Published in G3 (Bethesda) on August 07, 2013
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Identifying personal genomes by surname inference. Science (2013) 10.79
Protecting the privacy of family members in survey and pedigree research. JAMA (2001) 4.74
The genomic and transcriptomic landscape of a HeLa cell line. G3 (Bethesda) (2013) 3.82
Research ethics. The complexities of genomic identifiability. Science (2013) 3.23
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Biobanks, consent and claims of consensus. Nat Methods (2012) 1.66
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Predicting intention to biobank: a national survey. Eur J Public Health (2010) 1.17
Biobanking, consent, and control: a survey of Albertans on key research ethics issues. Biopreserv Biobank (2012) 1.07
Be prepared for the big genome leak. Nature (2013) 0.98
Bioethics in popular science: evaluating the media impact of The Immortal Life of Henrietta Lacks on the biobank debate. BMC Med Ethics (2013) 0.97
To the barricades! Am J Bioeth (2010) 0.85
Whose body is it anyway? Human cells and the strange effects of property and intellectual property law. Stanford Law Rev (2011) 0.82
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. Genet Med (2013) 22.73
Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy. N Engl J Med (2010) 13.57
Identifying personal genomes by surname inference. Science (2013) 10.79
Research ethics recommendations for whole-genome research: consensus statement. PLoS Biol (2008) 5.24
Exploring concordance and discordance for return of incidental findings from clinical sequencing. Genet Med (2012) 4.04
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Informed consent in research to improve the number and quality of deceased donor organs. Crit Care Med (2011) 2.18
The Human Microbiome Project: a community resource for the healthy human microbiome. PLoS Biol (2012) 2.17
The legal risks of returning results of genomics research. Genet Med (2012) 2.15
Experiences and attitudes of genome investigators regarding return of individual genetic test results. Genet Med (2013) 1.97
Personalized genomic information: preparing for the future of genetic medicine. Nat Rev Genet (2010) 1.87
The futility of genomic counseling: essential role of electronic health records. Genome Med (2009) 1.73
Principal investigator views of the IRB system. Int J Med Sci (2008) 1.63
The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine. Trials (2014) 1.62
Shaping patients' decisions. Chest (2011) 1.58
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Incidental copy-number variants identified by routine genome testing in a clinical population. Genet Med (2012) 1.33
Currents in contemporary ethics. Direct-to-consumer genetic testing: is it the practice of medicine? J Law Med Ethics (2009) 1.10
Beyond shared decision making: an expanded typology of medical decisions. Med Decis Making (2008) 1.06
Beneficent persuasion: techniques and ethical guidelines to improve patients' decisions. Ann Fam Med (2010) 1.05
Participants' recall and understanding of genomic research and large-scale data sharing. J Empir Res Hum Res Ethics (2013) 1.03
GINA, genetic discrimination, and genomic medicine. N Engl J Med (2015) 1.01
Personalized genomic disease risk of volunteers. Proc Natl Acad Sci U S A (2013) 0.99
The need for medical education reform: genomics and the changing nature of health information. Genome Med (2010) 0.97
Research results: preserving newborn blood samples. Sci Transl Med (2012) 0.97
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"Snake-oil," "quack medicine," and "industrially cultured organisms:" biovalue and the commercialization of human microbiome research. BMC Med Ethics (2012) 0.88
Pediatric data sharing in genomic research: attitudes and preferences of parents. Pediatrics (2014) 0.87
Beyond breaking bad news: the roles of hope and hopefulness. Cancer (2008) 0.86
Developing a tissue resource to characterize the genome of pancreatic cancer. World J Surg (2009) 0.86
Adult genetic risk screening. Annu Rev Med (2013) 0.84
Return of research results from genomic biobanks: a call for data. Genet Med (2013) 0.84
Clinical integration of next generation sequencing: a policy analysis. J Law Med Ethics (2014) 0.82
Why information alone is not enough: behavioral economics and the future of genomic medicine. Ann Intern Med (2014) 0.81
Do recent US Supreme Court rulings on patenting of genes and genetic diagnostics affect the practice of genetic screening and diagnosis in prenatal and reproductive care? Prenat Diagn (2014) 0.79
Erratum: Community crystal gazing. Nat Biotechnol (2016) 0.75
Consent: informed, simple, implied and presumed. Am J Bioeth (2007) 0.75
Please don't call my mom: pediatric consent and confidentiality. Clin Pediatr (Phila) (2008) 0.75