Jugessur, Shi, Gjessing, Lie, Wilcox, Weinberg, Christensen, Boyles, Daack-Hirsch, Nguyen, Christiansen, Lidral, Murray: "Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia." in: PLoS ONE, Vol. 5, Issue 7, pp. e11493, 2010 (PubMed).
Yerges, Klei, Cauley, Roeder, Kammerer, Moffett, Ensrud, Nestlerode, Marshall, Hoffman, Lewis, Lang, Barrett-Connor, Ferrell, Orwoll, Zmuda: "High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men." in: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, Vol. 24, Issue 12, pp. 2039-49, 2009 (PubMed).
Liu, Novosedlik, Wang, Hudson, Cohen, Chudley, Forster-Gibson, Lewis, Holden: "The DLX1and DLX2 genes and susceptibility to autism spectrum disorders." in: European journal of human genetics : EJHG, Vol. 17, Issue 2, pp. 228-35, 2009 (PubMed).
Laroche, Ramoz, Leroy, Fortin, Rousselot-Paillet, Philippe, Colleaux, Bresson, Mogenet, Golse, Mouren-Simeoni, Gorwood, Galli, Simonneau, Krebs, Robel: "Polymorphisms of coding trinucleotide repeats of homeogenes in neurodevelopmental psychiatric disorders." in: Psychiatric genetics, Vol. 18, Issue 6, pp. 295-301, 2008 (PubMed).
Espinoza, Ganga, Vadlamudi, Martin, Brooks, Semina, Murray, Amendt: "Protein kinase C phosphorylation modulates N- and C-terminal regulatory activities of the PITX2 homeodomain protein." in: Biochemistry, Vol. 44, Issue 10, pp. 3942-54, 2005 (PubMed).