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

Year Number of Results
1966 1
1970 1
1978 1
1981 1
1991 1
1992 2
1995 1
1997 1
2000 3
2002 2
2007 1
2011 3
2012 9
2013 15
2014 6
2015 8
2016 8
2017 5
2018 8
2019 15
2020 14
2021 10
2022 9
2023 7
2024 6

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124 results

Results by year

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Page 1
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.
Hamdan FF, Myers CT, Cossette P, Lemay P, Spiegelman D, Laporte AD, Nassif C, Diallo O, Monlong J, Cadieux-Dion M, Dobrzeniecka S, Meloche C, Retterer K, Cho MT, Rosenfeld JA, Bi W, Massicotte C, Miguet M, Brunga L, Regan BM, Mo K, Tam C, Schneider A, Hollingsworth G; Deciphering Developmental Disorders Study; FitzPatrick DR, Donaldson A, Canham N, Blair E, Kerr B, Fry AE, Thomas RH, Shelagh J, Hurst JA, Brittain H, Blyth M, Lebel RR, Gerkes EH, Davis-Keppen L, Stein Q, Chung WK, Dorison SJ, Benke PJ, Fassi E, Corsten-Janssen N, Kamsteeg EJ, Mau-Them FT, Bruel AL, Verloes A, Õunap K, Wojcik MH, Albert DVF, Venkateswaran S, Ware T, Jones D, Liu YC, Mohammad SS, Bizargity P, Bacino CA, Leuzzi V, Martinelli S, Dallapiccola B, Tartaglia M, Blumkin L, Wierenga KJ, Purcarin G, O'Byrne JJ, Stockler S, Lehman A, Keren B, Nougues MC, Mignot C, Auvin S, Nava C, Hiatt SM, Bebin M, Shao Y, Scaglia F, Lalani SR, Frye RE, Jarjour IT, Jacques S, Boucher RM, Riou E, Srour M, Carmant L, Lortie A, Major P, Diadori P, Dubeau F, D'Anjou G, Bourque G, Berkovic SF, Sadleir LG, Campeau PM, Kibar Z, Lafrenière RG, Girard SL, Mercimek-Mahmutoglu S, Boelman C, Rouleau GA, Scheffer IE, Mefford HC, An… See abstract for full author list ➔ Hamdan FF, et al. Among authors: ware t. Am J Hum Genet. 2017 Nov 2;101(5):664-685. doi: 10.1016/j.ajhg.2017.09.008. Am J Hum Genet. 2017. PMID: 29100083 Free PMC article.
SYNGAP1 encephalopathy: A distinctive generalized developmental and epileptic encephalopathy.
Vlaskamp DRM, Shaw BJ, Burgess R, Mei D, Montomoli M, Xie H, Myers CT, Bennett MF, XiangWei W, Williams D, Maas SM, Brooks AS, Mancini GMS, van de Laar IMBH, van Hagen JM, Ware TL, Webster RI, Malone S, Berkovic SF, Kalnins RM, Sicca F, Korenke GC, van Ravenswaaij-Arts CMA, Hildebrand MS, Mefford HC, Jiang Y, Guerrini R, Scheffer IE. Vlaskamp DRM, et al. Among authors: ware tl. Neurology. 2019 Jan 8;92(2):e96-e107. doi: 10.1212/WNL.0000000000006729. Epub 2018 Dec 12. Neurology. 2019. PMID: 30541864 Free PMC article.
Shape-morphing living composites.
Rivera-Tarazona LK, Bhat VD, Kim H, Campbell ZT, Ware TH. Rivera-Tarazona LK, et al. Among authors: ware th. Sci Adv. 2020 Jan 17;6(3):eaax8582. doi: 10.1126/sciadv.aax8582. eCollection 2020 Jan. Sci Adv. 2020. PMID: 32010767 Free PMC article.
Sheath-run artificial muscles.
Mu J, Jung de Andrade M, Fang S, Wang X, Gao E, Li N, Kim SH, Wang H, Hou C, Zhang Q, Zhu M, Qian D, Lu H, Kongahage D, Talebian S, Foroughi J, Spinks G, Kim H, Ware TH, Sim HJ, Lee DY, Jang Y, Kim SJ, Baughman RH. Mu J, et al. Among authors: ware th. Science. 2019 Jul 12;365(6449):150-155. doi: 10.1126/science.aaw2403. Science. 2019. PMID: 31296765
Stimuli-responsive engineered living materials.
Rivera-Tarazona LK , Campbell ZT , Ware TH . Rivera-Tarazona LK , et al. Among authors: ware th. Soft Matter. 2021 Jan 28;17(4):785-809. doi: 10.1039/d0sm01905d. Epub 2021 Jan 7. Soft Matter. 2021. PMID: 33410841 Review.
Juvenile Parkinsonism.
Ware TL, Srinivasan J, Gonzalez L, Hardikar W, Scheinberg AM, Baker L, Prakash C, Ryan MM. Ware TL, et al. J Paediatr Child Health. 2013 May;49(5):409-11. doi: 10.1111/j.1440-1754.2012.02555.x. Epub 2012 Sep 13. J Paediatr Child Health. 2013. PMID: 22970882
Endocannabinoid biosynthetic enzymes regulate pain response via LKB1-AMPK signaling.
Chen M, Shin M, Ware TB, Donvito G, Muchhala KH, Mischel R, Mustafa MA, Serbulea V, Upchurch CM, Leitinger N, Akbarali HI, Lichtman AH, Hsu KL. Chen M, et al. Among authors: ware tb. Proc Natl Acad Sci U S A. 2023 Dec 26;120(52):e2304900120. doi: 10.1073/pnas.2304900120. Epub 2023 Dec 18. Proc Natl Acad Sci U S A. 2023. PMID: 38109529
Functional correlates of clinical phenotype and severity in recurrent SCN2A variants.
Berecki G, Howell KB, Heighway J, Olivier N, Rodda J, Overmars I, Vlaskamp DRM, Ware TL, Ardern-Holmes S, Lesca G, Alber M, Veggiotti P, Scheffer IE, Berkovic SF, Wolff M, Petrou S. Berecki G, et al. Among authors: ware tl. Commun Biol. 2022 May 30;5(1):515. doi: 10.1038/s42003-022-03454-1. Commun Biol. 2022. PMID: 35637276 Free PMC article.
124 results