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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2019 | 1 |
2020 | 1 |
2021 | 1 |
2022 | 2 |
2024 | 0 |
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A genome-first approach to rare variants in hypertrophic cardiomyopathy genes MYBPC3 and MYH7 in a medical biobank.
Hum Mol Genet. 2022 Mar 3;31(5):827-837. doi: 10.1093/hmg/ddab249.
Hum Mol Genet. 2022.
PMID: 34542152
Free PMC article.
Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank.
Park J, MacLean MT, Lucas AM, Torigian DA, Schneider CV, Cherlin T, Xiao B, Miller JE, Bradford Y, Judy RL; Regeneron Genetics Center; Verma A, Damrauer SM, Ritchie MD, Witschey WR, Rader DJ.
Park J, et al.
Cell Rep Med. 2022 Dec 20;3(12):100855. doi: 10.1016/j.xcrm.2022.100855. Epub 2022 Dec 12.
Cell Rep Med. 2022.
PMID: 36513072
Free PMC article.
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A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes.
Park J, Levin MG, Haggerty CM, Hartzel DN, Judy R, Kember RL, Reza N; Regeneron Genetics Center; Ritchie MD, Owens AT, Damrauer SM, Rader DJ.
Park J, et al.
Genet Med. 2020 Jan;22(1):102-111. doi: 10.1038/s41436-019-0625-8. Epub 2019 Aug 6.
Genet Med. 2020.
PMID: 31383942
Free PMC article.
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Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations.
Park J, Lucas AM, Zhang X, Chaudhary K, Cho JH, Nadkarni G, Dobbyn A, Chittoor G, Josyula NS, Katz N, Breeyear JH, Ahmadmehrabi S, Drivas TG, Chavali VRM, Fasolino M, Sawada H, Daugherty A, Li Y, Zhang C, Bradford Y, Weaver J, Verma A, Judy RL, Kember RL, Overton JD, Reid JG, Ferreira MAR, Li AH, Baras A, LeMaire SA, Shen YH, Naji A, Kaestner KH, Vahedi G, Edwards TL, Chen J, Damrauer SM, Justice AE, Do R, Ritchie MD, Rader DJ.
Park J, et al.
Nat Med. 2021 Jan;27(1):66-72. doi: 10.1038/s41591-020-1133-8. Epub 2021 Jan 11.
Nat Med. 2021.
PMID: 33432171
Free PMC article.
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