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The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer., Pomerantz, Mark M., Ahmadiyeh Nasim, Jia Li, Herman Paula, Verzi Michael P., Doddapaneni Harshavardhan, Beckwith Christine A., Chan Jennifer A., Hills Adam, Davis Matt, et al. , Nature genetics, 2009 Aug, Volume 41, Issue 8, p.882-4, (2009) Abstract
A
Aggressive tumor growth and clinical evolution in a patient with X-linked acro-gigantism syndrome., Naves, Luciana A., Daly Adrian F., Dias Luiz Augusto, Yuan Bo, Zakir Juliano Coelho Oliveira, Barra Gustavo Barcellos, Palmeira Leonor, Villa Chiara, Trivellin Giampaolo, Júnior Armindo Jreige, et al. , Endocrine, 2015 Nov 25, (2015) Abstract
Allelic Mutations of KITLG, Encoding KIT Ligand, Cause Asymmetric and Unilateral Hearing Loss and Waardenburg Syndrome Type 2., Zazo Seco, Celia, Serrão de Castro Luciana, van Nierop Josephine W., Morín Matías, Jhangiani Shalini, Verver Eva J. J., Schraders Margit, Maiwald Nadine, Wesdorp Mieke, Venselaar Hanka, et al. , American journal of human genetics, 2015 Nov 5, Volume 97, Issue 5, p.647-60, (2015) Abstract
Ampullary Cancers Harbor the Tumor Suppressor Gene ELF3 and Exhibit Frequent WNT Dysregulation., Gingras, Marie-Claude, Covington Kyle R., Chang David K., Donehower Lawrence A., Gill Anthony J., Ittmann Michael M., Creighton Chad J., Johns Amber L., Shinbrot Eve, Dewal Ninad, et al. , Cell reports, 2016 Jan 19, (2016) Abstract
Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome., Margulies, Elliott H., Cooper Gregory M., Asimenos George, Thomas Daryl J., Dewey Colin N., Siepel Adam, Birney Ewan, Keefe Damian, Schwartz Ariel S., Hou Minmei, et al. , Genome research, 2007 Jun, Volume 17, Issue 6, p.760-74, (2007) Abstract
Assemblathon 2: evaluating de novo methods of genome assembly in three vertebrate species., Bradnam, Keith R., Fass Joseph N., Alexandrov Anton, Baranay Paul, Bechner Michael, Birol Inanç, Boisvert Sébastien, Chapman Jarrod A., Chapuis Guillaume, Chikhi Rayan, et al. , GigaScience, 2013 Jul 22, Volume 2, Issue 1, p.10, (2013) Abstract
Association of exome sequences with plasma C-reactive protein levels in >9000 participants, Schick, U. M., Auer P. L., Bis J. C., Lin H., Wei P., Pankratz N., Lange L. A., Brody J., Stitziel N. O., Kim D. S., et al. , Human Molecular Genetics, (2014)
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks., Peloso, Gina M., Auer Paul L., Bis Joshua C., Voorman Arend, Morrison Alanna C., Stitziel Nathan O., Brody Jennifer A., Khetarpal Sumeet A., Crosby Jacy R., Fornage Myriam, et al. , American journal of human genetics, 2014 Feb 6, Volume 94, Issue 2, p.223-32, (2014) Abstract
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
Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3., Chong, Jessica X., Burrage Lindsay C., Beck Anita E., Marvin Colby T., McMillin Margaret J., Shively Kathryn M., Harrell Tanya M., Buckingham Kati J., Bacino Carlos A., Jain Mahim, et al. , American journal of human genetics, 2015 May 7, Volume 96, Issue 5, p.841-9, (2015) Abstract
B
A BAC-based physical map of the major autosomes of Drosophila melanogaster., Hoskins, R. A., Nelson C. R., Berman B. P., Laverty T. R., George R. A., Ciesiolka L., Naeemuddin M., Arenson A. D., Durbin J., David R. G., et al. , Science (New York, N.Y.), 2000 Mar 24, Volume 287, Issue 5461, p.2271-4, (2000) Abstract
Bacterial discrimination by dictyostelid amoebae reveals the complexity of ancient interspecies interactions., Nasser, Waleed, Santhanam Balaji, Miranda Edward Roshan, Parikh Anup, Juneja Kavina, Rot Gregor, Dinh Chris, Chen Rui, Zupan Blaz, Shaulsky Gad, et al. , Current biology : CB, 2013 May 20, Volume 23, Issue 10, p.862-72, (2013) Abstract
Beta 2 adrenergic receptor 5' haplotypes influence promoter activity., Johnatty, Sharon E., Abdellatif Maha, Shimmin Lawrence, Clark Richard B., and Boerwinkle Eric , British journal of pharmacology, 2002 Dec, Volume 137, Issue 8, p.1213-6, (2002) Abstract
Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability., Stray-Pedersen, Asbjørg, Cobben Jan-Maarten, Prescott Trine E., Lee Sora, Cang Chunlei, Aranda Kimberly, Ahmed Sohnee, Alders Marielle, Gerstner Thorsten, Aslaksen Kathinka, et al. , American journal of human genetics, 2015 Dec 16, (2015) Abstract
Bioactivity and Bioavailability of Ginsenosides are Dependent on the Glycosidase Activities of the A/J Mouse Intestinal Microbiome Defined by Pyrosequencing., Niu, Tao, Smith Diane L., Yang Zhen, Gao Song, Yin Taijun, Jiang Zhi-Hong, You Ming, Gibbs Richard A., Petrosino Joseph F., and Hu Ming , Pharmaceutical research, 2013 Mar, Volume 30, Issue 3, p.836-46, (2013) Abstract
Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway., Jin, Peng, Zarnescu Daniela C., Ceman Stephanie, Nakamoto Mika, Mowrey Julie, Jongens Thomas A., Nelson David L., Moses Kevin, and Warren Stephen T. , Nature neuroscience, 2004 Feb, Volume 7, Issue 2, p.113-7, (2004) Abstract
Biological characterization and next-generation genome sequencing of the unclassified Cotia virus SPAn232 (Poxviridae)., Afonso, Priscila P., Silva Patrícia M., Schnellrath Laila C., Jesus Desyreé M., Hu Jianhong, Yang Yajie, Renne Rolf, Attias Marcia, Condit Richard C., Moussatché Nissin, et al. , Journal of virology, 2012 May, Volume 86, Issue 9, p.5039-54, (2012) Abstract
Bos taurus genome assembly., Liu, Yue, Qin Xiang, Song Xing-Zhi Henry, Jiang Huaiyang, Shen Yufeng, Durbin James K., Lien Sigbjørn, Kent Matthew Peter, Sodeland Marte, Ren Yanru, et al. , BMC genomics, 2009, Volume 10, p.180, (2009) Abstract
C
Calpain-10 is a component of the obesity-related quantitative trait locus Adip1., Cheverud, James M., Fawcett Gloria L., Jarvis Joseph P., Norgard Elizabeth A., Pavlicev Mihaela, Pletscher Susan L., Polonsky Kenneth S., Ye Honggang, Bell Graeme I., and Semenkovich Clay F. , Journal of lipid research, 2010 May, Volume 51, Issue 5, p.907-13, (2010) Abstract
The Cancer Genome Atlas Pan-Cancer analysis project., Chang, Kyle, Creighton Chad J., Davis Caleb F., Donehower Lawrence, Drummond Jennifer, Wheeler David, Ally Adrian, Balasundaram Miruna, Birol Inanc, Butterfield Yaron S. N., et al. , Nature genetics, 2013 Sep 26, Volume 45, Issue 10, p.1113-20, (2013)
A catalog of reference genomes from the human microbiome., Nelson, Karen E., Weinstock George M., Highlander Sarah K., Worley Kim C., Creasy Heather Huot, Wortman Jennifer Russo, Rusch Douglas B., Mitreva Makedonka, Sodergren Erica, Chinwalla Asif T., et al. , Science (New York, N.Y.), 2010 May 21, Volume 328, Issue 5981, p.994-9, (2010) Abstract
Characterization of HPV and host genome interactions in primary head and neck cancers., Parfenov, Michael, Pedamallu Chandra Sekhar, Gehlenborg Nils, Freeman Samuel S., Danilova Ludmila, Bristow Christopher A., Lee Semin, Hadjipanayis Angela G., Ivanova Elena V., Wilkerson Matthew D., et al. , Proceedings of the National Academy of Sciences of the United States of America, 2014 Oct 13, (2014) Abstract
Characterizing the cancer genome in lung adenocarcinoma., Weir, Barbara A., Woo Michele S., Getz Gad, Perner Sven, Ding Li, Beroukhim Rameen, Lin William M., Province Michael A., Kraja Aldi, Johnson Laura A., et al. , Nature, 2007 Dec 6, Volume 450, Issue 7171, p.893-8, (2007) Abstract
Chromosome rearrangement and diversification of Francisella tularensis revealed by the type B (OSU18) genome sequence., Petrosino, Joseph F., Xiang Qin, Karpathy Sandor E., Jiang Huaiyang, Yerrapragada Shailaja, Liu Yamei, Gioia Jason, Hemphill Lisa, Gonzalez Arely, Raghavan T. M., et al. , Journal of bacteriology, 2006 Oct, Volume 188, Issue 19, p.6977-85, (2006) Abstract
Color-blind fluorescence detection for four-color DNA sequencing., Lewis, Ernest K., Haaland Wade C., Nguyen Freddy, Heller Daniel A., Allen Matthew J., MacGregor Robert R., Berger Scott C., Willingham Britain, Burns Lori A., Scott Graham B. I., et al. , Proceedings of the National Academy of Sciences of the United States of America, 2005 Apr 12, Volume 102, Issue 15, p.5346-51, (2005) Abstract


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