Center-Authored Papers
Filters: Author is Völker, Uwe [Clear All Filters]
Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study.. PloS one. 12(1):e0167742. Abstract
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2017.
Discovery of novel heart rate-associated loci using the Exome Chip.. Human molecular genetics. Abstract
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2017.
Fifteen Genetic Loci Associated With the Electrocardiographic P Wave.. Circulation. Cardiovascular genetics. 10(4) Abstract
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2017.
Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-wide Association Studies.. Gastroenterology. 151(2):351-363. Abstract
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2016.
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.. Nature communications. 7:10023. Abstract
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2016.
Genetic studies of body mass index yield new insights for obesity biology.. Nature. 518(7538):197-206. Abstract
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2015.
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.. Nature. 478(7367):103-9. Abstract
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2011.
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2016.
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.. Nature genetics. 41(11):1182-90. Abstract
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2009.
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.. PLoS genetics. 13(4):e1006528. Abstract
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2017.
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2015.
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.. Nature genetics. 49(6):946-952. Abstract
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2017.
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.. Nature genetics. 48(10):1162-1170. Abstract
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2016.
A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration.. Human molecular genetics. 25(2):358-70. Abstract
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2016.
New genetic loci link adipose and insulin biology to body fat distribution.. Nature. 518(7538):187-96. Abstract
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2015.
Novel Genetic Markers Associate with Atrial Fibrillation Risk in Europeans and Japanese.. Journal of the American College of Cardiology. Abstract
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2014.
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study.. The lancet. Diabetes & endocrinology. Abstract
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2016.
Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.. American journal of human genetics. Abstract
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2016.
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.
Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.. Nature genetics. 46(6):629-34. Abstract
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2014.
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2015.
Rare coding variants and X-linked loci associated with age at menarche.. Nature communications. 6:7756. Abstract
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2015.
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. Doing Business with Arnold Library
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