Brilliant M - Search Results

1

Advancing artificial intelligence-assisted pre-screening for fragile X syndrome.

Movaghar A, Page D, Brilliant M, Mailick M. Movaghar A, et al. Among authors: brilliant m. BMC Med Inform Decis Mak. 2022 Jun 10;22(1):152. doi: 10.1186/s12911-022-01896-5. BMC Med Inform Decis Mak. 2022. PMID: 35689224 Free PMC article.

2

Artificial intelligence-assisted phenotype discovery of fragile X syndrome in a population-based sample.

Movaghar A, Page D, Scholze D, Hong J, DaWalt LS, Kuusisto F, Stewart R, Brilliant M, Mailick M. Movaghar A, et al. Among authors: brilliant m. Genet Med. 2021 Jul;23(7):1273-1280. doi: 10.1038/s41436-021-01144-7. Epub 2021 Mar 26. Genet Med. 2021. PMID: 33772223 Free PMC article.

3

Prevalence of Underdiagnosed Fragile X Syndrome in 2 Health Systems.

Movaghar A, Page D, Brilliant M, Mailick M. Movaghar A, et al. Among authors: brilliant m. JAMA Netw Open. 2021 Dec 1;4(12):e2141516. doi: 10.1001/jamanetworkopen.2021.41516. JAMA Netw Open. 2021. PMID: 34967885 Free PMC article.

4

Health Profiles of Mosaic Versus Non-mosaic FMR1 Premutation Carrier Mothers of Children With Fragile X Syndrome.

Mailick MR, Movaghar A, Hong J, Greenberg JS, DaWalt LS, Zhou L, Jackson J, Rathouz PJ, Baker MW, Brilliant M, Page D, Berry-Kravis E. Mailick MR, et al. Among authors: brilliant m. Front Genet. 2018 May 16;9:173. doi: 10.3389/fgene.2018.00173. eCollection 2018. Front Genet. 2018. PMID: 29868121 Free PMC article.

5

Data-driven phenotype discovery of FMR1 premutation carriers in a population-based sample.

Movaghar A, Page D, Brilliant M, Baker MW, Greenberg J, Hong J, DaWalt LS, Saha K, Kuusisto F, Stewart R, Berry-Kravis E, Mailick MR. Movaghar A, et al. Among authors: brilliant m. Sci Adv. 2019 Aug 21;5(8):eaaw7195. doi: 10.1126/sciadv.aaw7195. eCollection 2019 Aug. Sci Adv. 2019. PMID: 31457090 Free PMC article.

6

Health profiles of adults with autism spectrum disorder: Differences between women and men.

DaWalt LS, Taylor JL, Movaghar A, Hong J, Kim B, Brilliant M, Mailick MR. DaWalt LS, et al. Among authors: brilliant m. Autism Res. 2021 Sep;14(9):1896-1904. doi: 10.1002/aur.2563. Epub 2021 Jul 2. Autism Res. 2021. PMID: 34213066 Free PMC article.

7

Response to Timothé Ménard.

Movaghar A, Page D, Brilliant M, Mailick M. Movaghar A, et al. Among authors: brilliant m. Genet Med. 2022 Mar;24(3):752-753. doi: 10.1016/j.gim.2021.10.023. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906516 Free article. No abstract available.

8

Using machine learning to identify patterns of lifetime health problems in decedents with autism spectrum disorder.

Bishop-Fitzpatrick L, Movaghar A, Greenberg JS, Page D, DaWalt LS, Brilliant MH, Mailick MR. Bishop-Fitzpatrick L, et al. Autism Res. 2018 Aug;11(8):1120-1128. doi: 10.1002/aur.1960. Epub 2018 May 7. Autism Res. 2018. PMID: 29734508 Free PMC article.

9

Mild Neurological Signs in FMR1 Premutation Women in an Unselected Community-Based Cohort.

Mailick MR, Hong J, Movaghar A, DaWalt L, Berry-Kravis EM, Brilliant MH, Boero J, Todd PK, Hall D. Mailick MR, et al. Among authors: brilliant mh. Mov Disord. 2021 Oct;36(10):2378-2386. doi: 10.1002/mds.28683. Epub 2021 Jun 12. Mov Disord. 2021. PMID: 34117786 Free PMC article.

10

FMR1 Low Zone CGG Repeats: Phenotypic Associations in the Context of Parenting Stress.

Mailick MR, Hong J, DaWalt LS, Greenberg JS, Movaghar A, Baker MW, Rathouz PJ, Brilliant MH. Mailick MR, et al. Front Pediatr. 2020 May 14;8:223. doi: 10.3389/fped.2020.00223. eCollection 2020. Front Pediatr. 2020. PMID: 32478017 Free PMC article.

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