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Items: 1 to 50 of 183

1.

Third-Party Genetic Interpretation Tools: A Mixed-Methods Study of Consumer Motivation and Behavior.

Nelson SC, Bowen DJ, Fullerton SM.

Am J Hum Genet. 2019 Jun 7. pii: S0002-9297(19)30201-0. doi: 10.1016/j.ajhg.2019.05.014. [Epub ahead of print]

PMID:
31204012
2.

Contemporary Trends in Percutaneous Nephrolithomy Across New York State: A Review of the Statewide Planning and Research Cooperative System (SPARCS).

Patel NH, Parikh S, Bloom J, Schulman A, Wagmaister J, Fullerton S, Phillips JL, Choudhury M, Eshghi M.

J Endourol. 2019 Jun 10. doi: 10.1089/end.2019.0115. [Epub ahead of print]

PMID:
31179737
3.

Ethics of inclusion: Cultivate trust in precision medicine.

Lee SS, Fullerton SM, Saperstein A, Shim JK.

Science. 2019 Jun 7;364(6444):941-942. doi: 10.1126/science.aaw8299. No abstract available.

PMID:
31171685
4.

The Two-point Technique for Fluoroscopic Guided Endoscopic Procedures in Urology - A Validation Study.

Wagmaister J, Iorga M, Huang R, Patel NH, Fullerton S, Schulman A, Phillips JL, Choudhury M, Eshghi M.

J Endourol. 2019 Jun 4. doi: 10.1089/end.2019.0077. [Epub ahead of print]

PMID:
31161786
5.

The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research.

Horowitz CR, Orlando LA, Slavotinek AM, Peterson J, Angelo F, Biesecker B, Bonham VL, Cameron LD, Fullerton SM, Gelb BD, Goddard KAB, Hailu B, Hart R, Hindorff LA, Jarvik GP, Kaufman D, Kenny EE, Knight SJ, Koenig BA, Korf BR, Madden E, McGuire AL, Ou J, Wasserstein MP, Robinson M, Leventhal H, Sanderson SC.

Am J Hum Genet. 2019 Jun 6;104(6):1088-1096. doi: 10.1016/j.ajhg.2019.04.006. Epub 2019 May 16.

PMID:
31104772
6.

Consent insufficient for data release.

Nicol D, Eckstein L, Bentzen HB, Borry P, Burgess M, Burke W, Chalmers D, Cho M, Dove E, Fullerton S, Ida R, Kato K, Kaye J, Koenig B, Manson S, McGrail K, Meslin E, O'Doherty K, Prainsack B, Shabani M, Tabor H, Thorogood A, de Vries J.

Science. 2019 May 3;364(6439):445-446. doi: 10.1126/science.aax0892. No abstract available.

PMID:
31048483
7.

Device Malfunctions and Complications Associated with Benign Prostatic Hyperplasia Surgery: Review of the Manufacturer and User Facility Device Experience Database.

Patel NH, Uppaluri N, Iorga M, Schulman A, Bloom JB, Phillips J, Fullerton S, Konno S, Choudhury M, Eshghi M.

J Endourol. 2019 Jun;33(6):448-454. doi: 10.1089/end.2019.0067. Epub 2019 May 24.

PMID:
30990073
8.

The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation.

Li M, Bennette CS, Amendola LM, Ragan Hart M, Heagerty P, Comstock B, Tarczy-Hornoch P, Fullerton SM, Regier DA, Burke W, Trinidad SB, Jarvik GP, Veenstra DL, Patrick DL.

J Genet Couns. 2019 Apr;28(2):477-490. doi: 10.1007/s10897-018-0286-9. Epub 2018 Dec 14.

PMID:
30964586
9.

You Are Just Now Telling Us About This? African American Perspectives of Testing for Genetic Susceptibility to Kidney Disease.

Umeukeje EM, Young BA, Fullerton SM, Cavanaugh K, Owens D, Wilson JG, Burke W, Blacksher E.

J Am Soc Nephrol. 2019 Apr;30(4):526-530. doi: 10.1681/ASN.2018111091. Epub 2019 Mar 11. No abstract available.

PMID:
30858224
10.

"It would be so much easier": health system-led genetic risk notification-feasibility and acceptability of cascade screening in an integrated system.

Henrikson NB, Blasi PR, Fullerton SM, Grafton J, Leppig KA, Jarvik GP, Larson EB.

J Community Genet. 2019 Mar 6. doi: 10.1007/s12687-019-00412-z. [Epub ahead of print]

PMID:
30843145
11.

Practice Implications of Expanded Genetic Testing in Oncology.

Korngiebel DM, Zech JM, Chappelle A, Burke W, Carline JD, Gallagher TH, Fullerton SM.

Cancer Invest. 2019;37(1):39-45. doi: 10.1080/07357907.2018.1564926. Epub 2019 Jan 24.

PMID:
30676118
12.

The clinical imperative for inclusivity: Race, ethnicity, and ancestry (REA) in genomics.

Popejoy AB, Ritter DI, Crooks K, Currey E, Fullerton SM, Hindorff LA, Koenig B, Ramos EM, Sorokin EP, Wand H, Wright MW, Zou J, Gignoux CR, Bonham VL, Plon SE, Bustamante CD; Clinical Genome Resource (ClinGen) Ancestry and Diversity Working Group (ADWG).

Hum Mutat. 2018 Nov;39(11):1713-1720. doi: 10.1002/humu.23644.

PMID:
30311373
13.

Parents' attitudes toward consent and data sharing in biobanks: A multisite experimental survey.

Antommaria AHM, Brothers KB, Myers JA, Feygin YB, Aufox SA, Brilliant MH, Conway P, Fullerton SM, Garrison NA, Horowitz CR, Jarvik GP, Li R, Ludman EJ, McCarty CA, McCormick JB, Mercaldo ND, Myers MF, Sanderson SC, Shrubsole MJ, Schildcrout JS, Williams JL, Smith ME, Clayton EW, Holm IA.

AJOB Empir Bioeth. 2018 Jul-Sep;9(3):128-142. doi: 10.1080/23294515.2018.1505783. Epub 2018 Sep 21.

PMID:
30240342
14.

Cumulative Antidepressant Use and Risk of Dementia in a Prospective Cohort Study.

Heath L, Gray SL, Boudreau DM, Thummel K, Edwards KL, Fullerton SM, Crane PK, Larson EB.

J Am Geriatr Soc. 2018 Oct;66(10):1948-1955. doi: 10.1111/jgs.15508. Epub 2018 Sep 17.

PMID:
30221747
15.

The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.

Amendola LM, Berg JS, Horowitz CR, Angelo F, Bensen JT, Biesecker BB, Biesecker LG, Cooper GM, East K, Filipski K, Fullerton SM, Gelb BD, Goddard KAB, Hailu B, Hart R, Hassmiller-Lich K, Joseph G, Kenny EE, Koenig BA, Knight S, Kwok PY, Lewis KL, McGuire AL, Norton ME, Ou J, Parsons DW, Powell BC, Risch N, Robinson M, Rini C, Scollon S, Slavotinek AM, Veenstra DL, Wasserstein MP, Wilfond BS, Hindorff LA; CSER consortium, Plon SE, Jarvik GP.

Am J Hum Genet. 2018 Sep 6;103(3):319-327. doi: 10.1016/j.ajhg.2018.08.007.

16.

The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation.

Li M, Bennette CS, Amendola LM, Ragan Hart M, Heagerty P, Comstock B, Tarczy-Hornoch P, Fullerton SM, Regier DA, Burke W, Trinidad SB, Jarvik GP, Veenstra DL, Patrick DL.

J Genet Couns. 2018 Sep 1. doi: 10.1007/s10897-018-0286-9. [Epub ahead of print]

PMID:
30173308
17.

Informed Consent in Translational Genomics: Insufficient Without Trustworthy Governance.

Burke W, Beskow LM, Trinidad SB, Fullerton SM, Brelsford K.

J Law Med Ethics. 2018 Mar;46(1):79-86. doi: 10.1177/1073110518766023. Epub 2018 Mar 27. No abstract available.

18.

Prostate Cancer Screening Trends After United States Preventative Services Task Force Guidelines in an Underserved Population.

Patel NH, Bloom J, Hillelsohn J, Fullerton S, Allman D, Matthews G, Eshghi M, Phillips JL.

Health Equity. 2018 May 1;2(1):55-61. doi: 10.1089/heq.2018.0004. eCollection 2018.

19.

Hereditary cancer gene panel test reports: wide heterogeneity suggests need for standardization.

Makhnoon S, Shirts BH, Bowen DJ, Fullerton SM.

Genet Med. 2018 Nov;20(11):1438-1445. doi: 10.1038/gim.2018.23. Epub 2018 Mar 1.

PMID:
29493582
20.

"Bridge to the Literature"? Third-Party Genetic Interpretation Tools and the Views of Tool Developers.

Nelson SC, Fullerton SM.

J Genet Couns. 2018 Aug;27(4):770-781. doi: 10.1007/s10897-018-0217-9. Epub 2018 Feb 7.

PMID:
29411211
21.

Clinical verification of genetic results returned to research participants: findings from a Colon Cancer Family Registry.

Laurino MY, Truitt AR, Tenney L, Fisher D, Lindor NM, Veenstra D, Jarvik GP, Newcomb PA, Fullerton SM.

Mol Genet Genomic Med. 2017 Nov;5(6):700-708. doi: 10.1002/mgg3.328. Epub 2017 Aug 23.

22.

Clinical Genetic Testing for APOL1: Are we There Yet?

Young BA, Fullerton SM, Wilson JG, Cavanaugh K, Blacksher E, Spigner C, Himmelfarb J, Burke W.

Semin Nephrol. 2017 Nov;37(6):552-557. doi: 10.1016/j.semnephrol.2017.07.009. Review.

PMID:
29110763
23.

Sepsis after elective ureteroscopy.

Bloom J, Fox C, Fullerton S, Matthews G, Phillips J.

Can J Urol. 2017 Oct;24(5):9017-9023.

PMID:
28971790
24.

Clinical and palliative care outcomes for patients of poor performance status treated with antiprogrammed death-1 monoclonal antibodies for advanced melanoma.

Wong A, Williams M, Milne D, Morris K, Lau P, Spruyt O, Fullerton S, McArthur G.

Asia Pac J Clin Oncol. 2017 Dec;13(6):385-390. doi: 10.1111/ajco.12702. Epub 2017 Jun 29.

PMID:
28661584
25.

Discordance in selected designee for return of genomic findings in the event of participant death and estate executor.

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

Mol Genet Genomic Med. 2017 Jan 16;5(2):172-176. doi: 10.1002/mgg3.274. eCollection 2017 Mar.

26.

Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.

Sanderson SC, Brothers KB, Mercaldo ND, Clayton EW, Antommaria AHM, Aufox SA, Brilliant MH, Campos D, Carrell DS, Connolly J, Conway P, Fullerton SM, Garrison NA, Horowitz CR, Jarvik GP, Kaufman D, Kitchner TE, Li R, Ludman EJ, McCarty CA, McCormick JB, McManus VD, Myers MF, Scrol A, Williams JL, Shrubsole MJ, Schildcrout JS, Smith ME, Holm IA.

Am J Hum Genet. 2017 Mar 2;100(3):414-427. doi: 10.1016/j.ajhg.2017.01.021. Epub 2017 Feb 9.

27.

Subcutaneous Lidocaine Infusion for Pain in Patients with Cancer.

Seah DSE, Herschtal A, Tran H, Thakerar A, Fullerton S.

J Palliat Med. 2017 Jun;20(6):667-671. doi: 10.1089/jpm.2016.0298. Epub 2016 Dec 20.

PMID:
27996364
28.

No Panacea: Next-Gen Sequencing Will Not Mitigate Adoptees' Lack of Genetic Family Health History.

Fullerton SM.

Am J Bioeth. 2016 Dec;16(12):41-43. No abstract available.

29.

Conducting a large, multi-site survey about patients' views on broad consent: challenges and solutions.

Smith ME, Sanderson SC, Brothers KB, Myers MF, McCormick J, Aufox S, Shrubsole MJ, Garrison NA, Mercaldo ND, Schildcrout JS, Clayton EW, Antommaria AH, Basford M, Brilliant M, Connolly JJ, Fullerton SM, Horowitz CR, Jarvik GP, Kaufman D, Kitchner T, Li R, Ludman EJ, McCarty C, McManus V, Stallings S, Williams JL, Holm IA.

BMC Med Res Methodol. 2016 Nov 24;16(1):162.

30.

Patient safety in genomic medicine: an exploratory study.

Korngiebel DM, Fullerton SM, Burke W.

Genet Med. 2016 Nov;18(11):1136-1142. doi: 10.1038/gim.2016.16. Epub 2016 Mar 24.

31.

Genomics is failing on diversity.

Popejoy AB, Fullerton SM.

Nature. 2016 Oct 13;538(7624):161-164. doi: 10.1038/538161a. No abstract available.

32.

Allocation of Resources to Communication of Research Result Summaries.

Richards JE, Bane E, Fullerton SM, Ludman EJ, Jarvik G.

J Empir Res Hum Res Ethics. 2016 Oct;11(4):364-369. doi: 10.1177/1556264616667126. Epub 2016 Sep 19.

33.

Using Genetic Technologies To Reduce, Rather Than Widen, Health Disparities.

Smith CE, Fullerton SM, Dookeran KA, Hampel H, Tin A, Maruthur NM, Schisler JC, Henderson JA, Tucker KL, Ordovás JM.

Health Aff (Millwood). 2016 Aug 1;35(8):1367-73. doi: 10.1377/hlthaff.2015.1476. Review.

34.

Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era.

Chalmers D, Nicol D, Kaye J, Bell J, Campbell AV, Ho CW, Kato K, Minari J, Ho CH, Mitchell C, Molnár-Gábor F, Otlowski M, Thiel D, Fullerton SM, Whitton T.

BMC Med Ethics. 2016 Jul 12;17(1):39. doi: 10.1186/s12910-016-0124-2. Review.

35.

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.

Green RC, Goddard KA, Jarvik GP, Amendola LM, Appelbaum PS, Berg JS, Bernhardt BA, Biesecker LG, Biswas S, Blout CL, Bowling KM, Brothers KB, Burke W, Caga-Anan CF, Chinnaiyan AM, Chung WK, Clayton EW, Cooper GM, East K, Evans JP, Fullerton SM, Garraway LA, Garrett JR, Gray SW, Henderson GE, Hindorff LA, Holm IA, Lewis MH, Hutter CM, Janne PA, Joffe S, Kaufman D, Knoppers BM, Koenig BA, Krantz ID, Manolio TA, McCullough L, McEwen J, McGuire A, Muzny D, Myers RM, Nickerson DA, Ou J, Parsons DW, Petersen GM, Plon SE, Rehm HL, Roberts JS, Robinson D, Salama JS, Scollon S, Sharp RR, Shirts B, Spinner NB, Tabor HK, Tarczy-Hornoch P, Veenstra DL, Wagle N, Weck K, Wilfond BS, Wilhelmsen K, Wolf SM, Wynn J, Yu JH; CSER Consortium.

Am J Hum Genet. 2016 Jul 7;99(1):246. doi: 10.1016/j.ajhg.2016.06.002. No abstract available.

36.

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.

Green RC, Goddard KAB, Jarvik GP, Amendola LM, Appelbaum PS, Berg JS, Bernhardt BA, Biesecker LG, Biswas S, Blout CL, Bowling KM, Brothers KB, Burke W, Caga-Anan CF, Chinnaiyan AM, Chung WK, Clayton EW, Cooper GM, East K, Evans JP, Fullerton SM, Garraway LA, Garrett JR, Gray SW, Henderson GE, Hindorff LA, Holm IA, Lewis MH, Hutter CM, Janne PA, Joffe S, Kaufman D, Knoppers BM, Koenig BA, Krantz ID, Manolio TA, McCullough L, McEwen J, McGuire A, Muzny D, Myers RM, Nickerson DA, Ou J, Parsons DW, Petersen GM, Plon SE, Rehm HL, Roberts JS, Robinson D, Salama JS, Scollon S, Sharp RR, Shirts B, Spinner NB, Tabor HK, Tarczy-Hornoch P, Veenstra DL, Wagle N, Weck K, Wilfond BS, Wilhelmsen K, Wolf SM, Wynn J, Yu JH; CSER Consortium.

Am J Hum Genet. 2016 Jun 2;98(6):1051-1066. doi: 10.1016/j.ajhg.2016.04.011. Epub 2016 May 12. Erratum in: Am J Hum Genet. 2016 Jul 7;99(1):246.

37.

Integration of Immuno-Oncology and Palliative Care.

Wong A, Fullerton S, Spruyt O, Brady B, McArthur G, Sandhu S.

J Clin Oncol. 2016 May 1;34(13):1561-2. doi: 10.1200/JCO.2015.64.4146. Epub 2016 Feb 29. No abstract available.

PMID:
26926686
38.

Engaging Study Participants in Research Dissemination at a Center for Population Health and Health Disparities.

Knerr S, Hohl SD, Molina Y, Neuhouser ML, Li CI, Coronado GD, Fullerton SM, Thompson B.

Prog Community Health Partnersh. 2016;10(4):569-576. doi: 10.1353/cpr.2016.0065.

39.

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.

40.

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.

41.

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.

42.

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.

43.

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.

44.

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.

45.

"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.

46.

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.

47.

Daily subcutaneous parecoxib injection for cancer pain: an open label pilot study.

Kenner DJ, Bhagat S, Fullerton SL.

J Palliat Med. 2015 Apr;18(4):366-72. doi: 10.1089/jpm.2014.0249. Epub 2015 Feb 19.

PMID:
25695199
48.

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.

49.

Measuring physical inactivity: do current measures provide an accurate view of "sedentary" video game time?

Fullerton S, Taylor AW, Dal Grande E, Berry N.

J Obes. 2014;2014:287013. doi: 10.1155/2014/287013. Epub 2014 Jun 4.

50.

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.

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