Anu Reigo

5.3k total citations
14 papers, 62 citations indexed

About

Anu Reigo is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Anu Reigo has authored 14 papers receiving a total of 62 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Surgery. Recurrent topics in Anu Reigo's work include Genomics and Rare Diseases (3 papers), BRCA gene mutations in cancer (3 papers) and RNA regulation and disease (2 papers). Anu Reigo is often cited by papers focused on Genomics and Rare Diseases (3 papers), BRCA gene mutations in cancer (3 papers) and RNA regulation and disease (2 papers). Anu Reigo collaborates with scholars based in Estonia, Finland and Switzerland. Anu Reigo's co-authors include Andres Metspalu, Mart Kals, Tiit Nikopensius, Liis Leitsalu, Tōnu Esko, Kalle Pärn, Neeme Tõnisson, Peeter Padrik, Evelin Mihailov and Eva Reinmaa and has published in prestigious journals such as Nature Communications, Scientific Reports and Journal of Clinical Epidemiology.

In The Last Decade

Anu Reigo

11 papers receiving 61 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Anu Reigo Estonia	5	26	15	11	9	8	14	62
Saskia Haitjema Netherlands	2	10 0.4×	11 0.7×	16 1.5×	6 0.7×		4	48
Jin Fang Chai China	5	27 1.0×	32 2.1×	4 0.4×	5 0.6×	1 0.1×	13	72
Reeta Metta United States	2	23 0.9×	16 1.1×	6 0.5×	6 0.7×	1 0.1×	2	74
Andrea Seeley United States	5	31 1.2×	17 1.1×	3 0.3×	5 0.6×		8	57
Fausto Poddie Italy	3	22 0.8×	22 1.5×	2 0.2×	6 0.7×	4 0.5×	3	46
Jun Hosoe Japan	4	34 1.3×	46 3.1×	6 0.5×	31 3.4×	1 0.1×	7	93
Xiuqing Guo United States	4	37 1.4×	17 1.1×	3 0.3×	7 0.8×		8	74
C. J. Weber United States	3	18 0.7×	40 2.7×	9 0.8×	6 0.7×		6	82
Abolfazl Heidari Iran	4	13 0.5×	17 1.1×	4 0.4×	3 0.3×	1 0.1×	8	59
Ulvi Gerst Talas United Kingdom	2	9 0.3×	15 1.0×	2 0.2×	7 0.8×	2 0.3×	4	39

Countries citing papers authored by Anu Reigo

Since Specialization

Citations

This map shows the geographic impact of Anu Reigo'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 Anu Reigo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anu Reigo more than expected).

Fields of papers citing papers by Anu Reigo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anu Reigo. 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 Anu Reigo. The network helps show where Anu Reigo may publish in the future.

Co-authorship network of co-authors of Anu Reigo

This figure shows the co-authorship network connecting the top 25 collaborators of Anu Reigo. A scholar is included among the top collaborators of Anu Reigo 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 Anu Reigo. Anu Reigo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

Pezzullo, Angelo Maria, Péter Pikó, Markus Perola, et al.. (2025). A scoping review of the assessment reports of genetic or genomic tests reveals inconsistent consideration of key dimensions of clinical utility. Journal of Clinical Epidemiology. 181. 111729–111729. 1 indexed citations

Salminen, Aino, Kati Hyvärinen, Jarmo Ritari, et al.. (2025). Genome-wide association study of pulpal and apical diseases. Nature Communications. 16(1). 6774–6774. 2 indexed citations

Kals, Mart, Anu Reigo, Maris Teder‐Laving, et al.. (2025). Polygenic Risk Score Combined with Transcranial Sonography Refines Parkinson's Disease Risk Prediction. Movement Disorders Clinical Practice. 12(7). 928–937. 1 indexed citations

Reigo, Anu, Tarmo Annilo, Toomas Toomsoo, et al.. (2024). Use of Estonian Biobank data and participant recall to improve Wilson’s disease management. European Journal of Human Genetics. 33(11). 1499–1508.

Jaagura, Madis, Jaanika Kronberg, Anu Reigo, et al.. (2024). Comorbidities confound metabolomics studies of human disease. Scientific Reports. 14(1). 24810–24810. 2 indexed citations

Sliz, Eeva, Laura Huilaja, Kadri Reis, et al.. (2024). Genetic Study of Psoriasis Highlights its Close Link with Socioeconomic Status and Affective Symptoms. Journal of Investigative Dermatology. 144(12). 2719–2729.

Kajanne, Risto, Abdelrahman G. Elnahas, Anu Reigo, et al.. (2024). Genome-wide association study of anterior uveitis. British Journal of Ophthalmology. 109(6). 660–667.

Teder‐Laving, Maris, Mart Kals, Anu Reigo, et al.. (2023). Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris. European Journal of Human Genetics. 32(9). 1136–1143. 11 indexed citations

Reigo, Anu, Sven Laur, Ardi Tampuu, et al.. (2023). Common clinical blood and urine biomarkers for ischemic stroke: an Estonian Electronic Health Records database study. European journal of medical research. 28(1). 133–133. 3 indexed citations

10.

Reigo, Anu, Margit Nõukas, Liis Leitsalu, et al.. (2022). Do Biobank Recall Studies Matter? Long-Term Follow-Up of Research Participants With Familial Hypercholesterolemia. Frontiers in Genetics. 13. 936131–936131. 2 indexed citations

11.

Leitsalu, Liis, Anu Reigo, Mart Kals, et al.. (2020). Genotype-first approach to the detection of hereditary breast and ovarian cancer risk, and effects of risk disclosure to biobank participants. European Journal of Human Genetics. 29(3). 471–481. 19 indexed citations

12.

Urgard, Egon, Anu Reigo, Eva Reinmaa, Ana Rebane, & Andres Metspalu. (2017). Human basonuclin 2 up-regulates a cascade set of interferon-stimulated genes with anti-cancerous properties in a lung cancer model. Cancer Cell International. 17(1). 18–18. 7 indexed citations

13.

Mihailov, Evelin, Tiit Nikopensius, Anu Reigo, et al.. (2016). Whole-exome sequencing identifies a potential TTN mutation in a multiplex family with inguinal hernia. Hernia. 21(1). 95–100. 6 indexed citations

14.

Leitsalu, Liis, Helene Alavere, Sébastien Jacquemont, et al.. (2016). Reporting incidental findings of genomic disorder-associated copy number variants to unselected biobank participants. Personalized Medicine. 13(4). 303–314. 8 indexed citations

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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