ASHG 2026 · Tier 1 Academic

Institute for Molecular Medicine Finland at ASHG 2026

Helsinki, Finland

Institute for Molecular Medicine Finland at ASHG 2026 in Montréal: 6 presentations (5 posters, 1 platform talk); 3 research groups.

6
presentations on the program
3
research groups identified

Explore everyone at ASHG 2026 →

OrganizationASHG 2026 Attendance
Institute for Molecular Medicine Finland
Helsinki, Finland
2 PhD Students · 2 Postdocs · 1 PI
Ollila Labollilalab.org
Dry lab~13 people
Analyzes FinnGen genetic data and electronic health records alongside population genetics, GWAS and bioinformatics. Studies circadian rhythms and brain autoimmunity with Massachusetts General Hospital.
73 papers since 2024
Genome-wide association study of long COVID
Nature Genetics, 2025
Genetic drivers and cellular selection of female mosaic X chromosome loss
Nature, 2024
An immunogenetic basis for lung cancer risk
Science, 2024
Source: OpenAlex author A5045290512
12 platforms and techniques
Analyzes
FinnGen, UK Biobank, Electronic health records, Single-cell RNA sequencing, Transcriptomics, Metabolomics
Techniques
GWAS, Exome-wide association analyses, Mendelian randomization, PheWAS, CRISPR Cas9-engineered iPSC models, Neuronal cell models
Source: lab pages
Currently hiring
“We are always looking for talented post-docs and students.”
Source: lab positions page
No funding stated
Poster
Thu Oct 22
4:15 pm
Age-dependent APOE associations with UK Biobank sleep questionnaire response suggest late-life neurodegenerative selection
Statistical Genetics and Genetic Epidemiology
Collaborators: Massachusetts General Hospital, University of Helsinki
Genome-wide association studyGenetic epidemiologyNeurodegenerationLarge-scale biobanks
Poster
Fri Oct 23
2:30 pm
Multiomic analysis of circadian and seasonal biomarkers
Statistical Genetics and Genetic Epidemiology
Collaborators: University of Helsinki, Massachusetts General Hospital +1 more
BioinformaticsBrain/nervous systemProteomicsMetabolomics
Translational Genomics Labtranslationalgenomics.eu
Dry lab~15 people
Analyzes germline genomics, Finnish biobank/registry, clinical and multi-omic data. Develops disease-risk, cancer-screening and medication-response prediction tools.
24 papers since 2024
Evaluation of polygenic scoring methods in five biobanks shows larger variation between biobanks than methods and finds benefits of ensemble learning
The American Journal of Human Genetics, 2024
An immunogenetic basis for lung cancer risk
Science, 2024
Comprehensive Inherited Risk Estimation for Risk-Based Breast Cancer Screening in Women
Journal of Clinical Oncology, 2024
Source: OpenAlex author A5061885811
2 platforms and techniques
Techniques
Polygenic risk scores, Mendelian randomization
Source: lab pages
No funding stated · No openings posted
Talk
Thu Oct 22
11:00 am
Germline polygenic susceptibility shapes somatic mutational signatures across common cancers
Cancer Susceptibility: Germline Effects on Risk, Mechanisms, and Mutations
Collaborators: University of Helsinki
CancerPolygenic risk scoreSomatic variantsStatistical genetics
Poster
Thu Oct 22
4:15 pm
Genome-wide association study identifies 13 loci for ovarian mature teratoma and implicates meiotic cell cycle regulators
Statistical Genetics and Genetic Epidemiology
Collaborators: University of Helsinki
Genome-wide association studyPopulation geneticsWomen's health
Data Science - Genetic Epidemiology Labdsgelab.org
Dry lab~17 people
Develops statistical and deep-learning methods on EHR, national registries, genetic, proteomics and single-cell transcriptomic data. Uses them for early disease detection, biomarker discovery and prevention.
64 papers since 2024
Genetic drivers and cellular selection of female mosaic X chromosome loss
Nature, 2024
Family-GWAS reveals effects of environment and mating on genetic associations
medRxiv, 2024
Evaluation of polygenic scoring methods in five biobanks shows larger variation between biobanks than methods and finds benefits of ensemble learning
The American Journal of Human Genetics, 2024
Source: OpenAlex author A5073500794
13 platforms and techniques
Analyzes
Electronic Health Records (EHRs), National health registries, Whole-exome sequencing, Single-cell transcriptomics, Proteomics
Techniques
Statistical methods, Deep learning, GWAS, Polygenic scores, Self-supervised foundation models, Transformer-based models, Multi-omics, Longitudinal and survival analysis
Source: lab pages
No funding stated · No openings posted
Poster
Fri Oct 23
2:30 pm
Large-Scale GWAS of Lab Value Trajectories Reveals Genetic Effects Distinct from Mean Levels
Statistical Genetics and Genetic Epidemiology
Collaborators: Hue University of Education, University of Tartu +5 more
Complex diseasesGenome-wide association studyPolygenic risk score
1 more presenter — research group not yet identified

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