CDC Science Clips

Genetics and Genomics

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


2. Analysis of whole genome sequences of 16 strains of rubella virus from the United States, 1961-2009
   Abernathy E, Chen MH, Bera J, Shrivastava S, Kirkness E, Zheng Q, Bellini W, Icenogle J.
   Virol J. 2013 ;10:32.


3. Core gene set as the basis of multilocus sequence analysis of the subclass Actinobacteridae
   Adekambi T, Butler RW, Hanrahan F, Delcher AL, Drancourt M, Shinnick TM.
   PLoS One. 2011 ;6(3):e14792.


4. 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.


5. Genomic comparison of Escherichia coli O104:H4 isolates from 2009 and 2011 reveals plasmid, and prophage heterogeneity, including Shiga toxin encoding phage stx2
   Ahmed SA, Awosika J, Baldwin C, Bishop-Lilly KA, Biswas B, Broomall S, Chain PS, Chertkov O, Chokoshvili O, Coyne S, Davenport K, Detter JC, Dorman W, Erkkila TH, Folster JP, Frey KG, George M, Gleasner C, Henry M, Hill KK, Hubbard K, Insalaco J, Johnson S, Kitzmiller A, Krepps M, Lo CC, Luu T, McNew LA, Minogue T, Munk CA, Osborne B, Patel M, Reitenga KG, Rosenzweig CN, Shea A, Shen X, Strockbine N, Tarr C, Teshima H, van Gieson E, Verratti K, Wolcott M, Xie G, Sozhamannan S, Gibbons HS.
   PLoS One. 2012 ;7(11):e48228.


6. Selective sweeps and genetic lineages of Plasmodium falciparum drug -resistant alleles in Ghana
   Alam MT, de Souza DK, Vinayak S, Griffing SM, Poe AC, Duah NO, Ghansah A, Asamoa K, Slutsker L, Wilson MD, Barnwell JW, Udhayakumar V, Koram KA.
   J Infect Dis. 2011 Jan;203(2):220-7.


7. Efficient rescue of recombinant Lassa virus reveals the influence of S segment non-coding regions on virus replication and virulence
   Albarino CG, Bird BH, Chakrabarti AK, Dodd KA, Erickson BR, Nichol ST.
   J Virol. 2011 Feb 9.


8. Reverse genetics generation of chimeric infectious Junin/Lassa virus is dependent on interaction of homologous glycoprotein stable signal peptide and G2 cytoplasmic domains
   Albarino CG, Bird BH, Chakrabarti AK, Dodd KA, White DM, Bergeron E, Shrivastava-Ranjan P, Nichol ST.
   J Virol. 2010 Oct 27.


9. 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.


10. Molecular characterization of diarrheagenic Escherichia coli from Libya
    Ali MM, Mohamed ZK, Klena JD, Ahmed SF, Moussa TA, Ghenghesh KS.
    Am J Trop Med Hyg. 2012 May;86(5):866-71.


11. Age-associated DNA methylation in pediatric populations
    Alisch RS, Barwick BG, Chopra P, Myrick LK, Satten GA, Conneely KN, Warren ST.
    Genome Res. 2012 Apr;22(4):623-32.


12. 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.


13. 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.


14. Pharmacogenomics: will the promise be fulfilled?
    Altman RB, Kroemer HK, McCarty CA, Ratain MJ, Roden D.
    Nat Rev Genet. 2010 Nov 30.


15. 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.


16. 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.


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


18. 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.


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


20. Inclusion of gene-gene and gene-environment interactions unlikely to dramatically improve risk prediction for complex diseases
    Aschard H, Chen J, Cornelis MC, Chibnik LB, Karlson EW, Kraft P.
    Am J Hum Genet. 2012 May 23.


21. Genome medicine: past, present and future
    Auffray C, Caulfield T, Khoury MJ, Lupski JR, Schwab M, Veenstra T.
    Genome Med. 2011 Jan 31;3(1):6.


22. Looking back at genomic medicine in 2011
    Auffray C, Caulfield T, Khoury MJ, Lupski JR, Schwab M, Veenstra T.
    Genome Med. 2012 Jan 30;4(1):9.


23. New gene variants associated with venous thrombosis - a replication study in United States Whites and Blacks
    Austin H, De Staercke C, Lally C, Bezemer ID, Rosendaal FR, Hooper WC.
    J Thromb Haemost. 2011 Jan 13.


24. Association between family history and coronary heart disease death across long-term follow-up in men: the Cooper Center Longitudinal Study
    Bachmann JM, Willis BL, Ayers CR, Khera A, Berry JD.
    Circulation. 2012 May 23.


25. A risk-benefit analysis of factor V Leiden testing to improve pregnancy outcomes: a case study of the capabilities of decision modeling in genomics
    Bajaj PS, Veenstra DL.
    Genet Med. 2012 Nov 8.


26. Genetic characterization of measles vaccine strains
    Bankamp B, Takeda M, Zhang Y, Xu W, Rota PA.
    J Infect Dis. 2011 Jul;204 Suppl 1:S533-48.


27. 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
    Banyai K, Mijatovic-Rustempasic S, Hull JJ, Esona MD, Freeman MM, Frace AM, Bowen MD, Gentsch JR.
    J Med Virol. 2011 Mar;83(3):532-9.


28. Single nucleotide polymorphism in the promoter region of the CD209 gene is associated with human predisposition to severe forms of tick-borne encephalitis
    Barkhash AV, Perelygin AA, Babenko VN, Brinton MA, Voevoda MI.
    Antiviral Res. 2012 Jan;93(1):64-8.


29. A hybrid approach for the automated finishing of bacterial genomes
    Bashir A, Klammer AA, Robins WP, Chin CS, Webster D, Paxinos E, Hsu D, Ashby M, Wang S, Peluso P, Sebra R, Sorenson J, Bullard J, Yen J, Valdovino M, Mollova E, Luong K, Lin S, Lamay B, Joshi A, Rowe L, Frace M, Tarr CL, Turnsek M, Davis BM, Kasarskis A, Mekalanos JJ, Waldor MK, Schadt EE.
    Nat Biotechnol. 2012 Jul 1.


30. Impact of CYP2C19 variant genotypes on clinical efficacy of antiplatelet treatment with clopidogrel: systematic review and meta-analysis
    Bauer T, Bouman HJ, van Werkum JW, Ford NF, Ten Berg JM, Taubert D.
    BMJ. 2011 ;343:d4588.


31. Shifting genetic structure of invasive serotype 19A pneumococci in the United States
    Beall BW, Gertz RE, Hulkower RL, Whitney CG, Moore MR, Brueggemann AB.
    J Infect Dis. 2011 Mar 11.


32. Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease
    Bean CJ, Boulet SL, Ellingsen D, Pyle ME, Barron-Casella EA, Casella JF, Payne AB, Driggers J, Trau HA, Yang G, Jones K, Ofori-Acquah SF, Hooper WC, Debaun MR.
    Blood. 2012 Sep 10.


33. Increased risk of venous thromboembolism is associated with genetic variation in heme oxygenase-1 in Blacks
    Bean CJ, Boulet SL, Ellingsen D, Trau H, Ghaji N, Hooper WC, Austin H.
    Thromb Res. 2012 Sep 6.


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


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


36. Implementing screening for Lynch syndrome among patients with newly diagnosed with colorectal cancer: summary of a public health/clinical collaborative meeting
    Bellcross CA, Bedrosian SR, Daniels E, Duquette D, Hampel H, Jasperson K, Joseph DA, Kaye C, Lubin I, Meyer LJ, Reyes M, Scheuner MT, Schully SD, Senter L, Stewart SL, St Pierre J, Westman J, Wise P, Yang VW, Khoury MJ.
    Genet Med. 2011 Oct 21.


37. Awareness and utilization of BRCA1/2 testing among U.S. primary care physicians
    Bellcross CA, Kolor K, Goddard KA, Coates RJ, Reyes M, Khoury MJ.
    Am J Prev Med. 2011 Jan;40(1):61-6.


38. Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time
    Berg JS, Khoury MJ, Evans JP.
    Genet Med. 2011 May 9.


39. Reverse genetics recovery of Lujo virus and role of virus RNA secondary structures in efficient virus growth
    Bergeron E, Chakrabarti AK, Bird BH, Dodd KA, McMullan LK, Spiropoulou CF, Nichol ST, Albarino CG.
    J Virol. 2012 Jul 25.


40. CTNNA3 (alpha-catenin) gene variants are associated with diisocyanate asthma: a replication study in a caucasian worker population
    Bernstein DI, Kashon M, Lummus ZL, Johnson VJ, Fluharty K, Gautrin D, Malo JL, Cartier A, Boulet LP, Sastre J, Quirce S, Germolec D, Tarlo SM, Cruz MJ, Munoz X, Luster MI, Yucesoy B.
    Toxicol Sci. 2012 Jan;131(1):242-6.


41. 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.


42. Offering aggregate results to participants in genomic research: opportunities and challenges
    Beskow LM, Burke W, Fullerton SM, Sharp RR.
    Genet Med. 2012 Jan 19.


43. Recommendations for ethical approaches to genotype-driven research recruitment
    Beskow LM, Fullerton SM, Namey EE, Nelson DK, Davis AM, Wilfond BS.
    Hum Genet. 2012 May 24.


44. 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.


45. The genetics of type 2 diabetes: what have we learned from GWAS?
    Billings LK, Florez JC.
    Ann N Y Acad Sci. 2010 Nov;1212(1):59-77.


46. The impact of family history of breast cancer on knowledge, attitudes, and early detection practices of Mexican women along the Mexico-US border
    Bird Y, Banegas MP, Moraros J, King S, Prapasiri S, Thompson B.
    J Immigr Minor Health. 2010 Nov 21.


47. Analysis of a non-structural gene reveals evidence of possible hepatitis C virus (HCV) compartmentalization
    Blackard JT, Ma G, Welge JA, Martin CM, Sherman KE, Taylor LE, Mayer KH, Jamieson DJ.
    J Med Virol. 2012 February;84(2):242-252.


48. [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.


49. Citizens' values regarding research with stored samples from newborn screening in Canada
    Bombard Y, Miller FA, Hayeems RZ, Carroll JC, Avard D, Wilson BJ, Little J, et al.
    Pediatrics. 2012 Jan 16.


50. Phylogeny of shiga toxin-producing Escherichia coli O157 isolated from cattle and clinically ill humans
    Bono JL, Smith TP, Keen JE, Harhay GP, McDaneld TG, Mandrell RE, Jung WK, Besser TE, Gerner-Smidt P, Bielaszewska M, Karch H, Clawson ML.
    Mol Biol Evol. 2012 Aug;29(8):2047-62.


51. 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.


52. Public attitudes regarding the use of residual newborn screening specimens for research
    Botkin JR, Rothwell E, Anderson R, Stark L, Goldenberg A, Lewis M, Burbank M, et al.
    Pediatrics. 2012 Jan 16.


53. 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.


54. Public health action in genomics is now needed beyond newborn screening
    Bowen MS, Kolor K, Dotson WD, Ned RM, Khoury MJ.
    Public Health Genomics. 2012 Sep 11.


55. RIG-I goes beyond naked recognition
    Bowzard JB, Ranjan P, Sambhara S.
    Cell Host Microbe. 2013 Mar 13;13(3):247-9.


56. RIG-I goes beyond naked recognition
    Bowzard JB, Ranjan P, Sambhara S.
    Cell Host Microbe. 2013 Mar 13;13(3):247-9.


57. Intragenic ATM methylation in peripheral blood DNA as a biomarker of breast cancer risk
    Brennan K, Garcia-Closas M, Orr N, Fletcher O, Jones M, Ashworth A, Swerdlow A, et al.
    Cancer Res. 2012 May 1;72(9):2304-2313.


58. 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.


59. 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?
    Broekhuizen K, Jelsma JG, van Poppel MN, Koppes LL, Brug J, van Mechelen W.
    BMC Public Health. 2012 May 14;12(1):348.


60. KPC-4 is encoded within a truncated Tn4401 in an IncL/M plasmid, pNE1280, isolated from Enterobacter cloacae and Serratia marcescens
    Bryant KA, Van Schooneveld TC, Thapa I, Bastola D, Williams LO, Safranek TJ, Hinrichs SH, Rupp ME, Fey PD.
    Antimicrob Agents Chemother. 2013 Jan;57(1):37-41.


61. Extending the reach of public health genomics: what should be the agenda for public health in an era of genome-based and "personalized" medicine?
    Burke W, Burton H, Hall AE, Karmali M, Khoury MJ, Knoppers B, Meslin EM, Stanley F, Wright CF, Zimmern RL.
    Genet Med. 2010 Dec;12(12):785-91.


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


63. 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.


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. Public health implications from COGS and potential for risk stratification and screening
    Burton H, Chowdhury S, Dent T, Hall A, Pashayan N, Pharoah P.
    Nat Genet. 2013 Apr;45(4):349-51.


66. Human monoclonal antibodies to West Nile virus identify epitopes on the prM protein
    Calvert AE, Kalantarov GF, Chang GJ, Trakht I, Blair CD, Roehrig JT.
    Virology. 2010 Nov 15.


67. Molecular detection of mutations associated with first and second-line drug resistance compared with conventional drug susceptibility testing in M. tuberculosis
    Campbell PJ, Morlock GP, Sikes RD, Dalton TL, Metchock B, Starks AM, Hooks DP, Cowan LS, Plikaytis BB, Posey JE.
    Antimicrob Agents Chemother. 2011 Feb 7.


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


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


70. Molecular evolution of viruses of the family Filoviridae based on 97 whole-genome sequences
    Carroll SA, Towner JS, Sealy TK, McMullan LK, Khristova ML, Burt FJ, Swanepoel R, Rollin PE, Nichol ST.
    J Virol. 2013 Mar;87(5):2608-16.


71. Race/ethnic variation in the association of lipid-related genetic variants with blood lipids in the adult U.S. population
    Chang MH, Ned RM, Hong Y, Yesupriya A, Yang Q, Liu T, Janssens AC, Dowling NF.
    Circ Cardiovasc Genet. 2011 Aug 10.


72. Needs assessment in genomic education: a survey of health educators in the United States
    Chen LS, Kim M.
    Health Promot Pract. 2013 Apr 1.


73. 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.


74. Japanese encephalitis virus genotype replacement, Taiwan, 2009-2010
    Chen YY, Fan YC, Tu WC, Chang RY, Shih CC, Lu IH, Chien MS, Lee WC, Chen TH, Chang GJ, Chiou SS.
    Emerg Infect Dis. 2011 Dec;17(12):2354-6.


75. Mutation analysis of the cross-reactive epitopes of Japanese encephalitis virus envelope glycoprotein
    Chiou SS, Fan YC, Crill WD, Chang RY, Chang GJ.
    J Gen Virol. 2012 Jun;93(Pt 6):1185-92.


76. The use of a family history risk assessment tool within a community health care system: views of primary care providers
    Christianson CA, Powell KP, Hahn SE, Blanton SH, Bogacik J, Henrich VC, The Genomedical Connection.
    J Genet Couns. 2012 Jan 21.


77. 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.


78. 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.


79. CFTR mutation analysis and haplotype associations in CF patients
    Cordovado SK, Hendrix M, Greene CN, Mochal S, Earley MC, Farrell PM, Kharrazi M, Hannon WH, Mueller PW.
    Mol Genet Metab. 2012 Feb;105(2):249-54.


80. Patterns of cancer genetic testing: a randomized survey of Oregon clinicians
    Cox SL, Zlot AI, Silvey K, Elliott D, Horn T, Johnson A, Leman RF.
    J Cancer Epidemiol. 2012 ;2012:294730.


81. Rapid pneumococcal evolution in response to clinical interventions
    Croucher NJ, Harris SR, Fraser C, Quail MA, Burton J, van der Linden M, McGee L, von Gottberg A, Song JH, Ko KS, Pichon B, Baker S, Parry CM, Lambertsen LM, Shahinas D, Pillai DR, Mitchell TJ, Dougan G, Tomasz A, Klugman KP, Parkhill J, Hanage WP, Bentley SD.
    Science. 2011 Jan 28;331(6016):430-4.


82. Rapid hepatitis C virus divergence among chronically infected individuals
    Cruz-Rivera M, Carpio-Pedroza JC, Escobar-Gutierrez A, Lozano D, Vergara-Castaneda A, Rivera-Osorio P, Martinez-Guarneros A, Chacon CA, Fonseca-Coronado S, Vaughan G.
    J Clin Microbiol. 2013 Feb;51(2):629-32.


83. Trypanosoma cruzi I genotypes in different geographical regions and transmission cycles based on a microsatellite motif of the intergenic spacer of spliced-leader genes
    Cura CI, Mejia-Jaramillo AM, Duffy T, Burgos JM, Rodriguero M, Cardinal MV, Kjos S, Gurgel-Goncalves R, Blanchet D, De Pablos LM, Tomasini N, da Silva A, Russomando G, Cuba CA, Aznar C, Abate T, Levin MJ, Osuna A, Gurtler RE, Diosque P, Solari A, Triana-Chavez O, Schijman AG.
    Int J Parasitol. 2010 Dec;40(14):1599-607.


84. 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.


85. 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.


86. 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.


87. The 3' untranslated regions of influenza genomic sequences are 5'PPP-independent ligands for RIG-I
    Davis WG, Bowzard JB, Sharma SD, Wiens ME, Ranjan P, Gangappa S, Stuchlik O, Pohl J, Donis RO, Katz JM, Cameron CE, Fujita T, Sambhara S.
    PLoS One. 2012 ;7(3):e32661.


88. Analysis of circulating tumor DNA to monitor metastatic breast cancer
    Dawson SJ, Tsui DW, Murtaza M, Biggs H, Rueda OM, Chin SF, Dunning MJ, et al..
    N Engl J Med. 2013 Mar 28;368(13):1199-209.


89. 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.


90. Health benefits and cost-effectiveness of primary genetic screening for Lynch syndrome in the general population
    Dinh TA, Rosner BI, Atwood JC, Boland CR, Syngal S, Vasen HF, Gruber SB, et al.
    Cancer Prev Res (Phila). 2010 Nov 18.


91. Synopsis of preterm birth genetic association studies: the preterm birth genetics knowledge base (PTBGene)
    Dolan SM, Hollegaard MV, Merialdi M, Betran AP, Allen T, Abelow C, Nace J, Lin BK, Khoury MJ, Ioannidis JP, Bagade S, Zheng X, Dubin RA, Bertram L, Velez Edwards DR, Menon R.
    Public Health Genomics. 2010 ;13(7-8):514-23.


92. 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.


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


94. IRB perspectives on the return of individual results from genomic research
    Dressler LG, Smolek S, Ponsaran R, Markey JM, Starks H, Gerson N, Lewis S, et al.
    Genet Med. 2012 Jan 5.


95. Genetics researchers' and IRB professionals' attitudes toward genetic research review: a comparative analysis
    Edwards KL, Lemke AA, Trinidad SB, Lewis SM, Starks H, Snapinn KW, Griffin MQ, et al.
    Genet Med. 2012 Jan 12.


96. Detection of the first G6P[14] human rotavirus strain from a child with diarrhea in Egypt
    El Sherif M, Esona MD, Wang Y, Gentsch JR, Jiang B, Glass RI, Baker SA, Klena JD.
    Infect Genet Evol. 2011 Aug;11(6):1436-42.


97. 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.


98. Next-generation sequencing of Coccidioides immitis isolated during cluster investigation
    Engelthaler DM, Chiller T, Schupp JA, Colvin J, Beckstrom-Sternberg SM, Driebe EM, Moses T, Tembe W, Sinari S, Beckstrom-Sternberg JS, Christoforides A, Pearson JV, Carpten J, Keim P, Peterson A, Terashita D, Balajee SA.
    Emerg Infect Dis. 2011 Feb;17(2):227-232.


99. A permutation procedure to correct for confounders in case-control studies, including tests of rare variation
    Epstein MP, Duncan R, Jiang Y, Conneely KN, Allen AS, Satten GA.
    Am J Hum Genet. 2012 Aug 10;91(2):215-23.


100. 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.


101. 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.


102. Whole genome sequence typing to investigate the Apophysomyces outbreak following a tornado in Joplin, Missouri, 2011
     Etienne KA, Gillece J, Hilsabeck R, Schupp JM, Colman R, Lockhart SR, Gade L, Thompson EH, Sutton DA, Neblett-Fanfair R, Park BJ, Turabelidze G, Keim P, Brandt ME, Deak E, Engelthaler DM.
     PLoS One. 2012 ;7(11):e49989.


103. The arrival of genomic medicine to the clinic is only the beginning of the journey
     Evans JP, Khoury MJ.
     Genet Med. 2013 Apr;15(4):268-9.


104. Nocardia amikacinitolerans sp. nov., an amikacin-resistant human pathogen
     Ezeoke I, Klenk HP, Potter G, Schumann P, Moser BD, Lasker BA, Nicholson A, Brown JM.
     Int J Syst Evol Microbiol. 2012 Jun 15.


105. Functional genomics of serotonin receptor 2A (HTR2A): interaction of polymorphism, methylation, expression and disease association
     Falkenberg VR, Gurbaxani BM, Unger ER, Rajeevan MS.
     Neuromolecular Med. 2010 Oct 13.


106. 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.


107. A pilot study of host genetic variants associated with influenza-associated deaths among children and young adults
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108. CrcZ and CrcX regulate carbon source utilization in Pseudomonas syringae pathovar tomato strain DC3000
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109. Regulation of the expression of the varicella-zoster virus open reading frame 66 gene
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110. Gene mapping and phylogenetic analysis of the complete genome from 30 single-stranded RNA male-specific coliphages (family Leviviridae)
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111. Assessing causal relationships in genomics: from Bradford-Hill criteria to complex gene-environment interactions and directed acyclic graphs
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112. 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)
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113. Public health genomics and the new molecular epidemiology of bacterial pathogens
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114. Developmental genetics of secretory vesicle acidification during Caenorhabditis elegans spermatogenesis
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115. Adapting the logical basis of tests for Hardy-Weinberg Equilibrium to the real needs of association studies in human and medical genetics
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116. Pneumococcal genome sequencing tracks a vaccine escape variant formed through a multi-fragment recombination event
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117. F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis
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118. Detection of G3P[3] and G3P[9] rotavirus strains in American Indian children with evidence of gene reassortment between human and animal rotaviruses
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119. Charting a course for genomic medicine from base pairs to bedside
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120. Historical shifts in Brazilian P. falciparum population structure and drug resistance alleles
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121. Modeling uncertain outcomes of genetic testing: factor V Leiden mutation and pregnant women
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122. Evaluation of the validity and utility of genetic testing for rare diseases
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123. Personal utility and genomic information: look before you leap
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124. Testing of VKORC1 and CYP2C9 alleles to guide warfarin dosing
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125. TREM2 variants in Alzheimer's disease
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126. Genome-wide association studies in pharmacogenomics: untapped potential for translation
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127. Multiwalled carbon nanotube-induced gene signatures in the mouse lung: potential predictive value for human lung cancer risk and prognosis
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128. PLoS Currents: Evidence on genomic tests - at the crossroads of translation
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129. Horizon scanning for new genomic tests
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130. Invited commentary: genes, environment, and hybrid vigor
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131. Recent advances in research of HIV infection: implications of viral and host genetics on treatment and prevention
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132. Survey of US public attitudes toward pharmacogenetic testing
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133. Cystic fibrosis newborn screening: using experience to optimize the screening algorithm
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134. 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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135. Whole-genome sequencing for analysis of an outbreak of meticillin-resistant Staphylococcus aureus: a descriptive study
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136. Ethnicity interacts with the OPRM1 gene in experimental pain sensitivity
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137. Implications of Internet availability of genomic information for public health practice
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138. Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: a report from the National Down Syndrome Project
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139. Putting genomics into practice
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140. Utility of genetic determinants of lipids and cardiovascular events in assessing risk
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141. Complications associated with carrier status among people with blood disorders: a commentary
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142. The benefits of using genetic information to design prevention trials
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143. Are randomized trials obsolete or more important than ever in the genomic era?
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144. Genetic bases of the temperature-sensitive phenotype of a master donor virus used in live attenuated influenza vaccines: A/Leningrad/134/17/57 (H2N2)
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145. Incidental findings in genetic research and clinical diagnostic tests: a systematic review
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146. Detectable clonal mosaicism and its relationship to aging and cancer
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147. Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration
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148. Strengthening the reporting of genetic risk prediction studies: the GRIPS statement
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149. Assessment of improved prediction beyond traditional risk factors: when does a difference make a difference?
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150. An epidemiological perspective on the future of direct-to-consumer personal genome testing
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151. Qualitative assessment of study materials and communication strategies used in studies that include DNA collection
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152. Maternal attitudes toward DNA collection for gene-environment studies: a qualitative research study
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153. Genome sequences for five strains of the emerging pathogen Haemophilus haemolyticus
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154. Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
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155. Development of genomic DNA reference materials for genetic testing of disorders common in people of Ashkenazi Jewish descent
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156. Use of whole genome sequencing to determine the microevolution of mycobacterium tuberculosis during an outbreak
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157. Using single-nucleotide polymorphisms to discriminate disease-associated from carried genomes of Neisseria meningitidis
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158. 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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159. High degree of genetic diversity of non-polio enteroviruses identified in Georgia by environmental and clinical surveillance, 2002-2005
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160. CISH and susceptibility to infectious diseases
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161. Translation research is an essential but not sufficient ingredient for translation of genomic medicine into population health benefits
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162. Dealing with the evidence dilemma in genomics and personalized medicine
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163. Public health genomics: the end of the beginning
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164. Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases
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165. Current priorities for public health practice in addressing the role of human genomics in improving population health
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166. Evidence-based classification of recommendations on use of genomic tests in clinical practice: dealing with insufficient evidence
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167. Multilevel research and the challenges of implementing genomic medicine
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168. Family history and personal genomics as tools for improving health in an era of evidence-based medicine
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169. Beyond base pairs to bedside: a population perspective on how genomics can improve health
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170. Genetic epidemiology with a capital E, ten years after
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171. Is there a need for PGxceptionalism?
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172. Knowledge integration at the center of genomic medicine
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173. How can polygenic inheritance be used in population screening for common diseases?
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174. The scientific foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention Multidisciplinary Workshop
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175. A genetic test registry: Bringing credible and actionable data together
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176. Comparative effectiveness research and genomic medicine: an evolving partnership for 21st century medicine
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177. Molecular surveillance of hepatitis C
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178. Genetic factors associated with elevated carbapenem resistance in KPC-producing Klebsiella pneumoniae
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179. Framing genomics, public health research and policy: points to consider
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180. Public awareness and use of direct-to-consumer personal genomic tests from four state population-based surveys, and implications for clinical and public health practice
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181. Bartonella bacteria in nature: where does population variability end and a species start?
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182. Relationships between selected gene polymorphisms and blood pressure sensitivity to weight loss in elderly persons with hypertension
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183. Genome sequences for six Rhodanobacter strains, isolated from soils and the terrestrial subsurface, with variable denitrification capabilities
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184. Epistatic connectivity among HCV genomic sites as a genetic marker of interferon resistance
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185. Human leukocyte antigen class I supertypes and HIV-1 control in African Americans
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186. The influence of human leukocyte antigen class I alleles and their population frequencies on human immunodeficiency virus type 1 control among African Americans
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187. Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS genomewide association study 03)
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188. Relaxation of adaptive evolution during the HIV-1 infection owing to reduction of CD4+ T cell counts
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189. Atypical Listeria monocytogenes serotype 4b strains harboring a lineage II-specific gene cassette
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190. Steroid 5-{alpha}-reductase type 2 (SRD5a2) gene polymorphisms and risk of prostate cancer: a HuGE review
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191. The impact of positive cancer family history on the clinical features and outcome of patients with non-small cell lung cancer
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192. Physical activity attenuates the genetic predisposition to obesity in 20,000 men and women from EPIC-Norfolk prospective population study
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193. Population genetic analysis of Enterocytozoon bieneusi in humans
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194. Diversity of 16S-23S rDNA internal transcribed spacer (ITS) reveals phylogenetic relationships in Burkholderia pseudomallei and its near-neighbors
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195. Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: the PDGene database
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196. 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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197. Identifying host genetic risk factors in the context of public health surveillance for invasive pneumococcal disease
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198. On track? Using the Human Genome Epidemiology Roadmap
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199. STrengthening the REporting of Genetic Association Studies (STREGA)--an extension of the STROBE statement
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200. Genetic susceptibility to West Nile virus and dengue
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201. Genome-wide copy number alterations in subtypes of invasive breast cancers in young white and African American women
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202. Malaria diagnostics and surveillance in the post-genomic era
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203. Diverse mutational mechanisms cause pathogenic subtelomeric rearrangements
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204. Genetic diversity among Clostridium botulinum strains harboring bont/A2 and bont/A3 genes
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205. Pharmacogenetics, pharmacogenomics, and individualized medicine
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206. Erratum: Molecular monitoring of resistant dhfr and dhps allelic haplotypes in Morogoro and Mvomero districts in south eastern Tanzania
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207. Molecular epidemiology of anthrax cases associated with recreational use of animal hides and yarn in the United States
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208. Influence of family history of colorectal cancer on health behavior and performance of early detection procedures: the SUN Project
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209. Future health applications of genomics: priorities for communication, behavioral, and social sciences research
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210. Introduction to the 4th National Conference on Genomics and Public Health
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211. Diversity and relationships of cocirculating modern human rotaviruses revealed using large-scale comparative genomics
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212. Endurance, refuge, and reemergence of dengue virus type 2, Puerto Rico, 1986-2007
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213. Neonatal screening for lysosomal storage disorders: feasibility and incidence from a nationwide study in Austria
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214. Family history of cancer and cancer risks in women with BRCA1 or BRCA2 mutations
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215. F8 and F9 mutations in US haemophilia patients: correlation with history of inhibitor and race/ethnicity
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216. Personalized medicine in major depressive disorder - opportunities and pitfalls
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217. A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia
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218. Genetic diversity of HA1 domain of hemagglutinin gene of pandemic influenza H1N1pdm09 viruses in New Delhi, India
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219. Telomere length and variation in telomere biology genes in individuals with osteosarcoma
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220. Evidence of selective sweeps in genes conferring resistance to chloroquine and pyrimethamine in Plasmodium falciparum within India
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221. Permanent genetic resources added to Molecular Ecology Resources Database 1 October 2011 - 30 November 2011
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222. The genetics of obesity and the metabolic syndrome
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223. Estimating the contribution of genetic variants to difference in incidence of disease between population groups
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224. Genomic medicine and racial/ethnic health disparities: promises, perils, and the challenges for health care and public health policy
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225. Discriminative accuracy of genomic profiling comparing multiplicative and additive risk models
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226. Evaluation of the discriminative accuracy of genomic profiling in the prediction of common complex diseases
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227. Integrating mechanistic and polymorphism data to characterize human genetic susceptibility for environmental chemical risk assessment in the 21st century
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228. Microdeletions of 3q29 confer high risk for schizophrenia
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229. The cost-effectiveness of genetic testing strategies for Lynch syndrome among newly diagnosed patients with colorectal cancer
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230. Family history as a risk factor for early-onset stroke/transient Ischemic attack among adults in the United States
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231. The malaria parasite Plasmodium vivax exhibits greater genetic diversity than Plasmodium falciparum
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232. Patterns and rates of exonic de novo mutations in autism spectrum disorders
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233. Inflammation gene variants and susceptibility to albuminuria in the U.S. population: analysis in the Third National Health and Nutrition Examination Survey (NHANES III), 1991-1994
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234. Impact of colon cancer screening on family history phenotype
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235. Characterization and allelic polymorphisms of rhesus macaque (Macaca mulatta) IgG Fc receptor genes
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236. Evolution of highly pathogenic avian influenza (H5N1) virus populations in Vietnam between 2007 and 2010
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237. Evidence of gene-environment interactions between common breast cancer susceptibility loci and established environmental risk factors
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238. Association of nucleotide polymorphisms within the O-antigen gene cluster of Escherichia coli O26, O45, O103, O111, O121, and O145 with serogroups and genetic subtypes
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239. When is correlation coevolution?
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240. Communication about family members' risk of melanoma: self-reported practices of dermatologists in the United States
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241. Differential association of gene content polymorphisms of killer cell immunoglobulin-like receptors with placental malaria in HIV- and HIV+ mothers
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242. Preferences for genetic and behavioral health information: the impact of risk factors and disease attributions
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243. Critical role of an antiviral stress granule containing RIG-I and PKR in viral detection and innate immunity
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244. Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
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245. Evidence of purifying selection on merozoite surface protein 8 (MSP8) and 10 (MSP10) in Plasmodium spp
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246. Evidence for negative selection on the gene encoding rhoptry-associated protein 1 (RAP-1) in Plasmodium spp
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247. Consolidating newborn screening efforts in the Asia Pacific region : networking and shared education
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248. Emergence and characterization of serotype G9 rotavirus strains from Africa
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249. 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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250. 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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251. Family history of cancer and risk of breast cancer in the black women's health study
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252. Association between 9p21 genomic markers and heart disease: a meta-analysis
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253. Use of genomic profiling to assess risk for cardiovascular disease and identify individualized prevention strategies-a targeted evidence-based review
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254. Whole genome single nucleotide polymorphism based phylogeny of Francisella tularensis and its application to the development of a strain typing assay
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255. Genomics for public health improvement: relevant international ethical and policy issues around genome-wide association studies and biobanks
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256. Genetic characterization of measles viruses that circulated in Thailand from 1998 to 2008
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257. Utility of multiplex ligation-dependent probe amplification (mlpa) for hemophilia mutation screening
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258. The CDC Hemophilia A Mutation Project (CHAMP) Mutation List: a new online resource
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259. Association between a literature-based genetic risk score and cardiovascular events in women
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260. Phylogeographic reconstruction of a bacterial species with high levels of lateral gene transfer
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261. Genetic variability, phylogenetic relationships and gene flow in Triatoma infestans dark morphs from the Argentinean Chaco
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262. Does a screening questionnaire for familial and hereditary colorectal cancer risk work in a health insurance population?
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263. Functional impact of global rare copy number variation in autism spectrum disorders
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264. Characterization of 107 genomic DNA reference materials for CYP2D6, CYP2C19, CYP2C9, VKORC1, and UGT1A1. A GeT-RM and Association for Molecular Pathology collaborative project
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265. Evolution of the hepatitis E virus polyproline region: order from disorder
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266. Evolutionary history and population dynamics of hepatitis E virus
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267. The molecular epidemiology of hepatitis E virus infection
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268. Genome-wide association study of glioma and meta-analysis
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269. Evaluation of intra-host variants of the entire hepatitis B virus genome
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270. Personal genomics: information can be harmful
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271. Risk of cardiovascular disease in family members of young sudden cardiac death victims
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272. Detection and differentiation of Clostridium botulinum type A strains using a focused DNA microarray
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273. Genetic backgrounds of the Plasmodium falciparum chloroquine resistant transporter (pfcrt) alleles in Pakistan
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274. Genetic polymorphisms associated with acute lung injury
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275. Estrogen-related genes and their contribution to racial differences in breast cancer risk
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276. An efficient method for generating poxvirus recombinants in the absence of selection
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277. Genomic basis of a polyagglutinating isolate of Neisseria meningitidis
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278. Evolution of canine and equine influenza (H3N8) viruses co-circulating between 2005 and 2008
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279. 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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280. Genetic variation and exchange in Trypanosoma cruzi isolates from the United States
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281. Challenges of translating genetic tests into clinical and public health practice
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282. Global distribution of measles genotypes and measles molecular epidemiology
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283. Trends in population-based studies of human genetics in infectious diseases
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284. The genetics of susceptibility to variant Creutzfeldt-Jakob disease
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285. Mycobacterium shinjukuense sp. nov., a slowly growing, non-chromogenic species isolated from human clinical specimens
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286. Turning of COGS moves forward findings for hormonally mediated cancers
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287. De novo mutations revealed by whole-exome sequencing are strongly associated with autism
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288. Genomic privacy and limits of individual detection in a pool
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289. Re-emergence and decline of dengue virus serotype 3 in Puerto Rico
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290. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
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291. Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions
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292. A report template for molecular genetic tests designed to improve communication between the clinician and laboratory
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293. General cardiovascular risk profile identifies advanced coronary artery calcium and is improved by family history: the multiethnic study of atherosclerosis
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294. Caffeine, selected metabolic gene variants, and risk for neural tube defects
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297. How can we stimulate translational research in cancer genomics beyond bench to bedside?
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298. Cancer GAMAdb: database of cancer genetic associations from meta-analyses and genome-wide association studies
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299. Genome-based knowledge and public health: the vision of tomorrow and the challenge of today
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300. Prevalence of CGG expansions of the FMR1 gene in a US population-based sample
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301. Epigenome-wide association study in the European Prospective Investigation into Cancer and Nutrition (EPIC-Turin) identifies novel genetic loci associated with smoking
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302. Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy
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303. Genetic variability of wild-type measles viruses, circulating in the Russian Federation during the implementation of the National Measles Elimination Program, 2003-2007
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304. Common ancestry and novel genetic traits of Francisella novicida-like isolates from North America and Australia as revealed by comparative genomic analyses
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307. Genetic variability and the classification of hepatitis E virus
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308. Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa Heart Study
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309. Binding of cellular p32 protein to the rubella virus P150 replicase protein via PxxPxR motifs
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311. Computational analysis suggests that lyssavirus glycoprotein gene plays a minor role in viral adaptation
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312. Genetic determinants of sensitivity to beryllium in mice
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313. Draft genome sequences of Bordetella holmesii strains from blood (F627) and nasopharynx (H558)
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317. Characterization of novel Brucella strains originating from wild native rodent species in North Queensland, Australia
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318. Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations
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323. Improving the efficiency and relevance of evidence-based recommendations in the era of whole-genome sequencing: an EGAPP methods update
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352. Variants in ABCB1, TGFB1, and XRCC1 genes and susceptibility to viral hepatitis A infection in Mexican Americans
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354. Natural type 3/type 2 intertypic vaccine-related poliovirus recombinants with the first crossover sites within the VP1 capsid coding region
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356. Survival among people with Down syndrome: a nationwide population-based study in Denmark
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