Author

Walid Fazeli

University Hospital BonnORCID 0000-0002-9425-5535Unclaimed 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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Approach:statistical model· 2 Research Focus:cell type annotation· 1 Assay:electronic health records· 1 Research Focus:genome assembly· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

Alba Sanchis‐JuaniD· 1 shared Amélie PitoniD· 1 shared Amy McTagueiD· 1 shared Anne de Saint MartiniD· 1 shared Argirios DinopoulosiD· 1 shared Arthur J. CampbelliD· 1 shared Birgit EngelandiD· 1 shared Damien LedereriD· 1 shared

Activity by Year

2021-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alba Sanchis‐JuanORCID

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintJun 29, 2025

Early postnatal CA3 hyperexcitability drives hippocampal development and epileptogenesis in SCN2A developmental and epileptic encephalopathy

Yana Reva, Katharina Ulrich, Xian Xin…·Dirk Isbrandt

This study shows that early postnatal CA3 hyperexcitability drives hippocampal development and epileptogenesis in SCN2A-DEE, suggesting it as a therapeutic target.

2 citations

mouseelectronic health records

Genetic & Genomic MedicineGenetics in MedicinePeer-reviewedDec 6, 2021

Structural mapping of GABRB3 variants reveals genotype-phenotype correlation

Katrine M. Johannesen, Sumaiya Iqbal, Milena Guazzi…·Elena Gardella

The paper analyzes GABRB3 variants in a cohort of 71 individuals to identify genotype-phenotype correlations, finding associations between variant locations and specific clinical features.

23 citations

humanstatistical model