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Delobel, Bruno
398
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Online (398)
Mediatypes
Articles (Online) (87)
OpenAccess-fulltext (311)
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1
Missense variants in ANO4 cause sporadic encephalopathic or..:
Yang, Fang
;
Begemann, Anais
;
Reichhart, Nadine
...
The American Journal of Human Genetics. 111 (2024) 6 - p. 1184-1205 , 2024
Link:
https://doi.org/10.1016/..
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2
Novel pathogenic variants in SLCO2A1 causing autosomal domi..:
Bloch, Adrien
;
Couture, Guillaume
;
Isidor, Bertrand
...
European Journal of Medical Genetics. 66 (2023) 2 - p. 104689 , 2023
Link:
https://doi.org/10.1016/..
?
3
Growth charts in DYRK1A syndrome:
Lanvin, Pierre‐Louis
;
Goronflot, Thomas
;
Isidor, Bertrand
...
American Journal of Medical Genetics Part A. 194 (2023) 1 - p. 9-16 , 2023
Link:
https://doi.org/10.1002/..
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4
Mathematical Modeling of Energy-Dense NMC Electrodes: I. De..:
Nguyen, Tuan-Tu
;
Delobel, Bruno
;
Berthe, Maxime
...
Journal of The Electrochemical Society. 169 (2022) 4 - p. 040546 , 2022
Link:
https://doi.org/10.1149/..
?
5
3D Operando Monitoring of Lithiation Spatial Composition in..:
Nguyen, Tuan-Tu
;
Xu, Jiahui
;
Su, Zeliang
...
Microscopy and Microanalysis. 28 (2022) S1 - p. 194-196 , 2022
Link:
https://doi.org/10.1017/..
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6
Understanding the new BRD4‐related syndrome: Clinical and g..:
Jouret, Guillaume
;
Heide, Solveig
;
Sorlin, Arthur
...
Clinical Genetics. 102 (2022) 2 - p. 117-122 , 2022
Link:
https://doi.org/10.1111/..
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7
1p36 deletion syndrome: Review and mapping with further cha..:
Jacquin, Clémence
;
Landais, Emilie
;
Poirsier, Céline
...
American Journal of Medical Genetics Part A. 191 (2022) 2 - p. 445-458 , 2022
Link:
https://doi.org/10.1002/..
?
8
Mathematical Modeling of Energy-dense NMC Electrodes: Part ..:
Nguyen, Tuan-Tu
;
Delobel, Bruno
;
Demortière, Arnaud
.
Journal of The Electrochemical Society. 169 (2022) 6 - p. 060510 , 2022
Link:
https://doi.org/10.1149/..
?
9
3D Quantification of Microstructural Properties of LiNi0.5M..:
Nguyen, Tuan‐Tu
;
Villanova, Julie
;
Su, Zeliang
...
Advanced Energy Materials. 11 (2021) 8 - p. , 2021
Link:
https://doi.org/10.1002/..
?
10
Integrative approach to interpret DYRK1A variants, leading ..:
Courraud, Jérémie
;
Chater-Diehl, Eric
;
Durand, Benjamin
...
Genetics in Medicine. 23 (2021) 11 - p. 2150-2159 , 2021
Link:
https://doi.org/10.1038/..
?
11
Neurodevelopmental phenotype in 36 new patients with 8p inv..:
Vibert, Roseline
;
Mignot, Cyril
;
Keren, Boris
...
Clinical Genetics. 101 (2021) 3 - p. 307-316 , 2021
Link:
https://doi.org/10.1111/..
?
12
The electrode tortuosity factor: why the conventional tortu..:
Nguyen, Tuan-Tu
;
Demortière, Arnaud
;
Fleutot, Benoit
...
npj Computational Materials. 6 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1038/..
?
13
Further delineation of the female phenotype with KDM5C dise..:
Carmignac, Virginie
;
Nambot, Sophie
;
Lehalle, Daphné
...
Clinical Genetics. 98 (2020) 1 - p. 43-55 , 2020
Link:
https://doi.org/10.1111/..
?
14
A new mutational hotspot in the SKI gene in the context of ..:
Arnaud, Pauline
;
Racine, Caroline
;
Hanna, Nadine
...
Human Genetics. 139 (2020) 4 - p. 461-472 , 2020
Link:
https://doi.org/10.1007/..
?
15
BLOC1S5 pathogenic variants cause a new type of Hermansky–P..:
Pennamen, Perrine
;
Le, Linh
;
Tingaud-Sequeira, Angèle
...
Genetics in Medicine. 22 (2020) 10 - p. 1613-1622 , 2020
Link:
https://doi.org/10.1038/..
1-15