Canine models of human rare disorders

por Hytönen, Marjo K., Lohi, Hannes
Publicado 2016

A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions

por Hytönen, Marjo K., Lohi, Hannes
Publicado 2019

webGQT: A Shiny Server for Genotype Query Tools for Model-Based Variant Filtering

por Arumilli, Meharji, Layer, Ryan M., Hytönen, Marjo K., Lohi, Hannes
Publicado 2020

Toxoplasma gondii seroprevalence varies by cat breed

por Must, Kärt, Hytönen, Marjo K., Orro, Toomas, Lohi, Hannes, Jokelainen, Pikka
Publicado 2017

Canine models of human amelogenesis imperfecta: identification of novel recessive ENAM and ACP4 variants

por Hytönen, Marjo K., Arumilli, Meharji, Sarkiala, Eva, Nieminen, Pekka, Lohi, Hannes
Publicado 2019

Novel Locus Associated with Symmetrical Lupoid Onychodystrophy in the Bearded Collie

por Gershony, Liza C., Belanger, Janelle M., Hytönen, Marjo K., Lohi, Hannes, Oberbauer, Anita M.
Publicado 2019

Whole Genome Sequencing Reveals Multiple Linked Genetic Variants on Canine Chromosome 12 Associated with Risk for Symmetrical Lupoid Onychodystrophy (SLO) in the Bearded Collie

por Gershony, Liza C., Belanger, Janelle M., Hytönen, Marjo K., Lohi, Hannes, Oberbauer, Anita M.
Publicado 2021

Intronic variant in POU1F1 associated with canine pituitary dwarfism

por Kyöstilä, Kaisa, Niskanen, Julia E., Arumilli, Meharji, Donner, Jonas, Hytönen, Marjo K., Lohi, Hannes
Publicado 2021

Canine MPV17 truncation without clinical manifestations

por Hänninen, Reetta L., Ahonen, Saija, Màrquez, Merce, Myöhänen, Maarit J., Hytönen, Marjo K., Lohi, Hannes
Publicado 2015

Nonsense variant in COL7A1 causes recessive dystrophic epidermolysis bullosa in Central Asian Shepherd dogs

por Niskanen, Julia, Dillard, Kati, Arumilli, Meharji, Salmela, Elina, Anttila, Marjukka, Lohi, Hannes, Hytönen, Marjo K.
Publicado 2017

A Novel GUSB Mutation in Brazilian Terriers with Severe Skeletal Abnormalities Defines the Disease as Mucopolysaccharidosis VII

por Hytönen, Marjo K., Arumilli, Meharji, Lappalainen, Anu K., Kallio, Heli, Snellman, Marjatta, Sainio, Kirsi, Lohi, Hannes
Publicado 2012

ANLN truncation causes a familial fatal acute respiratory distress syndrome in Dalmatian dogs

por Holopainen, Saila, Hytönen, Marjo K., Syrjä, Pernilla, Arumilli, Meharji, Järvinen, Anna-Kaisa, Rajamäki, Minna, Lohi, Hannes
Publicado 2017

An across-breed validation study of 46 genetic markers in canine hip dysplasia

por Mikkola, Lea, Kyöstilä, Kaisa, Donner, Jonas, Lappalainen, Anu K., Hytönen, Marjo K., Lohi, Hannes, Iivanainen, Antti
Publicado 2021

Missense variant in LOXHD1 is associated with canine nonsyndromic hearing loss

por Hytönen, Marjo K., Niskanen, Julia E., Arumilli, Meharji, Brookhart-Knox, Casey A., Donner, Jonas, Lohi, Hannes
Publicado 2021

Assembly and Analysis of Unmapped Genome Sequence Reads Reveal Novel Sequence and Variation in Dogs

por Holden, Lindsay A., Arumilli, Meharji, Hytönen, Marjo K., Hundi, Sruthi, Salojärvi, Jarkko, Brown, Kim H., Lohi, Hannes
Publicado 2018

Author Correction: Assembly and Analysis of Unmapped Genome Sequence Reads Reveal Novel Sequence and Variation in Dogs

por Holden, Lindsay A., Arumilli, Meharji, Hytönen, Marjo K., Hundi, Sruthi, Salojärvi, Jarkko, Brown, Kim H., Lohi, Hannes
Publicado 2018

Genetic dissection of canine hip dysplasia phenotypes and osteoarthritis reveals three novel loci

por Mikkola, Lea, Holopainen, Saila, Pessa-Morikawa, Tiina, Lappalainen, Anu K., Hytönen, Marjo K., Lohi, Hannes, Iivanainen, Antti
Publicado 2019

Genetic characterization of Addison’s disease in Bearded Collies

por Gershony, Liza C., Belanger, Janelle M., Hytönen, Marjo K., Lohi, Hannes, Famula, Thomas R., Oberbauer, Anita M.
Publicado 2020

Correction to: Genetic characterization of Addison’s disease in Bearded Collies

por Gershony, Liza C., Belanger, Janelle M., Hytönen, Marjo K., Lohi, Hannes, Famula, Thomas R., Oberbauer, Anita M.
Publicado 2020

Canine DVL2 variant contributes to brachycephalic phenotype and caudal vertebral anomalies

por Niskanen, Julia E., Reunanen, Vilma, Salonen, Milla, Bannasch, Danika, Lappalainen, Anu K., Lohi, Hannes, Hytönen, Marjo K.
Publicado 2021