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
Fingerprint
- 1 Similar Profiles
Network
Projects
- 2 Finished
-
Characterisation of genetic variance induced fetal structural anomalies using deep-phenotyping and deep-genotyping
Krūmiņa, Z., Gailīte, L., Auzenbaha, M., Grīnfelde, I., Rots, D. & Vogel, S.
1/09/20 → 31/08/21
Project: RSU grants
-
Characteristics of Genetic Variations Causing Structural Foetal Malformations, Using Deep Phenotyping and Genotyping
Gailīte, L., Auzenbaha, M., Grīnfelde, I., Mālniece, I., Kempa, I., Rota, A., Dobele, Z. & Rots, D.
1/04/19 → 31/03/20
Project: RSU grants
-
Implication of Genetic Testing and Pregnancy Outcome in a Woman with Unbalanced Translocation t(1;6)
Jurčenko, M., 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 AccessFile1 Downloads (Pure) -
Monogenic Versus Multifactorial Inheritance in the Development of Isolated Cleft Palate: A Whole Genome Sequencing Study
Lace, B., 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 AccessFile1 Citation (Scopus)3 Downloads (Pure) -
Overview of Neuromuscular Disorder Molecular Diagnostic Experience for the Population of Latvia
Lace, B., 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 AccessFile1 Citation (Scopus)1 Downloads (Pure) -
Treatment of latent tuberculosis in a child with mucopolysaccharidosis type I receiving enzyme replacement therapy: A case report
Vasilevska, L., Kreile, M., Grinfelde, I. & Skangale, A., 16 Aug 2022, In: Frontiers in Pediatrics. 10, p. 01-03 3 p., 973193.Research output: Contribution to journal › Article › peer-review
Open AccessFile3 Downloads (Pure) -
Analysis of referrals to genetic investigations in children 0–3 months old in Children’s Clinical University Hospital (Riga, Latvia) in year 2019
Liepa, J., Kreile, M., Tauriņa, G., Mičule, I., Grīnfelde, I. & Mūrmane, D., 24 Mar 2021, p. 29.Research output: Contribution to conference › Abstract › peer-review
Activities
- 1 Oral presentation
-
Diagnostic challenges in patients with suspicions for primary immunodeficiencies in Latvia
Nataļja Kurjāne (Speaker), Daiga Murmane (Speaker), Ieva Mičule (Co-author), Madara Kreile (Co-author), Ieva Grīnfelde (Co-author), Inga Nartiša (Co-author), Dmitrijs Rots (Co-author), Linda Gailīte (Co-author) & Gita Taurina (Co-author)
Apr 2021Activity: Talk or presentation types › Oral presentation