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The human genome: genes, pseudogenes, and variation on chromosome 7., Waterston, R. H., Hillier L. W., Fulton L. A., Fulton R. S., Graves T. A., Pepin K. H., Bork P., Suyama M., Torrents D., Chinwalla A. T., et al. , Cold Spring Harbor symposia on quantitative biology, 2003, Volume 68, p.13-22, (2003)
A computational/functional genomics approach for the enrichment of the retinal transcriptome and the identification of positional candidate retinopathy genes., Katsanis, Nicholas, Worley Kim C., Gonzalez Guillermo, Ansley Stephen J., and Lupski James R. , Proceedings of the National Academy of Sciences of the United States of America, 2002 Oct 29, Volume 99, Issue 22, p.14326-31, (2002) Abstract
Molecular evidence of HIV-1 transmission in a criminal case., Metzker, Michael L., Mindell David P., Liu Xiao-Mei, Ptak Roger G., Gibbs Richard A., and Hillis David M. , Proceedings of the National Academy of Sciences of the United States of America, 2002 Oct 29, Volume 99, Issue 22, p.14292-7, (2002) Abstract
Mutation screening of two candidate genes from 13q32 in families affected with Bipolar disorder: human peptide transporter (SLC15A1) and human glypican5 (GPC5)., Maheshwari, Manjula, Christian S. L., Liu C., Badner J. A., Detera-Wadleigh S., Gershon E. S., and Gibbs Richard A. , BMC genomics, 2002 Oct 22, Volume 3, Issue 1, p.30, (2002) Abstract
Efficient isolation of targeted Caenorhabditis elegans deletion strains using highly thermostable restriction endonucleases and PCR., Wei, Aguan, Yuan Alex, Fawcett Gloria, Butler Alice, Davis Theodore, Xu Shuang-yong, and Salkoff Lawrence , Nucleic acids research, 2002 Oct 15, Volume 30, Issue 20, p.e110, (2002) 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
PTPN11 mutations in Noonan syndrome type I: detection of recurrent mutations in exons 3 and 13., Maheshwari, M., Belmont J., Fernbach S., Ho T., Molinari L., Yakub I., Yu F., Combes A., Towbin J., Craigen W. J., et al. , Human mutation, 2002 Oct, Volume 20, Issue 4, p.298-304, (2002) Abstract
Virulence effect of Enterococcus faecalis protease genes and the quorum-sensing locus fsr in Caenorhabditis elegans and mice., Sifri, Costi D., Mylonakis Eleftherios, Singh Kavindra V., Qin Xiang, Garsin Danielle A., Murray Barbara E., Ausubel Frederick M., and Calderwood Stephen B. , Infection and immunity, 2002 Oct, Volume 70, Issue 10, p.5647-50, (2002) Abstract
DNA polymerase III from Escherichia coli cells expressing mutA mistranslator tRNA is error-prone., Al Mamun, Abu Amar M., Marians Kenneth J., and Humayun Zafri M. , The Journal of biological chemistry, 2002 Nov 29, Volume 277, Issue 48, p.46319-27, (2002) Abstract
The latency-associated nuclear antigen of Kaposi's sarcoma-associated herpesvirus supports latent DNA replication in dividing cells., Hu, Jianhong, Garber Alexander C., and Renne Rolf , Journal of virology, 2002 Nov, Volume 76, Issue 22, p.11677-87, (2002) Abstract
Neighboring-nucleotide effects on single nucleotide polymorphisms: a study of 2.6 million polymorphisms across the human genome., Zhao, Zhongming, and Boerwinkle Eric , Genome research, 2002 Nov, Volume 12, Issue 11, p.1679-86, (2002) Abstract
Generalized T2 test for genome association studies., Xiong, Momiao, Zhao Jinying, and Boerwinkle Eric , American journal of human genetics, 2002 May, Volume 70, Issue 5, p.1257-68, (2002) Abstract
LPL polymorphism predicts stroke risk in men., Morrison, Alanna C., Ballantyne Christie M., Bray Molly, Chambless Lloyd E., Sharrett Richey A., and Boerwinkle Eric , Genetic epidemiology, 2002 Mar, Volume 22, Issue 3, p.233-42, (2002) Abstract
TREM-1, MDL-1, and DAP12 expression is associated with a mature stage of myeloid development., Gingras, Marie-Claude, Lapillonne Hélène, and Margolin Judith F. , Molecular immunology, 2002 Mar, Volume 38, Issue 11, p.817-24, (2002) Abstract
The cloning, genomic organization and tissue expression profile of the human DLG5 gene: Correction., Shah, Gopi, Brugada Ramon, Gonzalez Oscar, Czernuszewicz Grazyna, Gibbs Richard A., Bachinski Linda, and Roberts Robert , BMC genomics, 2002 Jun 11, Volume 3, p.14, (2002)
ADD1 460W allele associated with cardiovascular disease in hypertensive individuals., Morrison, Alanna C., Bray Molly S., Folsom Aaron R., and Boerwinkle Eric , Hypertension, 2002 Jun, Volume 39, Issue 6, p.1053-7, (2002) Abstract
Loader Lite: a new software tool for the ABI PRISM 3700 DNA sequencer., Scott, G. B. I., Steffen D. L., Edgar D., Warren J. T., Kovár C. L., Scherer S. E., Havlak P. H., and Gibbs R. A. , BioTechniques, 2002 Jun, Volume 32, Issue 6, p.1366, 1368, 1370-1, (2002) Abstract
Intron-size constraint as a mutational mechanism in Rothmund-Thomson syndrome., Wang, Lisa L., Worley Kim, Gannavarapu Anu, Chintagumpala Murali M., Levy Moise L., and Plon Sharon E. , American journal of human genetics, 2002 Jul, Volume 71, Issue 1, p.165-7, (2002) Abstract
Factor XIIIA Val34Leu polymorphism does not predict risk of coronary heart disease: The Atherosclerosis Risk in Communities (ARIC) Study., Aleksic, Nena, Ahn Chul, Wang Yao-Wei, Juneja Harinder, Folsom Aaron R., Boerwinkle Eric, and Wu Kenneth K. , Arteriosclerosis, thrombosis, and vascular biology, 2002 Feb 1, Volume 22, Issue 2, p.348-52, (2002) Abstract
Initial sequencing and comparative analysis of the mouse genome., Waterston, Robert H., Lindblad-Toh Kerstin, Birney Ewan, Rogers Jane, Abril Josep F., Agarwal Pankaj, Agarwala Richa, Ainscough Rachel, Alexandersson Marina, An Peter, et al. , Nature, 2002 Dec 5, Volume 420, Issue 6915, p.520-62, (2002) Abstract
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences., Strausberg, Robert L., Feingold Elise A., Grouse Lynette H., Derge Jeffery G., Klausner Richard D., Collins Francis S., Wagner Lukas, Shenmen Carolyn M., Schuler Gregory D., Altschul Stephen F., et al. , Proceedings of the National Academy of Sciences of the United States of America, 2002 Dec 24, Volume 99, Issue 26, p.16899-903, (2002) 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
Haplotype and linkage disequilibrium architecture for human cancer-associated genes., Bonnen, Penelope E., Wang Peggy J., Kimmel Marek, Chakraborty Ranajit, and Nelson David L. , Genome research, 2002 Dec, Volume 12, Issue 12, p.1846-53, (2002) Abstract
The beta-globin C-->G mutation at 6 bp 3' to the termination codon causes beta-thalassaemia by decreasing the mRNA level., Sgourou, Argyro, Papachatzopoulou Adamandia, Psiouri Lambrini, Antoniou Michael, Zoumbos Nicholas, Gibbs Richard, and Athanassiadou Aglaia , British journal of haematology, 2002 Aug, Volume 118, Issue 2, p.671-6, (2002) Abstract

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