Sarah Vergult
Universiteit Gent
H-index: 22
Europe-Belgium
Top articles of Sarah Vergult
Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability
The American Journal of Human Genetics
2024/2/26
Sadegheh Haghshenas
H-Index: 2
Aidin Foroutan
H-Index: 5
Xia Wang
H-Index: 6
Pankaj Agrawal
H-Index: 25
Katrin Hoffmann
H-Index: 4
Jason Hom
H-Index: 17
Julie Jones
H-Index: 4
Pengfei Liu
H-Index: 4
Philippe Lysy
H-Index: 18
Nicole Revencu
H-Index: 21
Eleanor G Seaby
H-Index: 13
Siddharth Srivastava
H-Index: 2
Olivier Vanakker
H-Index: 24
Nan Wu
H-Index: 2
Sen Zhao
H-Index: 13
Bekim Sadikovic
H-Index: 27
Björn Menten
H-Index: 38
Bo Yuan
H-Index: 23
Sarah Vergult
H-Index: 18
A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development
Nature Communications
2024/1/2
Emma Wentworth Winchester
H-Index: 3
Sarah Vergult
H-Index: 18
Differential 3D genome topology shapes the regulatory landscapes of IRD genes in human neural retina and retinal pigment epithelium
Investigative Ophthalmology & Visual Science
2023/6/1
Eva D'Haene
H-Index: 4
Sarah Vergult
H-Index: 18
A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene
medRxiv
2023
Long-read sequencing and optical genome mapping enable full characterization of previously unresolved structural variation
2023
P50. Long-read sequencing resolves (complex) cryptic structural variation in patients with syndromic intellectual disability
2023
A comprehensive comparison of different seeding densities and the use of microscaffolds to establish a reproducible protocol for unguided neural organoid differentiation.
2023
Comparative 3D genome analysis between neural retina and RPE reveals differential cis-regulatory interactions at retinal disease loci
bioRxiv
2023
Eva D'Haene
H-Index: 4
Sarah Vergult
H-Index: 18
Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy
The American Journal of Human Genetics
2022/11/3
Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models
The American Journal of Human Genetics
2022/11/3
HDAC9 structural variants disrupting TWIST1 transcriptional regulation lead to craniofacial and limb malformations
Genome Research
2022/7/1
Eva D'Haene
H-Index: 4
Sarah Vergult
H-Index: 18
Francesco Brancati
H-Index: 35
Benedikt Hallgrímsson
H-Index: 40
Expanding the phenotype of B3GALNT2-related disorders
Genes
2022/4/14
Sarah Vergult
H-Index: 18
Björn Menten
H-Index: 38
Multi-omics profiling, in vitro and in vivo enhancer assays dissect the cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal …
bioRxiv
2022/3/9
An optimized workflow for CRISPR/Cas9-mediated generation of indels and large deletions in induced pluripotent stem cells and neural stem cells.
2022
Eva D'Haene
H-Index: 4
Sarah Vergult
H-Index: 18
Long-read sequencing resolves cryptic structural variation in patients with syndromic intellectual disability
2022
Mapping the 3D genome of the human retina and its role in retinal disease
2022
Eva D'Haene
H-Index: 4
Sarah Vergult
H-Index: 18
MYT1L-associated neurodevelopmental disorder: description of 40 new cases and literature review of clinical and molecular aspects
2022/1/1
A reassessment of copy number variations in congenital heart defects: picturing the whole genome
Genes
2021/7/8
Sarah Vergult
H-Index: 18
Björn Menten
H-Index: 38
Whole genome sequencing and UMI-4C provide novel insights into the genetic architecture and mechanisms underlying North Carolina macular dystrophy, a cis-regulatory disease
Investigative Ophthalmology & Visual Science
2021/6/21
Phenotypic spectrum of the RBM10‐mediated intellectual disability and congenital malformation syndrome beyond classic TARP syndrome features
Clinical genetics
2021/3
Sarah Vergult
H-Index: 18
