Browse by People

Pervjakova, Natalia, Kasela, Silva, Morris, Andrew P, Kals, Mart, Metspalu, Andres, Lindgren, Cecilia M, Salumets, Andres and Magi, Reedik (2016) Imprinted genes and imprinting control regions show predominant intermediate methylation in adult somatic tissues. EPIGENOMICS, 8 (6). pp. 789-799.

Collapse authors list.
Esteki, Masoud Zamani, Viltrop, Triin, Tsuiko, Olga, Tiirats, Airi, Koel, Mariann, Noukas, Margit, Zilina, Olga, Teearu, Katre, Marjonen, Heidi, Kahila, Hanna et al (show 11 more authors) , Meekels, Jeroen, Soderstrom-Anttila, Viveca, Suikkari, Anne-Maria, Tiitinen, Aila, Magi, Reedik, Koks, Sulev ORCID: 0000-0001-6087-6643, Kaminen-Ahola, Nina, Kurg, Ants, Voet, Thierry, Vermeesch, Joris Robert and Salumets, Andres (2019) In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineages. NATURE MEDICINE, 25 (11). 1699-+.

Collapse authors list.
Rahmioglu, Nilufer, Mortlock, Sally, Ghiasi, Marzieh, Moller, Peter L, Stefansdottir, Lilja, Galarneau, Genevieve, Turman, Constance, Danning, Rebecca, Law, Matthew H, Sapkota, Yadav et al (show 123 more authors) , Christofidou, Paraskevi, Skarp, Sini, Giri, Ayush, Banasik, Karina, Krassowski, Michal, Lepamets, Maarja, Marciniak, Blazej, Noukas, Margit, Perro, Danielle, Sliz, Eeva, Sobalska-Kwapis, Marta, Thorleifsson, Gudmar, Topbas-Selcuki, Nura F, Vitonis, Allison, Westergaard, David, Arnadottir, Ragnheidur, Burgdorf, Kristoffer S, Campbell, Archie, Cheuk, Cecilia SK, Clementi, Caterina, Cook, James, De Vivo, Immaculata, DiVasta, Amy, Dorien, O, Donoghue, Jacqueline F, Edwards, Todd, Fontanillas, Pierre, Fung, Jenny N, Geirsson, Reynir T, Girling, Jane E, Harkki, Paivi, Harris, Holly R, Healey, Martin, Heikinheimo, Oskari, Holdsworth-Carson, Sarah, Hostettler, Isabel C, Houlden, Henry, Houshdaran, Sahar, Irwin, Juan C, Jarvelin, Marjo-Riitta, Kamatani, Yoichiro, Kennedy, Stephen H, Kepka, Ewa, Kettunen, Johannes, Kubo, Michiaki, Kulig, Bartosz, Kurra, Venla, Laivuori, Hannele, Laufer, Marc R, Lindgren, Cecilia M, MacGregor, Stuart, Mangino, Massimo, Martin, Nicholas G, Matalliotaki, Charoula, Matalliotakis, Michail, Murray, Alison D, Ndungu, Anne, Nezhat, Camran, Olsen, Catherine M, Opoku-Anane, Jessica, Padmanabhan, Sandosh, Paranjpe, Manish, Peters, Maire, Polak, Grzegorz, Porteous, David J, Rabban, Joseph, Rexrode, Kathyrn M, Romanowicz, Hanna, Saare, Merli, Saavalainen, Liisu, Schork, Andrew J, Sen, Sushmita, Shafrir, Amy L, Siewierska-Gorska, Anna, Slomka, Marcin, Smith, Blair H, Smolarz, Beata, Szaflik, Tomasz, Szyllo, Krzysztof, Takahashi, Atsushi, Terry, Kathryn L, Tomassetti, Carla, Treloar, Susan A, Vanhie, Arne, Vincent, Katy, Vo, Kim C, Werring, David J, Zeggini, Eleftheria, Zervou, Maria I, Stefansson, Kari, Nyegaard, Mette, Uimari, Outi, Yurttas-Beim, Piraye, Tung, Joyce Y, Adachi, Sosuke, Buring, Julie E, Ridker, Paul M, D'Hooghe, Thomas, Goulielmos, George N, Hapangama, Dharani K ORCID: 0000-0003-0270-0150, Hayward, Caroline, Horne, Andrew W, Low, Siew-Kee, Martikainen, Hannu, Chasman, Daniel I, Rogers, Peter AW, Saunders, Philippa T, Sirota, Marina, Spector, Tim, Strapagiel, Dominik, Whiteman, David C, Giudice, Linda C, Velez-Edwards, Digna R, Kraft, Peter, Salumets, Andres, Nyholt, Dale R, Magi, Reedik, Becker, Christian M, Steinthorsdottir, Valgerdur, Missmer, Stacey A, Montgomery, Grant W, Morris, Andrew P and Zondervan, Krina T (2023) The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. NATURE GENETICS, 55 (3). 423-+.

Tiirats, Airi, Viltrop, Triin, Noukas, Margit, Reimann, Ene, Salumets, Andres and Koks, Sulev ORCID: 0000-0001-6087-6643 (2016) <i>C14orf132</i> gene is possibly related to extremely low birth weight. BMC GENETICS, 17 (1). 132-.

Collapse authors list.
Marjonen, Heidi, Auvinen, Pauliina, Kahila, Hanna, Tsuiko, Olga, Koks, Sulev ORCID: 0000-0001-6087-6643, Tiirats, Airi, Viltrop, Triin, Tuuri, Timo, Soderstrom-Anttila, Viveca, Suikkari, Anne-Maria et al (show 3 more authors) , Salumets, Andres, Tiitinen, Aila and Kaminen-Ahola, Nina (2018) rs10732516 polymorphism at the IGF2/H19 locus associates with genotype-specific effects on placental DNA methylation and birth weight of newborns conceived by assisted reproductive technology. CLINICAL EPIGENETICS, 10 (1). 80-.