Outi Tuovila

Turku Centre for Biotechnology — Finland

Biochemistry, Genetics and Molecular Biology · Life Sciences

19h-index4.3kcitations32works7.42yr avg
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Research Topics

Genetic Associations and Epidemiology(7), Sleep and related disorders(3), BRCA gene mutations in cancer(3), Bioinformatics and Genomic Networks(3), Lipid metabolism and biosynthesis(3)

Publications19 total

Large-scale genome-wide analyses with proteomics integration reveal novel loci and biological insights into frailty
Nature Aging·2025· 2 citedOpen Access
Narcolepsy as a potential risk factor for Schizophrenia
Translational Psychiatry·2025· 3 citedOpen Access
Genome-wide meta-analysis conducted in three large biobanks expands the genetic landscape of lumbar disc herniations
Nature Communications·2024· 7 citedOpen Access
Genetic Susceptibility to Acute Viral Bronchiolitis
The Journal of Infectious Diseases·2024· 5 citedOpen Access
Comprehensive Inherited Risk Estimation for Risk-Based Breast Cancer Screening in Women
Journal of Clinical Oncology·2024· 29 citedOpen Access
High-Resolution Genotyping of Formalin-Fixed Tissue Accurately Estimates Polygenic Risk Scores in Human Diseases
Laboratory Investigation·2024· 5 citedOpen Access
NTHL1 is a recessive cancer susceptibility gene
Scientific Reports·2023· 6 citedOpen Access
Data Resource Profile: Nationwide registry data for high-throughput epidemiology and machine learning (FinRegistry)
International Journal of Epidemiology·2023· 24 citedOpen Access
The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections
EBioMedicine·2023· 26 citedOpen Access
Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy
JAMA Cardiology·2023· 114 citedOpen Access
Major Genetic Risk Factors for Dupuytren's Disease Are Inherited From Neandertals
Molecular Biology and Evolution·2023· 13 citedOpen Access
Risk of Midlife Stroke After Adverse Pregnancy Outcomes: The FinnGen Study
Stroke·2023· 23 citedOpen Access
Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy
Nature Communications·2023· 54 citedOpen Access
Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata
Nature Communications·2023· 19 citedOpen Access
Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis
Communications Biology·2022· 16 citedOpen Access
Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes
Communications Biology·2022· 50 citedOpen Access
An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease
European Journal of Human Genetics·2020· 26 citedOpen Access
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells
Nature·2020· 145 citedOpen Access
Genetic architecture of human plasma lipidome and its link to cardiovascular disease
Nature Communications·2019· 189 citedOpen Access

Frequent Co-authors

Heiko Runz(24), Petri Virolainen(19), Sally John(19), Raimo Pakkanen(19), Anders Mälarstig(19), Jaakko Kaprio(18), Terhi Kilpi(18), Markus Perola(17), Johanna Schleutker(17), Tomi P. Mäkelä(17), Robert Graham(17), Joseph Maranville(16), Reetta Hinttala(16), Margaret G. Ehm(16), Antti Hakanen(16), Jari A. Laukkanen(16), Nicole Renaud(16), Adam Ziemann(15), Aarno Palotie(15), Dawn Waterworth(15)