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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 7
2013 8
2014 10
2015 8
2016 9
2017 9
2018 14
2019 5
2020 2
2021 4
2022 4
2023 3
2024 4
2025 5
2026 1

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159 results

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Page 1
Congenital Myasthenic Syndromes in Belgium: Genetic and Clinical Characterization of Pediatric and Adult Patients.
Smeets N, Gheldof A, Dequeker B, Poleur M, Maldonado Slootjes S, Van Parijs V, Deconinck N, Dontaine P, Alonso-Jimenez A, De Bleecker J, De Ridder W, Herdewyn S, Paquay S, Vanlander A, De Waele L, Peirens G, Beysen D, Claeys KG, Dubuisson N, Hansen I, Remiche G, Seneca S, Bissay V, Régal L. Smeets N, et al. Among authors: seneca s. Pediatr Neurol. 2024 Sep;158:57-65. doi: 10.1016/j.pediatrneurol.2024.06.002. Epub 2024 Jun 11. Pediatr Neurol. 2024. PMID: 38964204 Free article.
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.
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
Biallelic variants in COX18 cause a mitochondrial disorder primarily manifesting as peripheral neuropathy.
Armirola-Ricaurte C, Morant L, Adant I, Hamed SA, Pipis M, Efthymiou S, Amor-Barris S, Atkinson D, Van de Vondel L, Tomic A, Seneca S, de Vriendt E, Zuchner S, Ghesquiere B, Hanna M, Houlden H, Lunn MP, Reilly MM, Rasic VM, Jordanova A. Armirola-Ricaurte C, et al. Among authors: seneca s. Brain. 2025 Aug 20:awaf300. doi: 10.1093/brain/awaf300. Online ahead of print. Brain. 2025. PMID: 40830826
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
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.
159 results