- ORCID iD
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0000-0002-5936-8294
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TurboID proximity interactome mapping reveals NR2E3 association with AP-1 and retinal developmental complexes
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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
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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 regulatory elements steering FOXG1 transcription in early neurodevelopment
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Structural variants disrupt a critical regulatory region downstream of FOXG1
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Structural variants disrupt a critical regulatory region downstream of FOXG1
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Systematic comparative analysis of 3D genome structure between neuronal and clinically accessible tissues highlights tissue-specific chromatin features at disease loci
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Tissue-specific 3D genome and splicing signatures of clinically accessible tissues inform sample selection for assessing the impact of genomic aberrations in neurodevelopmental disorders