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)

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|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 <i>RNU2-2</i> cause the most prevalent known recessive neurodevelopmental disorder.

Daniel Greene, Rodrigo Mendez, Jon Lees

|Apr 16, 2025

De novo variants in <i>KDM2A</i> 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

Matthew T Wheeler

Stephen B Montgomery

Pagé C Goddard

Rachel A Ungar

Tanner D Jensen

Jennefer N Kohler

Euan A Ashley

Rodrigo Mendez

Chloe M Reuter

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