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Items: 1 to 20 of 66


Patient safety in genomic medicine: an exploratory study.

Korngiebel DM, Fullerton SM, Burke W.

Genet Med. 2016 Mar 24. doi: 10.1038/gim.2016.16. [Epub ahead of print]


Patients' Choices for Return of Exome Sequencing Results to Relatives in the Event of Their Death.

Amendola LM, Horike-Pyne M, Trinidad SB, Fullerton SM, Evans BJ, Burke W, Jarvik GP.

J Law Med Ethics. 2015 Fall;43(3):476-85. doi: 10.1111/jlme.12290.


Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network.

Gallego CJ, Burt A, Sundaresan AS, Ye Z, Shaw C, Crosslin DR, Crane PK, Fullerton SM, Hansen K, Carrell D, Kuivaniemi H, Derr K, de Andrade M, McCarty CA, Kitchner TE, Ragon BK, Stallings SC, Papa G, Bochenek J, Smith ME, Aufox SA, Pacheco JA, Patel V, Friesema EM, Erwin AL, Gottesman O, Gerhard GS, Ritchie M, Motulsky AG, Kullo IJ, Larson EB, Tromp G, Brilliant MH, Bottinger E, Denny JC, Roden DM, Williams MS, Jarvik GP.

Am J Hum Genet. 2015 Oct 1;97(4):512-20. doi: 10.1016/j.ajhg.2015.08.008. Epub 2015 Sep 10.


Broad Consent for Research With Biological Samples: Workshop Conclusions.

Grady C, Eckstein L, Berkman B, Brock D, Cook-Deegan R, Fullerton SM, Greely H, Hansson MG, Hull S, Kim S, Lo B, Pentz R, Rodriguez L, Weil C, Wilfond BS, Wendler D.

Am J Bioeth. 2015;15(9):34-42. doi: 10.1080/15265161.2015.1062162.


Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network.

Crosslin DR, Robertson PD, Carrell DS, Gordon AS, Hanna DS, Burt A, Fullerton SM, Scrol A, Ralston J, Leppig K, Hartzler A, Baldwin E, Andrade Md, Kullo IJ, Tromp G, Doheny KF, Ritchie MD, Crane PK, Nickerson DA, Larson EB, Jarvik GP.

Genome Med. 2015 Jul 3;7(1):67. doi: 10.1186/s13073-015-0181-z. eCollection 2015.


Looking for Trouble and Finding It.

Trinidad SB, Fullerton SM, Burke W.

Am J Bioeth. 2015;15(7):15-7. doi: 10.1080/15265161.2015.1039731. No abstract available.


Rural Mexican-Americans' perceptions of family health history, genetics, and disease risk: implications for disparities-focused research dissemination.

Malen R, Knerr S, Delgado F, Fullerton SM, Thompson B.

J Community Genet. 2016 Jan;7(1):91-6. doi: 10.1007/s12687-015-0245-1. Epub 2015 Jul 4.


"Getting off the Bus Closer to Your Destination": Patients' Views about Pharmacogenetic Testing.

Trinidad SB, Coffin TB, Fullerton SM, Ralston J, Jarvik GP, Larson EB.

Perm J. 2015 Summer;19(3):21-7. doi: 10.7812/TPP/15-046. Epub 2015 Jun 1.


Awareness of Federal Regulatory Mechanisms Relevant to Community-Engaged Research: Survey of Health Disparities-Oriented NIH-Funded Investigators.

Fullerton SM, Anderson EE, Cowan K, Malen RC, Brugge D.

J Empir Res Hum Res Ethics. 2015 Feb;10(1):13-21. doi: 10.1177/1556264614561964. Epub 2014 Dec 10.


Actionable exomic incidental findings in 6503 participants: challenges of variant classification.

Amendola LM, Dorschner MO, Robertson PD, Salama JS, Hart R, Shirts BH, Murray ML, Tokita MJ, Gallego CJ, Kim DS, Bennett JT, Crosslin DR, Ranchalis J, Jones KL, Rosenthal EA, Jarvik ER, Itsara A, Turner EH, Herman DS, Schleit J, Burt A, Jamal SM, Abrudan JL, Johnson AD, Conlin LK, Dulik MC, Santani A, Metterville DR, Kelly M, Foreman AK, Lee K, Taylor KD, Guo X, Crooks K, Kiedrowski LA, Raffel LJ, Gordon O, Machini K, Desnick RJ, Biesecker LG, Lubitz SA, Mulchandani S, Cooper GM, Joffe S, Richards CS, Yang Y, Rotter JI, Rich SS, O'Donnell CJ, Berg JS, Spinner NB, Evans JP, Fullerton SM, Leppig KA, Bennett RL, Bird T, Sybert VP, Grady WM, Tabor HK, Kim JH, Bamshad MJ, Wilfond B, Motulsky AG, Scott CR, Pritchard CC, Walsh TD, Burke W, Raskind WH, Byers P, Hisama FM, Rehm H, Nickerson DA, Jarvik GP.

Genome Res. 2015 Mar;25(3):305-15. doi: 10.1101/gr.183483.114. Epub 2015 Jan 30.


Comparative effectiveness of next generation genomic sequencing for disease diagnosis: design of a randomized controlled trial in patients with colorectal cancer/polyposis syndromes.

Gallego CJ, Bennette CS, Heagerty P, Comstock B, Horike-Pyne M, Hisama F, Amendola LM, Bennett RL, Dorschner MO, Tarczy-Hornoch P, Grady WM, Fullerton SM, Trinidad SB, Regier DA, Nickerson DA, Burke W, Patrick DL, Jarvik GP, Veenstra DL.

Contemp Clin Trials. 2014 Sep;39(1):1-8. doi: 10.1016/j.cct.2014.06.016. Epub 2014 Jul 3.


Return of genomic results to research participants: the floor, the ceiling, and the choices in between.

Jarvik GP, Amendola LM, Berg JS, Brothers K, Clayton EW, Chung W, Evans BJ, Evans JP, Fullerton SM, Gallego CJ, Garrison NA, Gray SW, Holm IA, Kullo IJ, Lehmann LS, McCarty C, Prows CA, Rehm HL, Sharp RR, Salama J, Sanderson S, Van Driest SL, Williams MS, Wolf SM, Wolf WA; eMERGE Act-ROR Committee and CERC Committee; CSER Act-ROR Working Group, Burke W.

Am J Hum Genet. 2014 Jun 5;94(6):818-26. doi: 10.1016/j.ajhg.2014.04.009. Epub 2014 May 8.


Refining the structure and content of clinical genomic reports.

Dorschner MO, Amendola LM, Shirts BH, Kiedrowski L, Salama J, Gordon AS, Fullerton SM, Tarczy-Hornoch P, Byers PH, Jarvik GP.

Am J Med Genet C Semin Med Genet. 2014 Mar;166C(1):85-92. doi: 10.1002/ajmg.c.31395. Epub 2014 Mar 10.


Returning pleiotropic results from genetic testing to patients and research participants.

Kocarnik JM, Fullerton SM.

JAMA. 2014 Feb 26;311(8):795-6. doi: 10.1001/jama.2014.369. No abstract available.


Stakeholder engagement: a key component of integrating genomic information into electronic health records.

Hartzler A, McCarty CA, Rasmussen LV, Williams MS, Brilliant M, Bowton EA, Clayton EW, Faucett WA, Ferryman K, Field JR, Fullerton SM, Horowitz CR, Koenig BA, McCormick JB, Ralston JD, Sanderson SC, Smith ME, Trinidad SB.

Genet Med. 2013 Oct;15(10):792-801. doi: 10.1038/gim.2013.127. Epub 2013 Sep 12. Review.


Forensic familial searching: scientific and social implications.

Garrison NA, Rohlfs RV, Fullerton SM.

Nat Rev Genet. 2013 Jul;14(7):445. No abstract available.


Using genetically informed, randomized prevention trials to test etiological hypotheses about child and adolescent drug use and psychopathology.

Brody GH, Beach SR, Hill KG, Howe GW, Prado G, Fullerton SM.

Am J Public Health. 2013 Oct;103 Suppl 1:S19-24. doi: 10.2105/AJPH.2012.301080. Epub 2013 Aug 8.


Return of incidental findings in genomic medicine: measuring what patients value--development of an instrument to measure preferences for information from next-generation testing (IMPRINT).

Bennette CS, Trinidad SB, Fullerton SM, Patrick D, Amendola L, Burke W, Hisama FM, Jarvik GP, Regier DA, Veenstra DL.

Genet Med. 2013 Nov;15(11):873-81. doi: 10.1038/gim.2013.63. Epub 2013 May 30.


Informed Consent in Genome-Scale Research: What Do Prospective Participants Think?

Trinidad SB, Fullerton SM, Bares JM, Jarvik GP, Larson EB, Burke W.

AJOB Prim Res. 2012 Jul 1;3(3):3-11. Epub 2012 Jun 19.


Values in translation: how asking the right questions can move translational science toward greater health impact.

Kelley M, Edwards K, Starks H, Fullerton SM, James R, Goering S, Holland S, Disis ML, Burke W.

Clin Transl Sci. 2012 Dec;5(6):445-51. doi: 10.1111/j.1752-8062.2012.00441.x. Epub 2012 Aug 7. Review.

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