- ORCID iD
-
0000-0002-0117-9255
Show
Sort by
-
Non-coding structural variants disrupt FOXG1 transcriptional regulation in early neurodevelopment
-
- Journal Article
- A1
- open access
Non-coding structural variants disrupt FOXG1 transcriptional regulation in early neurodevelopment
-
Non-coding structural variants disrupt regulatory elements steering FOXG1 transcription in early neurodevelopment (Award Candidate)
(2025) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 33(Supplement 1). p.745-746 -
Non-coding structural variants identify a commonly affected regulatory region steering FOXG1 transcription in early neurodevelopment
-
Non-coding structural variants disrupt a critical regulatory region steering FOXG1 transcription during early neurodevelopment
-
Non-coding structural variants identify a commonly affected regulatory region steering FOXG1 transcription in early neurodevelopment
-
Non-coding structural variants disrupt regulatory elements steering FOXG1 transcription in early neurodevelopment
-
Structural variants disrupt a critical regulatory region downstream of FOXG1
-
Structural variants disrupt a critical regulatory region downstream of FOXG1
-
- Journal Article
- A1
- open access
Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder