Eija Hämäläinen

Analysis of shared heritability in common disorders of the brain

Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane et al. · Science · 2018 · 2K citations · Full text

Brain Function, Psychiatric Disorders, Genetics +23

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

Genome-wide association analysis identifies susceptibility loci for migraine without aura

Tobias Freilinger, Verneri Anttila, Boukje de Vries et al. · Nature Genetics · 2012 · 339 citations · Full text

Genome-wide Association Study, Cluster Headache, Neurogenomics +5

Metabonomic, transcriptomic, and genomic variation of a population cohort

Michael Inouye, Johannes Kettunen, Pasi Soininen et al. · Molecular Systems Biology · 2010 · 272 citations · Full text

Genomic Variation, Molecular Ecology, Medicine +6

Use of cancer‐specific genomic rearrangements to quantify disease burden in plasma from patients with solid tumors

David J. McBride, Arto Orpana, Christos Sotiriou et al. · Genes Chromosomes and Cancer · 2010 · 194 citations