A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY

Kettunen, J. L. T., Rantala, E., Dwivedi, O. P., Isomaa, B., Sarelin, L., Kokko, P., Hakaste, L., Miettinen, P. J., Groop, L. C. & Tuomi, T., Apr 2022, In: Diabetologia. 65, 4, p. 632–643 12 p.

Research output: Contribution to journal › Article › Scientific › peer-review

How Communicating Polygenic and Clinical Risk for Atherosclerotic Cardiovascular Disease Impacts Health Behavior: an Observational Follow-up Study

Widen, E., Junna, N., Ruotsalainen, S., Surakka, I., Mars, N., Ripatti, P., Partanen, J. J., Aro, J., Mustonen, P., Tuomi, T., Palotie, A., Salomaa, V., Kaprio, J., Partanen, J., Hotakainen, K., Pöllänen, P. & Ripatti, S., Apr 2022, In: Circulation-Genomic and precision medicine. 15, 2, p. 91-99 9 p., 003459.

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Lipid-Associated Variants near ANGPTL3 and LPL Show Parent-of-Origin Specific Effects on Blood Lipid Levels and Obesity

Lessmark, A., Hatem, G., Kovacs, G., Vitai, M., Ahlqvist, E., Tuomi, T., Koranyi, L., Groop, L. & Prasad, R. B., Jan 2022, In: Genes. 13, 1, 15 p., 91.

Research output: Contribution to journal › Article › Scientific › peer-review

Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes

Pervjakova, N., Moen, G-H., Borges, M-C., Ferreira, T., Cook, J. P., Allard, C., Beaumont, R. N., Canouil, M., Hatem, G., Heiskala, A., Joensuu, A., Karhunen, V., Kwak, S. H., Lin, F. T. J., Liu, J., Rifas-Shiman, S., Tam, C. H., Tam, W. H., Thorleifsson, G., Andrew, T. & 53 others, Auvinen, J., Bhowmik, B., Bonnefond, A., Delahaye, F., Demirkan, A., Froguel, P., Haller-Kikkatalo, K., Hardardottir, H., Hummel, S., Hussain, A., Kajantie, E., Keikkala, E., Khamis, A., Lahti, J., Lekva, T., Mustaniemi, S., Sommer, C., Tagoma, A., Tzala, E., Uibo, R., Vaarasmaki, M., Villa, P. M., Birkeland, K., Bouchard, L., Duijn, C. M., Finer, S., Groop, L., Hämäläinen, E., Hayes, G. M., Hitman, G. A., Jang, H. C., Järvelin, M-R., Jenum, A. K., Laivuori, H., Ma, R. C., Melander, O., Oken, E., Park, K. S., Perron, P., Prasad, R. B., Qvigstad, E., Sebert, S., Stefansson, K., Steinthorsdottir, V., Tuomi, T., Hivert, M-F., Franks, P. W., McCarthy, M., Lindgren, C. M., Freathy, R. M., Lawlor, D. A., Morris, A. P. & Mägi, R., 26 Feb 2022, (E-pub ahead of print) In: Human Molecular Genetics. 15 p.

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Subgroups of patients with young-onset type 2 diabetes in India reveal insulin deficiency as a major driver

Prasad, R. B., Asplund, O., Shukla, S. R., Wagh, R., Kunte, P., Bhat, D., Parekh, M., Shah, M., Phatak, S., Karajamaki, A., Datta, A., Kakati, S., Tuomi, T., Saboo, B., Ahlqvist, E., Groop, L. & Yajnik, C. S., Jan 2022, In: Diabetologia. 65, 1, p. 65-78 14 p.

Research output: Contribution to journal › Article › Scientific › peer-review