Elina Hypponen

Prof Elina Hypponen

Professor of Nutritional and Genetic Epidemiology

School of Public Health

College of Health

Eligible to supervise Masters and PhD - email supervisor to discuss availability.

Available For Media Comment.


Professor Hyppönen is the Director of the Australian Centre for Precision Health at the University of South Australia. She was recruited to the UniSA as the Professor in Nutritional and Genetic Epidemiology in 2013, following 12 years at the University College London, Great Ormond Street Institute of Child Health (London, UK).She is a NHMRC Leadership (L2) Investigator and holds appointments as a Senior Principal Research Fellow at the South Australian Health and Medical Research Institute (SAHMRI) and as an Adjunct Professor in Epidemiology at the University of Tampere, Finland. Professor Hyppönen has an interdisciplinary academic background, with academic qualifications in epidemiology, medical statistics, nutrition and public health. Professor Hyppönen has a H-factor of 90, and her work has been cited over 51,000 times.  She has authored more than 230 high-profile refereed publications and several book chapters. She leads the Nutritional and Genetic Epidemiology group which has a focus on using genetic tools to inform on dietary and lifestyle guidelines for optimal health. She has a long-term research interest in life-course and intergenerational epidemiology, and an extensive track record in gene and risk factor discovery. Her current interests are related to methods of causal analyses, machine learning, and implementing systems epidemiology approaches to establish effective strategies for prediction and prevention of chronic diseases.  

Year Citation
2026 Pham, K., Mulugeta, A., Lumsden, A., & Hyppӧnen, E. (2026). A multivariable Mendelian randomization study of serum lipids and dementia risk within the UK Biobank. Journal of Nutritional Biochemistry, 148(110160), 1-9.
DOI
2025 Byrne, S., Hypponen, E., Benyamin, B., & Boyle, T. (2025). Greater adherence to lifestyle recommendations after cancer diagnosis is associated with lower mortality in the UK Biobank. Cancer Epidemiology, Biomarkers and Prevention, 34(5), 669-675.
DOI
2025 Stacey, D., Gaziano, L., Eldi, P., Toben, C., Benyamin, B., Lee, S. H., & Hyppönen, E. (2025). A Transcriptome-Wide Mendelian Randomization Study in Isolated Human Immune Cells Highlights Risk Genes Involved in Viral Infections and Potential Drug Repurposing Opportunities for Schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 198(6), 19-31.
DOI
2025 Amente, L. D., Mills, N. T., Le, T. D., Hyppönen, E., & Lee, S. H. (2025). A latent outcome variable approach for Mendelian randomization using the stochastic expectation maximization algorithm. Human Genetics, 144(5), 559-574.
DOI Scopus1 WoS1 Europe PMC1
2025 Mulugeta, A., Stacey, D., Lumsden, A. L., Madakkatel, I., Lee, S. H., Mäenpää, J., . . . Hyppönen, E. (2025). Protein markers of ovarian cancer and its subtypes: insights from proteome-wide Mendelian randomisation analysis. British Journal Of Cancer, 133(8), 1208-1217.
DOI
2025 Dewau, R., Byrne, S., Hyppönen, E., Lee, S. H., & Benyamin, B. (2025). Genetic and Environmental Contributions to Child Height in Low- and Middle-Income Countries. American Journal of Human Biology, 37(9), e70134.
DOI Europe PMC1
2025 Amente, L. D., Mills, N. T., Le, T. D., Hypponen, E., & Lee, S. H. (2025). Disentangling horizontal and vertical Pleiotropy in genetic correlation estimation: introducing the HVP model. Human Genetics, 144(8), 861-876.
DOI Europe PMC1
2025 Pham, K., Kassaw, N. A., Mulugeta, A., Zhou, A., & Hyppӧnen, E. (2025). Coffee and health outcomes: a systematic review of Mendelian randomisation studies. Nutrition Research Reviews, online(2), 21 pages.
DOI
2025 Hypponen, E., & Madakkatel, I. (2025). Response to Oka and Takefuji's correspondence on the article "Large-scale analysis to identify risk factors for ovarian cancer" by Madakkatel et al. International Journal Of Gynecological Cancer, 35(9, article no. 102000), 1.
DOI
2025 Lumsden, A. L., Mulugeta, A., & Hypponen, E. (2025). Dementia risk across distinct metabolic profiles in the UK Biobank. Geroscience, online, 1-25.
DOI
2025 Sutherland, J. P., Zhou, A., & Hyppönen, E. (2025). Vitamin D, C-reactive protein, and increased fall risk: a genetic epidemiological study. Nutrients, 17(1), 1-16.
DOI Scopus1 Europe PMC1
2025 Yeshaw, Y., Madakkatel, I., Mulugeta, A., Lumsden, A., & Hypponen, E. (2025). Machine learning to discover factors predicting volume of white matter hyperintensities: insights from the UK Biobank. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring, 17(1, article no. e70090), 1-12.
DOI
2025 Hyppönen, E., Mulugeta, A., & Zhou, A. (2025). Reanalysis of the vitamin D and dementia association using the doubly-ranked nonlinear Mendelian randomization approach. The American Journal of Clinical Nutrition, 122(3), 894-897.
DOI Scopus1
2025 Hypponen, E. (2025). Challenges with Mendelian randomization and its application to the study of vitamins. International Journal Of Epidemiology, 54(5, article no. dyaf165), 1-3.
DOI
2025 Zhou, A., & Hyppönen, E. (2025). A reanalysis of the bidirectional association between vitamin D and C-reactive protein using the doubly-ranked non-linear Mendelian randomization approach. International Journal of Epidemiology, 54(5, article no. dyaf166), 1-5.
DOI Scopus1 Europe PMC1
2024 Hypponen, E., Sutherland, J. P., & Zhou, A. (2024). Vitamin D deficiency increases mortality risk in the UK Biobank. Annals Of Internal Medicine, 177(12), 1743-1746.
DOI
2024 Kassaw, N. A., Zhou, A., Mulugeta, A., Lee, S. H., Burgess, S., & Hyppönen, E. (2024). Alcohol consumption and the risk of all-cause and cause-specific mortality-a linear and nonlinear Mendelian randomization study. International Journal of Epidemiology, 53(2), 1-8.
DOI Scopus14 Europe PMC9
2024 Yeshaw, Y., Madakkatel, I., Mulugeta, A., Lumsden, A., & Hyppönen, E. (2024). Uncovering predictors of low hippocampal volume: evidence from a large-scale machine-learning-based study in the UK biobank. Neuroepidemiology, 58(5), 369-382.
DOI
2024 Eshetie, S., Choi, K. W., Hyppönen, E., Benyamin, B., & Lee, S. H. (2024). Integrative multi-omics analysis to gain new insights into COVID-19. Scientific Reports, 14(1), 14 pages.
DOI Scopus1 WoS2 Europe PMC1
2024 Momin, M. M., Zhou, X., Hyppönen, E., Benyamin, B., & Lee, S. H. (2024). Cross-ancestry genetic architecture and prediction for cholesterol traits. Human Genetics, 143(5), 635-648.
DOI Scopus1 WoS2 Europe PMC3
2024 Verhoef, E., Allegrini, A. G., Jansen, P. R., Lange, K., Hypponen, E., & St. Pourcain, B. (2024). Genome-wide analyses of vocabulary size in infancy and toddlerhood: associations with attention-deficit/hyperactivity disorder, literacy, and cognition-related traits. Biological Psychiatry, 95(9), 859-869.
DOI Scopus8 Europe PMC13
2024 Madakkatel, I., & Hyppönen, E. (2024). LLpowershap: logistic loss-based automated Shapley values feature selection method. BMC Medical Research Methodology, 24(1, article no. 247), 1-14.
DOI
2024 Bradfeld, J. P., Kember, R. L., Ulrich, A., Balkhiyarova, Z., Alyass, A., Aris, I. M., . . . Hakonarson, H. (2024). Correction to: Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes (Genome Biology, (2024), 25, 1, (22), 10.1186/s13059-023-03136-z). Genome Biology, 25(1), 129.
DOI
2024 Bradfield, J. P., Kember, R. L., Ulrich, A., Balkiyarova, Z., Hypponen, E., & Cousminer, D. L. (2024). Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes. Genome biology, 25(22), 1-19.
DOI Scopus9 WoS8 Europe PMC10
2024 Dewau, R., Boomsma, A., Doyle, C., Byrne, S., Hyppönen, E., Lee, S. H., & Benyamin, B. (2024). Meta-Analysis of the Heritability of Childhood Height From 560 000 Pairs of Relatives Born Between 1929 and 2004. American Journal of Human Biology, 37(1), e24188-1-e24188-15.
DOI Scopus3 WoS3 Europe PMC3
2024 Jayasinghe, D., Momin, M. M., Beckmann, K., Hyppönen, E., Benyamin, B., & Lee, S. H. (2024). Mitigating type 1 error inflation and power loss in GxE PRS: Genotype–environment interaction in polygenic risk score models. Genetic Epidemiology, 48(2), 85-100.
DOI Scopus6 WoS7 Europe PMC8
2024 Amente, L. D., Mills, N. T., Le, T. D., Hyppönen, E., & Lee, S. H. (2024). Unraveling phenotypic variance in metabolic syndrome through multi-omics. Human Genetics, 143(1), 35-47.
DOI Scopus4 WoS4 Europe PMC2
2024 Byrne, S., Boyle, T., Ahmed, M., Lee, S. H., Benyamin, B., & Hyppönen, E. (2024). Response to: Adherence to the World Cancer Research Fund lifestyle recommendations and incidence of prostate cancer in the UK Biobank.. Int J Epidemiol, 53(1), 1-2.
DOI Scopus1 WoS1 Europe PMC1
2024 Mulugeta, A., Lumsden, A., Madakkatel, I., Stacey, D., Lee, S. H., Mäenpää, J., . . . Hypponen, E. (2024). Phenome-wide association study of ovarian cancer identifies common comorbidities and reveals shared genetics with complex diseases and biomarkers. Cancer Medicine, 13(4, article no. e7051), 1-13.
DOI Scopus2 Europe PMC3
2024 Stacey, D., Benyamin, B., Lee, S. H., & Hyppönen, E. (2024). A metabolome-wide Mendelian randomization study identifies dysregulated arachidonic acid synthesis as a potential causal risk factor for bipolar disorder. Biological Psychiatry, 96(6), 455-462.
DOI Scopus13 WoS14 Europe PMC14
2024 Stacey, D., Suppiah, V., Benyamin, B., Lee, S. H., & Hyppönen, E. (2024). In-silico functional analyses identify TMPRSS15-mediated intestinal absorption of lithium as a modulator of lithium response in bipolar disorder. Journal of Affective Disorders, 358, 416-421.
DOI Scopus2 WoS2 Europe PMC2
2024 Madakkatel, I., Lumsden, A. L., Mulugeta, A., Mäenpää, J., Oehler, M. K., & Hyppönen, E. (2024). Large-scale analysis to identify risk factors for ovarian cancer. International Journal of Gynecological Cancer, 35(8, article no. 101844), 005424-1-005424-9.
DOI Scopus6 WoS6 Europe PMC5
2024 Duko, B., Mengistu, T. S., Stacey, D., Moran, L. J., Tessema, G., Pereira, G., . . . Hyppönen, E. (2024). Associations between maternal preconception and pregnancy adiposity and neuropsychiatric and behavioral outcomes in the offspring: a systematic review and meta-analysis. Psychiatry Research, 342(116149), 1-20.
DOI Scopus9 WoS6 Europe PMC4
2024 Yalew, M., Mulugeta, A., Lumsden, A. L., Madakkatel, I., Lee, S. H., Oehler, M. K., . . . Hyppönen, E. (2024). Circulating Phylloquinone and the Risk of Four Female-Specific Cancers: A Mendelian Randomization Study. Nutrients, 16(21), nu16213680-1-nu16213680-9.
DOI
2023 Ahmed, M., Mäkinen, V. -P., Lumsden, A., Boyle, T., Mulugeta, A., Lee, S. H., . . . Hyppönen, E. (2023). Metabolic profile predicts incident cancer: A large-scale population study in the UK Biobank.. Metabolism: clinical and experimental, 138(155342), 1-9.
DOI Scopus8 WoS8 Europe PMC4
2023 Byrne, S., Boyle, T., Ahmed, M., Lee, S. H., Benyamin, B., & Hyppönen, E. (2023). Lifestyle, genetic risk and incidence of cancer: a prospective cohort study of 13 cancer types.. International journal of epidemiology, 52(3), 817-826.
DOI Scopus67 WoS62 Europe PMC59
2023 Solé Navais, P., Flatley, C., Steinthorsdottir, V., Vaudel, M., Jacobsson, B., & Hypponen, E. (2023). Genetic effects on the timing of parturition and links to fetal birth weight. Nature Genetics, 55(4), 559-567.
DOI Scopus52 WoS51 Europe PMC66
2023 Solé-Navais, P., Flatley, C., Steinthorsdottir, V., Vaudel, M., Juodakis, J., Chen, J., . . . Jacobsson, B. (2023). Author Correction: Genetic effects on the timing of parturition and links to fetal birth weight (Nature Genetics, (2023), 55, 4, (559-567), 10.1038/s41588-023-01343-9). Nature Genetics, 55(7), 1250.
DOI
2023 Madakkatel, I., Lumsden, A. L., Mulugeta, A., Olver, I., & Hyppönen, E. (2023). Hypothesis-free discovery of novel cancer predictors using machine learning. European Journal of Clinical Investigation, 53(10), 1-13.
DOI Scopus4 WoS4 Europe PMC4
2023 Mulugeta, A., Suppiah, V., & Hyppönen, E. (2023). Schizophrenia and co-morbidity risk: Evidence from a data driven phenomewide association study. Journal of Psychiatric Research, 162, 1-10.
DOI Scopus10 WoS8 Europe PMC8
2023 Mulugeta, A., Suppiah, V., & Hypponen, E. (2023). Schizophrenia and co-morbidity risk: Evidence from a data driven phenomewide association study (vol 162, pg 1, 2023]. JOURNAL OF PSYCHIATRIC RESEARCH, 165, 344.
DOI
2023 Pham, K., Mulugeta, A., Lumsden, A., & Hyppӧnen, E. (2023). Genetically instrumented LDL-cholesterol lowering and multiple disease outcomes: A Mendelian randomization phenome-wide association study in the UK Biobank. British Journal of Clinical Pharmacology, 89(10), 2992-3004.
DOI Scopus5 WoS4 Europe PMC4
2023 Mathieson, I., Day, F. R., Barban, N., Tropf, F. C., Hyppӧnen, E., & Perry, J. R. B. (2023). Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus. Nature Human Behaviour, 7(5), 790-801.
DOI Scopus25 Europe PMC35
2023 Zhou, A., & Hyppönen, E. (2023). Vitamin D deficiency and C-reactive protein: a bidirectional Mendelian randomization study. International journal of epidemiology, 52(1), 260-271.
DOI Scopus85 Europe PMC70
2023 Lumme, J., Morin Papunen, L., Pesonen, P., Sebert, S., Hyppönen, E., Järvelin, M. R., . . . Niinimäki, M. (2023). Vitamin D status in women with a history of infertility and decreased fecundability: a population-based study. Nutrients, 15(11), 1-13.
DOI
2023 Sutherland, J. P., Zhou, A., & Hyppönen, E. (2023). Muscle traits, sarcopenia, and sarcopenic obesity: a vitamin D Mendelian randomization study. Nutrients, 15(12), 1-13.
DOI Scopus16 Europe PMC12
2023 Lumsden, A. L., Mulugeta, A., Makinen, V. P., & Hypponen, E. (2023). Metabolic profile-based subgroups can identify differences in brain volumes and brain iron deposition. Diabetes Obesity & Metabolism, 25(1), 121-131.
DOI
2022 Mulugeta, A., Navale, S. S., Lumsden, A. L., Llewellyn, D. J., & Hyppönen, E. (2022). Healthy lifestyle, genetic risk and brain health: a gene-environment interaction study in the UK Biobank. Nutrients, 14(19, article no. 3907), 1-13.
DOI
2022 Sutherland, J. P., Zhou, A., & Hyppönen, E. (2022). Vitamin D deficiency increases mortality risk in the UK biobank: a nonlinear Mendelian Randomization Study. Annals of Internal Medicine, 175(11), 1552-1559.
DOI Scopus99 Europe PMC84
2022 Hyppönen, E., Vimaleswaran, K. S., & Zhou, A. (2022). Genetic determinants of 25-hydroxyvitamin D concentrations and their relevance to public health. Nutrients, 14(20, article no. 4408), 1-14.
DOI Scopus32 Europe PMC31
2022 Lumsden, A. L., Mulugeta, A., & Hyppönen, E. (2022). Milk consumption and risk of twelve cancers: a large-scale observational and Mendelian randomisation study. Clinical Nutrition, 42(1), 1-8.
DOI
2022 Mulugeta, A., Eshetie, T. C., Kassie, G. M., Erku, D., Mekonnen, A., Lumsden, A., & Hypponen, E. (2022). Association between metabolically different adiposity subtypes and osteoarthritis: a Mendelian Randomization Study. Arthritis Care & Research, 75(4), 885-892.
DOI
2022 Navale, S. S., Mulugeta, A., Zhou, A., Llewellyn, D. J., & Hyppönen, E. (2022). Vitamin D and brain health: an observational and Mendelian randomization study. The American Journal of Clinical Nutrition, 116(2), 531-540.
DOI Scopus70 Europe PMC57
2022 Mulugeta, A., Hypponen, E., Ala Korpela, M., & Makinen, V. P. (2022). Cross-sectional metabolic subgroups and 10-year follow-up of cardiometabolic multimorbidity in the UK Biobank. Scientific Reports, 12(1, article no. 8590), 1-11.
DOI
2022 Hyppönen, E., Carslake, D., Berry, D. J., Power, C., & Davey Smith, G. (2022). Estimating the influence of body mass index (BMI) on mortality using offspring BMI as an instrumental variable. International Journal of Obesity, 46(1), 77.
DOI Scopus6 Europe PMC6
2022 Darooghegi Mofrad, M., Naghshi, S., Lotfi, K., Beyene, J., Hypponen, E., Pirouzi, A., & Sadeghi, O. (2022). Egg and dietary cholesterol intake and risk of all-cause, cardiovascular, and cancer mortality: a systematic review and dose-response meta-analysis of prospective cohort studies. Frontiers in Nutrition, 9(878979), 1-16.
DOI
2022 Pham, K., Mulugeta, A., Zhou, A., O'Brien, J. T., Llewellyn, D. J., & Hyppönen, E. (2022). High coffee consumption, brain volume and risk of dementia and stroke.. Nutritional Neuroscience, 25(10), 2111-2122.
DOI Scopus26 WoS29 Europe PMC25
2022 Yengo, L., Vedantam, S., Marouli, E., Sidorenko, J., Hypponen, E., & Hirschhorn, J. N. (2022). A saturated map of common genetic variants associated with human height. Nature, 610(7933), 704-712.
DOI Scopus456 WoS427 Europe PMC574
2022 Dickson, C., Zhou, A., MacIntyre, E., & Hyppönen, E. (2022). Do chronic low back pain and chronic widespread pain differ in their association with depression symptoms in the 1958 British Cohort?. Pain Med, 24(6), 23 pages.
DOI Scopus7 WoS8 Europe PMC6
2022 Wang, Z., Emmerich, A., Pillon, N. J., Moore, T., Hyppönen, E., & den Hoed, M. (2022). Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Nature Genetics, 54(9), 1332-1344.
DOI Scopus142 WoS145 Europe PMC169
2022 Shin, J., Zhou, X., Tan, J. T. M., Hyppönen, E., Benyamin, B., & Lee, S. H. (2022). Lifestyle Modifies the Diabetes-Related Metabolic Risk, Conditional on Individual Genetic Differences. Frontiers in Genetics, 13(759309), 759309-1-759309-10.
DOI Scopus7 WoS7 Europe PMC8
2022 Ahmed, M., Mäkinen, V. -P., Mulugeta, A., Shin, J., Boyle, T., Hyppönen, E., & Lee, S. H. (2022). Considering hormone-sensitive cancers as a single disease in the UK biobank reveals shared aetiology. Communications biology, 5(1, article no. 614), 1-14.
DOI Scopus13 WoS12 Europe PMC12
2022 Neumann, A., Nolte, I. M., Pappa, I., Ahluwalia, T. S., Pettersson, E., Rodriguez, A., . . . Tiemeier, H. (2022). A genome-wide association study of total child psychiatric problems scores. Plos One, 17(8 August), 23 pages.
DOI Scopus18 WoS16 Europe PMC23
2022 Jami, E. S., Hammerschlag, A. R., Ip, H. F., Allegrini, A. G., Benyamin, B., Border, R., . . . Middeldorp, C. M. (2022). Genome-wide Association Meta-analysis of Childhood and Adolescent Internalizing Symptoms. Journal of the American Academy of Child and Adolescent Psychiatry, 61(7), 934-945.
DOI Scopus40 WoS36 Europe PMC48
2021 Byrne, S., Boyle, T., Benyamin, B., Lee, S. H., Ahmed, M., & Hypponen, E. (2021). Do associations between a healthy lifestyle and incidence of cancer differ by genetic risk?. INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 50(Supplement_1), 40.
DOI
2021 Sutherland, J. P., Zhou, A., Leach, M. J., & Hypponen, E. (2021). Differences and determinants of vitamin D deficiency among UK biobank participants: a cross-ethnic and socioeconomic study. Clinical Nutrition, 40(5), 3436-3447.
DOI Scopus44 WoS40 Europe PMC35
2021 Ahmed, M., Mulugeta, A., Lee, S. H., Mäkinen, V. P., Boyle, T., & Hyppönen, E. (2021). Adiposity and cancer: a Mendelian randomization analysis in the UK biobank. International Journal of Obesity, 45(12), 2657-2665.
DOI Scopus32 WoS27 Europe PMC26
2021 Madakkatel, I., Zhou, A., McDonnell, M. D., & Hyppönen, E. (2021). Combining machine learning and conventional statistical approaches for risk factor discovery in a large cohort study. Scientific Reports, 11(1, article no. 22997), 11 pages.
DOI Scopus46 WoS42 Europe PMC38
2021 Zhou, A., Selvanayagam, J. B., & Hyppönen, E. (2021). Non-linear Mendelian randomization analyses support a role for vitamin D deficiency in cardiovascular disease risk. European heart journal, 43(18), 1731-1739.
DOI Scopus155 Europe PMC125
2021 Vimaleswaran, K. S., Zhou, A., Cavadino, A., & Hyppönen, E. (2021). Evidence for a causal association between milk intake and cardiometabolic disease outcomes using a two-sample Mendelian Randomization analysis in up to 1,904,220 individuals. International Journal of Obesity, 45(8), 1751-1762.
DOI Scopus22 Europe PMC19
2021 Lumme, J. E., Savukoski, S. M., Suvanto, E. T. J., Pesonen, P. R. O., Auvinen, J. P., Sebert, S., . . . Niinimäki, M. (2021). Early-onset climacterium is not associated with impaired vitamin D status: a population-based study. Menopause (New York, N.Y.), 28(8), 899-908.
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2021 Mills, M. C., Tropf, F. C., Brazel, D. M., van Zuydam, N., Vaez, A., Pers, T. H., . . . Hyppӧnen, E. (2021). Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour. Nature Human Behaviour, 5(12), 1717-1730.
DOI Scopus103 Europe PMC102
2021 Zhou, A., & Hyppönen, E. (2021). Habitual coffee intake and plasma lipid profile: evidence from UK Biobank. Clinical Nutrition, 40(6), 4404-4413.
DOI Scopus26 Europe PMC20
2021 Mulugeta, A., Lumsden, A., & Hyppönen, E. (2021). Relationship between serum 25(Oh)d and depression: causal evidence from a bi-directional mendelian randomization study. Nutrients, 13(1), 1-13.
DOI
2021 Mulugeta, A., Lumsden, A., & Hyppönen, E. (2021). Unlocking the causal link of metabolically different adiposity subtypes with brain volumes and the risks of dementia and stroke: a Mendelian randomization study. Neurobiology of Aging, 102, 161-169.
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2021 Hyppönen, E., & Zhou, A. (2021). Cardiovascular symptoms affect the patterns of habitual coffee consumption. American Journal of Clinical Nutrition, 114(1), 214-219.
DOI Scopus14 Europe PMC7
2021 Bejar, C. A., Goyal, S., Afzal, S., Mangino, M., Zhou, A., Hyppönen, E., & Sanghera, D. K. (2021). A Bidirectional Mendelian Randomization Study to evaluate the causal role of reduced blood vitamin D levels with type 2 diabetes risk in South Asians and Europeans. Nutrition Journal, 20(1), 1-11.
DOI Scopus15 Europe PMC14
2021 Najjar, L., Sutherland, J., Zhou, A., & Hyppönen, E. (2021). Vitamin D and type 1 diabetes risk: a systematic review and meta-analysis of genetic evidence. Nutrients, 13(12, article no. 4260), 1-15.
DOI Scopus14 Europe PMC12
2020 Ranson, J. M., Lourida, I., Hannon, E., Littlejohns, T. J., Ballard, C., Langa, K. M., . . . Llewellyn, D. J. (2020). Genetic risk, education and incidence of dementia. Alzheimer S & Dementia, 16(S10), 1.
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2020 Ranson, J. M., Lourida, I., Hannon, E., Littlejohns, T. J., Ballard, C., Langa, K. M., . . . Llewellyn, D. J. (2020). Stroke, genetic risk and incidence of dementia. Alzheimer S & Dementia, 16(S10), 1.
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2020 King, C., Mulugeta, A., Nabi, F., Walton, R., Zhou, A., & Hyppönen, E. (2020). Mendelian randomization case-control PheWAS in UK Biobank shows evidence of causality for smoking intensity in 28 distinct clinical conditions. EClinicalMedicine, 26(100488), 1-7.
DOI Scopus20 WoS20 Europe PMC17
2020 Lumsden, A. L., Mulugeta, A., Zhou, A., & Hyppönen, E. (2020). Apolipoprotein E (APOE) genotype-associated disease risks: a phenome-wide, registry-based, case-control study utilising the UK Biobank. EBioMedicine, 59(102954), 1-11.
DOI Scopus202 Europe PMC207
2020 Stasinopoulos, L. C., Zhou, A., & Hypponen, E. (2020). Association of supplemental calcium and dairy milk intake with all-cause and cause-specific mortality in the UK Biobank: a prospective cohort study. British Journal of Nutrition, 123(5), 574-582.
DOI Scopus9 Europe PMC9
2020 Nicolopoulos, K., Mulugeta, A., Zhou, A., & Hypponen, E. (2020). Association between habitual coffee consumption and multiple disease outcomes: a Mendelian randomisation phenome-wide association study in the UK Biobank. Clinical Nutrition, 39(11), 3467-3476.
DOI Scopus36 Europe PMC33
2020 Hypponen, E. (2020). Commentary: Intergenerational BMI association: Is there a role for fetal programming?. International Journal of Epidemiology, 49(1), 244-245.
DOI
2020 Mulugeta, A., Zhou, A., King, C., & Hyppönen, E. (2020). Association between major depressive disorder and multiple disease outcomes: a phenome-wide Mendelian randomisation study in the UK Biobank. Molecular psychiatry, 25(7), 1469-1476.
DOI Scopus71 WoS72 Europe PMC72
2020 Palaniswamy, S., Gill, D., De Silva, N. M., Lowry, E., Jokelainen, J., Karhu, T., . . . Järvelin, M. R. (2020). Could vitamin D reduce obesity-associated inflammation? Observational and Mendelian randomization study. The American journal of clinical nutrition, 111(5), 1036-1047.
DOI
2020 Zheng, Y., Huang, T., Wang, T., Mei, Z., Zhou, A., Hypponen, E., & Qi, L. (2020). Mendelian randomization analysis does not support causal associations of birth weight with hypertension risk and blood pressure in adulthood. European Journal of Epidemiology, 35(7), 685-697.
DOI Scopus11 WoS11 Europe PMC9
2020 Zhou, X., van der Werf, J., Carson-Chahhoud, K., Ni, G., McGrath, J., Hyppönen, E., & Lee, S. H. (2020). Whole-genome approach discovers novel genetic and nongenetic variance components modulated by lifestyle for cardiovascular health. Journal of the American Heart Association, 9(8), 1-42.
DOI Scopus11 WoS11 Europe PMC13
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2019 Tyrrell, J., Mulugeta, A., Wood, A. R., Zhou, A., Beaumont, R. N., Tuke, M. A., . . . Hyppӧnen, E. (2019). Using genetics to understand the causal influence of higher BMI on depression. International journal of epidemiology, 48(3), 834-848.
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2018 He, Y., Timofeeva, M., Farrington, S. M., Vaughan Shaw, P., Hypponen, E., & Dunlop, M. G. (2018). Exploring causality in the association between circulating 25-hydroxyvitamin D and colorectal cancer risk: a large Mendelian randomisation study. BMC medicine, 16(1), 1-11.
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2018 Zhou, A., Taylor, A. E., Karhunen, V., Zhan, Y., & Hypponen, E. (2018). Habitual coffee consumption and cognitive function: a Mendelian randomization meta-analysis in up to 415,530 participants. Scientific reports, 8(7526), 1-9.
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2018 Lee, J. J., Wedow, R., Okbay, A., Kong, E., Cesarini, D., & Hyppönen, E. (2018). Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. Nature genetics, 50(8), 1112-1121.
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2015 Vimaleswaran, K., Cavadino, A., Verweij, N., Nolte, I., Leach, I., Auvinen, J., . . . Hyppönen, E. (2015). Interactions between uncoupling protein 2 gene polymorphisms, obesity and alcohol intake on liver function: a large meta-analysed population-based study. European Journal of Endocrinology, 173(6), 863-872.
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2014 Williams, D., Fraser, A., Sayers, A., Fraser, W., Hyppönen, E., Smith, G., . . . Lawlor, D. (2014). Associations of childhood 25-hydroxyvitamin D₂ and D₃ and cardiovascular risk factors in adolescence: prospective findings from the Avon Longitudinal Study of Parents and Children. European Journal of Preventive Cardiology, 21(3), 281-290.
DOI Scopus25 WoS24 Europe PMC17
2014 Mutt, S. J., Hyppönen, E., Saarnio, J., Järvelin, M. R., & Herzig, K. H. (2014). Vitamin D and adipose tissue-more than storage. Frontiers in physiology, 5(article no. 228), 1-9.
DOI
2013 Kuan, V., Martineau, A. R., Griffiths, C. J., Hyppönen, E., & Walton, R. (2013). DHCR7 mutations linked to higher vitamin D status allowed early human migration to Northern latitudes. BMC evolutionary biology, 13(144), 1-10.
DOI
2013 Brouwer Brolsma, E. M., Bischoff Ferrari, H. A., Bouillon, R., Feskens, E. J. M., Gallagher, C. J., Hypponen, E. T., . . . de Groot, L. C. P. G. M. (2013). Vitamin D: do we get enough? A discussion between vitamin D experts in order to make a step towards the harmonisation of dietary reference intakes for vitamin D across Europe. Osteoporosis International, 24(5), 1567-1577.
DOI
2013 Alfred, T., Ben Shlomo, Y., Cooper, R., Hardy, R., Deary, I. J., Elliott, J., . . . Day, I. N. M. (2013). Genetic variants influencing biomarkers of nutrition are not associated with cognitive capability in middle-aged and older adults. Journal of nutrition, 143(5), 606-612.
DOI
2013 Cooper, R., Pinto Pereira, S. M., Power, C., & Hypponen, E. (2013). Parental obesity and risk factors for cardiovascular disease among their offspring in mid-life: findings from the 1958 British Birth Cohort Study. International journal of obesity, 37(12), 1590-1596.
DOI
2013 Vimaleswaran, K. S., Cavadino, A., & Hypponen, E. T. (2013). APOA5 genotype influences the association between 25-hydroxyvitamin D and high density lipoprotein cholesterol. Atherosclerosis, 228(1), 188-192.
DOI
2013 Maddock, J., Berry, D. J., Geoffroy, M. C., Power, C., & Hyppönen, E. (2013). Vitamin D and common mental disorders in mid-life : cross-sectional and prospective findings. Clinical nutrition, 32(5), 758-764.
DOI
2013 Hyppönen, E., Cavadino, A., Williams, D., Fraser, A., Vereczkey, A., Fraser, W., . . . Czeizel, A. (2013). Vitamin D and pre-eclampsia: original data, systematic review and meta-analysis. Annals of Nutrition and Metabolism, 63(4), 331-340.
DOI Scopus135 WoS130 Europe PMC114
2013 Williams, D., Fraser, A., Fraser, W., Hyppon̈en, E., Smith, G., Deanfield, J., . . . Lawlor, D. (2013). Associations of maternal 25-hydroxyvitamin D in pregnancy with offspring cardiovascular risk factors in childhood and adolescence: findings from the Avon Longitudinal Study of Parents and Children. Heart, 99(24), 1849-1856.
DOI Scopus41 WoS34 Europe PMC34
2013 Shah, T., Engmann, J., Dale, C., Shah, S., White, J., Giambartolomei, C., . . . Hingorani, A. (2013). Population genomics of cardiometabolic traits: design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) Consortium. PLoS One, 8(8), e71345-1-e71345-12.
DOI Scopus33 WoS33 Europe PMC37
2013 Horikoshi, M., Yaghootkar, H., Mook-Kanamori, D., Sovio, U., Taal, H., Hennig, B., . . . Geller, F. (2013). New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism. Nature Genetics, 45(1), 76-82.
DOI Scopus264 WoS252 Europe PMC244
2013 Randall, J., Winkler, T., Kutalik, Z., Berndt, S., Jackson, A., Monda, K., . . . Vedantam, S. (2013). Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits. PLoS Genetics, 9(6), e1003500-1-e1003500-19.
DOI Scopus337 WoS338 Europe PMC338
2013 Berndt, S., Gustafsson, S., Mägi, R., Ganna, A., Wheeler, E., Feitosa, M., . . . Wood, A. (2013). Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nature Genetics, 45(5), 501-512.
DOI Scopus529 WoS511 Europe PMC494
2013 Vimaleswaran, K., & Palmer, L. (2013). Causal relationship between obesity and vitamin D status: bi-directional Mendelian randomization analysis of multiple cohorts. PLoS Medicine, 10(2), 1001383-1-1001383-1 3.
DOI Scopus829 WoS609 Europe PMC659
2013 Cousminer, D., Berry, D., Timpson, N., Ang, W., Thiering, E., Byrne, E., . . . Palmer, L. (2013). Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity. Human Molecular Genetics, 22(13), 2735-2747.
DOI Scopus166 WoS156 Europe PMC152
2013 Do, R., Willer, C. J., Schmidt, E. M., Sengupta, S., Hyppönen, E., & Kathiresan, S. (2013). Common variants associated with plasma triglycerides and risk for coronary artery disease. Nature genetics, 45(11), 1345-1353.
DOI Scopus728 WoS692 Europe PMC684
2013 Willer, C., Schmidt, E., Sengupta, S., Peloso, G., Hypponen, E. T., & Abecasis, G. R. (2013). Discovery and refinement of loci associated with lipid levels. Nature genetics, 45(11), 1274-1285.
DOI Scopus2444 WoS2239 Europe PMC2444
2013 Fall, T., Hagg, S., Magi, R., Ploner, A., Benyamin, B., Hypponen, E. T., & Pokoppenko, I. (2013). The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis. PLoS medicine, 10(6), 1-16.
DOI Scopus176 WoS156 Europe PMC157
2013 Vimaleswaran, K. S., Cavadino, A., Berry, D. J., Whittaker, J. C., Power, C., Jarvelin, M. R., & Hypponen, E. T. (2013). Genetic association analysis of vitamin D pathway with obesity traits. International journal of obesity, 37(10), 1399-1406.
DOI
2013 Maddock, J., Geoffroy, M. C., Power, C., & Hypponen, E. (2013). 25-Hydroxyvitamin D and cognitive performance in mid-life. Annals of nutrition and metabolism, 63, 849.
2013 Berry, D. J., Hypponen, E., & Cortina Borja, M. (2013). Investigating the association of vitamin D seasonality on inflammatory and hemostatic markers. Chronobiology international, 30(6), 786-795.
DOI
2012 Okada, Y., Sim, X., Go, M. J., Wu, J. Y., Gu, D., Takeuchi, F., . . . Peltonen, L. (2012). Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations. Nature Genetics, 44(8), 904-909.
DOI Scopus253 Europe PMC241
2012 Ikram, M., Fornage, M., Smith, A., Seshadri, S., Schmidt, R., Debette, S., . . . Uitterlinden, A. (2012). Common variants at 6q22 and 17q21 are associated with intracranial volume. Nature Genetics, 44(5), 539-544.
DOI Scopus100 WoS112 Europe PMC114
2012 Bradfield, J., Taal, H., Timpson, N., Scherag, A., Lecoeur, C., Warrington, N., . . . St Pourcain, B. (2012). A genome-wide association meta-analysis identifies new childhood obesity loci. Nature Genetics, 44(5), 526-531.
DOI Scopus342 WoS323 Europe PMC312
2012 Taal, H., St Pourcain, B., Thiering, E., Das, S., Mook-Kanamori, D., Warrington, N., . . . Chawes, B. (2012). Common variants at 12q15 and 12q24 are associated with infant head circumference. Nature Genetics, 44(5), 532-538.
DOI Scopus99 WoS102 Europe PMC107
2012 Tyrrell, J., Huikari, V., Christie, J., Cavadino, A., Bakker, R., Brion, M., . . . Freathy, R. (2012). Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weight. Human Molecular Genetics, 21(24), 5344-5358.
DOI Scopus60 WoS60 Europe PMC57
2012 Vimaleswaran, K. S., Cavadino, A., & Hypponen, E. (2012). Evidence for a genetic interaction in allergy-related responsiveness to vitamin D deficiency. Allergy, 67(8), 1033-1040.
DOI
2012 Mutt, S. J., Karhu, T., Lehtonen, S., Lehenkari, P., Carlberg, C., Saarnio, J., . . . Herzig, K. H. (2012). Inhibition of cytokine secretion from adipocytes by 1,25-dihydroxyvitamin D3 via the NF-KB pathway. The FASEB journal, 26(11), 4400-4407.
DOI
2012 Angelakopoulou, A., Shah, T., Sofat, R., Shah, S., Hypponen, E., & Hingorani, A. D. (2012). Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration. European heart journal, 33(3), 393-407.
DOI
2012 Disanto, G., Chaplin, G., Morahan, J. M., Giovannoni, G., Hyppönen, E., Ebers, G. C., & Ramagopalan, S. V. (2012). Month of birth, vitamin D and risk of immune-mediated disease: a case control study. BMC medicine, 10(article no. 69), 1-7.
DOI
2012 Tripkovic, L., Lambert, H., Hart, K., Smith, C. P., Bucca, G., Penson, S., . . . Lanham New, S. (2012). Comparison of vitamin D2 and vitamin D3 supplementation in raising serum 25-hydroxyvitamin D status: a systematic review and meta-analysis. American journal of clinical nutrition, 95(6), 1357-1364.
DOI
2012 Berry, D. J., Vimaleswaran, K. S., Whittaker, J. C., Hingorani, A. D., & Hyppönen, E. (2012). Evaluation of genetic markers as instruments for Mendelian randomization studies on vitamin D. PLoS one, 7(5), e37465.
DOI
2011 Cooper, J. D., Smyth, D. J., Walker, N. M., Stevens, H., Burren, O. S., Wallace, C., . . . Todd, J. A. (2011). Inherited variation in vitamin D genes is associated with predisposition to autoimmune disease type 1 diabetes. Diabetes, 60(5), 1624-1631.
DOI
2011 Hypponen, E. T. (2011). Preventing vitamin D deficiency in pregnancy - importance for the mother and child. Annals of nutrition and metabolism, 59(1), 28-31.
DOI
2011 Ward, M., Berry, D. J., Power, C., & Hyppönen, E. (2011). Working patterns and vitamin D status in mid-life: a cross-sectional study of the 1958 British birth cohort. Occupational and environmental medicine, 68(12), 902-907.
DOI
2011 Hypponen, E. T., & Boucher, B. (2011). Need to be implemented in UK. BMJ, 342(7791), 244.
DOI
2011 Berry, D. J., Hesketh, K., Power, C., & Hypponen, E. T. (2011). Vitamin D status has a linear association with seasonal infections and lung function in British adults. British journal of nutrition, 106(9), 1433-1440.
DOI
2011 Hypponen, E., Fararouei, M., Sovio, U., Hartikainen, A., Pouta, A., Robertson, C., . . . Jarvelin, M. (2011). High-dose vitamin D supplements are not associated with linear growth in a large Finnish cohort. Journal of nutrition, 141(5), 843-848.
DOI
2011 Berry, D., & Hypponen, E. (2011). Determinants of vitamin D status: focus on genetic variations. Current opinion in nephrology and hypertension, 20(4), 331-336.
DOI
2011 Zabaneh, D., Gaunt, T., Kumari, M., Drenos, F., Shah, S., Berry, D., . . . Humphries, S. (2011). Genetic Variants Associated with von Willebrand Factor Levels in Healthy Men and Women Identified Using the HumanCVD BeadChip. Annals of Human Genetics, 75(4), 456-467.
DOI Scopus27 WoS25 Europe PMC23
2011 Kilpeläinen, T., Qi, L., Brage, S., Sharp, S., Sonestedt, E., Demerath, E., . . . Marmot, M. (2011). Physical activity attenuates the influence of FTO variants on obesity risk: A meta-analysis of 218,166 adults and 19,268 children. PLoS Medicine, 8(11), 14 pages.
DOI Scopus469 WoS427 Europe PMC369
2011 Chambers, J., & Palmer, L. (2011). Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. Nature Genetics, 43(11), 1131-1138.
DOI Scopus466 WoS449 Europe PMC448
2011 Kilpelainen, T., den Hoed, M., Ong, K., Grontved, A., Brage, S., Early Growth Genetics Consortium., . . . Loos, R. (2011). Obesity-susceptibility loci have a limited influence on birth weight: A meta-analysis of up to 28,219 individuals. American Journal of Clinical Nutrition, 93(4), 851-860.
DOI Scopus55 WoS51 Europe PMC43
2011 Lanham New, S. A., Buttriss, J. L., Miles, L. M., Ashwell, M., Hyppöpnen, E., & Williams, C. M. (2011). Proceedings of the rank forum on vitamin D. British journal of nutrition, 105(1), 144-156.
DOI
2011 Disanto, G., Handel, A. E., Morahan, J. M., Deluca, G. C., Kimball, S. M., Hypponen, E., . . . Ramagopalan, S. V. (2011). Vitamin D and multiple sclerosis hospital admissions in Scotland. QJM, 104(11), 1001-1003.
DOI
2010 Freathy, R., Mook-Kanamori, D., Sovio, U., Prokopenko, I., Timpson, N., Berry, D., . . . Bennett, A. (2010). Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. Nature Genetics, 42(5), 430-435.
DOI Scopus206 WoS195 Europe PMC179
2010 Chambers, J. C., Zhang, W., Lord, G. M., Van der Harst, P., Hypponen, E., & Kooner, J. S. (2010). Genetic loci influencing kidney function and chronic kidney disease. Nature genetics, 42(5), 373-375.
DOI Scopus243 WoS228 Europe PMC211
2010 Hypponen, E., Berry, D., Cortina Borja, M., & Power, C. (2010). 25-Hydroxyvitamin D and pre-clinical alterations in inflammatory and hemostatic markers: a cross sectional analysis in the 1958 British birth cohort. PLoS one, 5(5), 1-8.
DOI
2010 Wang, T., Zhang, F., Richards, J. B., Kestenbaum, B., Hypponen, E., & Spector, T. D. (2010). Common genetic determinants of vitamin D insufficiency : a genome-wide association study. The lancet, 376(9736), 180-188.
DOI
2010 Hypponen, E., & Boucher, B. J. (2010). Avoidance of vitamin D deficiency in pregnancy in the United Kingdom: the case for a unified approach in National policy. British Journal of Nutrition, 104(3), 309-314.
DOI
2010 Hyppönen, E. (2010). Vitamin D and increasing incidence of type 1 diabetes - evidence for an association?. Diabetes, obesity and metabolism, 12(9), 737-743.
DOI
2010 Cooper, R., Hypponen, E., Berry, D., & Power, C. (2010). Associations between parental and offspring adiposity up to midlife: the contribution of adult lifestyle factors in the 1958 british birth cohort study. American Journal of Clinical Nutrition, 92(4), 946-953.
DOI
2010 Harville, E. W., Boynton Jarrett, R., Power, C., & Hypponen, E. (2010). Childhood hardship, maternal smoking, and birth outcomes: a prospective cohort study. Archives of Pediatrics and Adolescent Medicine, 164(6), 533-539.
DOI
2010 Fararouei, M., Robertson, C., Whittaker, J., Sovio, U., Ruokonen, A., Hartikainen, A. L., . . . Hypponen, E. (2010). Maternal Hb during pregnancy and offspring's educational achievement: a prospective cohort study over 30 years. British Journal of Nutrition, 104(9), 1363-1368.
DOI
2009 Atherton, K., Berry, D. J., Parsons, T., Macfarlane, G. J., Power, C., & Hyppönen, E. (2009). Vitamin D and chronic widespread pain in a white middle-aged British population: Evidence from a cross-sectional population survey. Annals of the rheumatic diseases, 68(6), 817-822.
DOI
2009 Hyppönen, E., Berry, D. J., Wjst, M., & Power, C. (2009). Serum 25-hydroxyvitamin D and IgE - a significant but nonlinear relationship. Allergy, 64(4), 613-620.
DOI
2009 Freathy, R. M., Bennett, A. J., Ring, S. M., Shields, B., Hypponen, E., & Hattersley, A. T. (2009). Type 2 diabetes risk alleles are associated with reduced size at birth. Diabetes, 58(6), 1428-1433.
DOI
2008 Hypponen, E., Boucher, B. J., Berry, D. J., & Power, C. (2008). 25-hydroxyvitamin D, IGF-1, and metabolic syndrome at 45 years of age: a cross-sectional study in the 1958 British birth cohort. Diabetes, 57(2), 298-305.
DOI
2008 Hypponen, E. T. (2008). Birth weight and risk of type 2 diabetes a systematic review. JAMA : journal of the American Medical Association, 300(24), 2886-2897.
DOI Scopus813 WoS734 Europe PMC649
2008 Thomas, C., Hyppönen, E., & Power, C. (2008). Obesity and type 2 diabetes risk in midadult life: the role of childhood adversity. Pediatrics, 121(5), 1240-1249.
DOI

Year Citation
2021 Sutherland, J., Zhou, A., Leach, M., & Hypponen, E. (2021). Ethnic differences and determinants of vitamin D deficiency in the UK Biobank. In INTERNATIONAL JOURNAL OF EPIDEMIOLOGY Vol. 50 (pp. 227). OXFORD UNIV PRESS.
2018 Li, L., Williams, M., Johnston, K., Frith, P., Hypponen, E., & Paquet, C. (2018). PARENTAL RESPIRATORY DISEASE IS ASSOCIATED WITH REDUCED OFFSPRING LUNG HEALTH AT AGE 45 VIA PATHWAY OF MATERNAL AND PERSONAL SMOKING. In RESPIROLOGY Vol. 23 (pp. 75). WILEY.
2014 Tripkovic, L., Wilson, L. R., Hart, K., Elliott, R., Smith, C. P., Bucca, G., . . . Lanham-New, S. (2014). DAILY SUPPLEMENTATION WITH VITAMIN D3 IS COMPREHENSIVELY MORE EFFECTIVE THAN VITAMIN D2 IN RAISING 25OHD STATUS AND CONCOMITANTLY REDUCING PARATHYROID HORMONE LEVELS: IMPLICATIONS FOR BONE HEALTH. In OSTEOPOROSIS INTERNATIONAL Vol. 25 (pp. S665). Birmingham, ENGLAND: SPRINGER LONDON LTD.
  • Assessing the feasibility and laying the groundwork for applying the ‘recall by genotype’ design in MS research, Multiple Sclerosis Australia, 01/08/2025 - 31/07/2026

  • Predicting and Preventing Ovarian Cancer: a machine learning approach, MRFF- 2020 PHCRI - Primary Health Care Research, 01/06/2021 - 31/08/2025

  • Whole-genome multivariate reaction norm model for complex traits, ARC - Discovery Projects, 17/06/2019 - 16/06/2024

  • The dark side of vitamin D supplementation, NHMRC - Project Grant, 01/01/2017 - 31/12/2022

  • Machine learning to predict and prevent cancer, Tour de Cure Ltd, 01/07/2019 - 31/12/2022

  • Identifying pathways to dementia: a large scale genetic study, NHMRC - Project Grant, 01/01/2019 - 31/12/2021

Courses I teach

  • REHB 6014 Participatory Community Practice GE: Planning (2024)

Date Role Research Topic Program Degree Type Student Load Student Name
2025 Co-Supervisor - Doctor of Philosophy Doctorate Full Time Mrs Honey Rahmanian
2024 Co-Supervisor - - Master Full Time Mr Rory Shepherd
2024 Principal Supervisor - Doctor of Philosophy Doctorate Full Time Mr Liam Veltman
2023 Principal Supervisor - Doctor of Philosophy Doctorate Full Time Mr Endeshaw Chekol Abebe
2023 Principal Supervisor - Doctor of Philosophy Doctorate Full Time Mr Melaku Anagaw
2022 Co-Supervisor - Doctor of Philosophy Doctorate Full Time Miss Caitlin Doyle
2022 Co-Supervisor - Doctor of Philosophy Doctorate Full Time Mr Reta Yimer
2022 Co-Supervisor - Doctor of Philosophy Doctorate Full Time Lamessa Amente
2022 Principal Supervisor - Doctor of Philosophy Doctorate Full Time Mr Yigizie Yeshaw Mihiretie
2017 Co-Supervisor - Master of Philosophy Master Full Time Ms Natasha Jane Radcliffe
  • Position: Professor of Nutritional and Genetic Epidemiology
  • Email: elina.hypponen@adelaide.edu.au
  • Alternative Contact: ACPreH Administrative assistant t: +61 8 8302 1135 |e: acpreh@unisa.edu.au 

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