Author

Laura R. Nementzik

University of Auckland

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:cell type annotation· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Assay:protein structure· 1 Research Focus:spatial domain detection· 1 Approach:statistical model· 1

Frequent Co-Authors

Emma L. ScotteriD· 2 shared Garth A. NicholsoniD· 2 shared Ian P. BlairiD· 2 shared Kyrah M. ThumbadooiD· 2 shared Maurice A. CurtisiD· 2 shared Richard L. M. FaulliD· 2 shared Birger Victor DieriksiD· 1 shared Catriona McLeaniD· 1 shared

Activity by Year

2023-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 42 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Emma L. ScotterORCID

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2 papers

Recent·Most cited

A meta-analysis of genetic variant pathogenicity and sex differences in UBQLN2-linked amyotrophic lateral sclerosis and frontotemporal dementia

Kyrah M. Thumbadoo, Laura R. Nementzik, Molly E.V. Swanson, Birger Victor Dieriks, Michael Dragunow, Richard L. M. Faull, Maurice A. Curtis, Ian P. Blair, Garth A. Nicholson, Kelly L. Williams, Emma L. Scotter

This paper performs a meta-analysis of UBQLN2 genetic variants in ALS/FTD, finding sex-specific differences in age at onset and aggregate burden in brain tissue.

medRxiv · Oct 25, 2024 · PreprintGenetic & Genomic Medicine

Distribution of ubiquilin 2 and TDP-43 aggregates throughout the CNS in UBQLN2 p.T487I-linked amyotrophic lateral sclerosis and frontotemporal dementia

Laura R. Nementzik, Kyrah M. Thumbadoo, Helen C. Murray, David Gordon, Shu Yang, Ian P. Blair, Clinton P. Turner, Richard L. M. Faull, Maurice A. Curtis, Catriona McLean, Garth A. Nicholson, Molly E. V. Swanson, Emma L. Scotter

The paper compares ubiquilin 2 and TDP-43 aggregate distribution in UBQLN2-linked and sporadic ALS/FTD cases across the CNS.

bioRxiv · Feb 10, 2023 · PreprintNeuroscience