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

Year Number of Results
2004 1
2005 1
2006 1
2007 2
2008 1
2009 2
2010 1
2011 2
2012 5
2013 3
2014 4
2016 3
2017 7
2018 7
2019 4
2020 2
2021 2
2022 4
2023 3
2024 0

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48 results

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Page 1
Colorectal Cancer Archaeome: A Metagenomic Exploration, Tunisia.
Mathlouthi NEH, Oumarou Hama H, Belguith I, Charfi S, Boudawara T, Lagier JC, Ammar Keskes L, Grine G, Gdoura R. Mathlouthi NEH, et al. Among authors: ammar keskes l. Curr Issues Mol Biol. 2023 Sep 19;45(9):7572-7581. doi: 10.3390/cimb45090477. Curr Issues Mol Biol. 2023. PMID: 37754261 Free PMC article.
Analysis of Genetic Alterations in Tunisian Patients with Lung Adenocarcinoma.
Dhieb D, Belguith I, Capelli L, Chiadini E, Canale M, Bravaccini S, Yangui I, Boudawara O, Jlidi R, Boudawara T, Calistri D, Keskes LA, Ulivi P. Dhieb D, et al. Among authors: keskes la. Cells. 2019 May 28;8(6):514. doi: 10.3390/cells8060514. Cells. 2019. PMID: 31141932 Free PMC article.
An unusual familial Xp22.12 microduplication including EIF1AX: A novel candidate dosage-sensitive gene for premature ovarian insufficiency.
Sakka R, Abdelhedi F, Sellami H, Pichon B, Lajmi Y, Mnif M, Kebaili S, Derbel R, Kamoun H, Gdoura R, Delbaere A, Desir J, Abramowicz M, Vialard F, Dupont JM, Ammar-Keskes L. Sakka R, et al. Among authors: ammar keskes l. Eur J Med Genet. 2022 Nov;65(11):104613. doi: 10.1016/j.ejmg.2022.104613. Epub 2022 Sep 14. Eur J Med Genet. 2022. PMID: 36113757
A novel TBX1 missense mutation in patients with syndromic congenital heart defects.
Jaouadi A, Tabebi M, Abdelhedi F, Abid D, Kamoun F, Chabchoub I, Maatoug S, Doukali H, Belghuith N, Ksentini MA, Keskes LA, Triki C, Hachicha M, Kamoun S, Kamoun H. Jaouadi A, et al. Among authors: keskes la. Biochem Biophys Res Commun. 2018 May 15;499(3):563-569. doi: 10.1016/j.bbrc.2018.03.190. Epub 2018 Mar 28. Biochem Biophys Res Commun. 2018. PMID: 29596833
48 results