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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
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
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
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 genomic analysis of 962 whole genome sequences of humans reveals natural selection in non-coding regions., Yu, Fuli, Lu Jian, Liu Xiaoming, Gazave Elodie, Chang Diana, Raj Srilakshmi, Hunter-Zinck Haley, Blekhman Ran, Arbiza Leonardo, Van Hout Cris, et al. , PloS one, 2015, Volume 10, Issue 3, p.e0121644, (2015) Abstract
Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series., Hattori, Eiji, Liu Chunyu, Badner Judith A., Bonner Tom I., Christian Susan L., Maheshwari Manjula, Detera-Wadleigh Sevilla D., Gibbs Richard A., and Gershon Elliot S. , American journal of human genetics, 2003 May, Volume 72, Issue 5, p.1131-40, (2003) 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
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
Pol iota is a candidate for the mouse pulmonary adenoma resistance 2 locus, a major modifier of chemically induced lung neoplasia., Wang, Min, Devereux Theodora R., Vikis Haris G., McCulloch Scott D., Holliday Wanda, Anna Colleen, Wang Yian, Bebenek Katarzyna, Kunkel Thomas A., Guan Kunliang, et al. , Cancer research, 2004 Mar 15, Volume 64, Issue 6, p.1924-31, (2004) 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
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
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)
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
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
Phylogeny of the macaques (Cercopithecidae: Macaca) based on Alu elements., Li, Jing, Han Kyudong, Xing Jinchuan, Kim Heui-Soo, Rogers Jeffrey, Ryder Oliver A., Disotell Todd, Yue Bisong, and Batzer Mark A. , Gene, 2009 Dec 15, Volume 448, Issue 2, p.242-9, (2009) 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
PhenoDB: a new web-based tool for the collection, storage, and analysis of phenotypic features., Hamosh, Ada, Sobreira Nara, Hoover-Fong Julie, Sutton Reid V., Boehm Corinne, Schiettecatte François, and Valle David , Human mutation, 2013 Apr, Volume 34, Issue 4, p.566-71, (2013) Abstract
Pharmacogenetics of response to statins: where do we stand?, Maitland-van der Zee, Anke-Hilse, and Boerwinkle Eric , Current atherosclerosis reports, 2005 May, Volume 7, Issue 3, p.204-8, (2005) 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)
Personalized copy number and segmental duplication maps using next-generation sequencing., Alkan, Can, Kidd Jeffrey M., Marques-Bonet Tomas, Aksay Gozde, Antonacci Francesca, Hormozdiari Fereydoun, Kitzman Jacob O., Baker Carl, Malig Maika, Mutlu Onur, et al. , Nature genetics, 2009 Oct, Volume 41, Issue 10, p.1061-7, (2009) Abstract
Peroxisome proliferator-activated receptor [alpha] genetic variation interacts with n-6 and long-chain n-3 fatty acid intake to affect total cholesterol and LDL-cholesterol concentrations in the Atherosclerosis Risk in Communities Study., Volcik, Kelly A., Nettleton Jennifer A., Ballantyne Christie M., and Boerwinkle Eric , The American journal of clinical nutrition, 2008 Jun, Volume 87, Issue 6, p.1926-31, (2008) Abstract
Pediatric Cancer Genetics Research and an Evolving Preventive Ethics Approach for Return of Results after Death of the Subject., Scollon, Sarah, Bergstrom Katie, McCullough Laurence B., McGuire Amy L., Gutierrez Stephanie, Kerstein Robin, Parsons Williams D., and Plon Sharon E. , The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics, 2015 Sep, Volume 43, Issue 3, p.529-37, (2015) 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
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


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