Author

Anna M. Karydas

University of California, San Francisco

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

Frequent Co-Authors

Brittany N. LasseigneiD· 1 shared Bruce L. MilleriD· 1 shared Erik D. RobersoniD· 1 shared Ethan G. Geier· 1 shared Gil Dan RabinoviciiD· 1 shared Gregory M. CooperiD· 1 shared J. Nicholas CochraniD· 1 shared J. Scott Newberry· 1 shared

Activity by Year

2020-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperNeuroscience

Brittany N. LasseigneORCID

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1 paper

Recent·Most cited

Non-Coding and Loss-of-Function Coding Variants in TET2 are Associated with Multiple Neurodegenerative Diseases

J. Nicholas Cochran, Ethan G. Geier, Luke W. Bonham, J. Scott Newberry, Michelle D. Amaral, Michelle L. Thompson, Brittany N. Lasseigne, Anna M. Karydas, Erik D. Roberson, Gregory M. Cooper, Gil Dan Rabinovici, Bruce L. Miller, R Myers, Jennifer S. Yokoyama

The paper identifies rare variants in TET2 associated with early-onset Alzheimer's disease and frontotemporal dementia, highlighting both coding and non-coding variants as risk factors.

The American Journal of Human Genetics · Apr 23, 2020Peer-reviewedNeuroscience