Ghent University Academic Bibliography

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Your filters: cql: author="Jacobs, Eva" or (type any "bookEditor journalEditor issueEditor" and editor="Jacobs, Eva")

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- Journal Article
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
- open access
A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene

Maria del Rocio Pérez Baca (UGent) , Eva Jacobs, Lies Vantomme (UGent) , Pontus LeBlanc (UGent) , Elke Bogaert (UGent) , Annelies Dheedene (UGent) , Laurenz De Cock, Bart Dermaut (UGent) , Aidin Foroutan, Jennifer Kerkhof, et al.

(2022) Joint BeSHG / NVHG meeting 2022, Abstracts.
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Luminescent human iPSC-derived neurospheroids enable modeling of neurotoxicity after oxygen-glucose deprivation

Elise Van Breedam, Aleksandra Nijak, Tamariche Buyle-Huybrecht, Julia Di Stefano, Marlies Boeren, Jonas Govaerts, Alessandra Quarta, Tine Swartenbroekx, Eva Jacobs, Björn Menten (UGent) , et al.

(2022) NEUROTHERAPEUTICS. 19(2). p.550-569
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- PhD Thesis
CRISPR-ing the gap between discovery and validation of candidate genes for neurodevelopmental disorders

Eva Jacobs

(2021)
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Expanding the molecular spectrum and the neurological phenotype related to CAMTA1 variants

Eva Jacobs, Kathleen Brown, Melissa C. Byler, Erika D'haenens (UGent) , Annelies Dheedene (UGent) , Lindsay B. Henderson, Jennifer B. Humberson, Richard H. Jaarsveld, Farah Kanani, Robert Roger Lebel, et al.

(2021) CLINICAL GENETICS. 99(2). p.259-268
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Recurrent chromosomal imbalances provide selective advantage to human embryonic stem cells under enhanced replicative stress conditions

Liselot Mus (UGent) , Stéphane Van Haver (UGent) , Mina Popovic, Wim Trypsteen (UGent) , Steve Lefever (UGent) , Nadja Zeltner, Yudelca Ogando, Eva Jacobs, Geertrui Denecker (UGent) , Ellen Sanders (UGent) , et al.

(2021) GENES CHROMOSOMES & CANCER. 60(4). p.272-281
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- Conference Paper
- C3
A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 gene (ZFHX3)

Maria del Rocio Pérez Baca (UGent) , Eva Jacobs, Lies Vantomme (UGent) , Mareike Bauer, Melissa Bellini, Claire Beneteau, Natasha Brown, David Coman, Laurenz De Cock (UGent) , Annelies Dheedene (UGent) , et al.

(2021) Online Research Day 2021, Abstracts.
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- Conference Paper
- C3
Exploring the contribution of gene dosage effects of 17q gain genes on hESC and neuroblastoma proliferation

Liselot Mus (UGent) , Geertrui Denecker (UGent) , Stéphane Van Haver (UGent) , Nadja Zeltner, Yudelca Ogando, Ellen Sanders (UGent) , Eva Jacobs, Mina Popovic, Christophe Van Neste (UGent) , Suzanne Vanhauwaert (UGent) , et al.

(2019) Pediatric Oncology and Hematology, 2nd KiTZ symposium, Abstracts.
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- Conference Paper
- C3
17q gain provides proliferative advantage to human embryonic stem cells under conditions of replicative stress

Liselot Mus (UGent) , Geertrui Denecker (UGent) , Stéphane Van Haver (UGent) , Nadja Zeltner, Yudelca Ogando, Ellen Sanders (UGent) , Eva Jacobs, Mina Popovic, Christophe Van Neste (UGent) , Suzanne Vanhauwaert (UGent) , et al.

(2019) OncoPoint, 7th Research seminar, Abstracts.
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- Conference Paper
- C3
17q gain provides proliferative advantage to human embryonic stem cells under replicative stress

Liselot Mus (UGent) , Stéphane Van Haver (UGent) , Geertrui Denecker (UGent) , Nadja Zeltner, Yudelca Ogando, Ellen Sanders (UGent) , Eva Jacobs, Mina Popovic, Christophe Van Neste (UGent) , Suzanne Vanhauwaert (UGent) , et al.

(2019) The DNA-damage response in cell physiology and disease, EMBO Workshop, Abstracts.

Academic Bibliography

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

A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene

Luminescent human iPSC-derived neurospheroids enable modeling of neurotoxicity after oxygen-glucose deprivation

CRISPR-ing the gap between discovery and validation of candidate genes for neurodevelopmental disorders

Expanding the molecular spectrum and the neurological phenotype related to CAMTA1 variants

Recurrent chromosomal imbalances provide selective advantage to human embryonic stem cells under enhanced replicative stress conditions

A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 gene (ZFHX3)

Exploring the contribution of gene dosage effects of 17q gain genes on hESC and neuroblastoma proliferation

17q gain provides proliferative advantage to human embryonic stem cells under conditions of replicative stress

17q gain provides proliferative advantage to human embryonic stem cells under replicative stress

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