Author

Randi Jenssen Hagerman

University of California Davis Medical CenterORCID 0000-0001-5029-8448Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1 Genomics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

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

Frequent Co-Authors

Reymundo LozanoiD· 2 shared Verónica Martínez‐CerdeñoiD· 2 shared Adel AzghadiiD· 1 shared Allan L. ReissiD· 1 shared Amy A. LightbodyiD· 1 shared Amy EsleriD· 1 shared Amy L. Talboy· 1 shared Andrea Lynne GropmaniD· 1 shared

Activity by Year

2018-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenomics

Reymundo LozanoORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

GenomicsbioRxivPreprintJul 10, 2026

DNA Methylation and Proteomic Profiling of Postmortem Brain Tissue Reveals Epigenetic Dysregulation and Neuroinflammatory in Fragile X-associated Tremor/Ataxia Syndrome (FXTAS)

Reymundo Lozano, Xiao Lin, Randi Jenssen Hagerman…·Dalila Pinto

This study identifies epigenetic and proteomic changes in FXTAS brains, linking DNA methylation and inflammation to neurodegeneration.

DOI 10.64898/2026.07.06.736649

humanDNA methylation

𝕏 PostBluesky

Genetic & Genomic MedicineJournal of Autism and Developmental DisordersPeer-reviewedNov 28, 2022

Latent class analysis identifies distinctive behavioral subtypes in children with fragile X syndrome

Walter E. Kaufmann, Melissa Raspa, Carla Bann…·Stephanie M. Morris

The paper uses latent class analysis to identify distinct behavioral subtypes in children with fragile X syndrome, revealing clinically meaningful groups with unique cognitive and behavioral profiles.

14 citations

humanstatistical model

𝕏 PostBluesky

NeuroscienceNature NeurosciencePeer-reviewedDec 7, 2018

Widespread RNA editing dysregulation in Autism Spectrum Disorders

Stephen S. Tran, Hyun-Ik Jun, Jae Hoon Bahn…·Xinshu Grace Xiao

This study identifies widespread hypo-editing in ASD brains and links RNA editing dysregulation to Fragile X syndrome through FMRP/FXR1P-ADAR interactions.

219 citationstop 1%

humanbulk RNA-seq

𝕏 PostBluesky