Author

Anne Blomhoff

Oslo University Hospital

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· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Ada HamoshiD· 1 shared Alan H. BeggsiD· 1 shared Alice PoissoniD· 1 shared André ReisiD· 1 shared Anita M. RauchiD· 1 shared Antonio NovelliiD· 1 shared Aubrie SoucyiD· 1 shared Audrey LabalmeiD· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Ada HamoshORCID

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1 paper

Recent·Most cited

Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior

Holly K. Harris, Tojo Nakayama, Jenny F. Lai, Boxun Zhao, Nikoleta Argyrou, Cynthia Sophia Gubbels, Aubrie Soucy, Casie A. Genetti, Victoria Suslovitch, Lance H. Rodan, George E. Tiller, Gaëtan Lesca, Karen Webster Gripp, Reza Asadollahi, Ada Hamosh, , Timothy W. Yu

The paper identifies RFX3, RFX4, and RFX7 mutations as causes of neurodevelopmental disorders including autism, ADHD, and intellectual disability, and links these genes to ASD risk genes through bioinformatic analysis.

Genetics in Medicine · Mar 3, 2021Peer-reviewedGenetic & Genomic Medicine