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A list of all the posts and pages found on the site. For you robots out there is an XML version available for digesting as well.
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Posts
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Blog Post number 4
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Blog Post number 1
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portfolio
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publications
Non-invasive prenatal diagnosis of beta-thalassemia by semiconductor sequencing: a feasibility study in the sardinian population
Published in European Journal of Human Genetics volume 25, pages 600–607 (2017), 2017
Recommended citation: Saba L, Masala M, Capponi V, Marceddu G, Massidda M, Rosatelli MC. (2017). European journal of human genetics : EJHG, 25(5), 600–607. doi:10.1038/ejhg.2017.26.
Circulating Levels of MiRNAs From 320 Family in Subjects With Lipodystrophy: Disclosing Novel Signatures of the Disease
Published in Frontiers in Endocrinology volume 13 (June 2022), 2022
Recommended citation: Dattilo A, Ceccarini G, Scabia G, Magno S, Quintino L, Pelosini C, Salvetti G, Cusano R, Massidda M, Montanelli L, Gilio D, Gatti G, Giacomina A, Costa M, Santini F, Maffei M (2022). Circulating Levels of MiRNAs From 320 Family in Subjects With Lipodystrophy: Disclosing Novel Signatures of the Disease. Frontiers in endocrinology, 13, 866679. https://doi.org/10.3389/fendo.2022.866679
VariantAlert: a web-based tool to notify updates in genetic variant annotations
Published in Human Mutation (Oct 2022), 2022
Recommended citation: Atzeni, R., Massidda, M., Fotia, G., & Uva, P. (2022). VariantAlert: A web-based tool to notify updates in genetic variant annotations. Human mutation, 10.1002/humu.24495. Advance online publication. https://doi.org/10.1002/humu.24495
Next Generation Sequencing for miRNA Detection on the Exhaled Breath Condensate: A Pilot Study
Published in Epigenetics Insights, 2023
Recommended citation: Cherchi R, Cusano R, Orrù S, Ferrari PA, Massidda M, Fotia G, De Matteis S and Cocco P. (2023). Next Generation Sequencing for miRNA Detection on the Exhaled Breath Condensate: A Pilot Study. Epigenetics Insights. 2023;16. https://doi.org/10.1177/25168657231160985
Whole genome sequencing in ROHHAD trios proved inconclusive: what’s beyond?
Published in Frontiers in Genetics, 2023
Recommended citation: Grossi A. , Rusmini M. , Cusano R. , Massidda M. , Santamaria G. , Napoli F. , Angelelli A. , Fava D. , Uva P. , Ceccherini I. , Maghnie M. (2024). Whole genome sequencing in ROHHAD trios proved inconclusive: what’s beyond? Frontiers in Genetics, Sec. Genetics of Common and Rare Diseases. 2023,14. https://doi.org/10.3389/fgene.2023.1031074
Harnessing Minimal Residual Disease as a Predictor for Colorectal Cancer: Promising Horizons Amidst Challenges
Published in Medicina, 2023
Recommended citation: Wen, X., Coradduzza, D., Shen, J., Scanu, A. M., Muroni, M. R., Massidda, M., Rallo, V., Carru, C., Angius, A., & De Miglio, M. R. (2023). Harnessing Minimal Residual Disease as a Predictor for Colorectal Cancer: Promising Horizons Amidst Challenges. Medicina, 59(10), 1886. https://doi.org/10.3390/medicina59101886
Esophageal Cancer with Early Onset in a Patient with Cri du Chat Syndrome
Published in Diseases 2024, 12(1), 9, 2023
Recommended citation: Danesino, C., Gualtierotti, M., Origi, M., Cistaro, A., Malacarne, M., Massidda, M., Bencardino, K., Coviello, D., Albani, G., Schiera, I. G., Liava, A., & Guala, A. (2024). Esophageal Cancer with Early Onset in a Patient with Cri du Chat Syndrome. Diseases, 12(1), 9. https://doi.org/10.3390/diseases12010009
A Novel Affordable and Reliable Framework for Accurate Detection and Comprehensive Analysis of Somatic Mutations in Cancer
Published in Int. J. Mol. Sci, 2024
Recommended citation: Atzeni, R., Massidda, M., Pieroni, E., Rallo, V., Pisu, M., & Angius, A. (2024). A Novel Affordable and Reliable Framework for Accurate Detection and Comprehensive Analysis of Somatic Mutations in Cancer. International Journal of Molecular Sciences, 25(15), 8044., 10.3390/ijms25158044.
talks
teaching
Molecular Structure of Proteins - BIO/11
Master Degree course, University of Cagliari, Faculty of Biology and Pharmacy, 2018
The course was held as part of the Master Degree in Cellular and Molecular Biology