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

Year Number of Results
1988 1
1991 1
1992 2
1993 1
1995 5
1996 4
1997 4
1998 7
1999 3
2000 2
2001 3
2002 1
2003 5
2004 6
2005 3
2006 5
2007 5
2008 6
2009 10
2010 8
2011 3
2012 6
2013 7
2014 10
2015 8
2016 9
2017 9
2018 14
2019 5
2020 2
2021 4
2022 4
2023 3
2024 2

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151 results

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Page 1
EDIR: exome database of interspersed repeats.
Vo Ngoc LDT, Osei R, Dohr K, Olsen C, Seneca S, Gheldof A. Vo Ngoc LDT, et al. Among authors: seneca s. Bioinformatics. 2023 Jan 1;39(1):btac771. doi: 10.1093/bioinformatics/btac771. Bioinformatics. 2023. PMID: 36453866 Free PMC article.
PEGylating poly(p-phenylene vinylene)-based bioimaging nanoprobes.
Peters M, Desta D, Seneca S, Reekmans G, Adriaensens P, Noben JP, Hellings N, Junkers T, Ethirajan A. Peters M, et al. Among authors: seneca s. J Colloid Interface Sci. 2021 Jan 1;581(Pt B):566-575. doi: 10.1016/j.jcis.2020.07.145. Epub 2020 Aug 2. J Colloid Interface Sci. 2021. PMID: 32818676
Genetic causes of male infertility.
Stouffs K, Seneca S, Lissens W. Stouffs K, et al. Among authors: seneca s. Ann Endocrinol (Paris). 2014 May;75(2):109-11. doi: 10.1016/j.ando.2014.03.004. Epub 2014 Apr 24. Ann Endocrinol (Paris). 2014. PMID: 24768008 Review.
Children born after assisted reproduction more commonly carry a mitochondrial genotype associating with low birthweight.
Mertens J, Belva F, van Montfoort APA, Regin M, Zambelli F, Seneca S, Couvreu de Deckersberg E, Bonduelle M, Tournaye H, Stouffs K, Barbé K, Smeets HJM, Van de Velde H, Sermon K, Blockeel C, Spits C. Mertens J, et al. Among authors: seneca s. Nat Commun. 2024 Feb 9;15(1):1232. doi: 10.1038/s41467-024-45446-1. Nat Commun. 2024. PMID: 38336715 Free PMC article.
Primary ovarian insufficiency in RMND1 mitochondrial disease.
Boros E, Elilié Mawa Ongoth F, Heinrichs C, Mansbach AL, Seneca S, Aeby A, Ismaïli K, Brachet C. Boros E, et al. Among authors: seneca s. Mitochondrion. 2022 Sep;66:51-53. doi: 10.1016/j.mito.2022.07.004. Epub 2022 Jul 25. Mitochondrion. 2022. PMID: 35901949
DNA diagnosis of X-linked adrenoleukodystrophy.
Seneca S, Lissens W. Seneca S, et al. J Inherit Metab Dis. 1995;18 Suppl 1:34-44. doi: 10.1007/BF00711427. J Inherit Metab Dis. 1995. PMID: 9053554 Review.
Expanding the clinical spectrum of biallelic ZNF335 variants.
Stouffs K, Stergachis AB, Vanderhasselt T, Dica A, Janssens S, Vandervore L, Gheldof A, Bodamer O, Keymolen K, Seneca S, Liebaers I, Jayaraman D, Hill HE, Partlow JN, Walsh CA, Jansen AC. Stouffs K, et al. Among authors: seneca s. Clin Genet. 2018 Aug;94(2):246-251. doi: 10.1111/cge.13260. Epub 2018 May 3. Clin Genet. 2018. PMID: 29652087 Free PMC article.
Sertoli Cell-Only Syndrome: Behind the Genetic Scenes.
Stouffs K, Gheldof A, Tournaye H, Vandermaelen D, Bonduelle M, Lissens W, Seneca S. Stouffs K, et al. Among authors: seneca s. Biomed Res Int. 2016;2016:6191307. doi: 10.1155/2016/6191307. Epub 2016 Jan 26. Biomed Res Int. 2016. PMID: 26925412 Free PMC article.
151 results