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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 4
2011 3
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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92 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
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 Jun 2;98(6):1271. doi: 10.1016/j.ajhg.2016.05.009. Epub 2016 Jun 2. Am J Hum Genet. 2016. PMID: 27259058 Free PMC article. No abstract available.
Rare susceptibility variants for bipolar disorder suggest a role for G protein-coupled receptors.
Cruceanu C, Schmouth JF, Torres-Platas SG, Lopez JP, Ambalavanan A, Darcq E, Gross F, Breton B, Spiegelman D, Rochefort D, Hince P, Petite JM, Gauthier J, Lafrenière RG, Dion PA, Greenwood CM, Kieffer BL, Alda M, Turecki G, Rouleau GA. Cruceanu C, et al. Among authors: rochefort d. Mol Psychiatry. 2018 Oct;23(10):2050-2056. doi: 10.1038/mp.2017.223. Epub 2017 Nov 21. Mol Psychiatry. 2018. PMID: 29158579
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.
92 results