Author

Princess Carter

University of Alabama at Birmingham

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

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Belle A. MoyersiD· 1 shared Carter WrightiD· 1 shared David GeldmacheriD· 1 shared Erik D. RobersoniD· 1 shared J. Nicholas CochraniD· 1 shared James M.J. LawloriD· 1 shared Jared W. Taylor· 1 shared Marissa Natelson LoveiD· 1 shared

Activity by Year

2023-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Belle A. MoyersORCID

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1 paper

Recent·Most cited

Contributions of rare and common variation to early-onset and atypical dementia risk

Carter Wright, Jared W. Taylor, J. Nicholas Cochran, James M.J. Lawlor, Belle A. Moyers, Michelle D. Amaral, Zachary T Bonnstetter, Princess Carter, Veronika Solomon, R Myers, Marissa Natelson Love, David Geldmacher, Sara J. Cooper, Erik D. Roberson

The paper analyzes genomic data from early-onset and atypical dementia patients to show that both rare and common genetic variations contribute to dementia risk.

Molecular Case Studies · Jun 1, 2023Peer-reviewedGenetic & Genomic Medicine