Author

Emily McKinley

University of Alabama at BirminghamORCID 0000-0002-7265-480XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Brittany N. LasseigneiD· 1 shared Bryan A. Moyers· 1 shared David E. Gray· 1 shared David GeldmacheriD· 1 shared Elizabeth A. WortheyiD· 1 shared Erik D. RobersoniD· 1 shared Ethan G. Geier· 1 shared Gregory M. CooperiD· 1 shared

Activity by Year

2019-2019 · 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

Mutual co-authors in cluster

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1 paper

Recent·Most cited

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