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

Year Number of Results
1998 2
1999 2
2000 2
2001 1
2002 2
2003 3
2004 2
2008 2
2009 3
2010 2
2011 7
2012 5
2013 6
2014 6
2015 8
2016 8
2017 8
2018 6
2019 8
2020 4
2021 3
2022 5
2023 6
2024 16
2025 7

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112 results

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Page 1
Sex Differences in Natural History and Health Outcomes Among Individuals With Tic Disorders.
Dy-Hollins ME, Chibnik LB, Tracy NA, Osiecki L, Budman CL, Cath DC, Grados MA, King RA, Lyon GJ, Rouleau GA, Sandor P, Singer HS, Sharma N, Mathews CA, Scharf JM. Dy-Hollins ME, et al. Among authors: lyon gj. Neurology. 2025 Feb 11;104(3):e210249. doi: 10.1212/WNL.0000000000210249. Epub 2025 Jan 15. Neurology. 2025. PMID: 39813627 Free PMC article.
DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders.
Lessel I, Baresic A, Chinn IK, May J, Goenka A, Chandler KE, Posey JE, Afenjar A, Averdunk L, Bedeschi MF, Besnard T, Brager R, Brick L, Brugger M, Brunet T, Byrne S, Calle-Martín O, Capra V, Cardenas P, Chappé C, Chong HJ, Cogne B, Conboy E, Cope H, Courtin T, Deb W, Dilena R, Dubourg C, Elgizouli M, Fernandes E, Fitzgerald KK, Gangi S, George-Abraham JK, Gucsavas-Calikoglu M, Haack TB, Hadonou M, Hanker B, Hüning I, Iascone M, Isidor B, Järvelä I, Jin JJ, Jorge AAL, Josifova D, Kalinauskiene R, Kamsteeg EJ, Keren B, Kessler E, Kölbel H, Kozenko M, Kubisch C, Kuechler A, Leal SM, Leppälä J, Luu SM, Lyon GJ, Madan-Khetarpal S, Mancardi M, Marchi E, Mehta L, Menendez B, Morel CF, Harasink SM, Nevay DL, Nigro V, Odent S, Oegema R, Pappas J, Pastore MT, Perilla-Young Y, Platzer K, Powell-Hamilton N, Rabin R, Rekab A, Rezende RC, Robert L, Romano F, Scala M, Poths K, Schrauwen I, Sebastian J, Short J, Sidlow R, Sullivan J, Szakszon K, Tan QKG; Undiagnosed Diseases Network; Wagner M, Wieczorek D, Yuan B, Maeding N, Strunk D, Begtrup A, Banka S, Lupski JR, Tolosa E, Lessel D. Lessel I, et al. Among authors: lyon gj. Am J Hum Genet. 2025 Feb 6;112(2):394-413. doi: 10.1016/j.ajhg.2024.12.012. Epub 2025 Jan 10. Am J Hum Genet. 2025. PMID: 39798569 Free PMC article.
A framework for N-of-1 trials of individualized gene-targeted therapies for genetic diseases.
Kim-McManus O, Gleeson JG, Mignon L, Smith Fine A, Yan W, Nolen N, Demarest S, Berry-Kravis E, Finkel R, Leonard S, Finlayson S, Augustine E, Lyon GJ, Schule R, Yu T. Kim-McManus O, et al. Among authors: lyon gj. Nat Commun. 2024 Nov 12;15(1):9802. doi: 10.1038/s41467-024-54077-5. Nat Commun. 2024. PMID: 39532857 Free PMC article. Review.
A repository of Ogden syndrome patient derived iPSC lines and isogenic pairs by X-chromosome screening and genome-editing.
Wesely J, Rusielewicz T, Chen YR, Hartley B, McKenzie D, Yim MK, Maguire C, Bia R, Franklin S, Makwana R, Marchi E, Nikte M, Patil S, Sapar M, Moroziewicz D; NYSCF Global Stem Cell Array® Team; Bauer L, Lee JT, Monsma FJ Jr, Paull D, Lyon GJ. Wesely J, et al. Among authors: lyon gj. bioRxiv [Preprint]. 2024 Sep 28:2024.09.28.615067. doi: 10.1101/2024.09.28.615067. bioRxiv. 2024. PMID: 39386428 Free PMC article. Preprint.
112 results