Author

Stefanie Caroline Linden

Cardiff UniversityORCID 0000-0003-2120-3811Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Assay:imaging· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1

Frequent Co-Authors

David E.J. LindeniD· 3 shared Jérémy HalliD· 3 shared Marianne B. M. van den BreeiD· 3 shared Michael John OweniD· 3 shared Jacqueline SmithiD· 2 shared Mark DrakesmithiD· 2 shared Nigel M. WilliamsiD· 2 shared Adrian J. HarwoodiD· 1 shared

Activity by Year

2019-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersNeuroscience

David E.J. LindenORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

NeuroscienceMolecular PsychiatryPeer-reviewedJun 10, 2021

Using induced pluripotent stem cells to investigate human neuronal phenotypes in 1q21.1 deletion and duplication syndrome.

Gareth Chapman, Mouhamed Alsaqati, Sharna Lunn…·Yasir Ahmed Syed

This study investigates the effects of 1q21.1 deletion and duplication on neuronal development using induced pluripotent stem cells and shows reciprocal phenotypes and potential therapeutic targets.

27 citations

humanexperimental assay

𝕏 PostBluesky

NeuroscienceTranslational PsychiatryPeer-reviewedSep 21, 2020

Electrophysiological network alterations in adults with copy number variants associated with high neurodevelopmental risk

Diana C. Dima, Rachael Adams, Stefanie Caroline Linden…·Krish D. Singh

This study investigates electrophysiological network changes in adults with neurodevelopmental risk copy number variants using MEG, finding decreased connectivity and network segregation differences.

14 citations

humanimaging

𝕏 PostBluesky

NeuroscienceTranslational PsychiatryPeer-reviewedFeb 25, 2019

Genetic risk for schizophrenia and developmental delay is associated with shape and microstructure of midline white matter structures

Mark Drakesmith, Greg D. Parker, Jacqueline Smith…·David E.J. Linden

The paper investigates how genetic risk for schizophrenia and developmental delay relates to structural brain abnormalities in midline white matter.

31 citations

humanimaging

𝕏 PostBluesky