prof. dr. ir. Sarah Vergult
- ORCID iD
- 0000-0002-0816-6262
Show
Sort by
-
- 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
-
Long-read sequencing and optical genome mapping enable full characterization of previously unresolved structural variation
-
Long-read sequencing resolves (complex) cryptic structural variation in patients with syndromic intellectual disability
-
Long-read sequencing resolves (complex) cryptic structural variation in patients with syndromic intellectual disability
-
- Conference Paper
- C3
- open access
Long-read sequencing resolves (complex) cryptic structural variation in patients with syndromic intellectual disability
-
- Miscellaneous
- open access
Comparative 3D genome analysis between neural retina and RPE reveals differential cis-regulatory interactions at retinal disease loci
(2023) -
Comparative 3D genome analysis between neural retina and RPE reveals differential cis-regulatory interactions at retinal disease loci
-
Differential 3D genome topology shapes the regulatory landscapes of IRD genes in human neural retina and retinal pigment epithelium
-
Structural variants disrupt a critical regulatory region downstream of FOXG1
(2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.28-28 -
Mapping the 3D genome of the human retina and its role in retinal disease
(2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.57-57