Moises Serrano - Search Results

Year	Number of Results
2009	1
2011	1
2013	1
2014	1
2015	2
2016	3
2017	1
2018	1
2019	3
2020	1
2022	1
2023	1
2024	0

1

Rehm HL, Berg JS, Brooks LD, Bustamante CD, Evans JP, Landrum MJ, Ledbetter DH, Maglott DR, Martin CL, Nussbaum RL, Plon SE, Ramos EM, Sherry ST, Watson MS; ClinGen. Rehm HL, et al. N Engl J Med. 2015 Jun 4;372(23):2235-42. doi: 10.1056/NEJMsr1406261. Epub 2015 May 27. N Engl J Med. 2015. PMID: 26014595 Free PMC article.

2

Parent-of-Origin Effects in 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome.

Davis KW, Serrano M, Loddo S, Robinson C, Alesi V, Dallapiccola B, Novelli A, Butler MG. Davis KW, et al. Among authors: serrano m. Int J Mol Sci. 2019 Mar 22;20(6):1459. doi: 10.3390/ijms20061459. Int J Mol Sci. 2019. PMID: 30909440 Free PMC article.

3

Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders.

Costain G, Walker S, Argiropoulos B, Baribeau DA, Bassett AS, Boot E, Devriendt K, Kellam B, Marshall CR, Prasad A, Serrano MA, Stavropoulos DJ, Twede H, Vermeesch JR, Vorstman JAS, Scherer SW. Costain G, et al. Among authors: serrano ma. J Neurodev Disord. 2019 Feb 7;11(1):3. doi: 10.1186/s11689-019-9263-3. J Neurodev Disord. 2019. PMID: 30732576 Free PMC article.

4

NeuroSCORE is a genome-wide omics-based model that identifies candidate disease genes of the central nervous system.

Davis KW, Bilancia CG, Martin M, Vanzo R, Rimmasch M, Hom Y, Uddin M, Serrano MA. Davis KW, et al. Among authors: serrano ma. Sci Rep. 2022 Mar 31;12(1):5427. doi: 10.1038/s41598-022-08938-y. Sci Rep. 2022. PMID: 35361823 Free PMC article.

5

Comparative Benchmarking of Optical Genome Mapping and Chromosomal Microarray Reveals High Technological Concordance in CNV Identification and Additional Structural Variant Refinement.

Barseghyan H, Pang AWC, Clifford B, Serrano MA, Chaubey A, Hastie AR. Barseghyan H, et al. Among authors: serrano ma. Genes (Basel). 2023 Sep 26;14(10):1868. doi: 10.3390/genes14101868. Genes (Basel). 2023. PMID: 37895217 Free PMC article.

6

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. Among authors: serrano ma. Neurol Genet. 2019 Dec 6;5(6):e378. doi: 10.1212/NXG.0000000000000378. eCollection 2019 Dec. Neurol Genet. 2019. PMID: 32042908 Free PMC article.

7

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: serrano ma. J Pers Med. 2020 Dec 29;11(1):21. doi: 10.3390/jpm11010021. J Pers Med. 2020. PMID: 33383702 Free PMC article.

8

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: serrano ma. 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.

9

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: serrano m. Biomed Res Int. 2016;2016:3284534. doi: 10.1155/2016/3284534. Epub 2016 Nov 16. Biomed Res Int. 2016. PMID: 27975050 Free PMC article.

10

ATR Plays a Direct Antiapoptotic Role at Mitochondria, which Is Regulated by Prolyl Isomerase Pin1.

Hilton BA, Li Z, Musich PR, Wang H, Cartwright BM, Serrano M, Zhou XZ, Lu KP, Zou Y. Hilton BA, et al. Among authors: serrano m. Mol Cell. 2015 Oct 1;60(1):35-46. doi: 10.1016/j.molcel.2015.08.008. Epub 2015 Sep 18. Mol Cell. 2015. PMID: 26387736 Free PMC article.

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