Mads V. Hollegaard
Statens Serum Institut(DK)
Publications by Year
Research Areas
Genetic Associations and Epidemiology, Birth, Development, and Health, Epigenetics and DNA Methylation, Neonatal Respiratory Health Research, Genetics and Neurodevelopmental Disorders
Most-Cited Works
- → Identification of common genetic risk variants for autism spectrum disorder(2019)2,550 cited
- → Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder(2018)2,287 cited
- → A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations(2013)576 cited
- → Genome-wide associations for birth weight and correlations with adult disease(2016)536 cited
- → Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population(2016)390 cited
- → Polygenic Risk Score, Parental Socioeconomic Status, Family History of Psychiatric Disorders, and the Risk for Schizophrenia(2015)330 cited
- → New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism(2012)318 cited
- → An epigenetic clock for gestational age at birth based on blood methylation data(2016)309 cited
- → Cytokine gene polymorphism in human disease: on-line databases, Supplement 3(2006)219 cited
- → Common variants at VRK2 and TCF4 conferring risk of schizophrenia(2011)216 cited