Ronen Schneider
4PUBLICATIONS
25CO-AUTHORS
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Publications (4)
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|Nov 15, 2022
X-linked variations in SHROOM4 are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems.Caroline M Kolvenbach, Tim Felger, Luca Schierbaum
|Feb 01, 2021
Recessive NOS1AP variants impair actin remodeling and cause glomerulopathy in humans and mice.Amar J Majmundar, Florian Buerger, Thomas A Forbes
|Jul 08, 2020
DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes.Jonathan Marquez, Nina Mann, Kathya Arana
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Frequent Collaborators
2 joint publications
Eugen Widmeier
1 joint publications
Jonathan Marquez
1 joint publications
Saquib Ali Lakhani
1 joint publications
Heiko M Reutter
1 joint publications
Gabriel C Dworschak
1 joint publications
Amar J Majmundar
1 joint publications
Florian Buerger
1 joint publications
Thomas A Forbes
1 joint publications
Konstantin Deutsch
1 joint publications
Ihsan Ullah
