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Issue DateTitleAuthor(s)
1-Jan-2019The cancer aneuploidy paradox : In the light of evolutionSalmina, Kristine; Huna, Anda; Kalejs, Martins; Pjanova, Dace; Scherthan, Harry; Cragg, Mark S.; Erenpreisa, Jekaterina; Scientific Laboratory of Biomechanics
13-Dec-2018Significantly altered peripheral blood cell DNA methylation profile as a result of immediate effect of metformin use in healthy individualsElbere, Ilze; Silamikelis, Ivars; Ustinova, Monta; Kalnina, Ineta; Zaharenko, Linda; Peculis, Raitis; Konrade, Ilze; Ciuculete, Diana Maria; Zhukovsky, Christina; Gudra, Dita; Radovica-Spalvina, Ilze; Fridmanis, Davids; Pirags, Valdis; Schiöth, Helgi B.; Klovins, Janis
21-Dec-2019Association of variants in the CP, ATOX1 and COMMD1 genes with Wilson disease symptoms in LatviaZarina, A.; Tolmane, I.; Krumina, Z.; Tutane, A. I.; Gailite, L.; Scientific Laboratory of Molecular Genetics; Department of Biology and Microbiology
Jul-2017Genetic variation spectrum in ATP7B gene identified in Latvian patients with Wilson diseaseZarina, 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-2011Genotype-phenotype correlations among BRCA1 4153delA and 5382insC mutation carriers from LatviaPlakhins, 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-2013BRCA1/2 mutation screening in high-risk breast/ovarian cancer families and sporadic cancer patient surveilling for hidden high-risk familiesBerzina, Dace; Nakazawa-Miklasevica, Miki; Zestkova, Jekaterina; Aksenoka, Karina; Irmejs, Arvids; Gardovskis, Andris; Kalniete, Dagnija; Gardovskis, Janis; Miklasevics, Edvins; RSU Institute of Oncology
1-Aug-2018Performance comparison of two whole genome amplification techniques in frame of multifactor preimplantation genetic testingVolozonoka, Ludmila; Perminov, Dmitry; Korņejeva, Liene; Alkšere, Baiba; Novikova, Natālija; Pīmane, Evija Jokste; Blumberga, Arita; Kempa, Inga; Miskova, Anna; Gailīte, Linda; Fodina, Violeta; Scientific Laboratory of Molecular Genetics; Department of Obstetrics and Gynaecology
13-Aug-2019Meta-analysis of cancer triploidy : Rearrangements of genome complements in male human tumors are characterized by XXY karyotypesVainshelbaum, Ninel M.; Zayakin, Pawel; Kleina, Regina; Giuliani, Alessandro; Erenpreisa, Jekaterina; Department of Pathology
Dec-2012Strategies to work with HLA data in human populations for histocompatibility, clinical transplantation, epidemiology and population genetics : HLA-NET methodological recommendationsSanchez-Mazas, A.; Vidan-Jeras, B.; Nunes, J. M.; Fischer, G.; Little, A. M.; Bekmane, U.; Buhler, S.; Buus, S.; Claas, F. H.J.; Dormoy, A.; Dubois, V.; Eglite, E.; Eliaou, J. F.; Gonzalez-Galarza, F.; Grubic, Z.; Ivanova, M.; Lie, B.; Ligeiro, D.; Lokki, M. L.; da Silva, B. Martins; Martorell, J.; Mendonça, D.; Middleton, D.; Voniatis, D. Papioannou; Papasteriades, C.; Poli, F.; Riccio, M. E.; Vlachou, M. Spyropoulou; Sulcebe, G.; Tonks, S.; Nevessignsky, M. Toungouz; Vangenot, C.; van Walraven, A. M.; Tiercy, J. M.; Rīga Stradiņš University
Sep-2011Whole Xp deletion in a girl with mental retardation, epilepsy, and biochemical features of OTC deficiencyJoost, K.; Tammur, P.; Teek, R.; Žilina, O.; Peters, M.; Kreile, M.; Lace, B.; Žordania, R.; Talvik, I.; Õunap, K.

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