Vermeulen, Sita H.
Radboud University Medical Center · Radboud Institute for Health Sciences
16 papers on CoChatORCID 0000-0003-4913-8601
Most cited papers
- Verified
Genetic studies of body mass index yield new insights for obesity biology
Study, T. L. C., Locke, A. E., The ADIPOGen Consortium, The AGEN-BMI Working Group, The CARDIOGRAMplusC4D Consortium, The CKDGen Consortium, The, G. L. G. C., The, I. C. B. P., The MAGIC Investigators, The MuTHER Consortium, et al. (2015) · Nature
Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals
Cited by 4,534
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Defining the role of common variation in the genomic and biological architecture of adult human height
The Electronic Medical Records and Genomics (eMERGE) Consortium, Wood, A. R., The MIGen Consortium, The PAGE Consortium, Study, T. L. C., Esko, T., Yang, J., Vedantam, S., Pers, T. H., Gustafsson, S., et al. (2014) · Nature Genetics
Genetic Associations and EpidemiologyGenetics and Physical Performance
Cited by 1,853
- Verified
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
Berndt, S. I., Gustafsson, S., Mägi, R., Ganna, A., Wheeler, E., Feitosa, M. F., Justice, A. E., Monda, K. L., Croteau-Chonka, D. C., Day, F. R., et al. (2013) · Nature Genetics
Genetic Associations and EpidemiologyGenetics and Physical Performance
Cited by 646
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Rare and low-frequency coding variants alter human adult height
Marouli, E., Graff, M., Medina-Gomez, C., Lo, K. S., Wood, A. R., Kjaer, T. R., Fine, R. S., Lu, Y., Schurmann, C., Highland, H. M., et al. (2017) · Nature
Genetic Associations and EpidemiologyGenetics and Physical Performance
Cited by 610
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Two newly identified genetic determinants of pigmentation in Europeans
Sulem, P., Gudbjartsson, D. F., Stacey, S. N., Helgason, A., Rafnar, T., Jakobsdottir, M., Steinberg, S., Gudjonsson, S. A., Palsson, A., Thorleifsson, G., et al. (2008) · Nature Genetics
melanin and skin pigmentationGenetic Associations and Epidemiology
Cited by 368
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Meta-analysis of genome-wide association studies for neuroticism, and the polygenic association with major depressive disorder
de Moor, M. H. M., van den Berg, S. M., Verweij, K. J. H., Krueger, R. F., Luciano, M., Arias Vasquez, A., Matteson, L. K., Derringer, J., Esko, T., Amin, N., et al. (2015) · JAMA Psychiatry
Genetic Associations and EpidemiologyNeurotransmitter Receptor Influence on Behavior
Cited by 345
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Genetic evidence of assortative mating in humans
Robinson, M. R., Kleinman, A., Graff, M., Vinkhuyzen, A. A. E., Couper, D., Miller, M. B., Peyrot, W. J., Abdellaoui, A., Zietsch, B. P., Nolte, I. M., et al. (2017) · Nature Human Behaviour
Genetic Associations and EpidemiologyGenetic and phenotypic traits in livestock
Cited by 326
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Serum hepcidin: reference ranges and biochemical correlates in the general population
Galesloot, T. E., Vermeulen, S. H., Geurts-Moespot, A. J., Klaver, S. M., Kroot, J. J., van Tienoven, D., Wetzels, J. F. M., Kiemeney, L. A. L. M., Sweep, F. C., den Heijer, M., et al. (2011) · Blood
Iron Metabolism and DisordersTrace Elements in Health
Cited by 303
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Ultra-sensitive Sequencing Identifies High Prevalence of Clonal Hematopoiesis-Associated Mutations throughout Adult Life
Acuna-Hidalgo, R., Sengul, H., Steehouwer, M., van de Vorst, M., Vermeulen, S. H., Kiemeney, L. A. L. M., Veltman, J. A., Gilissen, C., & Hoischen, A. (2017) · The American Journal of Human Genetics
Acute Myeloid Leukemia ResearchCancer Genomics and Diagnostics
Cited by 264
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Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease
Medici, M., Porcu, E., Pistis, G., Teumer, A., Brown, S. J., Jensen, R. A., Rawal, R., Roef, G. L., Plantinga, T. S., Vermeulen, S. H., et al. (2014) · PLoS Genetics
Thyroid Disorders and TreatmentsGenetic Associations and Epidemiology
Cited by 218
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Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease
van Meurs, J. B., Pare, G., Schwartz, S. M., Hazra, A., Tanaka, T., Vermeulen, S. H., Cotlarciuc, I., Yuan, X., Mälarstig, A., Bandinelli, S., et al. (2013) · The American Journal of Clinical Nutrition
Folate and B Vitamins ResearchGenetic Associations and Epidemiology
Cited by 198
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Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity
Joshi, P. K., Pirastu, N., Kentistou, K. A., Fischer, K., Hofer, E., Schraut, K. E., Clark, D. W., Nutile, T., Barnes, C. L. K., Timmers, P. R. H. J., et al. (2017) · Nature Communications
Genetic Associations and EpidemiologyGenetics, Aging, and Longevity in Model Organisms
Cited by 161
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ADHD and Poor Motor Performance From a Family Genetic Perspective
Fliers, E., Vermeulen, S., Rijsdijk, F., Altink, M., Buschgens, C., Rommelse, N., Faraone, S., Sergeant, J., Buitelaar, J., & Franke, B. (2009) · Journal of the American Academy of Child & Adolescent Psychiatry
Attention Deficit Hyperactivity DisorderChildren's Physical and Motor Development
Cited by 89
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A large-scale association analysis of 68 thyroid hormone pathway genes with serum TSH and FT4 levels
Medici, M., van der Deure, W. M., Verbiest, M., Vermeulen, S. H., Hansen, P. S., Kiemeney, L. A., Hermus, A. R. M. M., Breteler, M. M., Hofman, A., Hegedüs, L., et al. (2011) · European Journal of Endocrinology
Thyroid Disorders and TreatmentsGenetic Associations and Epidemiology
Cited by 68
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Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis
Benyamin, B., Esko, T., Ried, J. S., Radhakrishnan, A., Vermeulen, S. H., Traglia, M., Gögele, M., Anderson, D., Broer, L., Podmore, C., et al. (2014) · Nature Communications
Iron Metabolism and DisordersGenetic Associations and Epidemiology
Cited by 30
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Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations
van de Putte, R., Wijers, C. H. W., Reutter, H., Vermeulen, S. H., Marcelis, C. L. M., Brosens, E., Broens, P. M. A., Homberg, M., Ludwig, M., Jenetzky, E., et al. (2019) · PLOS ONE
Congenital gastrointestinal and neural anomaliesGenetic Associations and Epidemiology
Cited by 6
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