Aarhus University at ASHG 2026

Oct 20–24, 2026 Montréal, Canada ~7.5k attendees Website

Aarhus University brings 4 presentations from 3 research groups to ASHG 2026 in Montréal. Its program centres on population genetics, computational methods, and clinical and reproductive genetics. Center for Registerforskning brings a simulation study of inverse probability weighting, SMARTbiomed brings genetic-correlation estimates from variant effects, and Neuropsychiatric and Statistical Genomics Lab brings genetically distinct depression trajectories from longitudinal health records.

OrganizationASHG 2026 Attendance
Aarhus University
Aarhus, Denmark
2 PhD Students · 1 Postdoc
Center for Registerforskningncrr.au.dk
Dry lab~70 people
Studies Danish registers, iPSYCH2012 and bio-banked genetic data. Focuses on psychiatric epidemiology and gene-environment interactions in mental disorders.
Funded by Danish National Research Foundation, Lundbeck Foundation +7 more
›
Aarhus University, CIRRAU · active
“CIRRAU; a centre for interdisciplinary register-based research funded by Aarhus University”
Lundbeck Foundation, CIRRAU scientific programs · active
“supported financially by the Lundbeck Foundation, TrygFonden, The Stanley Medical Research Institute, EU, The Simon Foundation and NordForsk.”
TrygFonden, CIRRAU scientific programs · active
“supported financially by the Lundbeck Foundation, TrygFonden, The Stanley Medical Research Institute, EU, The Simon Foundation and NordForsk.”
+6 more on the lab page
Source: lab pages
8 platforms and techniques
›
Analyzes
Danish registers, iPSYCH2012 case-cohort sample, Danish Neonatal Screening Bank, Statistics Denmark database
Techniques
Population-based epidemiology, Gene-environment interaction studies, Population-based genetic studies, Register-based research
Source: lab pages
No openings posted
Poster
Fri Oct 23
2:30 pm
Weight with caution: a simulation study on inverse probability weighting (IPW) adjustment
Statistical geneticsMethodologyGenetic epidemiologyPopulation genetics
SMARTbiomedsmartbiomed.dk
Dry lab~38 people
Develops statistical methods for omics, biobank/EHR and clinical imaging data. Applies causal inference, risk prediction and machine learning to cardiometabolic, brain and reproductive traits.
Funded by Lundbeck Foundation, Novo Nordisk Foundation +3 more
›
Lundbeck Foundation, Pioneer Centre for SMARTbiomed · starting June 2024
“from the Lundbeck Foundation”
Novo Nordisk Foundation, Pioneer Centre for SMARTbiomed · starting June 2024
“the Novo Nordisk Foundation”
Villum Foundation, Pioneer Centre for SMARTbiomed · starting June 2024
“the Villum Foundation”
+2 more on the lab page
Source: lab pages
14 platforms and techniques
›
Analyzes
perturb-seq data, electronic health records, multiomics data, single-cell CRISPR screens, cell-free DNA fragments, wearable device data, continuous glucose monitoring data, clinical imaging data
Techniques
causal inference, risk prediction, machine learning, polygenic risk scoring, causal discovery, deep learning
Source: lab pages
Currently hiring
›
“At SMARTbiomed, we are regularly looking for postdoctoral fellows or PhD students.”
Source: lab positions page
Poster
Thu Oct 22
4:15 pm
Estimating genetic correlation using posterior sampling variant effects
Collaborators: Institute for Molecular Bioscience
Genotype-phenotype correlationsPolygenic risk scoreStatistical genetics
Neuropsychiatric and Statistical Genomics Labyafenglab.com
Works in computational genetics.
1 more presenter — research group not yet identified

Explore the full ASHG 2026 dataset

Get in-depth attendee and institution profiles and research, to plan your meetings in Montréal. Leave your work email and we’ll be in touch.

Privacy

Download the full ASHG 2026 CSV

Leave your work email and we’ll be in touch. The CSV adds attendee names, roles and contact details to the company and session data shown here.

Privacy

Instantly find 20 buyers from Aarhus University

Get a list of who you should contact, their contact info, and what to say.

Totally free and instant, no sign up necessary!

Not affiliated with or endorsed by the American Society of Human Genetics. Submit a correction