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Researcher
Lies Vantomme
Profile
Projects
Publications
Activities
Awards & Distinctions
22
Results
2022
A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene
Maria del Rocio Pérez Baca
Eva Jacobs
Lies Vantomme
Pontus LeBlanc
Elke Bogaert
Annelies Dheedene
Laurenz De Cock
Bart Dermaut
Aidin Foroutan
Jennifer Kerkhof
et al.
C3
Conference
2022
Benchmarking of long read structural variant callers using Oxford Nanopore data
Griet De Clercq
Bram Van Gaever
Lies Vantomme
Annelies Dheedene
Björn Menten
C3
Conference
2022
Benchmarking of long-read structural variant callers using Oxford Nanopore data
Griet De Clercq
Bram Van Gaever
Lies Vantomme
Annelies Dheedene
Björn Menten
C3
Conference
2022
Benchmarking of long-read structural variant callers using Oxford Nanopore data
Griet De Clercq
Bram Van Gaever
Lies Vantomme
Annelies Dheedene
Björn Menten
C3
Conference
2022
Benchmarking of long-read structural variant callers using in-house generated Oxford Nanopore data
Griet De Clercq
Bram Van Gaever
Lies Vantomme
Annelies Dheedene
Björn Menten
C3
Conference
2022
Long-read sequencing resolves cryptic structural variation in patients with syndromic intellectual disability
Griet De Clercq
Lies Vantomme
Bert Callewaert
Sarah Vergult
Annelies Dheedene
Björn Menten
C3
Conference
2022
Mapping the 3D genome of the human retina and its role in retinal disease
Eva D'haene
Victor Lopez Soriano
Lies Vantomme
Bernd Wissinger
Susanne Kohl
Sarah Vergult
Elfride De Baere
C3
Conference
2022
Mapping the 3D genome of the human retina and its role in retinal disease
Eva D'haene
Victor Lopez Soriano
Lies Vantomme
Bernd Wissinger
Susanne Kohl
Sarah Vergult
Elfride De Baere
C3
Conference
2022
2021
A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 gene (ZFHX3)
Maria del Rocio Pérez Baca
Eva Jacobs
Lies Vantomme
Mareike Bauer
Melissa Bellini
Claire Beneteau
Natasha Brown
David Coman
Laurenz De Cock
Annelies Dheedene
et al.
C3
Conference
2021
Benchmarking of long-read structural variant callers on a recently released truth set using Oxford Nanopore data
Griet De Clercq
Bram Van Gaever
Lies Vantomme
Annelies Dheedene
Björn Menten
C3
Conference
2021
Benchmarking of long-read structural variant callers on a recently released truth set using Oxford Nanopore data
Griet De Clercq
Bram Van Gaever
Lies Vantomme
Annelies Dheedene
Björn Menten
C3
Conference
2021
Structural variants disrupt a critical regulatory region downstream of FOXG1
Eva D'haene
Lies Vantomme
Björn Menten
Bert Callewaert
Elfride De Baere
Sarah Vergult
C3
Conference
2021
2019
A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett-like characteristics
Eva D'haene
Reut Bar-Yaacov
Inbar Bariah
Lies Vantomme
Sien Van Loo
Francisco Avila Cobos
Karen Verboom
Reut Eshel
Rawan Alatawna
Björn Menten
et al.
A1
Journal Article
in
HUMAN MOLECULAR GENETICS
2019
Noncoding structural variants disrupt the regulatory architecture of Rett genes
Eva D'haene
Reut Bar-Yaacov
Inbar Bariah
Lies Vantomme
Sien Van Loo
Francisco Avila Cobos
Karen Verboom
Reut Eshel
Rawan Alatawna
Björn Menten
et al.
C3
Conference
2019
Noncoding structural variants disrupt the regulatory architecture of Rett genes
Eva D'haene
Reut Bar-Yaacov
Inbar Bariah
Lies Vantomme
Sien Van Loo
Francisco Avila Cobos
Karen Verboom
Reut Eshel
Rawan Alatawna
Björn Menten
et al.
C3
Conference
2019
2018
A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett-like characteristics
Eva D'haene
Reut Bar-Yaacov
Inbar Bariah
Lies Vantomme
Sien Van Loo
Francisco Avila Cobos
Karen Verboom
Reut Eshel
Rawan Alatawna
Björn Menten
et al.
C3
Conference
2018
CRISPR/Cas9-mediated genome editing in naïve human embryonic stem cells
Eva Jacobs
Sharat Warrier
Pieter-Jan Volders
Eva D'haene
Eva Vanlombergen
Lies Vantomme
Margot Van der Jeught
Björn Heindryckx
Björn Menten
Sarah Vergult
C3
Conference
2018
CRISPR/Cas9-mediated genome editing in naïve human embryonic stem cells
Eva Jacobs
Sharat Warrier
Pieter-Jan Volders
Eva D'haene
Eva Vanlombergen
Lies Vantomme
Margot Van der Jeught
Björn Heindryckx
Björn Menten
Sarah Vergult
C3
Conference
2018
The MEF2C regulatory network is disrupted in patients with Rett-like characteristics
Eva D'haene
Sarah Vergult
Reut Bar-Yaakov
Inbar Bariah
Lies Vantomme
Sien Van Loo
Francisco Avila Cobos
Reut Eshel
Rowan Alatawna
Ramon Birnbaum
et al.
C3
Conference
2018
The MEF2C regulatory network is disrupted in patients with Rett-like characteristics
Eva D'haene
Reut Bar-Yaakov
Inbar Bariah
Sien Van Loo
Lies Vantomme
Francisco Avila Cobos
Reut Eshel
Rowan Alatawna
Björn Menten
Ramon Birnbaum
et al.
C3
Conference
2018
2017
CRISPR/Cas9-mediated genome editing in naïve human embryonic stem cells
Eva Jacobs
Sharat Warrier
Pieter-Jan Volders
Eva D'haene
Eva Van Lombergen
Lies Vantomme
Margot Van der Jeught
Björn Heindryckx
Björn Menten
Sarah Vergult
A1
Journal Article
in
SCIENTIFIC REPORTS
2017
2015
Two siblings with homozygous pathogenic splice-site variant in mitochondrial asparaginyl-tRNA synthetase (NARS2)
Arnaud Vanlander
Björn Menten
Joél Smet
Linda De Meirleir
Tom Sante
Boel De Paepe
Sara Seneca
Sarah F Pearce
Christopher A Powell
Sarah Vergult
et al.
A1
Journal Article
in
HUMAN MUTATION
2015