Publications by authors named "Heiko M Reutter"

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is implicated in central nervous system, orofacial and maxillofacial anomalies.
Jeshurun C Kalanithy, Enrico Mingardo, Jil D Stegmann, Ramgopal Dhakar, Tikam Chand Dakal, Heiko M Reutter

J Med Genet· January 2025

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Common variants increase risk for congenital diaphragmatic hernia within the context of de novo variants.
Lu Qiao, Carrie L Welch, Rebecca Hernan, Julia Wynn, Usha S Krishnan, Heiko Martin Reutter

Am J Hum Genet· November 2024

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Centralization as the key survival benefit in acute neonatal surgery.
Manuel Besendörfer, Simone Günster, Katja Linz, Heiko Martin Reutter, Sonja Diez

Front Pediatr· March 2024

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Is Involved in Congenital Chylothorax.
Jonathan B Whitchurch, Sophia Schneider, Alina C Hilger, Ricarda Köllges, Jil D Stegmann, Heiko M Reutter

Cells· January 2024

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X-linked variations in are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems.
Caroline M Kolvenbach, Tim Felger, Luca Schierbaum, Isabelle Thiffault, Tomi Pastinen, Heiko M Reutter

J Med Genet· June 2023

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Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing Challenge.
Erwin Brosens, Nina C J Peters, Kim S van Weelden, Charlotte Bendixen, Rutger W W Brouwer, Heiko Martin Reutter

Front Pediatr· February 2022

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Genetic Counseling for Birth Defects.
Heiko M Reutter

Eur J Pediatr Surg· December 2021

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A Prevalence Estimation of Exstrophy and Epispadias in Germany From Public Health Insurance Data.
Anne-Karoline Ebert, Nadine Zwink, Heiko Martin Reutter, Ekkehart Jenetzky

Front Pediatr· October 2021

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

Pediatr Blood Cancer· September 2021

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

Genes (Basel)· August 2021

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

Orphanet J Rare Dis· April 2021

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Lessons Learned from CNV Analysis of Major Birth Defects.
Alina Christine Hilger, Gabriel Clemens Dworschak, Heiko Martin Reutter

Int J Mol Sci· November 2020

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Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.
Dervla M Connaughton, Rufeng Dai, Danielle J Owen, Jonathan Marquez, Nina Mann, Heiko M Reutter

Am J Hum Genet· October 2020

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A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies.
Romy van de Putte, Gabriel C Dworschak, Erwin Brosens, Heiko M Reutter, Carlo L M Marcelis

Front Pediatr· June 2020

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Treatment Strategies and Outcome of the Exstrophy-Epispadias Complex in Germany: Data From the German CURE-Net.
Anne-Karoline Ebert, Nadine Zwink, Heiko M Reutter, Ekkehart Jenetzky, Raimund Stein

Front Pediatr· May 2020

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AUTHOR REPLY.
Anne-Karoline Ebert, Nadine Zwink, Heiko Martin Reutter

Urology· January 2019

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Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
Amelie T van der Ven, Dervla M Connaughton, Hadas Ityel, Nina Mann, Makiko Nakayama, Heiko M Reutter

J Am Soc Nephrol· September 2018

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Circulating microRNAs are associated with Pulmonary Hypertension and Development of Chronic Lung Disease in Congenital Diaphragmatic Hernia.
Marisol Herrera-Rivero, Rong Zhang, Stefanie Heilmann-Heimbach, Andreas Mueller, Soyhan Bagci, Heiko M Reutter

Sci Rep· July 2018

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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.
Stefan Kohl, Jing Chen, Asaf Vivante, Daw-Yang Hwang, Shirlee Shril, Heiko M Reutter

Nephrol Dial Transplant· August 2016

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Loss of Function of GALNT2 Lowers High-Density Lipoproteins in Humans, Nonhuman Primates, and Rodents.
Sumeet A Khetarpal, Katrine T Schjoldager, Christina Christoffersen, Avanthi Raghavan, Andrew C Edmondson, Heiko M Reutter

Cell Metab· August 2016

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More than fetal urine: enteral uptake of amniotic fluid as a major predictor for fetal growth during late gestation.
Soyhan Bagci, Erwin Brosens, Dick Tibboel, Annelies De Klein, Hanneke Ijsselstijn, Heiko M Reutter

Eur J Pediatr· June 2016

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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.
Daw-Yang Hwang, Stefan Kohl, Xueping Fan, Asaf Vivante, Stefanie Chan, Heiko M Reutter

Hum Genet· August 2015

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Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development.
Asaf Vivante, Marc-Jens Kleppa, Julian Schulz, Stefan Kohl, Amita Sharma, Heiko M Reutter

Am J Hum Genet· August 2015

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

Cardiol Young· March 2015

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Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract.
Stefan Kohl, Daw-Yang Hwang, Gabriel C Dworschak, Alina C Hilger, Pawaree Saisawat, Heiko M Reutter

J Am Soc Nephrol· September 2014

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