Amelie van der Ven

Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract

Asaf Vivante, Daw‐Yang Hwang, Stefan Kohl et al. · Journal of the American Society of Nephrology · 2016 · 98 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate<i>ZIC3</i>and<i>FOXF1</i>in Human VATER/VACTERL Association

Alina C. Hilger, Jan Halbritter, Tracie Pennimpede et al. · Human Mutation · 2015 · 56 citations

Life Sciences, Genetics, Molecular Genetics +14

Preventing Preterm Birth with Progesterone in Women with a Short Cervical Length from a Low-Risk Population: A Multicenter Double-Blind Placebo-Controlled Randomized Trial

Amelie van der Ven, C. Emily Kleinrouweler, Ewoud Schuit et al. · American Journal of Perinatology · 2015 · 51 citations · Full text

Medicine, Maternal Health, Obstetrics +15

Array‐based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL‐like patients identifies disease‐causing copy number variations

Rong Zhang, Florian Marsch, Franziska Kause et al. · Birth Defects Research · 2017 · 30 citations

Medicine, Molecular Biology, Molecular Genetics +17

Modulating effects of FGF12 variants on NaV1.2 and NaV1.6 being associated with developmental and epileptic encephalopathy and Autism spectrum disorder: A case series

Simone Seiffert, Manuela Pendziwiat, Tatjana Bierhals et al. · EBioMedicine · 2022 · 30 citations · Full text

Life Sciences, Genetics, Neuroscience +17