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Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error.
Nat Genet. 2018 Jun;50(6):834-848. doi: 10.1038/s41588-018-0127-7. Epub 2018 May 28.
Nat Genet. 2018.
PMID: 29808027
Free PMC article.
Rare structural variation of synapse and neurotransmission genes in autism.
Gai X, Xie HM, Perin JC, Takahashi N, Murphy K, Wenocur AS, D'arcy M, O'Hara RJ, Goldmuntz E, Grice DE, Shaikh TH, Hakonarson H, Buxbaum JD, Elia J, White PS.
Gai X, et al. Among authors: wenocur as.
Mol Psychiatry. 2012 Apr;17(4):402-11. doi: 10.1038/mp.2011.10. Epub 2011 Mar 1.
Mol Psychiatry. 2012.
PMID: 21358714
Free PMC article.
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CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics.
Gai X, Perin JC, Murphy K, O'Hara R, D'arcy M, Wenocur A, Xie HM, Rappaport EF, Shaikh TH, White PS.
Gai X, et al. Among authors: wenocur a.
BMC Bioinformatics. 2010 Feb 4;11:74. doi: 10.1186/1471-2105-11-74.
BMC Bioinformatics. 2010.
PMID: 20132550
Free PMC article.
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Evaluating sequence data quality from the Swift Accel-Amplicon CFTR Panel.
Leung ML, Watson DJ, Vaccaro CN, Mafra F, Wenocur A, Wang T, Hakonarson H, Santani A.
Leung ML, et al. Among authors: wenocur a.
Sci Data. 2020 Jan 8;7(1):8. doi: 10.1038/s41597-019-0339-4.
Sci Data. 2020.
PMID: 31913291
Free PMC article.
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