Author

Jennifer K. Forsyth

University of California, Los AngelesORCID 0000-0002-8786-0024Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Neuroscience· 1 Systems Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 4 Organism:human· 4 Approach:statistical model· 4 Research Focus:differential expression· 3 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Organism:Drosophila· 1

Frequent Co-Authors

Carrie E. BeardeniD· 3 shared Michael J. GandaliD· 2 shared Aaron F. Alexander‐BlochiD· 1 shared Amanda A. H. FreemaniD· 1 shared Amanda J. CrockeriD· 1 shared Ariana AndersoniD· 1 shared Avanti GokhaleiD· 1 shared Benjamin JungiD· 1 shared

Activity by Year

2018-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Carrie E. BeardenORCID

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Author profile →

4 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMay 14, 2024

The copy number variant architecture of psychopathology and cognitive development in the ABCD study

Zhiqiang Sha, Kevin Y. Sun, Benjamin Jung…·Aaron F. Alexander‐Bloch

This study identifies copy number variants (CNVs) associated with child psychopathology and cognitive function using data from the ABCD study.

2 citations

humanwhole-genome sequencing

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Genetic & Genomic MedicinemedRxivPreprintFeb 19, 2024

Attention-mediated genetic influences on psychotic symptomatology in adolescence

Sarah E. Chang, Dylan Hughes, Jinhan Zhu…·Carrie E. Bearden

The paper examines how genetic risk scores relate to attentional variability and psychotic-like experiences in adolescents, finding partial mediation through attentional variability.

1 citation

humanGWAS summary statistics

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Systems BiologyBiological PsychiatryPeer-reviewedJul 11, 2019

Synaptic and Gene Regulatory Mechanisms in Schizophrenia, Autism, and 22q11.2 CNV Mediated Risk for Neuropsychiatric Disorders

Jennifer K. Forsyth, Daniel C. Nachun, Michael J. Gandal…·Carrie E. Bearden

The paper integrates transcriptomic, genomic, and proteomic data to identify gene networks and pathways involved in schizophrenia and autism risk, with a focus on 22q11.2 CNVs.

60 citationstop 2%

humanbulk RNA-seq

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NeuroscienceJournal of NeurosciencePeer-reviewedJan 1, 2018

Systems Analysis of the 22q11.2 Microdeletion Syndrome Converges on a Mitochondrial Interactome Necessary for Synapse Function and Behavior

Avanti Gokhale, Cortnie L. Hartwig, Amanda A. H. Freeman…·Victor Faúndez

The paper identifies a mitochondrial transporter interactome disruption in 22q11.2 syndrome, linking it to synapse function and behavior.

60 citationstop 3%

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