Ruth Loos

Ruth Loos

Professor

  • Loos Group

    Blegdamsvej 3B, Mærsk Tårnet, 7. sal

    2200 København N.

    Phone: +4535337781Mobile: +4530589681
ORCID: 0000-0002-8532-5087

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  1. Published

    Understanding risk and causal mechanisms for developing obesity in infants and young children: A National Institutes of Health workshop

    Aagaard, K. M., Barkin, S. L., Burant, C. F., Carnell, S., Demerath, E., Donovan, S. M., Eneli, I., Francis, L. A., Gilbert-Diamond, D., Hivert, M. F., LeBourgeois, M. K., Loos, R. J. F., Lumeng, J. C., Miller, A. L., Okely, A. D., Osganian, S. K., Ramirez, A. G., Trasande, L., Van Horn, L. V., Wake, M. & 2 others, Wright, R. J. & Yanovski, S. Z., 2024, In: Obesity Reviews. 25, 4, 21 p., e13690.

    Research output: Contribution to journal › Review › Research › peer-review

  2. Univariate and multivariate genetic analysis of subcutaneous fatness and fat distribution in early adolescence

    Beunen, G., Maes, H. H., Vlietinck, R., Malina, R. M., Thomis, M., Feys, E., Loos, Ruth & Derom, C., Jul 1998, In: Behavior Genetics. 28, 4, p. 279-88 10 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  3. Utilisation and cost of professional care and assistance according to disability of patients with multiple sclerosis in Flanders (Belgium)

    Carton, H., Loos, Ruth, Pacolet, J., Versieck, K. & Vlietinck, R., Apr 1998, In: Journal of neurology, neurosurgery, and psychiatry. 64, 4, p. 444-50 7 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  4. Published

    Variants in the fat mass- and obesity-associated (FTO) gene are not associated with obesity in a Chinese Han population

    Li, H., Wu, Y., Loos, Ruth, Hu, F. B., Liu, Y., Wang, J., Yu, Z. & Lin, X., Jan 2008, In: Diabetes. 57, 1, p. 264-8 5 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  5. Published

    Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma

    Kachroo, P., Hecker, J., Chawes, B. L., Ahluwalia, T. S., Cho, M. H., Qiao, D., Kelly, R. S., Chu, S. H., Virkud, Y. V., Huang, M., Barnes, K. C., Burchard, E. G., Eng, C., Hu, D., Celedón, J. C., Daya, M., Levin, A. M., Gui, H., Williams, L. K., Forno, E. & 31 others, Mak, A. C. Y., Avila, L., Soto-Quiros, M. E., Cloutier, M. M., Acosta-Pérez, E., Canino, G., Bønnelykke, Klaus, Bisgaard, H., Raby, B. A., Lange, C., Weiss, S. T., Lasky-Su, J. A., Abe, N., Abecasis, G., Albert, C., Palmer Allred, N. (., Almasy, L., Alonso, A., Ament, S., Anderson, P., Anugu, P., Applebaum-Bowden, D., Arking, D., Arnett, D. K., Ashley-Koch, A., Aslibekyan, S., Assimes, T., Auer, P., Avramopoulos, D., Loos, Ruth & National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Consortium, N. H. L. A. B. I. T. F. P. M. (. C., 2019, In: Chest. 156, 6, p. 1068-1079 12 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  6. Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine program

    Armstrong, N. D., Srinivasasainagendra, V., Ammous, F., Assimes, T. L., Beitelshees, A. L., Brody, J., Cade, B. E., Ida Chen, Y-D., Chen, H., de Vries, P. S., Floyd, J. S., Franceschini, N., Guo, X., Hellwege, J. N., House, J. S., Hwu, C-M., Kardia, S. L. R., Lange, E. M., Lange, L. A., McDonough, C. W. & 24 others, Montasser, M. E., O'Connell, J. R., Shuey, M. M., Sun, X., Tanner, R. M., Wang, Z., Zhao, W., Carson, A. P., Edwards, T. L., Kelly, T. N., Kenny, E. E., Kooperberg, C., Loos, Ruth, Morrison, A. C., Motsinger-Reif, A., Psaty, B. M., Rao, D. C., Redline, S., Rich, S. S., Rotter, J. I., Smith, J. A., Smith, A. V., Irvin, M. R. & Arnett, D. K., 2023, In: Frontiers in Genetics. 14, 1278215.

    Research output: Contribution to journal › Journal article › Research › peer-review

  7. Published

    Whole genome sequence analysis of blood lipid levels in >66,000 individuals

    Selvaraj, M. S., Li, X., Li, Z., Pampana, A., Zhang, D. Y., Park, J., Aslibekyan, S., Bis, J. C., Brody, J. A., Cade, B. E., Chuang, L. M., Chung, R. H., Curran, J. E., de las Fuentes, L., de Vries, P. S., Duggirala, R., Freedman, B. I., Graff, M., Guo, X., Heard-Costa, N. & 27 others, Hidalgo, B., Hwu, C. M., Irvin, M. R., Kelly, T. N., Kral, B. G., Lange, L., Li, X., Lisa, M., Lubitz, S. A., Manichaikul, A. W., Michael, P., Montasser, M. E., Morrison, A. C., Naseri, T., O’Connell, J. R., Palmer, N. D., Peyser, P. A., Reupena, M. S., Smith, J. A., Sun, X., Taylor, K. D., Tracy, R. P., Tsai, M. Y., Wang, Z., Wang, Y., Loos, Ruth & NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, N. T. F. P. M. (. C., 2022, In: Nature Communications. 13, 18 p., 5995.

    Research output: Contribution to journal › Journal article › Research › peer-review

  8. Published

    Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

    Wheeler, M. M., Stilp, A. M., Rao, S., Halldórsson, B. V., Beyter, D., Wen, J., Mihkaylova, A. V., McHugh, C. P., Lane, J., Jiang, M. Z., Raffield, L. M., Jun, G., Sedlazeck, F. J., Metcalf, G., Yao, Y., Bis, J. B., Chami, N., de Vries, P. S., Desai, P., Floyd, J. S. & 39 others, Gao, Y., Kammers, K., Kim, W., Moon, J. Y., Ratan, A., Yanek, L. R., Almasy, L., Becker, L. C., Blangero, J., Cho, M. H., Curran, J. E., Fornage, M., Kaplan, R. C., Lewis, J. P., Loos, Ruth, Mitchell, B. D., Morrison, A. C., Preuss, M., Psaty, B. M., Rich, S. S., Rotter, J. I., Tang, H., Tracy, R. P., Boerwinkle, E., Abecasis, G. R., Blackwell, T. W., Smith, A. V., Johnson, A. D., Mathias, R. A., Nickerson, D. A., Conomos, M. P., Li, Y., Þorsteinsdóttir, U., Magnússon, M. K., Stefansson, K., Pankratz, N. D., Bauer, D. E., Auer, P. L. & Reiner, A. P., 2022, In: Nature Communications. 13, 18 p., 7592.

    Research output: Contribution to journal › Journal article › Research › peer-review

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ID: 183694311