Ligia Mateiu
Ligia Mateiu
Center for Medical Genetics - University of Antwerp
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Cited by
Cited by
Concurrent whole-genome haplotyping and copy-number profiling of single cells
MZ Esteki, E Dimitriadou, L Mateiu, C Melotte, N Van der Aa, P Kumar, ...
The American Journal of Human Genetics 96 (6), 894-912, 2015
Single-cell paired-end genome sequencing reveals structural variation per cell cycle
T Voet, P Kumar, P Van Loo, SL Cooke, J Marshall, ML Lin, ...
Nucleic acids research 41 (12), 6119-6138, 2013
A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer’s disease
J Verheijen, T Van den Bossche, J van der Zee, S Engelborghs, ...
Acta neuropathologica 132 (2), 213-224, 2016
Frequency and pattern of heteroplasmy in the complete human mitochondrial genome
A Ramos, C Santos, L Mateiu, MM Gonzalez, L Alvarez, L Azevedo, ...
PloS one 8 (10), e74636, 2013
Genome-wide copy number profiling of single cells in S-phase reveals DNA-replication domains
N Van der Aa, J Cheng, L Mateiu, MZ Esteki, P Kumar, E Dimitriadou, ...
Nucleic acids research 41 (6), e66-e66, 2013
Nuclear insertions of mitochondrial origin: database updating and usefulness in cancer studies
A Ramos, E Barbena, L Mateiu, M del Mar Gonzalez, Q Mairal, M Lima, ...
Mitochondrion 11 (6), 946-953, 2011
Inferring complex DNA substitution processes on phylogenies using uniformization and data augmentation
L Mateiu, B Rannala
Systematic biology 55 (2), 259-269, 2006
Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative disease
T Geuens, V De Winter, N Rajan, T Achsel, L Mateiu, L Almeida-Souza, ...
Acta neuropathologica communications 5, 1-15, 2017
Validated primer set that prevents nuclear DNA sequences of mitochondrial origin co‐amplification: A revision based on the New Human Genome Reference Sequence (GRCh37)
A Ramos, C Santos, E Barbena, L Mateiu, L Alvarez, R Nogués, MP Aluja
Electrophoresis 32 (6‐7), 782-783, 2011
Induced pluripotent stem cell-derived motor neurons of CMT type 2 patients reveal progressive mitochondrial dysfunction
J Van Lent, P Verstraelen, B Asselbergh, E Adriaenssens, L Mateiu, ...
Brain 144 (8), 2471-2485, 2021
The role of endothelial autocrine NRG1/ERBB4 signaling in cardiac remodeling
L Dugaucquier, E Feyen, L Mateiu, TAM Bruyns, GW De Keulenaer, ...
American Journal of Physiology-Heart and Circulatory Physiology 319 (2 …, 2020
Bayesian inference of errors in ancient DNA caused by postmortem degradation
LM Mateiu, BH Rannala
Molecular Biology and Evolution 25 (7), 1503-1511, 2008
Transcriptional dysregulation by a nucleus-localized aminoacyl-tRNA synthetase associated with Charcot-Marie-Tooth neuropathy
S Bervoets, N Wei, ML Erfurth, S Yusein-Myashkova, B Ermanoska, ...
Nature communications 10 (1), 5045, 2019
Charcot–Marie–Tooth disease type 2G redefined by a novel mutation in LRSAM1
K Peeters, P Palaima, AL Pelayo‐Negro, A García, E Gallardo, ...
Annals of Neurology 80 (6), 823-833, 2016
Cardiac endothelial cell transcriptome in neonatal, adult, and remodeling hearts
Z Vermeulen, L Mateiu, L Dugaucquier, GW De Keulenaer, VFM Segers
Physiological genomics 51 (6), 186-196, 2019
Shared brain transcriptomic signature in TDP-43 type A FTLD patients with or without GRN mutations
C Pottier, L Mateiu, MC Baker, M DeJesus-Hernandez, C Teixeira Vicente, ...
Brain 145 (7), 2472-2485, 2022
An Additional Lrp4 High Bone Mass Mutation Mitigates the Sost-Knockout Phenotype in Mice by Increasing Bone Remodeling
G Hendrickx, E Boudin, L Mateiu, TA Yorgan, E Steenackers, M Kneissel, ...
Calcified Tissue International 114 (2), 171-181, 2024
Identification of a DLG3 stop mutation in the MRX20 family
J Huyghebaert, L Mateiu, E Elinck, KE Van Rossem, B Christiaenssen, ...
European Journal of Human Genetics, 1-7, 2024
Heterozygous variants in CTR9, which encodes a major component of the PAF1 complex, are associated with a neurodevelopmental disorder
M Meuwissen, A Verstraeten, E Ranza, J Iwaszkiewicz, M Bastiaansen, ...
Genetics in Medicine 24 (7), 1583-1591, 2022
ADNP dysregulates methylation and mitochondrial gene expression in the cerebellum of a Helsmoortel–Van der Aa syndrome autopsy case
C D’Incal, A Van Dijck, J Ibrahim, K De Man, L Bastini, A Konings, E Elinck, ...
Acta Neuropathologica Communications 12 (1), 1-32, 2024
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