prof. dr. ir. Sarah Vergult
- ORCID iD
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0000-0002-0816-6262
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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 -
Stress attenuation by the adrenergic-specific lncRNA NESPR prevents cell death in neuroblastoma cells
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Multi-omics profiling of human ovarian granulosa cells uncovers cell type-specific regulatory landscapes
(2025) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 33(Supplement 1). p.573-573 -
RNA-sequencing unveils novel FLT4 splice site variants in isolated CHD
(2025) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 33(Supplement 1). p.691-691 -
Assessing the effect of aberrant FOXG1 expression in neural organoids
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Assessing the effect of aberrant FOXG1 expression in neural organoids
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Assessing the effect of aberrant FOXG1 expression in neural organoids
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Heterochronic HOXD13 activation due to 2q31.1 microdeletion results in isolated forearm mesomelic dysplasia
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Non-coding structural variants identify a commonly affected regulatory region steering FOXG1 transcription in early neurodevelopment
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Non-coding structural variants disrupt a critical regulatory region steering FOXG1 transcription during early neurodevelopment