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  1. 1.   The GTEx Consortium atlas of genetic regulatory effects across human tissues
  2. Aguet, Francois; Barbeira, Alvaro N.; Bonazzola, Rodrigo; Brown, Andrew; Castel, Stephane E.; Jo, Brian; Kasela, Silva; Kim-Hellmuth, Sarah; Liang, Yanyu; Parsana, Princy; Flynn, Elise; Fresard, Laure; Gamazon, Eric R.; Hamel, Andrew R.; He, Yuan; Hormozdiari, Farhad; Mohammadi, Pejman; Munoz-Aguirre, Manuel; Ardlie, Kristin G.; Battle, Alexis; Bonazzola, Rodrigo; Brown, Christopher D.; Cox, Nancy; Dermitzakis, Emmanouil T.; Engelhardt, Barbara E.; Garrido-Martin, Diego; Gay, Nicole R.; Getz, Gad; Guigo, Roderic; Hamel, Andrew R.; Handsaker, Robert E.; He, Yuan; Hoffman, Paul J.; Hormozdiari, Farhad; Im, Hae Kyung; Jo, Brian; Kasela, Silva; Kashin, Seva; Kim-Hellmuth, Sarah; Kwong, Alan; Lappalainen, Tuuli; Li, Xiao; Liang, Yanyu; MacArthur, Daniel G.; Mohammadi, Pejman; Montgomery, Stephen B.; Munoz-Aguirre, Manuel; Rouhana, John M.; Hormozdiari, Farhad; Im, Hae Kyung; Kim-Hellmuth, Sarah; Ardlie, Kristin G.; Getz, Gad; Guigo, Roderic; Im, Hae Kyung; Lappalainen, Tuuli; Montgomery, Stephen B.; Im, Hae Kyung; Lappalainen, Tuuli; Lappalainen, Tuuli; Anand, Shankara; Gabriel, Stacey; Getz, Gad; Graubert, Aaron; Hadley, Kane; Handsaker, Robert E.; Huang, Katherine H.; Kashin, Seva; Li, Xiao; MacArthur, Daniel G.; Meier, Samuel R.; Nedzel, Jared L.; Balliu, Brunilda; Conrad, Don; Cotter, Daniel J.; Das, Sayantan; de Goede, Olivia M.; Eskin, Eleazar; Eulalio, Tiffany Y.; Ferraro, Nicole M.; Garrido-Martin, Diego; Gay, Nicole R.; Getz, Gad; Graubert, Aaron; Guigo, Roderic; Hadley, Kane; Hamel, Andrew R.; Handsaker, Robert E.; He, Yuan; Hoffman, Paul J.; Hormozdiari, Farhad; Hou, Lei; Huang, Katherine H.; Im, Hae Kyung; Jo, Brian; Kasela, Silva; Kashin, Seva; Kellis, Manolis; Kim-Hellmuth, Sarah; Kwong, Alan; Lappalainen, Tuuli; Li, Xiao; Li, Xin; Liang, Yanyu; MacArthur, Daniel G.; Mangul, Serghei; Meier, Samuel R.; Mohammadi, Pejman; Montgomery, Stephen B.; Munoz-Aguirre, Manuel; Nachun, Daniel C.; Nedzel, Jared L.; Nguyen, Duyen Y.; Nobel, Andrew B.; Park, YoSon; Reverter, Ferran; Sabatti, Chiara; Saha, Ashis; Segre, Ayellet; Stephens, Matthew; Strober, Benjamin J.; Teran, Nicole A.; Todres, Ellen; Vinuela, Ana; Wang, Gao; Wen, Xiaoquan; Wright, Fred; Wucher, Valentin; Zou, Yuxin; Ferreira, Pedro G.; Li, Gen; Mele, Marta; Yeger-Lotem, Esti; Barcus, Mary E.; Bradbury, Debra; Krubit,Tanya; McLean,Jeff; Qi,Liqun; Robinson, Karna; Roche,Nancy; Smith, Anna M.; Tabor,David; Undale, Anita; Bridge, Jason; Brigham, Lori E.; Foster, Barbara A.; Gillard, Bryan M.; Hasz, Richard; Hunter, Marcus; Johns, Christopher; Johnson, Mark; Karasik, Ellen; Kopen, Gene; Leinweber, William F.; McDonald, Alisa; Moser, Michael T.; Myer, Kevin; Ramsey, Kimberley D.; Roe, Brian; Shad, Saboor; Thomas, Jeffrey A.; Walters, Gary; Washington, Michael; Wheeler, Joseph; Jewell, Scott D.; Rohrer, Daniel C.; Valley, Dana R.; Davis, David A.; Mash, Deborah C.; Branton, Philip A.; Sobin, Leslie; Barker, Laura K.; Gardiner, Heather M.; Mosavel, Maghboeba; Siminoff, Laura A.; Flicek, Paul; Haeussler, Maximilian; Juettemann, Thomas; Kent, W. James; Lee, Christopher M.; Powell, Conner C.; Rosenbloom, Kate R.; Ruffier, Magali; Sheppard, Dan; Taylor, Kieron; Trevanion, Stephen J.; Zerbino, Daniel R.; Abell, Nathan S.; Akey, Joshua; Chen, Lin; Demanelis, Kathryn; Doherty, Jennifer A.; Feinberg, Andrew P.; Hansen, Kasper D.; Hickey, Peter F.; Hou, Lei; Jasmine, Farzana; Jiang, Lihua; Kaul, Rajinder; Kellis, Manolis; Kibriya, Muhammad G.; Li, Jin Billy; Li, Qin; Lin, Shin; Linder, Sandra E.; Montgomery, Stephen B.; Oliva, Meritxell; Park, Yongjin; Pierce, Brandon L.; Rizzardi, Lindsay F.; Skol, Andrew D.; Smith, Kevin S.; Snyder, Michael; Stamatoyannopoulos, John; Tang, Hua; Wang, Meng; Carithers, Latarsha J.; Guan, Ping; Koester, Susan E.; Little, A. Roger; Moore, Helen M.; Nierras, Concepcion R.; Rao, Abhi K.; Vaught, Jimmie B.; Volpi, Simona
  3. SCIENCE. 2020, SEP 11; 369(6509): 1318-+.
  1. 2.   The MHC in the era of next-generation sequencing: Implications for bridging structure with function
  2. Petersdorf, Effie W.; Ohuigin,Colm
  3. HUMAN IMMUNOLOGY. 2019, Jan; 80(1): 67-78.
  1. 3.   Ultrasensitive single-genome sequencing: accurate, targeted, next generation sequencing of HIV-1 RNA.
  2. Boltz, Valerie; Rausch, Jason; Shao, Wei; Hattori, Takaaki; Luke, Brian; Maldarelli, Frank; Mellors, John W; Kearney, Mary F; Coffin, John
  3. Retrovirology. 2016, Dec 20; 13(1): 87.
  1. 4.   Fine mapping of 14q24.1 breast cancer susceptibility locus
  2. Lee, P.; Fu, Y. P.; Figueroa, J. D.; Prokunina-Olsson, L.; Gonzalez-Bosquet, J.; Kraft, P.; Wang, Z. M.; Jacobs, K. B.; Yeager, M.; Horner, M. J.; Hankinson, S. E.; Hutchinson, A.; Chatterjee, N.; Garcia-Closas, M.; Ziegler, R. G.; Berg, C. D.; Buys, S. S.; McCarty, C. A.; Feigelson, H. S.; Thun, M. J.; Diver, R.; Prentice, R.; Jackson, R.; Kooperberg, C.; Chlebowski, R.; Lissowska, J.; Peplonska, B.; Brinton, L. A.; Tucker, M.; Fraumeni, J. F.; Hoover, R. N.; Thomas, G.; Hunter, D. J.; Chanock, S. J.
  3. Human Genetics. 2012, Mar; 131(3): 479-490.
  1. 5.   MiR-886-3p Regulates Cell Proliferation and Migration, and Is Dysregulated in Familial Non-Medullary Thyroid Cancer
  2. Xiong, Y.; Zhang, L.; Holloway, A. K.; Wu, X. L.; Su, L.; Kebebew, E.
  3. Plos One. 2011, Oct; 6(10): 11.
  1. 6.   Von Hippel-Lindau (VHL) Inactivation in Sporadic Clear Cell Renal Cancer: Associations with Germline VHL Polymorphisms and Etiologic Risk Factors
  2. Moore, L. E.; Nickerson, M. L.; Brennan, P.; Toro, J. R.; Jaeger, E.; Rinsky, J.; Han, S. S.; Zaridze, D.; Matveev, V.; Janout, V.; Kollarova, H.; Bencko, V.; Navratilova, M.; Szeszenia-Dabrowska, N.; Mates, D.; Schmidt, L. S.; Lenz, P.; Karami, S.; Linehan, W. M.; Merino, M.; Chanock, S.; Boffetta, P.; Chow, W. H.; Waldman, F. M.; Rothman, N.
  3. Plos Genetics. 2011, Oct; 7(10): 13.
  1. 7.   SHAPE analysis of the FIV Leader RNA reveals a structural switch potentially controlling viral packaging and genome dimerization
  2. Kenyon, J. C.; Tanner, S. J.; Legiewicz, M.; Phillip, P. S.; Rizvi, T. A.; Le Grice, S. F. J.; Lever, A. M. L.
  3. Nucleic Acids Research. 2011, Aug; 39(15): 6692-6704.
  1. 8.   Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer
  2. Chung, C. C.; Ciampa, J.; Yeager, M.; Jacobs, K. B.; Berndt, S. I.; Hayes, R. B.; Gonzalez-Bosquet, J.; Kraft, P.; Wacholder, S.; Orr, N.; Yu, K.; Hutchinson, A.; Boland, J.; Chen, Q.; Feigelson, H. S.; Thun, M. J.; Diver, W. R.; Albanes, D.; Virtamo, J.; Weinstein, S.; Schumacher, F. R.; Cancel-Tassin, G.; Cussenot, O.; Valeri, A.; Andriole, G. L.; Crawford, E. D.; Haiman, C. A.; Henderson, B. E.; Kolonel, L.; Le Marchand, L.; Siddiq, A.; Riboli, E.; Key, T. J.; Kaaks, R.; Isaacs, W. B.; Isaacs, S. D.; Gronberg, H.; Wiklund, F.; Xu, J. F.; Vatten, L. J.; Hveem, K.; Njolstad, I.; Gerhard, D. S.; Tucker, M.; Hoover, R. N.; Fraumeni, J. F.; Hunter, D. J.; Thomas, G.; Chatterjee, N.; Chanock, S. J.
  3. Human Molecular Genetics. 2011, Jul; 20(14): 2869-2878.
  1. 9.   Genomewide Linkage Scan for Diabetic Renal Failure and Albuminuria: The FIND Study
  2. Igo, R. P.; Iyengar, S. K.; Nicholas, S. B.; Goddard, K. A. B.; Langefeld, C. D.; Hanson, R. L.; Duggirala, R.; Divers, J.; Abboud, H.; Adler, S. G.; Arar, N. H.; Horvath, A.; Elston, R. C.; Bowden, D. W.; Guo, X. Q.; Ipp, E.; Kao, W. H. L.; Kimmel, P. L.; Knowler, W. C.; Meoni, L. A.; Molineros, J.; Nelson, R. G.; Pahl, M. V.; Parekh, R. S.; Rasooly, R. S.; Schelling, J. R.; Shah, V. O.; Smith, M. W.; Winkler, C. A.; Zager, P. G.; Sedor, J. R.; Freedman, B. I.; Family Invest Nephropathy, D.
  3. American Journal of Nephrology. 2011, May; 33(5): 381-389.
  1. 10.   Similarity in Recombination Rate Estimates Highly Correlates with Genetic Differentiation in Humans
  2. Laayouni, H. L. H.; Montanucci, L.; Sikora, M.; Mele, M.; Dall'Olio, G. M.; Lorente-Galdos, B.; McGee, K. M.; Graffelman, J.; Awadalla, P.; Bosch, E.; Comas, D.; Navarro, A.; Calafell, F.; Casals, F.; Bertranpetit, J.
  3. Plos One. 2011, Mar; 6(3): 8.
  1. 11.   Accounting for multiple comparisons in a genome-wide association study (GWAS)
  2. Johnson, R. C.; Nelson, G. W.; Troyer, J. L.; Lautenberger, J. A.; Kessing, B. D.; Winkler, C. A.; O'Brien, S. J.
  3. Bmc Genomics. 2010, Dec; 11: 6.
  1. 12.   Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations
  2. Yang, X. R.; Liang, X. Y.; Pfeiffer, R. M.; Wheeler, W.; Maeder, D.; Burdette, L.; Yeager, M.; Chanock, S.; Tucker, M. A.; Goldstein, A. M.
  3. Familial Cancer. 2010, Dec; 9(4): 625-633.
  1. 13.   Widespread retinal degenerative disease mutation (rdAc) discovered among a large number of popular cat breeds
  2. Menotti-Raymond, M.; David, V. A.; Pflueger, S.; Roelke, M. E.; Kehler, J.; O'Brien, S. I.; Narfstrom, K.
  3. Veterinary Journal. 2010, Oct; 186(1): 32-38.
  1. 14.   Admixture Mapping Comes of Age
  2. Winkler, C. A.; Nelson, G. W.; Smith, M. W.
  3. Annual review of genomics and human genetics. 2010, Sep 22; 11: 65-89.
  1. 15.   Worldwide Distribution of the MYH9 Kidney Disease Susceptibility Alleles and Haplotypes: Evidence of Historical Selection in Africa
  2. Oleksyk, T. K.; Nelson, G. W.; An, P.; Kopp, J. B.; Winkler, C. A.
  3. Plos One. 2010, Jul; 5(7): 12.
  1. 16.   African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans
  2. Behar, D. M.; Rosset, S.; Tzur, S.; Selig, S.; Yudkovsky, G.; Bercovici, S.; Kopp, J. B.; Winkler, C. A.; Nelson, G. W.; Wasser, W. G.; Skorecki, K.
  3. Human Molecular Genetics. 2010, May; 19(9): 1816-1827.
  1. 17.   Host Determinants of HIV-1 Control in African Americans
  2. Pelak, K.; Goldstein, D. B.; Walley, N. M.; Fellay, J.; Ge, D.; Shianna, K. V.; Gumbs, C.; Gao, X.; Maia, J. M.; Cronin, K. D.; Hussain, S. K.; Carrington, M.; Michael, N. L.; Weintrob, A. C.; Natl Inst Allergy Infect, D.
  3. Journal of Infectious Diseases. 2010, Apr; 201(8): 1141-1149.
  1. 18.   Diversity in the Glucose Transporter-4 Gene (SLC2A4) in Humans Reflects the Action of Natural Selection along the Old-World Primates Evolution
  2. Tarazona-Santos, E.; Fabbri, C.; Yeager, M.; Magalhaes, W. C.; Burdett, L.; Crenshaw, A.; Pettener, D.; Chanock, S. J.
  3. Plos One. 2010, Mar; 5(3): 10.
  1. 19.   Genetics of Focal Segmental Glomerulosclerosis and Human Immunodeficiency Virus-Associated Collapsing Glomerulopathy: The Role of MYH9 Genetic Variation
  2. Winkler, C. A.; Nelson, G.; Oleksyk, T. K.; Nava, M. B.; Kopp, J. B.
  3. Seminars in Nephrology. 2010, Mar; 30(2): 111-125.
  1. 20.   Defining and Mapping Mammalian Coat Pattern Genes: Multiple Genomic Regions Implicated in Domestic Cat Stripes and Spots
  2. Eizirik, E.; David, V. A.; Buckley-Beason, V.; Roelke, M. E.; Schaffer, A. A.; Hannah, S. S.; Narfstrom, K.; O'Brien, S. J.; Menotti-Raymond, M.
  3. Genetics. 2010, Jan; 184(1): 267-U422.
  1. 21.   Multiplex Manager 1.0: a cross-platform computer program that plans and optimizes multiplex PCR
  2. Holleley, C. E.; Geerts, P. G.
  3. Biotechniques. 2009 46(7): 511-517.
  1. 22.   Mapping of the Domestic Cat "SILVER" Coat Color Locus Identifies a Unique Genomic Location for Silver in Mammals
  2. Menotti-Raymond, M.; David, V. A.; Eizirik, E.; Roelke, M. E.; Ghaffari, H.; O'Brien, S. J.
  3. Journal of Heredity. 2009 100: S8-S13.
  1. 23.   An autosomal genetic linkage map of the domestic cat, Felis silvestris catus
  2. Menotti-Raymond, M.; David, V. A.; Schaffer, A. A.; Tomlin, J. F.; Eizirik, E.; Phillip, C.; Wells, D.; Pontius, J. U.; Hannah, S. S.; O'Brien, S. J.
  3. Genomics. 2009 93(4): 305-313.
  1. 24.   Association of human leukocyte antigens with nasopharyngeal carcinoma in high-risk multiplex families in Taiwan
  2. Yu, K. J.; Gao, X. J.; Chen, C. J.; Yang, X. H.; Diehl, S. R.; Goldstein, A.; Hsu, W. L.; Liang, X. Y.; Marti, D.; Liu, M. Y.; Chen, J. Y.; Carrington, M.; Hildesheim, A.
  3. Human Immunology. 2009 70(11): 910-914.
  1. 25.   Pooled analysis of genetic variation at chromosome 8q24 and colorectal neoplasia risk
  2. Berndt, S. I.; Potter, J. D.; Hazra, A.; Yeager, M.; Thomas, G.; Makar, K. W.; Welch, R.; Cross, A. J.; Huang, W. Y.; Schoen, R. E.; Giovannucci, E.; Chan, A. T.; Chanock, S. J.; Peters, U.; Hunter, D. J.; Hayes, R. B.
  3. Human Molecular Genetics. 2008 17(17): 2665-2672.
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