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Publications

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Journal Article
Association of Rare Loss-Of-Function Alleles in HAL, Serum Histidine Levels and Incident Coronary Heart Disease., Yu, Bing, Li Alexander H., Muzny Donna, Veeraraghavan Narayanan, de Vries Paul S., Bis Joshua C., Musani Solomon K., Alexander Danny, Morrison Alanna C., Franco Oscar H., et al. , Circulation. Cardiovascular genetics, 2015 Jan 8, (2015) Abstract
Association of the complement factor H Y402H polymorphism with cardiovascular disease is dependent upon hypertension status: The ARIC study., Volcik, Kelly A., Ballantyne Christie M., Braun Michael C., Coresh Josef, Mosley Thomas H., and Boerwinkle Eric , American journal of hypertension, 2008 May, Volume 21, Issue 5, p.533-8, (2008) Abstract
Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease., Ueda, Hironori, Howson Joanna M. M., Esposito Laura, Heward Joanne, Snook Hywel, Chamberlain Giselle, Rainbow Daniel B., Hunter Kara M. D., Smith Annabel N., Di Genova Gianfranco, et al. , Nature, 2003 May 29, Volume 423, Issue 6939, p.506-11, (2003) Abstract
Association studies for next-generation sequencing., Luo, Li, Boerwinkle Eric, and Xiong Momiao , Genome research, 2011 Jul, Volume 21, Issue 7, p.1099-108, (2011) Abstract
Associations between dietary patterns and flow cytometry-measured biomarkers of inflammation and cellular activation in the Atherosclerosis Risk in Communities (ARIC) Carotid Artery MRI Study., Nettleton, Jennifer A., Matijevic Nena, Follis Jack L., Folsom Aaron R., and Boerwinkle Eric , Atherosclerosis, 2010 Sep, Volume 212, Issue 1, p.260-7, (2010) Abstract
Associations between metabolomic compounds and incident heart failure among African Americans: the ARIC Study., Zheng, Yan, Yu Bing, Alexander Danny, Manolio Teri A., Aguilar David, Coresh Josef, Heiss Gerardo, Boerwinkle Eric, and Nettleton Jennifer A. , American journal of epidemiology, 2013 Aug 15, Volume 178, Issue 4, p.534-42, (2013) Abstract
The Atlas genome assembly system., Havlak, Paul, Chen Rui, Durbin James K., Egan Amy, Ren Yanru, Song Xing-Zhi, Weinstock George M., and Gibbs Richard A. , Genome research, 2004 Apr, Volume 14, Issue 4, p.721-32, (2004) Abstract
Atlas2 Cloud: a framework for personal genome analysis in the cloud., Evani, Uday S., Challis Danny, Yu Jin, Jackson Andrew R., Paithankar Sameer, Bainbridge Matthew N., Jakkamsetti Adinarayana, Pham Peter, Coarfa Cristian, Milosavljevic Aleksandar, et al. , BMC genomics, 2012, Volume 13 Suppl 6, p.S19, (2012) Abstract
Atypical angiopoietin-like protein that regulates ANGPTL3., Quagliarini, Fabiana, Wang Yan, Kozlitina Julia, Grishin Nick V., Hyde Rhonda, Boerwinkle Eric, Valenzuela David M., Murphy Andrew J., Cohen Jonathan C., and Hobbs Helen H. , Proceedings of the National Academy of Sciences of the United States of America, 2012 Nov 27, Volume 109, Issue 48, p.19751-6, (2012) Abstract
Automated DNA sequencing methods for detection and analysis of mutations: applications to the Lesch-Nyhan syndrome., Edwards, A., Gibbs R. A., Nguyen P. N., Ansorge W., and Caskey C. T. , Transactions of the Association of American Physicians, 1989, Volume 102, p.185-94, (1989)
Automated MeSH indexing of the World-Wide Web., Fowler, J., Kouramajian V., Maram S., and Devadhar V. , Proceedings / the ... Annual Symposium on Computer Application [sic] in Medical Care. Symposium on Computer Applications in Medical Care, 1995, p.893-7, (1995) Abstract
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel., Zhuchenko, O., Bailey J., Bonnen P., Ashizawa T., Stockton D. W., Amos C., Dobyns W. B., Subramony S. H., Zoghbi H. Y., and Lee C. C. , Nature genetics, 1997 Jan, Volume 15, Issue 1, p.62-9, (1997) Abstract


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