-
1
-
-
80053030497
-
Exome sequencing: A transformative technology
-
Singleton AB: Exome sequencing: a transformative technology. Lancet Neurol 2011; 10: 942-946.
-
(2011)
Lancet Neurol
, vol.10
, pp. 942-946
-
-
Singleton, A.B.1
-
3
-
-
84859566974
-
Managing incidental findings and research results in genomic research involving biobanks and archived data sets
-
Wolf SM, Crock BN, Van Ness B et al: Managing incidental findings and research results in genomic research involving biobanks and archived data sets. Genet Med 2012; 14: 361-384.
-
(2012)
Genet Med
, vol.14
, pp. 361-384
-
-
Wolf, S.M.1
Crock, B.N.2
Van Ness, B.3
-
4
-
-
84859591508
-
Return of individual research results and incidental findings in the clinical trials cooperative group setting
-
Ferriere M, Van Ness B: Return of individual research results and incidental findings in the clinical trials cooperative group setting. Genet Med 2012; 14: 411-416.
-
(2012)
Genet Med
, vol.14
, pp. 411-416
-
-
Ferriere, M.1
Van Ness, B.2
-
5
-
-
84859619831
-
Return of individual research results from genome-wide association studies: Experience of the Electronic Medical Records and Genomics (eMERGE) Network
-
Fullerton SM, Wolf WA, Brothers KB et al: Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network. Genet Med 2012; 14: 424-431.
-
(2012)
Genet Med
, vol.14
, pp. 424-431
-
-
Fullerton, S.M.1
Wolf, W.A.2
Brothers, K.B.3
-
6
-
-
77951914791
-
Personal genome research: What should the participant be told?
-
McGuire AL, Lupski JR: Personal genome research: what should the participant be told? Trends Genet 2010; 26: 199-201.
-
(2010)
Trends Genet
, vol.26
, pp. 199-201
-
-
McGuire, A.L.1
Lupski, J.R.2
-
7
-
-
38549163811
-
Gene information opens new frontier in privacy debate
-
Dizikes P: Gene information opens new frontier in privacy debate. Boston Globe 2007. http://www.boston.com/news/globe/health-science/articles/2007/09/24/ gene-information-opens-new-frontier-in-privacy-debate/.
-
(2007)
Boston Globe
-
-
Dizikes, P.1
-
8
-
-
35648976118
-
The diploid genome sequence of an individual human
-
Levy S, Sutton G, Ng PC et al: The diploid genome sequence of an individual human. PLoS Biol 2007; 5: 2113-2144.
-
(2007)
PLoS Biol
, vol.5
, pp. 2113-2144
-
-
Levy, S.1
Sutton, G.2
Ng, P.C.3
-
9
-
-
69749108657
-
The ClinSeq Project: Piloting large-scale genome sequencing for research in genomic medicine
-
Biesecker LG, Mullikin JC, Facio FM et al: The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine. Genome Res 2009; 19: 1665-1674.
-
(2009)
Genome Res
, vol.19
, pp. 1665-1674
-
-
Biesecker, L.G.1
Mullikin, J.C.2
Facio, F.M.3
-
10
-
-
33646254125
-
Reporting genetic results in research studies: Summary and recommendations of an NHLBI Working Group
-
Bookman EB, Langehorne AA, Eckfeldt JH et al: Reporting genetic results in research studies: Summary and recommendations of an NHLBI Working Group. Am J Med Genet 2006; 140A: 1033-1040.
-
(2006)
Am J Med Genet
, vol.140 A
, pp. 1033-1040
-
-
Bookman, E.B.1
Langehorne, A.A.2
Eckfeldt, J.H.3
-
11
-
-
79951863517
-
Ethical and practical guidelines for reporting genetic research results to study participants: Updated guidelines from a national heart, lung, and blood institute working group
-
Fabsitz RR, McGuire A, Sharp RR et al: Ethical and practical guidelines for reporting genetic research results to study participants: Updated guidelines from a national heart, lung, and blood institute working group. Circ Cardiovasc Genet 2010; 3: 574-580.
-
(2010)
Circ Cardiovasc Genet
, vol.3
, pp. 574-580
-
-
Fabsitz, R.R.1
McGuire, A.2
Sharp, R.R.3
-
12
-
-
44949211505
-
Managing incidental findings in human subjects research: Analysis and recommendations
-
Wolf SM, Lawrenz FP, Nelson CA et al: Managing incidental findings in human subjects research: analysis and recommendations. J Law Med Ethics 2008; 36: 219-248.
-
(2008)
J Law Med Ethics
, vol.36
, pp. 219-248
-
-
Wolf, S.M.1
Lawrenz, F.P.2
Nelson, C.A.3
-
13
-
-
77955610460
-
Multidimensional results reporting to participants in genomic studies: Getting it right
-
Kohane IS, Taylor PL: Multidimensional results reporting to participants in genomic studies: Getting it right. Sci Transl Med 2010; 2: 37cm19.
-
(2010)
Sci Transl Med
, vol.2
-
-
Kohane, I.S.1
Taylor, P.L.2
-
14
-
-
67650391208
-
Disclosure of research results from cancer genomic studies: State of the science
-
Dressler LG: Disclosure of research results from cancer genomic studies: state of the science. Clin Cancer Res 2009; 15: 4270-4276.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 4270-4276
-
-
Dressler, L.G.1
-
15
-
-
33750631748
-
Disclosing individual genetic results to research participants
-
Ravitsky V, Wilfond BS: Disclosing individual genetic results to research participants. Am J Bioethics 2006; 6: 8-17.
-
(2006)
Am J Bioethics
, vol.6
, pp. 8-17
-
-
Ravitsky, V.1
Wilfond, B.S.2
-
16
-
-
57449115536
-
Subjects matter: A survey of public opinions about a large genetic cohort study
-
Kaufman D, Murphy J, Scott J, Hudson K: Subjects matter: a survey of public opinions about a large genetic cohort study. Genet Med 2008; 10: 831-839.
-
(2008)
Genet Med
, vol.10
, pp. 831-839
-
-
Kaufman, D.1
Murphy, J.2
Scott, J.3
Hudson, K.4
-
17
-
-
84859608971
-
Public preferences regarding the return of individual genetic research results: Findings from a qualitative focus group study
-
Bollinger JM, Scott J, Dvoskin R, Kaufman D: Public preferences regarding the return of individual genetic research results: findings from a qualitative focus group study. Genet Med 2012; 14: 451-457.
-
(2012)
Genet Med
, vol.14
, pp. 451-457
-
-
Bollinger, J.M.1
Scott, J.2
Dvoskin, R.3
Kaufman, D.4
-
18
-
-
81555203460
-
Motivators for participation in a whole-genome sequencing study: Implications for translational genomics research
-
Facio FM, Brooks S, Loewenstein J, Green S, Biesecker LG, Biesecker BB: Motivators for participation in a whole-genome sequencing study: implications for translational genomics research. Eur J Hum Genet 2011; 19: 1213-1217.
-
(2011)
Eur J Hum Genet
, vol.19
, pp. 1213-1217
-
-
Facio, F.M.1
Brooks, S.2
Loewenstein, J.3
Green, S.4
Biesecker, L.G.5
Biesecker, B.B.6
-
19
-
-
79959276553
-
Deploying whole genome sequencing in clinical practice and public health: Meeting the challenge one bin at a time
-
Berg JS, Khoury MJ, Evans JP: Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time. Genet Med 2011; 13: 499-504.
-
(2011)
Genet Med
, vol.13
, pp. 499-504
-
-
Berg, J.S.1
Khoury, M.J.2
Evans, J.P.3
-
21
-
-
80052273655
-
Exome sequencing supports a de novo mutational paradigm for schizophrenia
-
Xu B, Roos JL, Dexheimer P et al: Exome sequencing supports a de novo mutational paradigm for schizophrenia. Nat Genet 2011; 43: 864-868.
-
(2011)
Nat Genet
, vol.43
, pp. 864-868
-
-
Xu, B.1
Roos, J.L.2
Dexheimer, P.3
-
23
-
-
33744992691
-
Attitudes and uptake of a screening test: The moderating role of ambivalence
-
Dormandy E, Hankins M, Marteau T: Attitudes and uptake of a screening test: the moderating role of ambivalence. Psychol Health 2006; 21: 499-511.
-
(2006)
Psychol Health
, vol.21
, pp. 499-511
-
-
Dormandy, E.1
Hankins, M.2
Marteau, T.3
-
24
-
-
84859583108
-
Opportunities and challenges for the integration of massively parallel genomic sequencing into clinical practice: Lessons from the ClinSeq project
-
Biesecker LG: Opportunities and challenges for the integration of massively parallel genomic sequencing into clinical practice: lessons from the ClinSeq project. Genet Med 2012; 14: 393-398.
-
(2012)
Genet Med
, vol.14
, pp. 393-398
-
-
Biesecker, L.G.1
-
26
-
-
79953286746
-
Exome sequencing allows for rapid gene identification in a Charcot-Marie-Tooth family
-
Montenegro G, Powell E, Huang J et al: Exome sequencing allows for rapid gene identification in a Charcot-Marie-Tooth family. Ann Neurol 2011; 69: 464-470.
-
(2011)
Ann Neurol
, vol.69
, pp. 464-470
-
-
Montenegro, G.1
Powell, E.2
Huang, J.3
-
27
-
-
84859313496
-
Modelling decisions to undergo genetic testing for susceptibility to common health conditions: An ancillary study of the multiplex initiative
-
Wade CH, Shiloh S, Woolford SW et al: Modelling decisions to undergo genetic testing for susceptibility to common health conditions: an ancillary study of the Multiplex Initiative. Psychol Health 2011; 27: 430-444.
-
(2011)
Psychol Health
, vol.27
, pp. 430-444
-
-
Wade, C.H.1
Shiloh, S.2
Woolford, S.W.3
-
28
-
-
77950832782
-
Future health applications of genomics: Priorities for communication, behavioral, and social sciences research
-
McBride CM, Bowen D, Brody LC et al: Future health applications of genomics: priorities for communication, behavioral, and social sciences research. Am J Prev Med 2010; 38: 556-565.
-
(2010)
Am J Prev Med
, vol.38
, pp. 556-565
-
-
McBride, C.M.1
Bowen, D.2
Brody, L.C.3
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