Author

Dinesh C. Soares

Western General HospitalORCID 0000-0001-7557-0495Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Organism:human· 1 Assay:imaging· 1 Organism:mouse· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Andrew Mark McIntoshiD· 1 shared Caroline ThaungiD· 1 shared Catherine M. AbbottiD· 1 shared David John PorteousiD· 1 shared Douglas BlackwoodiD· 1 shared Ian J. DearyiD· 1 shared Ian J. JacksoniD· 1 shared J. Kirsty Millar· 1 shared

Activity by Year

2017-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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1 shared paperGenetics

Andrew Mark McIntoshORCID

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3 papers

Recent·Most cited

GeneticsBioscience ReportsPeer-reviewedJan 1, 2020

Translation elongation factor 1A2 (eEF1A2) is encoded by one of four closely related eef1a genes and is dispensable for survival in zebrafish

Nwamaka J. Idigo, Dinesh C. Soares, Catherine M. Abbott

The paper investigates the role of eEF1A2 in zebrafish by generating null mutations and compares phenotypes with morphants and mice, finding zebrafish can survive without eEF1A2.

6 citations

zebrafishexperimental assay

𝕏 PostBluesky

Molecular BiologyInvestigative Ophthalmology & Visual SciencePeer-reviewedJul 2, 2019

Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse

Sally H. Cross, Lisa McKie, Margaret Keighren…·Ian J. Jackson

The paper identifies TMEM98 mutations in mice that cause retinal defects similar to human nanophthalmos, showing localized photoreceptor laminar disruption rather than small eyes.

19 citations

mouseimaging

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GeneticsMolecular PsychiatryPeer-reviewedJun 20, 2017

Rare disruptive variants in the DISC1 Interactome and Regulome: association with cognitive ability and schizophrenia

Shaolei Teng, Pippa A. Thomson, S McCarthy…·William Richard McCombie

The paper investigates rare disruptive variants in the DISC1 Interactome and Regulome, finding associations with schizophrenia and cognitive ability in psychiatric patients.

45 citationstop 4%

humanwhole-exome sequencing

𝕏 PostBluesky