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

Year Number of Results
2002 2
2003 7
2004 11
2005 13
2006 7
2007 12
2008 9
2009 11
2010 14
2011 19
2012 10
2013 9
2014 13
2015 12
2016 13
2017 11
2018 11
2019 9
2020 23
2021 6
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194 results
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Page 1
De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes.
Rivière JB, Mirzaa GM, O'Roak BJ, Beddaoui M, Alcantara D, Conway RL, St-Onge J, Schwartzentruber JA, Gripp KW, Nikkel SM, Worthylake T, Sullivan CT, Ward TR, Butler HE, Kramer NA, Albrecht B, Armour CM, Armstrong L, Caluseriu O, Cytrynbaum C, Drolet BA, Innes AM, Lauzon JL, Lin AE, Mancini GM, Meschino WS, Reggin JD, Saggar AK, Lerman-Sagie T, Uyanik G, Weksberg R, Zirn B, Beaulieu CL; Finding of Rare Disease Genes (FORGE) Canada Consortium, Majewski J, Bulman DE, O'Driscoll M, Shendure J, Graham JM Jr, Boycott KM, Dobyns WB. Rivière JB, et al. Among authors: sullivan ct. Nat Genet. 2012 Jun 24;44(8):934-40. doi: 10.1038/ng.2331. Nat Genet. 2012. PMID: 22729224 Free PMC article.
De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome.
Rivière JB, van Bon BW, Hoischen A, Kholmanskikh SS, O'Roak BJ, Gilissen C, Gijsen S, Sullivan CT, Christian SL, Abdul-Rahman OA, Atkin JF, Chassaing N, Drouin-Garraud V, Fry AE, Fryns JP, Gripp KW, Kempers M, Kleefstra T, Mancini GM, Nowaczyk MJ, van Ravenswaaij-Arts CM, Roscioli T, Marble M, Rosenfeld JA, Siu VM, de Vries BB, Shendure J, Verloes A, Veltman JA, Brunner HG, Ross ME, Pilz DT, Dobyns WB. Rivière JB, et al. Among authors: sullivan ct. Nat Genet. 2012 Feb 26;44(4):440-4, S1-2. doi: 10.1038/ng.1091. Nat Genet. 2012. PMID: 22366783 Free PMC article.
A consensus-based transparency checklist.
Aczel B, Szaszi B, Sarafoglou A, Kekecs Z, Kucharský Š, Benjamin D, Chambers CD, Fisher A, Gelman A, Gernsbacher MA, Ioannidis JP, Johnson E, Jonas K, Kousta S, Lilienfeld SO, Lindsay DS, Morey CC, Munafò M, Newell BR, Pashler H, Shanks DR, Simons DJ, Wicherts JM, Albarracin D, Anderson ND, Antonakis J, Arkes HR, Back MD, Banks GC, Beevers C, Bennett AA, Bleidorn W, Boyer TW, Cacciari C, Carter AS, Cesario J, Clifton C, Conroy RM, Cortese M, Cosci F, Cowan N, Crawford J, Crone EA, Curtin J, Engle R, Farrell S, Fearon P, Fichman M, Frankenhuis W, Freund AM, Gaskell MG, Giner-Sorolla R, Green DP, Greene RL, Harlow LL, de la Guardia FH, Isaacowitz D, Kolodner J, Lieberman D, Logan GD, Mendes WB, Moersdorf L, Nyhan B, Pollack J, Sullivan C, Vazire S, Wagenmakers EJ. Aczel B, et al. Among authors: sullivan c. Nat Hum Behav. 2020 Jan;4(1):4-6. doi: 10.1038/s41562-019-0772-6. Nat Hum Behav. 2020. PMID: 31792401 Free article. No abstract available.
Risks of and risk factors for COVID-19 disease in people with diabetes: a cohort study of the total population of Scotland.
McGurnaghan SJ, Weir A, Bishop J, Kennedy S, Blackbourn LAK, McAllister DA, Hutchinson S, Caparrotta TM, Mellor J, Jeyam A, O'Reilly JE, Wild SH, Hatam S, Höhn A, Colombo M, Robertson C, Lone N, Murray J, Butterly E, Petrie J, Kennon B, McCrimmon R, Lindsay R, Pearson E, Sattar N, McKnight J, Philip S, Collier A, McMenamin J, Smith-Palmer A, Goldberg D, McKeigue PM, Colhoun HM; Public Health Scotland COVID-19 Health Protection Study Group; Scottish Diabetes Research Network Epidemiology Group. McGurnaghan SJ, et al. Lancet Diabetes Endocrinol. 2021 Feb;9(2):82-93. doi: 10.1016/S2213-8587(20)30405-8. Epub 2020 Dec 23. Lancet Diabetes Endocrinol. 2021. PMID: 33357491 Free PMC article. Clinical Trial.
Virus-encoded microRNAs.
Grundhoff A, Sullivan CS. Grundhoff A, et al. Among authors: sullivan cs. Virology. 2011 Mar 15;411(2):325-43. doi: 10.1016/j.virol.2011.01.002. Epub 2011 Jan 31. Virology. 2011. PMID: 21277611 Free PMC article. Review.
194 results
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