Vanzo RJ - Search Results

1

Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis.

Prasad A, Sdano MA, Vanzo RJ, Mowery-Rushton PA, Serrano MA, Hensel CH, Wassman ER. Prasad A, et al. Among authors: vanzo rj. BMC Med Genet. 2018 Mar 20;19(1):46. doi: 10.1186/s12881-018-0555-3. BMC Med Genet. 2018. PMID: 29554876 Free PMC article.

2

Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.

Ho KS, Twede H, Vanzo R, Harward E, Hensel CH, Martin MM, Page S, Peiffer A, Mowery-Rushton P, Serrano M, Wassman ER. Ho KS, et al. Biomed Res Int. 2016;2016:3284534. doi: 10.1155/2016/3284534. Epub 2016 Nov 16. Biomed Res Int. 2016. PMID: 27975050 Free PMC article.

3

Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf-Hirschhorn syndrome.

Ho KS, South ST, Lortz A, Hensel CH, Sdano MR, Vanzo RJ, Martin MM, Peiffer A, Lambert CG, Calhoun A, Carey JC, Battaglia A. Ho KS, et al. Among authors: vanzo rj. J Med Genet. 2016 Apr;53(4):256-63. doi: 10.1136/jmedgenet-2015-103626. Epub 2016 Jan 8. J Med Genet. 2016. PMID: 26747863 Free PMC article.

4

Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.

Ho KS, Wassman ER, Baxter AL, Hensel CH, Martin MM, Prasad A, Twede H, Vanzo RJ, Butler MG. Ho KS, et al. Among authors: vanzo rj. Int J Mol Sci. 2016 Dec 9;17(12):2070. doi: 10.3390/ijms17122070. Int J Mol Sci. 2016. PMID: 27941670 Free PMC article.

5

Clinical significance of copy number variants involving KANK1 in patients with neurodevelopmental disorders.

Vanzo RJ, Twede H, Ho KS, Prasad A, Martin MM, South ST, Wassman ER. Vanzo RJ, et al. Eur J Med Genet. 2019 Jan;62(1):15-20. doi: 10.1016/j.ejmg.2018.04.012. Epub 2018 May 3. Eur J Med Genet. 2019. PMID: 29729439 Free article.

6

Clinical Utility of a Comprehensive, Whole Genome CMA Testing Platform in Pediatrics: A Prospective Randomized Controlled Trial of Simulated Patients in Physician Practices.

Peabody J, Martin M, DeMaria L, Florentino J, Paculdo D, Paul M, Vanzo R, Wassman ER, Burgon T. Peabody J, et al. PLoS One. 2016 Dec 30;11(12):e0169064. doi: 10.1371/journal.pone.0169064. eCollection 2016. PLoS One. 2016. PMID: 28036350 Free PMC article. Clinical Trial.

7

Analytical and Clinical Validity Study of FirstStepDx PLUS: A Chromosomal Microarray Optimized for Patients with Neurodevelopmental Conditions.

Hensel C, Vanzo R, Martin M, Dixon S, Lambert C, Levy B, Nelson L, Peiffer A, Ho KS, Rushton P, Serrano M, South S, Ward K, Wassman E. Hensel C, et al. PLoS Curr. 2017 Feb 27;9:ecurrents.eogt.7d92ce775800ef3fbc72e3840fb1bc22. doi: 10.1371/currents.eogt.7d92ce775800ef3fbc72e3840fb1bc22. PLoS Curr. 2017. PMID: 28357155 Free PMC article.

8

Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders.

Wassman ER, Ho KS, Bertrand D, Davis KW, Martin MM, Page S, Peiffer A, Prasad A, Serrano MA, Twede H, Vanzo R, Scherer SW, Uddin M, Hensel CH. Wassman ER, et al. Neurol Genet. 2019 Dec 6;5(6):e378. doi: 10.1212/NXG.0000000000000378. eCollection 2019 Dec. Neurol Genet. 2019. PMID: 32042908 Free PMC article.

9

The Temple Grandin Genome: Comprehensive Analysis in a Scientist with High-Functioning Autism.

Vanzo RJ, Prasad A, Staunch L, Hensel CH, Serrano MA, Wassman ER, Kaplun A, Grandin T, Boles RG. Vanzo RJ, et al. J Pers Med. 2020 Dec 29;11(1):21. doi: 10.3390/jpm11010021. J Pers Med. 2020. PMID: 33383702 Free PMC article.

10

A Novel Partial Duplication of ZEB2 and Review of ZEB2 Involvement in Mowat-Wilson Syndrome.

Baxter AL, Vivian JL, Hagelstrom RT, Hossain W, Golden WL, Wassman ER, Vanzo RJ, Butler MG. Baxter AL, et al. Among authors: vanzo rj. Mol Syndromol. 2017 Jun;8(4):211-218. doi: 10.1159/000473693. Epub 2017 May 3. Mol Syndromol. 2017. PMID: 28690488 Free PMC article.

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