Author

Nancy J. Minshew

University of PittsburghORCID 0000-0001-7875-1929Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Assay:imaging· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aarno V. PalotieiD· 1 shared Alexander KolevzoniD· 1 shared Alfredo BruscoiD· 1 shared Andreas G. ChiocchettiiD· 1 shared Ángel CarracedoiD· 1 shared Antonio Maria PersicoiD· 1 shared Aparna BhaduriiD· 1 shared Astanand JugessuriD· 1 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Aarno V. PalotieORCID

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2 papers

Recent·Most cited

Uncharacteristic task-evoked pupillary responses implicate atypical locus coeruleus activity in autism

Michael C. Granovetter, Charlie S. Burlingham, Nicholas M. Blauch, Nancy J. Minshew, David J. Heeger, Marlene Behrmann

This study finds that individuals with ASD show atypical pupillary responses to distractor stimuli, suggesting altered locus coeruleus activity during attentional tasks.

Journal of Neuroscience · Apr 6, 2020Peer-reviewedNeuroscience

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