M. Kraatari

Heterozygous TLR3 Mutation in Patients with Hantavirus Encephalitis

V. Anttila, J. Casanova, Shen-Ying Zhang, 2020, Journal of Clinical Immunology.

The heritability and genetic risk factors of Modic changes

Minna Kraatari, M. Kraatari, 2018 .

A Whole Exome Study Identifies Novel Candidate Genes for Vertebral Bone Marrow Signal Changes (Modic Changes)

J. Niinimäki, J. Karppinen, M. Männikkö, 2017, Spine.

Vertebral endplate change as a feature of intervertebral disc degeneration: a heritability study

J. Niinimäki, F. Williams, J. Karppinen, 2014, European Spine Journal.

Genome-wide meta-analysis identifies genetic locus on chromosome 9 associated with Modic changes

J. Niinimäki, J. Kettunen, F. Williams, 2019, Journal of Medical Genetics.

X-linked myotubular myopathy mimics hereditary spastic paraplegia in two female manifesting carriers of pathogenic MTM1 variant.

S. Tuupanen, T. Haapaniemi, H. Tuominen, 2020, European Journal of Medical Genetics.

Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant

S. Leal, I. Schrauwen, E. Rahikkala, 2022, Molecular genetics & genomic medicine.

Herpes simplex virus 2 encephalitis in a patient heterozygous for a TLR3 mutation

J. Casanova, U. Huuskonen, Shen-Ying Zhang, 2020, Neurology: Genetics.