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C. Heymanslaan 10, ingang 34 (MRB)
9000 Gent - Lies.Vantomme@UGent.be
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Mapping the 3D genome of the human retina and its role in retinal disease
(2022) -
Mapping the 3D genome of the human retina and its role in retinal disease
(2022) -
Structural variants disrupt a critical regulatory region downstream of FOXG1
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Benchmarking of long-read structural variant callers on a recently released truth set using Oxford Nanopore data
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Benchmarking of long-read structural variant callers on a recently released truth set using Oxford Nanopore data
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A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 gene (ZFHX3)
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Noncoding structural variants disrupt the regulatory architecture of Rett genes
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Noncoding structural variants disrupt the regulatory architecture of Rett genes
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- Journal Article
- A1
- open access
A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett-like characteristics
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CRISPR/Cas9-mediated genome editing in naïve human embryonic stem cells