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TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities., Wiszniewski, Wojciech, Hunter Jill V., Hanchard Neil A., Willer Jason R., Shaw Chad, Tian Qi, Illner Anna, Wang Xueqing, Cheung Sau W., Patel Ankita, et al. , American journal of human genetics, 2013 Aug 8, Volume 93, Issue 2, p.197-210, (2013) Abstract
Tissue-specific transcriptome sequencing analysis expands the non-human primate reference transcriptome resource (NHPRTR)., Peng, Xinxia, Thierry-Mieg Jean, Thierry-Mieg Danielle, Nishida Andrew, Pipes Lenore, Bozinoski Marjan, Thomas Matthew J., Kelly Sara, Weiss Jeffrey M., Raveendran Muthuswamy, et al. , Nucleic acids research, 2014 Nov 11, (2014) Abstract
Three common CFTR mutations should be included in a neonatal screening programme for cystic fibrosis in Sweden., Schaedel, C., Hjelte L., de Monestrol I., Johannesson M., Kollberg H., Kornfält R., and Holmberg L. , Clinical genetics, 1999 Oct, Volume 56, Issue 4, p.318-22, (1999) Abstract
TET2 and CSMD1 genes affect SBP response to hydrochlorothiazide in never-treated essential hypertensives., Chittani, Martina, Zaninello Roberta, Lanzani Chiara, Frau Francesca, Ortu Maria F., Salvi Erika, Fresu Giovanni, Citterio Lorena, Braga Daniele, Piras Daniela A., et al. , Journal of hypertension, 2015 Feb 18, (2015) Abstract
Targeted sequencing in candidate genes for atrial fibrillation: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing Study., Lin, Honghuang, Sinner Moritz F., Brody Jennifer A., Arking Dan E., Lunetta Kathryn L., Rienstra Michiel, Lubitz Steven A., Magnani Jared W., Sotoodehnia Nona, McKnight Barbara, et al. , Heart rhythm : the official journal of the Heart Rhythm Society, 2014 Mar, Volume 11, Issue 3, p.452-7, (2014) Abstract
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A systematic survey of loss-of-function variants in human protein-coding genes., MacArthur, Daniel G., Balasubramanian Suganthi, Frankish Adam, Huang Ni, Morris James, Walter Klaudia, Jostins Luke, Habegger Lukas, Pickrell Joseph K., Montgomery Stephen B., et al. , Science (New York, N.Y.), 2012 Feb 17, Volume 335, Issue 6070, p.823-8, (2012) Abstract
Subtle genetic changes enhance virulence of methicillin resistant and sensitive Staphylococcus aureus., Highlander, Sarah K., Hultén Kristina G., Qin Xiang, Jiang Huaiyang, Yerrapragada Shailaja, Mason Edward O., Shang Yue, Williams Tiffany M., Fortunov Régine M., Liu Yamei, et al. , BMC microbiology, 2007, Volume 7, p.99, (2007) Abstract
Strict evolutionary conservation followed rapid gene loss on human and rhesus Y chromosomes., Hughes, Jennifer F., Skaletsky Helen, Brown Laura G., Pyntikova Tatyana, Graves Tina, Fulton Robert S., Dugan Shannon, Ding Yan, Buhay Christian J., Kremitzki Colin, et al. , Nature, 2012 Mar 1, Volume 483, Issue 7387, p.82-6, (2012) Abstract
Strategic transformation of population studies: recommendations of the working group on epidemiology and population sciences from the national heart, lung, and blood advisory council and board of external experts., Roger, Véronique L., Boerwinkle Eric, Crapo James D., Douglas Pamela S., Epstein Jonathan A., Granger Christopher B., Greenland Philip, Kohane Isaac, and Psaty Bruce M. , American journal of epidemiology, 2015 Mar 15, Volume 181, Issue 6, p.363-8, (2015) Abstract
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)., Gerhard, Daniela S., Wagner Lukas, Feingold Elise A., Shenmen Carolyn M., Grouse Lynette H., Schuler Greg, Klein Steven L., Old Susan, Rasooly Rebekah, Good Peter, et al. , Genome research, 2004 Oct, Volume 14, Issue 10B, p.2121-7, (2004) Abstract
Somatic mutations affect key pathways in lung adenocarcinoma., Ding, Li, Getz Gad, Wheeler David A., Mardis Elaine R., McLellan Michael D., Cibulskis Kristian, Sougnez Carrie, Greulich Heidi, Muzny Donna M., Morgan Margaret B., et al. , Nature, 2008 Oct 23, Volume 455, Issue 7216, p.1069-75, (2008) Abstract
The Somatic Genomic Landscape of Chromophobe Renal Cell Carcinoma., Davis, Caleb F., Ricketts Christopher J., Wang Min, Yang Lixing, Cherniack Andrew D., Shen Hui, Buhay Christian, Kang Hyojin, Kim Sang Cheol, Fahey Catherine C., et al. , Cancer cell, 2014 Sep 8, Volume 26, Issue 3, p.319-330, (2014) Abstract
Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10., Matsuura, Tohru, Fang Ping, Lin Xi, Khajavi Mehrdad, Tsuji Kuniko, Rasmussen Astrid, Grewal Raji P., Achari Madhureeta, Alonso Maria E., Pulst Stefan M., et al. , American journal of human genetics, 2004 Jun, Volume 74, Issue 6, p.1216-24, (2004) Abstract
Software for automated analysis of DNA fingerprinting gels., Fuhrmann, Daniel R., Krzywinski Martin I., Chiu Readman, Saeedi Parvaneh, Schein Jacqueline E., Bosdet Ian E., Chinwalla Asif, Hillier Ladeana W., Waterston Robert H., McPherson John D., et al. , Genome research, 2003 May, Volume 13, Issue 5, p.940-53, (2003) Abstract
Single stimulus fMRI produces a neural individual difference measure for Autism Spectrum Disorder., Lu, James, Kishida Ken, De Asis Cruz Josepheen, Lohrenz Terry, Deering Diane Treadwell, Beauchamp Michael, and Montague Read P. , Clinical psychological science : a journal of the Association for Psychological Science, 2015 May 1, Volume 3, Issue 3, p.422-432, (2015) Abstract
Single nucleotide polymorphism in RECQL and survival in resectable pancreatic adenocarcinoma., Cotton, Ronald T., Li Donghui, Scherer Steven E., Muzny Donna M., Hodges Sally E., Catania Robbi L., Witkiewicz Agnieszka K., Brody Jonathan R., Kennedy Eugene P., Yeo Charles J., et al. , HPB : the official journal of the International Hepato Pancreato Biliary Association, 2009 Aug, Volume 11, Issue 5, p.435-44, (2009) Abstract
The sheep genome illuminates biology of the rumen and lipid metabolism., Jiang, Yu, Xie Min, Chen Wenbin, Talbot Richard, Maddox Jillian F., Faraut Thomas, Wu Chunhua, Muzny Donna M., Li Yuxiang, Zhang Wenguang, et al. , Science (New York, N.Y.), 2014 Jun 6, Volume 344, Issue 6188, p.1168-73, (2014) 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
Serotonin transporter binding and genotype in the nonhuman primate brain using [C-11]DASB PET., Christian, B. T., Fox A. S., Oler J. A., Vandehey N. T., Murali D., Rogers J., Oakes T. R., Shelton S. E., Davidson R. J., and Kalin N. H. , NeuroImage, 2009 Oct 1, Volume 47, Issue 4, p.1230-6, (2009) Abstract
Sequence, assembly and analysis of pX01 and pX02., Okinaka, R., Cloud K., Hampton O., Hoffmaster A., Hill K., Keim P., Koehler T., Lamke G., Kumano S., Manter D., et al. , Journal of applied microbiology, 1999 Aug, Volume 87, Issue 2, p.261-2, (1999) Abstract
Sequence variation in DOCK9 and heterogeneity in bipolar disorder., Detera-Wadleigh, Sevilla D., Liu Chun-yu, Maheshwari Manjula, Cardona Imer, Corona Winston, Akula Nirmala, Steele C. J. M., Badner Judith A., Kundu Mukta, Kassem Layla, et al. , Psychiatric genetics, 2007 Oct, Volume 17, Issue 5, p.274-86, (2007) Abstract
Sequence and structure of the extrachromosomal palindrome encoding the ribosomal RNA genes in Dictyostelium., Sucgang, Richard, Chen Guokai, Liu Wen, Lindsay Ryan, Lu Jing, Muzny Donna, Shaulsky Gad, Loomis William, Gibbs Richard, and Kuspa Adam , Nucleic acids research, 2003 May 1, Volume 31, Issue 9, p.2361-8, (2003) Abstract
Sequence and organization of pXO1, the large Bacillus anthracis plasmid harboring the anthrax toxin genes., Okinaka, R. T., Cloud K., Hampton O., Hoffmaster A. R., Hill K. K., Keim P., Koehler T. M., Lamke G., Kumano S., Mahillon J., et al. , Journal of bacteriology, 1999 Oct, Volume 181, Issue 20, p.6509-15, (1999) Abstract
Section V. Application of Chimeras in Monitoring and Manipulating Cell Physiology-37 Use of Fusions to Green Fluorescent Protein in the Detection of Apoptosis, Shinbrot, Eve, Spencer Collin, Natale Valerie, and Kain Steven R. , Methods in Enzymology, Volume 327, p.513–521, (2000)
A second generation human haplotype map of over 3.1 million SNPs., Frazer, Kelly A., Ballinger Dennis G., Cox David R., Hinds David A., Stuve Laura L., Gibbs Richard A., Belmont John W., Boudreau Andrew, Hardenbol Paul, Leal Suzanne M., et al. , Nature, 2007 Oct 18, Volume 449, Issue 7164, p.851-61, (2007) Abstract


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