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De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation.
Mao D, Reuter CM, Ruzhnikov MRZ, Beck AE, Farrow EG, Emrick LT, Rosenfeld JA, Mackenzie KM, Robak L, Wheeler MT, Burrage LC, Jain M, Liu P, Calame D, Küry S, Sillesen M, Schmitz-Abe K, Tonduti D, Spaccini L, Iascone M, Genetti CA, Koenig MK, Graf M, Tran A, Alejandro M; Undiagnosed Diseases Network; Lee BH, Thiffault I, Agrawal PB, Bernstein JA, Bellen HJ, Chao HT. Mao D, et al. Among authors: wheeler mt. Am J Hum Genet. 2020 Apr 2;106(4):570-583. doi: 10.1016/j.ajhg.2020.02.016. Epub 2020 Mar 19. Am J Hum Genet. 2020. PMID: 32197074 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: wheeler mt. 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.
Gene coexpression network topology of cardiac development, hypertrophy, and failure.
Dewey FE, Perez MV, Wheeler MT, Watt C, Spin J, Langfelder P, Horvath S, Hannenhalli S, Cappola TP, Ashley EA. Dewey FE, et al. Among authors: wheeler mt. Circ Cardiovasc Genet. 2011 Feb;4(1):26-35. doi: 10.1161/CIRCGENETICS.110.941757. Epub 2010 Dec 2. Circ Cardiovasc Genet. 2011. PMID: 21127201 Free PMC article.
Systems biology of heart failure, challenges and hopes.
Dewey FE, Wheeler MT, Ashley EA. Dewey FE, et al. Among authors: wheeler mt. Curr Opin Cardiol. 2011 Jul;26(4):314-21. doi: 10.1097/HCO.0b013e328346597d. Curr Opin Cardiol. 2011. PMID: 21478745 Review.
234 results