Author

David Adams

Children's Hospital of Orange CountyPrimary ORCID profile (0000-0001-6776-0336 · 1 paper)Unclaimed ORCID profile · follow to get notified of new preprints

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Same name, identified by ORCID

David AdamsiD1 paper · Wellcome Sanger Institute

Biology Disciplines

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Genomics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Research Focus:cell-cell communication· 1 Assay:electronic health records· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1

Frequent Co-Authors

Anthony DoraniD· 1 shared Beth A. LopouriD· 1 shared Blanca Romero MilàiD· 1 shared Clare SkoraiD· 1 shared Daniel W. ShreyiD· 1 shared Derek K. HuiD· 1 shared Donald Phillips· 1 shared Jonathan Flint· 1 shared

Activity by Year

2016-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenomics

Anthony DoranORCID

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Author profile →

2 papers

Recent·Most cited

EEG Functional Connectivity as a Marker of Evolution from Infantile Epileptic Spasms Syndrome to Lennox-Gastaut Syndrome

Blanca Romero Milà, Virginia B. Liu, Rachel June Smith, Derek K. Hu, Natalie A. Benneian, Shaun A. Hussain, Maija Steenari, Donald Phillips, David Adams, Clare Skora, Beth A. Lopour, Daniel W. Shrey

The paper uses EEG functional connectivity to track progression from infantile epileptic spasms syndrome to Lennox-Gastaut Syndrome and identifies patterns associated with treatment response and disease markers.

Epilepsia · Nov 24, 2025Peer-reviewedNeuroscience

Deep genome sequencing and variation analysis of 13 inbred mouse strains defines candidate phenotypic alleles, private variation, and homozygous truncating mutations

Thomas Keane, Anthony Doran, David Adams, Kent Hunter, Jonathan Flint, Kim Wong

The paper deep sequences 13 inbred mouse strains to identify SNPs, indels, and private mutations linked to disease phenotypes.

Genome Biology · Aug 1, 2016Peer-reviewedGenomics