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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
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61 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
MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotype.
Smol T, Petit F, Piton A, Keren B, Sanlaville D, Afenjar A, Baker S, Bedoukian EC, Bhoj EJ, Bonneau D, Boudry-Labis E, Bouquillon S, Boute-Benejean O, Caumes R, Chatron N, Colson C, Coubes C, Coutton C, Devillard F, Dieux-Coeslier A, Doco-Fenzy M, Ewans LJ, Faivre L, Fassi E, Field M, Fournier C, Francannet C, Genevieve D, Giurgea I, Goldenberg A, Green AK, Guerrot AM, Heron D, Isidor B, Keena BA, Krock BL, Kuentz P, Lapi E, Le Meur N, Lesca G, Li D, Marey I, Mignot C, Nava C, Nesbitt A, Nicolas G, Roche-Lestienne C, Roscioli T, Satre V, Santani A, Stefanova M, Steinwall Larsen S, Saugier-Veber P, Picker-Minh S, Thuillier C, Verloes A, Vieville G, Wenzel M, Willems M, Whalen S, Zarate YA, Ziegler A, Manouvrier-Hanu S, Kalscheuer VM, Gerard B, Ghoumid J. Smol T, et al. Among authors: le meur n. Neurogenetics. 2018 May;19(2):93-103. doi: 10.1007/s10048-018-0541-0. Epub 2018 Mar 6. Neurogenetics. 2018. PMID: 29511999
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
queryMed: Semantic Web functions for linking pharmacological and medical knowledge to data.
Rivault Y, Dameron O, Le Meur N. Rivault Y, et al. Among authors: le meur n. Bioinformatics. 2019 Sep 1;35(17):3203-3205. doi: 10.1093/bioinformatics/btz034. Bioinformatics. 2019. PMID: 30657867 Free article.
A Simple, Universal, and Cost-Efficient Digital PCR Method for the Targeted Analysis of Copy Number Variations.
Cassinari K, Quenez O, Joly-Hélas G, Beaussire L, Le Meur N, Castelain M, Goldenberg A, Guerrot AM, Brehin AC, Deleuze JF, Boland A, Rovelet-Lecrux A, Campion D, Saugier-Veber P, Gruchy N, Frebourg T, Nicolas G, Sarafan-Vasseur N, Chambon P. Cassinari K, et al. Among authors: le meur n. Clin Chem. 2019 Sep;65(9):1153-1160. doi: 10.1373/clinchem.2019.304246. Epub 2019 Jul 10. Clin Chem. 2019. PMID: 31292136
Postmortem Diagnosis of Heart-hand Syndrome Associated With a 7p22.1p22.3 Deletion in a 16-week-old Fetus.
Tessier A, Callier P, LeMeur N, Frebourg T, Sabourin JC, Patrier S. Tessier A, et al. Pediatr Dev Pathol. 2019 Mar-Apr;22(2):146-151. doi: 10.1177/1093526618799293. Epub 2018 Sep 7. Pediatr Dev Pathol. 2019. PMID: 30193563
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.
Categorical state sequence analysis and regression tree to identify determinants of care trajectory in chronic disease: Example of end-stage renal disease.
Le Meur N, Vigneau C, Lefort M, Lebbah S, Jais JP, Daugas E, Bayat S. Le Meur N, et al. Stat Methods Med Res. 2019 Jun;28(6):1731-1740. doi: 10.1177/0962280218774811. Epub 2018 May 9. Stat Methods Med Res. 2019. PMID: 29742976 Free article.
Does the edge effect impact on the measure of spatial accessibility to healthcare providers?
Gao F, Kihal W, Le Meur N, Souris M, Deguen S. Gao F, et al. Among authors: le meur n. Int J Health Geogr. 2017 Dec 11;16(1):46. doi: 10.1186/s12942-017-0119-3. Int J Health Geogr. 2017. PMID: 29228961 Free PMC article.
[The use of administrative health databases in infectious disease epidemiology and public health].
Fonteneau L, Le Meur N, Cohen-Akenine A, Pessel C, Brouard C, Delon F, Desjeux G, Durand J, Kirchgesner J, Lapidus N, Lemaitre M, Tala S, Thiébaut A, Watier L, Rudant J, Guillon-Grammatico L. Fonteneau L, et al. Among authors: le meur n. Rev Epidemiol Sante Publique. 2017 Oct;65 Suppl 4:S174-S182. doi: 10.1016/j.respe.2017.03.131. Epub 2017 Jun 16. Rev Epidemiol Sante Publique. 2017. PMID: 28624133 French.
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