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Issue DateTitleAuthor(s)
14-May-2019Analysis of the Spatiotemporal Development of Hematopoietic Stem and Progenitor Cells in the Early Human EmbryoEasterbrook, Jennifer; Rybtsov, Stanislav; Gordon-Keylock, Sabrina; Ivanovs, Andrejs; Taoudi, Samir; Anderson, Richard A.; Medvinsky, Alexander
2019Anthropometric characteristics of females in different age groups in Latvia from childhood to adulthoodPļaviņa, Liāna; Kārkliņa, Helena; Umbraško, Silvija; Stankeviča, Jekaterīna; Kachlik, David; Department of Morphology; Institute of Anatomy and Anthropology
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
29-Oct-2010Population screening for hereditary and familial cancer syndromes in Valka district of LatviaVanags, Andrejs; Štrumfa, Ilze; Gardovskis, Andris; Borošenko, Viktors; Aboliņš, Arnis; Teibe, Uldis; Trofimovičs, Genadijs; Miklaševičs, Edvins; Gardovskis, Janis; Hereditary Cancer Research Department
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-Dec-2018Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targetsLempiäinen, Harri; Brænne, Ingrid; Michoel, Tom; Tragante, Vinicius; Vilne, Baiba; Webb, Tom R.; Kyriakou, Theodosios; Eichner, Johannes; Zeng, Lingyao; Willenborg, Christina; Franzen, Oscar; Ruusalepp, Arno; Goel, Anuj; Van Der Laan, Sander W.; Biegert, Claudia; Hamby, Stephen; Talukdar, Husain A.; Foroughi Asl, Hassan; Dichgans, Martin; Dreker, Tobias; Graettinger, Mira; Gribbon, Philip; Kessler, Thorsten; Malik, Rainer; Prestel, Matthias; Stiller, Barbara; Schofield, Christine; Pasterkamp, Gerard; Watkins, Hugh; Samani, Nilesh J.; Wittenberger, Timo; Erdmann, Jeanette; Schunkert, Heribert; Asselbergs, Folkert W.; Björkegren, Johan L.M.
1-Jul-2016The impact of genome-wide association studies on the pathophysiology and therapy of cardiovascular diseaseKessler, Thorsten; Vilne, Baiba; Schunkert, Heribert
2019Novel variant of the androgen receptor gene in a patient with complete androgen insensitivity syndrome and polyorchidismKonrade, Ilze; Zavorikina, Julija; Fridvalde, Aija; Rots, Dmitrijs; Kalere, Ieva; Strumfa, Ilze; Dambrova, Maija; Gailite, Linda; Department of Internal Diseases; Scientific Laboratory of Molecular Genetics; Faculty of Pharmacy; Department of Pathology; Department of Human Physiology and Biochemistry
2019Methods for detection of direct oral anticoagulants and their role in clinical practicePukite, Katrina; Apsite, Ketija; Pupkevica, Irina; Cernevska, Ilze; Boichuk, Oksana; Meisters, Janis; Straupmane, Dagnija; Urtane, Inga; Lejnieks, Aivars; Kalejs, Oskars; Faculty of Medicine; Department of Pharmaceutical Chemistry; Department of Internal Diseases

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