Common variants conferring risk of schizophreniaLambertus A. Kiemeney, Preben Bo Mortensen, Engilbert Sigurðsson et al.|Nature|2009Cited by 1.7k
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysisNigel Williams, Anita Thapar, Irina Zaharieva et al.|The Lancet|2010Cited by 575
Disruption of the neurexin 1 gene is associated with schizophreniaDan Rujescu, Leena Peltonen, Andrés Ingason et al.|Human Molecular Genetics|2008Cited by 485
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degenerationYi Yu, Johanna M. Seddon, Tushar Bhangale et al.|Human Molecular Genetics|2011Cited by 257
Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and CognitionDennis van der Meer, Ómar Gústafsson, Ida E. Sønderby et al.|JAMA Psychiatry|2019Cited by 91