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FBN1 Coding Variants and Nonsyndromic Aortic Disease.
Damrauer SM, Hardie K, Kember RL, Judy R, Birtwell D, Williams H, Rader DJ, Pyeritz RE. Damrauer SM, et al. Among authors: pyeritz re. Circ Genom Precis Med. 2019 Jun;12(6):e002454. doi: 10.1161/CIRCGEN.119.002454. Epub 2019 Jun 18. Circ Genom Precis Med. 2019. PMID: 31211626 Free PMC article. No abstract available.
Medical management of Marfan syndrome.
Keane MG, Pyeritz RE. Keane MG, et al. Among authors: pyeritz re. Circulation. 2008 May 27;117(21):2802-13. doi: 10.1161/CIRCULATIONAHA.107.693523. Circulation. 2008. PMID: 18506019 Review. No abstract available.
Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1.
LeMaire SA, McDonald ML, Guo DC, Russell L, Miller CC 3rd, Johnson RJ, Bekheirnia MR, Franco LM, Nguyen M, Pyeritz RE, Bavaria JE, Devereux R, Maslen C, Holmes KW, Eagle K, Body SC, Seidman C, Seidman JG, Isselbacher EM, Bray M, Coselli JS, Estrera AL, Safi HJ, Belmont JW, Leal SM, Milewicz DM. LeMaire SA, et al. Among authors: pyeritz re. Nat Genet. 2011 Sep 11;43(10):996-1000. doi: 10.1038/ng.934. Nat Genet. 2011. PMID: 21909107 Free PMC article.
Gene-environment interactions.
Pyeritz RE. Pyeritz RE. Genet Med. 2015 Nov;17(11):943-5. doi: 10.1038/gim.2015.126. Epub 2015 Sep 10. Genet Med. 2015. PMID: 26355661 Free article. No abstract available.
307 results