Author

Jan Doering

German Center for Neurodegenerative DiseasesORCID 0000-0001-9731-0790Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:imaging· 1 Organism:mouse· 1 Research Focus:spatial domain detection· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Albrecht StrohiD· 1 shared Alejandro LealiD· 1 shared Annemarie Schwan· 1 shared Bernt PoppiD· 1 shared Carsten FinkeiD· 1 shared Christian RothiD· 1 shared Diana Le DuciD· 1 shared Harald PrüßiD· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperNeuroscience

Albrecht StrohORCID

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintNov 30, 2023

Maternofetal transfer of human NMDAR-antibodies leads to cortical network defect in adolescence

Saleh Altahini, Jan Doering, Joseph Kuchling…·Albrecht Stroh

This study shows that maternal-fetal transfer of NMDAR-antibodies causes lasting impairments in adolescent brain network function and connectivity.

DOI 10.1101/2023.11.30.569370

𝕏 PostBluesky

Genetic & Genomic MedicineEuropean Journal of Human GeneticsPeer-reviewedOct 25, 2021

Prenatal phenotype of PNKP-related primary microcephaly associated with variants in the FHA and Phosphatase domain

Sonja Neuser, Ilona Krey, Annemarie Schwan…·Bernt Popp

The paper describes the prenatal phenotype of PNKP-related primary microcephaly and characterizes the effects of variants using RNA analysis and structural modeling.

8 citations

humanwhole-exome sequencing

𝕏 PostBluesky