Author

Alexandra K. Davies

Manchester Academic Health Science CentreORCID 0000-0002-1594-8780Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cell Biology· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Organism:human· 2 Approach:experimental assay· 1 Approach:genetic perturbation / CRISPR· 1 Assay:proteomics· 1

Frequent Co-Authors

Afshin SaffariiD· 1 shared Barbora Kuttichova· 1 shared Cedric Böger· 1 shared Clemens M. SauteriD· 1 shared Darius Ebrahimi‐FakhariiD· 1 shared Hyo‐Min KimiD· 1 shared Jared L. SterneckertiD· 1 shared Julian E. AlecuiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperCell Biology

Afshin SaffariORCID

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintJul 19, 2026

Deep axonal proteomics of human iPSC-derived neurons by microfluidic separation and DIA-MS

Clemens M. Sauter, Zac Sandy, Milena Korneck…·Stefan Hauser

This paper reports the deepest human axonal proteome to date using microfluidic separation and DIA-MS on iPSC-derived neurons, identifying axon-enriched proteins and disease-related pathways.

DOI 10.64898/2026.07.17.739061

humanproteomics

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Cell BiologybioRxivPreprintFeb 22, 2025

Arrayed CRISPR/Cas9 Loss-Of-Function Screen in a Neuronal Model of Adaptor Protein Complex 4 Deficiency Identifies Modulators of ATG9A Trafficking

Marvin Ziegler, Cedric Böger, Julian E. Alecu…·Darius Ebrahimi‐Fakhari

The paper uses a CRISPR/Cas9 screen to identify genes modulating ATG9A trafficking in a neuronal model of AP-4 deficiency, revealing ANPEP and NPM1 as key regulators.

DOI 10.1101/2025.02.22.639634

humangenetic perturbation / CRISPR

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