Björn Menten

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)

Implicit bias in diagnosing mosaicism amongst preimplantation genetic testing providers : results from a multicenter study of 36 395 blastocysts

Mina Popovic, Lorena Borot, Aline R. Lorenzon, Ana Luiza Rossi de Castro Lopes, Denny Sakkas, Belen Lledo, Ruth Morales, Jose Antonio Ortiz, Nikolaos Polyzos (UGent) , Monica Parriego, et al.

(2024) HUMAN REPRODUCTION. 39(1). p.258-274

Journal Article
A1
open access

Pronuclear transfer rescues poor embryo development of in vitro-grown secondary mouse follicles

Antonia Christodoulaki (UGent) , Haitang He, Min Zhou (UGent) , Chloë De Roo (UGent) , Machteld Baetens (UGent) , Tine De Pretre (UGent) , Muhammad Fakhar-I-Adil (UGent) , Björn Menten (UGent) , Ann Van Soom (UGent) , Dominic Stoop (UGent) , et al.

(2024) HUMAN REPRODUCTION OPEN. 2024(1).

Journal Article
A1
open access

Neoantigen-targeted dendritic cell vaccination in lung cancer patients induces long-lived T cells exhibiting the full differentiation spectrum

Joline Ingels (UGent) , Laurenz De Cock (UGent) , Dieter Stevens (UGent) , Rupert Mayer (UGent) , Fabien Henri Thery (UGent) , Guillem Sanchez Sanchez, David Vermijlen, Karin Weening (UGent) , Saskia De Smet (UGent) , Nele Lootens (UGent) , et al.

(2024) CELL REPORTS MEDICINE. 5(5).

Long-read sequencing enables full characterization of previously unresolved structural variation

Griet De Clercq (UGent) , Lies Vantomme (UGent) , Bert Callewaert (UGent) , Annelies Dheedene (UGent) and Björn Menten (UGent)

(2023) Nanopore Day Paris 2023, Abstracts.

Academic Bibliography

Björn Menten

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

Implicit bias in diagnosing mosaicism amongst preimplantation genetic testing providers : results from a multicenter study of 36 395 blastocysts

Pronuclear transfer rescues poor embryo development of in vitro-grown secondary mouse follicles

Neoantigen-targeted dendritic cell vaccination in lung cancer patients induces long-lived T cells exhibiting the full differentiation spectrum

Long-read sequencing enables full characterization of previously unresolved structural variation

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