Author

Woojin Scott Kim

The University of SydneyORCID 0000-0002-4707-933XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 3 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 3 Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Approach:statistical model· 2 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1 Assay:protein structure· 1

Frequent Co-Authors

Glenda Margaret HallidayiD· 2 shared Ahmet Aydogan· 1 shared Angela S. LairdiD· 1 shared Anthony Choi· 1 shared Anthony Simon DoniD· 1 shared Aykut Göktürk ÜneriD· 1 shared Barbara J. CaldaroneiD· 1 shared Benedikt FriegiD· 1 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 13 mutual co-author links

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2 shared papersNeuroscience

Glenda Margaret HallidayORCID

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4 papers

Recent·Most cited

Reduced plasma hexosylceramides in frontotemporal dementia are a biomarker of white matter integrity

Oana C. Marian, Sophie Matis, Carol Dobson‐Stone, Woojin Scott Kim, John B. Kwok, Olivier Piguet, Glenda Margaret Halliday, Ramón Landín-Romero, Anthony Simon Don

Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring · Apr 1, 2025Peer-reviewedNeuroscience

GABAergic LRP1 is a key link between obesity and memory function

Aykut Göktürk Üner, Zhi-Shuai Hou, Ahmet Aydogan, KELLEN RODRIGUES, Jennie Young, Anthony Choi, Won‐Mo Yang, Woojin Scott Kim, Vincent Prévot, Barbara J. Caldarone, Bradley T. Hyman, Hyon Lee, Young‐Bum Kim

This study shows that deleting LRP1 in GABAergic neurons causes memory impairments and obesity in mice, linking LRP1 function to metabolic and cognitive health.

bioRxiv · Sep 17, 2022 · PreprintNeuroscience

α-Synuclein polymorphism determines oligodendroglial dysfunction

Benedikt Frieg, James A. Geraets, Timo Strohäker, Christian Dienemann, Panagiota Mavroeidi, Byung Chul Jung, Woojin Scott Kim, Seung‐Jae Lee, Maria Xilouri, Markus Zweckstetter, G.F. Schroeder

This study compares α-synuclein fibril structures from Parkinson's disease and Multiple System Atrophy patients, showing differences in their quaternary arrangement and effects on oligodendroglial cells.

bioRxiv · Jul 9, 2021 · PreprintNeuroscience

Accelerated loss of hypoxia response in zebrafish with familial Alzheimer's disease-like mutation of Presenilin 1.

Morgan Newman, Seyyed Hani Moussavi Nik, Greg Trevor Sutherland, Nhi Hin, Woojin Scott Kim, Glenda Margaret Halliday, Suman Jayadev, Carole Smith, Angela S. Laird, Caitlin W. Lucas, Thaksaon Kittipassorn, Dan Peet, Michael T. Lardelli

This study shows that zebrafish with PSEN1 mutations exhibit accelerated hypoxia response loss with age, suggesting a link between PSEN1 dysfunction and Alzheimer's disease pathogenesis.

Human Molecular Genetics · Jun 16, 2020Peer-reviewedGenomics