Author

Stephen J. Guter

University of Illinois ChicagoORCID 0000-0002-4476-2045Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:gene regulatory network inference· 1 Assay:GWAS summary statistics· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alfredo BruscoiD· 2 shared Andreas G. ChiocchettiiD· 2 shared Ángel CarracedoiD· 2 shared Benjamin M. NealeiD· 2 shared Chiara FalleriniiD· 2 shared Christine Margarete FreitagiD· 2 shared Christine R. StevensiD· 2 shared F. Kyle SatterstromiD· 2 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Alfredo BruscoORCID

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2 papers

Recent·Most cited

Rare variation illuminates the distinct and pleiotropic genetic architecture of autism across neuropsychiatric traits

F. Kyle Satterstrom, Chiara Auwerx, Jack M. Fu, Zhancheng Zhang, Susan S. Kuo, Emily Hang, Wenhan Lu, Michelle M. Morrow, Julia Sealock, Calwing Liao, Marina Natividad Avila, Caroline M. Cusick, Christine R. Stevens, Juha M Karjalainen, Stephen J. Guter, , Mark J. Daly

The paper identifies 253 autism-associated genes using rare variation from 62,429 individuals and finds pleiotropy across physiological systems and developmental disorders.

medRxiv · Aug 26, 2026 · PreprintGenetic & Genomic Medicine

Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

F. Kyle Satterstrom, Jack A. Kosmicki, Jiebiao Wang, Michael S. Breen, Silvia De Rubeis, Joon‐Yong An, Minshi Peng, Ryan L. Collins, Jakob Grove, Lambertus Klei, Christine R. Stevens, Jennifer G. Reichert, Maureen Mulhern, Mykyta Artomov, Sherif Gerges, , Kaija Puura

This study identifies 99 genes associated with autism spectrum disorder through large-scale exome sequencing, showing differences in mutation frequencies between ASD and severe neurodevelopmental delay groups.

Cell · Jan 1, 2019Peer-reviewedGenetics