Author

Stephanie Millin

University of Oxford

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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Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:Bayesian inference· 1 Research Focus:clustering· 1 Assay:electronic health records· 1 Organism:human· 1

Frequent Co-Authors

Andrew DahliD· 1 shared Bobby Bojovic· 1 shared Caleb WebberiD· 1 shared Christine BlancheriD· 1 shared Cynthia SandoriD· 1 shared Donald G. GrossetiD· 1 shared Hannah Matten· 1 shared Jonathan MarchiniiD· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperNeuroscience

Andrew DahlORCID

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1 paper

Recent·Most cited

Universal latent axes capturing Parkinson's patient deep phenotypic variation reveals patients with a high genetic risk for Alzheimer's disease are more likely to develop a more aggressive form of Parkinson's.

Cynthia Sandor, Stephanie Millin, Andrew Dahl, Michael Lawton, Leon Hubbard, Bobby Bojovic, Marine Peyret Guzzon, Hannah Matten, Christine Blancher, Nigel M. Williams, Yoav Ben‐Shlomo, Michele T. Hu, Donald G. Grosset, Jonathan Marchini, Caleb Webber

bioRxiv · Feb 18, 2021 · PreprintNeuroscience