Beckmann, Matthias W.

Associations of breast cancer risk factors with tumor subtypes: A pooled analysis from the breast cancer association consortium studies

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Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

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Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

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Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

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Prenatal correction of x-linked hypohidrotic ectodermal dysplasia

Schneider, H., Faschingbauer, F., Schuepbach-Mallepell, S., Körber, I., Wohlfart, S., Dick, A., Wahlbuhl, M., Kowalczyk-Quintas, C., Vigolo, M., Kirby, N., et al. (2018) · New England Journal of Medicine

dental development and anomaliesGenetic and rare skin diseases.

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Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170

EMBRACE, Dunning, A. M., Collaborators, G. S., HEBON, kConFab Investigators, Michailidou, K., Kuchenbaecker, K. B., Thompson, D., French, J. D., Beesley, J., et al. (2016) · Nature Genetics

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A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density

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Digital Radiography and Breast ImagingGenetic Associations and Epidemiology

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The Role of Artificial Intelligence in Gynecologic Oncology Decision-Making: A Feasibility Study

Psilopatis, I., Sipulina, N., Stuebs, F. A., Heindl, F., Poeschke, P., Bader, S., Krueckel, A., Fasching, P. A., Beckmann, M. W., & Emons, J. (2025) · Gynecologic and Obstetric Investigation

Artificial Intelligence in Healthcare and EducationArtificial Intelligence in Healthcare

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