SEARCH

SEARCH BY CITATION

References

  • 1
    Hur J, Schuyler AD, States DJ, Feldman EL: SciMiner: web-based literature mining tool for target identification and functional enrichment analysis. Bioinformatics 2009; 25:838840.
  • 2
    International HapMap Consortium: A haplotype map of the human genome. Nature 2005; 437:12991320.
  • 3
    Donner A, Klar N: The statistical analysis of kappa statistics in multiple samples. J Clin Epidemiol 1996; 49:10531058.
  • 4
    Reed JF 3rd: Homogeneity of kappa statistics in multiple samples. Comput Methods Programs Biomed 2000; 63:4346.
  • 5
    Enquobahrie DA, Williams MA, Qiu C, Muhie SY, Slentz-Kesler K, Ge Z, Sorenson T: Early pregnancy peripheral blood gene expression and risk of preterm delivery: a nested case control study. BMC Pregnancy Childbirth 2009; 9:56.
  • 6
    Weiner CP, Mason CW, Dong Y, Buhimschi IA, Swaan PW, Buhimschi CS: Human effector/initiator gene sets that regulate myometrial contractility during term and preterm labor. Am J Obstet Gynecol 2010; 202:474.e1e20.
  • 7
    Buhimschi CS, Dulay AT, Abdel-Razeq S, Zhao G, Lee S, Hodgson EJ, Bhandari V, Buhimschi IA: Fetal inflammatory response in women with proteomic biomarkers characteristic of intra-amniotic inflammation and preterm birth. BJOG 2009; 116:257267.
  • 8
    Adams KM, Eschenbach DA: The genetic contribution towards preterm delivery. Semin Fetal Neonatal Med 2004; 9:445452.
  • 9
    Crider KS, Whitehead N, Buus RM: Genetic variation associated with preterm birth: a HuGE review. Genet Med 2005; 7:593604.
  • 10
    Menon R, Fortunato SJ, Thorsen P, Williams S: Genetic associations in preterm birth: a primer of marker selection, study design, and data analysis. J Soc Gynecol Investig 2006; 13:531541.
  • 11
    Pennell CE, Jacobsson B, Williams SM, Buus RM, Muglia LJ, Dolan SM, Morken NH, Ozcelik H, Lye SJ, Relton C: Genetic epidemiologic studies of preterm birth: guidelines for research. Am J Obstet Gynecol 2007; 196:107118.
  • 12
    Plunkett J, Muglia LJ: Genetic contributions to preterm birth: implications from epidemiological and genetic association studies. Ann Med 2008; 40:167195.
  • 13
    Romero R, Espinoza J, Gotsch F, Kusanovic JP, Friel LA, Erez O, Mazaki-Tovi S, Than NG, Hassan S, Tromp G: The use of high-dimensional biology (genomics, transcriptomics, proteomics, and metabolomics) to understand the preterm parturition syndrome. BJOG 2006; 113(Suppl. 3):118135.
  • 14
    Weinberg CR, Shi M: The genetics of preterm birth: using what we know to design better association studies. Am J Epidemiol 2009; 170:13731381.
  • 15
    Aidoo M, McElroy PD, Kolczak MS, Terlouw DJ, ter Kuile FO, Nahlen B, Lal AA, Udhayakumar V: Tumor necrosis factor-alpha promoter variant 2 (TNF2) is associated with pre-term delivery, infant mortality, and malaria morbidity in western Kenya: Asembo Bay Cohort Project IX. Genet Epidemiol 2001; 21:201211.
  • 16
    Fujimoto T, Parry S, Urbanek M, Sammel M, Macones G, Kuivaniemi H, Romero R, Strauss JF 3rd: A single nucleotide polymorphism in the matrix metalloproteinase-1 (MMP-1) promoter influences amnion cell MMP-1 expression and risk for preterm premature rupture of the fetal membranes. J Biol Chem 2002; 277:62966302.
  • 17
    Genc MR, Gerber S, Nesin M, Witkin SS: Polymorphism in the interleukin-1 gene complex and spontaneous preterm delivery. Am J Obstet Gynecol 2002; 187:157163.
  • 18
    Kalish RB, Vardhana S, Gupta M, Perni SC, Witkin SS: Interleukin-4 and -10 gene polymorphisms and spontaneous preterm birth in multifetal gestations. Am J Obstet Gynecol 2004; 190:702706.
  • 19
    Landau R, Xie HG, Dishy V, Stein CM, Wood AJ, Emala CW, Smiley RM: beta2-Adrenergic receptor genotype and preterm delivery. Am J Obstet Gynecol 2002; 187:12941298.
  • 20
    Lorenz E, Hallman M, Marttila R, Haataja R, Schwartz DA: Association between the Asp299Gly polymorphisms in the Toll-like receptor 4 and premature births in the Finnish population. Pediatr Res 2002; 52:373376.
  • 21
    Ozkur M, Dogulu F, Ozkur A, Gokmen B, Inaloz SS, Aynacioglu AS: Association of the Gln27Glu polymorphism of the beta-2-adrenergic receptor with preterm labor. Int J Gynaecol Obstet 2002; 77:209215.
  • 22
    Papazoglou D, Galazios G, Koukourakis MI, Kontomanolis EN, Maltezos E: Association of -634G/C and 936C/T polymorphisms of the vascular endothelial growth factor with spontaneous preterm delivery. Acta Obstet Gynecol Scand 2004; 83:461465.
  • 23
    Roberts AK, Monzon-Bordonaba F, Van Deerlin PG, Holder J, Macones GA, Morgan MA, Strauss JF 3rd, Parry S: Association of polymorphism within the promoter of the tumor necrosis factor alpha gene with increased risk of preterm premature rupture of the fetal membranes. Am J Obstet Gynecol 1999; 180:12971302.
  • 24
    Simhan HN, Krohn MA, Roberts JM, Zeevi A, Caritis SN: Interleukin-6 promoter -174 polymorphism and spontaneous preterm birth. Am J Obstet Gynecol 2003; 189:915918.
  • 25
    Witkin SS, Vardhana S, Yih M, Doh K, Bongiovanni AM, Gerber S: Polymorphism in intron 2 of the fetal interleukin-1 receptor antagonist genotype influences midtrimester amniotic fluid concentrations of interleukin-1beta and interleukin-1 receptor antagonist and pregnancy outcome. Am J Obstet Gynecol 2003; 189:14131417.
  • 26
    Gibson G: Hints of hidden heritability in GWAS. Nat Genet 2010; 42:558560.
  • 27
    Varmus H: Getting ready for gene-based medicine. N Engl J Med 2002; 347:15261527.
  • 28
    Collins FS, Green ED, Guttmacher AE, Guyer MS: A vision for the future of genomics research. Nature 2003; 422:835847.
  • 29
    Feero WG, Guttmacher AE, Collins FS: Genomic medicine–an updated primer. N Engl J Med 2010; 362:20012011.
  • 30
    Dewan A, Liu M, Hartman S, Zhang SS, Liu DT, Zhao C, Tam PO, Chan WM, Lam DS, Snyder M, Barnstable C, Pang CP, Hoh J: HTRA1 promoter polymorphism in wet age-related macular degeneration. Science 2006; 314:989992.
  • 31
    Mathew CG: New links to the pathogenesis of Crohn disease provided by genome-wide association scans. Nat Rev Genet 2008; 9:914.
  • 32
    Glessner JT, Bradfield JP, Wang K, Takahashi N, Zhang H, Sleiman PM, Mentch FD, Kim CE, Hou C, Thomas KA, Garris ML, Deliard S, Frackelton EC, Otieno FG, Zhao J, Chiavacci RM, Li M, Buxbaum JD, Berkowitz RI, Hakonarson H, Grant SF: A genome-wide study reveals copy number variants exclusive to childhood obesity cases. Am J Hum Genet 2010; 87:661666.
  • 33
    Gui J, Andrew AS, Andrews P, Nelson HM, Kelsey KT, Karagas MR, Moore JH: A robust multifactor dimensionality reduction method for detecting gene–gene interactions with application to the genetic analysis of bladder cancer susceptibility. Ann Hum Genet 2011; 75:2028.
  • 34
    Cordell HJ: Detecting gene–gene interactions that underlie human diseases. Nat Rev Genet 2009; 10:392404.
  • 35
    Moore JH: Detecting, characterizing, and interpreting nonlinear gene–gene interactions using multifactor dimensionality reduction. Adv Genet 2010; 72:101116.