Publications by authors named "Laura Vandervore"

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Aztreonam-avibactam synergy, a validation and comparison of diagnostic tools.
Gil Verschelden, Maxim Noeparast, Anke Stoefs, Eveline Van Honacker, Kristof Vandoorslaer, Laura Vandervore

Front Microbiol· November 2023

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False positive Herpes Simplex IgM serology in COVID-19 patients correlates with SARS-CoV-2 IgM/IgG seropositivity.
Laura Vandervore, Eugénie Van Mieghem, Vicky Nowé, Sofie Schouwers, Charlotte Steger

Diagn Microbiol Infect Dis· May 2022

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TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental Abnormalities.
Laura V Vandervore, Rachel Schot, Chiara Milanese, Daphne J Smits, Esmee Kasteleijn

Am J Hum Genet· December 2019

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Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis.
Pamela Magini, Daphne J Smits, Laura Vandervore, Rachel Schot, Marta Columbaro

Am J Hum Genet· October 2019

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Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamics.
Laura V Vandervore, Rachel Schot, Esmee Kasteleijn, Renske Oegema, Katrien Stouffs

Brain· April 2019

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Biallelic mutations in RTTN are associated with microcephaly, short stature and a wide range of brain malformations.
Katrien Stouffs, Stéphanie Moortgat, Tim Vanderhasselt, Laura Vandervore, Alice Dica

Eur J Med Genet· December 2018

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Mutated zinc finger protein of the cerebellum 1 leads to microcephaly, cortical malformation, callosal agenesis, cerebellar dysplasia, tethered cord and scoliosis.
Laura V Vandervore, Rachel Schot, A Jeannette M Hoogeboom, Carsten Lincke, Irenaeus F de Coo

Eur J Med Genet· December 2018

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MACF1 Mutations Encoding Highly Conserved Zinc-Binding Residues of the GAR Domain Cause Defects in Neuronal Migration and Axon Guidance.
William B Dobyns, Kimberly A Aldinger, Gisele E Ishak, Ghayda M Mirzaa, Andrew E Timms, Laura Vandervore

Am J Hum Genet· December 2018

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Bi-allelic variants in encoding the ligand to GPR56 are associated with cobblestone-like cortical malformation, white matter changes and cerebellar cysts.
Laura Vandervore, Katrien Stouffs, Ibrahim Tanyalçin, Tim Vanderhasselt, Filip Roelens

J Med Genet· June 2017

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