Suvi Mäkeläinen

Swedish University of Agricultural Sciences — Sweden

Biochemistry, Genetics and Molecular Biology · Life Sciences

5h-index252citations17works0.02yr avg
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Research Topics

Retinal Development and Disorders(4), Genomics and Phylogenetic Studies(3), Genomics and Chromatin Dynamics(3), Genetic and Kidney Cyst Diseases(3), Genetic Syndromes and Imprinting(3)

Publications17 total

A nonsense mutation in the PRKG2 gene in dalmatian dogs with chondrodysplasia
PLoS ONE·2025Open Access
A Nonsense Mutation in the PRKG2 Gene in Dalmatian Dogs with Chondrodysplasia
2025Open Access
CNSC-40. HARNESSING EVOLUTIONARY CONSTRAINT IDENTIFIES POTENTIAL NON-CODING DRIVERS IN BRAIN TUMORS
Neuro-Oncology·2023Open Access
Using evolutionary constraint to define novel candidate driver genes in medulloblastoma
Proceedings of the National Academy of Sciences·2023· 4 citedOpen Access
Abnormal Appearance of the Area Centralis in Labrador Retrievers With an <i>ABCA4</i> Loss-of-function Mutation
Translational Vision Science & Technology·2022· 4 citedOpen Access
A novel canine reference genome resolves genomic architecture and uncovers transcript complexity
Communications Biology·2021· 159 citedOpen Access
Deletion in the Bardet–Biedl Syndrome Gene TTC8 Results in a Syndromic Retinal Degeneration in Dogs
Genes·2020· 10 citedOpen Access
&lt;strong&gt;Deletion in the Bardet-Biedl Syndrome Gene &lt;em&gt;TTC8&lt;/em&gt; Results in a Syndromic Retinal Degeneration in Dogs&lt;/strong&gt;
Preprints.org·2020· 2 citedOpen Access
GSD_1.0 (canFam4): A novel canine reference genome resolves genomic architecture and uncovers transcript complexity
2020· 1 citedOpen Access
A new long-read dog assembly uncovers thousands of exons and functional elements missing in the previous reference
2020· 6 citedOpen Access
Fundus autofluorescence and foveal appearance in Labrador Retriever dogs with an ABCA4 loss-of-function mutation.
Investigative Ophthalmology & Visual Science·2020Open Access
Canine inherited retinal degenerations: a model for visual impairment in humans
Epsilon Open Archive (Sveriges lantbruksuniversitet biblioteket (Swedish University of Agricultural Sciences))·2020Open Access
An ABCA4 loss-of-function mutation causes a canine form of Stargardt disease
PLoS Genetics·2019· 40 citedOpen Access
An ABCA4 loss-of-function mutation causes a canine form of Stargardt disease
2018Open Access
Abstract 2426: Oncopig soft-tissue sarcomas recapitulate key transcriptional features of human sarcomas
Cancer Research·2017Open Access
Oncopig Soft-Tissue Sarcomas Recapitulate Key Transcriptional Features of Human Sarcomas
Scientific Reports·2017· 26 citedOpen Access
P6000 Whole genome sequencing of canine family trios to identify rare alleles for Mendelian diseases.
Journal of Animal Science·2016

Frequent Co-authors

Tomas F. Bergström(12), Göran Andersson(7), Kerstin Lindblad‐Toh(6), Björn Ekesten(6), Jessika Nordin(5), Ingrid Ljungvall(5), Jens Häggström(5), Åke Hedhammar(5), Elisabeth Sundström(4), Jennifer R. S. Meadows(4), Minas Hellsand(4), Cathryn S. Mellersh(4), Finn Hallböök(4), Chao Wang(3), Ola Wallerman(3), Maja L. Arendt(3), Åsa Karlsson(3), Gerli Pielberg(3), Jeanette Hanson(3), Sara Saellström(3)