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Mapping a locus for familial thoracic aortic aneurysms and dissections (TAAD2) to 3p24-25., Hasham, Sumera N., Willing Marcia C., Guo Dong-Chuan, Muilenburg Ann, He Rumin, Tran Van T., Scherer Steven E., Shete Sanjay S., and Milewicz Dianna M. , Circulation, 2003 Jul 1, Volume 107, Issue 25, p.3184-90, (2003) Abstract
Evolutionary genetics and implications of small size and twinning in callitrichine primates., Harris, Alan R., Tardif Suzette D., Vinar Tomas, Wildman Derek E., Rutherford Julienne N., Rogers Jeffrey, Worley Kim C., and Aagaard Kjersti M. , Proceedings of the National Academy of Sciences of the United States of America, 2014 Jan 28, Volume 111, Issue 4, p.1467-72, (2014) Abstract
Human-specific changes of genome structure detected by genomic triangulation., Harris, R. A., Rogers J., and Milosavljevic A. , Science (New York, N.Y.), 2007 Apr 13, Volume 316, Issue 5822, p.235-7, (2007) Abstract
WormBase: a multi-species resource for nematode biology and genomics., Harris, Todd W., Chen Nansheng, Cunningham Fiona, Tello-Ruiz Marcela, Antoshechkin Igor, Bastiani Carol, Bieri Tamberlyn, Blasiar Darin, Bradnam Keith, Chan Juancarlos, et al. , Nucleic acids research, 2004 Jan 1, Volume 32, Issue Database issue, p.D411-7, (2004) Abstract
Building a comprehensive genomic program for hepatocellular carcinoma., Harring, Theresa R., Guiteau Jacfranz J., Nguyen Thao N. T., Cotton Ron T., Gingras Marie-Claude, Wheeler David A., O'Mahony Christine A., Gibbs Richard A., Brunicardi Charles F., and Goss John A. , World journal of surgery, 2011 Aug, Volume 35, Issue 8, p.1746-50, (2011) Abstract
Treponema pallidum infection in the wild baboons of East Africa: distribution and genetic characterization of the strains responsible., Harper, Kristin N., Fyumagwa Robert D., Hoare Richard, Wambura Philemon N., Coppenhaver Dorian H., Sapolsky Robert M., Alberts Susan C., Tung Jenny, Rogers Jeffrey, Kilewo Morris, et al. , PloS one, 2012, Volume 7, Issue 12, p.e50882, (2012) Abstract
Association of glycemic index and glycemic load with risk of incident coronary heart disease among Whites and African Americans with and without type 2 diabetes: the Atherosclerosis Risk in Communities study., Hardy, Dale S., Hoelscher Deanna M., Aragaki Corinne, Stevens June, Steffen Lyn M., Pankow James S., and Boerwinkle Eric , Annals of epidemiology, 2010 Aug, Volume 20, Issue 8, p.610-6, (2010) Abstract
Highly multiplexed molecular inversion probe genotyping: over 10,000 targeted SNPs genotyped in a single tube assay., Hardenbol, Paul, Yu Fuli, Belmont John, Mackenzie Jennifer, Bruckner Carsten, Brundage Tiffany, Boudreau Andrew, Chow Steve, Eberle Jim, Erbilgin Ayca, et al. , Genome research, 2005 Feb, Volume 15, Issue 2, p.269-75, (2005) Abstract
Mutational analysis of the latency-associated nuclear antigen DNA-binding domain of Kaposi's sarcoma-associated herpesvirus reveals structural conservation among gammaherpesvirus origin-binding proteins., Han, Soo-Jin, Hu Jianhong, Pierce Brian, Weng Zhiping, and Renne Rolf , The Journal of general virology, 2010 Sep, Volume 91, Issue Pt 9, p.2203-15, (2010) Abstract
A sequence-level map of chromosomal breakpoints in the MCF-7 breast cancer cell line yields insights into the evolution of a cancer genome., Hampton, Oliver A., Den Hollander Petra, Miller Christopher A., Delgado David A., Li Jian, Coarfa Cristian, Harris Ronald A., Richards Stephen, Scherer Steven E., Muzny Donna M., et al. , Genome research, 2009 Feb, Volume 19, Issue 2, p.167-77, (2009) Abstract
Long-range massively parallel mate pair sequencing detects distinct mutations and similar patterns of structural mutability in two breast cancer cell lines., Hampton, Oliver A., Koriabine Maxim, Miller Christopher A., Coarfa Cristian, Li Jian, Den Hollander Petra, Schoenherr Caroline, Carbone Lucia, Nefedov Mikhail, Ten Hallers Boudewijn F. H., et al. , Cancer genetics, 2011 Aug, Volume 204, Issue 8, p.447-57, (2011) 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
A genome-wide linkage scan for diabetic retinopathy susceptibility genes in Mexican Americans with type 2 diabetes from Starr County, Texas., Hallman, Michael D., Boerwinkle Eric, Gonzalez Victor H., Klein Barbara E. K., Klein Ronald, and Hanis Craig L. , Diabetes, 2007 Apr, Volume 56, Issue 4, p.1167-73, (2007) Abstract
Relation of PCSK9 mutations to serum low-density lipoprotein cholesterol in childhood and adulthood (from The Bogalusa Heart Study)., Hallman, Michael D., Srinivasan Sathanur R., Chen Wei, Boerwinkle Eric, and Berenson Gerald S. , The American journal of cardiology, 2007 Jul 1, Volume 100, Issue 1, p.69-72, (2007) Abstract
The beta(2)-adrenergic receptor Arg16-gly polymorphism and interactions involving beta(2)- and beta(3)-adrenergic receptor polymorphisms are associated with variations in longitudinal serum lipid profiles: the Bogalusa Heart Study., Hallman, Michael D., Srinivasan Sathanur R., Chen Wei, Boerwinkle Eric, and Berenson Gerald S. , Metabolism: clinical and experimental, 2004 Sep, Volume 53, Issue 9, p.1184-91, (2004) Abstract
Relationship between low-density lipoprotein subclasses and asymptomatic atherosclerosis in subjects from the Atherosclerosis Risk in Communities (ARIC) Study., Hallman, Michael D., Brown Spencer A., Ballantyne Christie M., Sharrett Richey A., and Boerwinkle Eric , Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals, 2004 Mar-Apr, Volume 9, Issue 2, p.190-202, (2004) Abstract
Longitudinal analysis of haplotypes and polymorphisms of the APOA5 and APOC3 genes associated with variation in serum triglyceride levels: the Bogalusa Heart Study., Hallman, Michael D., Srinivasan Sathanur R., Chen Wei, Boerwinkle Eric, and Berenson Gerald S. , Metabolism: clinical and experimental, 2006 Dec, Volume 55, Issue 12, p.1574-81, (2006) Abstract
Adverse outcomes in clear cell renal cell carcinoma with mutations of 3p21 epigenetic regulators BAP1 and SETD2: a report by MSKCC and the KIRC TCGA research network., Hakimi, Ari A., Ostrovnaya Irina, Reva Boris, Schultz Nikolaus, Chen Ying-Bei, Gonen Mithat, Liu Han, Takeda Shugaku, Voss Martin H., Tickoo Satish K., et al. , Clinical cancer research : an official journal of the American Association for Cancer Research, 2013 Jun 15, Volume 19, Issue 12, p.3259-67, (2013) Abstract
Large-scale identification of chemically induced mutations in Drosophila melanogaster., Haelterman, Nele A., Jiang Lichun, Li Yumei, Bayat Vafa, Sandoval Hector, Ugur Berrak, Tan Kai Li, Zhang Ke, Bei Danqing, Xiong Bo, et al. , Genome research, 2014 Oct, Volume 24, Issue 10, p.1707-18, (2014) Abstract
Ago HITS-CLIP expands understanding of Kaposi's sarcoma-associated herpesvirus miRNA function in primary effusion lymphomas., Haecker, Irina, Gay Lauren A., Yang Yajie, Hu Jianhong, Morse Alison M., McIntyre Lauren M., and Renne Rolf , PLoS pathogens, 2012, Volume 8, Issue 8, p.e1002884, (2012) Abstract
A-beta-subtype of ketosis-prone diabetes is not predominantly a monogenic diabetic syndrome., Haaland, Wade C., Scaduto Diane I., Maldonado Mario R., Mansouri Dena L., Nalini Ramaswami, Iyer Dinakar, Patel Sanjeet, Guthikonda Anu, Hampe Christiane S., Balasubramanyam Ashok, et al. , Diabetes care, 2009 May, Volume 32, Issue 5, p.873-7, (2009) Abstract
Genomic scanning for expressed sequences in Xp21 identifies the glycerol kinase gene., Guo, W., Worley K., Adams V., Mason J., Sylvester-Jackson D., Zhang Y. H., Towbin J. A., Fogt D. D., Madu S., and Wheeler D. A. , Nature genetics, 1993 Aug, Volume 4, Issue 4, p.367-72, (1993) Abstract
Bayesian estimation of genomic copy number with single nucleotide polymorphism genotyping arrays., Guo, Beibei, Villagran Alejandro, Vannucci Marina, Wang Jian, Davis Caleb F., Man Tsz-Kwong, Lau Ching, and Guerra Rudy , BMC research notes, 2010, Volume 3, p.350, (2010) Abstract
Familial thoracic aortic aneurysms and dissections: identification of a novel locus for stable aneurysms with a low risk for progression to aortic dissection., Guo, Dong-Chuan, Regalado Ellen S., Minn Charles, Tran-Fadulu Van, Coney Joshua, Cao Jiumei, Wang Min, Yu Robert K., Estrera Anthony L., Safi Hazim J., et al. , Circulation. Cardiovascular genetics, 2011 Feb, Volume 4, Issue 1, p.36-42, (2011) Abstract
Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease., Guo, Dong-Chuan, Papke Christina L., Tran-Fadulu Van, Regalado Ellen S., Avidan Nili, Johnson Ralph Jay, Kim Dong H., Pannu Hariyadarshi, Willing Marcia C., Sparks Elizabeth, et al. , American journal of human genetics, 2009 May, Volume 84, Issue 5, p.617-27, (2009) Abstract

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