Center-Authored Papers

Filters: Author is Amendola, Laura M  [Clear All Filters]
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Amendola LM, Horike-Pyne M, Trinidad SB, Fullerton SM, Evans BJ, Burke W, Jarvik GP.  2015.  Patients' Choices for Return of Exome Sequencing Results to Relatives in the Event of Their Death.. The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics. 43(3):476-85. Abstract
Amendola LM, Dorschner MO, Robertson PD, Salama JS, Hart R, Shirts BH, Murray ML, Tokita MJ, Gallego CJ, Kim DS et al..  2015.  Actionable exomic incidental findings in 6503 participants: challenges of variant classification.. Genome research. 25(3):305-15. Abstract
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Berg JS, Amendola LM, Eng C, Van Allen E, Gray SW, Wagle N, Rehm HL, Dechene ET, Dulik MC, Hisama FM et al..  2013.  Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium.. Genetics in medicine : official journal of the American College of Medical Genetics. 15(11):860-7. Abstract
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Chen D-H, Méneret A, Friedman JR, Korvatska O, Gad A, Bonkowski ES, Stessman HA, Doummar D, Mignot C, Anheim M et al..  2015.  ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlations.. Neurology. Abstract
D
Dorschner MO, Amendola LM, Turner EH, Robertson PD, Shirts BH, Gallego CJ, Bennett RL, Jones KL, Tokita MJ, Bennett JT et al..  2013.  Actionable, pathogenic incidental findings in 1,000 participants' exomes.. American journal of human genetics. 93(4):631-40. Abstract
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Gallego CJ, Bennette CS, Heagerty P, Comstock B, Horike-Pyne M, Hisama F, Amendola LM, Bennett RL, Dorschner MO, Tarczy-Hornoch P et al..  2014.  Comparative effectiveness of next generation genomic sequencing for disease diagnosis: Design of a randomized controlled trial in patients with colorectal cancer/polyposis syndromes.. Contemporary clinical trials. Abstract
Gallego CJ, Shirts BH, Bennette CS, Guzauskas G, Amendola LM, Horike-Pyne M, Hisama FM, Pritchard CC, Grady WM, Burke W et al..  2015.  Next-Generation Sequencing Panels for the Diagnosis of Colorectal Cancer and Polyposis Syndromes: A Cost-Effectiveness Analysis.. Journal of clinical oncology : official journal of the American Society of Clinical Oncology. Abstract
Goodman JL, Amendola LM, Horike-Pyne M, Trinidad SB, Fullerton SM, Burke W, Jarvik GP.  2017.  Discordance in selected designee for return of genomic findings in the event of participant death and estate executor.. Molecular genetics & genomic medicine. 5(2):172-176. Abstract
Green RC, Goddard KAB, Jarvik GP, Amendola LM, Appelbaum PS, Berg JS, Bernhardt BA, Biesecker LG, Biswas S, Blout CL et al..  2016.  Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.. American journal of human genetics. 98(6):1051-1066. Abstract
J
Jarvik GP, Amendola LM, Berg JS, Brothers K, Clayton EW, Chung W, Evans BJ, Evans JP, Fullerton SM, Gallego CJ et al..  2014.  Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between.. American journal of human genetics. Abstract
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Tan N, Amendola LM, O'Daniel JM, Burt A, Horike-Pyne MJ, Boshe L, Henderson GE, Rini C, Roche MI, Hisama FM et al..  2016.  Is "incidental finding" the best term?: a study of patients' preferences. Genetics in medicine : official journal of the American College of Medical Genetics. Abstract