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

Year Number of Results
1961 1
1962 1
1963 1
1965 1
1975 2
1976 4
1977 5
1979 1
1984 1
1985 1
1987 1
1990 2
1994 1
1995 1
1997 2
1998 2
2002 2
2003 1
2004 1
2005 1
2006 2
2008 1
2010 2
2011 1
2012 2
2013 1
2014 8
2015 4
2016 4
2017 3
2018 2
2019 3
2020 4
2021 0
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64 results
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Page 1
De Novo Frameshift Variants in the Neuronal Splicing Factor NOVA2 Result in a Common C-Terminal Extension and Cause a Severe Form of Neurodevelopmental Disorder.
Mattioli F, Hayot G, Drouot N, Isidor B, Courraud J, Hinckelmann MV, Mau-Them FT, Sellier C, Goldman A, Telegrafi A, Boughton A, Gamble C, Moutton S, Quartier A, Jean N, Van Ness P, Grotto S, Nambot S, Douglas G, Si YC, Chelly J, Shad Z, Kaplan E, Dineen R, Golzio C, Charlet-Berguerand N, Mandel JL, Piton A. Mattioli F, et al. Among authors: jean n. Am J Hum Genet. 2020 Apr 2;106(4):438-452. doi: 10.1016/j.ajhg.2020.02.013. Epub 2020 Mar 19. Am J Hum Genet. 2020. PMID: 32197073 Free PMC article.
Normal-weight obesity: implications for cardiovascular health.
Jean N, Somers VK, Sochor O, Medina-Inojosa J, Llano EM, Lopez-Jimenez F. Jean N, et al. Curr Atheroscler Rep. 2014 Dec;16(12):464. doi: 10.1007/s11883-014-0464-7. Curr Atheroscler Rep. 2014. PMID: 25342492 Review.
Associations between cognitive performance and the rehabilitation, medical care and social support provided to French children with Prader-Willi syndrome.
Roux-Levy PH, Bournez M, Masurel A, Jean N, Chancenotte S, Bordes M, Debomy F, Minot D, Schmitt E, Vinault S, Gautier E, Lacombe D, Odent S, Mikaty M, Manouvrier S, Ghoumid J, Geneviève D, Lehman N, Philip N, Edery P, Cornaton J, Gallard J, Héron D, Rastel C, Huet F, Thauvin-Robinet C, Verloes A, Binquet C, Tauber M, Lejeune C, Faivre L. Roux-Levy PH, et al. Among authors: jean n. Eur J Med Genet. 2020 Dec;63(12):104064. doi: 10.1016/j.ejmg.2020.104064. Epub 2020 Sep 28. Eur J Med Genet. 2020. PMID: 32998064
64 results
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