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Influences of rare copy-number variation on human complex traits.
Hujoel MLA, Sherman MA, Barton AR, Mukamel RE, Sankaran VG, Terao C, Loh PR. Hujoel MLA, et al. Among authors: barton ar. Cell. 2022 Oct 27;185(22):4233-4248.e27. doi: 10.1016/j.cell.2022.09.028. Cell. 2022. PMID: 36306736 Free PMC article.
Hidden protein-altering variants influence diverse human phenotypes.
Hujoel MLA, Handsaker RE, Sherman MA, Kamitaki N, Barton AR, Mukamel RE, Terao C, McCarroll SA, Loh PR. Hujoel MLA, et al. Among authors: barton ar. bioRxiv [Preprint]. 2023 Jun 9:2023.06.07.544066. doi: 10.1101/2023.06.07.544066. bioRxiv. 2023. PMID: 37333244 Free PMC article. Updated. Preprint.
Large mosaic copy number variations confer autism risk.
Sherman MA, Rodin RE, Genovese G, Dias C, Barton AR, Mukamel RE, Berger B, Park PJ, Walsh CA, Loh PR. Sherman MA, et al. Among authors: barton ar. Nat Neurosci. 2021 Feb;24(2):197-203. doi: 10.1038/s41593-020-00766-5. Epub 2021 Jan 11. Nat Neurosci. 2021. PMID: 33432194 Free PMC article.
Linked-read analysis identifies mutations in single-cell DNA-sequencing data.
Bohrson CL, Barton AR, Lodato MA, Rodin RE, Luquette LJ, Viswanadham VV, Gulhan DC, Cortés-Ciriano I, Sherman MA, Kwon M, Coulter ME, Galor A, Walsh CA, Park PJ. Bohrson CL, et al. Among authors: barton ar. Nat Genet. 2019 Apr;51(4):749-754. doi: 10.1038/s41588-019-0366-2. Epub 2019 Mar 18. Nat Genet. 2019. PMID: 30886424 Free PMC article.
Protein-coding repeat polymorphisms strongly shape diverse human phenotypes.
Mukamel RE, Handsaker RE, Sherman MA, Barton AR, Zheng Y, McCarroll SA, Loh PR. Mukamel RE, et al. Among authors: barton ar. bioRxiv [Preprint]. 2021 Jan 19:2021.01.19.427332. doi: 10.1101/2021.01.19.427332. bioRxiv. 2021. PMID: 33501449 Free PMC article. Updated. Preprint.
17 results