TRIP12

Publications

Iossifov I et al. The contribution of de novo coding mutations to autism spectrum disorder. Nature.  2014; 515:216-221. doi:10.1038/nature13908. PMID:25363768.

O’Roak BJ et al. Recurrent de novo mutations implicate novel genes underlying simplex autism risk. Nat Commun. 2014; 5:5595. doi:10.1038/ncomms6595. PMID:25418537.

Lelieveld SH et al. Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability. Nat Neurosci. 2016; 19(9):1194-6. doi:10.1038/nn.4352. PMID: 27479843.

Bramswig NC et al. Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autism. Hum Genet. 2016; 136(2):179-192. doi:10.1007/s00439-016-1743-x. PMID: 27848077.