Author

Peter Bergin

Auckland City HospitalORCID 0000-0003-0181-1959Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Assay:electronic health records· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Adam T. HigginsiD· 1 shared Alexander D. ShawiD· 1 shared Anna V. Derrick· 1 shared Charlotte A. Jones· 1 shared Cynthia M. SharpeiD· 1 shared Ed Dudley· 1 shared Ingrid Eileen SchefferiD· 1 shared Jeffrey S. DaviesiD· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Adam T. HigginsORCID

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintAug 10, 2025

Females with epilepsy show abnormal changes to perimenstrual sensory induced long-term potentiation

Malak Alshakhouri, Cynthia M. Sharpe, Peter Bergin…·Rachael L. Sumner

This study shows that females with epilepsy exhibit enhanced visual long-term potentiation (LTP) in the perimenstrual phase compared to mid-follicular and mid-luteal phases, suggesting increased glutamatergic excitation.

DOI 10.1101/2025.08.10.669555

humanelectronic health records

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintApr 1, 2025

Pathogenic ultra-rare variants in SLC6A1, SLC6A11, GAD1 and GAD2 are new & recurrent GABAergic loci for GGE syndromes

Seo‐Kyung Chung, Kate V. Everett, Rhys Huw Thomas…·Mark I. Rees

The paper identifies ultra-rare variants in GABAergic genes associated with genetic generalized epilepsy syndromes and links their functional impact to epilepsy severity.

DOI 10.1101/2025.04.01.24316792

humanwhole-exome sequencing

𝕏 PostBluesky