Pharmacoepigenetics of hypertension: genome-wide methylation analysis of responsiveness to four classes of antihypertensive drugs using a double-blind crossover study design

Nuotio, M-L., Tähtisalo, H. S., Lahtinen, A., Donner, K., Fyhrquist, F., Perola, M., Kontula, K. K. & Hiltunen, T. P., 27 Feb 2022, (E-pub ahead of print) In: Epigenetics. 14 p., 2038418.

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

Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

Nhlbi Trans-Omics Precision Med To, Natarajan, P., Pampana, A., Graham, S. E., Ruotsalainen, S. E., Perry, J. A., de Vries, P. S., Broome, J. G., Palotie, A., Ripatti, S., Daly, M., Kaprio, J., Pulkki, K., Ripatti, S., Kettunen, J., Laaksonen, R., Rinne, J., Pikkarainen, S., Eklund, K., Kauppi, P. & 30 others, Sinisalo, J., Taskinen, M-R., Tuomi, T., Joensuu, H., Meretoja, T., Aaltonen, L., Turunen, J., Seitsonen, S., Hannula-Jouppi, K., Jalanko, A., Kajanne, R., Lyhs, U., Kaunisto, M., Kurki, M., Karjalainen, J., Havulinna, A., Palta, P., Parolo, P. D. B., Harju, J., Lehisto, A., Ganna, A., Llorens, V., Koskinen, M., Heikkinen, S., Loukola, A., Donner, K., Nunez-Fontarnau, J., Brein, G., Laivuori, H. & Kiiskinen, T., 12 Apr 2021, In: Nature Communications. 12, 1, 14 p., 2182.

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Dominant Distal Myopathy 3 (MPD3) Caused by a Deletion in the HNRNPA1 Gene

Hackman, P., Rusanen, S. M., Johari, M., Vihola, A., Jonson, P. H., Sarparanta, J., Donner, K., Lahermo, P., Koivunen, S., Luque, H., Soininen, M., Mahjneh, I., Auranen, M., Arumilli, M., Savarese, M. & Udd, B., Dec 2021, In: Neurology Genetics. 7, 6, 10 p., 632.

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Mapping the human genetic architecture of COVID-19

Covid 19 Host Genetics Initiative, 23andMe COVID-19 Team, Norwegian SARS-CoV-2 Study Grp, Humanitas COVID-19 Task Force, Humanitas Gavazzeni COVID-19 Task, FHoGID, RegCOVID, P-PredictUs, SeroCOVID, CRiPSI, Genes & Hlth Res Team, UCLA Hlth ATLAS Data Mart Working, Niemi, M. E. K., Karjalainen, J., Liao, R. G., Neale, B. M., Daly, M. J., Ganna, A., Marttila, M., Mehtonen, J. & 3 others, Niemi, M. E. K., Cordioli, M. & Nakanishi, T., 8 Jul 2021, (E-pub ahead of print) In: Nature. 36 p.

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Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusions

Johari, M., Sarparanta, J., Vihola, A., Jonson, P. H., Savarese, M., Jokela, M., Torella, A., Piluso, G., Said, E., Vella, N., Cauchi, M., Magot, A., Magri, F., Mauri, E., Kornblum, C., Reimann, J., Stojkovic, T., Romero, N. B., Luque, H., Huovinen, S. & 6 others, Lahermo, P., Donner, K., Comi, G. P., Nigro, V., Hackman, P. & Udd, B., Aug 2021, In: Acta Neuropathologica. 142, p. 375-393 19 p.

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