-
Conti, V, Carabalona, A, Pallesi-Pocachard, E, Leventer, RJ, Schaller, F, Parrini, E, Deparis, AA, Watrin, F, Buhler, E, Novara, F, et al.
A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations.
Journal of Visualized Experiments
2024
view publication
-
Soon, E, Siffredi, V, Anderson, PJ, Anderson, VA, McIlroy, A, Leventer, RJ, Wood, AG, Spencer-Smith, MM.
Inhibitory control in children with agenesis of the corpus callosum compared with typically developing children..
J Int Neuropsychol Soc
30(1)
:
18 -26
2024
view publication
-
Spyrou, J, Aung, KP, Vanyai, H, Leventer, RJ, Maljevic, S, Lockhart, PJ, Howell, KB, Reid, CA.
Slc35a2 mosaic knockout impacts cortical development, dendritic arborisation, and neuronal firing in the developing brain.
2024
view publication
-
Kooshavar, D, Amor, DJ, Boggs, K, Baker, N, Barnett, C, de Silva, MG, Edwards, S, Fahey, MC, Marum, JE, Snell, P, et al.
Diagnostic utility of exome sequencing followed by research reanalysis in human brain malformations..
Brain Commun
6(2)
:
fcae056
2024
view publication
-
Ha, TT, Burgess, R, Newman, M, Moey, C, Mandelstam, SA, Gardner, AE, Ivancevic, AM, Pham, D, Kumar, R, Smith, N, et al.
Aicardi Syndrome Is a Genetically Heterogeneous Disorder..
Genes (Basel)
14(8)
:
2023
view publication