Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disordersDavid J. Roberts, Jaana Suvisaari, Himanshu Chheda et al.|Nature Neuroscience|2016Cited by 476
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencingThomas Pickardt, Alejandro Sifrim, Marc‐Phillip Hitz et al.|Nature Genetics|2016Cited by 467
The genetic architecture and evolution of the human skeletal formEucharist Kun, Vagheesh M. Narasimhan, Emily Javan et al.|Science|2023Cited by 79
The impact of rare protein coding genetic variation on adult cognitive functionChia‐Yen Chen, Martta Kerkelä, Ruoyu Tian et al.|Nature Genetics|2023Cited by 64