Julian Schröter

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 8

Top Topics

Intellectual Disability

Congenital Heart Disease

Functional Connectivity

Artificial Intelligence

Top Venues

Scientific data

Journal of inherited metabolic disease

European journal of human genetics : EJHG

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

Publications

Julian Schröter, Luca Deininger, Blaz Lupse, Petra Richter, Steffen Syrbe, Ralf Mikut, Sabine Jung-Klawitter
A large and diverse brain organoid dataset of 1,400 cross-laboratory images of 64 trackable brain organoids. Scientific data 11 (1) (2024)
Julian Schröter, Luca Deininger, Blaz Lupse, Petra Richter, Steffen Syrbe, Ralf Mikut, Sabine Jung-Klawitter
A large and diverse brain organoid dataset of 1,400 cross-laboratory images of 64 trackable brain organoids. Scientific data 11 (1) (2024)
Julian Schröter, Luca Deininger, Blaz Lupse, Petra Richter, Steffen Syrbe, Ralf Mikut, Sabine Jung-Klawitter
A large and diverse brain organoid dataset of 1,400 cross-laboratory images of 64 trackable brain organoids. Scientific data 11 (1) (2024)
Imke M E Schuurmans, Bianca Dimitrov, Julian Schröter, Antonia Ribes, Rubén Pérez de la Fuente, Berta Zamora, Clara D M van Karnebeek, Stefan Kölker, Alejandro Garanto
Exploring genotype-phenotype correlations in glutaric aciduria type 1. Journal of inherited metabolic disease (2023)
Julian Schröter, Bernt Popp, Heiko Brennenstuhl, Jan H Döring, Stephany H Donze, Emilia K Bijlsma, Arie van Haeringen, Dagmar Huhle, Leonie Jestaedt, Andreas Merkenschlager, Maria Arelin, Daniel Gräfe, Sonja Neuser, Stephanie Oates, Deb K Pal, Michael J Parker, Johannes R Lemke, Georg F Hoffmann, Stefan Kölker, Inga Harting, Steffen Syrbe
Complementing the phenotypical spectrum of TUBA1A tubulinopathy and its role in early-onset epilepsies. European journal of human genetics : EJHG 30 (3) (2022)
Francesca Semino, Julian Schröter, Marjolein H Willemsen, Thomas Bast, Saskia Biskup, Stefanie Beck-Woedl, Heiko Brennenstuhl, Christian P Schaaf, Stefan Kölker, Georg F Hoffmann, Tobias B Haack, Steffen Syrbe
Further evidence for de novo variants in SYNCRIP as the cause of a neurodevelopmental disorder. Human mutation 42 (9) (2021)
Jan H Döring, Julian Schröter, Jerome Jüngling, Saskia Biskup, Kerstin Alexandra Klotz, Thomas Bast, Tobias Dietel, G Christoph Korenke, Sophie Christoph, Heiko Brennenstuhl, Guido Rubboli, Rikke Steensjerre Moller, Gaetan Lesca, Yves Chaix, Stefan Kölker, Georg Friedrich Hoffmann, Johannes R Lemke, Steffen Syrbe
Refining Genotypes and Phenotypes in KCNA2-Related Neurological Disorders. International journal of molecular sciences 22 (6) (2021)
Julian Schröter, Jan H Döring, Sven F Garbade, Georg F Hoffmann, Stefan Kölker, Markus Ries, Steffen Syrbe
Cross-sectional quantitative analysis of the natural history of TUBA1A and TUBB2B tubulinopathies. Genetics in medicine : official journal of the American College of Medical Genetics 23 (3) (2020)