Henrike Heyne
Hasso Plattner Institute(DE)Institute for Molecular Medicine Finland(FI)Icahn School of Medicine at Mount Sinai(US)
Publications by Year
Research Areas
Genomics and Rare Diseases, Genetic Associations and Epidemiology, Genetics and Neurodevelopmental Disorders, Genomic variations and chromosomal abnormalities, Epilepsy research and treatment
Most-Cited Works
- → FinnGen provides genetic insights from a well-phenotyped isolated population(2023)3,864 cited
- → Rare coding variants in ten genes confer substantial risk for schizophrenia(2022)840 cited
- → FinnGen: Unique genetic insights from combining isolated population and national health register data(2022)412 cited
- → De novo variants in neurodevelopmental disorders with epilepsy(2018)312 cited
- → STXBP1 encephalopathy(2016)310 cited
- → Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals(2019)299 cited
- → GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects