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
- 3.1 Basic medicine
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Dive into the research topics where Inga Nartiša is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 1 Similar Profiles
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
- 3 Finished
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Hereditary angioedema: Research of genetic etiology
Kurjāne, N. (Project leader), Gailīte, L. (Participant), Kaņepa, A. (Participant), Rots, D. (Participant), Nartiša, I. (Participant) & Vīksne, K. (Participant)
12/07/21 → 11/07/22
Project: RSU grants
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Predominantly primary antibody deficiencies among adults: solving etiology and causes of clinical variability
Kurjāne, N. (Project leader), Gailīte, L. (Leading expert), Rots, D. (Participant), Kaņepa, A. (Assistant (student)), Lucāne, Z. (Assistant (student)), Nartiša, I. (Assistant (student)), Neiburga, K. D. (Assistant (student)), Ozola, L. (Participant) & Ķēniņa, V. (Expert)
1/01/21 → 31/12/23
Project: Fundamental and Applied Research Programme
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Predominant antibody deficiencies: in search of causes for clinical phenotypes and etiological diversity
Nartiša, I. (Project leader) & Kurjāne, N. (Supervisor)
1/10/20 → 30/09/24
Project: PhD projects
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Hereditary or acquired? Comprehensive genetic testing assists in stratifying angioedema patients
Rozevska, M., Kaņepa, A., Puriņa, S., Gailīte, L., Nartiša, I., Farkas, H., Rots, D. & Kurjāne, N. (Corresponding Author), 30 Mar 2024, In: Allergy, Asthma & Clinical Immunology. 20, 1, p. 1-6 6 p., 28.Research output: Contribution to journal › Article › peer-review
Open AccessFile1 Citation (Scopus)6 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 AccessFile41 Downloads (Pure) -
National survey on clinical and genetic characteristics of patients with hereditary angioedema in Latvia
Kanepa, A. (Corresponding Author), Nartisa, I., Rots, D., Gailite, L., Farkas, H. & Kurjane, N., 8 Apr 2023, In: Allergy, Asthma and Clinical Immunology. 19, 1, 28.Research output: Contribution to journal › Article › peer-review
Open AccessFile4 Citations (Scopus)6 Downloads (Pure) -
Newborn screening for biotidinase deficiency experience in Latvia
Laktina, S. (Corresponding Author), Auzenbaha, M., Nartisa, I., Konika, M. & Vetra, A., 2022, In: Journal of Inherited Metabolic Disease. 45, Suppl.1, p. 397 1 p., SSIEM22-2743.Research output: Contribution to journal › Meeting Abstract › peer-review
Open Access -
Urinary organic acids spectra in children with altered gut microbiota composition and autistic spectrum disorder
Daneberga, Z. (Corresponding Author), Nakazawa-Miklasevica, M., Berga-svitina, E., Murmane, D., Isarova, D., Cupane, L., Masinska, M., Nartiša, I., Lazdane, A. & Miklasevics, E., 3 Oct 2022, In: Nordic Journal Of Psychiatry. 76, 7, p. 523-529Research output: Contribution to journal › Article › peer-review
9 Citations (Scopus)
Datasets
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Clinical data for primary immunodeficiency patients
Gailīte, L. (Creator), Kurjāne, N. (Creator), Rots, D. (Creator), Nartiša, I. (Creator) & Lucāne, Z. (Creator), Riga Stradins University, 31 Jan 2024
DOI: 10.48510/FK2/4EMT9P, https://doi.org/10.48510/FK2/4EMT9P
Dataset
Activities
- 4 Oral presentation
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Opportunities of RNA-seq in Molecular Diagnosis of Primary Immunodeficiencies
Neiburga, K. D. (Speaker), Lucāne, Z. (Co-author), Nartiša, I. (Co-author), Rots, D. (Co-author), Gailīte, L. (Co-author), Kisand, K. (Co-author), Pajusalu, S. (Co-author), Vilne, B. (Co-author) & Kurjāne, N. (Co-author)
29 Mar 2023Activity: Talk or presentation types › Oral presentation
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First Results of Using Genome Sequencing in Discovering the Molecular Cause of Primary Immunodeficiencies
Gailīte, L. (Speaker), Nartiša, I. (Co-author), Lucāne, Z. (Co-author), Vilne, B. (Co-author), Rots, D. (Co-author) & Kurjāne, N. (Co-author)
29 Mar 2023Activity: Talk or presentation types › Oral 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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Genetic testing for primary immunodeficiencies: 2 years’ experience in Latvia
Nartiša, I. (Speaker)
24 Mar 2021Activity: Talk or presentation types › Oral presentation