Spremljaj
Matthieu Moisse
Matthieu Moisse
CTO - Unicle Biomedical Data Science
Preverjeni e-poštni naslov na vib-kuleuven.be - Domača stran
Naslov
Navedeno
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Leto
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
K Michailidou, P Hall, A Gonzalez-Neira, M Ghoussaini, J Dennis, ...
Nature genetics 45 (4), 353-361, 2013
13082013
Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations
YC Lin, M Boone, L Meuris, I Lemmens, N Van Roy, A Soete, J Reumers, ...
Nature communications 5 (1), 4767, 2014
7302014
Genome-wide analyses identify KIF5A as a novel ALS gene
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1267-1288, 2018
6662018
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
W Van Rheenen, RAA Van Der Spek, MK Bakker, JJFA Van Vugt, PJ Hop, ...
Nature genetics 53 (12), 1636-1648, 2021
4012021
Genome-wide meta-analyses of breast, ovarian, and prostate cancer association studies identify multiple new susceptibility loci shared by at least two cancer types
SP Kar, J Beesley, A Amin Al Olama, K Michailidou, J Tyrer, ZS Kote-Jarai, ...
Cancer discovery 6 (9), 1052-1067, 2016
2022016
Meta-analysis of epigenome-wide association studies in neonates reveals widespread differential DNA methylation associated with birthweight
LK Küpers, C Monnereau, GC Sharp, P Yousefi, LA Salas, A Ghantous, ...
Nature communications 10 (1), 1893, 2019
1952019
Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis
European Journal of Human Genetics 26 (10), 1537-1546, 2018
1552018
Progranulin functions as a cathepsin D chaperone to stimulate axonal outgrowth in vivo
S Beel, M Moisse, M Damme, L De Muynck, W Robberecht, ...
Human molecular genetics 26 (15), 2850-2863, 2017
1332017
Mismatch repair deficiency endows tumors with a unique mutation signature and sensitivity to DNA double-strand breaks
H Zhao, B Thienpont, BT Yesilyurt, M Moisse, J Reumers, L Coenegrachts, ...
Elife 3, e02725, 2014
1092014
Comprehensive characterization of the prostate tumor microenvironment identifies CXCR4/CXCL12 crosstalk as a novel antiangiogenic therapeutic target in prostate cancer
I Heidegger, G Fotakis, A Offermann, J Goveia, S Daum, S Salcher, ...
Molecular cancer 21 (1), 132, 2022
1042022
Salivary DNA methylation profiling: aspects to consider for biomarker identification
SAS Langie, M Moisse, K Declerck, G Koppen, L Godderis, ...
Basic & clinical pharmacology & toxicology 121, 93-101, 2017
1012017
Genetic modifiers of CHEK2* 1100delC-associated breast cancer risk
TA Muranen, D Greco, C Blomqvist, K Aittomäki, S Khan, F Hogervorst, ...
Genetics in medicine 19 (5), 599-603, 2017
972017
HDAC6 inhibition restores TDP‐43 pathology and axonal transport defects in human motor neurons with TARDBP mutations
R Fazal, S Boeynaems, A Swijsen, M De Decker, L Fumagalli, M Moisse, ...
The EMBO journal 40 (7), e106177, 2021
942021
Restoration of histone acetylation ameliorates disease and metabolic abnormalities in a FUS mouse model
E Rossaert, E Pollari, T Jaspers, L Van Helleputte, M Jarpe, ...
Acta neuropathologica communications 7, 1-19, 2019
932019
C9orf72-derived arginine-containing dipeptide repeats associate with axonal transport machinery and impede microtubule-based motility
L Fumagalli, FL Young, S Boeynaems, M De Decker, AR Mehta, ...
Science advances 7 (15), eabg3013, 2021
912021
Integrated genome analysis of uterine leiomyosarcoma to identify novel driver genes and targetable pathways
T Cuppens, M Moisse, J Depreeuw, D Annibali, E Colas, A Gil‐Moreno, ...
International journal of cancer 142 (6), 1230-1243, 2018
852018
Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients
F Perrone, HP Nguyen, S Van Mossevelde, M Moisse, A Sieben, ...
Neurobiology of aging 51, 177. e9-177. e16, 2017
832017
The project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public
RAA van der Spek, W van Rheenen, SL Pulit, KP Kenna, ...
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 20 (5-6), 432-440, 2019
782019
Mutations in the glycosyltransferase domain of GLT8D1 are associated with familial amyotrophic lateral sclerosis
J Cooper-Knock, T Moll, T Ramesh, L Castelli, A Beer, H Robins, I Fox, ...
Cell reports 26 (9), 2298-2306. e5, 2019
762019
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS
PJ Hop, RAJ Zwamborn, E Hannon, GL Shireby, MF Nabais, EM Walker, ...
Science translational medicine 14 (633), eabj0264, 2022
732022
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