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Genetics and Genomics

  1. Genetic relationships deduced from emm and multilocus sequence typing of invasive Streptococcus dysgalactiae subsp. equisimilis and S. canis recovered from isolates collected in the United States
    Ahmad Y, Gertz RE, Li Z, Sakota V, Broyles LN, Van Beneden C, Facklam R, Shewmaker PL, Reingold A, Farley MM, Beall BW.
    J Clin Microbiol. 2009 Jul;47(7):2046-54.

  2. First isolation of an H1N1 avian influenza virus from wild terrestrial non-migratory birds in Argentina
    Alvarez P, Mattiello R, Rivailler P, Pereda A, Davis CT, Boado L, D'Ambrosio E, Aguirre S, Espinosa C, La Torre J, Donis R, Mattion N.
    Virology. 2010 Jan 5;396(1):76-84.

  3. The NS1 protein of the 1918 pandemic influenza virus blocks host interferon and lipid metabolism pathways
    Billharz R, Zeng H, Proll SC, Korth MJ, Lederer S, Albrecht R, Goodman AG, Rosenzweig E, Tumpey TM, Garcia-Sastre A, Katze MG.
    J Virol. 2009 Oct;83(20):10557-70.

  4. Outcomes of interest in evidence-based evaluations of genetic tests
    Botkin JR, Teutsch SM, Kaye CI, Hayes M, Haddow JE, Bradley LA, Szegda K, Dotson WD, on behalf of the EGAPP Working Group.
    Genet Med. 2010 Jan 28.

  5. Genetic inactivation of poliovirus infectivity by increasing the frequencies of CpG and UpA dinucleotides within and across synonymous capsid region codons
    Burns CC, Campagnoli R, Shaw J, Vincent A, Jorba J, Kew O.
    J Virol. 2009 Jul 15.

  6. Ancient common ancestry of Crimean-Congo hemorrhagic fever virus
    Carroll SA, Bird BH, Rollin PE, Nichol ST.
    Mol Phylogenet Evol. 2010 Jan 11.

  7. Synergy of BMI and family history on diabetes: the Humboldt Study
    Chen Y, Rennie DC, Dosman JA.
    Public Health Nutr. 2009 Aug 26:1-5.

  8. Novel human leukocyte antigen class I and class II alleles identified by sequence-based typing in the Genetics of Kidneys in Diabetes (GoKinD) study population
    Cordovado SK, Hancock LN, Hendrix M, Greene CN, Mueller PW.
    Hum Immunol. 2009 Sep;70(9):747-9.

  9. Incorporating genetics and genomics in risk assessment for inhaled manganese: from data to policy
    Curran CP, Park RM, Ho SM, Haynes EN.
    Neurotoxicology. 2009 Sep;30(5):754-60.

  10. Genomic events underlying the changes in adamantane resistance among influenza A(H3N2) viruses during 2006-2008
    Deyde V, Garten R, Sheu T, Smith C, Myrick A, Barnes J, Xu X, Shaw M, Klimov A, Gubareva L.
    Influenza Other Respi Viruses. 2009 Nov;3(6):297-314.

  11. Human genomics and preparedness for infectious threats
    Dowling NF, Gwinn M, Mawle A.
    Genome Med. 2009 ;1(12):119.

  12. The phylogenetics and ecology of the orthopoxviruses endemic to North America
    Emerson GL, Li Y, Frace MA, Olsen-Rasmussen MA, Khristova ML, Govil D, Sammons SA, Regnery RL, Karem KL, Damon IK, Carroll DS.
    PLoS One. 2009 ;4(10):e7666.

  13. Gene mapping and phylogenetic analysis of the complete genome from 30 single-stranded RNA male-specific coliphages (family Leviviridae)
    Friedman SD, Genthner FJ, Gentry J, Sobsey MD, Vinje J.
    J Virol. 2009 Nov;83(21):11233-43.

  14. Adapting the logical basis of tests for Hardy-Weinberg Equilibrium to the real needs of association studies in human and medical genetics
    Goddard KA, Ziegler A, Wellek S.
    Genet Epidemiol. 2009 Nov;33(7):569-80.

  15. Personal utility and genomic information: look before you leap
    Grosse SD, McBride CM, Evans JP, Khoury MJ.
    Genet Med. 2009 Aug;11(8):575-6.

  16. Genome-wide association studies in pharmacogenomics: untapped potential for translation
    Guessous I, Gwinn M, Khoury MJ.
    Genome Med. 2009 ;1(4):46.

  17. Invited commentary: genes, environment, and hybrid vigor
    Gwinn M, Guessous I, Khoury MJ.
    Am J Epidemiol. 2009 Sep 15;170(6):703-7.

  18. Maternal attitudes toward DNA collection for gene-environment studies: a qualitative research study
    Jenkins MM, Reed-Gross E, Rasmussen SA, Barfield WD, Prue CE, Gallagher ML, Honein MA.
    Am J Med Genet A. 2009 Oct 16.

  19. Development of genomic DNA reference materials for genetic testing of disorders common in people of Ashkenazi Jewish descent
    Kalman L, Wilson JA, Buller A, Dixon J, Edelmann L, Geller L, Highsmith WE, Holtegaard L, Kornreich R, Rohlfs EM, Payeur TL, Sellers T, Toji L, Muralidharan K.
    J Mol Diagn. 2009 Oct 8.

  20. Translation research is an essential but not sufficient ingredient for translation of genomic medicine into population health benefits
    Khoury MJ.
    Genet Med. 2009 Dec;11(12):899.

  21. Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases
    Khoury MJ, Bertram L, Boffetta P, Butterworth AS, Chanock SJ, Dolan SM, Fortier I, Garcia-Closas M, Gwinn M, Higgins JP, Janssens AC, Ostell J, Owen RP, Pagon RA, Rebbeck TR, Rothman N, Bernstein JL, Burton PR, Campbell H, Chockalingam A, Furberg H, Little J, O'Brien TR, Seminara D, Vineis P, Winn DM, Yu W, Ioannidis JP.
    Am J Epidemiol. 2009 Aug 1;170(3):269-79.

  22. The scientific foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention Multidisciplinary Workshop
    Khoury MJ, McBride C, Schully SD, Ioannidis JP, Feero WG, Janssens AC, Gwinn M, Simons-Morton DG, Bernhardt JM, Cargill M, Chanock SJ, Church GM, Coates RJ, Collins FS, Croyle RT, Davis BR, Downing GJ, Duross A, Friedman S, Gail MH, Ginsburg GS, Green RC, Greene MH, Greenland P, Gulcher JR, Hsu A, Hudson KL, Kardia SL, Kimmel PL, Lauer MS, Miller AM, Offit K, Ransohoff DF, Roberts HS, Rasooly RS, Stefansson K, Terry SF, Teutsch SM, Trepanier A, Wanke KL, Witte JS, Xu J.
    Genet Med. 2009 Jul 16;11(8):559-67.

  23. A genetic test registry: Bringing credible and actionable data together
    Khoury MJ, Reyes M, Gwinn M, Feero WG.
    Public Health Genomics. 2009 Nov 26.

  24. Comparative effectiveness research and genomic medicine: an evolving partnership for 21st century medicine
    Khoury MJ, Rich EC, Randhawa G, Teutsch SM, Niederhuber J.
    Genet Med. 2009 Sep 11;11(10):707-11.

  25. Human leukocyte antigen class I supertypes and HIV-1 control in African Americans
    Lazaryan A, Song W, Lobashevsky E, Tang J, Shrestha S, Zhang K, Gardner LI, McNicholl JM, Wilson CM, Klein RS, Rompalo A, Mayer K, Sobel J, Richard AK.
    J Virol. 2009 Dec 23.

  26. Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS genomewide association study 03)
    Le Clerc S, Limou S, Coulonges C, Carpentier W, Dina C, Taing L, Delaneau O, Labib T, Sladek R, Group AG, Deveau C, Guillemain H, Ratsimandresy R, Montes M, Spadoni JL, Therwath A, Schachter F, Matsuda F, Gut I, Lelievre JD, Levy Y, Froguel P, Delfraissy JF, Hercberg S, Zagury JF.
    J Infect Dis. 2009 Oct 15;200(8):1194-1201.

  27. Steroid 5-{alpha}-reductase type 2 (SRD5a2) gene polymorphisms and risk of prostate cancer: a HuGE review
    Li J, Coates RJ, Gwinn M, Khoury MJ.
    Am J Epidemiol. 2010 Jan 1;171(1):1-13.

  28. STrengthening the REporting of Genetic Association Studies (STREGA)--an extension of the STROBE statement
    Little J, Higgins JP, Ioannidis JP, Moher D, Gagnon F, von Elm E, Khoury MJ, Cohen B, Davey-Smith G, Grimshaw J, Scheet P, Gwinn M, Williamson RE, Zou GY, Hutchings K, Johnson CY, Tait V, Wiens M, Golding J, van Duijn C, McLaughlin J, Paterson A, Wells G, Fortier I, Freedman M, Zecevic M, King R, Infante-Rivard C, Stewart A, Birkett N.
    Genet Epidemiol. 2009 Nov;33(7):581-98.

  29. Evidence of selective sweeps in genes conferring resistance to chloroquine and pyrimethamine in Plasmodium falciparum within India
    Mixson-Hayden T, Jain V, McCollum AM, Poe A, Nagpal AC, Dash AP, Stiles JK, Udhayakumar V, Singh N.
    Antimicrob Agents Chemother. 2009 Dec 28.

  30. Genomic medicine and racial/ethnic health disparities: promises, perils, and the challenges for health care and public health policy
    Moonesinghe R, Jones W, Honore PA, Truman BI, Graham G.
    Ethn Dis. 2009 Autumn;19(4):473-8.

  31. Evaluation of the discriminative accuracy of genomic profiling in the prediction of common complex diseases
    Moonesinghe R, Liu T, Khoury MJ.
    Eur J Hum Genet. 2009 Nov 25.

  32. The cost-effectiveness of genetic testing strategies for Lynch syndrome among newly diagnosed patients with colorectal cancer
    Mvundura M, Grosse SD, Hampel H, Palomaki GE.
    Genet Med. 2010 Jan 15.

  33. Family history as a risk factor for early-onset stroke/transient Ischemic attack among adults in the United States
    Mvundura M, McGruder H, Khoury MJ, Valdez R, Yoon PW.
    Public Health Genomics. 2010 ;13(1):13-20.

  34. Family history of cancer and risk of breast cancer in the black women's health study
    Palmer JR, Boggs DA, Adams-Campbell LL, Rosenberg L.
    Cancer Causes Control. 2009 Sep 17;20(9):1733-7.

  35. Whole genome single nucleotide polymorphism based phylogeny of Francisella tularensis and its application to the development of a strain typing assay
    Pandya GA, Holmes MH, Petersen JM, Pradhan S, Karamycheva SA, Wolcott MJ, Molins C, Jones M, Schriefer ME, Fleischmann RD, Peterson SN.
    BMC Microbiol. 2009 ;9:213.

  36. Phylogeographic reconstruction of a bacterial species with high levels of lateral gene transfer
    Pearson T, Giffard P, Beckstrom-Sternberg S, Auerbach R, Hornstra H, Tuanyok A, Price EP, Glass MB, Leadem B, Beckstrom-Sternberg JS, Allan GJ, Foster JT, Wagner DM, Okinaka RT, Sim SH, Pearson O, Wu Z, Chang J, Kaul R, Hoffmaster AR, Brettin TS, Robison RA, Mayo M, Gee JE, Tan P, Currie BJ, Keim P.
    BMC Biol. 2009 ;7:78.

  37. Detection and differentiation of Clostridium botulinum type A strains using a focused DNA microarray
    Raphael BH, Joseph LA, McCroskey LM, Luquez C, Maslanka SE.
    Mol Cell Probes. 2010 Jan 6.

  38. Genetic polymorphisms associated with acute lung injury
    Reddy AJ, Kleeberger SR.
    Pharmacogenomics. 2009 Sep;10(9):1527-39.

  39. Challenges of translating genetic tests into clinical and public health practice
    Rogowski WH, Grosse SD, Khoury MJ.
    Nat Rev Genet. 2009 Jul;10(7):489-95.

  40. Genomic privacy and limits of individual detection in a pool
    Sankararaman S, Obozinski G, Jordan MI, Halperin E.
    Nat Genet. 2009 Sep;41(9):965-7.

  41. Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy
    Shuldiner AR, O'Connell JR, Bliden KP, Gandhi A, Ryan K, Horenstein RB, Damcott CM, Pakyz R, Tantry US, Gibson Q, Pollin TI, Post W, Parsa A, Mitchell BD, Faraday N, Herzog W, Gurbel PA.
    JAMA. 2009 Aug 26;302(8):849-57.

  42. Genetic variability of wild-type measles viruses, circulating in the Russian Federation during the implementation of the National Measles Elimination Program, 2003-2007
    Shulga SV, Rota PA, Kremer JR, Naumova MA, Muller CP, Tikhonova NT, Lopareva EN, Mamaeva TA, Tsvirkun OV, Mulders MN, Lipskaya GY, Gerasimova AG.
    Clin Microbiol Infect. 2009 Jun;15(6):528-37.

  43. Genetic determinants of sensitivity to beryllium in mice
    Tarantino-Hutchison LM, Sorrentino C, Nadas A, Zhu Y, Rubin EM, Tinkle SS, Weston A, Gordon T.
    J Immunotoxicol. 2009 Jun;6(2):130-5.

  44. Family history in public health practice: A genomic tool for disease prevention and health promotion
    Valdez R, Yoon PW, Qureshi N, Green RF, Khoury MJ.
    Annu Rev Public Health. 2010 Jan 12.

  45. Synthetic viruses: a new opportunity to understand and prevent viral disease
    Wimmer E, Mueller S, Tumpey TM, Taubenberger JK.
    Nat Biotechnol. 2009 Dec;27(12):1163-72.

  46. Using lifetime risk estimates in personal genomic profiles: estimation of uncertainty
    Yang Q, Flanders WD, Moonesinghe R, Ioannidis JP, Guessous I, Khoury MJ.
    Am J Hum Genet. 2009 Nov 18.

  47. Phenopedia and Genopedia: disease-centered and gene-centered views of the evolving knowledge of human genetic associations
    Yu W, Clyne M, Khoury MJ, Gwinn M.
    Bioinformatics. 2009 Oct 27.

  48. Systems-based candidate genes for human response to influenza infection
    Zhang L, Katz JM, Gwinn M, Dowling NF, Khoury MJ.
    Infect Genet Evol. 2009 Jul 29.

  49. Genetic characterization of Chinese measles vaccines by analysis of complete genomic sequences
    Zhang Y, Zhou J, Bellini WJ, Xu W, Rota PA.
    J Med Virol. 2009 Aug;81(8):1477-83.

  50. Assessment of improved prediction beyond traditional risk factors: when does a difference make a difference?
    Janssens AC, Khoury MJ.
    Circ Cardiovasc Genet. 2010 Feb 1;3(1):3-5.

  51. Personal genomics: information can be harmful
    Ransohoff DF, Khoury MJ.
    Eur J Clin Invest. 2010 Jan;40(1):64-8.

  52. Association between 9p21 genomic markers and heart disease: a meta-analysis
    Palomaki GE, Melillo S, Bradley LA.
    JAMA. 2010 Feb 17;303(7):648-56.

  53. Association between a literature-based genetic risk score and cardiovascular events in women
    Paynter NP, Chasman DI, Pare G, Buring JE, Cook NR, Miletich JP, Ridker PM.
    JAMA. 2010 Feb 17;303(7):631-7.

  54. General cardiovascular risk profile identifies advanced coronary artery calcium and is improved by family history: the multiethnic study of atherosclerosis
    Scheuner MT, Setodji CM, Pankow JS, Blumenthal RS, Keeler E.
    Circ Cardiovasc Genet. 2010 Feb 1;3(1):97-105.

  55. Host genes associated with HIV/AIDS: advances in gene discovery
    An P, Winkler CA.
    Trends Genet. 2010 Feb 9.

  56. Complications associated with carrier status among people with blood disorders: a commentary
    Hooper WC, Miller CH, Key NS.
    Am J Prev Med. 2010 Apr;38(4 Suppl):S456-8.

  57. Gene polymorphisms in association with emerging cardiovascular risk markers in adult women
    Fan AZ, Yesupriya A, Chang MH, House M, Fang J, Ned R, Hayes D, Dowling NF, Mokdad AH.
    BMC Med Genet. 2010 ;11:6.

  58. Common genetic variants and cancer risk in Mendelian cancer syndromes
    Antoniou AC, Chenevix-Trench G.
    Curr Opin Genet Dev. 2010 Apr 15.

  59. Mendelian disorders and multifactorial traits: the big divide or one for all?
    Antonarakis SE, Chakravarti A, Cohen JC, Hardy J.
    Nat Rev Genet. 2010 May;11(5):380-4.

  60. Genetics and cardiac channelopathies
    Campuzano O, Beltran-Alvarez P, Iglesias A, Scornik F, Perez G, Brugada R.
    Genet Med. 2010 Apr 8.

  61. Warfarin genotyping reduces hospitalization rates: results from the MM-WES (Medco-Mayo Warfarin Effectiveness Study)
    Epstein RS, Moyer TP, Aubert RE, O'Kane DJ, Xia F, Verbrugge RR, Gage BF, et al.
    J Am Coll Cardiol. 2010 Apr 7.

  62. International network of cancer genome projects
    Nature. 2010 Apr 15;464(7291):993-8.

  63. Debating clinical utility
    Burke W, Laberge AM, Press N.
    Public Health Genomics. 2010 ;13(4):215-23.

  64. Mainstreaming genetics: a comparative review of clinical services for inherited cardiovascular conditions in the UK
    Burton H, Alberg C, Stewart A.
    Public Health Genomics. 2010 ;13(4):235-45.

  65. Framing genomics, public health research and policy: points to consider
    Knoppers BM, Leroux T, Doucet H, Godard B, Laberge C, Stanton-Jean M, Fortin S, et al.
    Public Health Genomics. 2010 ;13(4):224-34.

  66. On track? Using the Human Genome Epidemiology Roadmap
    Little J, Hawken S.
    Public Health Genomics. 2010 ;13(4):256-66.

  67. Future health applications of genomics: priorities for communication, behavioral, and social sciences research
    McBride CM, Bowen D, Brody LC, Condit CM, Croyle RT, Gwinn M, Khoury MJ, Koehly LM, Korf BR, Marteau TM, McLeroy K, Patrick K, Valente TW.
    Am J Prev Med. 2010 May;38(5):556-65.

  68. Dealing with the evidence dilemma in genomics and personalized medicine
    Khoury MJ.
    Clin Pharmacol Ther. 2010 Jun;87(6):635-8.

  69. Role of human immunodeficiency virus type 1 integrase in uncoating of the viral core
    Briones MS, Dobard CW, Chow SA.
    J Virol. 2010 May;84(10):5181-90.

  70. Lethal dissemination of H5N1 influenza virus is associated with dysregulation of inflammation and lipoxin signaling in a mouse model of infection
    Cilloniz C, Pantin-Jackwood MJ, Ni C, Goodman AG, Peng X, Proll SC, Carter VS, Rosenzweig ER, Szretter KJ, Katz JM, Korth MJ, Swayne DE, Tumpey TM, Katze MG.
    J Virol. 2010 May 26.

  71. Improvements in ability to detect undiagnosed diabetes by using information on family history among adults in the United States
    Yang Q, Liu T, Valdez R, Moonesinghe R, Khoury MJ.
    Am J Epidemiol. 2010 May 15;171(10):1079-89.

  72. Preferences for genetic and behavioral health information: the impact of risk factors and disease attributions
    O'Neill SC, McBride CM, Alford SH, Kaphingst KA.
    Ann Behav Med. 2010 Jun 8.

  73. SNPs in CAST are associated with Parkinson disease: a confirmation study
    Allen AS, Satten GA.
    Am J Med Genet B Neuropsychiatr Genet. 2010 Jun 5;153B(4):973-9.

  74. The clinical utility of molecular diagnostic testing for primary immune deficiency disorders: a case based review
    Ameratunga R, Woon ST, Neas K, Love DR.
    Allergy Asthma Clin Immunol. 2010 Jun 8;6(1):12.

  75. Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA
    Bostrom MA, Lu L, Chou J, Hicks PJ, Xu J, Langefeld CD, Bowden DW, et al.
    Hum Genet. 2010 Jun 8.

  76. Advancing public health genomics in Africa through prospective cohort studies
    Dalal S, Holmes MD, Ramesar RS.
    J Epidemiol Community Health. 2010 Jul;64(7):585-6.

  77. The genetics of obesity and the metabolic syndrome
    Monda KL, North KE, Hunt SC, Rao DC, Province MA, Kraja AT.
    Endocr Metab Immune Disord Drug Targets. 2010 Jun 1;10(2):86-108.

  78. Cystic fibrosis newborn screening: using experience to optimize the screening algorithm
    Hale JE, Parad RB, Dorkin HL, Gerstle R, Lapey A, O'Sullivan BP, Spencer T, et al.
    J Inherit Metab Dis. 2010 Jun 3.

  79. CISH and susceptibility to infectious diseases
    Khor CC, Vannberg FO, Chapman SJ, Guo H, Wong SH, Walley AJ, Vukcevic D, et al.
    N Engl J Med. 2010 Jun 3;362(22):2092-101.

  80. Functional impact of global rare copy number variation in autism spectrum disorders
    Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, et al.
    Nature. 2010 Jun 9.

  81. Microprocessor of microRNAs: regulation and potential for therapeutic intervention
    Beezhold KJ, Castranova V, Chen F.
    Mol Cancer. 2010 ;9:134.

  82. High diversity and ancient common ancestry of lymphocytic choriomeningitis virus
    Albarino CG, Palacios G, Khristova ML, Erickson BR, Carroll SA, Comer JA, Hui J, Briese T, St George K, Ksiazek TG, Lipkin WI, Nichol ST.
    Emerg Infect Dis. 2010 Jul;16(7):1093-100.

  83. Molecular epidemiology of group A rotavirus in Buenos Aires, Argentina 2004-2007: reemergence of G2P[4] and emergence of G9P[8] strains
    Esteban LE, Rota RP, Gentsch JR, Jiang B, Esona M, Glass RI, Glikmann G, Castello AA.
    J Med Virol. 2010 May;82(6):1083-1093.

  84. Family history and personal genomics as tools for improving health in an era of evidence-based medicine
    Khoury MJ, Feero WG, Valdez R.
    Am J Prev Med. 2010 Aug;39(2):184-8.

  85. When is correlation coevolution?
    Nuismer SL, Gomulkiewicz R, Ridenhour BJ.
    Am Nat. 2010 May;175(5):525-37.

  86. Evidence for negative selection on the gene encoding rhoptry-associated protein 1 (RAP-1) in Plasmodium spp
    Pacheco MA, Ryan EM, Poe AC, Basco L, Udhayakumar V, Collins WE, Escalante AA.
    Infect Genet Evol. 2010 Jul;10(5):655-61.

  87. Characterization of novel Brucella strains originating from wild native rodent species in North Queensland, Australia
    Tiller RV, Gee JE, Frace MA, Taylor TK, Setubal JC, Hoffmaster AR, De BK.
    Appl Environ Microbiol. 2010 Jul 16.

  88. Score-based adjustment for confounding by population stratification in genetic association studies
    Allen A, Epstein MP, Satten GA.
    Genet Epidemiol. 2010 Jul;34(5):383-5.

  89. Genetic factors associated with elevated carbapenem resistance in KPC-producing Klebsiella pneumoniae
    Kitchel B, Rasheed JK, Endimiani A, Hujer AM, Anderson KF, Bonomo RA, Patel JB.
    Antimicrob Agents Chemother. 2010 Jul 26.

  90. High degree of genetic diversity of non-polio enteroviruses identified in Georgia by environmental and clinical surveillance, 2002-2005
    Khetsuriani N, Kutateladze T, Zangaladze E, Shutkova T, Penaranda S, Nix WA, Pallansch M, Oberste MS.
    J Med Microbiol. 2010 Jul 29.

  91. Caffeine, selected metabolic gene variants, and risk for neural tube defects
    Schmidt RJ, Romitti PA, Burns TL, Murray JC, Browne ML, Druschel CM, Olney RS.
    Birth Defects Res A Clin Mol Teratol. 2010 Jul;88(7):560-9.

  92. A breast cancer prognostic signature predicts clinical outcomes in multiple tumor types
    Wan YW, Qian Y, Rathnagiriswaran S, Castranova V, Guo NL.
    Oncol Rep. 2010 Aug;24(2):489-94.

  93. [The example of cystic fibrosis to highlight the complexity of genetic screening] [in French]
    Bochud M, Fellmann F, Vader JP, Grosse S, Paccaud F, Guessous I.
    Rev Med Suisse. 2010 Jul 14;6(256):1395-9.

  94. Racial/ethnic differences in association of fasting glucose-associated genomic loci with fasting glucose, HOMA-B and impaired fasting glucose in U.S. adult population
    Yang Q, Liu T, Shrader P, Yesupriya A, Chang MH, Dowling NF, Ned RM, Dupuis J, Florez JC, Khoury MJ, Meigs JB.
    Diabetes Care. 2010 Aug 30.

  95. Evaluation of the validity and utility of genetic testing for rare diseases
    Grosse SD, Kalman L, Khoury MJ.
    Adv Exp Med Biol. 2010 ;686:115-31.

  96. Microdeletions of 3q29 confer high risk for schizophrenia
    Mulle JG, Dodd AF, McGrath JA, Wolyniec PS, Mitchell AA, Shetty AC, Sobreira NL, Valle D, Rudd MK, Satten G, Cutler DJ, Pulver AE, Warren ST.
    Am J Hum Genet. 2010 Aug 13;87(2):229-36.

  97. Molecular epidemiology of infectious diseases - expanding horizons for IJMEG
    Xiao L, Kehoe PG.
    Int J Mol Epidemiol Genet. 2010 ;1 (3):245-247.

  98. Emergence and characterization of serotype G9 rotavirus strains from Africa
    Page N, Esona M, Armah G, Nyangao J, Mwenda J, Sebunya T, Basu G, Pyndiah N, Potgieter N, Geyer A, Steele AD.
    J Infect Dis. 2010 Sep 1;202 Suppl:S55-63.

  99. Hybrid models identified a 12-gene signature for lung cancer prognosis and chemoresponse prediction
    Wan YW, Sabbagh E, Raese R, Qian Y, Luo D, Denvir J, Vallyathan V, Castranova V, Guo NL.
    PLoS ONE. 2010 ;5(8).

  100. Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality
    Domchek SM, Friebel TM, Singer CF, Evans DG, Lynch HT, Isaacs C, Garber JE, et al.
    JAMA. 2010 Sep 1;304(9):967-75.

  101. Physical activity attenuates the genetic predisposition to obesity in 20,000 men and women from EPIC-Norfolk prospective population study
    Li S, Zhao JH, Luan J, Ekelund U, Luben RN, Khaw KT, Wareham NJ, et al.
    PLoS Med. 2010 ;7(8).

  102. Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease
    Davila S, Wright VJ, Khor CC, Sim KS, Binder A, Breunis WB, Inwald D, et al.
    Nat Genet. 2010 Sep;42(9):772-6.

  103. Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2
    Thye T, Vannberg FO, Wong SH, Owusu-Dabo E, Osei I, Gyapong J, Sirugo G, et al.
    Nat Genet. 2010 Sep;42(9):739-41.

  104. Genome-wide association study identifies 1p36.22 as a new susceptibility locus for hepatocellular carcinoma in chronic hepatitis B virus carriers
    Zhang H, Zhai Y, Hu Z, Wu C, Qian J, Jia W, Ma F, et al.
    Nat Genet. 2010 Sep;42(9):755-8.

  105. An interferon-inducible neutrophil-driven blood transcriptional signature in human tuberculosis
    Berry MP, Graham CM, McNab FW, Xu Z, Bloch SA, Oni T, Wilkinson KA, et al.
    Nature. 2010 Aug 19;466(7309):973-7.

  106. Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa Heart Study
    Smith EN, Chen W, Kahonen M, Kettunen J, Lehtimaki T, Peltonen L, Raitakari OT, et al.
    PLoS Genet. 2010 ;6(9).

  107. PLoS Currents: Evidence on genomic tests - at the crossroads of translation
    Gwinn M, Dotson .D, Khoury MJ.
    PLoS Curr. 2010 .

  108. Tumor gene expression profiling in women with breast cancer
    Bellcross C, Dotson W.
    PLoS Curr. 2010 .

  109. Testing of VKORC1 and CYP2C9 alleles to guide warfarin dosing
    Grossniklaus D.
    PLoS Curr. 2010 .

  110. Family history of diabetes and prevalence of the metabolic syndrome in U.S. adults without diabetes: 6-year results from the National Health and Nutrition Examination Survey (1999-2004)
    Ghosh A, Liu T, Khoury MJ, Valdez R.
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  146. Sequencing and phylogenetic analysis of the coding region of six common rotavirus strains: evidence for intragenogroup reassortment among co-circulating G1P[8] and G2P[4] strains from the United States
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  187. Erratum: Molecular monitoring of resistant dhfr and dhps allelic haplotypes in Morogoro and Mvomero districts in south eastern Tanzania
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  196. Implementing screening for Lynch syndrome among patients with newly diagnosed with colorectal cancer: summary of a public health/clinical collaborative meeting
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  220. The association of variants in the FTO gene with longitudinal body mass index profiles in non-Hispanic white children and adolescents
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  221. Genetic diversity of HA1 domain of hemagglutinin gene of pandemic influenza H1N1pdm09 viruses in New Delhi, India
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  222. Permanent genetic resources added to Molecular Ecology Resources Database 1 October 2011 - 30 November 2011
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  224. Looking back at genomic medicine in 2011
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  225. Estimating the contribution of genetic variants to difference in incidence of disease between population groups
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  230. Genetic backgrounds of the Plasmodium falciparum chloroquine resistant transporter (pfcrt) alleles in Pakistan
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  231. The 3' untranslated regions of influenza genomic sequences are 5'PPP-independent ligands for RIG-I
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  235. Genetic characterization of measles viruses that circulated in Thailand from 1998 to 2008
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  236. Binding of cellular p32 protein to the rubella virus P150 replicase protein via PxxPxR motifs
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  238. Prospective study of methylenetetrahydrofolate reductase (MTHFR) variant C677T and risk of all-cause and cardiovascular disease mortality among 6000 US adults
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  243. Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: the PDGene database
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  244. Implications of Internet availability of genomic information for public health practice
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  245. Introduction to the 4th National Conference on Genomics and Public Health
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  247. Knowledge integration at the center of genomic medicine
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  248. Convergence and coevolution of Hepatitis B virus drug resistance
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  249. Evidence of purifying selection on merozoite surface protein 8 (MSP8) and 10 (MSP10) in Plasmodium spp
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  250. Molecular characterization of diarrheagenic Escherichia coli from Libya
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  251. Detectable clonal mosaicism and its relationship to aging and cancer
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  253. A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia
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  254. Prevalence of CGG expansions of the FMR1 gene in a US population-based sample
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  255. Mutation analysis of the cross-reactive epitopes of Japanese encephalitis virus envelope glycoprotein
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  256. Inclusion of gene-gene and gene-environment interactions unlikely to dramatically improve risk prediction for complex diseases
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  259. Intragenic ATM methylation in peripheral blood DNA as a biomarker of breast cancer risk
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  260. Is the process of delivery of an individually tailored lifestyle intervention associated with improvements in LDL cholesterol and multiple lifestyle behaviours in people with Familial Hypercholesterolemia?
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  261. Influence of family history of colorectal cancer on health behavior and performance of early detection procedures: the SUN Project
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  264. Influence of HLA-DRB1 and HLA-DQB1 alleles on IgG antibody response to the P. vivax MSP-1, MSP-3alpha and MSP-9 in individuals from Brazilian endemic area
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  266. Differential association of gene content polymorphisms of killer cell immunoglobulin-like receptors with placental malaria in HIV- and HIV+ mothers
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  271. Genetic variants in IGF-I, IGF-II, IGFBP-3, and adiponectin genes and colon cancer risk in African Americans and Whites
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  272. Estrogen-related genes and their contribution to racial differences in breast cancer risk
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  275. Relaxation of adaptive evolution during the HIV-1 infection owing to reduction of CD4+ T cell counts
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  277. Reverse genetics recovery of Lujo virus and role of virus RNA secondary structures in efficient virus growth
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  278. Ethnicity interacts with the OPRM1 gene in experimental pain sensitivity
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  279. A report template for molecular genetic tests designed to improve communication between the clinician and laboratory
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  280. A smoking-associated 7-gene signature for lung cancer diagnosis and prognosis
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  281. Evolutionary history and phylodynamics of influenza A and B neuraminidase (NA) genes inferred from large-scale sequence analyses
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  282. Virological and molecular characterization of a simian human immunodeficiency virus (SHIV) encoding the envelope and reverse transcriptase genes from HIV-1
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  283. Phylogeny of shiga toxin-producing Escherichia coli O157 isolated from cattle and clinically ill humans
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  285. A permutation procedure to correct for confounders in case-control studies, including tests of rare variation
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  286. Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease
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  289. Multilocus sequence subtyping and genetic structure of Cryptosporidium muris and Cryptosporidium andersoni
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  294. Multiwalled carbon nanotube-induced gene signatures in the mouse lung: potential predictive value for human lung cancer risk and prognosis
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  295. The malaria parasite Plasmodium vivax exhibits greater genetic diversity than Plasmodium falciparum
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  297. Genome sequences for six Rhodanobacter strains, isolated from soils and the terrestrial subsurface, with variable denitrification capabilities
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  303. Genome-wide association study of glioma and meta-analysis
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  304. Genomic comparison of Escherichia coli O104:H4 isolates from 2009 and 2011 reveals plasmid, and prophage heterogeneity, including Shiga toxin encoding phage stx2
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  306. Whole genome sequence typing to investigate the Apophysomyces outbreak following a tornado in Joplin, Missouri, 2011
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  324. Rapid hepatitis C virus divergence among chronically infected individuals
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  328. Hepatitis E virus isolated from rabbits is genetically heterogeneous but with very similar antigenicity to human HEV
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  329. Analysis of whole genome sequences of 16 strains of rubella virus from the United States, 1961-2009
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  331. Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: a report from the National Down Syndrome Project
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  332. Draft genome sequences of Bordetella holmesii strains from blood (F627) and nasopharynx (H558)
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  333. CrcZ and CrcX regulate carbon source utilization in Pseudomonas syringae pathovar tomato strain DC3000
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  336. Molecular evolution of viruses of the family Filoviridae based on 97 whole-genome sequences
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  338. Analysis of circulating tumor DNA to monitor metastatic breast cancer
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  340. Historical shifts in Brazilian P. falciparum population structure and drug resistance alleles
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  343. Genetic susceptibility to West Nile virus and dengue
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  346. Early onset breast cancer in a registry-based sample of African-American women: BRCA mutation prevalence, and other personal and system-level clinical characteristics
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  347. Genomics for public health improvement: relevant international ethical and policy issues around genome-wide association studies and biobanks
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  352. Relationships between selected gene polymorphisms and blood pressure sensitivity to weight loss in elderly persons with hypertension
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  353. Mutation of the dengue virus type 2 envelope protein heparan sulfate binding sites or the domain III lateral ridge blocks replication in Vero cells prior to membrane fusion
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  358. Prevalence and healthcare actions of women in a large health system with a family history meeting the 2005 USPSTF recommendation for BRCA genetic counseling referral
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  359. Comparative effectiveness research in cancer genomics and precision medicine: current landscape and future prospects
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  360. Genome sequence of Salmonella enterica serotype Tennessee strain CDC07-0191, implicated in the 2006-2007 multistate food-borne outbreak linked to peanut butter in the United States
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  362. The genome sequence of Lone Star virus, a highly divergent bunyavirus found in the Amblyomma americanum tick
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  363. Isolation and full genomic characterization of Batai virus from mosquitoes, Italy 2009
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  364. Telomere length and elevated iron: the influence of phenotype and HFE genotype
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  365. Antimicrobial resistance genes in multidrug-resistant Salmonella enterica isolated from animals, retail meats, and humans in the United States and Canada
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  366. Human G9P[8] rotavirus strains circulating in Cameroon, 1999-2000: genetic relationships with other G9 strains and detection of a new G9 subtype
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  367. Plasmodium vivax merozoite surface protein-3 (PvMSP3): expression of an 11 member multigene family in blood-stage parasites
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  368. Current landscape and new paradigms of proficiency testing and external quality assessment for molecular genetics
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  369. One year survey of human rotavirus strains suggests the emergence of genotype g12 in Cameroon
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  370. The microRNA-200 family targets multiple non-small cell lung cancer prognostic markers in H1299 cells and BEAS-2B cells
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  371. Development of a genomic DNA reference material panel for myotonic dystrophy type 1 (DM1) genetic testing
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  373. Current landscape and new paradigms of proficiency testing and external quality assessment for molecular genetics
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  374. The microRNA-200 family targets multiple non-small cell lung cancer prognostic markers in H1299 cells and BEAS-2B cells
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  375. Development of a genomic DNA reference material panel for myotonic dystrophy type 1 (DM1) genetic testing
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  378. Shared Mycobacterium avium genotypes observed among unlinked clinical and environmental isolates
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  379. Reconstruction of viral population structure from next-generation sequencing data using multicommodity flows
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  380. Dihydropteroate synthase mutations in Pneumocystis pneumonia: impact of applying different definitions of prophylaxis, mortality endpoints and mutant in a single cohort
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  381. Phenotypic, genomic, and transcriptional characterization of Streptococcus pneumoniae interacting with human pharyngeal cells
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  382. Invasive methicillin-resistant staphylococcus aureus infections among chronic dialysis patients in the United States, 2005-2011
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  383. Molecular mechanisms of macrolide resistant invasive Streptococcus pneumoniae isolates from Alaska, 1986 to 2010
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  384. Joint effects between five identified risk variants, allergy, and autoimmune conditions on glioma risk
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  386. Standard enrichment methods for targeted next-generation sequencing in high-repeat genomic regions
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  387. Recommendations for returning genomic incidental findings? We need to talk!
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  388. Economic analyses of genetic tests in personalized medicine: clinical utility first, then cost utility
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  389. Internal transcribed spacer rRNA gene sequencing analysis of fungal diversity in Kansas City indoor environments
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  395. Expanding diagnostic testing beyond cytogenetics: implications for birth defects research and surveillance
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  396. Discovery and full genome characterization of two highly divergent simian immunodeficiency viruses infecting black-and-white colobus monkeys (Colobus guereza) in Kibale National Park, Uganda
    Lauck M, Baggett HC, Switzer WM, Sibley SD, Hyeroba D, Tumukunde A, Weny G, Taylor B, Shankar A, Ting N, Chapman CA, Friedrich TC, Goldberg TL, O. Connor DH.
    Retrovirology. 2013 Oct 21;10(1):107.

  397. DNA-DNA hybridization study of strains of Chryseobacterium, Elizabethkingia and Empedobacter and of other usually indole-producing non-fermenters of CDC groups IIc, IIe, IIh and IIi, mostly from human clinical sources, and proposals of Chryseobacterium bernardetii sp. nov., Chryseobacterium carnis sp. nov., Chryseobacterium lactis sp. nov., Chryseobacterium nakagawai sp. nov. and Chryseobacterium taklimakanense comb. nov
    Holmes B, Steigerwalt AG, Nicholson AC.
    Int J Syst Evol Microbiol. 2013 Dec;63(Pt 12):4639-62.

  398. Replacement and positive evolution of subtype A and B respiratory syncytial virus g-protein genotypes from 1997-2012 in South Africa
    Pretorius MA, van Niekerk S, Tempia S, Moyes J, Cohen C, Madhi SA, Venter M.
    J Infect Dis. 2013 Dec;208 Suppl 3:S227-37.

  399. Mutation analysis of a cohort of US patients with hemophilia B
    Li T, Miller CH, Driggers J, Payne AB, Ellingsen D, Hooper WC.
    Am J Hematol. 2013 Dec 4.

  400. Rotavirus G and P types circulating in the eastern region of Kenya: predominance of G9 and emergence of G12 genotypes
    Kiulia NM, Nyaga MM, Seheri ML, Wolfaardt M, van Zyl WB, Esona MD, Irimu G, Inoti M, Gatinu BW, Njenga PK, Taylor MB, Nyachieo A.
    Pediatr Infect Dis J. 2014 Jan;33 Suppl 1:S85-8.

  401. Full-length genome characterization and genetic relatedness analysis of hepatitis A virus outbreak strains associated with acute liver failure among children
    Vaughan G, Forbi JC, Xia GL, Fonseca-Ford M, Vazquez R, Khudyakov YE, Montiel S, Waterman S, Alpuche C, Goncalves Rossi LM, Luna N.
    J Med Virol. 2014 Feb;86(2):202-8.

  402. Horizon scanning for translational genomic research beyond bench to bedside
    Clyne M, Schully SD, Dotson WD, Douglas MP, Gwinn M, Kolor K, Wulf A, Bowen MS, Khoury MJ.
    Genet Med. 2014 Jan 9.

  403. Prioritizing genomic applications for action by level of evidence: a horizon-scanning method
    Dotson WD, Douglas MP, Kolor K, Stewart AC, Bowen MS, Gwinn M, Wulf A, Anders HM, Chang CQ, Clyne M, Lam TK, Schully SD, Marrone M, Feero WG, Khoury MJ.
    Clin Pharmacol Ther. 2013 Nov 14.

  404. Genetic analysis of G12P[8] rotaviruses detected in the largest U.S. G12 genotype outbreak on record
    Mijatovic-Rustempasic S, Teel EN, Kerin TK, Hull JJ, Roy S, Weinberg GA, Payne DC, Parashar UD, Gentsch JR, Bowen MD.
    Infect Genet Evol. 2013 Nov 21;21c:214-219.

  405. Scientific reporting is suboptimal for aspects that characterize genetic risk prediction studies: a review of published articles based on the Genetic RIsk Prediction Studies statement
    Iglesias AI, Mihaescu R, Ioannidis JP, Khoury MJ, Little J, van Duijn CM, Janssens AC.
    J Clin Epidemiol. 2014 Jan 7.

  406. Draft genome sequence of Mortierella alpina isolate CDC-B6842
    Etienne KA, Chibucos MC, Su Q, Orvis J, Daugherty S, Ott S, Sengamalay NA, Fraser CM, Lockhart SR, Bruno VM.
    Genome Announc. 2014 ;2(1).

  407. Development of a genomic DNA reference material panel for Rett syndrome (MECP2-related disorders) genetic testing
    Kalman LV, Tarleton JC, Percy AK, Aradhya S, Bale S, Barker SD, Bayrak-Toydemir P, Bridges C, Buller-Burckle AM, Das S, Iyer RK, Vo TD, Zvereff VV, Toji LH.
    J Mol Diagn. 2014 Mar;16(2):273-9.

  408. Robust regression analysis of copy number variation data based on a univariate score
    Satten GA, Allen AS, Ikeda M, Mulle JG, Warren ST.
    PLoS One. 2014 ;9(2):e86272.

  409. Cryptosporidium parvum IId family: clonal population and dispersal from Western Asia to other geographical regions
    Wang R, Zhang L, Axen C, Bjorkman C, Jian F, Amer S, Liu A, Feng Y, Li G, Lv C, Zhao Z, Qi M, Dong H, Wang H, Sun Y, Ning C, Xiao L.
    Sci Rep. 2014 ;4:4208.

  410. Characterizing tuberculosis genotype clusters along the United States-Mexico border
    Baker BJ, Moonan PK.
    Int J Tuberc Lung Dis. 2014 01 Mar;18(3):289-291.

  411. Evolution and structural organization of the C proteins of paramyxovirinae
    Lo MK, Sogaard TM, Karlin DG.
    PLoS One. 2014 ;9(2):e90003.

  412. Prothrombin G20210A mutation is associated with young-onset stroke: the Genetics of Early-Onset Stroke Study and Meta-Analysis
    Jiang B, Ryan KA, Hamedani A, Cheng Y, Sparks MJ, Koontz D, Bean CJ, Gallagher M, Hooper WC, McArdle PF, O'Connell JR, Stine OC, Wozniak MA, Stern BJ, Mitchell BD, Kittner SJ, Cole JW.
    Stroke. 2014 Mar 11.

  413. Recombinant viruses initiated the early HIV-1 epidemic in Burkina Faso
    Fonjungo PN, Kalish ML, Schaefer A, Rayfield M, Mika J, Rose LE, Heslop O, Soudre R, Pieniazek D.
    PLoS One. 2014 ;9(3):e92423.

  414. Characterization of Clostridium botulinum strains producing BoNT/F4 or BoNT/F5
    Raphael BH, Bradshaw M, Kalb SR, Joseph LA, Luquez C, Barr JR, Johnson EA, Maslanka SE.
    Appl Environ Microbiol. 2014 Mar 14.

  415. Genetic host specificity of hepatitis E virus
    Lara J, Purdy MA, Khudyakov YE.
    Infect Genet Evol. 2014 Mar 22.

  416. Full-genome sequence of a rare human G3P[9] rotavirus strain
    Mijatovic-Rustempasic S, Roy S, Sturgeon M, Rungsrisuriyachai K, Esona MD, Degroat D, Qin X, Cortese MM, Bowen MD.
    Genome Announc. 2014 ;2(2).

  417. Wild-type measles viruses with non-standard genome lengths
    Bankamp B, Liu C, Rivailler P, Bera J, Shrivastava S, Kirkness EF, Bellini WJ, Rota PA.
    PLoS One. 2014 Apr 18;9(4):e95470.

  418. Utilizing population controls in rare-variant case-parent association tests
    Jiang Y, Satten GA, Han Y, Epstein MP, Heinzen EL, Goldstein DB, Allen AS.
    Am J Hum Genet. 2014 May 14.

  419. Draft genome sequence of Bacillus cereus strain BcFL2013, a clinical isolate similar to G9241
    Gee JE, Marston CK, Sammons SA, Burroughs MA, Hoffmaster AR.
    Genome Announc. 2014 May 29;2(3).

  420. Translational research is a key to nongeneticist physicians' genomics education
    Feero WG, Manolio TA, Khoury MJ.
    Genet Med. 2014 May 29.

  421. Draft genome sequences of nine enteropathogenic Escherichia coli strains from Kenya
    Hazen TH, Humphrys MS, Ochieng JB, Parsons M, Bopp CA, O'Reilly CE, Mintz E, Rasko DA.
    Genome Announc. 2014 Jun 12;2(3).

  422. Real-time PCR assays for genotyping of Cryptococcus gattii in North America
    Kelley EJ, Driebe EM, Etienne K, Brandt ME, Schupp JM, Gillece JD, Trujillo JS, Lockhart SR, Deak E, Keim PS, Engelthaler DM.
    BMC Microbiol. 2014 May 13;14(1):125.

  423. Dense genotyping of immune-related loci identifies variants associated with clearance of HPV among HIV-positive women in the HIV Epidemiology Research Study (HERS)
    Sudenga SL, Wiener HW, King CC, Rompalo AM, Cu-Uvin S, Klein RS, Shah KV, Sobel JD, Jamieson DJ, Shrestha S.
    PLoS One. 2014 Jun 11;9(6):e99109.

  424. Evolutionary genetics of genotype H1 measles viruses in China from 1993-2012
    Xu S, Zhang Y, Rivailler P, Wang H, Ji Y, Zhen Z, Mao N, Li C, Bellini WJ, Xu W, Rota P.
    J Gen Virol. 2014 Jun 9.

  425. Deriving group A Streptococcus typing information from short-read whole-genome sequencing data
    Athey TB, Teatero S, Li A, Marchand-Austin A, Beall BW, Fittipaldi N.
    J Clin Microbiol. 2014 Jun;52(6):1871-6.

  426. Heterogeneity of the internal transcribed spacer region in Leishmania tropica isolates from southern Iran
    Ghatee MA, Sharifi I, Kuhls K, Kanannejad Z, Fasihi Harandi M, de Almeida ME, Hatam G, Mirhendi H.
    Exp Parasitol. 2014 Jun 14.

  427. Genome sequences of nine Bordetella holmesii strains isolated in the United States
    Harvill ET, Goodfield LL, Ivanov Y, Smallridge WE, Meyer JA, Cassiday PK, Tondella ML, Brinkac L, Sanka R, Kim M, Losada L.
    Genome Announc. 2014 Jun 19;2(3).

  428. Whole genome analysis of Exserohilum rostratum from the outbreak of fungal meningitis and other infections
    Litvintseva AP, Hurst S, Gade L, Frace MA, Hilsabeck R, Schupp JM, Gillece JD, Roe C, Smith D, Keim P, Lockhart SR, Changayil S, Weil MR, MacCannell DR, Brandt ME, Engelthaler DM.
    J Clin Microbiol. 2014 Jun 20.

  429. Evidence synthesis and guideline development in genomic medicine: current status and future prospects
    Schully SD, Lam TK, Dotson WD, Chang CQ, Aronson N, Birkeland ML, Brewster SJ, Boccia S, Buchanan AH, Calonge N, Calzone K, Djulbegovic B, Goddard KA, Klein RD, Klein TE, Lau J, Long R, Lyman GH, Morgan RL, Palmer CG, Relling MV, Rubinstein WS, Swen JJ, Terry SF, Williams MS, Khoury MJ.
    Genet Med. 2014 Jun 19.

  430. Immunoglobulin genes influence the magnitude of humoral immunity to cytomegalovirus glycoprotein B
    Pandey JP, Kistner-Griffin E, Radwan FF, Kaur N, Namboodiri AM, Black L, Butler MA, Carreon T, Ruder AM.
    J Infect Dis. 2014 Jun 27.

  431. Molecular analysis of single oocyst of Eimeria by whole genome amplification (WGA) based nested PCR
    Wang Y, Tao G, Cui Y, Lv Q, Xie L, Li Y, Suo X, Qin Y, Xiao L, Liu X.
    Exp Parasitol. 2014 Jul 1.

  432. Molecular analysis of single oocyst of Eimeria by whole genome amplification (WGA) based nested PCR
    Wang Y, Tao G, Cui Y, Lv Q, Xie L, Li Y, Suo X, Qin Y, Xiao L, Liu X.
    Exp Parasitol. 2014 Jul 1.


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