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United States
Prediction of coronary heart disease risk using a genetic risk score: the Atherosclerosis Risk in Communities Study., Morrison, Alanna C., Bare Lance A., Chambless Lloyd E., Ellis Stephen G., Malloy Mary, Kane John P., Pankow James S., Devlin James J., Willerson James T., and Boerwinkle Eric , American journal of epidemiology, 2007 Jul 1, Volume 166, Issue 1, p.28-35, (2007) Abstract
Imputing gene-treatment interactions when the genotype distribution is unknown using case-only and putative placebo analyses--a new method for the Genetics of Hypertension Associated Treatment (GenHAT) study., Davis, Barry R., Ford Charles E., Boerwinkle Eric, Arnett Donna, Eckfeldt John, and Black Henry , Statistics in medicine, 2004 Aug 15, Volume 23, Issue 15, p.2413-27, (2004) Abstract
The INSIG2 rs7566605 genetic variant does not play a major role in obesity in a sample of 24,722 individuals from four cohorts., Bressler, Jan, Fornage Myriam, Hanis Craig L., Kao Wen Hong Linda, Lewis Cora E., McPherson Ruth, Dent Robert, Mosley Thomas H., Pennacchio Len A., and Boerwinkle Eric , BMC medical genetics, 2009, Volume 10, p.56, (2009) 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
Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10., Matsuura, T., Yamagata T., Burgess D. L., Rasmussen A., Grewal R. P., Watase K., Khajavi M., McCall A. E., Davis Caleb F., Zu L., et al. , Nature genetics, 2000 Oct, Volume 26, Issue 2, p.191-4, (2000) Abstract
Unified Medical Language System
Integrating the UMLS into VNS Retriever., Barber, S., Fowler J., Long K. B., Dargahi R., and Meyer B. , Proceedings / the ... Annual Symposium on Computer Application [sic] in Medical Care. Symposium on Computer Applications in Medical Care, 1992, p.273-7, (1992) Abstract
Ultraviolet Rays
Paradoxical DNA repair and peroxide resistance gene conservation in Bacillus pumilus SAFR-032., Gioia, Jason, Yerrapragada Shailaja, Qin Xiang, Jiang Huaiyang, Igboeli Okezie C., Muzny Donna, Dugan-Rocha Shannon, Ding Yan, Hawes Alicia, Liu Wen, et al. , PloS one, 2007, Volume 2, Issue 9, p.e928, (2007) Abstract
Paradoxical DNA repair and peroxide resistance gene conservation in Bacillus pumilus SAFR-032., Gioia, Jason, Yerrapragada Shailaja, Qin Xiang, Jiang Huaiyang, Igboeli Okezie C., Muzny Donna, Dugan-Rocha Shannon, Ding Yan, Hawes Alicia, Liu Wen, et al. , PloS one, 2007, Volume 2, Issue 9, p.e928, (2007) Abstract
Ubiquitin-Protein Ligases
Exome sequencing of head and neck squamous cell carcinoma reveals inactivating mutations in NOTCH1., Agrawal, Nishant, Frederick Mitchell J., Pickering Curtis R., Bettegowda Chetan, Chang Kyle, Li Ryan J., Fakhry Carole, Xie Tong-Xin, Zhang Jiexin, Wang Jing, et al. , Science (New York, N.Y.), 2011 Aug 26, Volume 333, Issue 6046, p.1154-7, (2011) Abstract
Ubiquitin Thiolesterase
Adverse outcomes in clear cell renal cell carcinoma with mutations of 3p21 epigenetic regulators BAP1 and SETD2: a report by MSKCC and the KIRC TCGA research network., Hakimi, Ari A., Ostrovnaya Irina, Reva Boris, Schultz Nikolaus, Chen Ying-Bei, Gonen Mithat, Liu Han, Takeda Shugaku, Voss Martin H., Tickoo Satish K., et al. , Clinical cancer research : an official journal of the American Association for Cancer Research, 2013 Jun 15, Volume 19, Issue 12, p.3259-67, (2013) Abstract
Turner Syndrome
Pulmonary alveolar proteinosis caused by deletion of the GM-CSFRalpha gene in the X chromosome pseudoautosomal region 1., Martinez-Moczygemba, Margarita, Doan Minh L., Elidemir Okan, Fan Leland L., Cheung Sau Wai, Lei Jonathan T., Moore James P., Tavana Ghamartaj, Lewis Lora R., Zhu Yiming, et al. , The Journal of experimental medicine, 2008 Nov 24, Volume 205, Issue 12, p.2711-6, (2008) Abstract
Tumor Suppressor Proteins
Adverse outcomes in clear cell renal cell carcinoma with mutations of 3p21 epigenetic regulators BAP1 and SETD2: a report by MSKCC and the KIRC TCGA research network., Hakimi, Ari A., Ostrovnaya Irina, Reva Boris, Schultz Nikolaus, Chen Ying-Bei, Gonen Mithat, Liu Han, Takeda Shugaku, Voss Martin H., Tickoo Satish K., et al. , Clinical cancer research : an official journal of the American Association for Cancer Research, 2013 Jun 15, Volume 19, Issue 12, p.3259-67, (2013) Abstract
Gene therapy rescues cilia defects and restores olfactory function in a mammalian ciliopathy model., McIntyre, Jeremy C., Davis Erica E., Joiner Ariell, Williams Corey L., Tsai I-Chun, Jenkins Paul M., McEwen Dyke P., Zhang Lian, Escobado John, Thomas Sophie, et al. , Nature medicine, 2012 Sep, Volume 18, Issue 9, p.1423-8, (2012) Abstract
Activation of multiple proto-oncogenic tyrosine kinases in breast cancer via loss of the PTPN12 phosphatase., Sun, Tingting, Aceto Nicola, Meerbrey Kristen L., Kessler Jessica D., Zhou Chunshui, Migliaccio Ilenia, Nguyen Don X., Pavlova Natalya N., Botero Maria, Huang Jian, et al. , Cell, 2011 Mar 4, Volume 144, Issue 5, p.703-18, (2011) Abstract
Tumor Suppressor Protein p14ARF
SINE retrotransposons cause epigenetic reprogramming of adjacent gene promoters., Estécio, Marcos R. H., Gallegos Juan, Dekmezian Mhair, Lu Yue, Liang Shoudan, and Issa Jean-Pierre J. , Molecular cancer research : MCR, 2012 Oct, Volume 10, Issue 10, p.1332-42, (2012) Abstract
Tumor Cells, Cultured
Pol iota is a candidate for the mouse pulmonary adenoma resistance 2 locus, a major modifier of chemically induced lung neoplasia., Wang, Min, Devereux Theodora R., Vikis Haris G., McCulloch Scott D., Holliday Wanda, Anna Colleen, Wang Yian, Bebenek Katarzyna, Kunkel Thomas A., Guan Kunliang, et al. , Cancer research, 2004 Mar 15, Volume 64, Issue 6, p.1924-31, (2004) Abstract
Aberrant TGF-beta production and regulation in metastatic malignancy., Schwarz, L. C., Wright J. A., Gingras M. C., Kondaiah P., Danielpour D., Pimentel M., Sporn M. B., and Greenberg A. H. , Growth factors (Chur, Switzerland), 1990, Volume 3, Issue 2, p.115-27, (1990) Abstract
Tubulin
Gene therapy rescues cilia defects and restores olfactory function in a mammalian ciliopathy model., McIntyre, Jeremy C., Davis Erica E., Joiner Ariell, Williams Corey L., Tsai I-Chun, Jenkins Paul M., McEwen Dyke P., Zhang Lian, Escobado John, Thomas Sophie, et al. , Nature medicine, 2012 Sep, Volume 18, Issue 9, p.1423-8, (2012) Abstract
Trisomy
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
Trinucleotide Repeats
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel., Zhuchenko, O., Bailey J., Bonnen P., Ashizawa T., Stockton D. W., Amos C., Dobyns W. B., Subramony S. H., Zoghbi H. Y., and Lee C. C. , Nature genetics, 1997 Jan, Volume 15, Issue 1, p.62-9, (1997) Abstract
Triglycerides
A preliminary report on the feeding of cynomolgus monkeys (Macaca fascicularis) with a high-sugar high-fat diet for 33 weeks., Mubiru, James N., Garcia-Forey Magdalena, Higgins Paul B., Hemmat Peggah, Cavazos Nicole E., Dick Edward J., Owston Michael A., Bauer Cassondra A., Shade Robert E., Comuzzie Anthony G., et al. , Journal of medical primatology, 2011 Oct, Volume 40, Issue 5, p.335-41, (2011) Abstract
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks., Peloso, Gina M., Auer Paul L., Bis Joshua C., Voorman Arend, Morrison Alanna C., Stitziel Nathan O., Brody Jennifer A., Khetarpal Sumeet A., Crosby Jacy R., Fornage Myriam, et al. , American journal of human genetics, 2014 Feb 6, Volume 94, Issue 2, p.223-32, (2014) Abstract
Longitudinal changes in triglycerides according to ANGPTL4[E40K] genotype and longitudinal body weight change in the atherosclerosis risk in communities study., Nettleton, Jennifer A., Volcik Kelly A., Demerath Ellen W., Boerwinkle Eric, and Folsom Aaron R. , Annals of epidemiology, 2008 Nov, Volume 18, Issue 11, p.842-6, (2008) Abstract
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction., Do, Ron, Stitziel Nathan O., Won Hong-Hee, Jørgensen Anders Berg, Duga Stefano, Angelica Merlini Pier, Kiezun Adam, Farrall Martin, Goel Anuj, Zuk Or, et al. , Nature, 2015 Feb 5, Volume 518, Issue 7537, p.102-6, (2015) Abstract
Tribolium
The genome of the model beetle and pest Tribolium castaneum., Richards, Stephen, Gibbs Richard A., Weinstock George M., Brown Susan J., Denell Robin, Beeman Richard W., Gibbs Richard, Beeman Richard W., Brown Susan J., Bucher Gregor, et al. , Nature, 2008 Apr 24, Volume 452, Issue 7190, p.949-55, (2008) Abstract


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