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Year Number of Results
2007 1
2008 1
2009 2
2011 3
2012 2
2013 3
2014 3
2015 6
2016 4
2017 2
2018 4
2019 4
2020 2
2021 1
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33 results
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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, Andrade DM, Rossignol E, Minassian BA, Michaud JL. Hamdan FF, et al. Among authors: girard sl. 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.
Impact of Paternal Age at Conception on Human Health.
Simard M, Laprise C, Girard SL. Simard M, et al. Among authors: girard sl. Clin Chem. 2019 Jan;65(1):146-152. doi: 10.1373/clinchem.2018.294421. Clin Chem. 2019. PMID: 30602478 Review.
Polygenic risk scores of several subtypes of epilepsies in a founder population.
Moreau C, Rébillard RM, Wolking S, Michaud J, Tremblay F, Girard A, Bouchard J, Minassian B, Laprise C, Cossette P, Girard SL. Moreau C, et al. Among authors: girard sl. Neurol Genet. 2020 Mar 27;6(3):e416. doi: 10.1212/NXG.0000000000000416. eCollection 2020 Jun. Neurol Genet. 2020. PMID: 32337343 Free PMC article.
Testing association of rare genetic variants with resistance to three common antiseizure medications.
Wolking S, Moreau C, Nies AT, Schaeffeler E, McCormack M, Auce P, Avbersek A, Becker F, Krenn M, Møller RS, Nikanorova M, Weber YG, Weckhuysen S, Cavalleri GL, Delanty N, Depondt C, Johnson MR, Koeleman BPC, Kunz WS, Marson AG, Sander JW, Sills GJ, Striano P, Zara F, Zimprich F, Schwab M, Krause R, Sisodiya SM, Cossette P, Girard SL, Lerche H; EpiPGX Consortium. Wolking S, et al. Among authors: girard sl. Epilepsia. 2020 Apr;61(4):657-666. doi: 10.1111/epi.16467. Epub 2020 Mar 6. Epilepsia. 2020. PMID: 32141622
Genome-wide estimates of heritability and genetic correlations in essential tremor.
Diez-Fairen M, Bandres-Ciga S, Houle G, Nalls MA, Girard SL, Dion PA, Blauwendraat C, Singleton AB, Rouleau GA, Pastor P. Diez-Fairen M, et al. Among authors: girard sl. Parkinsonism Relat Disord. 2019 Jul;64:262-267. doi: 10.1016/j.parkreldis.2019.05.002. Epub 2019 May 4. Parkinsonism Relat Disord. 2019. PMID: 31085086 Free PMC article.
A Wee1 checkpoint inhibits anaphase onset.
Lianga N, Williams EC, Kennedy EK, Doré C, Pilon S, Girard SL, Deneault JS, Rudner AD. Lianga N, et al. Among authors: girard sl. J Cell Biol. 2013 Jun 10;201(6):843-62. doi: 10.1083/jcb.201212038. J Cell Biol. 2013. PMID: 23751495 Free PMC article.
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