Christine Søholm Hansen
Publications by Year
Research Areas
Genetic Associations and Epidemiology, Epigenetics and DNA Methylation, Birth, Development, and Health, Genetics and Neurodevelopmental Disorders, Autism Spectrum Disorder Research
Most-Cited Works
- → Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression(2018)3,232 cited
- → Identification of common genetic risk variants for autism spectrum disorder(2019)2,551 cited
- → Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder(2018)2,287 cited
- → Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection(2018)1,700 cited
- → Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders(2019)1,446 cited
- → The iPSYCH2012 case–cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders(2017)372 cited
- → An epigenetic clock for gestational age at birth based on blood methylation data(2016)309 cited
- → Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank(2020)215 cited
- → The Genetic Architecture of Depression in Individuals of East Asian Ancestry(2021)191 cited
- → Discovery of the first genome-wide significant risk loci for ADHD(2017)182 cited