari, Hossein Darvish, Heiko Martin Reutter, Gregor Hagelueken, Matthias Geyer, Adrian S Woolf, Jennifer E Posey, James R. Lupski, Benjamin Odermatt, Alina C Hilger
Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies. NPJ genomic medicine 9 (1) (2024)
Michael Karl Baumgartner, Anna-Lena Behr, Anne Christina Garbe, Christoph Quatember, Heiko Martin Reutter, Joachim Woelfle, Fabian Benedikt Fahlbusch, Gregor Hanslik
Diving into the Digital Landscape: Assessing the Quality of Online Information on Neonatal Jaundice for Parents. Children (Basel, Switzerland) 11 (7) (2024)
Fabian Ebach, Pauline Wagner, Raimund Stein, Ramona Dolscheid-Pommerich, Heiko Martin Reutter, Alina C Hilger
Familial congenital lower urinary tract obstruction (LUTO) suggested by screening for lower urinary tract dysfunction in parents of patients: A descriptive study. Health science reports 7 (3) (2024)
Judit H Schultewolter, Anke Rissmann, Dietrich von Schweinitz, Michael Christoph Frühwald, Claudia Blattmann, Lars Fischer, Björn Sönke Lange, Rüdiger Wessalowski, Birgit Fröhlich, Wolfgang Behnisch, Irene Schmid, Harald Reinhard, Matthias Dürken, Patrick Hundsdörfer, Martin Heimbrodt, Christian Vokuhl, Stefan Schönberger, Dominik T Schneider, Guido Seitz, Leendert Looijenga, Ulrich Göbel, Rüdiger von Kries, Heiko Martin Reutter, Gabriele Calaminus
Non-Syndromic and Syndromic Defects in Children with Extracranial Germ Cell Tumors: Data of 2610 Children Registered with the German MAKEI 96/MAHO 98 Registry Compared to the General Population. Cancers 16 (11) (2024)
Michael Karl Baumgartner, Anna-Lena Behr, Anne Christina Garbe, Christoph Quatember, Heiko Martin Reutter, Joachim Woelfle, Fabian Benedikt Fahlbusch, Gregor Hanslik
Diving into the Digital Landscape: Assessing the Quality of Online Information on Neonatal Jaundice for Parents. Children (Basel, Switzerland) 11 (7) (2024)
Jonathan B Whitchurch, Sophia Schneider, Alina C Hilger, Ricarda Köllges, Jil D Stegmann, Lea Waffenschmidt, Laura Dyer, Holger Thiele, Bhanupriya Dhabhai, Tikam Chand Dakal, Andreas Müller, Dominic P Norris, Heiko Martin Reutter
PKD1L1 Is Involved in Congenital Chylothorax. Cells 13 (2) (2024)
Jil D Stegmann, Jeshurun C Kalanithy, Gabriel C Dworschak, Nina Ishorst, Enrico Mingardo, Filipa M Lopes, Yee Mang Ho, Phillip Grote, Tobias T Lindenberg, Öznur Yilmaz, Khadija Channab, Steve Seltzsam, Shirlee Shril, Friedhelm Hildebrandt, Felix Boschann, André Heinen, Angad Jolly, Katherine Myers, Kim McBride, Mir Reza Bekheirnia, Nasim Bekheirnia, Marcello Scala, Manuela Morleo, Vincenzo Nigro, Annalaura Torella, null null, Michele Pinelli, Valeria Capra, Andrea Accogli, Silvia Maitz, Alice Spano, Rory J Olson, Eric W Klee, Brendan C Lanpher, Se Song Jang, Jong-Hee Chae, Philipp Steinbauer, Dietmar Rieder, Andreas R Janecke, Julia Vodopiutz, Ida Vogel, Jenny Blechingberg, Jennifer L Cohen, Kacie Riley, Victoria Klee, Laurence E Walsh, Matthias Begemann, Miriam Elbracht, Eggermann Thomas, Arzu Stoppe, Kyra Stuurman, Marjon van Slegtenhorst, Tahsin Stefan Barakat, Maureen S Mulhern, Tristan T Sands, Cheryl Cytrynbaum, Rosanna Weksberg, Federica Isidori, Tommaso Pippucci, Giulia Severi, Francesca Montanari, Michael C Kruer, Somayeh Bakhtiari, Hossein Darvish, Heiko Martin Reutter, Gregor Hagelueken, Matthias Geyer, Adrian S Woolf, Jennifer E Posey, James R. Lupski, Benjamin Odermatt, Alina C Hilger
Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies. NPJ genomic medicine 9 (1) (2024)
Fabian Ebach, Pauline Wagner, Raimund Stein, Ramona Dolscheid-Pommerich, Heiko Martin Reutter, Alina C Hilger
Familial congenital lower urinary tract obstruction (LUTO) suggested by screening for lower urinary tract dysfunction in parents of patients: A descriptive study. Health science reports 7 (3) (2024)
Maria Carla Borroto, Coralie Michaud, Chloé Hudon, Pankaj B Agrawal, Katherine Agre, Carolyn D Applegate, Alan H Beggs, Hans T Bjornsson, Bert Callewaert, Mei-Jan Chen, Cynthia Curry, Orrin Devinsky, Tracy Dudding-Byth, Kelly Fagan, Candice R Finnila, Ralitza Gavrilova, Casie A Genetti, Susan M Hiatt, Friedhelm Hildebrandt, Monica Hsiung Wojcik, Tjitske Kleefstra, Caroline M Kolvenbach, Bruce R Korf, Paul S Kruszka, Hong Li, Jessica Litwin, Julien Marcadier, Konrad Platzer, Patrick R Blackburn, Margot R F Reijnders, Heiko Martin Reutter, Ina Schanze, Joseph T Shieh, Cathy A Stevens, Zaheer Valivullah, Marie-José H van den Boogaard, Eric W Klee, Philippe M Campeau
A Genotype/Phenotype Study of KDM5B -Associated Disorders Suggests a Pathogenic Effect of Dominantly Inherited Missense Variants. Genes 15 (8) (2024)
Alisa Bär, Sabina Schmitt-Grohé, Jürgen Held, Julia Lubig, Gregor Hanslik, Fabian B Fahlbusch, Heiko Martin Reutter, Joachim Woelfle, Adriana van der Donk, Maria Schleier, Tobias Hepp, Patrick Morhart
Evaluating the Use of Neonatal Colonization Screening for Empiric Antibiotic Therapy of Sepsis and Pneumonia. Antibiotics (Basel, Switzerland) 12 (2) (2023)
Maria Schleier, Julia Lubig, Sven Kehl, Steven Hébert, Joachim Woelfle, Adriana van der Donk, Alisa Bär, Heiko Martin Reutter, Tobias Hepp, Patrick Morhart
Diagnostic Utility of Interleukin-6 in Early-Onset Sepsis among Term Newborns: Impact of Maternal Risk Factors and CRP Evaluation. Children (Basel, Switzerland) 11 (1) (2023)
Heiko Martin Reutter
High molecular diagnostic yields and novel phenotypic expansions involving syndromic anorectal malformations. European journal of human genetics : EJHG (2023)
Alisa Bär, Sabina Schmitt-Grohé, Jürgen Held, Julia Lubig, Gregor Hanslik, Fabian B Fahlbusch, Heiko Martin Reutter, Joachim Woelfle, Adriana van der Donk, Maria Schleier, Tobias Hepp, Patrick Morhart
Evaluating the Use of Neonatal Colonization Screening for Empiric Antibiotic Therapy of Sepsis and Pneumonia. Antibiotics (Basel, Switzerland) 12 (2) (2023)
Marius Schmidt, Steven Hébert, Gerd Wallukat, Rolf Ponader, Tobias Krickau, Matthias Galiano, Heiko Martin Reutter, Joachim Woelfle, Abbas Agaimy, Christian Mardin, André Hoerning, Bettina Hohberger
"Multisystem Inflammatory Syndrome in Children"-Like Disease after COVID-19 Vaccination (MIS-V) with Potential Significance of Functional Active Autoantibodies Targeting G-Protein-Coupled Receptors (GPCR-fAAb) for Pathophysiology and Therapy. Children (Basel, Switzerland) 10 (12) (2023)
Steven Hébert, Marius Schmidt, Georg Topf, Daniel Rieger, Jens Klinge, Jan Vermehren, Christoph Fusch, Christian Grillhösl, Michael Schroth, Irmgard Toni, Heiko Martin Reutter, Patrick Morhart, Gregor Hanslik, Linda Mulzer, Joachim Woelfle, Bettina Hohberger, André Hoerning
"Multisystem Inflammatory Syndrome in Children" (MIS-C) after COVID-19 Infection in the Metropolitan Area of Nuremberg-Erlangen, Germany-Expectations and Results of a Two-Year Period. Children (Basel, Switzerland) 10 (8) (2023)
Heiko Martin Reutter
High molecular diagnostic yields and novel phenotypic expansions involving syndromic anorectal malformations. European journal of human genetics : EJHG 31 (3) (2023)
Heiko Martin Reutter
High molecular diagnostic yields and novel phenotypic expansions involving syndromic anorectal malformations. European journal of human genetics : EJHG 31 (3) (2023)
Patrick Morhart, Roman G Gerlach, Caroline Kunz, Jürgen Held, Giuseppe Valenza, Joachim Woelfle, Heiko Martin Reutter, Gregor J Hanslik, Fabian B Fahlbusch
Application of Next-Generation Sequencing to Enterobacter Hormaechei Subspecies Analysis during a Neonatal Intensive Care Unit Outbreak. Children (Basel, Switzerland) 10 (10) (2023)
Ricarda Köllges, Jil Stegmann, Sophia Schneider, Lea Waffenschmidt, Julia Fazaal, Katinka Breuer, Alina C Hilger, Gabriel C Dworschak, Enrico Mingardo, Wolfgang Rösch, Aybike Hofmann, Claudia Neissner, Anne-Karolin Ebert, Raimund Stein, Nina Younsi, Karin Hirsch-Koch, Eberhard Schmiedeke, Nadine Zwink, Ekkehart Jenetzky, Holger Thiele, Kerstin U Ludwig, Heiko Martin Reutter
Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease Formation. Biomolecules 13 (7) (2023)
Heiko Martin Reutter
High molecular diagnostic yields and novel phenotypic expansions involving syndromic anorectal malformations. European journal of human genetics : EJHG 31 (3) (2023)
Marius Schmidt, Steven Hébert, Gerd Wallukat, Rolf Ponader, Tobias Krickau, Matthias Galiano, Heiko Martin Reutter, Joachim Woelfle, Abbas Agaimy, Christian Mardin, André Hoerning, Bettina Hohberger
"Multisystem Inflammatory Syndrome in Children"-Like Disease after COVID-19 Vaccination (MIS-V) with Potential Significance of Functional Active Autoantibodies Targeting G-Protein-Coupled Receptors (GPCR-fAAb) for Pathophysiology and Therapy. Children (Basel, Switzerland) 10 (12) (2023)
Heiko Martin Reutter
High molecular diagnostic yields and novel phenotypic expansions involving syndromic anorectal malformations. European journal of human genetics : EJHG (2023)
Alisa Bär, Sabina Schmitt-Grohé, Jürgen Held, Julia Lubig, Gregor Hanslik, Fabian B Fahlbusch, Heiko Martin Reutter, Joachim Woelfle, Adriana van der Donk, Maria Schleier, Tobias Hepp, Patrick Morhart
Evaluating the Use of Neonatal Colonization Screening for Empiric Antibiotic Therapy of Sepsis and Pneumonia. Antibiotics (Basel, Switzerland) 12 (2) (2023)
Maria Schleier, Julia Lubig, Sven Kehl, Steven Hébert, Joachim Woelfle, Adriana van der Donk, Alisa Bär, Heiko Martin Reutter, Tobias Hepp, Patrick Morhart
Diagnostic Utility of Interleukin-6 in Early-Onset Sepsis among Term Newborns: Impact of Maternal Risk Factors and CRP Evaluation. Children (Basel, Switzerland) 11 (1) (2023)
Heiko Martin Reutter
High molecular diagnostic yields and novel phenotypic expansions involving syndromic anorectal malformations. European journal of human genetics : EJHG 31 (3) (2023)
Sophia Schneider, Ricarda Köllges, Jil D Stegmann, Frederic Thieme, Alina C Hilger, Lea Waffenschmidt, Julia Fazaal, Jeshurun C Kalanithy, Annegret Geipel, Brigitte Strizek, Kerstin U Ludwig, Heiko Martin Reutter, Andreas Müller
Resequencing of VEGFR3 pathway genes implicate GJC2 and FLT4 in the formation of primary congenital chylothorax. American journal of medical genetics. Part A 188 (5) (2022)
Caroline M Kolvenbach, Tim Felger, Luca Schierbaum, Isabelle Thiffault, Tomi Pastinen, Maria Szczepańska, Marcin Zaniew, Piotr Adamczyk, Allan Bayat, Öznur Yilmaz, Tobias T Lindenberg, Holger Thiele, Friedhelm Hildebrandt, Katrin Hinderhofer, Ute Moog, Alina C Hilger, Bonnie Sullivan, Lauren Bartik, Piotr Gnyś, Phillip Grote, Benjamin Odermatt, Heiko Martin Reutter, Gabriel C Dworschak
X-linked variations in SHROOM4 are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems. Journal of medical genetics (2022)
Laura Guckert, Heiko Martin Reutter, Nadia Saleh, Rainer Ganschow, Andreas Müller, Fabian Ebach
Nonurgent Visits to the Pediatric Emergency Department before and during the First Peak of the COVID-19 Pandemic. International journal of pediatrics 2022 (2022)
Enrico Mingardo, Glenda Beaman, Phillip Grote, Agneta Nordenskjöld, William G Newman, Adrian S Woolf, Markus Eckstein, Alina C Hilger, Gabriel C Dworschak, Wolfgang Rösch, Anne-Karolin Ebert, Raimund Stein, Alfredo Brusco, Massimo Di Grazia, Ali Tamer, Federico M Torres, Jose L Hernandez, Philipp Erben, Carlo Maj, Jose M Olmos, Jose A Riancho, Carmen Valero, Isabel Charlotte Hostettler, Henry Houlden, David John Werring, Johannes Schumacher, Jan Gehlen, Ann-Sophie Giel, Benedikt C Buerfent, Samara Arkani, Elisabeth Åkesson, Emilia Rotstein, Michael Ludwig, Gundela Holmdahl, Elisa Giorgio, Alfredo Berettini, David Keene, Raimondo M Cervellione, Nina Younsi, Melissa Ortlieb, Josef Oswald, Bernhard Haid, Martin Promm, Claudia Neissner, Karin Hirsch, Maximilian Stehr, Frank-Mattias Schäfer, Eberhard Schmiedeke, Thomas M Boemers, Iris A L M van Rooij, Wouter F J Feitz, Carlo L M Marcelis, Martin Lacher, Jana Nelson, Benno Ure, Caroline Fortmann, Daniel P Gale, Melanie M Y Chan, Kerstin U Ludwig, Markus Maria Nöthen, Stefanie Heilmann-Heimbach, Nadine Zwink, Ekkehart Jenetzky, Benjamin Odermatt, Michael Knapp, Heiko Martin Reutter
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy. Communications biology 5 (1) (2022)
Katinka Breuer, Korbinian Maria Riedhammer, Nicole Müller, Birthe Schaidinger, Gregor Dombrowsky, Sven Dittrich, Susanne Zeidler, Ulrike M M Bauer, Dominik Sebastian Westphal, Thomas Meitinger, Tikam Chand Dakal, Marc Phillip Hitz, Johannes Breuer, Heiko Martin Reutter, Alina C Hilger, Julia Hoefele
Exome sequencing in individuals with cardiovascular laterality defects identifies potential candidate genes. European journal of human genetics : EJHG 30 (8) (2022)
Julia Fabian, Gabriel C Dworschak, Lea Waffenschmidt, Luca Schierbaum, Charlotte Bendixen, Stefanie Heilmann-Heimbach, Sugirthan Sivalingam, Andreas Buness, Nicole Schwarzer, Thomas M Boemers, Eberhard Schmiedeke, Jörg Neser, Johannes Leonhardt, Ferdinand Kosch, Sandra Weih, Helen Maya Gielen, Stuart Hosie, Carmen Kabs, Markus Palta, Stefanie Märzheuser, Lena Marie Bode, Martin Lacher, Frank-Mattias Schäfer, Maximilian Stehr, Christian Knorr, Benno Ure, Katharina Kleine, Udo Rolle, Marcin Zaniew, Phillip Grote, Nadine Zwink, Ekkehart Jenetzky, Heiko Martin Reutter, Alina C Hilger
Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations. European journal of human genetics : EJHG (2022)
Charlotte Bendixen, Heiko Martin Reutter
The Role of De Novo Variants in Patients with Congenital Diaphragmatic Hernia. Genes 12 (9) (2021)
Anna-Lina König, Hemmen Sabir, Brigitte Stritzek, Ulrich Gembruch, Ulrike Herberg, Miriam Bertrand, Ute Grasshoff, Gesa Wiegand, Cornelia Wiechers, Eugenia Bernis, Heiko Martin Reutter, Andreas Müller
Isolated cytokine-enriched pericardial effusion: A likely key feature for Aymé-Gripp syndrome. American journal of medical genetics. Part A (2021)
Caroline M Kolvenbach, Amelie T van der Ven, Franziska Kause, Shirlee Shril, Marcello Scala, Dervla M Connaughton, Nina Mann, Makiko Nakayama, Rufeng Dai, Thomas M Kitzler, Ronen Schneider, Luca Schierbaum, Sophia Schneider, Andrea Accogli, Annalaura Torella, Gianluca Piatelli, Vincenzo Nigro, Valeria Capra, Bernd Hoppe, Stefanie Märzheuser, Eberhard Schmiedeke, Heidi L Rehm, Shrikant Mane, Richard P Lifton, Gabriel C Dworschak, Alina C Hilger, Heiko Martin Reutter, Friedhelm Hildebrandt
Exome survey of individuals affected by VATER/VACTERL with renal phenotypes identifies phenocopies and novel candidate genes. American journal of medical genetics. Part A 185 (12) (2021)
Luca M Schierbaum, Sophia Schneider, Stefan Herms, Sugirthan Sivalingam, Julia Fabian, Heiko Martin Reutter, Stefanie Weber, Waltraut M Merz, Marcin Tkaczyk, Monika Miklaszewska, Przemysław Sikora, Agnieszka Szmigielska, Grazyna Krzemien, Katarzyna Zachwieja, Shaji K Kumar, Katarzyna Taranta-Janusz, Pawel Kroll, Marcin Polok, Marcin Zaniew, Alina C Hilger
Genome-Wide Survey for Microdeletions or -Duplications in 155 Patients with Lower Urinary Tract Obstructions (LUTO). Genes 12 (9) (2021)
Ilaria Parenti, Mark B Mallozzi, Irina Hüning, Cristina Gervasini, Alma Kuechler, Emanuele Agolini, Beate Albrecht, Carolina Baquero-Montoya, Axel Bohring, Nuria C Bramswig, Andreas Busche, Andreas Dalski, Yiran Guo, Britta Hanker, Yorck Hellenbroich, Denise Horn, A Micheil Innes, Chiara Leoni, Yun R Li, Sally-Ann Lynch, Milena Mariani, Livija Medne, Barbara Mikat, Donatella Milani, Roberta Onesimo, Xilma R Ortiz-González, Eva Christina Prott, Heiko Martin Reutter, Eva Rossier, Angelo Selicorni, Peter Wieacker, Alisha Wilkens, Dagmar Wieczorek, Elaine H Zackai, Giuseppe Zampino, Birgit Zirn, Hakon H Hakonarson, Matthew A Deardorff, Gabriele Gillessen-Kaesbach, Frank J Kaiser
ANKRD11 variants: KBG syndrome and beyond. Clinical genetics 100 (2) (2021)
Gabriel C Dworschak, Iris A L M van Rooij, Heiko Martin Reutter
The Role of De Novo Variants in Formation of Human Anorectal Malformations. Genes 12 (9) (2021)
Alina Christine Hilger, Gabriel Clemens Dworschak, Heiko Martin Reutter
Lessons Learned from CNV Analysis of Major Birth Defects. International journal of molecular sciences 21 (21) (2020)
Rong Zhang, Jan Gehlen, Amit Kawalia, Maria-Theodora Melissari, Tikam Chand Dakal, Athira M Menon, Julia Höfele, Korbinian Maria Riedhammer, Lea Waffenschmidt, Julia Fabian, Katinka Breuer, Jeshurun Kalanithy, Alina Christine Hilger, Ingo G H Schmidt-Wolf, Alice Hölscher, Thomas M Boemers, Markus Pauly, Andreas Leutner, Jörg Fuchs, Guido Seitz, Barbara M Ludwikowski, Barbara Gomez, Jochen Hubertus, Andreas Heydweiller, Ralf Kurz, Johannes Leonhardt, Ferdinand Kosch, Stefan Holland-Cunz, Oliver Münsterer, Beno Ure, Eberhard Schmiedeke, Jörg Neser, Petra Degenhardt, Stefanie Märzheuser, Katharina Kleine, Mattias Schäfer, Nicole Spychalski, Oliver J Deffaa, Jan-Hendrik Gosemann, Martin Lacher, Stefanie Heilmann-Heimbach, Nadine Zwink, Ekkehart Jenetzky, Michael Ludwig, Phillip Grote, Johannes Schumacher, Holger Thiele, Heiko Martin Reutter
Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia. PloS one 15 (6) (2020)
Franziska Kause, Rong Zhang, Michael Ludwig, Eberhard Schmiedeke, Anke Rissmann, Holger Thiele, Janine Altmueller, Stefan Herms, Alina C Hilger, Friedhelm Hildebrandt, Heiko Martin Reutter
HSPA6: A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrum. Birth defects research 111 (10) (2019)
Valerie Weitensteiner, Rong Zhang, Julia Bungenberg, Matthias Marks, Jan Gehlen, Damian J Ralser, Alina C Hilger, Amit Sharma, Johannes Schumacher, Ulrich Gembruch, Waltraut M Merz, Albert Becker, Janine Altmüller, Holger Thiele, Bernhard G Herrmann, Benjamin Odermatt, Michael Ludwig, Heiko Martin Reutter
Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate gene. Birth defects research 110 (7) (2018)
Nina Ishorst, Paola Francheschelli, Anne C Böhmer, Mohammad Faisal J Khan, Stefanie Heilmann-Heimbach, Nadine Fricker, Julian Little, Regine P M Steegers-Theunissen, Borut Peterlin, Stefanie Nowak, Markus Martini, Teresa Kruse, Anton Dunsche, Thomas Kreusch, Lina Gölz, Khalid Aldhorae, Esam S Halboub, Heiko Martin Reutter, Peter Mossey, Markus M Nöthen, Michele Rubini, Kerstin U Ludwig, Michael Knapp, Elisabeth Mangold
Nonsyndromic cleft palate: An association study at GWAS candidate loci in a multiethnic sample. Birth defects research 110 (10) (2018)
Ingo G H Schmidt-Wolf, Tikam Chand Dakal, Michael Ludwig, Holger Fröhlich, Riya Mathur, Heiko Martin Reutter
Towards a Central Role of ISL1 in the Bladder Exstrophy⁻Epispadias Complex (BEEC): Computational Characterization of Genetic Variants and Structural Modelling. Genes 9 (12) (2018)
Amelie T van der Ven, Dervla M Connaughton, Hadas Ityel, Nina Mann, Makiko Nakayama, Jing Chen, Asaf Vivante, Daw-Yang Hwang, Julian Schulz, Daniela A Braun, Johanna Magdalena Schmidt, David Schapiro, Ronen Schneider, Jillian K Warejko, Ankana Daga, Amar J Majmundar, Weizhen Tan, Tilman Jobst-Schwan, Tobias Hermle, Eugen Widmeier, Shazia Ashraf, Ali Amar, Charlotte A Hoogstraaten, Hannah Hugo, Thomas M Kitzler, Franziska Kause, Caroline M Kolvenbach, Rufeng Dai, Leslie Spaneas, Kassaundra Amann, Deborah R Stein, Michelle A Baum, Michael J G Somers, Nancy M Rodig, Michael A Ferguson, Avram Z Traum, Ghaleb H Daouk, Radovan Bogdanović, Natasa Stajić, Neveen A Soliman, Jameela A Kari, Sherif El Desoky, Hanan M Fathy, Danko Milosevic, Muna Al-Saffar, Hazem S Awad, Loai A Eid, Aravind Selvin, Prabha Senguttuvan, Simone Sanna-Cherchi, Heidi L Rehm, Daniel G MacArthur, Monkol Lek, Kristen M Laricchia, Michael W Wilson, Shrikant M Mane, Richard P Lifton, Richard S Lee, Stuart B Bauer, Weining Lu, Heiko Martin Reutter, Velibor Tasic, Shirlee Shril, Friedhelm Hildebrandt
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract. Journal of the American Society of Nephrology : JASN 29 (9) (2018)
Rong Zhang, Florian Marsch, Franziska Kause, Franziska Degenhardt, Eeberhard Schmiedeke, Stefanie Märzheuser, Bernd Hoppe, Haitham Bachour, Thomas M Boemers, Matthias Schäfer, Nicole Spychalski, Jörg Neser, Johannes Leonhardt, Ferdinand Kosch, Benno Ure, Barbara Gómez, Martin Lacher, Oliver J Deffaa, Markus Palta, Boris Wittekindt, Katharina Kleine, Andrea Schmedding, Sabine Grasshoff-Derr, Amelie van der Ven, Stefanie Heilmann-Heimbach, Nadine Zwink, Ekkehart Jenetzky, Michael Ludwig, Heiko Martin Reutter
Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations. Birth defects research 109 (13) (2017)

Heiko Martin Reutter.css-eqlu8i{font-size:small;padding-left:4px;} (Heiko Reutter, Heiko M Reutter)

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Heiko Martin Reutter (Heiko Reutter, Heiko M Reutter)