| DNA methylation and susceptibility to autism spectrum disorder MW Tremblay, Y Jiang Annual review of medicine 70, 151-166, 2019 | 117 | 2019 |
| Epigenetics and autism spectrum disorder: A report of an autism case with mutation in H1 linker histone HIST1H1E and literature review LJ Duffney, P Valdez, MW Tremblay, X Cao, S Montgomery, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177 …, 2018 | 73 | 2018 |
| Epigenetic dysregulation of Oxtr in Tet1-deficient mice has implications for neuropsychiatric disorders AJ Towers, MW Tremblay, L Chung, X Li, AL Bey, W Zhang, X Cao, ... JCI insight 3 (23), 2018 | 24 | 2018 |
| Enterovirus 2Apro Cleavage of the YTHDF m6A Readers Implicates YTHDF3 as a Mediator of Type I Interferon-Driven JAK/STAT Signaling JP Kastan, MW Tremblay, MC Brown, JD Trimarco, EY Dobrikova, ... Mbio 12 (2), e00116-21, 2021 | 21 | 2021 |
| Mutations of the histone linker H1–4 in neurodevelopmental disorders and functional characterization of neurons expressing C-terminus frameshift mutant H1. 4 MW Tremblay, MV Green, BM Goldstein, AI Aldridge, JA Rosenfeld, ... Human molecular genetics, 2021 | 5 | 2021 |
