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

Year Number of Results
2002 1
2004 2
2007 2
2009 1
2010 1
2012 2
2013 2
2014 1
2015 3
2017 1
2018 2
2020 7
2021 4
2022 4
2023 3
2024 1

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35 results

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Page 1
Epigenetic Clocks: In Aging-Related and Complex Diseases.
Margiotti K, Monaco F, Fabiani M, Mesoraca A, Giorlandino C. Margiotti K, et al. Cytogenet Genome Res. 2023;163(5-6):247-256. doi: 10.1159/000534561. Epub 2023 Oct 28. Cytogenet Genome Res. 2023. PMID: 37899027 Review.
Genomic biomarkers, androgen pathway and prostate cancer.
D'Amico F, Biancolella M, Margiotti K, Reichardt JK, Novelli G. D'Amico F, et al. Among authors: margiotti k. Pharmacogenomics. 2007 Jun;8(6):645-61. doi: 10.2217/14622416.8.6.645. Pharmacogenomics. 2007. PMID: 17559353 Review.
The genetics of sports injuries and athletic performance.
Maffulli N, Margiotti K, Longo UG, Loppini M, Fazio VM, Denaro V. Maffulli N, et al. Among authors: margiotti k. Muscles Ligaments Tendons J. 2013 Aug 11;3(3):173-89. Muscles Ligaments Tendons J. 2013. PMID: 24367777 Free PMC article. Review.
Evaluation of SARS-CoV-2 viral RNA in fecal samples.
Mesoraca A, Margiotti K, Viola A, Cima A, Sparacino D, Giorlandino C. Mesoraca A, et al. Among authors: margiotti k. Virol J. 2020 Jun 30;17(1):86. doi: 10.1186/s12985-020-01359-1. Virol J. 2020. PMID: 32605577 Free PMC article.
Pharmacogenetics of human androgens and prostate cancer--an update.
Novelli G, Margiotti K, Chiocca AM, Spera E, Micali F, Reichardt JK. Novelli G, et al. Among authors: margiotti k. Pharmacogenomics. 2004 Apr;5(3):283-94. doi: 10.1517/phgs.5.3.283.29828. Pharmacogenomics. 2004. PMID: 15102543 Review.
Agnathia-Otocephaly Complex Due to a De Novo Deletion in the OTX2 Gene.
Fabiani M, Libotte F, Margiotti K, Tannous DKI, Sparacino D, D'Aleo MP, Monaco F, Dello Russo C, Mesoraca A, Giorlandino C. Fabiani M, et al. Among authors: margiotti k. Genes (Basel). 2022 Dec 2;13(12):2269. doi: 10.3390/genes13122269. Genes (Basel). 2022. PMID: 36553536 Free PMC article.
Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect.
Ferese R, Bonetti M, Consoli F, Guida V, Sarkozy A, Lepri FR, Versacci P, Gambardella S, Calcagni G, Margiotti K, Piceci Sparascio F, Hozhabri H, Mazza T, Digilio MC, Dallapiccola B, Tartaglia M, Marino B, Hertog JD, De Luca A. Ferese R, et al. Among authors: margiotti k. Hum Mutat. 2018 Oct;39(10):1428-1441. doi: 10.1002/humu.23593. Epub 2018 Jul 30. Hum Mutat. 2018. PMID: 30007050
35 results