Center-Authored Papers
Filters: Author is Boerwinkle, Eric [Clear All Filters]
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol.. American journal of human genetics. 94(2):233-45. Abstract
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2014.
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.. American journal of human genetics. 99(2):481-8. Abstract
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2016.
Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans.. Human molecular genetics. 23(24):6607-15. Abstract
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2014.
Trans-ethnic Meta-analysis of White Blood Cell Phenotypes.. Human molecular genetics. 23(25):6944-60. Abstract
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2014.
Trans-ethnic Meta-Analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin.. American journal of human genetics. 99(1):56-75. Abstract
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2016.
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2013.
Targeted sequencing in candidate genes for atrial fibrillation: The Cohorts for Heart and Aging Research in Genomic Epidemiology Targeted Sequencing Study.. Heart rhythm : the official journal of the Heart Rhythm Society. Abstract
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2013.
Strategies to Design and Analyze Targeted Sequencing Data: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study.. Circulation. Cardiovascular genetics. 7(3):335-43. Abstract
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2014.
SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function.. Journal of the American Society of Nephrology : JASN. Abstract
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2016.
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2017.
Sequence Variation in TMEM18 in Association With Body Mass Index: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study.. Circulation. Cardiovascular genetics. 7(3):344-9. Abstract
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2014.
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk.. Circulation. Cardiovascular genetics. Abstract
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2015.
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2017.
Rare coding variants and X-linked loci associated with age at menarche.. Nature communications. 6:7756. Abstract
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2015.
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2015.
Rare and low-frequency coding variants alter human adult height.. Nature. 542(7640):186-190. Abstract
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2017.
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2014.
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape.. Nature communications. 7:13357. Abstract
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2016.
Predicting Stroke Through Genetic Risk Functions: The CHARGE Risk Score Project.. Stroke; a journal of cerebral circulation. 45(2):403-12. Abstract
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2014.
Polymorphisms within the C-reactive protein (CRP) promoter region are associated with plasma CRP levels.. American journal of human genetics. 77(1):64-77. Abstract
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2005.
Pleiotropic genes for metabolic syndrome and inflammation.. Molecular genetics and metabolism. Abstract
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2014.
Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.. American journal of human genetics. Abstract
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2016.
A phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains.. PLoS genetics. 7(10):e1002322. Abstract
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2011.
Novel Genetic Loci Associated With Retinal Microvascular Diameter.. Circulation. Cardiovascular genetics. 9(1):45-54. Abstract
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2016. Doing Business with Arnold Library
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