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Alice Hölscher

Charité - Universitätsmedizin Berlin · DE
Area of research
Surgery · Pulmonary and Respiratory Medicine
Research interest
Research interests include Atresia, Medicine, Tracheoesophageal fistula, Genetics, Fistula, and Internal medicine.
h-index
citations
166
works
9
NIH funding
primary concept
email

Recent publications

First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B
Human Genetics and Genomics Advances 2022cited by 9position: middledoi
Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia
PLoS ONE 2020cited by 17position: middledoi
Treatment Strategies and Outcome of the Exstrophy–Epispadias Complex in Germany: Data From the German CURE-Net
Frontiers in Pediatrics 2020cited by 12position: middledoi
Quality of Life after Surgical Treatment for Esophageal Atresia: Long-Term Outcome of 154 Patients
European Journal of Pediatric Surgery 2017cited by 25position: lastdoi
Esophageal Atresia with or without Tracheoesophageal Fistula (EA/TEF): Association of Different EA/TEF Subtypes with Specific Co-occurring Congenital Anomalies and Implications for Diagnostic Workup
European Journal of Pediatric Surgery 2017cited by 16position: middledoi
Copy number variations in 375 patients with oesophageal atresia and/or tracheoesophageal fistula
European Journal of Human Genetics 2016cited by 32position: middledoi
More than fetal urine: enteral uptake of amniotic fluid as a major predictor for fetal growth during late gestation
European Journal of Pediatrics 2016cited by 20position: middledoi
Comparison of environmental risk factors for esophageal atresia, anorectal malformations, and the combined phenotype in 263 German families
Diseases of the Esophagus 2015cited by 18position: middledoi
Second study on the recurrence risk of isolated esophageal atresia with or without trachea‐esophageal fistula among first‐degree relatives: No evidence for increased risk of recurrence of EA/TEF or for malformations of the VATER/VACTERL association spectrum
Birth Defects Research Part A Clinical and Molecular Teratology 2013cited by 17position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Heiko Reutter · Friedrich-Alexander-Universität Erlangen-Nürnberg4 papers (2013–2020)Ekkehart Jenetzky · Witten/Herdecke University4 papers (2013–2020)Nadine Zwink · Johannes Gutenberg University Mainz4 papers (2013–2020) · 3 papers (2013–2017) · 3 papers (2013–2017)Markus Pauly · University of California, Berkeley3 papers (2013–2017)Martin Lacher · University of Alabama at Birmingham3 papers (2017–2020) · 3 papers (2013–2017) · 3 papers (2013–2017) · 2 papers (2013–2017) · 2 papers (2013–2017)Benno Ure · Medizinische Hochschule Hannover2 papers (2017–2017)Oliver Münsterer · Johannes Gutenberg University Mainz2 papers (2017–2017) · 2 papers (2013–2017)Peter Bartmann · Nationwide Children's Hospital1 papers (2013–2013) · 1 papers (2017–2017)Anne‐Karoline Ebert · University of Regensburg1 papers (2020–2020)Wolfgang Rösch · University of Regensburg1 papers (2020–2020) · 1 papers (2020–2020)Martin Promm · University of Regensburg1 papers (2020–2020)