Devon E Bonner

10PUBLICATIONS
111CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene mappingNeurogeneticsGene expression (incl. microarray and other genome-wide approaches)
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Publications (10)

|Jun 22, 2026
Population-scale detection of methylation outliers from long-read genome sequencing.

|Apr 20, 2026
De Novo Variants Associated With Autosomal Recessive Conditions: Case Series and Implications for Genetic Testing and Counseling.

|Sep 05, 2025
Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder.

Daniel Greene, Rodrigo Mendez, Jon Lees

|Apr 16, 2025
De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.

Eric N Anderson, Stephan Drukewitz, Sukhleen Kour

|Mar 20, 2025
Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease.

Tanner D Jensen, Bohan Ni, Chloe M Reuter

|Jan 13, 2025
Transcriptome-wide outlier approach identifies individuals with minor spliceopathies.

Maggie T Arriaga, Rodrigo Mendez, Rachel A Ungar

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Frequent Collaborators

10 joint publications

Jonathan A Bernstein

9 joint publications

Matthew T Wheeler

6 joint publications

Stephen B Montgomery

4 joint publications

Pagé C Goddard