Genome-wide association study identifies five risk loci for pernicious anemia by Laisk, Triin, Lepamets, Maarja, Koel, Mariann, Abner, Erik, Mägi, Reedik

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Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations by Tambets, Kristiina, Yunusbayev, Bayazit, Hudjashov, Georgi, Ilumäe, Anne-Mai, Rootsi, Siiri, Honkola, Terhi, Vesakoski, Outi, Atkinson, Quentin, Skoglund, Pontus, Kushniarevich, Alena, Litvinov, Sergey, Reidla, Maere, Metspalu, Ene, Saag, Lehti, Rantanen, Timo, Karmin, Monika, Parik, Jüri, Zhadanov, Sergey I, Gubina, Marina, Damba, Larisa D, Bermisheva, Marina, Reisberg, Tuuli, Dibirova, Khadizhat, Evseeva, Irina, Nelis, Mari, Klovins, Janis, Metspalu, Andres, Esko, Tõnu, Balanovsky, Oleg, Balanovska, Elena, Khusnutdinova, Elza K, Osipova, Ludmila P, Voevoda, Mikhail, Villems, Richard, Kivisild, Toomas, Metspalu, Mait

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Genetic structure of Europeans: a view from the North-East by Nelis, Mari, Esko, Tõnu, Mägi, Reedik, Zimprich, Fritz, Zimprich, Alexander, Toncheva, Draga, Karachanak, Sena, Piskácková, Tereza, Balascák, Ivan, Peltonen, Leena, Jakkula, Eveliina, Rehnström, Karola, Lathrop, Mark, Heath, Simon, Galan, Pilar, Schreiber, Stefan, Meitinger, Thomas, Pfeufer, Arne, Wichmann, H-Erich, Melegh, Béla, Polgár, Noémi, Toniolo, Daniela, Gasparini, Paolo, D'Adamo, Pio, Klovins, Janis, Nikitina-Zake, Liene, Kucinskas, Vaidutis, Kasnauskiene, Jūrate, Lubinski, Jan, Debniak, Tadeusz, Limborska, Svetlana, Khrunin, Andrey, Estivill, Xavier, Rabionet, Raquel, Marsal, Sara, Julià, Antonio, Antonarakis, Stylianos E, Deutsch, Samuel, Borel, Christelle, Attar, Homa, Gagnebin, Maryline, Macek, Milan, Krawczak, Michael, Remm, Maido, Metspalu, Andres

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SARS-CoV-2 dual infection with Delta and Omicron variants in an immunocompetent host: a case report by Abroi, Aare, Gerst Talas, Ulvi, Pauskar, Merit, Shablinskaja, Arina, Reisberg, Tuuli, Niglas, Heiki, Päll, Taavi, Nelis, Mari, Tagen, Ingrid, Soodla, Pilleriin, Lutsar, Irja, Huik, Kristi

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A cross-disorder dosage sensitivity map of the human genome by Collins, Ryan L., Glessner, Joseph T., Porcu, Eleonora, Lepamets, Maarja, Brandon, Rhonda, Lauricella, Christopher, Han, Lide, Morley, Theodore, Niestroj, Lisa-Marie, Ulirsch, Jacob, Everett, Selin, Howrigan, Daniel P., Boone, Philip M., Fu, Jack, Karczewski, Konrad J., Kellaris, Georgios, Lowther, Chelsea, Lucente, Diane, Mohajeri, Kiana, Nõukas, Margit, Nuttle, Xander, Samocha, Kaitlin E., Trinh, Mi, Ullah, Farid, Võsa, Urmo, Metspalu, Andres, Mägi, Reedik, Nelis, Mari, Milani, Lili, Esko, Tõnu, Hurles, Matthew E., Aradhya, Swaroop, Davis, Erica E., Finucane, Hilary, Gusella, James F., Janze, Aura, Katsanis, Nicholas, Matyakhina, Ludmila, Neale, Benjamin M., Sanders, David, Warren, Stephanie, Hodge, Jennelle C., Lal, Dennis, Ruderfer, Douglas M., Meck, Jeanne, Mägi, Reedik, Esko, Tõnu, Reymond, Alexandre, Kutalik, Zoltán, Hakonarson, Hakon, Sunyaev, Shamil, Brand, Harrison, Talkowski, Michael E.

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Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity by Esko, Tõnu, Mezzavilla, Massimo, Nelis, Mari, Borel, Christelle, Debniak, Tadeusz, Jakkula, Eveliina, Julia, Antonio, Karachanak, Sena, Khrunin, Andrey, Kisfali, Peter, Krulisova, Veronika, Aušrelé Kučinskiené, Zita, Rehnström, Karola, Traglia, Michela, Nikitina-Zake, Liene, Zimprich, Fritz, Antonarakis, Stylianos E, Estivill, Xavier, Glavač, Damjan, Gut, Ivo, Klovins, Janis, Krawczak, Michael, Kučinskas, Vaidutis, Lathrop, Mark, Macek, Milan, Marsal, Sara, Meitinger, Thomas, Melegh, Béla, Limborska, Svetlana, Lubinski, Jan, Paolotie, Aarno, Schreiber, Stefan, Toncheva, Draga, Toniolo, Daniela, Wichmann, H-Erich, Zimprich, Alexander, Metspalu, Mait, Gasparini, Paolo, Metspalu, Andres, D'Adamo, Pio

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The individual and global impact of copy-number variants on complex human traits by Auwerx, Chiara, Lepamets, Maarja, Sadler, Marie C., Patxot, Marion, Stojanov, Miloš, Baud, David, Mägi, Reedik, Esko, Tõnu, Metspalu, Andres, Milani, Lili, Mägi, Reedik, Nelis, Mari, Porcu, Eleonora, Reymond, Alexandre, Kutalik, Zoltán

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Haplotype phasing and inheritance of copy number variants in nuclear families by Palta, Priit, Kaplinski, Lauris, Nagirnaja, Liina, Veidenberg, Andres, Möls, Märt, Nelis, Mari, Esko, Tõnu, Metspalu, Andres, Laan, Maris, Remm, Maido

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Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss by Trpchevska, Natalia, Freidin, Maxim B., Broer, Linda, Oosterloo, Berthe C., Yao, Shuyang, Zhou, Yitian, Vona, Barbara, Bishop, Charles, Bizaki-Vallaskangas, Argyro, Canlon, Barbara, Castellana, Fabio, Chasman, Daniel I., Cherny, Stacey, Christensen, Kaare, Concas, Maria Pina, Correa, Adolfo, Elkon, Ran, Metspalu, Andres, Nelis, Mari, Mägi, Reedik, Esko, Tõnu, Mengel-From, Jonas, Gao, Yan, Giersch, Anne B.S., Girotto, Giorgia, Gudjonsson, Alexander, Gudnason, Vilmundur, Heard-Costa, Nancy L., Hertzano, Ronna, Hjelmborg, Jacob v.B., Hjerling-Leffler, Jens, Hoffman, Howard J., Kaprio, Jaakko, Kettunen, Johannes, Krebs, Kristi, Kähler, Anna K., Lallemend, Francois, Launer, Lenore J., Lee, I-Min, Leonard, Hampton, Li, Chuan-Ming, Lowenheim, Hubert, Magnusson, Patrik K.E., van Meurs, Joyce, Milani, Lili, Morton, Cynthia C., Mäkitie, Antti, Nalls, Mike A., Nardone, Giuseppe Giovanni, Nygaard, Marianne, Palviainen, Teemu, Pratt, Sheila, Quaranta, Nicola, Rämö, Joel, Saarentaus, Elmo, Sardone, Rodolfo, Satizabal, Claudia L., Schweinfurth, John M., Seshadri, Sudha, Shiroma, Eric, Shulman, Eldad, Simonsick, Eleanor, Spankovich, Christopher, Tropitzsch, Anke, Lauschke, Volker M., Sullivan, Patrick F., Goedegebure, Andre, Cederroth, Christopher R., Williams, Frances M.K., Nagtegaal, Andries Paul

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HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases by Butler-Laporte, Guillaume, Farjoun, Joseph, Nakanishi, Tomoko, Lu, Tianyuan, Abner, Erik, Chen, Yiheng, Hultström, Michael, Metspalu, Andres, Milani, Lili, Mägi, Reedik, Nelis, Mari, Hudjashov, Georgi, Yoshiji, Satoshi, Ilboudo, Yann, Liang, Kevin Y. H., Su, Chen-Yang, Willet, Julian D. S., Esko, Tõnu, Zhou, Sirui, Forgetta, Vincenzo, Taliun, Daniel, Richards, J. Brent

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Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia by Brenner, Darren R, Amos, Christopher I, Brhane, Yonathan, Timofeeva, Maria N, Caporaso, Neil, Wang, Yufei, Christiani, David C, Bickeböller, Heike, Yang, Ping, Albanes, Demetrius, Stevens, Victoria L, Gapstur, Susan, McKay, James, Boffetta, Paolo, Zaridze, David, Szeszenia-Dabrowska, Neonilia, Lissowska, Jolanta, Rudnai, Peter, Fabianova, Eleonora, Mates, Dana, Bencko, Vladimir, Foretova, Lenka, Janout, Vladimir, Krokan, Hans E, Skorpen, Frank, Gabrielsen, Maiken E, Vatten, Lars, Njølstad, Inger, Chen, Chu, Goodman, Gary, Lathrop, Mark, Vooder, Tõnu, Välk, Kristjan, Nelis, Mari, Metspalu, Andres, Broderick, Peter, Eisen, Timothy, Wu, Xifeng, Zhang, Di, Chen, Wei, Spitz, Margaret R, Wei, Yongyue, Su, Li, Xie, Dong, She, Jun, Matsuo, Keitaro, Matsuda, Fumihiko, Ito, Hidemi, Risch, Angela, Heinrich, Joachim, Rosenberger, Albert, Muley, Thomas, Dienemann, Hendrik, Field, John K, Raji, Olaide, Chen, Ying, Gosney, John, Liloglou, Triantafillos, Davies, Michael P A, Marcus, Michael, McLaughlin, John, Orlow, Irene, Han, Younghun, Li, Yafang, Zong, Xuchen, Johansson, Mattias, Liu, Geoffrey, Tworoger, Shelley S, Le Marchand, Loic, Henderson, Brian E, Wilkens, Lynne R, Dai, Juncheng, Shen, Hongbing, Houlston, Richard S, Landi, Maria T, Brennan, Paul, Hung, Rayjean J

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A genome-wide analysis of populations from European Russia reveals a new pole of genetic diversity in northern Europe by Khrunin, Andrey V, Khokhrin, Denis V, Filippova, Irina N, Esko, Tõnu, Nelis, Mari, Bebyakova, Natalia A, Bolotova, Natalia L, Klovins, Janis, Nikitina-Zake, Liene, Rehnström, Karola, Ripatti, Samuli, Schreiber, Stefan, Franke, Andre, Macek, Milan, Krulišová, Veronika, Lubinski, Jan, Metspalu, Andres, Limborska, Svetlana A

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FinnGen provides genetic insights from a well-phenotyped isolated population by Kurki, Mitja I., Karjalainen, Juha, Palta, Priit, Sipilä, Timo P., Donner, Kati M., Reeve, Mary P., Laivuori, Hannele, Kaunisto, Mari A., Loukola, Anu, Lahtela, Elisa, Mattsson, Hannele, Laiho, Päivi, Della Briotta Parolo, Pietro, Lehisto, Arto A., Kanai, Masahiro, Mars, Nina, Heyne, Henrike O., Veerapen, Kumar, Rüeger, Sina, Lemmelä, Susanna, Zhou, Wei, Ruotsalainen, Sanni, Pärn, Kalle, Hiekkalinna, Tero, Koskelainen, Sami, Llorens, Vincent, Gracia-Tabuenca, Javier, Siirtola, Harri, Reis, Kadri, Elnahas, Abdelrahman G., Aalto-Setälä, Katriina, Biswas, Shameek, Dada, Oluwaseun A., Ding, Zhihao, Ehm, Margaret G., Eklund, Kari, Färkkilä, Martti, Finucane, Hilary, Ganna, Andrea, Ghazal, Awaisa, Hakanen, Antti, Hu, Xinli, Hunkapiller, Julie, Jacob, Howard, Jensen, Jan-Nygaard, Joensuu, Heikki, John, Sally, Junttila, Juhani, Kähönen, Mika, Kallio, Lila, Kaprio, Jaakko, Kettunen, Johannes, Kilpeläinen, Elina, Kosma, Veli-Matti, Kuopio, Teijo, Laisk, Triin, Laukkanen, Jari, Liu, Aoxing, Mägi, Reedik, Mäkitie, Antti, Malarstig, Anders, Maranville, Joseph, Niemi, Mari E. K., Niemi, Marianna, Obeidat, Ma´en, Okafo, George, Palomäki, Antti, Palotie, Tuula, Pitkäranta, Anne, Pulford, David, Raghavan, Neha, Rahimov, Fedik, Riley-Gillis, Bridget, Rodosthenous, Rodosthenis, Salminen, Eveliina, Salomaa, Veikko, Schleutker, Johanna, Serpi, Raisa, Shen, Huei-yi, Siegel, Richard, Sul, Jae Hoon, Tachmazidou, Ioanna, Tienari, Pentti, Tukiainen, Taru, Vaura, Felix, Virolainen, Petri, Waring, Jeffrey, Waterworth, Dawn, Yang, Robert, Nelis, Mari, Metspalu, Andres, Milani, Lili, Fox, Caroline, Havulinna, Aki S., Perola, Markus, Jalanko, Anu, Plenge, Robert, Runz, Heiko, Daly, Mark J., Palotie, Aarno

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Cohort Profile Update: Mental Health Online Survey in the Estonian Biobank (EstBB MHoS) by Ojalo, Triinu, Haan, Elis, Kõiv, Kadri, Kariis, Hanna Maria, Krebs, Kristi, Uusberg, Helen, Sedman, Tuuli, Võsa, Urmo, Puusepp, Mairo, Lind, Sirje, Hallik, Innar, Alavere, Helene, Milani, Lili, Lehto, Kelli

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Evolution of the Pygmy Phenotype: Evidence of Positive Selection from Genome-wide Scans in African, Asian, and Melanesian Pygmies by Migliano, Andrea Bamberg, Romero, Irene Gallego, Metspalu, Mait, Leavesley, Matthew, Pagani, Luca, Antao, Tiago, Huang, Da-Wei, Sherman, Brad T., Siddle, Katharine, Scholes, Clarissa, Hudjashov, Georgi, Kaitokai, Elton, Babalu, Avis, Belatti, Maggie, Cagan, Alex, Hopkinshaw, Bryony, Shaw, Colin, Nelis, Mari, Metspalu, Ene, Mägi, Reedik, Lempicki, Richard A., Villems, Richard, Lahr, Marta Mirazon, Kivisild, Toomas

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Long-range regulatory effects of Neandertal DNA in modern humans by Yermakovich, Danat, Pankratov, Vasili, Võsa, Urmo, Yunusbayev, Bayazit, Dannemann, Michael

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Prioritizing autoimmunity risk variants for functional analyses by fine-mapping mutations under natural selection by Pankratov, Vasili, Yunusbaeva, Milyausha, Ryakhovsky, Sergei, Zarodniuk, Maksym, Yunusbayev, Bayazit

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Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome by Alver, Maris, Mancini, Valentina, Läll, Kristi, Schneider, Maude, Romano, Luciana, Mägi, Reedik, Dermitzakis, Emmanouil T., Eliez, Stephan, Reymond, Alexandre

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Genetic determinants of plasma protein levels in the Estonian population by Kalnapenkis, Anette, Jõeloo, Maarja, Lepik, Kaido, Kukuškina, Viktorija, Kals, Mart, Alasoo, Kaur, Mägi, Reedik, Esko, Tõnu, Võsa, Urmo

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Rare copy-number variants as modulators of common disease susceptibility by Auwerx, Chiara, Jõeloo, Maarja, Sadler, Marie C, Tesio, Nicolò, Ojavee, Sven, Clark, Charlie J, Mägi, Reedik, Reymond, Alexandre, Kutalik, Zoltán

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