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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 2
2004 3
2005 1
2006 1
2007 1
2009 2
2010 1
2011 4
2012 4
2013 2
2014 8
2015 3
2016 3
2017 5
2018 6
2019 6
2020 11
2021 6
2022 12
2023 7
2024 3

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82 results

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Page 1
Oxytocin and its links through scientific lineage.
Jacob S. Jacob S. Compr Psychoneuroendocrinol. 2024 Mar 11;18:100230. doi: 10.1016/j.cpnec.2024.100230. eCollection 2024 May. Compr Psychoneuroendocrinol. 2024. PMID: 38550559 Free PMC article.
Learning signatures of decision making from many individuals playing the same game.
Mendelson MJ, Azabou M, Jacob S, Grissom N, Darrow D, Ebitz B, Herman A, Dyer EL. Mendelson MJ, et al. Among authors: jacob s. Int IEEE EMBS Conf Neural Eng. 2023 Apr;2023:10.1109/ner52421.2023.10123846. doi: 10.1109/ner52421.2023.10123846. Epub 2023 May 19. Int IEEE EMBS Conf Neural Eng. 2023. PMID: 37808228 Free PMC article.
The CBIT + TMS trial: study protocol for a two-phase randomized controlled trial testing neuromodulation to augment behavior therapy for youth with chronic tics.
Conelea C, Greene DJ, Alexander J, Houlihan K, Hodapp S, Wellen B, Francis S, Mueller B, Hendrickson T, Tseng A, Chen M, Fiecas M, Lim K, Opitz A, Jacob S. Conelea C, et al. Among authors: jacob s. Trials. 2023 Jul 3;24(1):439. doi: 10.1186/s13063-023-07455-1. Trials. 2023. PMID: 37400828 Free PMC article.
The CBIT+TMS Trial: study protocol for a two-phase randomized controlled trial testing neuromodulation to augment behavior therapy for youth with chronic tics.
Conelea C, Greene D, Alexander J, Houlihan K, Hodapp S, Wellen B, Francis S, Mueller B, Hendrickson T, Tseng A, Chen M, Fiecas M, Lim K, Opitz A, Jacob S. Conelea C, et al. Among authors: jacob s. Res Sq [Preprint]. 2023 Jun 13:rs.3.rs-2949388. doi: 10.21203/rs.3.rs-2949388/v1. Res Sq. 2023. PMID: 37398344 Free PMC article. Updated. Preprint.
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.
Fu JM, Satterstrom FK, Peng M, Brand H, Collins RL, Dong S, Wamsley B, Klei L, Wang L, Hao SP, Stevens CR, Cusick C, Babadi M, Banks E, Collins B, Dodge S, Gabriel SB, Gauthier L, Lee SK, Liang L, Ljungdahl A, Mahjani B, Sloofman L, Smirnov AN, Barbosa M, Betancur C, Brusco A, Chung BHY, Cook EH, Cuccaro ML, Domenici E, Ferrero GB, Gargus JJ, Herman GE, Hertz-Picciotto I, Maciel P, Manoach DS, Passos-Bueno MR, Persico AM, Renieri A, Sutcliffe JS, Tassone F, Trabetti E, Campos G, Cardaropoli S, Carli D, Chan MCY, Fallerini C, Giorgio E, Girardi AC, Hansen-Kiss E, Lee SL, Lintas C, Ludena Y, Nguyen R, Pavinato L, Pericak-Vance M, Pessah IN, Schmidt RJ, Smith M, Costa CIS, Trajkova S, Wang JYT, Yu MHC; Autism Sequencing Consortium (ASC); Broad Institute Center for Common Disease Genomics (Broad-CCDG); iPSYCH-BROAD Consortium; Cutler DJ, De Rubeis S, Buxbaum JD, Daly MJ, Devlin B, Roeder K, Sanders SJ, Talkowski ME. Fu JM, et al. Nat Genet. 2022 Sep;54(9):1320-1331. doi: 10.1038/s41588-022-01104-0. Epub 2022 Aug 18. Nat Genet. 2022. PMID: 35982160 Free PMC article.
82 results