AMY MCGUIRE to Sequence Analysis, DNA
This is a "connection" page, showing publications AMY MCGUIRE has written about Sequence Analysis, DNA.
Connection Strength
2.330
-
Clinical integration of next generation sequencing: a policy analysis. J Law Med Ethics. 2014; 42 Suppl 1:5-8.
Score: 0.290
-
The indispensable role of professional judgment in genomic medicine. JAMA. 2013 Apr 10; 309(14):1465-6.
Score: 0.276
-
Personal genome research : what should the participant be told? Trends Genet. 2010 May; 26(5):199-201.
Score: 0.224
-
Research ethics and the challenge of whole-genome sequencing. Nat Rev Genet. 2008 02; 9(2):152-6.
Score: 0.192
-
Genetics. No longer de-identified. Science. 2006 Apr 21; 312(5772):370-1.
Score: 0.170
-
Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project. Am J Hum Genet. 2019 01 03; 104(1):76-93.
Score: 0.103
-
Newborn Sequencing in Genomic Medicine and Public Health. Pediatrics. 2017 Feb; 139(2).
Score: 0.090
-
Developing context-specific next-generation sequencing policy. Nat Biotechnol. 2016 05 06; 34(5):466-70.
Score: 0.085
-
Participants and Study Decliners' Perspectives About the Risks of Participating in a Clinical Trial of Whole Genome Sequencing. J Empir Res Hum Res Ethics. 2016 02; 11(1):21-30.
Score: 0.084
-
Potential Psychosocial Risks of Sequencing Newborns. Pediatrics. 2016 Jan; 137 Suppl 1:S24-9.
Score: 0.083
-
Are physicians prepared for whole genome sequencing? a qualitative analysis. Clin Genet. 2016 Feb; 89(2):228-34.
Score: 0.080
-
The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine. Trials. 2014 Mar 20; 15:85.
Score: 0.074
-
Social and behavioral research in genomic sequencing: approaches from the Clinical Sequencing Exploratory Research Consortium Outcomes and Measures Working Group. Genet Med. 2014 Oct; 16(10):727-35.
Score: 0.073
-
Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate. PLoS Biol. 2013 Nov; 11(11):e1001699.
Score: 0.072
-
Adult genetic risk screening. Annu Rev Med. 2014; 65:1-17.
Score: 0.072
-
Personalized genomic disease risk of volunteers. Proc Natl Acad Sci U S A. 2013 Oct 15; 110(42):16957-62.
Score: 0.071
-
Policy uncertainty, sequencing, and cell lines. G3 (Bethesda). 2013 Aug 07; 3(8):1205-7.
Score: 0.070
-
Point-counterpoint. Ethics and genomic incidental findings. Science. 2013 May 31; 340(6136):1047-8.
Score: 0.069
-
Exploring concordance and discordance for return of incidental findings from clinical sequencing. Genet Med. 2012 Apr; 14(4):405-10.
Score: 0.064
-
The complete genome of an individual by massively parallel DNA sequencing. Nature. 2008 Apr 17; 452(7189):872-6.
Score: 0.049
-
Parental interest in genomic sequencing of newborns: enrollment experience from the BabySeq Project. Genet Med. 2019 03; 21(3):622-630.
Score: 0.025
-
Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy. N Engl J Med. 2010 Apr 01; 362(13):1181-91.
Score: 0.014