Bianciardi L - Search Results

1

TM9SF4 expression in tumor tissues: a novel diagnostic biomarker for gastrointestinal tumors.

Guazzi P, Zocco D, Isajevs S, Zarovni N, Bianciardi L, Toots M, Sivins A, Leja M, Chiesi A, Lozupone F. Guazzi P, et al. Among authors: bianciardi l. Transl Cancer Res. 2020 Nov;9(11):6652-6659. doi: 10.21037/tcr-20-516. Transl Cancer Res. 2020. PMID: 35117275 Free PMC article.

2

When Less Is More: Specific Capture and Analysis of Tumor Exosomes in Plasma Increases the Sensitivity of Liquid Biopsy for Comprehensive Detection of Multiple Androgen Receptor Phenotypes in Advanced Prostate Cancer Patients.

Foroni C, Zarovni N, Bianciardi L, Bernardi S, Triggiani L, Zocco D, Venturella M, Chiesi A, Valcamonico F, Berruti A. Foroni C, et al. Among authors: bianciardi l. Biomedicines. 2020 May 22;8(5):131. doi: 10.3390/biomedicines8050131. Biomedicines. 2020. PMID: 32455948 Free PMC article.

3

Isolation of extracellular vesicles improves the detection of mutant DNA from plasma of metastatic melanoma patients.

Zocco D, Bernardi S, Novelli M, Astrua C, Fava P, Zarovni N, Carpi FM, Bianciardi L, Malavenda O, Quaglino P, Foroni C, Russo D, Chiesi A, Fierro MT. Zocco D, et al. Among authors: bianciardi l. Sci Rep. 2020 Sep 25;10(1):15745. doi: 10.1038/s41598-020-72834-6. Sci Rep. 2020. PMID: 32978468 Free PMC article.

4

Revealing the complexity of a monogenic disease: rett syndrome exome sequencing.

Grillo E, Lo Rizzo C, Bianciardi L, Bizzarri V, Baldassarri M, Spiga O, Furini S, De Felice C, Signorini C, Leoncini S, Pecorelli A, Ciccoli L, Mencarelli MA, Hayek J, Meloni I, Ariani F, Mari F, Renieri A. Grillo E, et al. Among authors: bianciardi l. PLoS One. 2013;8(2):e56599. doi: 10.1371/journal.pone.0056599. Epub 2013 Feb 28. PLoS One. 2013. PMID: 23468869 Free PMC article.

5

Exome sequencing analysis in a pair of monozygotic twins re-evaluates the genetics behind their intellectual disability and reveals a CHD2 mutation.

Pinto AM, Bianciardi L, Mencarelli MA, Imperatore V, Di Marco C, Furini S, Suppiej A, Salviati L, Tenconi R, Ariani F, Mari F, Renieri A. Pinto AM, et al. Among authors: bianciardi l. Brain Dev. 2016 Jun;38(6):590-6. doi: 10.1016/j.braindev.2015.12.006. Epub 2016 Jan 2. Brain Dev. 2016. PMID: 26754451

6

MECP2 missense mutations outside the canonical MBD and TRD domains in males with intellectual disability.

Bianciardi L, Fichera M, Failla P, Di Marco C, Grozeva D, Mencarelli MA, Spiga O, Mari F, Meloni I, Raymond L, Renieri A, Romano C, Ariani F. Bianciardi L, et al. J Hum Genet. 2016 Feb;61(2):95-101. doi: 10.1038/jhg.2015.118. Epub 2015 Oct 22. J Hum Genet. 2016. PMID: 26490184 Free PMC article.

7

Potentially Treatable Disorder Diagnosed Post Mortem by Exome Analysis in a Boy with Respiratory Distress.

Imperatore V, Mencarelli MA, Fallerini C, Bianciardi L, Ariani F, Furini S, Renieri A, Mari F, Frullanti E. Imperatore V, et al. Among authors: bianciardi l. Int J Mol Sci. 2016 Feb 27;17(3):306. doi: 10.3390/ijms17030306. Int J Mol Sci. 2016. PMID: 26927095 Free PMC article.

8

Exploiting the potential of next-generation sequencing in genomic medicine.

Pinto AM, Ariani F, Bianciardi L, Daga S, Renieri A. Pinto AM, et al. Among authors: bianciardi l. Expert Rev Mol Diagn. 2016 Sep;16(9):1037-47. doi: 10.1080/14737159.2016.1224181. Expert Rev Mol Diagn. 2016. PMID: 27574853 Review.

9

Exome sequencing coupled with mRNA analysis identifies NDUFAF6 as a Leigh gene.

Bianciardi L, Imperatore V, Fernandez-Vizarra E, Lopomo A, Falabella M, Furini S, Galluzzi P, Grosso S, Zeviani M, Renieri A, Mari F, Frullanti E. Bianciardi L, et al. Mol Genet Metab. 2016 Nov;119(3):214-222. doi: 10.1016/j.ymgme.2016.09.001. Epub 2016 Sep 3. Mol Genet Metab. 2016. PMID: 27623250

10

Combined ultrasound and exome sequencing approach recognizes Opitz G/BBB syndrome in two malformed fetuses.

Pinto AM, Imperatore V, Bianciardi L, Baldassarri M, Galluzzi P, Furini S, Centini G, Renieri A, Mari F. Pinto AM, et al. Among authors: bianciardi l. Clin Dysmorphol. 2017 Jan;26(1):18-25. doi: 10.1097/MCD.0000000000000152. Clin Dysmorphol. 2017. PMID: 27749392

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

44 results

Search Page