Rose, Behm, Drgon, Johnson, Uhl: "Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score." in: Molecular medicine (Cambridge, Mass.), Vol. 16, Issue 7-8, pp. 247-53, 2010 (PubMed).
Medves, Duhoux, Ferrant, Toffalini, Ameye, Libouton, Poirel, Demoulin: "KANK1, a candidate tumor suppressor gene, is fused to PDGFRB in an imatinib-responsive myeloid neoplasm with severe thrombocythemia." in: Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K, Vol. 24, Issue 5, pp. 1052-5, 2010 (PubMed).
Hoppenbrouwers, Aulchenko, Janssens, Ramagopalan, Broer, Kayser, Ebers, Oostra, van Duijn, Hintzen: "Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis." in: Journal of human genetics, Vol. 54, Issue 11, pp. 676-80, 2009 (PubMed).
Kakinuma, Kiyama: "A major mutation of KIF21A associated with congenital fibrosis of the extraocular muscles type 1 (CFEOM1) enhances translocation of Kank1 to the membrane." in: Biochemical and biophysical research communications, Vol. 386, Issue 4, pp. 639-44, 2009 (PubMed).
DNetto, Ward, Morrison, Ramagopalan, Dyment, DeLuca, Handunnetthi, Sadovnick, Ebers: "Risk alleles for multiple sclerosis in multiplex families." in: Neurology, Vol. 72, Issue 23, pp. 1984-8, 2009 (PubMed).