Search results (8)
« Back to PublicationsBiallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.
Journal article
Rius R. et al, (2026), Nature genetics
Saturation editing of RNU4-2 reveals distinct dominant and recessive disorders.
Journal article
De Jonghe J. et al, (2026), Nature
Saturation genome editing of RNU4-2 reveals distinct dominant and recessive neurodevelopmental disorders.
Preprint
De Jonghe J. et al, (2025)
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome.
Journal article
Chen Y. et al, (2024), Nature, 632, 832 - 840
De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders
Conference paper
Chen Y. et al, (2024), EUROPEAN JOURNAL OF HUMAN GENETICS, 32, 854 - 854
LncRNAs Are Differentially Expressed between Wildtype and Cell Line Strains of African Trypanosomes.
Journal article
Kim HC. and Jolly ER., (2022), Non-coding RNA, 8
Multiomic analysis of Schistosoma mansoni reveals unique expression profiles in cercarial heads and tails.
Journal article
Hagerty JR. et al, (2021), Communications biology, 4
LncRNAs in molluscan and mammalian stages of parasitic schistosomes are developmentally-regulated and coordinately expressed with protein-coding genes.
Journal article
Kim HC. et al, (2020), RNA biology, 17, 805 - 815