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Deprez, Marie
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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