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Journal of Proteome Research|August 12, 2021
iBRET Screen of the ABCD1 Peroxisomal Network and Mutation-Induced Network PerturbationsAmelie S Lotz-Havla, Mathias Woidy, Philipp Guder, et al.Annals of Neurology|September 26, 2021
Dominant KPNA3 Mutations Cause Infantile-Onset Hereditary Spastic ParaplegiaClaudia Schob, Maja Hempel, Dana Safka Brozkova, et al.Frontiers in Immunology|August 1, 2022
Specific CD4+ T Cell Responses to Ancestral SARS-CoV-2 in Children Increase With Age and Show Cross-Reactivity to Beta VariantKevin Paul, Freya Sibbertsen, Daniela Weiskopf, et al.Journal of Clinical Immunology|September 19, 2022
Long-Term Antibody Response to SARS-CoV-2 in ChildrenGabor A Dunay, Madalena Barroso, Mathias Woidy, et al.The Journal of Clinical Investigation|April 4, 2023
Accumulation of α-synuclein mediates podocyte injury in Fabry nephropathyFabian Braun, Ahmed Abed, Dominik Sellung, et al.Brain : a Journal of Neurology|August 8, 2020
Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorderPauline E Schneeberger, Fanny Kortüm, Georg Christoph Korenke, et al.Brain : a Journal of Neurology|November 15, 2025
The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiencyKajus Merkevicius, Dmitrii Smirnov, Lea D Schlieben, et al.Pageof 2