MR/L011166/1 /MRC_/Medical Research Council/United Kingdom[Grants and Funding] - Search Results

Year	Number of Results
2017	1
2018	5
2019	8
2020	8
2021	9
2022	8
2023	7
2024	2

1

Skuse D, Printzlau F, Wolstencroft J. Skuse D, et al. Handb Clin Neurol. 2018;147:355-376. doi: 10.1016/B978-0-444-63233-3.00024-5. Handb Clin Neurol. 2018. PMID: 29325624 Review.

2

Behavioural and neurodevelopmental characteristics of SYNGAP1.

Bednarczuk N, Housby H, Lee IO, Consortium I, Skuse D, Wolstencroft J. Bednarczuk N, et al. J Neurodev Disord. 2024 Aug 15;16(1):46. doi: 10.1186/s11689-024-09563-8. J Neurodev Disord. 2024. PMID: 39148034 Free PMC article.

3

Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome.

Fiksinski AM, Schneider M, Zinkstok J, Baribeau D, Chawner SJRA, Vorstman JAS. Fiksinski AM, et al. Curr Psychiatry Rep. 2021 Feb 24;23(3):13. doi: 10.1007/s11920-021-01225-z. Curr Psychiatry Rep. 2021. PMID: 33625600 Free PMC article. Review.

4

Clinical evaluation of patients with a neuropsychiatric risk copy number variant.

Chawner SJ, Watson CJ, Owen MJ. Chawner SJ, et al. Curr Opin Genet Dev. 2021 Jun;68:26-34. doi: 10.1016/j.gde.2020.12.012. Epub 2021 Jan 15. Curr Opin Genet Dev. 2021. PMID: 33461126 Free PMC article. Review.

5

Genetic testing in children and adolescents with intellectual disability.

Bass N, Skuse D. Bass N, et al. Curr Opin Psychiatry. 2018 Nov;31(6):490-495. doi: 10.1097/YCO.0000000000000456. Curr Opin Psychiatry. 2018. PMID: 30138136 Review.

6

Cognitive, behavioral, and neural consequences of sex chromosome aneuploidy.

Printzlau F, Wolstencroft J, Skuse DH. Printzlau F, et al. J Neurosci Res. 2017 Jan 2;95(1-2):311-319. doi: 10.1002/jnr.23951. J Neurosci Res. 2017. PMID: 27870409 Review.

7

Sleep EEG in young people with 22q11.2 deletion syndrome: A cross-sectional study of slow-waves, spindles and correlations with memory and neurodevelopmental symptoms.

Donnelly NA, Bartsch U, Moulding HA, Eaton C, Marston H, Hall JH, Hall J, Owen MJ, van den Bree MBM, Jones MW. Donnelly NA, et al. Elife. 2022 Aug 30;11:e75482. doi: 10.7554/eLife.75482. Elife. 2022. PMID: 36039635 Free PMC article.

8

Copy number variants (CNVs): a powerful tool for iPSC-based modelling of ASD.

Drakulic D, Djurovic S, Syed YA, Trattaro S, Caporale N, Falk A, Ofir R, Heine VM, Chawner SJRA, Rodriguez-Moreno A, van den Bree MBM, Testa G, Petrakis S, Harwood AJ. Drakulic D, et al. Mol Autism. 2020 Jun 1;11(1):42. doi: 10.1186/s13229-020-00343-4. Mol Autism. 2020. PMID: 32487215 Free PMC article. Review.

9

Using induced pluripotent stem cells to investigate human neuronal phenotypes in 1q21.1 deletion and duplication syndrome.

Chapman G, Alsaqati M, Lunn S, Singh T, Linden SC, Linden DEJ, van den Bree MBM, Ziller M, Owen MJ, Hall J, Harwood AJ, Syed YA. Chapman G, et al. Mol Psychiatry. 2022 Feb;27(2):819-830. doi: 10.1038/s41380-021-01182-2. Epub 2021 Jun 10. Mol Psychiatry. 2022. PMID: 34112971 Free PMC article.

10

Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort study.

Wolstencroft J, Wicks F, Srinivasan R, Wynn S, Ford T, Baker K, Chawner SJRA, Hall J, van den Bree MBM, Owen MJ; IMAGINE Study; Skuse D, Raymond FL. Wolstencroft J, et al. Lancet Psychiatry. 2022 Sep;9(9):715-724. doi: 10.1016/S2215-0366(22)00207-3. Epub 2022 Aug 3. Lancet Psychiatry. 2022. PMID: 35932790 Free PMC article.

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