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Journal Article
Paradoxical DNA repair and peroxide resistance gene conservation in Bacillus pumilus SAFR-032., Gioia, Jason, Yerrapragada Shailaja, Qin Xiang, Jiang Huaiyang, Igboeli Okezie C., Muzny Donna, Dugan-Rocha Shannon, Ding Yan, Hawes Alicia, Liu Wen, et al. , PloS one, 2007, Volume 2, Issue 9, p.e928, (2007) Abstract
Parental history of stroke and myocardial infarction predicts coronary artery calcification: The Coronary Artery Risk Development in Young Adults (CARDIA) study., Fornage, Myriam, Lopez David S., Roseman Jeffrey M., Siscovick David S., Wong Nathan D., and Boerwinkle Eric , European journal of cardiovascular prevention and rehabilitation : official journal of the European Society of Cardiology, Working Groups on Epidemiology & Prevention and Cardiac Rehabilitation and Exercise Physiology, 2004 Oct, Volume 11, Issue 5, p.421-6, (2004) Abstract
Pas1c1 is a candidate for the mouse pulmonary adenoma susceptibility 1 locus., Wang, Min, Futamura Manabu, Wang Yian, and You Ming , Oncogene, 2005 Mar 10, Volume 24, Issue 11, p.1958-63, (2005) Abstract
Patterns and rates of exonic de novo mutations in autism spectrum disorders., Neale, Benjamin M., Kou Yan, Liu Li, Ma'ayan Avi, Samocha Kaitlin E., Sabo Aniko, Lin Chiao-Feng, Stevens Christine, Wang Li-San, Makarov Vladimir, et al. , Nature, 2012 May 10, Volume 485, Issue 7397, p.242-5, (2012) Abstract
PDX-1 acts as a potential molecular target for treatment of human pancreatic cancer., Liu, Shihe, Ballian Nikiforos, Belaguli Narasimhaswamy S., Patel Sanjeet, Li Min, Templeton Nancy Smyth, Gingras Marie-Claude, Gibbs Richard, Fisher William, and Brunicardi Charles F. , Pancreas, 2008 Aug, Volume 37, Issue 2, p.210-20, (2008) Abstract
PDX-1 is a therapeutic target for pancreatic cancer, insulinoma and islet neoplasia using a novel RNA interference platform., Liu, Shi-He, Rao Donald D., Nemunaitis John, Senzer Neil, Zhou Guisheng, Dawson David, Gingras Marie-Claude, Wang Zhaohui, Gibbs Richard, Norman Michael, et al. , PloS one, 2012, Volume 7, Issue 8, p.e40452, (2012) Abstract
PDX-1: demonstration of oncogenic properties in pancreatic cancer., Liu, Shi-He, Patel Sanjeet, Gingras Marie-Claude, Nemunaitis John, Zhou Guisheng, Chen Changyi, Li Min, Fisher William, Gibbs Richard, and Brunicardi Charles F. , Cancer, 2011 Feb 15, Volume 117, Issue 4, p.723-33, (2011) Abstract
PGM3 Mutations Cause a Congenital Disorder of Glycosylation with Severe Immunodeficiency and Skeletal Dysplasia, Stray-Pedersen, Asbjørg, Backe Paul H., Sorte Hanne S., Mørkrid Lars, Chokshi Niti Y., Erichsen Hans Christian, Gambin Tomasz, Elgstøen Katja B.P., Bjørås Magnar, Wlodarski Marcin W., et al. , The American Journal of Human Genetics, 07/2014, Volume 95, Issue 1, p.96 - 107, (2014)
PGRNseq: a targeted capture sequencing panel for pharmacogenetic research and implementation., Gordon, Adam S., Fulton Robert S., Qin Xiang, Mardis Elaine R., Nickerson Deborah A., and Scherer Steve , Pharmacogenetics and genomics, 2016 Jan 5, (2016) Abstract
Phosphorylated and sumoylation-deficient progesterone receptors drive proliferative gene signatures during breast cancer progression., Knutson, Todd P., Daniel Andrea R., Fan Danhua, Silverstein Kevin At, Covington Kyle R., Fuqua Suzanne A. W., and Lange Carol A. , Breast cancer research : BCR, 2012, Volume 14, Issue 3, p.R95, (2012) Abstract
Phosphorylation of the mutant K303R estrogen receptor alpha at serine 305 affects aromatase inhibitor sensitivity., Barone, I., Iacopetta D., Covington K. R., Cui Y., Tsimelzon A., Beyer A., Andò S., and Fuqua S. A. W. , Oncogene, 2010 Apr 22, Volume 29, Issue 16, p.2404-14, (2010) Abstract
Phosphorylation of the mutant K303R estrogen receptor alpha at serine 305 affects aromatase inhibitor sensitivity., Barone, I., Iacopetta D., Covington K. R., Cui Y., Tsimelzon A., Beyer A., Andò S., and Fuqua S. A. W. , Oncogene, 2010 Apr 22, Volume 29, Issue 16, p.2404-14, (2010) Abstract
A physical map of the chicken genome., Wallis, John W., Aerts Jan, Groenen Martien A. M., Crooijmans Richard P. M. A., Layman Dan, Graves Tina A., Scheer Debra E., Kremitzki Colin, Fedele Mary J., Mudd Nancy K., et al. , Nature, 2004 Dec 9, Volume 432, Issue 7018, p.761-4, (2004) Abstract
A physical map of the human genome., McPherson, J. D., Marra M., Hillier L., Waterston R. H., Chinwalla A., Wallis J., Sekhon M., Wylie K., Mardis E. R., Wilson R. K., et al. , Nature, 2001 Feb 15, Volume 409, Issue 6822, p.934-41, (2001) Abstract
PipMaker--a web server for aligning two genomic DNA sequences., Schwartz, S., Zhang Z., Frazer K. A., Smit A., Riemer C., Bouck J., Gibbs R., Hardison R., and Miller W. , Genome research, 2000 Apr, Volume 10, Issue 4, p.577-86, (2000) Abstract
PLD3 variants in population studies., van der Lee, Sven J., Holstege Henne, Wong Tsz Hang, Jakobsdottir Johanna, Bis Joshua C., Chouraki Vincent, van Rooij Jeroen G. J., Grove Megan L., Smith Albert V., Amin Najaf, et al. , Nature, 2015 Apr 2, Volume 520, Issue 7545, p.E2-3, (2015)
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
POGZ truncating alleles cause syndromic intellectual disability., White, Janson, Beck Christine R., Harel Tamar, Posey Jennifer E., Jhangiani Shalini N., Tang Sha, Farwell Kelly D., Powis Zöe, Mendelsohn Nancy J., Baker Janice A., et al. , Genome medicine, 2016, Volume 8, Issue 1, p.3, (2016) 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


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