Sophia Schneider

ORCID

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 14

Top Venues

American journal of medical genetics. Part A

Cells

Genes

Biomolecules

This page only lists publications with an associated author ORCID identifier.

Publications

Jonathan B Whitchurch, Sophia Schneider, Alina C Hilger, Ricarda Köllges, Jil D Stegmann, Lea Waffenschmidt, Laura Dyer, Holger Thiele, Bhanupriya Dhabhai, Tikam Chand Dakal, Andreas Müller, Dominic P Norris, Heiko Martin Reutter
PKD1L1 Is Involved in Congenital Chylothorax. Cells 13 (2) (2024)
Jonathan B Whitchurch, Sophia Schneider, Alina C Hilger, Ricarda Köllges, Jil D Stegmann, Lea Waffenschmidt, Laura Dyer, Holger Thiele, Bhanupriya Dhabhai, Tikam Chand Dakal, Andreas Müller, Dominic P Norris, Heiko Martin Reutter
PKD1L1 Is Involved in Congenital Chylothorax. Cells 13 (2) (2024)
Jonathan B Whitchurch, Sophia Schneider, Alina C Hilger, Ricarda Köllges, Jil D Stegmann, Lea Waffenschmidt, Laura Dyer, Holger Thiele, Bhanupriya Dhabhai, Tikam Chand Dakal, Andreas Müller, Dominic P Norris, Heiko Martin Reutter
PKD1L1 Is Involved in Congenital Chylothorax. Cells 13 (2) (2024)
Jonathan B Whitchurch, Sophia Schneider, Alina C Hilger, Ricarda Köllges, Jil D Stegmann, Lea Waffenschmidt, Laura Dyer, Holger Thiele, Bhanupriya Dhabhai, Tikam Chand Dakal, Andreas Müller, Dominic P Norris, Heiko Martin Reutter
PKD1L1 Is Involved in Congenital Chylothorax. Cells 13 (2) (2024)
Jonathan B Whitchurch, Sophia Schneider, Alina C Hilger, Ricarda Köllges, Jil D Stegmann, Lea Waffenschmidt, Laura Dyer, Holger Thiele, Bhanupriya Dhabhai, Tikam Chand Dakal, Andreas Müller, Dominic P Norris, Heiko Martin Reutter
PKD1L1 Is Involved in Congenital Chylothorax. Cells 13 (2) (2024)
Caroline M Kolvenbach, Aihua Zhang, Lea M Merz, Nils D Mertens, Bshara Mansour, Chunyan Wang, Steve Seltzsam, Sophia Schneider, Luca Schierbaum, Dalia Pantel, Jing Chen, Amelie T van der Ven, Jibril O Bello, Shirlee Shril, Friedhelm Hildebrandt
A homozygous truncating ETV4 variant in a Nigerian family with congenital anomalies of the kidney and urinary tract. American journal of medical genetics. Part A (2023)
Caroline M Kolvenbach, Aihua Zhang, Lea M Merz, Nils D Mertens, Bshara Mansour, Chunyan Wang, Steve Seltzsam, Sophia Schneider, Luca Schierbaum, Dalia Pantel, Jing Chen, Amelie T van der Ven, Jibril O Bello, Shirlee Shril, Friedhelm Hildebrandt
A homozygous truncating ETV4 variant in a Nigerian family with congenital anomalies of the kidney and urinary tract. American journal of medical genetics. Part A (2023)
Sophia Schneider, Luca Schierbaum, Wessel A C Burger, Steve Seltzsam, Chunyan Wang, Bixia Zheng, Chen-Han Wilfred Wu, Makiko Nakayama, Dervla M Connaughton, Nina Mann, Mohamed A Shalaby, Jameela A Kari, Sherif ElDesoky, Velibor Tasic, Loai A Eid, Shirlee Shril, David M Thal, Friedhelm Hildebrandt
Recessive CHRM5 variant as a potential cause of neurogenic bladder. American journal of medical genetics. Part A (2023)
Ricarda Köllges, Jil Stegmann, Sophia Schneider, Lea Waffenschmidt, Julia Fazaal, Katinka Breuer, Alina C Hilger, Gabriel C Dworschak, Enrico Mingardo, Wolfgang Rösch, Aybike Hofmann, Claudia Neissner, Anne-Karolin Ebert, Raimund Stein, Nina Younsi, Karin Hirsch-Koch, Eberhard Schmiedeke, Nadine Zwink, Ekkehart Jenetzky, Holger Thiele, Kerstin U Ludwig, Heiko Martin Reutter
Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease Formation. Biomolecules 13 (7) (2023)
Sophia Schneider, Ricarda Köllges, Jil D Stegmann, Frederic Thieme, Alina C Hilger, Lea Waffenschmidt, Julia Fazaal, Jeshurun C Kalanithy, Annegret Geipel, Brigitte Strizek, Kerstin U Ludwig, Heiko Martin Reutter, Andreas Müller
Resequencing of VEGFR3 pathway genes implicate GJC2 and FLT4 in the formation of primary congenital chylothorax. American journal of medical genetics. Part A 188 (5) (2022)
Chunyan Wang, Steve Seltzsam, Bixia Zheng, Chen-Han Wilfred Wu, Camille Nicolas-Frank, Kirollos Yousef, Kit Sing Au, Nina Mann, Dalia Pantel, Sophia Schneider, Luca Schierbaum, Thomas M Kitzler, Dervla M Connaughton, Youying Mao, Rufeng Dai, Makiko Nakayama, Jameela A Kari, Sherif El Desoky, Mohammed Shalaby, Loai A Eid, Hazem S Awad, Velibor Tasic, Shrikant M Mane, Richard P Lifton, Michelle A Baum, Shirlee Shril, Carlos R Estrada, Friedhelm Hildebrandt
Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models. American journal of medical genetics. Part A 188 (5) (2022)
Bixia Zheng, Chunyan Wang, Steve Seltzsam, Sophia Schneider, Luca Schierbaum, Wilfred Wu, Rufeng Dai, Dervla M Connaughton, Makiko Nakayama, Nina Mann, Stuart B Bauer, Hazem S Awad, Loai A Eid, Velibor Tasic, Shirlee Shril, Friedhelm Hildebrandt
A truncating NRIP1 variant in an Arabic family with congenital anomalies of the kidneys and urinary tract. American journal of medical genetics. Part A (2021)
Caroline M Kolvenbach, Amelie T van der Ven, Franziska Kause, Shirlee Shril, Marcello Scala, Dervla M Connaughton, Nina Mann, Makiko Nakayama, Rufeng Dai, Thomas M Kitzler, Ronen Schneider, Luca Schierbaum, Sophia Schneider, Andrea Accogli, Annalaura Torella, Gianluca Piatelli, Vincenzo Nigro, Valeria Capra, Bernd Hoppe, Stefanie Märzheuser, Eberhard Schmiedeke, Heidi L Rehm, Shrikant Mane, Richard P Lifton, Gabriel C Dworschak, Alina C Hilger, Heiko Martin Reutter, Friedhelm Hildebrandt
Exome survey of individuals affected by VATER/VACTERL with renal phenotypes identifies phenocopies and novel candidate genes. American journal of medical genetics. Part A 185 (12) (2021)
Luca M Schierbaum, Sophia Schneider, Stefan Herms, Sugirthan Sivalingam, Julia Fabian, Heiko Martin Reutter, Stefanie Weber, Waltraut M Merz, Marcin Tkaczyk, Monika Miklaszewska, Przemysław Sikora, Agnieszka Szmigielska, Grazyna Krzemien, Katarzyna Zachwieja, Shaji K Kumar, Katarzyna Taranta-Janusz, Pawel Kroll, Marcin Polok, Marcin Zaniew, Alina C Hilger
Genome-Wide Survey for Microdeletions or -Duplications in 155 Patients with Lower Urinary Tract Obstructions (LUTO). Genes 12 (9) (2021)

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Publication Activity (10 Years)

Top Topics

Top Venues

Sophia Schneider