Sarah Vergult

Structural variants disrupt a critical regulatory region downstream of FOXG1

Lisa Hamerlinck (UGent) , Eva D'haene (UGent) , Nore Van Loon (UGent) , Maria del Rocio Pérez Baca (UGent) , Sarah Vergult (UGent) , Bert Callewaert (UGent) , Elfride De Baere (UGent) , Björn Menten (UGent) , Lies Vantomme (UGent) and Michael B Vaughan (UGent)

(2024) Belgian Society for Human Genetics (BeSHG) Annual Symposium 2024 : Single Cells : to care or not to care, Abstracts.

Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability

Maria del Rocio Pérez Baca (UGent) , Eva Jacobs, Lies Vantomme (UGent) , Pontus LeBlanc (UGent) , Elke Bogaert (UGent) , Annelies Dheedene (UGent) , Laurenz De Cock (UGent) , Sadegheh Haghshenas, Aidin Foroutan, Michael A Levy, et al.

(2024) AMERICAN JOURNAL OF HUMAN GENETICS. 111(3). p.509-528

Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene causes a novel neurodevelopmental disorder

Maria del Rocio Pérez Baca (UGent) , Maria Palomares, Michiel Vanhooydonck (UGent) , Eva D'haene (UGent) , Eva Z. Jacobs, Lies Vantomme (UGent) , Fernando Santos-Simarro, Roser Lleuger-Pujol, Sixto García-Miñaúr, Itsaso Losantos-García, et al.

(2024) 18th Troina Meeting on Genetics of Neurodevelopmental Disorders, Abstracts.

Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene causes a novel neurodevelopmental disorder

Maria del Rocio Pérez Baca (UGent) , Maria Palomares, Michiel Vanhooydonck (UGent) , Eva D'haene (UGent) , Eva Jacobs, Lies Vantomme (UGent) , Fernando Santos-Simarro, Roser Lleuger-Pujol, Sixto García-Miñáur, Itsaso Losantos-García, et al.

(2024) Belgian Society for Human Genetics (BeSHG) Annual Symposium 2024 : Single Cells : to care or not to care, Abstracts.

Conference Paper

Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder

Maria del Rocio Pérez Baca (UGent) , Maria Palomares Bralo, Michiel Vanhooydonck (UGent) , Lisa Hamerlinck (UGent) , Eva D'haene (UGent) , Sebastian Leimbacher (UGent) , Eva Z. Jacobs, Laurenz De Cock (UGent) , Erika D'haenens (UGent) , Zoë Malfait (UGent) , et al.

(2024)

Miscellaneous

Loss-of-function of the Zinc Finger Homeobox 4 (<i>ZFHX4</i>) gene underlies a neurodevelopmental disorder

Maria del Rocio Pérez Baca (UGent) , María Palomares Bralo, Michiel Vanhooydonck (UGent) , Lisa Hamerlinck (UGent) , Eva D'haene (UGent) , Sebastian Leimbacher (UGent) , Eva Z. Jacobs, Laurenz De Cock (UGent) , Erika D'haenens (UGent) , Annelies Dheedene (UGent) , et al.

(2024)

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

Andrea Wilderman, Eva D'haene (UGent) , Machteld Baetens (UGent) , Tara N. Yankee, Emma Wentworth Winchester, Nicole Glidden, Ellen Roets (UGent) , Jo Van Dorpe (UGent) , Sandra Janssens (UGent) , Danny E. Miller, et al.

(2024) NATURE COMMUNICATIONS. 15.

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

Eva D'haene (UGent) , Victor Lopez Soriano (UGent) , Pedro Manuel Martínez-García, Soraya Kalayanamontri, Alfredo Dueñas Rey (UGent) , Ana Sousa-Ortega, Silvia Naranjo, Stijn Van de Sompele (UGent) , Lies Vantomme (UGent) , Quinten Mahieu (UGent) , et al.

(2024) GENOME BIOLOGY. 25(1).

Structural variants disrupt a critical regulatory region downstream of FOXG1

Eva D'haene (UGent) , Lies Vantomme (UGent) , Björn Menten (UGent) , Bert Callewaert (UGent) , Elfride De Baere (UGent) and Sarah Vergult (UGent)

(2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.28-28

Conference Paper
C3
open access

Structural variants disrupt a critical regulatory region downstream of FOXG1

Lisa Hamerlinck (UGent) , Eva D'haene (UGent) , Maria del Rocio Pérez Baca (UGent) , Lies Vantomme (UGent) , Nore Van Loon (UGent) , Björn Menten (UGent) , Bert Callewaert (UGent) , Elfride De Baere (UGent) and Sarah Vergult

(2023) 17th Troina Meeting on Genetics of Neurodevelopmental Disorders Abstract Book. p.9-9

Academic Bibliography

Sarah Vergult

Public URL

Structural variants disrupt a critical regulatory region downstream of FOXG1

Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability

Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene causes a novel neurodevelopmental disorder

Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene causes a novel neurodevelopmental disorder

Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder

Loss-of-function of the Zinc Finger Homeobox 4 (<i>ZFHX4</i>) gene underlies a neurodevelopmental disorder

A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development

Comparative 3D genome analysis between neural retina and retinal pigment epithelium reveals differential cis-regulatory interactions at retinal disease loci

Structural variants disrupt a critical regulatory region downstream of FOXG1

Structural variants disrupt a critical regulatory region downstream of FOXG1

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