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Journal Article
Pleiotropic patterns of quantitative trait loci for 70 murine skeletal traits., Kenney-Hunt, Jane P., Wang Bing, Norgard Elizabeth A., Fawcett Gloria, Falk Doug, Pletscher Susan L., Jarvis Joseph P., Roseman Charles, Wolf Jason, and Cheverud James M. , Genetics, 2008 Apr, Volume 178, Issue 4, p.2275-88, (2008) Abstract
PNPLA3 polymorphisms and liver aminotransferase levels in a Mexican American population., Li, Quan, Qu Hui-Qi, Rentfro Anne R., Grove Megan L., Mirza Shaper, Lu Yang, Hanis Craig L., Fallon Michael B., Boerwinkle Eric, Fisher-Hoch Susan P., et al. , Clinical and investigative medicine. Médecine clinique et experimentale, 2012, Volume 35, Issue 4, p.E237-45, (2012) Abstract
Polymorphism in soluble epoxide hydrolase and blood pressure in spontaneously hypertensive rats., Fornage, Myriam, Hinojos Cruz A., Nurowska Barbara W., Boerwinkle Eric, Hammock Bruce D., Morisseau Christophe H. P., and Doris Peter A. , Hypertension, 2002 Oct, Volume 40, Issue 4, p.485-90, (2002) Abstract
Polymorphism of the soluble epoxide hydrolase is associated with coronary artery calcification in African-American subjects: The Coronary Artery Risk Development in Young Adults (CARDIA) study., Fornage, Myriam, Boerwinkle Eric, Doris Peter A., Jacobs David, Liu Kiang, and Wong Nathan D. , Circulation, 2004 Jan 27, Volume 109, Issue 3, p.335-9, (2004) Abstract
Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL., Romeo, Stefano, Pennacchio Len A., Fu Yunxin, Boerwinkle Eric, Tybjaerg-Hansen Anne, Hobbs Helen H., and Cohen Jonathan C. , Nature genetics, 2007 Apr, Volume 39, Issue 4, p.513-6, (2007) Abstract
Population-based risk factors for elevated alanine aminotransferase in a South Texas Mexican-American population., Qu, Hui-Qi, Li Quan, Grove Megan L., Lu Yang, Pan Jen-Jung, Rentfro Anne R., Bickel Perry E., Fallon Michael B., Hanis Craig L., Boerwinkle Eric, et al. , Archives of medical research, 2012 Aug, Volume 43, Issue 6, p.482-8, (2012) Abstract
Positional cloning of the major quantitative trait locus underlying lung tumor susceptibility in mice., Zhang, Zhongqiu, Futamura Manabu, Vikis Haris G., Wang Min, Li Jie, Wang Yian, Guan Kun-Liang, and You Ming , Proceedings of the National Academy of Sciences of the United States of America, 2003 Oct 28, Volume 100, Issue 22, p.12642-7, (2003) Abstract
Positive selection of a pre-expansion CAG repeat of the human SCA2 gene., Yu, Fuli, Sabeti Pardis C., Hardenbol Paul, Fu Qing, Fry Ben, Lu Xiuhua, Ghose Sy, Vega Richard, Perez Ag, Pasternak Shiran, et al. , PLoS genetics, 2005 Sep, Volume 1, Issue 3, p.e41, (2005) Abstract
Possible race and gender divergence in association of genetic variations with plasma von Willebrand factor: a study of ARIC and 1000 genome cohorts., Zhou, Zhou, Yu Fuli, Buchanan Ashley, Fu Yuanyuan, Campos Marco, Wu Kenneth K., Chambless Lloyd E., Folsom Aaron R., Boerwinkle Eric, and Dong Jing-fei , PloS one, 2014, Volume 9, Issue 1, p.e84810, (2014) Abstract
Potassium channels in C. elegans, Eisenmann, David M., and Fawcett G. , WormBook, 2005, (2005)
Prepublication data sharing., Birney, Ewan, Hudson Thomas J., Green Eric D., Gunter Chris, Eddy Sean, Rogers Jane, Harris Jennifer R., Ehrlich Dusko S., Apweiler Rolf, Austin Christopher P., et al. , Nature, 2009 Sep 10, Volume 461, Issue 7261, p.168-70, (2009) Abstract
Pretranscriptional regulation of Tgf-beta1 by PI polyamide prevents scarring and accelerates wound healing of the cornea after exposure to alkali., Chen, Min, Matsuda Hiroyuki, Wang Linghua, Watanabe Takayoshi, Kimura Makoto T., Igarashi Jun, Wang Xiaofei, Sakimoto Tohru, Fukuda Noboru, Sawa Mitsuru, et al. , Molecular therapy : the journal of the American Society of Gene Therapy, 2010 Mar, Volume 18, Issue 3, p.519-27, (2010) Abstract
PrimerSNP: a web tool for whole-genome selection of allele-specific and common primers of phylogenetically-related bacterial genomic sequences., Yao, Jiqiang, Lin Hong, Van Deynze Allen, Doddapaneni Harshavardhan, Francis Martha, Lemos Eliana Gertrudes Macedo, and Civerolo Edwin L. , BMC microbiology, 2008, Volume 8, p.185, (2008) Abstract
Progress and prospects in rat genetics: a community view., Aitman, Timothy J., Critser John K., Cuppen Edwin, Dominiczak Anna, Fernandez-Suarez Xose M., Flint Jonathan, Gauguier Dominique, Geurts Aron M., Gould Michael, Harris Peter C., et al. , Nature genetics, 2008 May, Volume 40, Issue 5, p.516-22, (2008) Abstract
The prolonged effect of repeated maternal glucocorticoid exposure on the maternal and fetal leptin/insulin-like growth factor axis in Papio species., Schlabritz-Loutsevitch, Natalia E., Lopez-Alvarenga Juan C., Comuzzie Anthony G., Miller Myrna M., Ford Stephen P., Li Cun, Hubbard Gene B., Ferry Robert J., and Nathanielsz Peter W. , Reproductive sciences (Thousand Oaks, Calif.), 2009 Mar, Volume 16, Issue 3, p.308-19, (2009) Abstract
The promise of a personalized genomic approach to pancreatic cancer and why targeted therapies have missed the mark., Fisher, William E. , World journal of surgery, 2011 Aug, Volume 35, Issue 8, p.1766-9, (2011) Abstract
A proposed architecture for ambulatory systems development., Buffone, G. J., Petermann C. A., Bobroff R. B., Moore D. M., Dargahi R., Moreau D. R., Gilson H. S., Li Y., Fowler J., and Beck J. R. , Medinfo. MEDINFO, 1995, Volume 8 Pt 1, p.363-6, (1995) Abstract
Prospective associations of coronary heart disease loci in African Americans using the MetaboChip: the PAGE study., Franceschini, Nora, Hu Yijuan, Reiner Alex P., Buyske Steven, Nalls Mike, Yanek Lisa R., Li Yun, Hindorff Lucia A., Cole Shelley A., Howard Barbara V., et al. , PloS one, 2014, Volume 9, Issue 12, p.e113203, (2014) Abstract
PTPN11 mutations in Noonan syndrome type I: detection of recurrent mutations in exons 3 and 13., Maheshwari, M., Belmont J., Fernbach S., Ho T., Molinari L., Yakub I., Yu F., Combes A., Towbin J., Craigen W. J., et al. , Human mutation, 2002 Oct, Volume 20, Issue 4, p.298-304, (2002) Abstract
Pulmonary alveolar proteinosis caused by deletion of the GM-CSFRalpha gene in the X chromosome pseudoautosomal region 1., Martinez-Moczygemba, Margarita, Doan Minh L., Elidemir Okan, Fan Leland L., Cheung Sau Wai, Lei Jonathan T., Moore James P., Tavana Ghamartaj, Lewis Lora R., Zhu Yiming, et al. , The Journal of experimental medicine, 2008 Nov 24, Volume 205, Issue 12, p.2711-6, (2008) Abstract
Quantitative Genetics of Response to Novelty and Other Stimuli by Infant Rhesus Macaques (Macaca mulatta) Across Three Behavioral Assessments., Fawcett, G. L., Dettmer A. M., Kay D., Raveendran M., Higley J. D., Ryan N. D., Cameron J. L., and Rogers J. , International journal of primatology, 2014 Feb 1, Volume 35, Issue 1, p.325-339, (2014) Abstract
Quantitative loci regulating plasma levels of gamma glutamyl transferase and albumin and their genetic correlations with cardiovascular risk factors., Bose, Tanushree, Voruganti Saroja V., Tejero Elizabeth M., Proffitt Michael J., Cox Laura A., VandeBerg John L., Mahaney Michael C., Rogers Jeffrey, Freeland-Graves Jeanne H., Cole Shelley A., et al. , Experimental biology and medicine (Maywood, N.J.), 2009 Dec, Volume 234, Issue 12, p.vi, 1519-24, (2009) Abstract
Quantitative trait loci affecting liver fat content in mice., Minkina, Olga, Cheverud James M., Fawcett Gloria, Semenkovich Clay F., and Kenney-Hunt Jane P. , G3 (Bethesda, Md.), 2012 Sep, Volume 2, Issue 9, p.1019-25, (2012) Abstract
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders., Lim, Elaine T., Raychaudhuri Soumya, Sanders Stephan J., Stevens Christine, Sabo Aniko, MacArthur Daniel G., Neale Benjamin M., Kirby Andrew, Ruderfer Douglas M., Fromer Menachem, et al. , Neuron, 2013 Jan 23, Volume 77, Issue 2, p.235-42, (2013) Abstract
Recurrent chromosome 16p13.1 duplications are a risk factor for aortic dissections., Kuang, Shao-Qing, Guo Dong-Chuan, Prakash Siddharth K., McDonald Merry-Lynn N., Johnson Ralph J., Wang Min, Regalado Ellen S., Russell Ludivine, Cao Jiu-Mei, Kwartler Callie, et al. , PLoS genetics, 2011 Jun, Volume 7, Issue 6, p.e1002118, (2011) Abstract


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