Cited by

• Systems Epidemiology: What's in a Name?

  Dammann O, Gray P, Gressens P, Wolkenhauer O, Leviton A. Dammann O, et al. Online J Public Health Inform. 2014 Dec 15;6(3):e198. doi: 10.5210/ojphi.v6i3.5571. eCollection 2014. Online J Public Health Inform. 2014. PMID: 25598870 Free PMC article.
• Estrogen metabolism and exposure in a genotypic-phenotypic model for breast cancer risk prediction.

  Crooke PS, Justenhoven C, Brauch H; GENICA Consortium; Dawling S, Roodi N, Higginbotham KS, Plummer WD, Schuyler PA, Sanders ME, Page DL, Smith JR, Dupont WD, Parl FF. Crooke PS, et al. Cancer Epidemiol Biomarkers Prev. 2011 Jul;20(7):1502-15. doi: 10.1158/1055-9965.EPI-11-0060. Epub 2011 May 24. Cancer Epidemiol Biomarkers Prev. 2011. PMID: 21610218 Free PMC article.
• SNP-based pathway enrichment analysis for genome-wide association studies.

  Weng L, Macciardi F, Subramanian A, Guffanti G, Potkin SG, Yu Z, Xie X. Weng L, et al. BMC Bioinformatics. 2011 Apr 15;12:99. doi: 10.1186/1471-2105-12-99. BMC Bioinformatics. 2011. PMID: 21496265 Free PMC article.
• Nicotinic acetylcholine receptor beta2 subunit gene implicated in a systems-based candidate gene study of smoking cessation.

  Conti DV, Lee W, Li D, Liu J, Van Den Berg D, Thomas PD, Bergen AW, Swan GE, Tyndale RF, Benowitz NL, Lerman C; Pharmacogenetics of Nicotine Addiction and Treatment Consortium. Conti DV, et al. Hum Mol Genet. 2008 Sep 15;17(18):2834-48. doi: 10.1093/hmg/ddn181. Epub 2008 Jul 1. Hum Mol Genet. 2008. PMID: 18593715 Free PMC article. Clinical Trial.
• Data integration workflow for search of disease driving genes and genetic variants.

  Karinen S, Heikkinen T, Nevanlinna H, Hautaniemi S. Karinen S, et al. PLoS One. 2011 Apr 12;6(4):e18636. doi: 10.1371/journal.pone.0018636. PLoS One. 2011. PMID: 21533266 Free PMC article.