PubRank

A Pilot Project Exploring the Impact of Whole Genome Sequencing in Healthcare

Clinical Trial ID NCT01736566

PubWeight™ 49.76‹?›

🔗 Visit the ClinicalTrials.gov page for NCT01736566

Top papers

Rank Title Journal Year PubWeight™‹?›
1 ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. Genet Med 2013 22.73
2 Charting a course for genomic medicine from base pairs to bedside. Nature 2011 9.39
3 The incidentalome: a threat to genomic medicine. JAMA 2006 7.24
4 Diagnostic clinical genome and exome sequencing. N Engl J Med 2014 5.55
5 The Roter interaction analysis system (RIAS): utility and flexibility for analysis of medical interactions. Patient Educ Couns 2002 5.10
6 Measuring numeracy without a math test: development of the Subjective Numeracy Scale. Med Decis Making 2007 4.80
7 Exploring concordance and discordance for return of incidental findings from clinical sequencing. Genet Med 2012 4.04
8 Numeric, verbal, and visual formats of conveying health risks: suggested best practices and future recommendations. Med Decis Making 2007 3.74
9 Validation of a decision regret scale. Med Decis Making 2003 3.70
10 The evidence dilemma in genomic medicine. Health Aff (Millwood) 2008 3.58
11 Disease-targeted sequencing: a cornerstone in the clinic. Nat Rev Genet 2013 3.30
12 Opportunities and challenges for the integration of massively parallel genomic sequencing into clinical practice: lessons from the ClinSeq project. Genet Med 2012 2.83
13 Point-counterpoint. Ethics and genomic incidental findings. Science 2013 2.73
14 Return of genomic results to research participants: the floor, the ceiling, and the choices in between. Am J Hum Genet 2014 2.54
15 Genomics. Deflating the genomic bubble. Science 2011 2.20
16 Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium. Genet Med 2013 2.08
17 Measuring trust in medical researchers. Med Care 2006 1.69
18 The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine. Trials 2014 1.62
19 The indispensable role of professional judgment in genomic medicine. JAMA 2013 1.54
20 Ten years on--the human genome and medicine. N Engl J Med 2010 1.52
21 Fearing the unknown: a short version of the Intolerance of Uncertainty Scale. J Anxiety Disord 2006 1.41
22 Communicating genetic risk information for common disorders in the era of genomic medicine. Annu Rev Genomics Hum Genet 2013 1.33
23 Effects of informed consent for individual genome sequencing on relevant knowledge. Clin Genet 2012 1.20
24 GINA, genetic discrimination, and genomic medicine. N Engl J Med 2015 1.01
25 Are physicians prepared for whole genome sequencing? a qualitative analysis. Clin Genet 2015 1.00
26 Management of incidental findings in clinical genomic sequencing. Curr Protoc Hum Genet 2013 0.90
27 Genetic testing in cardiovascular diseases. Curr Opin Cardiol 2014 0.88
28 Prioritizing disease-linked variants, genes, and pathways with an interactive whole-genome analysis pipeline. Hum Mutat 2014 0.85
29 Patients' perceived utility of whole-genome sequencing for their healthcare: findings from the MedSeq project. Per Med 2016 0.81
30 How behavioral economics can help to avoid 'The last mile problem' in whole genome sequencing. Genome Med 2015 0.81
31 gSearch: a fast and flexible general search tool for whole-genome sequencing. Bioinformatics 2012 0.81
32 Action and the actionability in exome variation. Circ Cardiovasc Genet 2012 0.79
33 Reducing false-positive incidental findings with ensemble genotyping and logistic regression based variant filtering methods. Hum Mutat 2014 0.79
34 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 0.78
35 Genomic medicine in primary care: barriers and assets. Postgrad Med J 2013 0.76
Next 100