- ORCID iD
- 0000-0002-5936-8294
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Comparison of 3D genome structure between neuronal and clinically accessible tissues
(2024) -
The retina-specific 3D genome and the impact of structural variation in inherited retinal disease
(2024) -
- Miscellaneous
- open access
Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder
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Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder
(2024) -
Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene causes a novel neurodevelopmental disorder
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Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene causes a novel neurodevelopmental disorder
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Structural variants disrupt a critical regulatory region downstream of FOXG1
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- Journal Article
- A1
- open access
Comparative 3D genome analysis between neural retina and retinal pigment epithelium reveals differential cis-regulatory interactions at retinal disease loci
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- Journal Article
- A1
- open access
A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development
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An optimized workflow for CRISPR/Cas9-mediated generation of indels and large deletions in induced pluripotent stem cells and neural stem cells