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Results 1-10 of 14 (Search time: 0.002 seconds).
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Issue DateTitleAuthor(s)
2021The association of FMR1 gene (CGG)n variation with idiopathic female infertilityGrasmane, Adele; Rots, Dmitrijs; Vītiņa, Zane; Magomedova, Valerija; Gailīte, Linda; Rīga Stradiņš University
2021A higher polygenic risk score is associated with a higher recurrence rate of atrial fibrillation in direct current cardioversion-treated patientsVogel, Simon; Rudaka, Irina; Rots, Dmitrijs; Isakova, Jekaterīna; Kalējs, Oskars; Vīksne, Kristīne; Gailīte, Linda; Scientific Laboratory of Molecular Genetics
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
8-Apr-2023National survey on clinical and genetic characteristics of patients with hereditary angioedema in LatviaKanepa, Adine; Nartisa, Inga; Rots, Dmitrijs; Gailite, Linda; Farkas, Henriette; Kurjane, Natalja; Rīga Stradiņš University
2023The most common European HINT1 neuropathy variant phenotype and its case studiesRozevska, Marija; Rots, Dmitrijs; Gailite, Linda; Linde, Ronalds; Mironovs, Stanislavs; Timcenko, Maksims; Linovs, Viktors; Locmele, Dzintra; Micule, Ieva; Lace, Baiba; Kenina, Viktorija; Scientific Laboratory of Molecular Genetics
20-Jan-2021Clinical Phenotyping and Biomarkers in Spinal and Bulbar Muscular AtrophyMillere, Elīna; Rots, Dmitrijs; Glāzere, Ieva; Tauriņa, Gita; Kurjāne, Nataļja; Priedīte, Viktorija; Gailīte, Linda; Blennov, Kaj; Zetterberg, Henrik; Ķēniņa, Viktorija; Department of Doctoral Studies; Scientific Laboratory of Molecular Genetics; Department of Biology and Microbiology
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
3-Oct-2018Case report : Multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndromeGailite, Linda; Rots, Dmitrijs; Pukite, Ieva; Cernevska, Gunta; Kreile, Madara; Scientific Laboratory of Molecular Genetics
2014Lack of association between polymorphisms in genes MTHFR and MDR1 with risk of childhood acute lymphoblastic leukemiaKreile, Madara; Rots, Dmitrijs; Piekuse, Linda; Cebura, Elizabete; Grutupa, Marika; Kovalova, Zhanna; Lace, Baiba; Rīga Stradiņš University
2018Association of in-vitro fertilization twin pregnancy with maternal and perinatal complicationsGrasmane, Adele; Purina-Liberte, Katrina; Rots, Dmitrijs; Miltiņa, Ināra; Rezeberga, Dace; Faculty of Medicine; Scientific Laboratory of Molecular Genetics; Department of Obstetrics and Gynaecology