Author

Iveta Gažová

MRC Human Genetics UnitORCID 0000-0002-0787-9463Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Approach:experimental assay· 2 Organism:mouse· 2 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Assay:CUT&Tag· 1 Organism:human· 1 Assay:imaging· 1

Frequent Co-Authors

Angèle Tingaud‐Sequeira· 2 shared Benoı̂t ArveileriD· 2 shared Ian J. JacksoniD· 2 shared Lisa McKieiD· 2 shared Sophie JaverzatiD· 2 shared Vincent MichaudiD· 2 shared Alan L. ArchibaldiD· 1 shared Alex CaultoniD· 1 shared

Activity by Year

2020-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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2 shared papersGenetics

Angèle Tingaud‐Sequeira

Mutual co-authors in cluster

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3 papers

Recent·Most cited

The Dct-/- mouse model to unravel retinogenesis misregulation in patients with albinism

Angèle Tingaud‐Sequeira, Elina Mercier, Vincent Michaud, Benoı̂t Pinson, Iveta Gažová, Étienne Gontier, Fanny Decoeur, Lisa McKie, Ian J. Jackson, Benoı̂t Arveiler, Sophie Javerzat

This paper investigates the retinal phenotype of Dct-/- mice to understand retinogenesis misregulation in albinism patients.

Genes · Jun 27, 2022Peer-reviewedGenetics

Dopachrome tautomerase variants in patients with oculocutaneous albinism.

Perrine Pennamen, Angèle Tingaud‐Sequeira, Iveta Gažová, Margaret Keighren, Lisa McKie, Sandrine Marlin, Souad Gherbi, Josseline Kaplan, Cédric Delevoye, Didier Lacombe, Claudio Plaisant, Vincent Michaud, Eulalie Lasseaux, Sophie Javerzat, Ian J. Jackson, Benoı̂t Arveiler

The paper identifies DCT gene variants in two patients with oculocutaneous albinism, demonstrating their association with hypopigmentation and proposing a new subtype, OCA8.

Genetics in Medicine · Oct 25, 2020Peer-reviewedGenetics

Global analysis of transcription start sites in the new ovine reference genome (Oar rambouillet v1.0)

Mazdak Salavati, Alex Caulton, Richard C. Clark, Iveta Gažová, Timothy P. L. Smith, Kim C. Worley, Noelle E. Cockett, Alan L. Archibald, Shannon Clarke, Brenda M. Murdoch, Emily L. Clark

The paper performs a global analysis of transcription start sites (TSS) in the ovine reference genome using CAGE sequencing, identifying novel TSS and validating them with bisulfite sequencing.

Frontiers in Genetics · Oct 23, 2020Peer-reviewedGenomics