Ricarda Köllges

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

Da I Jung, M. Nöthen, I. V. van Rooij, 2022, HGG advances.

Re‐sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL‐like association, and isolated anorectal malformation

M. Lacher, E. Jenetzky, H. Reutter, 2022, Birth defects research.

Resequencing of VEGFR3 pathway genes implicate GJC2 and FLT4 in the formation of primary congenital chylothorax

B. Strizek, H. Reutter, K. Ludwig, 2022, American journal of medical genetics. Part A.

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

H. Thiele, N. Zwink, E. Jenetzky, 2023, Biomolecules.