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

Year Number of Results
1951 1
1971 1
1999 2
2001 1
2003 1
2004 1
2005 1
2006 1
2010 1
2011 2
2012 2
2013 1
2014 5
2015 2
2017 1
2018 1
2020 2
2021 2
2022 2
2023 2
2024 1

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31 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, An… See abstract for full author list ➔ Hamdan FF, et al. Among authors: massicotte c. 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.
De novo mutations in moderate or severe intellectual disability.
Hamdan FF, Srour M, Capo-Chichi JM, Daoud H, Nassif C, Patry L, Massicotte C, Ambalavanan A, Spiegelman D, Diallo O, Henrion E, Dionne-Laporte A, Fougerat A, Pshezhetsky AV, Venkateswaran S, Rouleau GA, Michaud JL. Hamdan FF, et al. Among authors: massicotte c. PLoS Genet. 2014 Oct 30;10(10):e1004772. doi: 10.1371/journal.pgen.1004772. eCollection 2014 Oct. PLoS Genet. 2014. PMID: 25356899 Free PMC article.
Psychoanalysis and Telepathic Processes.
Rabeyron T, Evrard R, Massicotte C. Rabeyron T, et al. Among authors: massicotte c. J Am Psychoanal Assoc. 2021 Jun;69(3):535-571. doi: 10.1177/00030651211022332. J Am Psychoanal Assoc. 2021. PMID: 34424070
An Unusual Cause of Worsening Obstructive Sleep Apnea.
Sunkonkit K, Go C, Alzaid M, Massicotte C, Narang I, Amin R. Sunkonkit K, et al. Among authors: massicotte c. Clin Pediatr (Phila). 2023 Mar;62(3):188-190. doi: 10.1177/00099228221118957. Epub 2022 Aug 25. Clin Pediatr (Phila). 2023. PMID: 36016488 No abstract available.
What is your diagnosis? Diskospondylitis.
Soltero-Rivera MM, Goggin JM, Massicotte C, Scarano JM. Soltero-Rivera MM, et al. Among authors: massicotte c. J Am Vet Med Assoc. 2010 Dec 1;237(11):1245-6. doi: 10.2460/javma.237.11.1245. J Am Vet Med Assoc. 2010. PMID: 21118008 Free article. No abstract available.
Positional obstructive sleep apnea in an obese pediatric population.
Selvadurai S, Voutsas G, Massicotte C, Kassner A, Katz SL, Propst EJ, Narang I. Selvadurai S, et al. Among authors: massicotte c. J Clin Sleep Med. 2020 Aug 15;16(8):1295-1301. doi: 10.5664/jcsm.8496. J Clin Sleep Med. 2020. PMID: 32807295 Free PMC article.
31 results