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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2021 | 2 |
2022 | 2 |
2023 | 2 |
2024 | 1 |
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7 results
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Page 1
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Nat Genet. 2021 Aug;53(8):1260-1269. doi: 10.1038/s41588-021-00892-1. Epub 2021 Jul 5.
Nat Genet. 2021.
PMID: 34226706
Free PMC article.
Repeat polymorphisms underlie top genetic risk loci for glaucoma and colorectal cancer.
Mukamel RE, Handsaker RE, Sherman MA, Barton AR, Hujoel MLA, McCarroll SA, Loh PR.
Mukamel RE, et al.
Cell. 2023 Aug 17;186(17):3659-3673.e23. doi: 10.1016/j.cell.2023.07.002. Epub 2023 Jul 31.
Cell. 2023.
PMID: 37527660
Free article.
Item in Clipboard
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.
Science. 2021 Sep 24;373(6562):1499-1505. doi: 10.1126/science.abg8289. Epub 2021 Sep 23.
Science. 2021.
PMID: 34554798
Free PMC article.
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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.
Cell. 2022 Oct 27;185(22):4233-4248.e27. doi: 10.1016/j.cell.2022.09.028.
Cell. 2022.
PMID: 36306736
Free PMC article.
Item in Clipboard
Protein-altering variants at copy number-variable regions 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.
Nat Genet. 2024 Apr;56(4):569-578. doi: 10.1038/s41588-024-01684-z. Epub 2024 Mar 28.
Nat Genet. 2024.
PMID: 38548989
Free PMC article.
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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.
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.
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A spectrum of recessiveness among Mendelian disease variants in UK Biobank.
Barton AR, Hujoel MLA, Mukamel RE, Sherman MA, Loh PR.
Barton AR, et al.
Am J Hum Genet. 2022 Jul 7;109(7):1298-1307. doi: 10.1016/j.ajhg.2022.05.008. Epub 2022 May 31.
Am J Hum Genet. 2022.
PMID: 35649421
Free PMC article.
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