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Hyperexcitability and translational phenotypes in a preclinical model of SYNGAP1 mutations.
Silverman JL, Fenton T, Haouchine O, Hallam E, Smith E, Jackson K, Rahbarian D, Canales C, Adhikari A, Nord A, Ben-Shalom R. Silverman JL, et al. Res Sq [Preprint]. 2023 Sep 13:rs.3.rs-3246655. doi: 10.21203/rs.3.rs-3246655/v1. Res Sq. 2023. Update in: Transl Psychiatry. 2024 Oct 2;14(1):405. doi: 10.1038/s41398-024-03077-6. PMID: 37790402 Free PMC article. Updated. Preprint.
Hyperexcitability and translational phenotypes in a preclinical mouse model of SYNGAP1-Related Intellectual Disability.
Fenton TA, Haouchine OY, Hallam EL, Smith EM, Jackson KC, Rahbarian D, Canales C, Adhikari A, Nord AS, Ben-Shalom R, Silverman JL. Fenton TA, et al. Among authors: nord as. Res Sq [Preprint]. 2024 Mar 19:rs.3.rs-4067746. doi: 10.21203/rs.3.rs-4067746/v1. Res Sq. 2024. Update in: Transl Psychiatry. 2024 Oct 2;14(1):405. doi: 10.1038/s41398-024-03077-6. PMID: 38562838 Free PMC article. Updated. Preprint.
Deletion of a non-canonical regulatory sequence causes loss of Scn1a expression and epileptic phenotypes in mice.
Haigh JL, Adhikari A, Copping NA, Stradleigh T, Wade AA, Catta-Preta R, Su-Feher L, Zdilar I, Morse S, Fenton TA, Nguyen A, Quintero D, Agezew S, Sramek M, Kreun EJ, Carter J, Gompers A, Lambert JT, Canales CP, Pennacchio LA, Visel A, Dickel DE, Silverman JL, Nord AS. Haigh JL, et al. Among authors: nord as. Genome Med. 2021 Apr 26;13(1):69. doi: 10.1186/s13073-021-00884-0. Genome Med. 2021. PMID: 33910599 Free PMC article.
Hyperexcitability and translational phenotypes in a preclinical model of SYNGAP1 mutations.
Fenton TA, Haouchine OY, Hallam EL, Smith EM, Jackson KC, Rahbarian D, Canales C, Adhikari A, Nord AS, Ben-Shalom R, Silverman JL. Fenton TA, et al. Among authors: nord as. bioRxiv [Preprint]. 2023 Jul 26:2023.07.24.550093. doi: 10.1101/2023.07.24.550093. bioRxiv. 2023. Update in: Transl Psychiatry. 2024 Oct 2;14(1):405. doi: 10.1038/s41398-024-03077-6. PMID: 37546838 Free PMC article. Updated. Preprint.
Complimentary vertebrate Wac models exhibit phenotypes relevant to DeSanto-Shinawi Syndrome.
Lee KH, Stafford AM, Pacheco-Vergara M, Cichewicz K, Canales CP, Seban N, Corea M, Rahbarian D, Bonekamp KE, Gillie GR, Cruz DP, Gill AM, Hwang HE, Uhl KL, Jager TE, Shinawi M, Li X, Obenaus A, Crandall SR, Jeong J, Nord AS, Kim CH, Vogt D. Lee KH, et al. Among authors: nord as. bioRxiv [Preprint]. 2024 May 26:2024.05.26.595966. doi: 10.1101/2024.05.26.595966. bioRxiv. 2024. PMID: 38826421 Free PMC article. Preprint.
Germline Chd8 haploinsufficiency alters brain development in mouse.
Gompers AL, Su-Feher L, Ellegood J, Copping NA, Riyadh MA, Stradleigh TW, Pride MC, Schaffler MD, Wade AA, Catta-Preta R, Zdilar I, Louis S, Kaushik G, Mannion BJ, Plajzer-Frick I, Afzal V, Visel A, Pennacchio LA, Dickel DE, Lerch JP, Crawley JN, Zarbalis KS, Silverman JL, Nord AS. Gompers AL, et al. Among authors: nord as. Nat Neurosci. 2017 Aug;20(8):1062-1073. doi: 10.1038/nn.4592. Epub 2017 Jun 26. Nat Neurosci. 2017. PMID: 28671691 Free PMC article.
Parallel functional testing identifies enhancers active in early postnatal mouse brain.
Lambert JT, Su-Feher L, Cichewicz K, Warren TL, Zdilar I, Wang Y, Lim KJ, Haigh JL, Morse SJ, Canales CP, Stradleigh TW, Castillo Palacios E, Haghani V, Moss SD, Parolini H, Quintero D, Shrestha D, Vogt D, Byrne LC, Nord AS. Lambert JT, et al. Among authors: nord as. Elife. 2021 Oct 4;10:e69479. doi: 10.7554/eLife.69479. Elife. 2021. PMID: 34605404 Free PMC article.
Sequential perturbations to mouse corticogenesis following in utero maternal immune activation.
Canales CP, Estes ML, Cichewicz K, Angara K, Aboubechara JP, Cameron S, Prendergast K, Su-Feher L, Zdilar I, Kreun EJ, Connolly EC, Seo JM, Goon JB, Farrelly K, Stradleigh TW, van der List D, Haapanen L, Van de Water J, Vogt D, McAllister AK, Nord AS. Canales CP, et al. Among authors: nord as. Elife. 2021 Mar 5;10:e60100. doi: 10.7554/eLife.60100. Elife. 2021. PMID: 33666173 Free PMC article.
75 results