Author

Akhil Velluva

Max Planck Institute for Evolutionary AnthropologyORCID 0000-0003-0859-3624Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Neuroscience· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Organism:Drosophila· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1

Frequent Co-Authors

Antje GarteniD· 3 shared Diana Le DuciD· 3 shared Linnaeus BundalianiD· 3 shared Achmed MrestaniiD· 2 shared Anna Sophia KirsteiniD· 2 shared Chen-Ching LiniD· 2 shared Johannes R. LemkeiD· 2 shared Julia HentscheliD· 2 shared

Activity by Year

2022-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Antje GartenORCID

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3 papers

Recent·Most cited

NeurosciencebioRxivPreprintOct 16, 2023

Drosophila Bchs overexpression recapitulates human WDFY3 neurodevelopmental phenotypes with implications for glial cell involvement in altered head circumference

Marek B. Körner, Akhil Velluva, Linnaeus Bundalian…·Diana Le Duc

This study shows that overexpression of the Drosophila Bchs gene, an ortholog of human WDFY3, causes neural developmental issues in both neurons and glial cells, mirroring human neurodevelopmental disorders.

DOI 10.1101/2023.10.16.562295

Drosophilabulk RNA-seq

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Genetic & Genomic MedicinemedRxivPreprintJan 17, 2023

The role of rare genetic variants enrichment in epilepsies of presumed genetic etiology

Linnaeus Bundalian, Yin-Yuan Su, Siwei Chen…·Epi25 Collaborative

The paper identifies rare genetic variants associated with different epilepsy types, finding the most enrichment in non-acquired focal epilepsy.

4 citations

humanwhole-exome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicineScientific ReportsPeer-reviewedAug 5, 2022

Altered gene expression profiles impair the nervous system development in individuals with 15q13.3 microdeletion

Marek B. Körner, Akhil Velluva, Linnaeus Bundalian…·Diana Le Duc

The paper identifies altered gene expression patterns in 15q13.3 microdeletion carriers, showing dysregulation of genes involved in brain development and contributing to phenotypic variability.

6 citations

mousebulk RNA-seq

𝕏 PostBluesky