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F
Common INSIG2 polymorphisms are associated with age-related changes in body size and high-density lipoprotein cholesterol from young adulthood to middle age., Fornage, Myriam, Papanicolaou George, Lewis Cora E., Boerwinkle Eric, and Siscovick David S. , Metabolism: clinical and experimental, 2010 Aug, Volume 59, Issue 8, p.1084-91, (2010) Abstract
The soluble epoxide hydrolase gene harbors sequence variation associated with susceptibility to and protection from incident ischemic stroke., Fornage, Myriam, Lee Craig R., Doris Peter A., Bray Molly S., Heiss Gerardo, Zeldin Darryl C., and Boerwinkle Eric , Human molecular genetics, 2005 Oct 1, Volume 14, Issue 19, p.2829-37, (2005) 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
Family-based association study of matrix metalloproteinase-3 and -9 haplotypes with susceptibility to ischemic white matter injury., Fornage, Myriam, Mosley Thomas H., Jack Clifford R., de Andrade Mariza, Kardia Sharon L. R., Boerwinkle Eric, and Turner Stephen T. , Human genetics, 2007 Jan, Volume 120, Issue 5, p.671-80, (2007) Abstract
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium., Fornage, Myriam, Debette Stephanie, Bis Joshua C., Schmidt Helena, Ikram Arfan M., Dufouil Carole, Sigurdsson Sigurdur, Lumley Thomas, DeStefano Anita L., Fazekas Franz, et al. , Annals of neurology, 2011 Jun, Volume 69, Issue 6, p.928-39, (2011) Abstract
Gene expression profiling and functional proteomic analysis reveal perturbed kinase-mediated signaling in genetic stroke susceptibility., Fornage, Myriam, Swank Michael W., Boerwinkle Eric, and Doris Peter A. , Physiological genomics, 2003 Sep 29, Volume 15, Issue 1, p.75-83, (2003) Abstract
Convergent evolution of the genomes of marine mammals., Foote, Andrew D., Liu Yue, Thomas Gregg W. C., Vinař Tomáš, Alföldi Jessica, Deng Jixin, Dugan Shannon, van Elk Cornelis E., Hunter Margaret E., Joshi Vandita, et al. , Nature genetics, 2015 Mar, Volume 47, Issue 3, p.272-5, (2015) Abstract
Analysis of microsatellite variation in Drosophila melanogaster with population-scale genome sequencing., Fondon, John W., Martin Andy, Richards Stephen, Gibbs Richard A., and Mittelman David , PloS one, 2012, Volume 7, Issue 3, p.e33036, (2012) Abstract
Internet Contig Explorer (iCE)--a tool for visualizing clone fingerprint maps., Fjell, Christopher D., Bosdet Ian, Schein Jacqueline E., Jones Steven J. M., and Marra Marco A. , Genome research, 2003 Jun, Volume 13, Issue 6A, p.1244-9, (2003) 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
Identification and removal of colanic acid from plasmid DNA preparations: implications for gene therapy., Firozi, P., Zhang W., Chen L., Quiocho F. A., Worley K. C., and Templeton N. S. , Gene therapy, 2010 Dec, Volume 17, Issue 12, p.1484-99, (2010) Abstract
l7Rn6 encodes a novel protein required for clara cell function in mouse lung development., Fernández-Valdivia, Rodrigo, Zhang Ying, Pai Sonia, Metzker Michael L., and Schumacher Armin , Genetics, 2006 Jan, Volume 172, Issue 1, p.389-99, (2006) Abstract
l7Rn6 encodes a novel protein required for clara cell function in mouse lung development., Fernández-Valdivia, Rodrigo, Zhang Ying, Pai Sonia, Metzker Michael L., and Schumacher Armin , Genetics, 2006 Jan, Volume 172, Issue 1, p.389-99, (2006) Abstract
Comparative genomics of Ceriporiopsis subvermispora and Phanerochaete chrysosporium provide insight into selective ligninolysis., Fernandez-Fueyo, Elena, Ruiz-Dueñas Francisco J., Ferreira Patricia, Floudas Dimitrios, Hibbett David S., Canessa Paulo, Larrondo Luis F., James Tim Y., Seelenfreund Daniela, Lobos Sergio, et al. , Proceedings of the National Academy of Sciences of the United States of America, 2012 Apr 3, Volume 109, Issue 14, p.5458-63, (2012) Abstract
Characterization of single-nucleotide variation in Indian-origin rhesus macaques (Macaca mulatta)., Fawcett, Gloria L., Raveendran Muthuswamy, Rio Deiros David, Chen David, Yu Fuli, Harris Ronald Alan, Ren Yanru, Muzny Donna M., Reid Jeffrey G., Wheeler David A., et al. , BMC genomics, 2011, Volume 12, p.311, (2011) Abstract
Genetic architecture of adiposity and organ weight using combined generation QTL analysis., Fawcett, Gloria L., Roseman Charles C., Jarvis Joseph P., Wang Bing, Wolf Jason B., and Cheverud James M. , Obesity (Silver Spring, Md.), 2008 Aug, Volume 16, Issue 8, p.1861-8, (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
Mutant analysis of the Shal (Kv4) voltage-gated fast transient K+ channel in Caenorhabditis elegans., Fawcett, Gloria L., Santi Celia M., Butler Alice, Harris Thanawath, Covarrubias Manuel, and Salkoff Lawrence , The Journal of biological chemistry, 2006 Oct 13, Volume 281, Issue 41, p.30725-35, (2006) Abstract
Whole-Exome Sequencing in Familial Parkinson Disease., Farlow, Janice L., Robak Laurie A., Hetrick Kurt, Bowling Kevin, Boerwinkle Eric, Coban-Akdemir Zeynep H., Gambin Tomasz, Gibbs Richard A., Gu Shen, Jain Preti, et al. , JAMA neurology, 2015 Nov 23, p.1-8, (2015) Abstract
Genomic and proteomic analysis of transcription factor TFII-I reveals insight into the response to cellular stress., Fan, Alex Xiucheng, Papadopoulos Giorgio L., Hossain Mir A., Lin I-Ju, Hu Jianhong, Tang Tommy Ming, Kilberg Michael S., Renne Rolf, Strouboulis John, and Bungert Jörg , Nucleic acids research, 2014, Volume 42, Issue 12, p.7625-41, (2014) Abstract
E
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
SINE retrotransposons cause epigenetic reprogramming of adjacent gene promoters., Estécio, Marcos R. H., Gallegos Juan, Dekmezian Mhair, Lu Yue, Liang Shoudan, and Issa Jean-Pierre J. , Molecular cancer research : MCR, 2012 Oct, Volume 10, Issue 10, p.1332-42, (2012) Abstract
Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathway., Enns, Gregory M., Shashi Vandana, Bainbridge Matthew, Gambello Michael J., Zahir Farah R., Bast Thomas, Crimian Rebecca, Schoch Kelly, Platt Julia, Cox Rachel, et al. , Genetics in medicine : official journal of the American College of Medical Genetics, 2014 Oct, Volume 16, Issue 10, p.751-8, (2014) Abstract
Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway, Enns, Gregory M., Shashi Vandana, Bainbridge Matthew, Gambello Michael J., Zahir Farah R., Bast Thomas, Crimian Rebecca, Schoch Kelly, Platt Julia, Cox Rachel, et al. , Genetics in Medicine, 03/2014, (2014)
Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathway., Enns, Gregory M., Shashi Vandana, Bainbridge Matthew, Gambello Michael J., Zahir Farah R., Bast Thomas, Crimian Rebecca, Schoch Kelly, Platt Julia, Cox Rachel, et al. , Genetics in medicine : official journal of the American College of Medical Genetics, 2014 Mar 20, (2014) Abstract


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