Author

Julian Goggi

Agency for Science, Technology and ResearchORCID 0000-0002-3021-3184Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:benchmarking· 1 Research Focus:drug response / drug discovery· 1 Organism:human· 1 Assay:imaging· 1 Organism:mouse· 1 Organism:zebrafish· 1

Frequent Co-Authors

Alexander P.A. StegmanniD· 1 shared Anna M. BarroniD· 1 shared Anselm Salvatore VincentiD· 1 shared Arnette Shi Wei WongiD· 1 shared Barry J. CoulliD· 1 shared Boominathan Ramasamy· 1 shared Chernis Guai Mun Low· 1 shared David J. AmoriD· 1 shared

Activity by Year

2018-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetics

Alexander P.A. StegmannORCID

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintAug 13, 2023

Mitochondrial complex I as a diagnostic and therapeutic target in a mouse model of tauopathy

Jia Hui Wong, Anselm Salvatore Vincent, Shivashankar Khanapur…·Anna M. Barron

This study uses MC-I-PET to assess mitochondrial dysfunction in a tauopathy mouse model and evaluates the therapeutic effects of Mdivi-1, finding no rescue of mitochondrial deficits despite tau reduction and harmful effects of Mdivi-1.

DOI 10.1101/2023.08.13.552232

mouseimaging

𝕏 PostBluesky

GeneticsHuman Molecular GeneticsPeer-reviewedMay 3, 2018

Functional analysis of a hypomorphic allele shows that MMP14 catalytic activity is the prime determinant of the Winchester syndrome phenotype

Ivo J. H. M. de Vos, Evelyn Yaqiong Tao, Sheena L. M. Ong…·Maurice A. M. Van Steensel

The paper identifies a hypomorphic MMP14 mutation in Winchester syndrome and shows its catalytic activity determines disease severity using in vitro and zebrafish models.

30 citations

humanzebrafish

𝕏 PostBluesky