Now showing items 21-23 of 23

    • Wavelet Screening identifies regions highly enriched for differentially methylated loci for orofacial clefts 

      Denault, William Robert Paul; Romanowska, Julia; Haaland, Øystein Ariansen; Lyle, Robert; Taylor, Jack A.; Xu, Zongli; Lie, Rolv T.; Gjessing, Håkon K.; Jugessur, Astanand (Journal article; Peer reviewed, 2021)
      DNA methylation is the most widely studied epigenetic mark in humans and plays an essential role in normal biological processes as well as in disease development. More focus has recently been placed on understanding ...
    • Wavelet Screening: a novel approach to analyzing GWAS data 

      Denault, William Robert Paul; Gjessing, Håkon K.; Juodakis, Julius; Jacobsson, Bo; Jugessur, Astanand (Journal article; Peer reviewed, 2021)
      Background Traditional methods for single-variant genome-wide association study (GWAS) incur a substantial multiple-testing burden because of the need to test for associations with a vast number of single-nucleotide ...
    • X-Linked Genes and Risk of Orofacial Clefts: Evidence from Two Population-Based Studies in Scandinavia 

      Jugessur, Astanand; Skare, Øivind; Lie, Rolv Terje; Wilcox, Allen James; Christensen, Kaare; Christiansen, Lene; Nguyen, Truc Trung; Murray, Jeffrey Clark; Gjessing, Håkon K. (Peer reviewed; Journal article, 2012-06-19)
      Background: Orofacial clefts are common birth defects of complex etiology, with an excess of males among babies with cleft lip and palate, and an excess of females among those with cleft palate only. Although genes on the ...