Author

Stefka Mincheva-Tasheva

South Australian Health and Medical Research InstituteORCID 0000-0002-1394-580XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:mouse· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Assay:electronic health records· 1 Organism:human· 1 Research Focus:spatial domain detection· 1 Assay:spatial transcriptomics· 1

Frequent Co-Authors

Daniel T. PederickiD· 2 shared Paul Quinton ThomasiD· 2 shared Sandra PiltziD· 2 shared Ingrid Eileen SchefferiD· 1 shared James Nicholas Hughes· 1 shared Jozef GécziD· 1 shared Julien BensalemiD· 1 shared Kay RichardsiD· 1 shared

Activity by Year

2018-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersNeuroscience

Daniel T. PederickORCID

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintMar 14, 2024

Functional analysis of the epilepsy gene Pcdh19 using a novel conditional GFP-reporter mouse model

Stefka Mincheva-Tasheva, Michaela A. Scherer, Louise J. Robertson…·Paul Quinton Thomas

This paper develops a conditional Pcdh19 knockout mouse model with GFP reporter to study PCDH19's role in brain development and disease.

DOI 10.1101/2024.03.14.584898

mouseexperimental assay

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Developmental BiologyNeuronPeer-reviewedJan 1, 2018

Abnormal cell sorting underlies the unique X-linked inheritance of PCDH19 Epilepsy

Daniel T. Pederick, Kay Richards, Sandra Piltz…·Paul Quinton Thomas

The paper shows that PCDH19 mutations in females cause abnormal cell sorting in the developing cortex, leading to epilepsy, while males are unaffected due to normal sorting.

122 citationstop 1%

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