Author

Aurea B. Martins-Bach

University of OxfordORCID 0000-0002-7378-0867Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 4

Signature Assays, Organisms & Methods

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Organism:mouse· 3 Approach:statistical model· 3 Research Focus:differential expression· 2 Organism:human· 2 Assay:imaging· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1

Frequent Co-Authors

Karla L. MilleriD· 4 shared Brian J. NiemaniD· 3 shared Elizabeth FisheriD· 3 shared Shoshana SpringiD· 3 shared Thomas J. CunninghamiD· 3 shared Irene García-ToledoiD· 2 shared Irene Jiménez-CocaiD· 2 shared Jason P. LerchiD· 2 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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4 shared papersNeuroscience

Karla L. MillerORCID

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Author profile →

4 papers

Recent·Most cited

Assigning Targetable Pathways to Transdiagnostic Subgroups Across Neurodevelopmental Disorders

Jacob Ellegood, Antoine Beauchamp, Yohan Yee, Gabe Devenyi, Justine Ziolkowski, Lily R. Qiu, Rand Askalan, Muhammad Ayub, Philipp Suetterlin, Alex P. A. Donovan, M. Albert Basson, Katherine Quesnel, Nathalie G. Bérubé, Taeseon Woo, David Quentin Beversdorf, , Jill L. Silverman

The paper identifies molecular pathways associated with neurodevelopmental disorder subgroups using neuroimaging data from mice and humans.

bioRxiv · Mar 4, 2025 · PreprintNeuroscience

TDP-43-M323K causes abnormal brain development and progressive cognitive and motor deficits associated with mislocalised and increased levels of TDP-43.

Juan Miguel Godoy-Corchuelo, Zeinab Ali, José Miguel Brito Armas, Aurea B. Martins-Bach, Irene García-Toledo, Luis C. Fernández-Beltrán, Juan Ignacio López‐Carbonero, Pablo Bascuñana, Shoshana Spring, Irene Jiménez-Coca, Ramón A. Muñoz de Bustillo Alfaro, María José Sánchez-Barrena, R. Nair, Brian J. Nieman, Jason P. Lerch, , Silvia Corrochano

This study characterizes a mouse model with TDP-43 M323K mutation, showing cognitive, motor, and structural brain abnormalities linked to TDP-43 mislocalization and increased levels.

Neurobiology of Disease · Feb 15, 2024Peer-reviewedNeuroscience

FUSDelta14 mutation impairs normal brain development and causes systemic metabolic alterations

Juan Miguel Godoy-Corchuelo, Zeinab Ali, Aurea B. Martins-Bach, Irene García-Toledo, Luis C. Fernández-Beltrán, R. Nair, Shoshana Spring, Brian J. Nieman, Irene Jiménez-Coca, Rasneer Sonia Bains, Hamish Forrest, Jason P. Lerch, Karla L. Miller, Elizabeth Fisher, Thomas J. Cunningham, Silvia Corrochano

This study shows that the FUSDelta14 mutation causes neurodevelopmental and systemic metabolic issues in mice, including brain structural abnormalities and metabolic pathway changes.

bioRxiv · Feb 24, 2023 · PreprintNeuroscience

Phenotypic and genetic associations of quantitative magnetic susceptibility in UK Biobank brain imaging

Chaoyue Wang, Aurea B. Martins-Bach, Fidel Alfaro‐Almagro, Gwenaëlle Douaud, Johannes Christian Klein, Alberto Llera, Cristiana Fiscone, Richard W Bowtell, Lloyd T. Elliott, Stephen M. Smith, Benjamin C. Tendler, Karla L. Miller

The paper develops a QSM pipeline to analyze brain magnetic susceptibility in UK Biobank data, finding associations with iron, disease, and genetic variants.

Nature Neuroscience · May 23, 2022Peer-reviewedNeuroscience