Henrike O Heyne

13PUBLICATIONS
95CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)NeurogeneticsDevelopmental genetics (incl. sex determination)Epidemiological modellingMajor global burdens of disease
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Publications (13)

|Jul 08, 2026
Polygenic scores as modifiers in Mendelian diseases.

|Nov 24, 2025
Leveraging a Genetic Proxy to Investigate the Effects of Lifelong Cardiac Sodium Channel Blockade.

Julian S Wanner, Maren Krafft, Teemu Niiranen

|Oct 01, 2025
Limited overlap between genetic effects on disease susceptibility and disease survival.

Zhiyu Yang, Fanny-Dhelia Pajuste, Kristina Zguro

|Aug 12, 2024
Rare developmental disorder caused by variants in a small RNA gene.

Henrike Heyne

|Jul 25, 2024
Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events.

Henrike O Heyne, Fanny-Dhelia Pajuste, Julian Wanner

|Jun 12, 2024
A unified framework for estimating country-specific cumulative incidence for 18 diseases stratified by polygenic risk.

Bradley Jermy, Kristi Läll, Brooke N Wolford

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Frequent Collaborators

6 joint publications

Julian Wanner

4 joint publications

Mark J Daly

3 joint publications

Joel Rämö

3 joint publications

Aarno Palotie