Serio VB - Search Results

1

The Evidence Base for Circulating Tumor DNA-Methylation in Non-Small Cell Lung Cancer: A Systematic Review and Meta-Analysis.

Maffeo D, Rina A, Serio VB, Markou A, Powrózek T, Constâncio V, Nunes SP, Jerónimo C, Calvo A, Mari F, Frullanti E, Rosati D, Palmieri M. Maffeo D, et al. Among authors: serio vb. Cancers (Basel). 2024 Oct 29;16(21):3641. doi: 10.3390/cancers16213641. Cancers (Basel). 2024. PMID: 39518079 Free PMC article. Review.

2

The Genetic Analysis and Clinical Therapy in Lung Cancer: Current Advances and Future Directions.

Rina A, Maffeo D, Minnai F, Esposito M, Palmieri M, Serio VB, Rosati D, Mari F, Frullanti E, Colombo F. Rina A, et al. Among authors: serio vb. Cancers (Basel). 2024 Aug 19;16(16):2882. doi: 10.3390/cancers16162882. Cancers (Basel). 2024. PMID: 39199653 Free PMC article. Review.

3

The Personalized Inherited Signature Predisposing to Non-Small-Cell Lung Cancer in Non-Smokers.

Serio VB, Rosati D, Maffeo D, Rina A, Ghisalberti M, Bellan C, Spiga O, Mari F, Palmieri M, Frullanti E. Serio VB, et al. Cancers (Basel). 2024 Aug 20;16(16):2887. doi: 10.3390/cancers16162887. Cancers (Basel). 2024. PMID: 39199663 Free PMC article.

4

Case report: PIK3CA somatic mutation leading to Klippel Trenaunay Syndrome and multiple tumors.

Serio VB, Palmieri M, Innamorato S, Loberti L, Fallerini C, Ariani F, Antolini E, Covarelli J, Vaghi M, Frullanti E, Renieri A, Pinto AM. Serio VB, et al. Front Genet. 2023 Aug 17;14:1213283. doi: 10.3389/fgene.2023.1213283. eCollection 2023. Front Genet. 2023. PMID: 37662840 Free PMC article.

5

Host genetics and COVID-19 severity: increasing the accuracy of latest severity scores by Boolean quantum features.

Martelloni G, Turchi A, Fallerini C, Degl'Innocenti A, Baldassarri M, Olmi S, Furini S, Renieri A; GEN-COVID Multicenter study. Martelloni G, et al. Front Genet. 2024 May 22;15:1362469. doi: 10.3389/fgene.2024.1362469. eCollection 2024. Front Genet. 2024. PMID: 38841724 Free PMC article.

6

Nosological and Theranostic Approach to Vascular Malformation through cfDNA NGS Liquid Biopsy.

Serio VB, Palmieri M, Loberti L, Granata S, Fallerini C, Vaghi M, Renieri A, Pinto AM. Serio VB, et al. J Clin Med. 2022 Jun 28;11(13):3740. doi: 10.3390/jcm11133740. J Clin Med. 2022. PMID: 35807022 Free PMC article.

7

Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder.

Bergantini L, Baldassarri M, d'Alessandro M, Brunelli G, Fabbri G, Zguro K, Degl'Innocenti A; GEN-COVID Multicenter study; Fallerini C, Bargagli E, Renieri A. Bergantini L, et al. Respir Res. 2023 Jun 16;24(1):158. doi: 10.1186/s12931-023-02458-7. Respir Res. 2023. PMID: 37328761 Free PMC article.

8

Gain- and Loss-of-Function CFTR Alleles Are Associated with COVID-19 Clinical Outcomes.

Baldassarri M, Zguro K, Tomati V, Pastorino C, Fava F, Croci S, Bruttini M, Picchiotti N, Furini S, Pedemonte N, Gabbi C, Renieri A, Fallerini C; Gen-Covid Multicenter Study. Baldassarri M, et al. Cells. 2022 Dec 16;11(24):4096. doi: 10.3390/cells11244096. Cells. 2022. PMID: 36552859 Free PMC article.

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