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Year Number of Results
1977 1
1987 1
1988 1
1989 1
1990 1
1991 2
1992 2
1994 1
1995 1
1996 5
1997 2
2004 1
2006 1
2008 6
2009 5
2010 5
2011 3
2012 7
2013 9
2014 7
2015 1
2016 3
2017 3
2018 2
2019 3
2020 1
2021 2
2022 6
2023 3
2024 3

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80 results

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Page 1
Thoracic outlet syndrome.
Oates SD, Daley RA. Oates SD, et al. Hand Clin. 1996 Nov;12(4):705-18. Hand Clin. 1996. PMID: 8953290 Review.
Clinical spectrum of STX1B-related epileptic disorders.
Wolking S, May P, Mei D, Møller RS, Balestrini S, Helbig KL, Altuzarra CD, Chatron N, Kaiwar C, Stöhr K, Widdess-Walsh P, Mendelsohn BA, Numis A, Cilio MR, Van Paesschen W, Svendsen LL, Oates S, Hughes E, Goyal S, Brown K, Sifuentes Saenz M, Dorn T, Muhle H, Pagnamenta AT, Vavoulis DV, Knight SJL, Taylor JC, Canevini MP, Darra F, Gavrilova RH, Powis Z, Tang S, Marquetand J, Armstrong M, McHale D, Klee EW, Kluger GJ, Lowenstein DH, Weckhuysen S, Pal DK, Helbig I, Guerrini R, Thomas RH, Rees MI, Lesca G, Sisodiya SM, Weber YG, Lal D, Marini C, Lerche H, Schubert J. Wolking S, et al. Among authors: oates s. Neurology. 2019 Mar 12;92(11):e1238-e1249. doi: 10.1212/WNL.0000000000007089. Epub 2019 Feb 8. Neurology. 2019. PMID: 30737342 Free PMC article.
GRB 130427A: a nearby ordinary monster.
Maselli A, Melandri A, Nava L, Mundell CG, Kawai N, Campana S, Covino S, Cummings JR, Cusumano G, Evans PA, Ghirlanda G, Ghisellini G, Guidorzi C, Kobayashi S, Kuin P, La Parola V, Mangano V, Oates S, Sakamoto T, Serino M, Virgili F, Zhang BB, Barthelmy S, Beardmore A, Bernardini MG, Bersier D, Burrows D, Calderone G, Capalbi M, Chiang J, D'Avanzo P, D'Elia V, De Pasquale M, Fugazza D, Gehrels N, Gomboc A, Harrison R, Hanayama H, Japelj J, Kennea J, Kopac D, Kouveliotou C, Kuroda D, Levan A, Malesani D, Marshall F, Nousek J, O'Brien P, Osborne JP, Pagani C, Page KL, Page M, Perri M, Pritchard T, Romano P, Saito Y, Sbarufatti B, Salvaterra R, Steele I, Tanvir N, Vianello G, Wiegand B, Wiersema K, Yatsu Y, Yoshii T, Tagliaferri G. Maselli A, et al. Among authors: oates s. Science. 2014 Jan 3;343(6166):48-51. doi: 10.1126/science.1242279. Epub 2013 Nov 21. Science. 2014. PMID: 24263134
ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder.
Oates S, Absoud M, Goyal S, Bayley S, Baulcomb J, Sims A, Riddett A, Allis K, Brasch-Andersen C, Balasubramanian M, Bai R, Callewaert B, Hüffmeier U, Le Duc D, Radtke M, Korff C, Kennedy J, Low K, Møller RS, Nielsen JEK, Popp B, Quteineh L, Rønde G, Schönewolf-Greulich B, Shillington A, Taylor MR, Todd E, Torring PM, Tümer Z, Vasileiou G, Yates TM, Zweier C, Rosch R, Basson MA, Pal DK. Oates S, et al. Clin Genet. 2021 Oct;100(4):412-429. doi: 10.1111/cge.14023. Epub 2021 Jul 16. Clin Genet. 2021. PMID: 34216016 Free article.
Christopher Peterson: "other people matter".
Park N, Oates S, Schwarzer R. Park N, et al. Among authors: oates s. Appl Psychol Health Well Being. 2013 Mar;5(1):1-4. doi: 10.1111/aphw.12007. Appl Psychol Health Well Being. 2013. PMID: 23457083 Free article. No abstract available.
A kilonova following a long-duration gamma-ray burst at 350 Mpc.
Rastinejad JC, Gompertz BP, Levan AJ, Fong WF, Nicholl M, Lamb GP, Malesani DB, Nugent AE, Oates SR, Tanvir NR, de Ugarte Postigo A, Kilpatrick CD, Moore CJ, Metzger BD, Ravasio ME, Rossi A, Schroeder G, Jencson J, Sand DJ, Smith N, Fernández JFA, Berger E, Blanchard PK, Chornock R, Cobb BE, De Pasquale M, Fynbo JPU, Izzo L, Kann DA, Laskar T, Marini E, Paterson K, Escorial AR, Sears HM, Thöne CC. Rastinejad JC, et al. Among authors: oates sr. Nature. 2022 Dec;612(7939):223-227. doi: 10.1038/s41586-022-05390-w. Epub 2022 Dec 7. Nature. 2022. PMID: 36477128
Complementing the phenotypical spectrum of TUBA1A tubulinopathy and its role in early-onset epilepsies.
Schröter J, Popp B, Brennenstuhl H, Döring JH, Donze SH, Bijlsma EK, van Haeringen A, Huhle D, Jestaedt L, Merkenschlager A, Arelin M, Gräfe D, Neuser S, Oates S, Pal DK, Parker MJ, Lemke JR, Hoffmann GF, Kölker S, Harting I, Syrbe S. Schröter J, et al. Among authors: oates s. Eur J Hum Genet. 2022 Mar;30(3):298-306. doi: 10.1038/s41431-021-01027-0. Epub 2022 Jan 11. Eur J Hum Genet. 2022. PMID: 35017693 Free PMC article.
80 results