Hanna M Ollila

Employment

• Institute for Molecular Medicine Finland (FIMM) FIMM-EMBL Group leader
  2019 - Present
• Massachusetts General Hospital Instructor
  2018 - Present
• University of Helsinki

Education

Education history is unavailable.

Projects & Funding

Projects & funding information is unavailable.

Publications (116)

• The genetic architecture of fibromyalgia across 2.5 million individuals
  Isabel Kerrebijn, Gyða Björnsdóttir, Keon Arbabi +53 more
  Nature Medicine 2026 DOI: 10.1038/s41591-026-04492-6
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• Genetic architecture of 67 oral diseases and their links to systemic diseases
  Human Genetics and Genomics Advances 2026 DOI: 10.1016/j.xhgg.2026.100633
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• Variants Near NOG and SOX9 Are Associated with Mandibular Retrognathia
  Journal of Dental Research 2026 DOI: 10.1177/00220345251397375
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• Sleep and circadian health in the UK Biobank
  Katrina Y. K. Tse, Hang Yuan, Charilaos Zisou

  +21 more

  • Jo Holliday
  • Colin Alexander Espie
  • Derk‐Jan Dijk
  • Angus C. Burns
  • Aiden Doherty
  • +16 more
  Sleep 2026 DOI: 10.1093/sleep/zsag068
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• Genetic variants affect diurnal glucose levels throughout the day
  Nature Communications 2026 DOI: 10.1038/s41467-026-72432-6
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• Genetic variation near ROBO1 is associated with craniofacial microsomia and related phenotypes in the Finnish population
  Human Molecular Genetics 2026 DOI: 10.1093/hmg/ddag020
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• Genetic architecture of lumbar spinal stenosis
  Nature Communications 2026 DOI: 10.1038/s41467-026-70935-w
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• The genetic basis of dermatophytosis skin infection susceptibility
  Nature Communications 2026 DOI: 10.1038/s41467-026-69670-z
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• Central role of glycosylation processes in human genetic susceptibility to SARS-CoV-2 infections with Omicron variants
  Nature Genetics 2026 DOI: 10.1038/s41588-025-02484-9
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• Genome-wide meta-analysis identifies genetic risk loci for mono- and polyneuropathies in 983 477 individuals
  Human Molecular Genetics 2026 DOI: 10.1093/hmg/ddaf200
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• Genetic insights of sleep apnea symptomatology and endotypes
  Sleep 2026 DOI: 10.1093/sleep/zsaf308
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• Perimä muovaa alaleukaa - uutta tietoa retrognatian geneettisestä taustasta
  Suomen hammaslääkärilehti 2026
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• Human genetics implicate thromboembolism in the pathogenesis of long COVID in individuals of European ancestry
  Nature Cardiovascular Research 2025 DOI: 10.1038/s44161-025-00749-4
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• Characterization of prevalent genetic variants in the Estonian Biobank body-mass index GWAS
  Nature Communications 2025 DOI: 10.1038/s41467-025-64006-9
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• Genetic associations between Serotonin Receptor 1F (HTR1F) regulatory variation and sleep apnea in non-obese individuals
  European Respiratory Journal 2025 DOI: 10.1183/13993003.01778-2024
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• Steroid hormone biosynthesis and dietary related metabolites associated with excessive daytime sleepiness
  EBioMedicine 2025 DOI: 10.1016/j.ebiom.2025.105881
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• Haplotype analysis reveals pleiotropic disease associations in the HLA region
  American Journal of Human Genetics 2025 DOI: 10.1016/j.ajhg.2025.06.011
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• Large-scale genome-wide analyses with proteomics integration reveal novel loci and biological insights into frailty
  Nature Aging 2025 DOI: 10.1038/s43587-025-00925-y
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• Increasing incidence and burden of obstructive sleep apnoea in the Finnish population
  Respiratory Medicine 2025 DOI: 10.1016/j.rmed.2025.108155
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• Polygenic scores for obstructive sleep apnoea reveal pathways contributing to cardiovascular disease
  EBioMedicine 2025 DOI: 10.1016/j.ebiom.2025.105790
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