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Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts.
Frésard L, Smail C, Ferraro NM, Teran NA, Li X, Smith KS, Bonner D, Kernohan KD, Marwaha S, Zappala Z, Balliu B, Davis JR, Liu B, Prybol CJ, Kohler JN, Zastrow DB, Reuter CM, Fisk DG, Grove ME, Davidson JM, Hartley T, Joshi R, Strober BJ, Utiramerur S; Undiagnosed Diseases Network; Care4Rare Canada Consortium; Lind L, Ingelsson E, Battle A, Bejerano G, Bernstein JA, Ashley EA, Boycott KM, Merker JD, Wheeler MT, Montgomery SB. Frésard L, et al. Among authors: ashley ea. Nat Med. 2019 Jun;25(6):911-919. doi: 10.1038/s41591-019-0457-8. Epub 2019 Jun 3. Nat Med. 2019. PMID: 31160820 Free PMC article.
Challenges in the clinical application of whole-genome sequencing.
Ormond KE, Wheeler MT, Hudgins L, Klein TE, Butte AJ, Altman RB, Ashley EA, Greely HT. Ormond KE, et al. Among authors: ashley ea. Lancet. 2010 May 15;375(9727):1749-51. doi: 10.1016/S0140-6736(10)60599-5. Epub 2010 Apr 29. Lancet. 2010. PMID: 20434765 No abstract available.
Genetics of arrhythmia: disease pathways beyond ion channels.
Perez MV, Wheeler M, Ho M, Pavlovic A, Wang P, Ashley EA. Perez MV, et al. Among authors: ashley ea. J Cardiovasc Transl Res. 2008 Jun;1(2):155-65. doi: 10.1007/s12265-008-9030-4. Epub 2008 May 15. J Cardiovasc Transl Res. 2008. PMID: 20559910 Review.
A new era in clinical genetic testing for hypertrophic cardiomyopathy.
Wheeler M, Pavlovic A, DeGoma E, Salisbury H, Brown C, Ashley EA. Wheeler M, et al. Among authors: ashley ea. J Cardiovasc Transl Res. 2009 Dec;2(4):381-91. doi: 10.1007/s12265-009-9139-0. Epub 2009 Oct 30. J Cardiovasc Transl Res. 2009. PMID: 20559996 Review.
Systems biology of heart failure, challenges and hopes.
Dewey FE, Wheeler MT, Ashley EA. Dewey FE, et al. Among authors: ashley ea. Curr Opin Cardiol. 2011 Jul;26(4):314-21. doi: 10.1097/HCO.0b013e328346597d. Curr Opin Cardiol. 2011. PMID: 21478745 Review.
537 results