Author

Lillian F. Hyde

Jackson LaboratoryORCID 0000-0001-6230-4630Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:mouse· 2 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1

Frequent Co-Authors

Gayle B. ColliniD· 2 shared Jürgen Κ. NaggertiD· 2 shared Lisa V. StoneiD· 2 shared Mark P. KrebsiD· 2 shared Gregory W. CarteriD· 1 shared James G. PetersoniD· 1 shared Jeremy R. Charette· 1 shared Nattaya DamkhamiD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

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10 top collaborators · 40 mutual co-author links

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2 shared papersGenetics

Gayle B. CollinORCID

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintOct 5, 2026

A new mouse model for a high-risk AMD variant, ARMS2A69S

Navdeep Gogna, Gayle B. Collin, Lillian F. Hyde…·Patsy Nishina

This paper creates a mouse model with the ARMS2A69S variant to study AMD, finding it causes mitochondrial dysfunction and AMD-like phenotypes.

DOI 10.64898/2026.10.02.756275

mouseexperimental assay

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GeneticsPLoS GeneticsPeer-reviewedJun 8, 2022

Identification of Arhgef12 and Prkci as Genetic Modifiers of Retinal Dysplasia in the Crb1rd8 Mouse Model

Sonia M. Weatherly, Gayle B. Collin, Jeremy R. Charette…·Patsy M. Nishina

This study identifies Arhgef12 and Prkci as genetic modifiers that influence the severity of retinal dysplasia in the Crb1rd8 mouse model, revealing differential disease progression and cellular mislocalization.

12 citations

mousestatistical model

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