Author

Elizabeth K. Ruzzo

University of California, Los AngelesORCID 0000-0003-4024-8556Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:gene regulatory network inference· 2 Assay:whole-genome sequencing· 2 Research Focus:cell type annotation· 1 Assay:scRNA-seq· 1 Research Focus:trajectory inference· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Daniel H. GeschwindiD· 3 shared Jennifer K. LoweiD· 3 shared Damon Polioudakis· 2 shared Dennis Paul WalliD· 2 shared Jae-Yoon JungiD· 2 shared Laura Pérez‐CanoiD· 2 shared Aaron GordoniD· 1 shared Andrew G. Elkins· 1 shared

Activity by Year

2018-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 32 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Daniel H. GeschwindORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Genetic & Genomic MedicineProceedings of the National Academy of SciencesPeer-reviewedJul 28, 2023

The Contributions of Rare Inherited and Polygenic Risk to ASD in Multiplex Families

Matilde Cirnigliaro, Timothy S. Chang, Stephanie A. Arteaga…·Daniel H. Geschwind

This study identifies 74 ASD risk genes using whole genome sequencing of multiplex families and finds polygenic risk interacts with rare inherited variants.

123 citationstop 1%

humanwhole-genome sequencing

𝕏 PostBluesky

NeurosciencebioRxivPreprintAug 28, 2018

A single cell transcriptomic analysis of human neocortical development

Damon Polioudakis, Luis de la Torre-Ubieta, Justin Langerman…·Daniel H. Geschwind

The paper defines single cell transcriptomic profiles of 40,000 human neocortical cells to identify cell types, developmental trajectories, and disease-related gene expression.

7 citations

humanscRNA-seq

𝕏 PostBluesky

GenomicsbioRxivPreprintJun 6, 2018

Whole genome sequencing in multiplex families reveals novel inherited and de novo genetic risk in autism

Elizabeth K. Ruzzo, Laura Pérez‐Cano, Jae-Yoon Jung…·Dennis Paul Wall

This study uses whole-genome sequencing in multiplex families to identify novel inherited and de novo genetic risk factors for autism, revealing 16 new ASD-risk genes and supporting 69 total genes.

7 citations

humanwhole-genome sequencing

𝕏 PostBluesky