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

Year Number of Results
2003 1
2005 1
2006 4
2007 4
2008 4
2009 6
2010 12
2011 14
2012 9
2013 6
2014 12
2015 9
2016 11
2017 14
2018 8
2019 14
2020 11
2021 18
2022 9
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152 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: frye re. 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.
Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.
Parikh S, Goldstein A, Karaa A, Koenig MK, Anselm I, Brunel-Guitton C, Christodoulou J, Cohen BH, Dimmock D, Enns GM, Falk MJ, Feigenbaum A, Frye RE, Ganesh J, Griesemer D, Haas R, Horvath R, Korson M, Kruer MC, Mancuso M, McCormack S, Raboisson MJ, Reimschisel T, Salvarinova R, Saneto RP, Scaglia F, Shoffner J, Stacpoole PW, Sue CM, Tarnopolsky M, Van Karnebeek C, Wolfe LA, Cunningham ZZ, Rahman S, Chinnery PF. Parikh S, et al. Among authors: frye re. Genet Med. 2017 Dec;19(12):10.1038/gim.2017.107. doi: 10.1038/gim.2017.107. Epub 2017 Jul 27. Genet Med. 2017. PMID: 28749475 Free PMC article. Review.
Introduction.
Frye RE, Slattery J. Frye RE, et al. Microb Ecol Health Dis. 2015 May 7;26:28168. doi: 10.3402/mehd.v26.28168. eCollection 2015. Microb Ecol Health Dis. 2015. PMID: 25956239 Free PMC article. No abstract available.
Editorial: Secondary vs. Idiopathic Autism.
Casanova MF, Casanova EL, Frye RE, Baeza-Velasco C, LaSalle JM, Hagerman RJ, Scherer SW, Natowicz MR. Casanova MF, et al. Front Psychiatry. 2020 Apr 14;11:297. doi: 10.3389/fpsyt.2020.00297. eCollection 2020. Front Psychiatry. 2020. PMID: 32346372 Free PMC article. No abstract available.
Editorial: Comorbidity and Autism Spectrum Disorder.
Casanova MF, Frye RE, Gillberg C, Casanova EL. Casanova MF, et al. Among authors: frye re. Front Psychiatry. 2020 Nov 20;11:617395. doi: 10.3389/fpsyt.2020.617395. eCollection 2020. Front Psychiatry. 2020. PMID: 33329163 Free PMC article. No abstract available.
Introduction to Part 1.
Frye RE. Frye RE. Semin Pediatr Neurol. 2020 Jul;34:100802. doi: 10.1016/j.spen.2020.100802. Epub 2020 Mar 7. Semin Pediatr Neurol. 2020. PMID: 32446436
Introduction to Part 2.
Frye RE. Frye RE. Semin Pediatr Neurol. 2020 Oct;35:100828. doi: 10.1016/j.spen.2020.100828. Epub 2020 Jun 22. Semin Pediatr Neurol. 2020. PMID: 32892955
152 results