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Issue DateTitleAuthor(s)
5-Oct-2022Alanyl-tRNA synthetase 1 gene variants in hereditary neuropathy genotype and phenotype overviewSetlere, Signe; Jurcenko, Marija; Gailite, Linda; Rots, Dmitrijs; Kenina, Viktorija; Department of Doctoral Studies; Scientific Laboratory of Molecular Genetics; Department of Biology and Microbiology
22-Apr-2022A systematic review and standardized clinical validity assessment of genes involved in female reproductive failureVolozonoka, Ludmila; Miskova, Anna; Kornejeva, Liene; Kempa, Inga; Bargatina, Veronika; Gailite, Linda; Scientific Laboratory of Molecular Genetics; Department of Obstetrics and Gynaecology
16-Jun-2022Overview of Neuromuscular Disorder Molecular Diagnostic Experience for the Population of LatviaLace, Baiba; Micule, Ieva; Kenina, Viktorija; Setlere, Signe; Strautmanis, Jurgis; Kazaine, Inese; Taurina, Gita; Murmane, Daiga; Grinfelde, Ieva; Kornejeva, Liene; Krumina, Zita; Sterna, Olga; Radovica-Spalvina, Ilze; Vasiljeva, Inta; Gailite, Linda; Stavusis, Janis; Livcane, Diana; Kidere, Dita; Malniece, Ieva; Inashkina, Inna; Rīga Stradiņš University; Scientific Laboratory of Molecular Genetics
Dec-2021A novel EDA variant causing X-linked hypohidrotic ectodermal dysplasia : Case reportAlksere, Baiba; Kornejeva, Liene; Grinfelde, Ieva; Dzalbs, Aigars; Enkure, Dace; Conka, Una; Andersone, Santa; Blumberga, Arita; Nikitina-Zake, Liene; Kangare, Liga; Radovica-Spalvina, Ilze; Vasiljeva, Inta; Gailite, Linda; Erenpreiss, Juris; Fodina, Violeta; Rīga Stradiņš University

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