Onderzoeker
Laura Vandervore
- Trefwoorden:Geneeskunde
- Disciplines:Ontwikkelingsgenetica, Neurologische en neuromusculaire ziekten
Affiliaties
- Klinische Biologie (Departement)
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Vanaf13 mei 2022 → 31 aug 2023 - Klinische Biologie (Departement)
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Vanaf1 sep 2019 → 29 feb 2020 - Observerende Klinische wetenschappen (Departement)
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Vanaf8 apr 2019 → 30 sep 2019 - Observerende Klinische wetenschappen (Departement)
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Vanaf1 okt 2015 → 31 aug 2019 - Faculteit van de Geneeskunde en Farmacie (Faculteit)
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Vanaf28 aug 2015 → 12 sep 2019 - Faculteit van de Geneeskunde en Farmacie (Faculteit)
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Vanaf12 sep 2013 → 24 jun 2015
Publicaties
1 - 10 van 11
- Aztreonam-avibactam synergy, a validation and comparison of diagnostic tools(2023)
Auteurs: Gil Verschelden, Maxim Noeparast, Laura Vandervore, Anke Stoefs, Margo Olbrecht, Eveline Van Honacker, Katleen Vandamme, Kristof Vandoorslaer, Thomas Demuyser, Denis Piérard, et al.
- TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental Abnormalities(2019)
Auteurs: Laura Vandervore, Rachel Schot, Chiara Milanese, Daphne J Smits, Esmee Kasteleijn, Andrew E Fry, Daniela T Pilz, Stefanie Brock, Esra Börklü-Yücel, Marco Post, et al.
Pagina's: 1126-1147 - Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis(2019)
Auteurs: Pamela Magini, Daphne J Smits, Laura Vandervore, Rachel Schot, Marta Columbaro, Esmee Kasteleijn, Mees van der Ent, Flavia Palombo, Maarten H Lequin, Marjolein Dremmen, et al.
Pagina's: 689-705 - Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamics (vol 142, pg 867, 2019)(2019)
Auteurs: Laura Vandervore, Rachel Schot, Esmee Kasteleijn, Renske Oegema, Katrien Stouffs, Alexander Gheldof, Martyna M Grochowska, Marianne L T van der Sterre, Leontine M A van Unen, Martina Wilke, et al.
Pagina's: 867-867 - Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamics(2019)
Auteurs: Laura Vandervore, Rachel Schot, Esmee Kasteleijn, Renske Oegema, Katrien Stouffs, Alexander Gheldof, Martyna M Grochowska, Marianne L T van der Sterre, Leontine M A van Unen, Martina Wilke, et al.
Pagina's: 867-884 - FUNCTIONAL CHARACTERIZATION OF GENES INVOLVED IN THE DEVELOPMENT OF THE HUMAN BRAIN.(2019)
Auteurs: Laura Vandervore, Alexander Gheldof, Grazia Mancini, Anna C Jansen
- MACF1 Mutations Encoding Highly Conserved Zinc-Binding Residues of the GAR Domain Cause Defects in Neuronal Migration and Axon Guidance(2018)
Auteurs: William B Dobyns, Kimberly A Aldinger, Gisele E Ishak, Ghayda M Mirzaa, Andrew E Timms, Megan E Grout, Marjolein H G Dremmen, Rachel Schot, Laura Vandervore, Marjon A van Slegtenhorst, et al.
Pagina's: 1009-1021 - Mutated zinc finger protein of the cerebellum 1 leads to microcephaly, cortical malformation, callosal agenesis, cerebellar dysplasia, tethered cord and scoliosis(2018)
Auteurs: Laura Vandervore, Rachel Schot, A Jeannette M Hoogeboom, Carsten Lincke, Irenaeus F M de Coo, Maarten H Lequin, Marjolein Dremmen, Leontine M A van Unen, Jasper J Saris, Anna C Jansen, et al.
Pagina's: 783-789 - Biallelic mutations in RTTN are associated with microcephaly, short stature and a wide range of brain malformations(2018)
Auteurs: Katrien Stouffs, Stéphanie Moortgat, Tim Vanderhasselt, Laura Vandervore, Alice Dica, Mikaël Mathot, K. Keymolen, Sara Seneca, Alexander Gheldof, Linda De Meirleir, et al.
Pagina's: 733-737 - Expanding the clinical spectrum of biallelic ZNF335 variants(2018)
Auteurs: Katrien Stouffs, A B Stergachis, Tim Vanderhasselt, A Dica, S Janssens, Laura Vandervore, Alexander Gheldof, Olaf Bodamer, Kathelijn Keymolen, Sara Seneca, et al.
Pagina's: 246-251