Author

Gustaf Brander

Broad InstituteORCID 0000-0002-9549-4909Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:DNA methylation· 1 Research Focus:fine-mapping· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Organism:mouse· 1 Research Focus:variant calling· 1

Frequent Co-Authors

James J. CrowleyiD· 2 shared Asa Karlsson· 1 shared Brittney Kenney· 1 shared Chao WangiD· 1 shared Christian RückiD· 1 shared Christina DalmaniD· 1 shared David Mataix-Cols· 1 shared David Mataix‐ColsiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersGenetics

James J. CrowleyORCID

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2 papers

Recent·Most cited

Dog-human gene network colocalization links synaptic signalling and ubiquitination to compulsive disorders

Katarina Tengvall, Vista Sohrab, Matthew J. Christmas, Gustaf Brander, Eric Pederson, Raphaela Pensch, Brittney Kenney, 宋诚诚, Ola Wallerman, Elisabeth Sundström, Chao Wang, Asa Karlsson, Linnea L Monsen, PGC TS/OCD working group, Kathryn A. Lord, , Kerstin Lindblad‐Toh

This paper uses GWAS in dogs and humans to identify a gene network linked to compulsive disorders, revealing biological pathways not detectable in human studies alone.

bioRxiv · Oct 12, 2026 · PreprintGenetics

Performance of the Illumina Infinium MethylationEPIC v.2 array with low DNA input from Swedish neonatal dry blood spots

Gustaf Brander, Håkan Karlsson, Christina Dalman, Jonas Bybjerg‐Grauholm, James J. Crowley, David Mataix‐Cols

The paper evaluates the performance of the Illumina Infinium MethylationEPIC v2.0 array using DNA from Swedish neonatal blood spots, showing high probe call rates with low DNA input.

medRxiv · Mar 10, 2025 · PreprintGenetic & Genomic Medicine