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

Year Number of Results
1995 1
2002 5
2003 7
2004 7
2005 6
2006 5
2007 7
2008 2
2009 3
2010 5
2011 5
2012 3
2013 3
2015 3
2016 5
2017 2
2019 1
2021 1
2022 0
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Search Results

69 results
Results by year
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Page 1
Mutations in PCSK9 cause autosomal dominant hypercholesterolemia.
Abifadel M, Varret M, Rabès JP, Allard D, Ouguerram K, Devillers M, Cruaud C, Benjannet S, Wickham L, Erlich D, Derré A, Villéger L, Farnier M, Beucler I, Bruckert E, Chambaz J, Chanu B, Lecerf JM, Luc G, Moulin P, Weissenbach J, Prat A, Krempf M, Junien C, Seidah NG, Boileau C. Abifadel M, et al. Among authors: junien c. Nat Genet. 2003 Jun;34(2):154-6. doi: 10.1038/ng1161. Nat Genet. 2003. PMID: 12730697
Molecular spectrum of autosomal dominant hypercholesterolemia in France.
Marduel M, Carrié A, Sassolas A, Devillers M, Carreau V, Di Filippo M, Erlich D, Abifadel M, Marques-Pinheiro A, Munnich A, Junien C; French ADH Research Network, Boileau C, Varret M, Rabès JP. Marduel M, et al. Among authors: junien c. Hum Mutat. 2010 Nov;31(11):E1811-24. doi: 10.1002/humu.21348. Hum Mutat. 2010. PMID: 20809525 Free PMC article.
Cancer nutrigenomics.
Junien C, Gallou C. Junien C, et al. World Rev Nutr Diet. 2004;93:210-69. doi: 10.1159/000081260. World Rev Nutr Diet. 2004. PMID: 15496809 Review. No abstract available.
Developmental programming and epigenetics.
Gabory A, Attig L, Junien C. Gabory A, et al. Among authors: junien c. Am J Clin Nutr. 2011 Dec;94(6 Suppl):1943S-1952S. doi: 10.3945/ajcn.110.000927. Epub 2011 Nov 2. Am J Clin Nutr. 2011. PMID: 22049164 Review.
Hyperinsulinemic hypoglycemia in children.
de Lonlay P, Giurgea I, Robert JJ, Fournet JC, Touati G, Nihoul-Fékété C, Brunelle F, Jaubert F, Rahier J, Sempoux C, Junien C, Saudubray JM, Dunne M, Otonkoski T, Ribeiro M, Bellané-Chantelot C; European Group of Hyperinsulinism. de Lonlay P, et al. Among authors: junien c. Ann Endocrinol (Paris). 2004 Feb;65(1):96-8. doi: 10.1016/s0003-4266(04)95640-5. Ann Endocrinol (Paris). 2004. PMID: 15122102 Review. No abstract available.
[DOhaD and epigenetic information: societal challenges].
Rial-Sebbag E, Guibet Lafaye C, Simeoni U, Junien C. Rial-Sebbag E, et al. Among authors: junien c. Med Sci (Paris). 2016 Jan;32(1):100-5. doi: 10.1051/medsci/20163201016. Epub 2016 Feb 5. Med Sci (Paris). 2016. PMID: 26850614 Free article. Review. French.
Genetics of congenital hyperinsulinism.
Fournet JC, Junien C. Fournet JC, et al. Among authors: junien c. Endocr Pathol. 2004 Fall;15(3):233-40. doi: 10.1385/ep:15:3:233. Endocr Pathol. 2004. PMID: 15640549 Review.
Sexual dimorphism in non-Mendelian inheritance.
Vigé A, Gallou-Kabani C, Junien C. Vigé A, et al. Among authors: junien c. Pediatr Res. 2008 Apr;63(4):340-7. doi: 10.1203/PDR.0b013e318165b896. Pediatr Res. 2008. PMID: 18356736 Review.
Sex in basic research: concepts in the cardiovascular field.
Ventura-Clapier R, Dworatzek E, Seeland U, Kararigas G, Arnal JF, Brunelleschi S, Carpenter TC, Erdmann J, Franconi F, Giannetta E, Glezerman M, Hofmann SM, Junien C, Katai M, Kublickiene K, König IR, Majdic G, Malorni W, Mieth C, Miller VM, Reynolds RM, Shimokawa H, Tannenbaum C, D'Ursi AM, Regitz-Zagrosek V. Ventura-Clapier R, et al. Among authors: junien c. Cardiovasc Res. 2017 Jun 1;113(7):711-724. doi: 10.1093/cvr/cvx066. Cardiovasc Res. 2017. PMID: 28472454 Review.
[Nutritional epigenomics of metabolic syndrome].
Junien C, Gallou-Kabani C, Vigé A, Gross MS. Junien C, et al. Med Sci (Paris). 2005 Apr;21(4):396-404. doi: 10.1051/medsci/2005214396. Med Sci (Paris). 2005. PMID: 15811305 Free article. Review. French.
69 results