Maria Kaukonen

University of Helsinki

Finland

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Articles (17)

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2025

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2025

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2024

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2024

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2024

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2023

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2023

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2023

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2022

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2022

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2021

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2021

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2021

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2021

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2021

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2021

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2020

Collaborators (15)

Jasmina Cehajic-Kapetanovic

University of Oxford

UNITED KINGDOM

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Veera Karkamo

University of Helsinki

FINLAND

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Marjo Hytönen

University of Helsinki

FINLAND

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N. Matthew Ellinwood

Iowa State University

UNITED STATES

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Anna Letko

University of Bern

SWITZERLAND

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Michelle McClements

University of Oxford

UNITED KINGDOM

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Sanna Malkamäki

University of Helsinki

FINLAND

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Joni Turunen

University of Helsinki

FINLAND

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Antti Kalle Kalervo Sukura

University of Helsinki

FINLAND

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Peter Leegwater

Assitant Professor

Utrecht University

NETHERLANDS

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Ileana Quintero

FINLAND

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Sanna J. Viitanen

FINLAND

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Saija Ahonen

University of Helsinki

FINLAND

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Inka-Tuulevi Vähämäki (Pettinen)

University of Helsinki

FINLAND

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Tarja Jokinen

University of Helsinki

FINLAND

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Maria Kaukonen

Research Interests

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Articles (17)

A feline model of human low‐density lipoprotein receptor‐related atherosclerosis

Common variants in the CPT1A gene are associated with cataracts in Northern breeds of domestic dog

Genetic therapies and potential therapeutic applications of CRISPR activators in the eye

In Silico CRISPR-Cas-Mediated Base Editing Strategies for Early-Onset, Severe Cone-Rod Retinal Degeneration in Three Crumbs homolog 1 Patients, including the Novel Variant c.2833G>A.

The DoGA consortium expression atlas of promoters and genes in 100 canine tissues

A frameshift deletion in F8 associated with hemophilia A in Labrador Retriever dogs

Hypomorphic CDHR1 variants may result in retinitis pigmentosa with relative preservation of cone function.

Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human.

CRISPR DNA Base Editing Strategies for Treating Retinitis Pigmentosa Caused by Mutations in <i>Rhodopsin</i>

Potential CRISPR Base Editing Therapeutic Options in a Sorsby Fundus Dystrophy Patient

In Silico Analysis of Pathogenic <i>CRB1</i> Single Nucleotide Variants and Their Amenability to Base Editing as a Potential Lead for Therapeutic Intervention

A Missense Variant in the Bardet-Biedl Syndrome 2 Gene (BBS2) Leads to a Novel Syndromic Retinal Degeneration in the Shetland Sheepdog

Dog colour patterns explained by modular promoters of ancient canid origin

Clinical and Genetic Findings in 28 American Cocker Spaniels with Aural Ceruminous Gland Hyperplasia and Ectasia

Multi-omic analyses in Abyssinian cats with primary renal amyloid deposits

A missense variant in IFT122 associated with a canine model of retinitis pigmentosa.

Formal commentary

Collaborators (15)

Jasmina Cehajic-Kapetanovic

Veera Karkamo

Marjo Hytönen

N. Matthew Ellinwood

Anna Letko

Michelle McClements

Sanna Malkamäki

Joni Turunen

Antti Kalle Kalervo Sukura

Peter Leegwater

Ileana Quintero

Sanna J. Viitanen

Saija Ahonen

Inka-Tuulevi Vähämäki (Pettinen)

Tarja Jokinen

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