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Deprez, Marie
267
results:
Search for persons
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Format
Online (267)
Mediatypes
Articles (Online) (70)
Bookchapter (Online) (2)
OpenAccess-fulltext (194)
Audio (Online) (1)
Languages
english (237)
french (11)
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?
1
Integration of Multimodal Data:
, In:
Machine Learning for Brain Disorders; Neuromethods
,
Lorenzi, Marco
;
Deprez, Marie
;
Balelli, Irene
.. - p. 573-597 , 2023
Link:
https://doi.org/10.1007/..
?
2
CAMTA1‐related disorder: Phenotypic and molecular character..:
Al‐Kateb, Hussam
;
Au, P. Y. Billie
;
Berland, Siren
...
Clinical Genetics. , 2023
Link:
https://doi.org/10.1111/..
?
3
The MIR34B/C genomic region contains multiple potential reg..:
Cavard, Amélie
;
Redman, Elisa
;
Mercey, Olivier
...
FEBS Letters. 597 (2023) 12 - p. 1623-1637 , 2023
Link:
https://doi.org/10.1002/..
?
4
Structural mapping of GABRB3 variants reveals genotype–phen..:
Johannesen, Katrine M.
;
Iqbal, Sumaiya
;
Guazzi, Milena
...
Genetics in Medicine. 24 (2022) 3 - p. 681-693 , 2022
Link:
https://doi.org/10.1016/..
?
5
Decoding Genetic Markers of Multiple Phenotypic Layers Thro..:
Deprez, Marie
;
Moreira, Julien
;
Sermesant, Maxime
.
Frontiers in Molecular Medicine. 2 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
6
Efficient Clustering Using Alternating Minimization And A P..:
, In:
2022 IEEE International Conference on Image Processing (ICIP)
,
Gilet, Cyprien
;
Deprez, Marie
;
Barbry, Pacal
.. - p. 176-180 , 2022
Link:
https://doi.org/10.1109/..
?
7
ASC1 complex related conditions: Two novel paediatric patie..:
Dembour, Alexis
;
Destrée, Anne
;
Deprez, Marie
...
European Journal of Medical Genetics. 65 (2022) 4 - p. 104469 , 2022
Link:
https://doi.org/10.1016/..
?
8
A second case of Okamoto syndrome caused by HNRNPK mutation:
Maystadt, Isabelle
;
Deprez, Marie
;
Moortgat, Stéphanie
..
American Journal of Medical Genetics Part A. 182 (2020) 6 - p. 1537-1539 , 2020
Link:
https://doi.org/10.1002/..
?
9
Novel dynamics of human mucociliary differentiation reveale..:
Ruiz García, Sandra
;
Deprez, Marie
;
Lebrigand, Kevin
...
Development. 146 (2019) 20 - p. , 2019
Link:
https://doi.org/10.1242/..
?
10
CDC20B is required for deuterosome-mediated centriole produ..:
Revinski, Diego R.
;
Zaragosi, Laure-Emmanuelle
;
Boutin, Camille
...
Nature Communications. 9 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1038/..
?
11
Expanding the phenotypic spectrum associated with OPHN1 mut..:
Moortgat, Stéphanie
;
Lederer, Damien
;
Deprez, Marie
...
European Journal of Medical Genetics. 61 (2018) 8 - p. 442-450 , 2018
Link:
https://doi.org/10.1016/..
?
12
STXBP1encephalopathy: A neurodevelopmental disorder includi..:
Stamberger, Hannah
;
Nikanorova, Marina
;
Willemsen, Marjolein H.
...
Neurology. 86 (2016) 10 - p. 954-962 , 2016
Link:
https://doi.org/10.1212/..
?
13
A new Turkish infant with clinical features of CS/CISS1 syn..:
Moortgat, Stephanie
;
Benoit, Valerie
;
Deprez, Marie
..
European Journal of Medical Genetics. 57 (2014) 5 - p. 212-215 , 2014
Link:
https://doi.org/10.1016/..
?
14
The nutrient-responsive CDK Pho85 primes the Sch9 kinase fo..:
Deprez, Marie-Anne
;
Caligaris, Marco
;
Rosseels, Joëlle
...
PLOS Genetics. 19 (2023) 2 - p. e1010641 , 2023
Link:
https://doi.org/10.1371/..
?
15
Snf1/AMPK fine-tunes TORC1 signaling in response to glucose..:
Caligaris, Marco
;
Nicastro, Raffaele
;
Hu, Zehan
...
eLife. 12 (2023) - p. , 2023
Link:
https://doi.org/10.7554/..
1-15