Jonas Gustafson

11PUBLICATIONS
102CO-AUTHORS
Gene mappingGenetic immunologyGenome structure and regulationEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (11)

|Jan 23, 2026
Using the linear references from the pangenome to discover missing autism variants.

Yang Sui, Jiadong Lin, Michelle D Noyes

|Sep 25, 2025
Deep Intronic SVA_E Insertion Identified as the Most Common Pathogenic Variant Associated With Canavan Disease: A Diagnostic Blind Spot.

Carlos A Dominguez Gonzalez, Katrina M Bell, Ramakrishnan Rajagopalan

|Aug 08, 2025
Pangenome discovery of missing autism variants.

Yang Sui, Jiadong Lin, Michelle D Noyes

|Jun 12, 2025
Principles and functional consequences of plasmid chromatinization in mammalian cells.

Benjamin J Mallory, Thomas W Tullius, Carina G Biar

|Feb 20, 2025
Long-Read Sequencing is Required for Precision Diagnosis of Incontinentia Pigmenti.

Monica H Wojcik, Robin D Clark, Abdallah F Elias

|Oct 02, 2024
High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation.

Jonas A Gustafson, Sophia B Gibson, Nikhita Damaraju

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Frequent Collaborators

6 joint publications

Danny E Miller

4 joint publications

Joy Goffena

4 joint publications

Miranda Pg Zalusky

4 joint publications

Evan E Eichler