Wassman ER - Search Results

1

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.

2

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. Among authors: wassman er. 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.

3

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.

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: wassman er. 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 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. Among authors: wassman er. Biomed Res Int. 2016;2016:3284534. doi: 10.1155/2016/3284534. Epub 2016 Nov 16. Biomed Res Int. 2016. PMID: 27975050 Free PMC article.

6

A case for cannabidiol in Wolf-Hirschhorn syndrome seizure management.

Ho KS, Wassman ER. Ho KS, et al. Among authors: wassman er. Am J Med Genet A. 2017 Feb;173(2):324-326. doi: 10.1002/ajmg.a.37979. Epub 2016 Nov 7. Am J Med Genet A. 2017. PMID: 28102593 Free PMC article.

7

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: wassman er. 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.

8

A comparison of genomic laboratory reports and observations that may enhance their clinical utility for providers and patients.

Davis KW, Hamby Erby L, Fiallos K, Martin M, Wassman ER. Davis KW, et al. Among authors: wassman er. Mol Genet Genomic Med. 2019 Jul;7(7):e00551. doi: 10.1002/mgg3.551. Epub 2019 May 21. Mol Genet Genomic Med. 2019. PMID: 31115190 Free PMC article.

9

OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion Syndrome.

Uddin M, Unda BK, Kwan V, Holzapfel NT, White SH, Chalil L, Woodbury-Smith M, Ho KS, Harward E, Murtaza N, Dave B, Pellecchia G, D'Abate L, Nalpathamkalam T, Lamoureux S, Wei J, Speevak M, Stavropoulos J, Hope KJ, Doble BW, Nielsen J, Wassman ER, Scherer SW, Singh KK. Uddin M, et al. Among authors: wassman er. Am J Hum Genet. 2018 Feb 1;102(2):278-295. doi: 10.1016/j.ajhg.2018.01.006. Am J Hum Genet. 2018. PMID: 29395074 Free PMC article.

10

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. Among authors: wassman er. J Pers Med. 2020 Dec 29;11(1):21. doi: 10.3390/jpm11010021. J Pers Med. 2020. PMID: 33383702 Free PMC article.

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