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Author

Anu Reigo

Observed names: A Reigo, A. Reigo, Reigo, A., Reigo, Anu
Observed institutions: University of Helsinki, Oulu University Hospital, Tartu University Hospital, Finnish Institute for Health and Welfare, Institute for Molecular Medicine Finland, HiLIFE – Elämäntieteiden Instituutti, University of Tartu
ORCID: 0009-0008-0226-3396
Observed ORCID: 0009-0008-0226-3396
OpenAlex ID: A5041008485
FinnGen provides genetic insights from a well-phenotyped isolated population
2023 · Mitja I. Kurki, Juha Karjalainen, et al. · Nature · 4,874
Copy Number Variations and Cognitive Phenotypes in Unselected Populations
2015 · Katrin Männik, Reedik Mägi, et al. · JAMA · 207
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The Estonian Biobank’s journey from biobanking to personalized medicine
2025 · Lili Milani, Maris Alver, et al. · Nature Communications · 142
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European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
2023 · Ashley Budu-Aggrey, Anna Kilanowski, et al. · Nature Communications · 140
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Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population
2023 · Mitja I. Kurki, Juha Karjalainen, et al. · Nature · 130
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Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes
2024 · Amanda Elliott, Raymond K. Walters, et al. · Nature Genetics · 111
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The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition
2015 · Loyse Hippolyte, Anne M. Maillard, et al. · Biological Psychiatry · 87
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Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from Estonia
2018 · Maris Alver, Marili Palover, et al. · Genetics in Medicine · 58
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Family-GWAS reveals effects of environment and mating on genetic associations
2024 · Tammy Tan, Hariharan Jayashankar, et al. · medRxiv · 56
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Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris
2023 · Maris Teder-Laving, Mart Kals, et al. · European Journal of Human Genetics · 47
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16p11.2 Locus modulates response to satiety before the onset of obesity
2015 · A M Maillard, L Hippolyte, et al. · International Journal of Obesity · 45
Genotype-first approach to the detection of hereditary breast and ovarian cancer risk, and effects of risk disclosure to biobank participants
2020 · Liis Leitsalu, Marili Palover, et al. · European Journal of Human Genetics · 44
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Lessons learned during the process of reporting individual genomic results to participants of a population-based biobank
2022 · Liis Leitsalu, Anu Reigo, et al. · European Journal of Human Genetics · 22
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Human basonuclin 2 up-regulates a cascade set of interferon-stimulated genes with anti-cancerous properties in a lung cancer model
2017 · Egon Urgard, Anu Reigo, et al. · Cancer Cell International · 16
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Genome-wide meta-analysis conducted in three large biobanks expands the genetic landscape of lumbar disc herniations
2024 · Ville Salo, Juhani Määttä, et al. · Nature Communications · 15
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Precise, Genotype-First Breast Cancer Prevention: Experience With Transferring Monogenic Findings From a Population Biobank to the Clinical Setting
2022 · Hannes Jürgens, Laura Roht, et al. · Frontiers in Genetics · 15
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Reporting incidental findings of genomic disorder-associated copy number variants to unselected biobank participants
2016 · Liis Leitsalu, Helene Alavere, et al. · Personalized Medicine · 15
Genome-wide association study of pulpal and apical diseases
2025 · Aino Salminen, Kati Hyvärinen, et al. · Nature Communications · 11
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Comorbidities confound metabolomics studies of human disease
2024 · Madis Jaagura, Jaanika Kronberg, et al. · Scientific Reports · 11
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Distinct Genetic Risk Profile in Aortic Stenosis Compared With Coronary Artery Disease
2024 · Teresa Trenkwalder, Carlo Maj, et al. · JAMA Cardiology · 10
Common clinical blood and urine biomarkers for ischemic stroke: an Estonian Electronic Health Records database study
2023 · Siim Kurvits, Ainika Harro, et al. · European journal of medical research · 10
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A scoping review of the assessment reports of genetic or genomic tests reveals inconsistent consideration of key dimensions of clinical utility
2025 · Angelo Maria Pezzullo, Angelica Valz Gris, et al. · Journal of Clinical Epidemiology · 9
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Whole-exome sequencing identifies a potential TTN mutation in a multiplex family with inguinal hernia
2016 · E. Mihailov, T. Nikopensius, et al. · Hernia · 9
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Use of Estonian Biobank data and participant recall to improve Wilson’s disease management
2024 · Miriam Nurm, Anu Reigo, et al. · European Journal of Human Genetics · 8
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Genetic Study of Psoriasis Highlights its Close Link with Socioeconomic Status and Affective Symptoms
2024 · Anni Heikkilä, Eeva Sliz, et al. · Journal of Investigative Dermatology · 8
Works count: 68
Citation count: 6,136
H-index: 15
I10-index: 21
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