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):
Field of Science
- 3.2 Clinical medicine
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- 1 Similar Profiles
Collaborations and top research areas from the last five years
Projects
- 2 Finished
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Characterisation of genetic variance induced fetal structural anomalies using deep-phenotyping and deep-genotyping
Krūmiņa, Z. (Project leader), Gailīte, L. (Participant), Auzenbaha, M. (Participant), Grīnfelde, I. (Participant), Rots, D. (Participant) & Vogel, S. (Participant)
1/09/20 → 31/08/21
Project: RSU grants
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Characteristics of Genetic Variations Causing Structural Foetal Malformations, Using Deep Phenotyping and Genotyping
Gailīte, L. (Project leader), Auzenbaha, M. (Leading expert), Grīnfelde, I. (Leading expert), Mālniece, I. (Leading expert), Kempa, I. (Participant), Rota, A. (Participant), Dobele, Z. (Participant) & Rots, D. (Participant)
1/04/19 → 31/03/20
Project: RSU grants
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A Mild form of Aromatic L-amino acid decarboxylase deficiency
Laktina, S., Auzenbaha, M., Grinfelde, I. & Zarina, A., 2023, In: Journal of Inherited Metabolic Disease. 46, Suppl.1, p. 561Research output: Contribution to journal › Meeting Abstract › peer-review
Open Access -
Exploring the role of the SHH gene in development: A case report of two children with Variant of Uncertain Significance
Rozevska, M., Lāce, B., Mičule, I., Grīnfelde, I., Mūrmane, D., Locmele, D., Masinska, M., Piruška, I., Skrabule, L. & Tauriņa, G., 2023, p. 230 - 230. 1 p.Research output: Contribution to conference › Poster › peer-review
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Implication of Genetic Testing and Pregnancy Outcome in a Woman with Unbalanced Translocation t(1;6)
Jurčenko, M. (Corresponding Author), Auzenbaha, M., Mičule, I., Grīnfelde, I., Dzalbs, A. & Mālniece, I., 22 Feb 2022, In: American Journal of Case Reports. 23, 1, p. e935370-1 - e935370-6 6 p., e935370.Research output: Contribution to journal › Article › peer-review
Open AccessFile17 Downloads (Pure) -
Monogenic Versus Multifactorial Inheritance in the Development of Isolated Cleft Palate: A Whole Genome Sequencing Study
Lace, B. (Corresponding Author), Pajusalu, S., Livcane, D., Grīnfelde, I., Akota, I., Mauliņa, I., Barkāne, B., Stavusis, J. & Inashkina, I., 24 Feb 2022, In: Frontiers in Genetics. 13, 6 p., 828534.Research output: Contribution to journal › Article › peer-review
Open AccessFile5 Citations (Scopus)33 Downloads (Pure) -
Overview of Neuromuscular Disorder Molecular Diagnostic Experience for the Population of Latvia
Lace, B. (Corresponding Author), Micule, I., Kenina, V., Setlere, S., Strautmanis, J., Kazaine, I., Taurina, G., Murmane, D., Grinfelde, I., Kornejeva, L., Krumina, Z., Sterna, O., Radovica-Spalvina, I., Vasiljeva, I., Gailite, L., Stavusis, J., Livcane, D., Kidere, D., Malniece, I. & Inashkina, I., 16 Jun 2022, In: Neurology: Genetics. 8, 3, p. 1-8 8 p., e685.Research output: Contribution to journal › Article › peer-review
Open AccessFile3 Citations (Scopus)27 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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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
Press/Media
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Trīs personu mazuļi: apaugļošanas metode palīdz izvairīties no slimību pārnešanas bērnam
5/06/23
1 Media contribution
Press/Media
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