検索結果 - Rots, Dmitrijs

Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome 著者: Gailite, Linda, Rots, Dmitrijs, Pukite, Ieva, Cernevska, Gunta, Kreile, Madara

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The association of FMR1 gene (CGG)n variation with idiopathic female infertility 著者: Grasmane, Adele, Rots, Dmitrijs, Vitina, Zane, Magomedova, Valerija, Gailite, Linda

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Analysis of possible genetic risk factors contributing to development of childhood acute lymphoblastic leukaemia in the Latvian population 著者: Kreile, Madara, Piekuse, Linda, Rots, Dmitrijs, Dobele, Zane, Kovalova, Zhanna, Lace, Baiba

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Genetic landscape of preterm birth due to cervical insufficiency: Comprehensive gene analysis and patient next-generation sequencing data interpretation 著者: Volozonoka, Ludmila, Rots, Dmitrijs, Kempa, Inga, Kornete, Anna, Rezeberga, Dace, Gailite, Linda, Miskova, Anna

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A Higher Polygenic Risk Score Is Associated with a Higher Recurrence Rate of Atrial Fibrillation in Direct Current Cardioversion-Treated Patients 著者: Vogel, Simon, Rudaka, Irina, Rots, Dmitrijs, Isakova, Jekaterīna, Kalējs, Oskars, Vīksne, Kristīne, Gailīte, Linda

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Association of ARID5B Genetic Variants with Risk of Childhood B Cell Precursor Acute Lymphoblastic Leukaemia in Latvia 著者: Kreile, Madara, Rots, Dmitrijs, Zarina, Agnese, Rautiainen, Linda, Visnevska-Preciniece, Zelma, Kovalova, Zhanna, Gailite, Linda

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UGT1A1 Variants c.864+5G>T and c.996+2_996+5del of a Crigler-Najjar Patient Induce Aberrant Splicing in Minigene Assays 著者: Gailite, Linda, Valenzuela-Palomo, Alberto, Sanoguera-Miralles, Lara, Rots, Dmitrijs, Kreile, Madara, Velasco, Eladio A.

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Novel Variant of the Androgen Receptor Gene in a Patient With Complete Androgen Insensitivity Syndrome and Polyorchidism 著者: Konrade, Ilze, Zavorikina, Julija, Fridvalde, Aija, Rots, Dmitrijs, Kalere, Ieva, Strumfa, Ilze, Dambrova, Maija, Gailite, Linda

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Clinical Phenotyping and Biomarkers in Spinal and Bulbar Muscular Atrophy 著者: Millere, Elina, Rots, Dmitrijs, Glazere, Ieva, Taurina, Gita, Kurjane, Natalja, Priedite, Viktorija, Gailite, Linda, Blennow, Kaj, Zetterberg, Henrik, Kenina, Viktorija

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Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature 著者: Rots, Dmitrijs, Chater-Diehl, Eric, Dingemans, Alexander J.M., Goodman, Sarah J., Siu, Michelle T., Cytrynbaum, Cheryl, Choufani, Sanaa, Hoang, Ny, Walker, Susan, Awamleh, Zain, Charkow, Joshua, Meyn, Stephen, Pfundt, Rolph, Rinne, Tuula, Gardeitchik, Thatjana, de Vries, Bert B.A., Deden, A. Chantal, Leenders, Erika, Kwint, Michael, Stumpel, Constance T.R.M., Stevens, Servi J.C., Vermeulen, Jeroen R., van Harssel, Jeske V.T., Bosch, Danielle G.M., van Gassen, Koen L.I., van Binsbergen, Ellen, de Geus, Christa M., Brackel, Hein, Hempel, Maja, Lessel, Davor, Denecke, Jonas, Slavotinek, Anne, Strober, Jonathan, Crunk, Amy, Folk, Leandra, Wentzensen, Ingrid M., Yang, Hui, Zou, Fanggeng, Millan, Francisca, Person, Richard, Xie, Yili, Liu, Shuxi, Ousager, Lilian B., Larsen, Martin, Schultz-Rogers, Laura, Morava, Eva, Klee, Eric W., Berry, Ian R., Campbell, Jennifer, Lindstrom, Kristin, Pruniski, Brianna, Neumeyer, Ann M., Radley, Jessica A., Phornphutkul, Chanika, Schmidt, Berkley, Wilson, William G., Õunap, Katrin, Reinson, Karit, Pajusalu, Sander, van Haeringen, Arie, Ruivenkamp, Claudia, Cuperus, Roos, Santos-Simarro, Fernando, Palomares-Bralo, María, Pacio-Míguez, Marta, Ritter, Alyssa, Bhoj, Elizabeth, Tønne, Elin, Tveten, Kristian, Cappuccio, Gerarda, Brunetti-Pierri, Nicola, Rowe, Leah, Bunn, Jason, Saenz, Margarita, Platzer, Konrad, Mertens, Mareike, Caluseriu, Oana, Nowaczyk, Małgorzata J.M., Cohn, Ronald D., Kannu, Peter, Alkhunaizi, Ebba, Chitayat, David, Scherer, Stephen W., Brunner, Han G., Vissers, Lisenka E.L.M., Kleefstra, Tjitske, Koolen, David A., Weksberg, Rosanna

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