Nicole Spychalski

Statistics

Publications

Citations

102

H-Index

Active since

2011

Affiliations

University Hospital Bonn(Current)

Cnopf´sche Kinderklinik

Leipzig University

University of Bonn

University Hospital Cologne

Nicole Spychalski is an author at University Hospital Bonn specializing in molecular genetics, congenital anorectal malformations, and congenital malformations.

Publications per year

2011–2022

Publications

Involvement of the WNT and FGF signaling pathways in non-isolated anorectal malformations: Sequencing analysis of WNT3A, WNT5A, WNT11, DACT1, FGF10, FGFR2 and the T gene

Markus Draaken, WIEBKE PRINS, Claudia Zeidler et al. · International Journal of Molecular Medicine · 2012 · 32 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

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

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

Rong Zhang, Jan Gehlen, Amit Kawalia et al. · PLoS ONE · 2020 · 17 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

German Network for Congenital Uro-REctal Malformations: first evaluation and interpretation of postoperative urological complications in anorectal malformations

Stefanie Maerzheuser, Ekkehart Jenetzky, Nadine Zwink et al. · Pediatric Surgery International · 2011 · 13 citations

Medicine, Surgery, Urology +14

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

Jan Gehlen, Ann-Sophie Giel, Ricarda Köllges et al. · Human Genetics and Genomics Advances · 2022 · 10 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

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