Author

Matt Johnson

Washington University in St. Louis

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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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:eQTL / molecular QTL mapping· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Carlos CruchagaiD· 2 shared Ahmet HökeiD· 1 shared Aiman Farzeen· 1 shared Alexis J. BattleiD· 1 shared Allan F. McRaeiD· 1 shared Ana Laura Hernández-LedesmaiD· 1 shared Ángel Martínez-PéreziD· 1 shared Anneke BrümmeriD· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Carlos CruchagaORCID

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2 papers

Recent·Most cited

Trans-eQTL mapping prioritises USP18 as a negative regulator of interferon response at a lupus risk locus

Krista Freimann, Anneke Brümmer, Robert Warmerdam, Tarran S. Rupall, Ana Laura Hernández-Ledesma, Joshua Chiou, Emily Rose Holzinger, Joseph Maranville, Nikolina Nakić, Halit Ongen, Luca Stefanucci, Michael C. Turchin, eQTLGen, Habibul Ahsan, Philip Awadalla, , Suvi Rovio

The paper identifies USP18 as a negative regulator of interferon response at a lupus risk locus through trans-eQTL analysis in lymphoblastoid cell lines.

Nature Communications · Oct 2, 2025Peer-reviewedGenetic & Genomic Medicine

Heterozygous and Homozygous RFC1 AAGGG Repeat Expansions are Common in Idiopathic Peripheral Neuropathy

Zitian Tang, Sinem Seleme Övünç, Ryo Iwase, Elle Mehinovic, Simone Thomas, Jenna Ulibarri, Zefan Li, Dustin Baldridge, Carlos Cruchaga, Matt Johnson, Jeffrey Milbrandt, Brian Christopher Callaghan, PNRR Study Group, Ahmet Höke, Peter K. Todd, Sheng Chih Jin

The paper identifies RFC1 AAGGG repeat expansions in idiopathic peripheral neuropathy patients using a new computational pipeline and finds both heterozygous and homozygous expansions contribute to the condition.

medRxiv · Apr 18, 2025 · PreprintGenetic & Genomic Medicine