Author

Sarah A. Dugger

Columbia University Irving Medical CenterORCID 0000-0002-8005-6754Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 3 Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Organism:mouse· 2 Research Focus:benchmarking· 1 Research Focus:clustering· 1 Assay:electronic health records· 1 Approach:experimental assay· 1

Frequent Co-Authors

David B. GoldsteiniD· 3 shared Andrew K. RessleriD· 2 shared Michael J. BolandiD· 2 shared Sabrina Petri· 2 shared Sophie ColomboiD· 2 shared Wayne N. FrankeliD· 2 shared Aaron D. GitleriD· 1 shared Andrew S. AlleniD· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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3 shared papersNeuroscience

David B. GoldsteinORCID

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3 papers

Recent·Most cited

NeurosciencebioRxivPreprintOct 24, 2023

Aberrant Local Synchrony in Distinct Mouse Models of Epileptic Encephalopathy

Andrew K. Ressler, Sarah A. Dugger, Sophie Colombo…·Michael J. Boland

The paper develops topological synchrony measures to identify disease-relevant phenotypes in mouse models of epileptic encephalopathies using MEAs.

DOI 10.1101/2023.10.24.563817

mouseelectronic health records

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NeurosciencebioRxivPreprintMay 1, 2020

Neurodevelopmental deficits and cell-type-specific transcriptomic perturbations in a mouse model of HNRNPU haploinsufficiency

Sarah A. Dugger, Ryan S. Dhindsa, Gabriela Louise de Almeida Sampaio…·David B. Goldstein

This study examines HNRNPU haploinsufficiency in mice, identifying neuroanatomical and transcriptomic changes, and highlights cell-type-specific gene expression dysregulation in excitatory neurons.

8 citations

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GeneticsGenome ResearchPeer-reviewedMay 1, 2019

Regional collapsing of rare variation implicates specific genic regions in ALS

Sahar Gelfman, Sarah A. Dugger, Cristiane Araújo Martins Moreno…·Matthew B. Harms

The paper applies two novel collapsing methods to ALS sequencing data to identify risk regions in known ALS genes and candidate genes.

26 citations

humanwhole-exome sequencing

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