Projects per year
Personal profile
Education/Academic qualification
3.2 Clinical medicine, Expert, Latvian Council of Science
1 Jul 2021 → 30 Jun 2024
Field of Science
- 3.2 Clinical medicine
Fingerprint
- 1 Similar Profiles
Network
-
Development of screening algorithm for high breast cancer risk by analysis of spectrum of predisposing mutations and their phenotypic manifestations
Irmejs, A., Daneberga, Z., Maksimenko, J., Loža, P., Berga-Švītiņa, E., Kuzņecova, E., Subatniece, S. & Petroviča, M.
7/02/22 → 31/01/23
Project: Other projects
-
Development of screening algorithm for high breast and ovarian cancer risk by analysis of spectrum of predisposing mutations and their phenotypic manifestations
Irmejs, A., Nakazawa (Miklasevica), M., Maksimenko, J., Loža, P., Līcīte, B., Tauvena, E., Ukleikins, S. & Subatniece, S.
12/07/21 → 11/07/22
Project: RSU grants
-
Pregnancy after breast cancer in BRCA1/2 mutation carriers
Maksimenko, J., Irmejs, A. & Gardovskis, J., 21 Jan 2022, In: Hereditary Cancer in Clinical Practice. 20, 1, 7 p., 3.Research output: Contribution to journal › Review article › peer-review
Open AccessFile -
Spectrum and frequency of CHEK2 variants in breast cancer affected and general population in the Baltic states region, initial results and literature review
Pavlovica, K., Irmejs, A., Noukas, M., Palover, M., Kals, M., Tonisson, N., Metspalu, A., Gronwald, J., Lubinski, J., Murmane, D., Kalnina, A., Loza, P., Maksimenko, J., Trofimovics, G., Subatniece, S., Daneberga, Z., Miklasevics, E. & Gardovskis, J., May 2022, In: European Journal of Medical Genetics. 65, 5, p. 104477 7 p., 104477.Research output: Contribution to journal › Article › peer-review
-
A novel frequent BRCA1 recurrent variant c.5117G > A (p.Gly1206Glu) identified after 20 years of BRCA1/2 research in the Baltic region: cohort study and literature review
Loza, P., Irmejs, A., Daneberga, Z., Miklasevics, E., Berga-Svitina, E., Subatniece, S., Maksimenko, J., Trofimovics, G., Tauvena, E., Ukleikins, S. & Gardovskis, J., 19 Jan 2021, In: Hereditary cancer in clinical practice. 19, 1, 8 p., 11.Research output: Contribution to journal › Review article › peer-review
Open AccessFile3 Downloads (Pure) -
Epidemiology of rare breast cancer predisposing pathogenic gene variants in high hereditary breast cancer risk of population of Latvia, initial results
Pavloviča, K., Irmejs, A., Mūrmane, D., Kalniņa, A., Loža, P., Maksimenko, J., Trofimovičs, G., Subatniece, S., Miklaševičs, E. & Gardovskis, J., 24 Mar 2021, p. 91.Research output: Contribution to conference › Abstract › peer-review
-
Novel recurrent BRCA1 pathogenic variants c.5117G>A (p.Gly1706Glu) and c.4675G>A (p.Glu1559Lys) identified after 20 years of BRCA1/2 research in Baltic region. Cohort study and a literature review
Loža, P., Irmejs, A., Daneberga, Z., Miklaševičs, E., Berga-Švītiņa, E., Subatniece, S., Maksimenko, J., Gardovskis, J., Tauvena, E., Trofimovičs, G. & Ukleikins, S., 24 Mar 2021, p. 103.Research output: Contribution to conference › Abstract › peer-review
-
RSU Research week 2021: Knowledge for Use in Practice (Event)
Jeļena Maksimenko (Reviewer of conference paper)
24 Mar 2021Activity: Publication peer-review and editorial work types › Publication Peer-review
-
Breast (Journal)
Jeļena Maksimenko (Reviewer of journal article)
2021Activity: Publication peer-review and editorial work types › Publication Peer-review
-
Latvian Association of Surgeons (External organisation)
Jeļena Maksimenko (Member)
1 Jan 2014 → …Activity: Membership types › Membership of NGOs
-
European School of oncology (External organisation)
Jeļena Maksimenko (Expert)
1 Jan 2014 → …Activity: Membership types › Membership of NGOs