Author

Stephanie A. Arteaga

University of California, Los AngelesORCID 0000-0003-1441-8849Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Daniel H. GeschwindiD· 2 shared Jennifer K. LoweiD· 2 shared Matilde CirnigliaroiD· 2 shared Aaron D. BestermaniD· 1 shared Aaron GordoniD· 1 shared Alexander O. Flynn-Carroll· 1 shared Amanda C. GulsrudiD· 1 shared Amaris N. Clay· 1 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Daniel H. GeschwindORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintNov 18, 2025

Common and rare variant genetic contributions in African Americans with autism.

Matilde Cirnigliaro, Jennifer K. Lowe, Alexander O. Flynn-Carroll…·Daniel H. Geschwind

This study examines common and rare variant genetic contributions to autism in African Americans, highlighting differences in genetic effects and polygenic score transferability between European and African ancestries.

4 citations

humanGWAS summary statistics

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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

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