Sophia Schneider
9PUBLICATIONS
22CO-AUTHORS
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Publications (9)
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|Jan 22, 2024
PKD1L1 Is Involved in Congenital Chylothorax.Jonathan B Whitchurch, Sophia Schneider, Alina C Hilger
|Jul 29, 2023
Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease Formation.Ricarda Köllges, Jil Stegmann, Sophia Schneider
|May 22, 2023
Recessive CHRM5 variant as a potential cause of neurogenic bladder.Sophia Schneider, Luca Schierbaum, Wessel A C Burger
|Jan 24, 2023
A homozygous truncating ETV4 variant in a Nigerian family with congenital anomalies of the kidney and urinary tract.Caroline M Kolvenbach, Bixia Zheng, Lea M Merz
|Jan 18, 2022
Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models.Chunyan Wang, Steve Seltzsam, Bixia Zheng
|Jan 07, 2022
Resequencing of VEGFR3 pathway genes implicate GJC2 and FLT4 in the formation of primary congenital chylothorax.Sophia Schneider, Ricarda Köllges, Jil D Stegmann
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Frequent Collaborators
5 joint publications
Heiko Reutter
5 joint publications
Friedhelm Hildebrandt
1 joint publications
Caroline M Kolvenbach
1 joint publications
Stefan Herms
1 joint publications
Sugirthan Sivalingam
1 joint publications
Marcin Tkaczyk
1 joint publications
Monika Miklaszewska
1 joint publications
Przemyslaw Sikora
1 joint publications
Maria Szczepanska
1 joint publications
Katarzyna Taranta-Janusz
