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Minna Kraatari‐Tiri

Observed names: Kraatari-Tiri, Minna, M. Kraatari, Minna Kraatari, Minna Kraatari-Tiri
ORCID: 0000-0002-8072-699X
Observed ORCID: 0000-0002-8072-699X
OpenAlex ID: A5035688284
Vertebral endplate change as a feature of intervertebral disc degeneration: a heritability study
2014 · Juhani H. Määttä, Minna Kraatari, et al. · European Spine Journal · 65
An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome
2022 · Sanaa Choufani, Vanda McNiven, et al. · The American Journal of Human Genetics · 44
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Heterozygous TLR3 Mutation in Patients with Hantavirus Encephalitis
2020 · Terhi Partanen, Jie Chen, et al. · Journal of Clinical Immunology · 20
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Genome-wide meta-analysis identifies genetic locus on chromosome 9 associated with Modic changes
2019 · Maxim Freidin, Minna Kraatari, et al. · Journal of Medical Genetics · 20
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A Whole Exome Study Identifies Novel Candidate Genes for Vertebral Bone Marrow Signal Changes (Modic Changes)
2016 · Minna Kraatari, Sini Skarp, et al. · Spine · 11
Pathogenic REST variant causing Jones syndrome and a review of the literature
2022 · Elisa Rahikkala, Johanna Julku, et al. · European Journal of Human Genetics · 9
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HIDEA syndrome is caused by biallelic, pathogenic, rare or founder P4HTM variants impacting the active site or the overall stability of the P4H‐TM protein
2022 · Minna Kraatari‐Tiri, Leila Soikkonen, et al. · Clinical Genetics · 9
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Clinical and Genetic Characteristics of Finnish Patients with Autosomal Recessive and Dominant Non-Syndromic Hearing Loss Due to Pathogenic TMC1 Variants
2022 · Minna Kraatari-Tiri, Maria K. Haanpää, et al. · Journal of Clinical Medicine · 9
Expanding the clinical spectrum of biglycan-related Meester-Loeys syndrome
2024 · Josephina A. N. Meester, Anne Hebert, et al. · npj Genomic Medicine · 7
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Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study
2024 · Alix Paulet, Cavan Bennett-Ness, et al. · European Journal of Human Genetics · 7
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Herpes simplex virus 2 encephalitis in a patient heterozygous for a TLR3 mutation
2020 · Timo Hautala, Jie Chen, et al. · Neurology Genetics · 7
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ATM c. 7570G >C is a high‐risk allele for breast cancer
2022 · Minna Kankuri‐Tammilehto, Anna Tervasmäki, et al. · International Journal of Cancer · 5
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X-linked myotubular myopathy mimics hereditary spastic paraplegia in two female manifesting carriers of pathogenic MTM1 variant
2020 · Minna Kraatari, Hannu Tuominen, et al. · European Journal of Medical Genetics · 5
Biallelic hexokinase 1 ( HK1 ) variants causative of non‐spherocytic haemolytic anaemia: A case series with emphasis on the HK1 promoter variant and literature review
2024 · Elli‐Maija Ukonmaanaho, Silvia Dell'Anna, et al. · British Journal of Haematology · 3
An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome
2025 · Sanaa Choufani, Vanda McNiven, et al. · The American Journal of Human Genetics · 2
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Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant
2022 · Thashi Bharadwaj, Isabelle Schrauwen, et al. · Molecular Genetics & Genomic Medicine · 2
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Vertebral Endplate Change as a Feature of Intervertebral Disc Degeneration: A Heritability Study
2014 · J. Määttä, M. Kraatari, et al. · Global Spine Journal · 2
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Clinical and genetic characterization of intellectual disability
2026 · Aarni Venetvaara, Minna Kraatari‐Tiri, et al. · Developmental Medicine & Child Neurology · 1
Clinical and genetic characterisation of childhood-onset sensorineural hearing loss reveal associated phenotypes and enrichment of pathogenic founder mutations in the Finnish population
2024 · Minna Kraatari-Tiri, Tyrni Pykälainen, et al. · International Journal of Audiology · 1
XXYLT1 and Mendelian Retinal Dystrophy
2026 · Minna Kraatari-Tiri, Hina Ishtiaq, et al. · JAMA Ophthalmology
Correction: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study
2024 · Alix Paulet, Cavan Bennett-Ness, et al. · European Journal of Human Genetics
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The heritability and genetic risk factors of Modic changes
2018 · Minna Kraatari
Works count: 25
Citation count: 229
H-index: 8
I10-index: 5
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