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APOA5 polymorphisms influence plasma triglycerides in young, healthy African Americans and whites of the CARDIA Study., Klos, Kathy L. E., Hamon Sara, Clark Andrew G., Boerwinkle Eric, Liu Kiang, and Sing Charles F. , Journal of lipid research, 2005 Mar, Volume 46, Issue 3, p.564-71, (2005) Abstract
ESR1 polymorphism is associated with plasma lipid and apolipoprotein levels in Caucasians of the Rochester Family Heart Study., Klos, Kathy L. E., Boerwinkle Eric, Ferrell Robert E., Turner Stephen T., and Morrison Alanna C. , Journal of lipid research, 2008 Aug, Volume 49, Issue 8, p.1701-6, (2008) 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
APOE/C1/C4/C2 hepatic control region polymorphism influences plasma apoE and LDL cholesterol levels., Klos, Kathy, Shimmin Lawrence, Ballantyne Christie, Boerwinkle Eric, Clark Andrew, Coresh Josef, Hanis Craig, Liu Kiang, Sayre Scott, and Hixson James , Human molecular genetics, 2008 Jul 1, Volume 17, Issue 13, p.2039-46, (2008) Abstract
Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy., Klassen, Tara, Davis Caleb F., Goldman Alica, Burgess Dan, Chen Tim, Wheeler David, McPherson John, Bourquin Traci, Lewis Lora, Villasana Donna, et al. , Cell, 2011 Jun 24, Volume 145, Issue 7, p.1036-48, (2011) Abstract
Evidence for alternative candidate genes near RB1 involved in clonal expansion of in situ urothelial neoplasia., Kim, Mi-Sook, Jeong Joon, Majewski Tadeusz, Kram Andrzej, Yoon Dong-Sup, Zhang Ruo-Dan, Li Jun-Zhi, Ptaszynski Konrad, Kuang Tang C., Zhou Jain-Hua, et al. , Laboratory investigation; a journal of technical methods and pathology, 2006 Feb, Volume 86, Issue 2, p.175-90, (2006) Abstract
The fms21 (pilA)-fms20 locus encoding one of four distinct pili of Enterococcus faecium is harboured on a large transferable plasmid associated with gut colonization and virulence., Kim, David S., Singh Kavindra V., Nallapareddy Sreedhar R., Qin Xiang, Panesso Diana, Arias Cesar A., and Murray Barbara E. , Journal of medical microbiology, 2010 Apr, Volume 59, Issue Pt 4, p.505-7, (2010)
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies., Khanna, Hemant, Davis Erica E., Murga-Zamalloa Carlos A., Estrada-Cuzcano Alejandro, Lopez Irma, den Hollander Anneke I., Zonneveld Marijke N., Othman Mohammad I., Waseem Naushin, Chakarova Christina F., et al. , Nature genetics, 2009 Jun, Volume 41, Issue 6, p.739-45, (2009) Abstract
Pleiotropic patterns of quantitative trait loci for 70 murine skeletal traits., Kenney-Hunt, Jane P., Wang Bing, Norgard Elizabeth A., Fawcett Gloria, Falk Doug, Pletscher Susan L., Jarvis Joseph P., Roseman Charles, Wolf Jason, and Cheverud James M. , Genetics, 2008 Apr, Volume 178, Issue 4, p.2275-88, (2008) Abstract
An evaluation of the draft human genome sequence., Katsanis, N., Worley K. C., and Lupski J. R. , Nature genetics, 2001 Sep, Volume 29, Issue 1, p.88-91, (2001) 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
Genome sequence of Fusobacterium nucleatum subspecies polymorphum - a genetically tractable fusobacterium., Karpathy, Sandor E., Qin Xiang, Gioia Jason, Jiang Huaiyang, Liu Yamei, Petrosino Joseph F., Yerrapragada Shailaja, Fox George E., Haake Susan Kinder, Weinstock George M., et al. , PloS one, 2007, Volume 2, Issue 7, p.e659, (2007) Abstract
Drosophila eyes absent is required for normal cone and pigment cell development., Karandikar, Umesh C., Jin Meng, Jusiak Barbara, Kwak SuJin, Chen Rui, and Mardon Graeme , PloS one, 2014, Volume 9, Issue 7, p.e102143, (2014) Abstract
Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease., Karaca, Ender, Harel Tamar, Pehlivan Davut, Jhangiani Shalini N., Gambin Tomasz, Akdemir Zeynep Coban, Gonzaga-Jauregui Claudia, Erdin Serkan, Bayram Yavuz, Campbell Ian M., et al. , Neuron, 2015 Nov 4, Volume 88, Issue 3, p.499-513, (2015) Abstract
Rare variants in the notch signaling pathway describe a novel type of autosomal recessive Klippel-Feil syndrome., Karaca, Ender, Yuregir Ozge O., Bozdogan Sevcan T., Aslan Huseyin, Pehlivan Davut, Jhangiani Shalini N., Akdemir Zeynep C., Gambin Tomasz, Bayram Yavuz, Atik Mehmed M., et al. , American journal of medical genetics. Part A, 2015 Aug 4, (2015) Abstract
Human CLP1 Mutations Alter tRNA Biogenesis, Affecting Both Peripheral and Central Nervous System Function., Karaca, Ender, Weitzer Stefan, Pehlivan Davut, Shiraishi Hiroshi, Gogakos Tasos, Hanada Toshikatsu, Jhangiani Shalini N., Wiszniewski Wojciech, Withers Marjorie, Campbell Ian M., et al. , Cell, 2014 Apr 24, Volume 157, Issue 3, p.636-50, (2014) Abstract
Resources for genetic management and genomics research on non-human primates at the National Primate Research Centers (NPRCs)., Kanthaswamy, S., Capitanio J. P., Dubay C. J., Ferguson B., Folks T., Ha J. C., Hotchkiss C. E., Johnson Z. P., Katze M. G., Kean L. S., et al. , Journal of medical primatology, 2009 Oct, Volume 38 Suppl 1, p.17-23, (2009) Abstract
Recurrent BCAM-AKT2 fusion gene leads to a constitutively activated AKT2 fusion kinase in high-grade serous ovarian carcinoma., Kannan, Kalpana, Coarfa Cristian, Chao Pei-Wen, Luo Liming, Wang Yan, Brinegar Amy E., Hawkins Shannon M., Milosavljevic Aleksandar, Matzuk Martin M., and Yen Laising , Proceedings of the National Academy of Sciences of the United States of America, 2015 Mar 17, Volume 112, Issue 11, p.E1272-7, (2015) Abstract
Integrated genomic characterization of endometrial carcinoma., Kandoth, Cyriac, Schultz Nikolaus, Cherniack Andrew D., Akbani Rehan, Liu Yuexin, Shen Hui, Robertson Gordon A., Pashtan Itai, Shen Ronglai, Benz Christopher C., et al. , Nature, 2013 May 2, Volume 497, Issue 7447, p.67-73, (2013) Abstract
The serotonin transporter genotype is associated with intermediate brain phenotypes that depend on the context of eliciting stressor., Kalin, N. H., Shelton S. E., Fox A. S., Rogers J., Oakes T. R., and Davidson R. J. , Molecular psychiatry, 2008 Nov, Volume 13, Issue 11, p.1021-7, (2008) Abstract
Pash: efficient genome-scale sequence anchoring by Positional Hashing., Kalafus, Ken J., Jackson Andrew R., and Milosavljevic Aleksandar , Genome research, 2004 Apr, Volume 14, Issue 4, p.672-8, (2004) Abstract
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Regulation of Drosophila eye development by the transcription factor Sine oculis., Jusiak, Barbara, Karandikar Umesh C., Kwak Su-Jin, Wang Feng, Wang Hui, Chen Rui, and Mardon Graeme , PloS one, 2014, Volume 9, Issue 2, p.e89695, (2014) Abstract
Genome-wide DNA binding pattern of the homeodomain transcription factor Sine oculis (So) in the developing eye of Drosophila melanogaster., Jusiak, Barbara, Wang Feng, Karandikar Umesh C., Kwak Su-Jin, Wang Hui, Chen Rui, and Mardon Graeme , Genomics data, 2014 Dec 1, Volume 2, p.153-155, (2014) Abstract
MAPK target sites of eyes absent are not required for eye development or survival in Drosophila., Jusiak, Barbara, Abulimiti Abuduaini, Haelterman Nele, Chen Rui, and Mardon Graeme , PloS one, 2012, Volume 7, Issue 12, p.e50776, (2012) Abstract


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