Academic Bibliography

Search 200 years of publications by Ghent University researchers.

Maria del Rocio Pérez Baca

Faculty of Medicine and Health Sciences > Department of Biomolecular Medicine

ORCID iD: 0000-0002-0117-9255

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- Miscellaneous
- open access
Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) 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 Jacobs, Laurenz De Cock (UGent) , Erika D'haenens (UGent) , Annelies Dheedene (UGent) , et al.

(2024) MEDRXIV.
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- 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)
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- Conference Paper
- C3
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.
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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.
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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.
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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
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- Conference Paper
- C3
An optimized workflow for CRISPR/Cas9-mediated generation of indels and large deletions in induced pluripotent stem cells and neural stem cells

Lisa Hamerlinck (UGent) , Maria del Rocio Pérez Baca (UGent) , Lies Vantomme (UGent) , Eva D'haene (UGent) and Sarah Vergult (UGent)

(2023) Belgian Society for Human Genetics (BeSHG) Annual Meeting 2023 : To DNA and beyond, Abstracts.
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- Conference Paper
- C3
Structural variants disrupt a critical regulatory region downstream of FOXG1

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

(2023) EMBO Workshop 'Gene regulatory mechanisms in neural fate decisions', Abstracts.
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- Conference Paper
- C3
Structural variants disrupt a critical regulatory region downstream of FOXG1

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

(2023) 15th Meeting of the Belgian Society for Neuroscience, Abstracts.
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- 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

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