1. Genome-wide meta-analysis identifies genetic locus on chromosome 9 associated with Modic changes. Issue 7 (26th February 2019) Authors: Freidin, Maxim; Kraatari, Minna; Skarp, Sini; Määttä, Juhani; Kettunen, Johannes; Niinimäki, Jaakko; Karppinen, Jaro; Williams, Frances; Männikkö, Minna Journal: Journal of medical genetics Issue: Volume 56:Issue 7(2019) Page Start: 420 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant. Issue 3 (11th February 2022) Authors: Bharadwaj, Thashi; Schrauwen, Isabelle; Acharya, Anushree; Nouel‐Saied, Liz M.; Väisänen, Marja‐Leena; Kraatari, Minna; Rahikkala, Elisa; Jarvela, Irma; Kotimäki, Jouko; Leal, Suzanne M. Journal: Molecular genetics & genomic medicine Issue: Volume 10:Issue 3(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Herpes simplex virus 2 encephalitis in a patient heterozygous for a TLR3 mutation. (December 2020) Authors: Hautala, Timo; Chen, Jie; Tervonen, Laura; Partanen, Terhi; Winqvist, Satu; Lehtonen, Johanna; Saarela, Janna; Kraatari, Minna; Kuismin, Outi; Vuorinen, Tytti; Glumoff, Virpi; Åström, Pirjo; Huuskonen, Usko; Lorenzo, Lazaro; Casanova, Jean-Laurent; Zhang, Shen-Ying; Seppänen, Mikko R.J. Journal: Neurology Issue: Volume 6:Number 6(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A Whole Exome Study Identifies Novel Candidate Genes for Vertebral Bone Marrow Signal Changes (Modic Changes). Issue 16 (15th August 2017) Authors: Kraatari, Minna; Skarp, Sini; Niinimäki, Jaakko; Karppinen, Jaro; Männikkö, Minna Journal: Spine Issue: Volume 42:Issue 16(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗