R37 HD029957/HD/NICHD NIH HHS/United States[Grants and Funding] - Search Results

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Subject: R37 HD029957/HD/NICHD NIH HHS/United States[Grant - PubMed

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Year	Number of Results
1999	1
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Altered pubertal timing in 7q11.23 copy number variations and associated genetic mechanisms.

Wei SM, Gregory MD, Nash T, de Abreu E Gouvêa A, Mervis CB, Cole KM, Garvey MH, Kippenhan JS, Eisenberg DP, Kolachana B, Schmidt PJ, Berman KF. Wei SM, et al. iScience. 2024 Feb 6;27(3):109113. doi: 10.1016/j.isci.2024.109113. eCollection 2024 Mar 15. iScience. 2024. PMID: 38375233 Free PMC article.

Concurrent predictors of mathematics achievement for 9-year-old children with Williams syndrome.

Guimaraes VN, Mervis CB. Guimaraes VN, et al. Sci Rep. 2024 Jan 30;14(1):2454. doi: 10.1038/s41598-024-52639-7. Sci Rep. 2024. PMID: 38291096 Free PMC article.

Longitudinal Predictors of Word Reading for Children with Williams Syndrome.

Richter CG, Cardoso-Martins C, Mervis CB. Richter CG, et al. Read Writ. 2023 Oct;36(8):2119-2145. doi: 10.1007/s11145-022-10370-7. Epub 2022 Nov 15. Read Writ. 2023. PMID: 37936600 Free PMC article.

DNA methylation profiles in individuals with rare, atypical 7q11.23 CNVs correlate with GTF2I and GTF2IRD1 copy number.

Strong E, Mervis CB, Tam E, Morris CA, Klein-Tasman BP, Velleman SL, Osborne LR. Strong E, et al. NPJ Genom Med. 2023 Sep 14;8(1):25. doi: 10.1038/s41525-023-00368-7. NPJ Genom Med. 2023. PMID: 37709781 Free PMC article.

Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndrome.

Kippenhan JS, Gregory MD, Nash T, Kohn P, Mervis CB, Eisenberg DP, Garvey MH, Roe K, Morris CA, Kolachana B, Pani AM, Sorcher L, Berman KF. Kippenhan JS, et al. J Neurodev Disord. 2023 Aug 26;15(1):29. doi: 10.1186/s11689-023-09493-x. J Neurodev Disord. 2023. PMID: 37633900 Free PMC article.

Early diagnostic indicators of childhood apraxia of speech in young children with 7q11.23 duplication syndrome: preliminary findings.

Abbiati CI, Velleman SL, Overby MS, Becerra AM, Mervis CB. Abbiati CI, et al. Clin Linguist Phon. 2023 Jun 3;37(4-6):330-344. doi: 10.1080/02699206.2022.2080590. Epub 2022 Jun 2. Clin Linguist Phon. 2023. PMID: 35652603

Spelling abilities of school-aged children with Williams syndrome.

Greiner de Magalhães C, Cardoso-Martins C, Mervis CB. Greiner de Magalhães C, et al. Res Dev Disabil. 2022 Jan;120:104129. doi: 10.1016/j.ridd.2021.104129. Epub 2021 Dec 4. Res Dev Disabil. 2022. PMID: 34875548 Free PMC article.

Executive function as measured by the Behavior Rating Inventory of Executive Function-2: children and adolescents with Williams syndrome.

Greiner de Magalhães C, Pitts CH, Mervis CB. Greiner de Magalhães C, et al. J Intellect Disabil Res. 2022 Jan;66(1-2):94-107. doi: 10.1111/jir.12858. Epub 2021 Jun 10. J Intellect Disabil Res. 2022. PMID: 34110652 Free PMC article.

Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype.

Qaiser F, Yin Y, Mervis CB, Morris CA, Klein-Tasman BP, Tam E, Osborne LR, Yuen RKC. Qaiser F, et al. Orphanet J Rare Dis. 2021 Jan 6;16(1):6. doi: 10.1186/s13023-020-01648-6. Orphanet J Rare Dis. 2021. PMID: 33407644 Free PMC article.

Development of rapid word-object associations in relation to expressive vocabulary: Shared commonalities in infants and toddlers with and without Williams syndrome.

Ha OR, Cashon CH, Holt NA, Mervis CB. Ha OR, et al. Dev Sci. 2020 Nov;23(6):e12966. doi: 10.1111/desc.12966. Epub 2020 Apr 7. Dev Sci. 2020. PMID: 32196857 Free PMC article.

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