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CRHR1 genotypes, neural circuits and the diathesis for anxiety and depression., Rogers, J., Raveendran M., Fawcett G. L., Fox A. S., Shelton S. E., Oler J. A., Cheverud J., Muzny D. M., Gibbs R. A., Davidson R. J., et al. , Molecular psychiatry, 2013 Jun, Volume 18, Issue 6, p.700-7, (2013) Abstract
Corticotropin releasing hormone (CRH) gene variation: comprehensive resequencing for variant and molecular haplotype discovery in monosomic hybrid cell lines., Shimmin, Lawrence C., Natarajan Sivamani, Ibarguen Heladio, Montasser May, Kim Do-Kyun, Hanis Craig L., Boerwinkle Eric, Wadhwa Pathik D., and Hixson James E. , DNA sequence : the journal of DNA sequencing and mapping, 2007 Dec, Volume 18, Issue 6, p.434-44, (2007) Abstract
Cortical sulcal areas in baboons (Papio hamadryas spp.) with generalized interictal epileptic discharges on scalp EEG., Szabó, C. A., Kochunov P., Knape K. D., McCoy K. J. M., Leland M. M., Lancaster J. L., Fox P. T., Williams J. T., and Rogers J. , Epilepsy research, 2011 Feb, Volume 93, Issue 2-3, p.91-5, (2011) Abstract
Coronary heart disease and genetic variants with low phospholipase A2 activity., Polfus, Linda M., Gibbs Richard A., and Boerwinkle Eric , The New England journal of medicine, 2015 Jan 15, Volume 372, Issue 3, p.295-6, (2015)
Copy number variation of CCL3-like genes affects rate of progression to simian-AIDS in Rhesus Macaques (Macaca mulatta)., Degenhardt, Jeremiah D., de Candia Paola, Chabot Adrien, Schwartz Stuart, Henderson Les, Ling Binhua, Hunter Meredith, Jiang Zhaoshi, Palermo Robert E., Katze Michael, et al. , PLoS genetics, 2009 Jan, Volume 5, Issue 1, p.e1000346, (2009) Abstract
Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion., Xi, Ruibin, Hadjipanayis Angela G., Luquette Lovelace J., Kim Tae-Min, Lee Eunjung, Zhang Jianhua, Johnson Mark D., Muzny Donna M., Wheeler David A., Gibbs Richard A., et al. , Proceedings of the National Academy of Sciences of the United States of America, 2011 Nov 15, Volume 108, Issue 46, p.E1128-36, (2011) Abstract
COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis., Watkin, Levi B., Jessen Birthe, Wiszniewski Wojciech, Vece Timothy J., Jan Max, Sha Youbao, Thamsen Maike, Santos-Cortez Regie L. P., Lee Kwanghyuk, Gambin Tomasz, et al. , Nature genetics, 2015 Apr 20, (2015) Abstract
Cooperation between the TNF receptors demonstrated by TNF receptor knockout mice, Shinbrot, Eve, and Moore Mark , Cytokine Knockouts. Humana Press, New Jersey, Volume 89, (1998)
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
Construction of small genome BAC library for functional and genomic applications., Smajs, David, Norris Steven J., and Weinstock George M. , Methods in molecular biology (Clifton, N.J.), 2004, Volume 255, p.47-56, (2004)
Construction of a high-resolution physical map of the chromosome 10q22-q23 dilated cardiomyopathy locus and analysis of candidate genes., Bowles, K. R., Abraham S. E., Brugada R., Zintz C., Comeaux J., Sorajja D., Tsubata S., Li H., Brandon L., Gibbs R. A., et al. , Genomics, 2000 Jul 15, Volume 67, Issue 2, p.109-27, (2000) Abstract
Consistent effects of genes involved in reverse cholesterol transport on plasma lipid and apolipoprotein levels in CARDIA participants., Klos, Kathy L. E., Sing Charles F., Boerwinkle Eric, Hamon Sara C., Rea Thomas J., Clark Andrew, Fornage Myriam, and Hixson James E. , Arteriosclerosis, thrombosis, and vascular biology, 2006 Aug, Volume 26, Issue 8, p.1828-36, (2006) Abstract
Conservation of virally encoded microRNAs in Kaposi sarcoma--associated herpesvirus in primary effusion lymphoma cell lines and in patients with Kaposi sarcoma or multicentric Castleman disease., Marshall, Vickie, Parks Thomas, Bagni Rachel, Wang Cheng Dian, Samols Mark A., Hu Jianhong, Wyvil Kathleen M., Aleman Karen, Little Richard F., Yarchoan Robert, et al. , The Journal of infectious diseases, 2007 Mar 1, Volume 195, Issue 5, p.645-59, (2007) Abstract
Conservation of human chromosome 18 in baboons (Papio hamadryas): a linkage map of eight human microsatellites., Perelygin, A. A., Kammerer C. M., Stowell N. C., and Rogers J. , Cytogenetics and cell genetics, 1996, Volume 75, Issue 4, p.207-9, (1996) Abstract
Concatenation cDNA sequencing for transcriptome analysis., Gunaratne, Preethi H., Wu Jiaqian, Garcia Angela M., Hulyk Steven, Worley Kim C., Margolin Judith F., and Gibbs Richard A. , Comptes rendus biologies, 2003 Oct-Nov, Volume 326, Issue 10-11, p.971-7, (2003) Abstract
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
Comprehensive Molecular Diagnosis of a Large Chinese Leber Congenital Amaurosis Cohort., Wang, Hui, Wang Xia, Zou Xuan, Xu Shan, Li Hui, Soens Zachry Tore, Wang Keqing, Li Yumei, Dong Fangtian, Chen Rui, et al. , Investigative ophthalmology & visual science, 2015 Jun, Volume 56, Issue 6, p.3642-55, (2015) Abstract
Comprehensive molecular diagnosis of 67 Chinese Usher syndrome probands: high rate of ethnicity specific mutations in Chinese USH patients., Jiang, Lichun, Liang Xiaofang, Li Yumei, Wang Jing, Zaneveld Jacques Eric, Wang Hui, Xu Shan, Wang Keqing, Wang Binbin, Chen Rui, et al. , Orphanet journal of rare diseases, 2015, Volume 10, Issue 1, p.110, (2015) Abstract
Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing., Wang, Xia, Wang Hui, Sun Vincent, Tuan Han-Fang, Keser Vafa, Wang Keqing, Ren Huanan, Lopez Irma, Zaneveld Jacques E., Siddiqui Sorath, et al. , Journal of medical genetics, 2013 Oct, Volume 50, Issue 10, p.674-88, (2013) Abstract
Comprehensive molecular characterization of human colon and rectal cancer., Shinbrot, Eve , Nature, 2012 Jul 19, Volume 487, Issue 7407, p.330-7, (2012) Abstract
Comprehensive molecular characterization of clear cell renal cell carcinoma., Davis, Caleb F. , Nature, 2013 Jul 4, Volume 499, Issue 7456, p.43-9, (2013) Abstract

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