Author

Brieana Fregeau

University of California, San Francisco

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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Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Organism:mouse· 1

Frequent Co-Authors

Elliott H. SherriD· 2 shared A. James BarkovichiD· 1 shared Alban C. ZiegleriD· 1 shared Alexandra AfenjariD· 1 shared Allan Micheil InnesiD· 1 shared Amy Sarah Kimball· 1 shared Ashley L. Lennox· 1 shared Atsushi FujitaiD· 1 shared

Activity by Year

2018-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

Elliott H. SherrORCID

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2 papers

Recent·Most cited

Pathogenic DDX3X mutations impair RNA metabolism and neurogenesis during fetal cortical development

Ashley L. Lennox, Mariah L. Hoye, Ruiji Jiang, Bethany Johnson-Kerner, Lindsey Suit, Srivats Venkataramanan, Charles J. Sheehan, Fernando C. Alsina, Brieana Fregeau, Kimberly A. Aldinger, Ching Moey, Iryna V. Lobach, Alexandra Afenjar, Dusica Babovic‐Vuksanovic, Stéphane Bezieau, , Elliott H. Sherr

This study identifies DDX3X mutations as causing neurodevelopmental disorders by disrupting RNA metabolism and neurogenesis during fetal cortical development.

Neuron · Mar 4, 2020Peer-reviewedGenetics

Abnormal Speech Motor Control in Individuals with 16p11.2 Deletions

Carly Demopoulos, Hardik Kothare, Danielle Mizuiri, Jennifer Henderson‐Sabes, Brieana Fregeau, Jennifer Tjernagel, John F. Houde, Elliott H. Sherr, Srikantan S. Nagarajan

This study investigates speech motor control impairments in individuals with 16p11.2 deletions, finding exaggerated pitch compensation and reduced sensorimotor adaptation to auditory feedback changes.

Scientific Reports · Jan 15, 2018Peer-reviewedNeuroscience