Baldo C - Search Results

1

Impact of NSD1 Alternative Transcripts in Actin Filament Formation and Cellular Division Pathways in Fibroblasts.

Conteduca G, Cangelosi D, Baldo C, Arado A, Testa B, Wagner RT, Robertson KD, Dequiedt F, Fitzsimmons L, Malacarne M, Filaci G, Coviello DA. Conteduca G, et al. Among authors: baldo c. Genes (Basel). 2024 Aug 24;15(9):1117. doi: 10.3390/genes15091117. Genes (Basel). 2024. PMID: 39336709 Free PMC article.

2

8p23.2-pter Microdeletions: Seven New Cases Narrowing the Candidate Region and Review of the Literature.

Catusi I, Garzo M, Capra AP, Briuglia S, Baldo C, Canevini MP, Cantone R, Elia F, Forzano F, Galesi O, Grosso E, Malacarne M, Peron A, Romano C, Saccani M, Larizza L, Recalcati MP. Catusi I, et al. Among authors: baldo c. Genes (Basel). 2021 Apr 27;12(5):652. doi: 10.3390/genes12050652. Genes (Basel). 2021. PMID: 33925474 Free PMC article.

3

NSD1 Mutations in Sotos Syndrome Induce Differential Expression of Long Noncoding RNAs, miR646 and Genes Controlling the G2/M Checkpoint.

Conteduca G, Cangelosi D, Coco S, Malacarne M, Baldo C, Arado A, Pinto R, Testa B, Coviello DA. Conteduca G, et al. Among authors: baldo c. Life (Basel). 2022 Jul 2;12(7):988. doi: 10.3390/life12070988. Life (Basel). 2022. PMID: 35888078 Free PMC article.

4

Identification of alternative transcripts of NSD1 gene in Sotos Syndrome patients and healthy subjects.

Conteduca G, Testa B, Baldo C, Arado A, Malacarne M, Candiano G, Garbarino A, Coviello DA, Cantoni C. Conteduca G, et al. Among authors: baldo c. Gene. 2023 Jan 30;851:146970. doi: 10.1016/j.gene.2022.146970. Epub 2022 Oct 17. Gene. 2023. PMID: 36261088 Free article.

5

Molecular Analysis and Reclassification of NSD1 Gene Variants in a Cohort of Patients with Clinical Suspicion of Sotos Syndrome.

Testa B, Conteduca G, Grasso M, Cecconi M, Lantieri F, Baldo C, Arado A, Andraghetti L, Malacarne M, Milani D, Coviello D, Sotos Collaborative Group. Testa B, et al. Among authors: baldo c. Genes (Basel). 2023 Jan 22;14(2):295. doi: 10.3390/genes14020295. Genes (Basel). 2023. PMID: 36833222 Free PMC article.

6

Pleomorphic Parotid Adenoma in a Child Affected with Cri du Chat Syndrome: Clinical, Cytogenetic, and Molecular Analysis.

Danesino C, Biglioli F, Moneghini L, Valli R, Olivieri C, Testa B, Baldo C, Malacarne M, Guala A. Danesino C, et al. Among authors: baldo c. Int J Mol Sci. 2024 Oct 3;25(19):10664. doi: 10.3390/ijms251910664. Int J Mol Sci. 2024. PMID: 39408992 Free PMC article.

7

First-trimester euploid miscarriages analysed by array-CGH.

Viaggi CD, Cavani S, Malacarne M, Floriddia F, Zerega G, Baldo C, Mogni M, Castagnetta M, Piombo G, Coviello DA, Camandona F, Lijoi D, Insegno W, Traversa M, Pierluigi M. Viaggi CD, et al. Among authors: baldo c. J Appl Genet. 2013 Aug;54(3):353-9. doi: 10.1007/s13353-013-0157-x. Epub 2013 Jun 19. J Appl Genet. 2013. PMID: 23780398

8

FXS-Like Phenotype in Two Unrelated Patients Carrying a Methylated Premutation of the FMR1 Gene.

Fernández E, Gennaro E, Pirozzi F, Baldo C, Forzano F, Turolla L, Faravelli F, Gastaldo D, Coviello D, Grasso M, Bagni C. Fernández E, et al. Among authors: baldo c. Front Genet. 2018 Nov 2;9:442. doi: 10.3389/fgene.2018.00442. eCollection 2018. Front Genet. 2018. PMID: 30450110 Free PMC article.

9

Clinical Manifestations in a Girl with NAA10-Related Syndrome and Genotype-Phenotype Correlation in Females.

Maini I, Caraffi SG, Peluso F, Valeri L, Nicoli D, Laurie S, Baldo C, Zuffardi O, Garavelli L. Maini I, et al. Among authors: baldo c. Genes (Basel). 2021 Jun 10;12(6):900. doi: 10.3390/genes12060900. Genes (Basel). 2021. PMID: 34200686 Free PMC article.

10

Expanding the phenotype of Wiedemann-Steiner syndrome: Craniovertebral junction anomalies.

Giangiobbe S, Caraffi SG, Ivanovski I, Maini I, Pollazzon M, Rosato S, Trimarchi G, Lauriello A, Marinelli M, Nicoli D, Baldo C, Laurie S, Flores-Daboub J, Provenzano A, Andreucci E, Peluso F, Rizzo R, Stewart H, Lachlan K, Bayat A, Napoli M, Carboni G, Baker J, Mendel A, Piatelli G, Pantaleoni C, Mattina T, Prontera P, Mendelsohn NJ, Giglio S, Zuffardi O, Garavelli L. Giangiobbe S, et al. Among authors: baldo c. Am J Med Genet A. 2020 Dec;182(12):2877-2886. doi: 10.1002/ajmg.a.61859. Epub 2020 Oct 11. Am J Med Genet A. 2020. PMID: 33043602

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

105 results

Search Page

Filters