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Structural deviations of the posterior fossa and the cerebellum and their cognitive links in a neurodevelopmental deletion syndrome.
Sefik E, Duan K, Li Y, Sholar B, Evans L, Pincus J, Ammar Z, Murphy MM, Klaiman C, Saulnier CA, Pulver SL, Goldman-Yassen AE, Guo Y, Walker EF, Li L, Mulle JG, Shultz S. Sefik E, et al. Among authors: saulnier ca. Mol Psychiatry. 2024 May 14. doi: 10.1038/s41380-024-02584-8. Online ahead of print. Mol Psychiatry. 2024. PMID: 38744992
Adaptive behaviour deficits in individuals with 3q29 deletion syndrome.
Pollak RM, Burrell TL, Cubells JF, Klaiman C, Murphy MM, Saulnier CA, Walker EF, White SP, Mulle JG. Pollak RM, et al. Among authors: saulnier ca. J Intellect Disabil Res. 2024 Feb;68(2):113-127. doi: 10.1111/jir.13094. Epub 2023 Sep 22. J Intellect Disabil Res. 2024. PMID: 37740553
Visual-Motor Integration Deficits in 3q29 Deletion Syndrome.
Pollak RM, Burrell TL, Cubells JF, Klaiman C, Murphy MM, Saulnier CA, Walker EF, White SP, Mulle JG. Pollak RM, et al. Among authors: saulnier ca. J Autism Dev Disord. 2023 Jun 24. doi: 10.1007/s10803-023-06034-2. Online ahead of print. J Autism Dev Disord. 2023. PMID: 37354284
Adaptive behavior deficits in individuals with 3q29 deletion syndrome.
Pollak RM, Burrell TL, Cubells JF, Klaiman C, Murphy MM, Saulnier CA, Walker EF, White SP, Mulle JG. Pollak RM, et al. Among authors: saulnier ca. medRxiv [Preprint]. 2023 Apr 3:2023.03.31.23288022. doi: 10.1101/2023.03.31.23288022. medRxiv. 2023. PMID: 37066139 Free PMC article. Updated. Preprint.
Adaptive Behavior Profiles in Autism Spectrum Disorder.
Saulnier CA, Klaiman C, McQueen E. Saulnier CA, et al. Curr Psychiatry Rep. 2022 Dec;24(12):749-756. doi: 10.1007/s11920-022-01381-w. Epub 2022 Nov 22. Curr Psychiatry Rep. 2022. PMID: 36417152 Review.
3q29 Recurrent Deletion.
Mulle JG, Gambello MJ, Sanchez Russo R, Murphy MM, Burrell TL, Klaiman C, White S, Saulnier CA, Walker EF, Cubells JF, Shultz S, Li L. Mulle JG, et al. Among authors: saulnier ca. 2016 Sep 22 [updated 2021 Jul 1]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2016 Sep 22 [updated 2021 Jul 1]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 27656750 Free Books & Documents. Review.
Deep phenotyping in 3q29 deletion syndrome: recommendations for clinical care.
Sanchez Russo R, Gambello MJ, Murphy MM, Aberizk K, Black E, Burrell TL, Carlock G, Cubells JF, Epstein MT, Espana R, Goines K, Guest RM, Klaiman C, Koh S, Leslie EJ, Li L, Novacek DM, Saulnier CA, Sefik E, Shultz S, Walker E, White SP; Emory 3q29 Project; Mulle JG. Sanchez Russo R, et al. Among authors: saulnier ca. Genet Med. 2021 May;23(5):872-880. doi: 10.1038/s41436-020-01053-1. Epub 2021 Feb 9. Genet Med. 2021. PMID: 33564151 Free PMC article.
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