Center-Authored Papers
Filters: Author is Jarvik, Gail P [Clear All Filters]
Actionable exomic incidental findings in 6503 participants: challenges of variant classification.. Genome research. 25(3):305-15. Abstract
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2015.
Actionable, pathogenic incidental findings in 1,000 participants' exomes.. American journal of human genetics. 93(4):631-40. Abstract
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2013.
Arterial remodeling in [corrected] subclinical carotid artery disease.. JACC. Cardiovascular imaging. 2(12):1381-9. Abstract
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2009.
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2016.
Beneficence, clinical urgency, and the return of individual research results to relatives.. The American journal of bioethics : AJOB. 12(10):9-10.
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2012.
Burden of potentially pathologic copy number variants is higher in children with isolated congenital heart disease and significantly impairs covariate-adjusted transplant-free survival.. The Journal of thoracic and cardiovascular surgery. 151(4):1147-1151.e4. Abstract
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2016.
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.. American journal of human genetics. 98(6):1051-1066. Abstract
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2016.
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.. Nature genetics. 43(5):436-41. Abstract
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2011.
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2014.
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2013.
The cost-effectiveness of returning incidental findings from next-generation genomic sequencing.. Genetics in medicine : official journal of the American College of Medical Genetics. Abstract
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2014.
Detectable clonal mosaicism from birth to old age and its relationship to cancer.. Nature genetics. 44(6):642-50. Abstract
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2012.
Discordance in selected designee for return of genomic findings in the event of participant death and estate executor.. Molecular genetics & genomic medicine. 5(2):172-176. Abstract
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2017.
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2017.
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2013.
The FDA and genomic tests--getting regulation right.. The New England journal of medicine. 372(23):2258-64.
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2015.
Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci.. American journal of human genetics. Abstract
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2014.
Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network.. Human genetics. 131(4):639-652. Abstract
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2012.
Genetic variation associated with circulating monocyte count in the eMERGE Network.. Human molecular genetics. 22(10):2119-2127. Abstract
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2013.
Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.. Circulation. 127(13):1377-85. Abstract
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2013.
High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE.. Clinical and translational science. 5(5):394-9. Abstract
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2012.
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2016.
Informed Consent in Genome-Scale Research: What Do Prospective Participants Think? AJOB primary research. 3(3):3-11. Abstract
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2012.
Is "incidental finding" the best term?: a study of patients' preferences. Genetics in medicine : official journal of the American College of Medical Genetics. Abstract
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2016.
Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci.. American journal of human genetics. 91(5):823-38. Abstract
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