Author

Sally J. Ozonoff

University of California, DavisORCID 0000-0002-1230-0794Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genomics· 2 Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 4 Approach:statistical model· 4 Research Focus:differential expression· 3 Assay:DNA methylation· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Charles E. MordauntiD· 3 shared Irva Hertz‐PicciottoiD· 3 shared Janine M. LaSalleiD· 3 shared Rebecca J. SchmidtiD· 3 shared Craig J. NewschafferiD· 2 shared Heather E. VolkiD· 2 shared Jason I. FeinbergiD· 2 shared Julia M. JianuiD· 2 shared

Activity by Year

2019-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 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

3 shared papersGenomics

Charles E. MordauntORCID

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMay 5, 2022

Genomic architecture of autism spectrum disorder from comprehensive whole-genome sequence annotation

Brett Trost, Bhooma Thiruvahindrapuram, Ada J. S. Chan…·Evdokia A. Anagnostou

This study identifies 135 ASD-associated protein-coding genes using whole-genome sequencing data from 11,312 individuals and exome sequencing from over 18,000 trios, with a false discovery rate of 80%.

3 citations

humanwhole-genome sequencing

GenomicsGenome MedicinePeer-reviewedOct 14, 2020

Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes

Charles E. Mordaunt, Julia M. Jianu, Benjamin I. Laufer…·Janine M. LaSalle

The paper identifies DNA methylation differences in cord blood samples from newborns later diagnosed with ASD, revealing sex-specific epigenomic signatures linked to neurodevelopmental and X-linked genes.

79 citationstop 2%

humanDNA methylation

GenomicsMolecular AutismPeer-reviewedOct 24, 2019

A meta-analysis of two high-risk prospective cohort studies reveals autism-specific transcriptional changes to chromatin, autoimmune, and environmental response genes in umbilical cord blood

Charles E. Mordaunt, Bo Young Park, Kelly M. Bakulski…·M. Daniele Fallin

This study identifies ASD-specific transcriptional changes in umbilical cord blood through a meta-analysis of two high-risk cohorts, highlighting environmental, immune, and epigenetic factors.

36 citations

humanbulk RNA-seq

GeneticsHuman Molecular GeneticsPeer-reviewedApr 17, 2019

Placental DNA methylation levels at CYP2E1 and IRS2 are associated with child outcome in a prospective autism study

Yihui Zhu, Charles E. Mordaunt, Dag H. Yasui…·Janine M. LaSalle

The paper identifies two placental DNA methylation markers, CYP2E1 and IRS2, associated with ASD risk and modulated by genetic and environmental factors.

82 citationstop 2%

humanDNA methylation