Projects per year
Personal profile
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
External positions
Clinical Geneticist, Children's Clinical University Hospital
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Dive into the research topics where Ieva Mičule is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
Projects
- 1 Finished
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The exploration of genetic factors underlying malformations of cortical development in patients with surgically treated refractory epilepsy
Mičule, I. (Project leader) & Lāce, B. (Supervisor)
1/10/20 → 30/09/24
Project: PhD projects
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Altered Splicing of LAMP2 in a Multigenerational Family from Latvia Affected by Danon Disease
Stavusis, J. (Corresponding Author), Mičule, I., Grīnfelde, I., Zdanovica, A., Pudulis, J., Valeina, S., Sepetiene, S., Lace, B. & Inashkina, I., Jan 2024, In: Medicina (Lithuania). 60, 1, 8 p., 99.Research output: Contribution to journal › Article › peer-review
Open AccessFile1 Citation (Scopus)1 Downloads (Pure) -
Evaluation of pathogenic repeat expansion detection from exome sequencing data
Bārdiņa, L., Zariņa, A., Žiravecka, I., Mičule, I., Tauriņa, G., Mūrmane, D., Ķēniņa, V., Rots, D. & Nartiša, I., Jan 2024, In: European Journal of Human Genetics. 32, Suppl.1, p. 658 1 p., P18.030.B.Research output: Contribution to journal › Meeting Abstract › peer-review
Open AccessFile2 Downloads (Pure) -
Laboratory challenges by the interpretation of slightly decreased branched chain amino acids concentrations: A case of BCKDK deficiency
Lazdane, A., Vorslova, S., Vevere, P., Micule, I., Daneberga, Z., Taurina, G., Laktina, S., Auzenbaha, M. & Nartisa, I., Jan 2024, In: European Journal of Human Genetics. 32, Suppl.1, p. 160-161 2 p., EP07.001.Research output: Contribution to journal › Meeting Abstract › peer-review
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The phenotypic spectrum of PTCD3 deficiency
Lāce, B. (Corresponding Author), Faqeih, E., Kaya, N., Krūmiņa, Z., Mayr, J. A., Mičule, I., Wright, N. T., Achleitner, M. T., AlQudairy, H., Pajusalu, S., Stavusis, J., Zayakin, P. & Inashkina, I., Sept 2024, In: JIMD Reports. 65, 5, p. 297-304 8 p.Research output: Contribution to journal › Article › peer-review
Open AccessFile1 Downloads (Pure) -
Clinical and genetic characterization of Netherton syndrome due to SPINK5 founder variant in Latvian population
Nartisa, I. (Corresponding Author), Kirsteina, R., Neiburga, K. D., Zigure, S., Ozola, L., Grantina, I., Micule, I., Murmane, D., Slisere, B., Gailite, L., Vilne, B., Rots, D., Taurina, G. & Kurjane, N., 1 Apr 2023, In: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology. 34, 4, e13937.Research output: Contribution to journal › Article › peer-review
Open AccessFile2 Citations (Scopus)73 Downloads (Pure)
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Genetic Characterisation of Retinoblastoma in Latvia from 2000 to 2022
Skrabule, L. (Speaker), Mičule, I. (Co-author), Mūrmane, D. (Co-author), Grīnfelde, I. (Co-author), Valeiņa, S. (Co-author), Vīksniņš, M. (Co-author) & Tauriņa, G. (Co-author)
29 Mar 2023Activity: Talk or presentation types › Poster presentation
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HINT1 Neuropathy in Latvia: Clinical, Genetic, and Functional Profiling
Rozevska, M. (Speaker), Rots, D. (Co-author), Gailīte, L. (Co-author), Linde, R. (Co-author), Mironovs, S. (Co-author), Timčenko, M. (Co-author), Ļiņovs, V. (Co-author), Locmele, D. (Co-author), Mičule, I. (Co-author), Lāce, B. (Co-author) & Ķēniņa, V. (Co-author)
29 Mar 2023Activity: Talk or presentation types › Poster presentation
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Analysis of Molecular Genetic Testing for Hereditary Forms of Cancer 2020–2022
Piruška, I. (Speaker), Lāce, B. (Co-author), Mūrmane, D. (Co-author), Mičule, I. (Co-author), Irmejs, A. (Co-author), Loža, P. (Co-author), Maksimenko, J. (Co-author) & Tauriņa, G. (Co-author)
29 Mar 2023Activity: Talk or presentation types › Poster presentation
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Diagnostic challenges in patients with suspicions for primary immunodeficiencies in Latvia
Kurjāne, N. (Speaker), Murmane, D. (Speaker), Mičule, I. (Co-author), Kreile, M. (Co-author), Grīnfelde, I. (Co-author), Nartiša, I. (Co-author), Rots, D. (Co-author), Gailīte, L. (Co-author) & Taurina, G. (Co-author)
23 Apr 2021 → 24 Apr 2021Activity: Talk or presentation types › Oral presentation
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Ģenētisko variāciju klasifikācija un to interpretēšana nākamās paaudzes sekvenēšanas laikmetā
Daneberga, Z. (Participant), Kiršteina, R. (Participant), Berga-Švītiņa, E. (Participant), Zvejniece, L. (Participant), Dobele, Z. (Participant), Nartiša, I. (Participant), Voložonoka, L. (Participant), Griķe, I. (Participant), Puzuka, A. (Participant), Zariņa, A. (Participant), Alkšere, B. (Participant), Mičule, I. (Participant), Līdaka, L. (Participant), Rota, A. (Participant) & Jurčenko, M. (Participant)
14 Nov 2020 → 12 Dec 2020Activity: Participating in or organising an event types › Participating in a conference, workshop, ...
Press/Media
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Children's Clinical University Hospital Researchers Reveal New Findings on Neuropathy (The most common European HINT1 neuropathy variant phenotype and its case studies)
Rots, D., Mičule, I. & Gailīte, L.
2/03/23
1 item of Media coverage
Press/Media