Associated Papers
Missense variant contribution to USP9X-female syndrome.
Jolly LA et al.
Npj Genomic Medicine, 2020
33298948 (PubMed )
Supplement: 41525_2020_162_MOESM1_ESM.pdf
Functional relationships between recessive inherited genes and genes with de novo variants in autism spectrum disorder.
Wang L et al.
Molecular Autism, 2020
33023636 (PubMed )
Supplement: 13229_2020_382_MOESM1_ESM.pdf
Prioritized High-Confidence Risk Genes for Intellectual Disability Reveal Molecular Convergence During Brain Development.
Liu Z et al.
Frontiers in Genetics, 2018
30279698 (PubMed )
Supplement: Table_2.XLS › Sheet1
Variation in a range of mTOR-related genes associates with intracranial volume and intellectual disability.
Reijnders MRF et al.
Nature Communications, 2017
29051493 (PubMed )
Supplement: 41467_2017_933_MOESM5_ESM.xlsx › All_de_novo_mutations
Select a paper to view details