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

Year Number of Results
1998 1
2004 5
2005 8
2006 8
2007 2
2008 3
2009 4
2010 2
2011 4
2012 3
2013 3
2014 4
2015 3
2016 5
2017 3
2018 4
2019 4
2020 5
2021 4
2022 5
2023 3
2024 1

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72 results

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Page 1
16p13.11 microduplication in 45 new patients: refined clinical significance and genotype-phenotype correlations.
Allach El Khattabi L, Heide S, Caberg JH, Andrieux J, Doco Fenzy M, Vincent-Delorme C, Callier P, Chantot-Bastaraud S, Afenjar A, Boute-Benejean O, Cordier MP, Faivre L, Francannet C, Gerard M, Goldenberg A, Masurel-Paulet A, Mosca-Boidron AL, Marle N, Moncla A, Le Meur N, Mathieu-Dramard M, Plessis G, Lesca G, Rossi M, Edery P, Delahaye-Duriez A, De Pontual L, Tabet AC, Lebbar A, Suiro L, Ioos C, Natiq A, Chafai Elalaoui S, Missirian C, Receveur A, François-Fiquet C, Garnier P, Yardin C, Laroche C, Vago P, Sanlaville D, Dupont JM, Benzacken B, Pipiras E. Allach El Khattabi L, et al. Among authors: le meur n. J Med Genet. 2020 May;57(5):301-307. doi: 10.1136/jmedgenet-2018-105389. Epub 2018 Oct 4. J Med Genet. 2020. PMID: 30287593
[A, not so robertsonian, translocation!].
Amiot J, Layet V, Talbot A, Castelain M, Frebourg T, Chambon P, Le Meur N, Joly Helas G, Cassinari K. Amiot J, et al. Among authors: le meur n. Ann Biol Clin (Paris). 2021 Jun 1;79(3):261-264. doi: 10.1684/abc.2021.1646. Ann Biol Clin (Paris). 2021. PMID: 34159905 French. No abstract available.
Modeling synthetic lethality.
Le Meur N, Gentleman R. Le Meur N, et al. Genome Biol. 2008;9(9):R135. doi: 10.1186/gb-2008-9-9-r135. Epub 2008 Sep 12. Genome Biol. 2008. PMID: 18789146 Free PMC article.
Data standards for flow cytometry.
Spidlen J, Gentleman RC, Haaland PD, Langille M, Le Meur N, Ochs MF, Schmitt C, Smith CA, Treister AS, Brinkman RR. Spidlen J, et al. Among authors: le meur n. OMICS. 2006 Summer;10(2):209-14. doi: 10.1089/omi.2006.10.209. OMICS. 2006. PMID: 16901228 Free PMC article. Review.
Gene expression profiling in human cardiovascular disease.
Steenman M, Lamirault G, Le Meur N, Léger JJ. Steenman M, et al. Among authors: le meur n. Clin Chem Lab Med. 2005;43(7):696-701. doi: 10.1515/CCLM.2005.118. Clin Chem Lab Med. 2005. PMID: 16207127 Review.
First clinical description of a pedigree with complete NAF1 deletion.
Galtier J, Dimicoli-Salazar S, Trimouille A, Lainey E, Revy P, Bidet A, Vial Y, Forcade E, Negrier-Leibreich ML, Rivière E, Tinat J, Le Meur N, Ménard C, Pigneux A, Leguay T, Dumas PY, Ibrahima B, Kannengiesser C. Galtier J, et al. Among authors: le meur n. Leuk Lymphoma. 2023 Feb;64(2):487-490. doi: 10.1080/10428194.2022.2148377. Epub 2022 Nov 23. Leuk Lymphoma. 2023. PMID: 36416722 No abstract available.
De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature.
Nambot S, Faivre L, Mirzaa G, Thevenon J, Bruel AL, Mosca-Boidron AL, Masurel-Paulet A, Goldenberg A, Le Meur N, Charollais A, Mignot C, Petit F, Rossi M, Metreau J, Layet V, Amram D, Boute-Bénéjean O, Bhoj E, Cousin MA, Kruisselbrink TM, Lanpher BC, Klee EW, Fiala E, Grange DK, Meschino WS, Hiatt SM, Cooper GM, Olivié H, Smith WE, Dumas M, Lehman A; CAUSES Study; Inglese C, Nizon M, Guerrini R, Vetro A, Kaplan ES, Miramar D, Van Gils J, Fergelot P, Bodamer O, Herkert JC, Pajusalu S, Õunap K, Filiano JJ, Smol T, Piton A, Gérard B, Chantot-Bastaraud S, Bienvenu T, Li D, Juusola J, Devriendt K, Bilan F, Poé C, Chevarin M, Jouan T, Tisserant E, Rivière JB, Tran Mau-Them F, Philippe C, Duffourd Y, Dobyns WB, Hevner R, Thauvin-Robinet C. Nambot S, et al. Among authors: le meur n. Eur J Hum Genet. 2020 Jun;28(6):770-782. doi: 10.1038/s41431-020-0571-6. Epub 2020 Jan 31. Eur J Hum Genet. 2020. PMID: 32005960 Free PMC article. Review.
72 results