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

Year Number of Results
1997 3
1998 1
1999 1
2000 3
2002 1
2003 3
2004 4
2005 1
2006 3
2007 2
2008 4
2009 4
2010 7
2011 3
2012 7
2013 2
2014 3
2015 3
2016 1
2017 1
2018 6
2019 1
2020 1
2021 7
2022 5
2023 3
2024 0

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71 results

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Page 1
APOE gene variants in primary dyslipidemia.
Khalil YA, Rabès JP, Boileau C, Varret M. Khalil YA, et al. Among authors: varret m. Atherosclerosis. 2021 Jul;328:11-22. doi: 10.1016/j.atherosclerosis.2021.05.007. Epub 2021 May 23. Atherosclerosis. 2021. PMID: 34058468 Free article. Review.
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: varret m. 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: varret m. Hum Mutat. 2010 Nov;31(11):E1811-24. doi: 10.1002/humu.21348. Hum Mutat. 2010. PMID: 20809525 Free PMC article.
Additive Effect of APOE Rare Variants on the Phenotype of Familial Hypercholesterolemia.
Marmontel O, Abou-Khalil Y, Bluteau O, Cariou B, Carreau V, Charrière S, Divry E, Gallo A, Moulin P, Paillard F, Peretti N, Rabès JP, Varret M, Carrié A, Di Filippo M. Marmontel O, et al. Among authors: varret m. Arterioscler Thromb Vasc Biol. 2023 Jul;43(7):e270-e278. doi: 10.1161/ATVBAHA.123.319146. Epub 2023 Apr 27. Arterioscler Thromb Vasc Biol. 2023. PMID: 37128917
Integrated omics approach for the identification of HDL structure-function relationships in PCSK9-related familial hypercholesterolemia.
Darabi M, Lhomme M, Ponnaiah M, Pučić-Baković M, Guillas I, Frisdal E, Bittar R, Croyal M, Matheron-Duriez L, Poupel L, Bonnefont-Rousselot D, Frere C, Varret M, Krempf M, Cariou B, Lauc G, Guerin M, Carrie A, Bruckert E, Giral P, Le Goff W, Kontush A. Darabi M, et al. Among authors: varret m. J Clin Lipidol. 2023 Sep-Oct;17(5):643-658. doi: 10.1016/j.jacl.2023.07.003. Epub 2023 Jul 27. J Clin Lipidol. 2023. PMID: 37550151
Circulating PCSK9 Linked to Dyslipidemia in Lebanese Schoolchildren.
Azar Y, Gannagé-Yared MH, Naous E, Ayoub C, Abou Khalil Y, Chahine E, Elbitar S, Ghaleb Y, Boileau C, Varret M, El Khoury P, Abifadel M. Azar Y, et al. Among authors: varret m. Metabolites. 2022 May 31;12(6):504. doi: 10.3390/metabo12060504. Metabolites. 2022. PMID: 35736437 Free PMC article.
Posttranscriptional Regulation of the Human LDL Receptor by the U2-Spliceosome.
Zanoni P, Panteloglou G, Othman A, Haas JT, Meier R, Rimbert A, Futema M, Abou Khalil Y, Norrelykke SF, Rzepiela AJ, Stoma S, Stebler M, van Dijk F, Wijers M, Wolters JC, Dalila N, Huijkman NCA, Smit M, Gallo A, Carreau V, Philippi A, Rabès JP, Boileau C, Visentin M, Vonghia L, Weyler J, Francque S, Verrijken A, Verhaegen A, Van Gaal L, van der Graaf A, van Rosmalen BV, Robert J, Velagapudi S, Yalcinkaya M, Keel M, Radosavljevic S, Geier A, Tybjaerg-Hansen A, Varret M, Rohrer L, Humphries SE, Staels B, van de Sluis B, Kuivenhoven JA, von Eckardstein A. Zanoni P, et al. Among authors: varret m. Circ Res. 2022 Jan 7;130(1):80-95. doi: 10.1161/CIRCRESAHA.120.318141. Epub 2021 Nov 23. Circ Res. 2022. PMID: 34809444 Free article.
71 results