Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis by Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A., Painter, J. N., Martin, N. G., Morris, A. P., Chasman, D. I., Missmer, S. A., Zondervan, K. T., Morton, C. C.

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Author Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis by Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A., Painter, J. N., Martin, N. G., Morris, A. P., Chasman, D. I., Missmer, S. A., Zondervan, K. T., Morton, C. C.

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Strong family history of uterine leiomyomatosis warrants fumarate hydratase mutation screening by Tolvanen, Jaana, Uimari, Outi, Ryynänen, Markku, Aaltonen, Lauri A., Vahteristo, Pia

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The impact of the new WHO Classification of renal cell carcinoma on the diagnosis of hereditary leiomyomatosis and renal cell carcinoma by Degenhardt, Jan, Tolkach, Yuri, Amin, Mahul B, Mosiello, Giovanni, Baydar, Dilek Ertoy, Gall, Emilie Cornec-Le, DiCola, Jason, Elhag, Dean, Frezza, Christian, Halbritter, Jan, Guillermo, Ignacio Blanco, Jewett, Michael A S, Lattouf, Jean-Baptise, Lovitt, Graham, Lundgren, Per-Olof, Maher, Eamonn R, Mulders, Peter, Shuch, Brian, Hartmann, Arndt, Müller, Roman-Ulrich

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MED12 mutations and FH inactivation are mutually exclusive in uterine leiomyomas by Kämpjärvi, Kati, Mäkinen, Netta, Mehine, Miika, Välipakka, Salla, Uimari, Outi, Pitkänen, Esa, Heinonen, Hanna-Riikka, Heikkinen, Tuomas, Tolvanen, Jaana, Ahtikoski, Anne, Frizzell, Norma, Sarvilinna, Nanna, Sjöberg, Jari, Bützow, Ralf, Aaltonen, Lauri A, Vahteristo, Pia

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Controlled ovarian hyperstimulation leads to high progesterone and estradiol levels during early pregnancy by Järvelä, Ilkka Y., Pelkonen, Sari, Uimari, Outi, Mäkikallio, Kaarin, Puukka, Katri, Ruokonen, Aimo, Tekay, Aydin, Martikainen, Hannu

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Natural history of familial myomas by Uimari, Outi, Suomalainen-König, Sanna, Sakkinen, Nina, Santala, Markku, Nieminen, Pentti, Ryynanen, Markku

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Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata by Sliz, Eeva, Tyrmi, Jaakko S., Rahmioglu, Nilufer, Zondervan, Krina T., Becker, Christian M., Uimari, Outi, Kettunen, Johannes

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New Paraoxonase 1 Polymorphism I102V and the Risk of Prostate Cancer in Finnish Men by Marchesani, Marja, Hakkarainen, Anna, Tuomainen, Tomi-Pekka, Kaikkonen, Jari, Pukkala, Eero, Uimari, Pekka, Seppälä, Eija, Matikainen, Mika, Kallioniemi, Olli-P., Schleutker, Johanna, Lehtimäki, Terho, Salonen, Jukka T.

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The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections by Jones, Samuel E, Maisha, Fahrisa I, Strausz, Satu J, Lammi, Vilma, Cade, Brian E, Tervi, Anniina, Helaakoski, Viola, Broberg, Martin E, Lane, Jacqueline M, Redline, Susan, Saxena, Richa, Ollila, Hanna M

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