Jonas Donner

Biochemistry, Genetics and Molecular Biology · Life Sciences

15h-index1.3kcitations67works0.82yr avg
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Research Topics

Human-Animal Interaction Studies(10), Genetic and phenotypic traits in livestock(9), Animal Genetics and Reproduction(9), Retinal Development and Disorders(8), Neurological diseases and metabolism(6)

Publications67 total

IP3 receptor depletion in a spontaneous canine model of Charcot-Marie-Tooth disease 1J with amelogenesis imperfecta
PLoS Genetics·2025Open Access
A <i>RETREG1</i> variant is associated with hereditary sensory and autonomic neuropathy with acral self‐mutilation in purebred German Spitz
Animal Genetics·2024· 1 citedOpen Access
IP3 receptor depletion in a spontaneous canine model of Charcot-Marie-Tooth disease 1J with amelogenesis imperfecta
2024Open Access
Frequency of <i>RPGRIP1</i> and <i>MAP9</i> genetic modifiers of canine progressive retinal atrophy, in 132 breeds of dog
Animal Genetics·2024Open Access
Association of FGF4L1 Retrogene Insertion with Prolapsed Gland of the Nictitans (Cherry Eye) in Dogs
Genes·2024· 3 citedOpen Access
Canine coat color E locus updates: Identification of a new <scp>MC1R</scp> variant causing ‘sable’ coat color in English Cocker Spaniels and a proposed update to the E locus dominance hierarchy
Animal Genetics·2024· 1 citedOpen Access
Global Frequency Analyses of Canine Progressive Rod-Cone Degeneration–Progressive Retinal Atrophy and Collie Eye Anomaly Using Commercial Genetic Testing Data
Genes·2023· 4 citedOpen Access
Association of the <i>FGF4L2</i> retrogene with fibrocartilaginous embolic myelopathy in dogs
Journal of Veterinary Internal Medicine·2023· 2 citedOpen Access
Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human
Genome Medicine·2023· 12 citedOpen Access
A frameshift deletion in<i>F8</i>associated with hemophilia A in Labrador Retriever dogs
Animal Genetics·2023· 1 citedOpen Access
A loss-of-function variant in canine GLRA1 associates with a neurological disorder resembling human hyperekplexia
Human Genetics·2023· 6 citedOpen Access
Genetic prevalence and clinical relevance of canine Mendelian disease variants in over one million dogs
PLoS Genetics·2023· 39 citedOpen Access
Genetic epidemiology of blood type, disease and trait variants, and genome-wide genetic diversity in over 11,000 domestic cats
PLoS Genetics·2022· 35 citedOpen Access
Genetic prevalence and clinical relevance of canine Mendelian disease variants in over one million dogs
2022· 4 citedOpen Access
Large scale across-breed genome-wide association study reveals a variant in HMGA2 associated with inguinal cryptorchidism risk in dogs
PLoS ONE·2022· 7 citedOpen Access
The effect of inbreeding, body size and morphology on health in dog breeds
Canine Medicine and Genetics·2021· 66 citedOpen Access
Genetic epidemiology of blood type, disease and trait variants, and genome-wide genetic diversity in over 11,000 domestic cats
2021· 4 citedOpen Access
Missense variant in LOXHD1 is associated with canine nonsyndromic hearing loss
Human Genetics·2021· 8 citedOpen Access
Gene Panel Screening Across Canine Eye Disorders Highlights Genetic Heterogeneity and the Need for Molecular Discoveries
Research Square (Research Square)·2021Open Access
In-frame deletion in canine PITRM1 is associated with a severe early-onset epilepsy, mitochondrial dysfunction and neurodegeneration
Human Genetics·2021· 14 citedOpen Access
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Frequent Co-authors

Heidi Anderson(20), Hannes Lohi(20), Marjo K. Hytönen(14), Oliver P. Forman(9), Meharji Arumilli(9), Stephen Davison(8), Kaisa Kyöstilä(8), Leena Honkanen(8), Iiris Hovatta(7), Maria Kaukonen(7), Jamie Freyer(6), Rebecca Chodroff Foran(6), Angela M. Hughes(5), Jouko Lönnqvist(5), Sami Pirkola(5), Julia E. Niskanen(5), Sruthi Hundi(5), Katherine M. Lytle(4), Balasubramanian Ganesan(4), Laura Kananen(4)