-
Levy, MA, Relator, R, McConkey, H, Pranckeviciene, E, Kerkhof, J, Barat‐Houari, M, Bargiacchi, S, Biamino, E, Bralo, MP, Cappuccio, G, et al.
Functional correlation of genome‐wide DNA methylation profiles in genetic neurodevelopmental disorders.
Human Mutation
43(11)
:
1609 -1628
2022
view publication
-
Levy, MA, McConkey, H, Kerkhof, J, Barat-Houari, M, Bargiacchi, S, Biamino, E, Bralo, MP, Cappuccio, G, Ciolfi, A, Clarke, A, et al.
Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders.
Human Genetics and Genomics Advances
3(1)
:
100075
2022
view publication
-
Kaur, S, Van Bergen, NJ, Ben-Zeev, B, Leonardi, E, Tan, TY, Coman, D, Kamien, B, White, SM, St John, M, Phelan, D, et al.
Expanding the genetic landscape of Rett syndrome to include lysine acetyltransferase 6A (KAT6A).
Journal of Genetics and Genomics
47(10)
:
650 -654
2020
view publication
-
St John, M, Columbus, G, Brignell, A, Carew, P, Skeat, J, Reilly, S, Morgan, AT.
Predicting speech‐sound disorder outcomes in school‐age children with hearing loss: The VicCHILD experience.
International Journal of Language & Communication Disorders
55(4)
:
537 -546
2020
view publication
-
Sanchez, K, Boyce, JO, Mei, C, St John, M, Smith, J, Leembruggen, L, Mills, S, Spittle, AJ, Morgan, AT.
Communication in children born very preterm: a prospective cohort study.
Developmental Medicine & Child Neurology
62(4)
:
506 -512
2020
view publication