Henrike Heyne

FinnGen provides genetic insights from a well-phenotyped isolated population

Mitja Kurki, Juha Karjalainen, Priit Palta et al. · Nature · 2023 · 3.8K citations · Full text

Rare coding variants in ten genes confer substantial risk for schizophrenia

Tarjinder Singh, Timothy Poterba, David Curtis et al. · Nature · 2022 · 823 citations · Full text

Allelic Variant, Psychiatry, Risk Prediction +11

FinnGen: Unique genetic insights from combining isolated population and national health register data

Mitja Kurki, Juha Karjalainen, Priit Palta et al. · 2022 · 412 citations · Full text

Genetic Testing, Genetics, Genetic Epidemiology +21

De novo variants in neurodevelopmental disorders with epilepsy

Henrike Heyne, Tarjinder Singh, Hannah Stamberger et al. · Nature Genetics · 2018 · 306 citations · Full text

Neurodevelopmental Disorders, Genetic Disorder, Neurology +5

Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

Yen‐Chen Anne Feng, Daniel P. Howrigan, Liam Abbott et al. · The American Journal of Human Genetics · 2019 · 298 citations · Full text

Allelic Variant, Ultra-rare Genetic Variation, Whole-exome Sequencing Study +10