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

Year Number of Results
1979 1
1981 1
1983 1
1984 1
1985 2
1987 1
1988 2
1990 1
1991 1
1992 2
1993 3
1995 1
1996 3
1997 2
1998 4
1999 2
2000 1
2001 2
2002 2
2003 5
2004 2
2005 2
2006 1
2007 1
2008 3
2009 2
2010 5
2011 4
2012 6
2013 7
2014 2
2015 3
2016 6
2017 4
2018 6
2019 5
2020 4
2022 1
2023 1
2024 0

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94 results

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Page 1
Diphenoquinones Redux.
Néron S, Morency M, Chen L, Maris T, Rochefort D, Iftimie R, Wuest JD. Néron S, et al. Among authors: rochefort d. J Org Chem. 2022 Jun 17;87(12):7673-7695. doi: 10.1021/acs.joc.2c00260. Epub 2022 Jun 6. J Org Chem. 2022. PMID: 35667025
Reimagining the Cuckoo's Nest.
Rochefort DA. Rochefort DA. J Med Humanit. 2018 Mar;39(1):3-14. doi: 10.1007/s10912-017-9481-1. J Med Humanit. 2018. PMID: 28956346
FOXP1-related intellectual disability syndrome: a recognisable entity.
Meerschaut I, Rochefort D, Revençu N, Pètre J, Corsello C, Rouleau GA, Hamdan FF, Michaud JL, Morton J, Radley J, Ragge N, García-Miñaúr S, Lapunzina P, Bralo MP, Mori MÁ, Moortgat S, Benoit V, Mary S, Bockaert N, Oostra A, Vanakker O, Velinov M, de Ravel TJ, Mekahli D, Sebat J, Vaux KK, DiDonato N, Hanson-Kahn AK, Hudgins L, Dallapiccola B, Novelli A, Tarani L, Andrieux J, Parker MJ, Neas K, Ceulemans B, Schoonjans AS, Prchalova D, Havlovicova M, Hancarova M, Budisteanu M, Dheedene A, Menten B, Dion PA, Lederer D, Callewaert B. Meerschaut I, et al. Among authors: rochefort d. J Med Genet. 2017 Sep;54(9):613-623. doi: 10.1136/jmedgenet-2017-104579. Epub 2017 Jul 22. J Med Genet. 2017. PMID: 28735298
Multiomics Analyses Identify Genes and Pathways Relevant to Essential Tremor.
Liao C, Sarayloo F, Rochefort D, Houle G, Akçimen F, He Q, Laporte AD, Spiegelman D, Poewe W, Berg D, Müller S, Hopfner F, Deuschl G, Kuhlenbäeumer G, Rajput A, Dion PA, Rouleau GA. Liao C, et al. Among authors: rochefort d. Mov Disord. 2020 Jul;35(7):1153-1162. doi: 10.1002/mds.28031. Epub 2020 Apr 6. Mov Disord. 2020. PMID: 32249994
Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia.
Tarabeux J, Kebir O, Gauthier J, Hamdan FF, Xiong L, Piton A, Spiegelman D, Henrion É, Millet B; S2D team; Fathalli F, Joober R, Rapoport JL, DeLisi LE, Fombonne É, Mottron L, Forget-Dubois N, Boivin M, Michaud JL, Drapeau P, Lafrenière RG, Rouleau GA, Krebs MO. Tarabeux J, et al. Transl Psychiatry. 2011 Nov 15;1(11):e55. doi: 10.1038/tp.2011.52. Transl Psychiatry. 2011. PMID: 22833210 Free PMC article.
[Night work].
Pépin-Lortie R, Durand M, Rochefort D. Pépin-Lortie R, et al. Among authors: rochefort d. Infirm Can. 1979 Oct;21(9):16-21. Infirm Can. 1979. PMID: 258194 French. No abstract available.
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.
Gan-Or Z, Bouslam N, Birouk N, Lissouba A, Chambers DB, Vérièpe J, Androschuk A, Laurent SB, Rochefort D, Spiegelman D, Dionne-Laporte A, Szuto A, Liao M, Figlewicz DA, Bouhouche A, Benomar A, Yahyaoui M, Ouazzani R, Yoon G, Dupré N, Suchowersky O, Bolduc FV, Parker JA, Dion PA, Drapeau P, Rouleau GA, Ouled Amar Bencheikh B. Gan-Or Z, et al. Among authors: rochefort d. Am J Hum Genet. 2016 May 5;98(5):1038-1046. doi: 10.1016/j.ajhg.2016.04.002. Am J Hum Genet. 2016. PMID: 27153400 Free PMC article.
94 results