Associated Papers
CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology.
Oppermann H et al.
European Journal of Human Genetics : Ejhg, 2023
Integrative analysis prioritised oxytocin-related biomarkers associated with the aetiology of autism spectrum disorder.
Wang T et al.
Ebiomedicine, 2022
35665681 (PubMed )
Supplement: mmc24.xlsx › Sheet1
De novo mutations in folate-related genes associated with common developmental disorders.
Luo T et al.
Computational and Structural Biotechnology Journal, 2021
33777337 (PubMed )
Supplement: mmc6.xlsx › Sheet1
Inactivating CUX1 mutations promote tumorigenesis.
Wong CC et al.
Nature Genetics, 2014
24316979 (PubMed )
Supplement: NIHMS55610-supplement-2.xlsx › Sup_Table_8
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