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Issue Date	Title	Author(s)
1-Jan-2019	The cancer aneuploidy paradox : In the light of evolution	Salmina, Kristine; Huna, Anda; Kalejs, Martins; Pjanova, Dace; Scherthan, Harry; Cragg, Mark S.; Erenpreisa, Jekaterina; Scientific Laboratory of Biomechanics
21-Dec-2019	Association of variants in the CP, ATOX1 and COMMD1 genes with Wilson disease symptoms in Latvia	Zarina, A.; Tolmane, I.; Krumina, Z.; Tutane, A. I.; Gailite, L.; Scientific Laboratory of Molecular Genetics; Department of Biology and Microbiology
Jul-2017	Genetic variation spectrum in ATP7B gene identified in Latvian patients with Wilson disease	Zarina, Agnese; Tolmane, Ieva; Kreile, Madara; Chernushenko, Aleksandrs; Cernevska, Gunta; Pukite, Ieva; Micule, Ieva; Krumina, Zita; Krumina, Astrida; Rozentale, Baiba; Piekuse, Linda; Scientific Laboratory of Molecular Genetics
27-Oct-2011	Genotype-phenotype correlations among BRCA1 4153delA and 5382insC mutation carriers from Latvia	Plakhins, Grigorijs; Irmejs, Arvids; Gardovskis, Andris; Subatniece, Signe; Rozite, Santa; Bitina, Marianna; Keire, Guntars; Purkalne, Gunta; Teibe, Uldis; Trofimovics, Genadijs; Miklasevics, Edvins; Gardovskis, Janis; Hereditary Cancer Research Department
14-Jun-2013	BRCA1/2 mutation screening in high-risk breast/ovarian cancer families and sporadic cancer patient surveilling for hidden high-risk families	Berzina, Dace; Nakazawa-Miklasevica, Miki; Zestkova, Jekaterina; Aksenoka, Karina; Irmejs, Arvids; Gardovskis, Andris; Kalniete, Dagnija; Gardovskis, Janis; Miklasevics, Edvins; RSU Institute of Oncology
13-Aug-2019	Meta-analysis of cancer triploidy : Rearrangements of genome complements in male human tumors are characterized by XXY karyotypes	Vainshelbaum, Ninel M.; Zayakin, Pawel; Kleina, Regina; Giuliani, Alessandro; Erenpreisa, Jekaterina; Department of Pathology
Sep-2011	Whole Xp deletion in a girl with mental retardation, epilepsy, and biochemical features of OTC deficiency	Joost, K.; Tammur, P.; Teek, R.; Žilina, O.; Peters, M.; Kreile, M.; Lace, B.; Žordania, R.; Talvik, I.; Õunap, K.

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