Inga Sakovich

441 total citations
6 papers, 35 citations indexed

About

Inga Sakovich is a scholar working on Immunology, Genetics and Molecular Biology. According to data from OpenAlex, Inga Sakovich has authored 6 papers receiving a total of 35 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Immunology, 3 papers in Genetics and 2 papers in Molecular Biology. Recurrent topics in Inga Sakovich's work include Immunodeficiency and Autoimmune Disorders (4 papers), Blood disorders and treatments (2 papers) and Immune Cell Function and Interaction (2 papers). Inga Sakovich is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (4 papers), Blood disorders and treatments (2 papers) and Immune Cell Function and Interaction (2 papers). Inga Sakovich collaborates with scholars based in Belarus, United States and Sweden. Inga Sakovich's co-authors include Svetlana Sharapova, Olga Aleinikova, Thomas L. Leto, Jolán E. Walter, Vedat Uygun, Ágnes Donkó, Анастасія Бондаренко, Larysa Kostyuchenko, Steven M. Holland and Alina Dulau‐Florea and has published in prestigious journals such as Journal of Clinical Investigation, Clinical Immunology and Immunogenetics.

In The Last Decade

Inga Sakovich

4 papers receiving 35 citations

Peers

Inga Sakovich
Mana Momenilandi Iran
Juhao Yang Germany
Jan Schroeder Australia
Paul Tuijnenburg Netherlands
Dante Acenas United States
Jeffrey Hsu United States
Kate McAllister United Kingdom
Matthew R. Schaner United States
Viola Fanfani United States
Clément Chatelain France
Mana Momenilandi Iran
Inga Sakovich
Citations per year, relative to Inga Sakovich Inga Sakovich (= 1×) peers Mana Momenilandi

Countries citing papers authored by Inga Sakovich

Since Specialization
Citations

This map shows the geographic impact of Inga Sakovich's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Inga Sakovich with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Inga Sakovich more than expected).

Fields of papers citing papers by Inga Sakovich

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Inga Sakovich. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Inga Sakovich. The network helps show where Inga Sakovich may publish in the future.

Co-authorship network of co-authors of Inga Sakovich

This figure shows the co-authorship network connecting the top 25 collaborators of Inga Sakovich. A scholar is included among the top collaborators of Inga Sakovich based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Inga Sakovich. Inga Sakovich is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

6 of 6 papers shown
1.
Sakovich, Inga, et al.. (2024). Infant with diffuse large B-cell lymphoma identified postmortem with homozygous founder Slavic RAG1 variant: a case report and literature review. Frontiers in Pediatrics. 12. 1415020–1415020. 2 indexed citations
2.
Sakovich, Inga, et al.. (2023). Diffuse large B-cell lymphoma in 1-year male with founder Slavic RAG1 mutation: case report. Clinical Immunology. 250. 109393–109393.
3.
Kuehn, Hye Sun, Inga Sakovich, Julie E. Niemela, et al.. (2023). Disease-associated AIOLOS variants lead to immune deficiency/dysregulation by haploinsufficiency and redefine AIOLOS functional domains. Journal of Clinical Investigation. 134(3). 8 indexed citations
4.
5.
Sharapova, Svetlana, Emma Haapaniemi, Inga Sakovich, et al.. (2019). Heterozygous activating mutation in RAC2 causes infantile-onset combined immunodeficiency with susceptibility to viral infections. Clinical Immunology. 205. 1–5. 21 indexed citations
6.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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2026