Author

J. Scott Newberry

HudsonAlpha Institute for Biotechnology

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· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Brittany N. LasseigneiD· 2 shared Erik D. RobersoniD· 2 shared Ethan G. Geier· 2 shared Gregory M. CooperiD· 2 shared J. Nicholas CochraniD· 2 shared Jennifer S. YokoyamaiD· 2 shared Michelle D. Amaral· 2 shared Michelle L. ThompsoniD· 2 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersNeuroscience

Brittany N. LasseigneORCID

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2 papers

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

Genome sequencing for early-onset dementia: high diagnostic yield and frequent observation of multiple contributory alleles

J. Nicholas Cochran, Emily McKinley, J. Nicholas Cochran, Michelle D. Amaral, Bryan A. Moyers, Brittany N. Lasseigne, David E. Gray, James M.J. Lawlor, Jeremy W. Prokop, Ethan G. Geier, James Holt, Michelle L. Thompson, J. Scott Newberry, Jennifer S. Yokoyama, Elizabeth A. Worthey, , Erik D. Roberson

Genome sequencing for early-onset dementia identified genetic variants in 50% of patients, including pathogenic variants and moderate penetrance alleles, supporting an oligogenic model.

Molecular Case Studies · Dec 13, 2019Peer-reviewedNeuroscience