Nadine Zwink

Mainz, RP 55131, Germany

Last Updated: 09/26/2026

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Found 45 publications

Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease Formation.

Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease Formation.

Journal: Biomolecules
Published: May 27, 2023

Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations.

Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations.

Journal: European journal of human genetics : EJHG
Published: March 18, 2022

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

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

Journal: Communications biology
Published: February 23, 2022

First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B.

First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B.

Journal: HGG advances
Published: October 25, 2021

Parental risk factors for congenital diaphragmatic hernia - a large German case-control study.

Parental risk factors for congenital diaphragmatic hernia - a large German case-control study.

Journal: BMC pediatrics
Published: March 04, 2021

A Prevalence Estimation of Exstrophy and Epispadias in Germany From Public Health Insurance Data.

A Prevalence Estimation of Exstrophy and Epispadias in Germany From Public Health Insurance Data.

Journal: Frontiers in pediatrics
Published: December 31, 2020

Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia.

Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia.

Journal: PloS one
Published: February 11, 2020

SLC20A1 Is Involved in Urinary Tract and Urorectal Development.

SLC20A1 Is Involved in Urinary Tract and Urorectal Development.

Journal: Frontiers in cell and developmental biology
Published: February 10, 2020

Treatment Strategies and Outcome of the Exstrophy-Epispadias Complex in Germany: Data From the German CURE-Net.

Treatment Strategies and Outcome of the Exstrophy-Epispadias Complex in Germany: Data From the German CURE-Net.

Journal: Frontiers in pediatrics
Published: November 04, 2019

Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations.

Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations.

Journal: PloS one
Published: November 21, 2018

Needs Assessment in Care of Adults With Anorectal Malformations and Exstrophy-Epispadias Complex in Germany.

Needs Assessment in Care of Adults With Anorectal Malformations and Exstrophy-Epispadias Complex in Germany.

Journal: Frontiers in pediatrics
Published: August 03, 2018

Utilization and determinants of follow-up colonoscopies within 6 years after screening colonoscopy: Prospective cohort study.

Utilization and determinants of follow-up colonoscopies within 6 years after screening colonoscopy: Prospective cohort study.

Journal: International journal of cancer
Published: May 04, 2018
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Last Updated: 09/26/2026