Author

Dave Parry

Institute of Genetics and Cancer

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Genetics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Alison M. MeynertiD· 1 shared Andrew Sofronis PapanastasiouiD· 1 shared Brianda Areli Hernández-MorániD· 1 shared David J. AdamsiD· 1 shared David R FitzPatrickiD· 1 shared Graeme R. GrimesiD· 1 shared Hemant BenganiiD· 1 shared Ian J. JacksoniD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Alison M. MeynertORCID

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1 paper

Recent·Most cited

Robust genetic analysis of the X-linked anophthalmic (Ie) mouse

Brianda Areli Hernández-Morán, Andrew Sofronis Papanastasiou, Dave Parry, Alison M. Meynert, Philippe Emmanuel Gautier, Graeme R. Grimes, Ian R. Adams, Violeta Trejo-Reveles, Hemant Bengani, Margaret Keighren, Ian J. Jackson, David J. Adams, David R FitzPatrick, Joe Rainger

This study identifies a critical genomic region on the X chromosome linked to anophthalmia in mice but finds no clear causative mutation, suggesting regulatory changes may underlie the phenotype.

Genes · Oct 5, 2022Peer-reviewedGenetics