Skip to Content

Publications

Filters: First Letter Of Last Name is F  [Clear All Filters]
Journal Article
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
Lactobacillus reuteri Strain Combination In Helicobacter pylori Infection: A Randomized, Double-Blind, Placebo-Controlled Study., Francavilla, Ruggiero, Polimeno Lorenzo, Demichina Antonella, Maurogiovanni Giovanni, Principi Beatrice, Scaccianoce Giuseppe, Ierardi Enzo, Russo Francesco, Riezzo Giuseppe, Di Leo Alfredo, et al. , Journal of clinical gastroenterology, 2014 May-Jun, Volume 48, Issue 5, p.407-13, (2014) Abstract
Large scale variation in Enterococcus faecalis illustrated by the genome analysis of strain OG1RF., Bourgogne, Agathe, Garsin Danielle A., Qin Xiang, Singh Kavindra V., Sillanpaa Jouko, Yerrapragada Shailaja, Ding Yan, Dugan-Rocha Shannon, Buhay Christian, Shen Hua, et al. , Genome biology, 2008, Volume 9, Issue 7, p.R110, (2008) Abstract
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair., Day, Felix R., Ruth Katherine S., Thompson Deborah J., Lunetta Kathryn L., Pervjakova Natalia, Chasman Daniel I., Stolk Lisette, Finucane Hilary K., Sulem Patrick, Bulik-Sullivan Brendan, et al. , Nature genetics, 2015 Nov, Volume 47, Issue 11, p.1294-303, (2015) Abstract
Leptin mediates tumor-stromal interactions that promote the invasive growth of breast cancer cells., Barone, Ines, Catalano Stefania, Gelsomino Luca, Marsico Stefania, Giordano Cinzia, Panza Salvatore, Bonofiglio Daniela, Bossi Gianluca, Covington Kyle R., Fuqua Suzanne A. W., et al. , Cancer research, 2012 Mar 15, Volume 72, Issue 6, p.1416-27, (2012) Abstract
Leveraging biological replicates to improve analysis in ChIP-seq experiments., Yang, Yajie, Fear Justin, Hu Jianhong, Haecker Irina, Zhou Lei, Renne Rolf, Bloom David, and McIntyre Lauren M. , Computational and structural biotechnology journal, 2014, Volume 9, p.e201401002, (2014) Abstract
Lipoprotein associated phospholipase A2 activity, apolipoprotein C3 loss-of-function variants and cardiovascular disease: The Atherosclerosis Risk In Communities Study., Pokharel, Yashashwi, Sun Wensheng, Polfus Linda M., Folsom Aaron R., Heiss Gerardo, Sharrett Richey A., Boerwinkle Eric, Ballantyne Christie M., and Hoogeveen Ron C. , Atherosclerosis, 2015 Aug, Volume 241, Issue 2, p.641-8, (2015) Abstract
Long HIV-1 incubation periods and dynamics of transmission within a family., Burger, H., Belman A. L., Grimson R., Kaell A., Flaherty K., Gulla J., Gibbs R. A., Nguyun P. N., and Weiser B. , Lancet, 1990 Jul 21, Volume 336, Issue 8708, p.134-6, (1990) Abstract
Longitudinal changes in triglycerides according to ANGPTL4[E40K] genotype and longitudinal body weight change in the atherosclerosis risk in communities study., Nettleton, Jennifer A., Volcik Kelly A., Demerath Ellen W., Boerwinkle Eric, and Folsom Aaron R. , Annals of epidemiology, 2008 Nov, Volume 18, Issue 11, p.842-6, (2008) Abstract
Longitudinal study shows increasing obesity and hyperglycemia in micronesia., Murdock, David, Salit Jacqueline, Stoffel Markus, Friedman Jeffrey M., Pe'er Itsik, Breslow Jan L., and Bonnen Penelope E. , Obesity (Silver Spring, Md.), 2013 Sep, Volume 21, Issue 9, p.E421-7, (2013) Abstract
Loss of Rho GDIα and resistance to tamoxifen via effects on estrogen receptor α., Barone, Ines, Brusco Lauren, Gu Guowei, Selever Jennifer, Beyer Amanda, Covington Kyle R., Tsimelzon Anna, Wang Tao, Hilsenbeck Susan G., Chamness Gary C., et al. , Journal of the National Cancer Institute, 2011 Apr 6, Volume 103, Issue 7, p.538-52, (2011) Abstract
Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm., Lindsay, Mark E., Schepers Dorien, Bolar Nikhita Ajit, Doyle Jefferson J., Gallo Elena, Fert-Bober Justyna, Kempers Marlies J. E., Fishman Elliot K., Chen Yichun, Myers Loretha, et al. , Nature genetics, 2012 Aug, Volume 44, Issue 8, p.922-7, (2012) Abstract
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility., Wessel, Jennifer, Chu Audrey Y., Willems Sara M., Wang Shuai, Yaghootkar Hanieh, Brody Jennifer A., Dauriz Marco, Hivert Marie-France, Raghavan Sridharan, Lipovich Leonard, et al. , Nature communications, 2015, Volume 6, p.5897, (2015) Abstract
The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes., Skaletsky, Helen, Kuroda-Kawaguchi Tomoko, Minx Patrick J., Cordum Holland S., Hillier Ladeana, Brown Laura G., Repping Sjoerd, Pyntikova Tatyana, Ali Johar, Bieri Tamberlyn, et al. , Nature, 2003 Jun 19, Volume 423, Issue 6942, p.825-37, (2003) Abstract
Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators, Bellott, Daniel W., Hughes Jennifer F., Skaletsky Helen, Brown Laura G., Pyntikova Tatyana, Cho Ting-Jan, Koutseva Natalia, Zaghlul Sara, Graves Tina, Rock Susie, et al. , Nature, 4/2014, Volume 508, Issue 7497, p.494 - 499, (2014)
A Massive Expansion of Effector Genes Underlies Gall-Formation in the Wheat Pest Mayetiola destructor., Zhao, Chaoyang, Escalante Lucio Navarro, Chen Hang, Benatti Thiago R., Qu Jiaxin, Chellapilla Sanjay, Waterhouse Robert M., Wheeler David, Andersson Martin N., Bao Riyue, et al. , Current biology : CB, 2015 Mar 2, Volume 25, Issue 5, p.613-20, (2015) Abstract
The Matchmaker Exchange: A Platform for Rare Disease Gene Discovery., Philippakis, Anthony A., Azzariti Danielle R., Beltran Sergi, Brookes Anthony J., Brownstein Catherine A., Brudno Michael, Brunner Han G., Buske Orion J., Carey Knox, Doll Cassie, et al. , Human mutation, 2015 Oct, Volume 36, Issue 10, p.915-21, (2015) Abstract
The Matchmaker Exchange: a platform for rare disease gene discovery., Philippakis, Anthony A., Azzariti Danielle R., Beltran Sergi, Brookes Anthony J., Brownstein Catherine A., Brudno Michael, Brunner Han G., Buske Orion J., Carey Knox, Doll Cassie, et al. , Human mutation, 2015 Oct, Volume 36, Issue 10, p.915-21, (2015) Abstract
The MEDLINE Retriever., Fowler, J., Barber S., Gilson H., Long K. B., and Gorry G. A. , Proceedings / the ... Annual Symposium on Computer Application [sic] in Medical Care. Symposium on Computer Applications in Medical Care, 1992, p.473-7, (1992) Abstract
Metagenomic analyses of alcohol induced pathogenic alterations in the intestinal microbiome and the effect of Lactobacillus rhamnosus GG treatment., Bull-Otterson, Lara, Feng Wenke, Kirpich Irina, Wang Yuhua, Qin Xiang, Liu Yanlong, Gobejishvili Leila, Joshi-Barve Swati, Ayvaz Tulin, Petrosino Joseph, et al. , PloS one, 2013, Volume 8, Issue 1, p.e53028, (2013) Abstract
Metastasis tumor-associated protein 2 enhances metastatic behavior and is associated with poor outcomes in estrogen receptor-negative breast cancer., Covington, Kyle R., Brusco Lauren, Barone Ines, Tsimelzon Anna, Selever Jennifer, Corona-Rodriguez Arnoldo, Brown Powel, Kumar Rakesh, Hilsenbeck Susan G., and Fuqua Suzanne A. W. , Breast cancer research and treatment, 2013 Sep 28, (2013) Abstract
Microarray analysis of somatostatin receptor 5-regulated gene expression profiles in murine pancreas., Patel, Sanjeet G., Zhou Guisheng, Liu Shi-He, Li Min, Jeong Jae-Wook, DeMayo Francesco J., Gingras Marie-Claude, Gibbs Richard A., Fisher William E., and Brunicardi Charles F. , World journal of surgery, 2009 Apr, Volume 33, Issue 4, p.630-7, (2009) Abstract
Minimum information about a marker gene sequence (MIMARKS) and minimum information about any (x) sequence (MIxS) specifications., Yilmaz, Pelin, Kottmann Renzo, Field Dawn, Knight Rob, Cole James R., Amaral-Zettler Linda, Gilbert Jack A., Karsch-Mizrachi Ilene, Johnston Anjanette, Cochrane Guy, et al. , Nature biotechnology, 2011 May, Volume 29, Issue 5, p.415-20, (2011) Abstract
MMP2 genetic variation is associated with measures of fibrous cap thickness: The Atherosclerosis Risk in Communities Carotid MRI Study., Volcik, Kelly A., Campbell Stephen, Chambless Lloyd E., Coresh Josef, Folsom Aaron R., Mosley Thomas H., Ni Hanyu, Wagenknecht Lynne E., Wasserman Bruce A., and Boerwinkle Eric , Atherosclerosis, 2010 May, Volume 210, Issue 1, p.188-93, (2010) Abstract
Monoallelic and Biallelic Mutations in MAB21L2 Cause a Spectrum of Major Eye Malformations, Rainger, Joe, Pehlivan Davut, Johansson Stefan, Bengani Hemant, Sanchez-Pulido Luis, Williamson Kathleen A., Ture Mehmet, Barker Heather, Rosendahl Karen, Spranger Jürgen, et al. , The American Journal of Human Genetics, 06/2014, Volume 94, Issue 6, p.915 - 923, (2014)


about seo