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

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Exploring disease-specific metabolite signatures in hereditary angioedema patients von Kanepa, Adine, Fan, Jingzhi, Rots, Dmitrijs, Vaska, Annija, Ansone, Laura, Briviba, Monta, Klovins, Janis, Kurjane, Natalja, Klavins, Kristaps

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National survey on clinical and genetic characteristics of patients with hereditary angioedema in Latvia von Kanepa, Adine, Nartisa, Inga, Rots, Dmitrijs, Gailite, Linda, Farkas, Henriette, Kurjane, Natalja

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

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Hereditary or acquired? Comprehensive genetic testing assists in stratifying angioedema patients von Rozevska, Marija, Kanepa, Adine, Purina, Signe, Gailite, Linda, Nartisa, Inga, Farkas, Henriette, Rots, Dmitrijs, Kurjane, Natalja

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

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Genetic Basis of Early Onset Atrial Fibrillation in Patients without Risk Factors von Rudaka, Irina, Vilne, Baiba, Isakova, Jekaterina, Kalejs, Oskars, Gailite, Linda, Rots, Dmitrijs

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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 von Gailite, Linda, Valenzuela-Palomo, Alberto, Sanoguera-Miralles, Lara, Rots, Dmitrijs, Kreile, Madara, Velasco, Eladio A

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The most common European HINT1 neuropathy variant phenotype and its case studies von Rozevska, Marija, Rots, Dmitrijs, Gailite, Linda, Linde, Ronalds, Mironovs, Stanislavs, Timcenko, Maksims, Linovs, Viktors, Locmele, Dzintra, Micule, Ieva, Lace, Baiba, Kenina, Viktorija

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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 von Vogel, Simon, Rudaka, Irina, Rots, Dmitrijs, Isakova, Jekaterīna, Kalējs, Oskars, Vīksne, Kristīne, Gailīte, Linda

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Long-Term Immunological Memory of SARS-CoV-2 Is Present in Patients with Primary Antibody Deficiencies for up to a Year after Vaccination von Lucane, Zane, Slisere, Baiba, Ozola, Lota, Rots, Dmitrijs, Papirte, Sindija, Vilne, Baiba, Gailite, Linda, Kurjane, Natalja

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P637: A newly derived DNA methylation signature for Koolen de Vries syndrome addresses the diagnostic challenges of the 17q21.31 locus von Awamleh, Zain, Choufani, Sanaa, Rots, Dmitrijs, Dingemans, Alexander, Ortigoza Escobar, Juan Dario, Koolen, David, de Vries, Bert, Weksberg, Rosanna

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

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

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Association of in-vitro fertilization twin pregnancy with maternal and perinatal complications von Grasmane Adele, Purina-Liberte Katrina, Rots Dmitrijs, Miltina Inara, Rezeberga Dace

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PREVALENCE OF OBSCN TRUNCATING VARIANTS IN LONE ATRIAL FIBRILLATION von Rudaka, Irina, Rots, Dmitrijs, Kalejs, Oskars, Gailite, Linda

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Plasma neurofilament light chain level is not a biomarker of Charcot–Marie–Tooth disease progression: Results of 3‐year follow‐up study von Setlere, Signe, Grosmane, Arta, Kurjane, Natalja, Gailite, Linda, Rots, Dmitrijs, Blennow, Kaj, Zetterberg, Henrik, Kenina, Viktorija

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Plasma neurofilament light chain as a potential biomarker in Charcot‐Marie‐Tooth disease von Millere, Elina, Rots, Dmitrijs, Simrén, Joel, Ashton, Nicholas J., Kupats, Einars, Micule, Ieva, Priedite, Viktorija, Kurjane, Natalja, Blennow, Kaj, Gailite, Linda, Zetterberg, Henrik, Kenina, Viktorija

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DeNovoCNN: a deep learning approach to de novo variant calling in next generation sequencing data von Khazeeva, Gelana, Sablauskas, Karolis, van der Sanden, Bart, Steyaert, Wouter, Kwint, Michael, Rots, Dmitrijs, Hinne, Max, van Gerven, Marcel, Yntema, Helger, Vissers, Lisenka, Gilissen, Christian

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Kohlschütter–Tönz syndrome: Case report with novel feature and detailed review of features associated with ROGDI variants von Liepina, Lelde, Kalnina, Marija Luize, Micule, Ieva, Gailite, Linda, Rots, Dmitrijs, Kalnina, Julija, Strautmanis, Jurgis, Celmina, Marta

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