U. Võsa

E-mail:
u.vosa umcg.nl

Research

Publications
  1. Allele specific expression identifies rare variants as cause for extreme allelic imbalance

    BIOS Consortium, Jul-2019, In : European Journal of Human Genetics. 27, p. 601 1 p.

    Research output: Contribution to journalMeeting AbstractAcademic

  2. Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits

    Porcu, E., Rueger, S., Lepik, K., eQTLgen Consortium & BIOS Consortium, 24-Jul-2019, In : Nature Communications. 10, 12 p., 3300.

    Research output: Contribution to journalArticleAcademicpeer-review

  3. Comprehensive Multiple eQTL Detection and Its Application to GWAS Interpretation

    Zeng, B., Lloyd-Jones, L. R., Montgomery, G. W., Metspalu, A., Esko, T., Franke, L., Vosa, U., Claringbould, A., Brigham, K. L., Quyyumi, A. A., Idaghdour, Y., Yang, J., Visscher, P. M., Powell, J. E. & Gibson, G., Jul-2019, In : Genetics. 212, 3, p. 905-918 14 p.

    Research output: Contribution to journalArticleAcademicpeer-review

  4. High-throughput identification of human SNPs affecting regulatory element activity

    van Arensbergen, J., Pagie, L., FitzPatrick, V. D., de Haas, M., Baltissen, M. P., Comoglio, F., van der Weide, R. H., Teunissen, H., Vosa, U., Franke, L., de Wit, E., Vermeulen, M., Bussemaker, H. J. & van Steensel, B., Jul-2019, In : Nature Genetics. 51, 7, p. 1160-+ 13 p.

    Research output: Contribution to journalArticleAcademicpeer-review

  5. Causal relationships among the gut microbiome, short-chain fatty acids and metabolic diseases

    Sanna, S., van Zuydam, N. R., Mahajan, A., Kurilshikov, A., Vich Vila, A., Võsa, U., Mujagic, Z., Masclee, A. A. M., Jonkers, D. M. A. E., Oosting, M., Joosten, L. A. B., Netea, M. G., Franke, L., Zhernakova, A., Fu, J., Wijmenga, C. & McCarthy, M. I., Apr-2019, In : Nature Genetics. 51, 4, p. 600-605 6 p.

    Research output: Contribution to journalLetterAcademicpeer-review

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