Author

Jonathan Sebat

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genomics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Abhishek Bhandari· 1 shared Alexandra G Moyzis· 1 shared Alysson R Muotri· 1 shared Amanda C Watts· 1 shared Amina NooriD· 1 shared Benjamin ClarkiD· 1 shared Bhooma ThiruvahindrapuramiD· 1 shared Celia M.T. GreenwoodiD· 1 shared

Activity by Year

2015-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenomics

Abhishek Bhandari

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2 papers

Recent·Most cited

Genomic deletion and duplication effects on cognitive ability lie at the opposing ends of the cortical sensorimotor-association hierarchy

Kuldeep Kumar, Sayeh Kazem, Jane Yang, Florian Bénitière, Mame Seynabou Diop, Benjamin Clark, Guillaume Huguet, Worrawat Engchuan, Jakub Kopál, Thomas Renne, Omar Shanta, Bhooma Thiruvahindrapuram, Jeffrey R. MacDonald, Josephine Mollon, Laura M. Schultz, , Sébastien Jacquemont

The paper develops a method to analyze genomic deletions and duplications across the cerebral cortex and finds opposing effects on cognitive ability depending on gene expression patterns in different cortical regions.

bioRxiv · Jan 6, 2025 · PreprintNeuroscience

Frequency and complexity of de novo structural mutation in autism

William M Brandler, Danny Antaki, Madhusudan Gujral, Amina Noor, Gabriel Rosanio, Timothy R Chapman, Daniel J Barrera, Guan Ning Lin, Dheeraj Malhotra, Amanda C Watts, Lawrence C Wong, Jasper A Estabillo, Therese E Gadomski, Oanh Hong, Karin V Fuentes Fajardo, , Jonathan Sebat

The paper identifies 1.2 million structural variants in 235 individuals, showing high de novo mutation diversity and complex mutation clusters, but finds no increased genome rearrangement rate for ASD.

bioRxiv · Oct 30, 2015Genomics