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

Year Number of Results
2007 2
2008 2
2009 4
2010 8
2011 7
2012 6
2013 4
2014 8
2015 9
2016 10
2017 7
2018 9
2019 13
2020 7
2021 7
2022 0
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Search Results

87 results
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Page 1
COVID-19: Discovery, diagnostics and drug development.
Asselah T, Durantel D, Pasmant E, Lau G, Schinazi RF. Asselah T, et al. Among authors: pasmant e. J Hepatol. 2021 Jan;74(1):168-184. doi: 10.1016/j.jhep.2020.09.031. Epub 2020 Oct 8. J Hepatol. 2021. PMID: 33038433 Free PMC article. Review.
"MPNST Epigenetics"-Letter.
Wassef M, Pasmant E, Margueron R. Wassef M, et al. Among authors: pasmant e. Mol Cancer Res. 2019 Oct;17(10):2139. doi: 10.1158/1541-7786.MCR-19-0680. Mol Cancer Res. 2019. PMID: 31575727 Free article. No abstract available.
One NF1 Mutation may Conceal Another.
Pacot L, Burin des Roziers C, Laurendeau I, Briand-Suleau A, Coustier A, Mayard T, Tlemsani C, Faivre L, Thomas Q, Rodriguez D, Blesson S, Dollfus H, Muller YG, Parfait B, Vidaud M, Gilbert-Dussardier B, Yardin C, Dauriat B, Derancourt C, Vidaud D, Pasmant E. Pacot L, et al. Among authors: pasmant e. Genes (Basel). 2019 Aug 22;10(9):633. doi: 10.3390/genes10090633. Genes (Basel). 2019. PMID: 31443423 Free PMC article.
[SUMMIT: a basket study scores points].
Luscan A, Pasmant É. Luscan A, et al. Among authors: pasmant e. Med Sci (Paris). 2018 Nov;34(11):910-913. doi: 10.1051/medsci/2018232. Epub 2018 Dec 10. Med Sci (Paris). 2018. PMID: 30526831 Free article. French. No abstract available.
Review and update of SPRED1 mutations causing Legius syndrome.
Brems H, Pasmant E, Van Minkelen R, Wimmer K, Upadhyaya M, Legius E, Messiaen L. Brems H, et al. Among authors: pasmant e. Hum Mutat. 2012 Nov;33(11):1538-46. doi: 10.1002/humu.22152. Epub 2012 Aug 1. Hum Mutat. 2012. PMID: 22753041 Review.
Chaperoning 5S RNA assembly.
Madru C, Lebaron S, Blaud M, Delbos L, Pipoli J, Pasmant E, Réty S, Leulliot N. Madru C, et al. Among authors: pasmant e. Genes Dev. 2015 Jul 1;29(13):1432-46. doi: 10.1101/gad.260349.115. Genes Dev. 2015. PMID: 26159998 Free PMC article.
KDM1A inactivation causes hereditary food-dependent Cushing syndrome.
Vaczlavik A, Bouys L, Violon F, Giannone G, Jouinot A, Armignacco R, Cavalcante IP, Berthon A, Letouzé E, Vaduva P, Barat M, Bonnet F, Perlemoine K, Ribes C, Sibony M, North MO, Espiard S, Emy P, Haissaguerre M, Tauveron I, Guignat L, Groussin L, Dousset B, Reincke M, Fragoso MC, Stratakis CA, Pasmant E, Libé R, Assié G, Ragazzon B, Bertherat J. Vaczlavik A, et al. Among authors: pasmant e. Genet Med. 2021 Nov 16:S1098-3600(21)05346-6. doi: 10.1016/j.gim.2021.09.018. Online ahead of print. Genet Med. 2021. PMID: 34906447
87 results