Author

Topun Austin

Cambridge University Hospitals NHS Foundation TrustORCID 0000-0002-8428-8624Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 2 Research Focus:clustering· 1 Approach:experimental assay· 1 Assay:imaging· 1 Assay:spatial transcriptomics· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

A. Edwards· 1 shared Adam PavlinekiD· 1 shared Alba Sanchis‐JuaniD· 1 shared Alex TsompanidisiD· 1 shared Alexander E. P. HeazelliD· 1 shared Alexandra HavdahliD· 1 shared Alice FrankliniD· 1 shared Andrew R. WebsteriD· 1 shared

Activity by Year

2018-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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1 shared paperNeuroscience

A. Edwards

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3 papers

Recent·Most cited

NeurosciencebioRxivPreprintMar 15, 2025

Co-Activation Patterns Characterize Early Resting-State Networks in Newborn Infants: A High-Density Diffuse Optical Tomography Study

Katharine Emily Lee, Julie Uchitel, C. Caballero-Gaudes…·Borja Blanco

This study applies co-activation pattern analysis to neonatal HD-DOT data to identify dynamic functional connectivity features in newborns.

DOI 10.1101/2025.03.15.643385

humanspatial transcriptomics

𝕏 PostBluesky

NeuroscienceBiology of Sex DifferencesPeer-reviewedOct 17, 2024

Sex Differences in Human Brain Structure at Birth

Yumnah T. Khan, Alex Tsompanidis, Marcin A. Radecki…·Simon Baron‐Cohen

The paper examines sex differences in brain structure at birth in newborns, finding larger brain volumes in males and specific regional differences in gray and white matter volumes between sexes.

28 citationstop 1%

𝕏 PostBluesky

GenomicsGenome MedicinePeer-reviewedDec 1, 2018

Complex Structural Variants Resolved by Short-Read and Long-Read Whole Genome Sequencing in Mendelian Disorders

Alba Sanchis‐Juan, Jonathan C. Stephens, Courtney E. French…·Keren Carss

The paper identifies complex structural variants in Mendelian disorders using short-read and long-read sequencing, showing their clinical significance and the utility of long-read technology for resolution.

174 citationstop 1%

humanwhole-genome sequencing

𝕏 PostBluesky