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TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum., Davis, Erica E., Zhang Qi, Liu Qin, Diplas Bill H., Davey Lisa M., Hartley Jane, Stoetzel Corinne, Szymanska Katarzyna, Ramaswami Gokul, Logan Clare V., et al. , Nature genetics, 2011 Mar, Volume 43, Issue 3, p.189-96, (2011) Abstract
Trisomy 17 in a baboon (Papio hamadryas) with polydactyly, patent foramen ovale and pyelectasis., Moore, Charleen M., Hubbard Gene B., Dick Edward, Dunn Betty G., Raveendran Muthuswamy, Rogers Jeffrey, Williams Vick, Gomez Jeremiah J., Butler Stephanie D., Leland Michelle M., et al. , American journal of primatology, 2007 Oct, Volume 69, Issue 10, p.1105-18, (2007) 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
Transcriptome of Treponema pallidum: gene expression profile during experimental rabbit infection., Smajs, David, McKevitt Matthew, Howell Jerrilyn K., Norris Steven J., Cai Wei-Wen, Palzkill Timothy, and Weinstock George M. , Journal of bacteriology, 2005 Mar, Volume 187, Issue 5, p.1866-74, (2005) Abstract
Trans-ancestry mutational landscape of hepatocellular carcinoma genomes, Totoki, Yasushi, Tatsuno Kenji, Covington Kyle R., Ueda Hiroki, Creighton Chad J., Kato Mamoru, Tsuji Shingo, Donehower Lawrence A., Slagle Betty L., Nakamura Hiromi, et al. , Nature Genetics, 11/2014, (2014)
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
Termination of DNA synthesis by N6-alkylated, not 3'-O-alkylated, photocleavable 2'-deoxyadenosine triphosphates., Wu, Weidong, Stupi Brian P., Litosh Vladislav A., Mansouri Dena, Farley Demetra, Morris Sidney, Metzker Sherry, and Metzker Michael L. , Nucleic acids research, 2007, Volume 35, Issue 19, p.6339-49, (2007) Abstract
Targeting iCre expression to murine progesterone receptor cell-lineages using bacterial artificial chromosome transgenesis., Mukherjee, Atish, Soyal Selma M., Wheeler David A., Fernandez-Valdivia Rodrigo, Nguyen Jonathan, DeMayo Francesco J., and Lydon John P. , Genesis (New York, N.Y. : 2000), 2006 Dec, Volume 44, Issue 12, p.601-10, (2006) Abstract
Targeted sequencing in chromosome 17q linkage region identifies familial glioma candidates in the Gliogene Consortium., Jalali, Ali, Amirian Susan E., Bainbridge Matthew N., Armstrong Georgina N., Liu Yanhong, Tsavachidis Spyros, Jhangiani Shalini N., Plon Sharon E., Lau Ching C., Claus Elizabeth B., et al. , Scientific reports, 2015, Volume 5, p.8278, (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
Taking DNA from the dead., McGuire, Amy L., Majumder Mary A., Halpern Scott D., Swindell J. S., Yaeger Laura V., Gibbs Richard A., and Wheeler Thomas M. , Nature reviews. Genetics, 2010 May, Volume 11, Issue 5, p.318, (2010)
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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
Systematic cloning of Treponema pallidum open reading frames for protein expression and antigen discovery., McKevitt, Matthew, Patel Krupa, Smajs David, Marsh Michael, McLoughlin Melanie, Norris Steven J., Weinstock George M., and Palzkill Timothy , Genome research, 2003 Jul, Volume 13, Issue 7, p.1665-74, (2003) Abstract
Successful diagnosis of HIBCH deficiency from exome sequencing and positive retrospective analysis of newborn screening cards in two siblings presenting with Leigh's disease., Stiles, Ashlee R., Ferdinandusse Sacha, Besse Arnaud, Appadurai Vivek, Leydiker Karen B., Cambray-Forker E. J., Bonnen Penelope E., and Abdenur Jose E. , Molecular genetics and metabolism, 2015 Aug, Volume 115, Issue 4, p.161-7, (2015) 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
Structure and function of the healthy pre-adolescent pediatric gut microbiome., Hollister, Emily B., Riehle Kevin, Luna Ruth Ann, Weidler Erica M., Rubio-Gonzales Michelle, Mistretta Toni-Ann, Raza Sabeen, Doddapaneni Harsha V., Metcalf Ginger A., Muzny Donna M., et al. , Microbiome, 2015, Volume 3, p.36, (2015) 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
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
SSTR5 P335L monoclonal antibody differentiates pancreatic neuroendocrine neuroplasms with different SSTR5 genotypes., Zhou, Guisheng, Gingras Marie-Claude, Liu Shi-He, Sanchez Robbi, Edwards Dean, Dawson David, Christensen Kurt, Paganelli Giovanni, Gibbs Richard, Fisher William, et al. , Surgery, 2011 Dec, Volume 150, Issue 6, p.1136-42, (2011) Abstract
Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation., Lalani, Seema R., Safiullah Arsalan M., Fernbach Susan D., Harutyunyan Karine G., Thaller Christina, Peterson Leif E., McPherson John D., Gibbs Richard A., White Lisa D., Hefner Margaret, et al. , American journal of human genetics, 2006 Feb, Volume 78, Issue 2, p.303-14, (2006) Abstract
Source identification in two criminal cases using phylogenetic analysis of HIV-1 DNA sequences., Scaduto, Diane I., Brown Jeremy M., Haaland Wade C., Zwickl Derrick J., Hillis David M., and Metzker Michael L. , Proceedings of the National Academy of Sciences of the United States of America, 2010 Dec 14, Volume 107, Issue 50, p.21242-7, (2010) 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


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