Author

Alex D. Jansen

University of Wisconsin–Madison

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Genetics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 1 Organism:human· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Daniel Navarro-Gomez· 1 shared David M. GammiD· 1 shared Elizabeth E. CapowskiiD· 1 shared Emily PlaceiD· 1 shared Eric A. PierceiD· 1 shared Kinga M. BujakowskaiD· 1 shared Mathew Maher· 1 shared Revital BronsteiniD· 1 shared

Activity by Year

2020-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Daniel Navarro-Gomez

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1 paper

Recent·Most cited

A combined RNA-seq and whole genome sequencing approach for identification of non-coding pathogenic variants in single families.

Revital Bronstein, Elizabeth E. Capowski, Sudeep Mehrotra, Alex D. Jansen, Daniel Navarro-Gomez, Mathew Maher, Emily Place, Riccardo Sangermano, Kinga M. Bujakowska, David M. Gamm, Eric A. Pierce

The paper combines whole genome sequencing and retinal organoid transcriptome analysis to identify and validate a novel non-coding pathogenic variant in a family with an unresolved genetic diagnosis.

Human Molecular Genetics · Jan 21, 2020Peer-reviewedGenetics