Author

Minas Hellsand

Uppsala UniversityORCID 0000-0002-1459-0377Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Agnese ViļumaiD· 1 shared Björn EkesteniD· 1 shared Caroline J. ZeissiD· 1 shared Cathryn S. MellershiD· 1 shared Daniela Hahn· 1 shared Finn HallböökiD· 1 shared Göran AnderssoniD· 1 shared Karim MakdoumiiD· 1 shared

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2019-2019 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

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1 paper

Recent·Most cited

GeneticsPLoS GeneticsPeer-reviewedMar 19, 2019

An ABCA4 loss-of-function mutation causes a canine form of Stargardt disease

Suvi Mäkeläinen, Marta Gòdia, Minas Hellsand…·Tomas F. Bergström

The paper identifies a loss-of-function mutation in the ABCA4 gene in Labrador retrievers with retinal degeneration, suggesting dogs as a model for human Stargardt disease.

41 citations

whole-genome sequencingstatistical model

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