Suchergebnisse - "Mihailov, Evelin"

The Genetic Legacy of the Expansion of Turkic-Speaking Nomads across Eurasia von Yunusbayev, Bayazit, Metspalu, Mait, Metspalu, Ene, Valeev, Albert, Litvinov, Sergei, Valiev, Ruslan, Akhmetova, Vita, Balanovska, Elena, Balanovsky, Oleg, Turdikulova, Shahlo, Dalimova, Dilbar, Nymadawa, Pagbajabyn, Bahmanimehr, Ardeshir, Sahakyan, Hovhannes, Tambets, Kristiina, Fedorova, Sardana, Barashkov, Nikolay, Khidiyatova, Irina, Mihailov, Evelin, Khusainova, Rita, Damba, Larisa, Derenko, Miroslava, Malyarchuk, Boris, Osipova, Ludmila, Voevoda, Mikhail, Yepiskoposyan, Levon, Kivisild, Toomas, Khusnutdinova, Elza, Villems, Richard

“… The Turkic peoples represent a diverse collection of ethnic groups defined by the Turkic languages. These groups have dispersed across a vast area, including …”
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Copy number variations and cognitive phenotypes in unselected populations von Männik, Katrin, Mägi, Reedik, Macé, Aurélien, Cole, Ben, Guyatt, Anna L, Shihab, Hashem A, Maillard, Anne M, Alavere, Helene, Kolk, Anneli, Reigo, Anu, Mihailov, Evelin, Leitsalu, Liis, Ferreira, Anne-Maud, Nõukas, Margit, Teumer, Alexander, Salvi, Erika, Cusi, Daniele, McGue, Matt, Iacono, William G, Gaunt, Tom R, Beckmann, Jacques S, Jacquemont, Sébastien, Kutalik, Zoltán, Pankratz, Nathan, Timpson, Nicholas, Metspalu, Andres, Reymond, Alexandre

“… The association of copy number variations (CNVs), differing numbers of copies of genetic sequence at locations in the genome, with phenotypes such as …”
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Demographic associations for autoantibodies in disease-free individuals of a European population von Haller-Kikkatalo, Kadri, Alnek, Kristi, Metspalu, Andres, Mihailov, Evelin, Metsküla, Kaja, Kisand, Kalle, Pisarev, Heti, Salumets, Andres, Uibo, Raivo

“… The presence of autoantibodies usually precedes autoimmune disease, but is sometimes considered an incidental finding with no clinical relevance. The …”
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Mapping the Genetic Architecture of Gene Regulation in Whole Blood von Schramm, Katharina, Marzi, Carola, Schurmann, Claudia, Carstensen, Maren, Reinmaa, Eva, Biffar, Reiner, Eckstein, Gertrud, Gieger, Christian, Grabe, Hans-Jörgen, Homuth, Georg, Kastenmüller, Gabriele, Mägi, Reedik, Metspalu, Andres, Mihailov, Evelin, Peters, Annette, Petersmann, Astrid, Roden, Michael, Strauch, Konstantin, Suhre, Karsten, Teumer, Alexander, Völker, Uwe, Völzke, Henry, Wang-Sattler, Rui, Waldenberger, Melanie, Meitinger, Thomas, Illig, Thomas, Herder, Christian, Grallert, Harald, Prokisch, Holger

“… We aimed to assess whether whole blood expression quantitative trait loci (eQTLs) with effects in cis and trans are robust and can be used to identify …”
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Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals von Okbay, Aysu, Wu, Yeda, Wang, Nancy, Jayashankar, Hariharan, Bennett, Michael, Nehzati, Seyed Moeen, Sidorenko, Julia, Kweon, Hyeokmoon, Goldman, Grant, Gjorgjieva, Tamara, Jiang, Yunxuan, Hicks, Barry, Tian, Chao, Hinds, David A., Ahlskog, Rafael, Magnusson, Patrik K. E., Oskarsson, Sven, Hayward, Caroline, Campbell, Archie, Porteous, David J., Freese, Jeremy, Herd, Pamela, Watson, Chelsea, Jala, Jonathan, Conley, Dalton, Koellinger, Philipp D., Johannesson, Magnus, Laibson, David, Meyer, Michelle N., Lee, James J., Kong, Augustine, Yengo, Loic, Cesarini, David, Turley, Patrick, Visscher, Peter M., Beauchamp, Jonathan P., Benjamin, Daniel J., Young, Alexander I.

“… We conduct a genome-wide association study (GWAS) of educational attainment (EA) in a sample of ~3 million individuals and identify 3,952 approximately …”
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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression von Ripke, Stephan, Trzaskowski, Maciej, Byrne, Enda M., Adams, Mark J., Andlauer, Till M. F., Bacanu, Silviu-Alin, Beekman, Aartjan F. T., Bigdeli, Tim B., Binder, Elisabeth B., Blackwood, Douglas R. H., Bybjerg-Grauholm, Jonas, Castelao, Enrique, Couvy-Duchesne, Baptiste, Craddock, Nick, Deary, Ian J., Finucane, Hilary K., Forstner, Andreas J., Frank, Josef, Gill, Michael, Goes, Fernando S., Grove, Jakob, Hall, Lynsey S., Hannon, Eilis, Hansen, Thomas F., Hickie, Ian B., Hoffmann, Per, Horn, Carsten, Hougaard, David M., Hyde, Craig L., Jorgenson, Eric, Knowles, James A., Kraft, Julia, Krogh, Jesper, Kutalik, Zoltán, Lane, Jacqueline M., Li, Yihan, Li, Yun, Liu, Xiaoxiao, Lu, Leina, MacIntyre, Donald J., MacKinnon, Dean F., Maier, Robert M., Marchini, Jonathan, Mbarek, Hamdi, McGrath, Patrick, Mehta, Divya, Montgomery, Grant W., Nauck, Matthias, Nivard, Michel G., Pedersen, Carsten Bøcker, Posthuma, Danielle, Purcell, Shaun M., Quiroz, Jorge A., Saeed Mirza, Saira, Schoevers, Robert, Schulte, Eva C., Shi, Jianxin, Shyn, Stanley I., Smit, Johannes H., Smith, Daniel J., Stockmeier, Craig A., Teumer, Alexander, Thompson, Wesley, Thomson, Pippa A., Thorgeirsson, Thorgeir E., Tian, Chao, Treutlein, Jens, van Hemert, Albert M., Viktorin, Alexander, Visscher, Peter M., Wang, Yunpeng, Weinsheimer, Shantel Marie, Wellmann, Jürgen, Witt, Stephanie H., Wu, Yang, Xi, Hualin S., Yang, Jian, Zhang, Futao, Baune, Bernhard T., Berger, Klaus, de Geus, E. C. J., Domschke, Katharina, Esko, Tõnu, Hinds, David A., Li, Qingqin S., McIntosh, Andrew M., Metspalu, Andres, Mors, Ole, Müller-Myhsok, Bertram, O’Donovan, Michael C., Paciga, Sara A., Pedersen, Nancy L., Perlis, Roy H., Potash, James B., Schaefer, Catherine, Schulze, Thomas G., Uher, Rudolf, Völzke, Henry, Winslow, Ashley R., Børglum, Anders D.

“… Major depressive disorder (MDD) is a common illness accompanied by considerable morbidity, mortality, costs, and heightened risk of suicide. We conducted a …”
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Assessment of Bidirectional Relationships Between Physical Activity and Depression Among Adults: A 2-Sample Mendelian Randomization Study von Choi, Karmel W, Chen, Chia-Yen, Stein, Murray B, Klimentidis, Yann C, Wang, Min-Jung, Koenen, Karestan C, Smoller, Jordan W

“… Increasing evidence shows that physical activity is associated with reduced risk for depression, pointing to a potential modifiable target for prevention …”
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A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease von Nikpay, Majid, Goel, Anuj, Won, Hong-Hee, Hall, Leanne M, Willenborg, Christina, Kanoni, Stavroula, Kyriakou, Theodosios, Nelson, Christopher P, Harris, Tamara B, Hazen, Stanley L, Hengstenberg, Christian, Hofman, Albert, Ingelsson, Erik, Iribarren, Carlos, Jukema, J Wouter, Karhunen, Pekka J, Kim, Bong-Jo, Webb, Thomas R, Kullo, Iftikhar J, Loos, Ruth JF, Melander, Olle, Metspalu, Andres, Palmer, Colin N, Quertermous, Thomas, Rader, Daniel J, Zeng, Lingyao, Ridker, Paul M, Roberts, Robert, Schwartz, Stephen M, Stewart, Alexandre F, Stott, David J, Thiery, Joachim, Dehghan, Abbas, Zalloua, Pierre A, O'Donnell, Christopher J, Thompson, John R, Erdmann, Jeanette, Clarke, Robert, Kathiresan, Sekar, McPherson, Ruth, Alver, Maris, Deloukas, Panos, Samani, Nilesh J, Farrall, Martin, Auro, Kirsi, Bjonnes, Andrew, Chasman, Daniel I, Chen, Shufeng, d, Ian, Franceschini, Nora, Gieger, Christian, Grace, Christopher, Gustafsson, Stefan, Huang, Jie, Kim, Yun Kyoung, Lau, King Wai, Lyytikäinen, Leo-Pekka, Morrison, Alanna C, Pervjakova, Natalia, Rose, Lynda M, Salfati, Elias, Saxena, Richa, Scholz, Markus, Tikkanen, Emmi, Uitterlinden, Andre, Zhang, Weihua, de Andrade, Mariza, van Zuydam, Natalie R, Dedoussis, George, Frossard, Philippe, Gauguier, Dominique, Goodall, Alison H, Gottesman, Omri, Haber, Marc, Huang, Jianfeng, König, Inke R, Lannfelt, Lars, Lind, Lars, Lindgren, Cecilia M, Magnusson, Patrik K, Mallick, Nadeem H, Meitinger, Thomas, Memon, Fazal-ur-Rehman, Morris, Andrew P, Nieminen, Markku S, Rallidis, Loukianos S, Rasheed, Asif, Sinisalo, Juha, Stirrups, Kathleen E, Wang, Laiyuan, Ardissino, Diego, Boerwinkle, Eric, Bottinger, Erwin P, Buring, Julie E, Chambers, John C, Cupples, L Adrienne, Danesh, John, Demuth, Ilja, Gudnason, Roberto, Hamsten, Anders

“… Hugh Watkins, Sekar Kathiresan, Ruth McPherson, Martin Farrall and colleagues report the results of a large genome-wide association meta-analysis of coronary …”
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Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error von Tedja, Milly S., Wojciechowski, Robert, Hysi, Pirro G., Eriksson, Nicholas, Furlotte, Nicholas A., Verhoeven, Virginie J. M., Iglesias, Adriana I., Meester-Smoor, Magda A., Tompson, Stuart W., Fan, Qiao, Khawaja, Anthony P., Cheng, Ching-Yu, Höhn, René, Yamashiro, Kenji, Wenocur, Adam, Grazal, Clare, Haller, Toomas, Metspalu, Andres, Wedenoja, Juho, Jonas, Jost B., Wang, Ya Xing, Xie, Jing, Mitchell, Paul, Foster, Paul J., Klein, Barbara E. K., Klein, Ronald, Paterson, Andrew D., Hosseini, S. Mohsen, Shah, Rupal L., Williams, Cathy, Teo, Yik Ying, Tham, Yih Chung, Gupta, Preeti, Zhao, Wanting, Shi, Yuan, Saw, Woei-Yuh, Tai, E-Shyong, Sim, Xue Ling, Huffman, Jennifer E., Polašek, Ozren, Hayward, Caroline, Bencic, Goran, Rudan, Igor, Wilson, James F., Joshi, Peter K., Tsujikawa, Akitaka, Matsuda, Fumihiko, Whisenhunt, Kristina N., Zeller, Tanja, van der Spek, Peter J., Haak, Roxanna, Meijers-Heijboer, Hanne, van Leeuwen, Elisabeth M., Iyengar, Sudha K., Lass, Jonathan H., Hofman, Albert, Rivadeneira, Fernando, Uitterlinden, André G., Vingerling, Johannes R., Lehtimäki, Terho, Raitakari, Olli T., Biino, Ginevra, Concas, Maria Pina, Schwantes-An, Tae-Hwi, Igo, Robert P., Cuellar-Partida, Gabriel, Martin, Nicholas G., Craig, Jamie E., Gharahkhani, Puya, Williams, Katie M., Nag, Abhishek, Rahi, Jugnoo S., Cumberland, Phillippa M., Delcourt, Cécile, Bellenguez, Céline, Ried, Janina S., Bergen, Arthur A., Meitinger, Thomas, Gieger, Christian, Wong, Tien Yin, Hewitt, Alex W., Mackey, David A., Simpson, Claire L., Pfeiffer, Norbert, Pärssinen, Olavi, Baird, Paul N., Vitart, Veronique, Amin, Najaf, van Duijn, Cornelia M., Bailey-Wilson, Joan E., Young, Terri L., Saw, Seang-Mei, Stambolian, Dwight, MacGregor, Stuart, Guggenheim, Jeremy A., Tung, Joyce Y., Hammond, Christopher J., Klaver, Caroline C. W.

“… Refractive errors, including myopia, are the most frequent eye disorders worldwide and an increasingly common cause of blindness. This genome-wide association …”
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Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA von Kettunen, Johannes, Demirkan, Ayşe, Würtz, Peter, Draisma, Harmen H.M., Haller, Toomas, Rawal, Rajesh, Vaarhorst, Anika, Kangas, Antti J., Lyytikäinen, Leo-Pekka, Pirinen, Matti, Pool, René, Sarin, Antti-Pekka, Soininen, Pasi, Tukiainen, Taru, Wang, Qin, Tiainen, Mika, Tynkkynen, Tuulia, Amin, Najaf, Zeller, Tanja, Beekman, Marian, Deelen, Joris, van Dijk, Ko Willems, Esko, Tõnu, Hottenga, Jouke-Jan, van Leeuwen, Elisabeth M, Lehtimäki, Terho, Mihailov, Evelin, Rose, Richard J., de Craen, Anton J.M., Gieger, Christian, Kähönen, Mika, Perola, Markus, Blankenberg, Stefan, Savolainen, Markku J., Verhoeven, Aswin, Viikari, Jorma, Willemsen, Gonneke, Boomsma, Dorret I., van Duijn, Cornelia M., Eriksson, Johan, Jula, Antti, Järvelin, Marjo-Riitta, Kaprio, Jaakko, Metspalu, Andres, Raitakari, Olli, Salomaa, Veikko, Slagboom, P. Eline, Waldenberger, Melanie, Ripatti, Samuli, Ala-Korpela, Mika

“… Genome-wide association studies have identified numerous loci linked with complex diseases, for which the molecular mechanisms remain largely unclear …”
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Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses von Okbay, Aysu, Baselmans, Bart M L, De Neve, Jan-Emmanuel, Turley, Patrick, Nivard, Michel G, Fontana, Mark Alan, Linnér, Richard Karlsson, Gratten, Jacob, Buchwald, Jadwiga, Cavadino, Alana, Frazier-Wood, Alexis C, Furlotte, Nicholas A, Gonzalez, Juan R, Haitjema, Saskia, Karlsson, Robert, van der Laan, Sander W, Ladwig, Karl-Heinz, Lahti, Jari, van der Lee, Sven J, Lind, Penelope A, Minica, Camelia C, Nolte, Ilja M, Raitakari, Olli, Rawal, Rajesh, Stergiakouli, Evie, Taylor, Kent, Wedenoja, Juho, Wellmann, Juergen, Zhao, Wei, Amin, Najaf, Bakshi, Andrew, Cherney, Samantha, Cox, Simon R, Davis, Oliver S P, Ding, Jun, Eibich, Peter, Emeny, Rebecca T, Forstner, Andreas J, Gupta, Richa, Harris, Tamara B, Harris, Juliette M, Holliday, Elizabeth G, De Jager, Philip L, Kaakinen, Marika A, Kajantie, Eero, Kolcic, Ivana, Launer, Lenore J, Franke, Lude, Li-Gao, Ruifang, Koini, Marisa, Loukola, Anu, Montgomery, Grant W, Paternoster, Lavinia, Pattie, Alison, Petrovic, Katja E, Pulkki-Råback, Laura, Quaye, Lydia, Rudan, Igor, Scott, Rodney J, Vinkhuyzen, Anna E, Zabaneh, Delilah, Bennett, David A, Berger, Klaus, Bertram, Lars, Boomsma, Dorret I, Cucca, Francesco, Deary, Ian J, van Duijn, Cornelia M, Eriksson, Johan G, de Geus, Eco J C, Hartman, Catharine A, Hayward, Caroline, Hinds, David A, Iacono, William G, Kaprio, Jaakko, Keltikangas-Järvinen, Liisa, Kubzansky, Laura D, Lehtimäki, Terho, Magnusson, Patrik K E, Pasterkamp, Gerard, Power, Christine, Rich, Stephen S, Schmidt, Helena, Svento, Rauli, Schmidt, Reinhold, Sørensen, Thorkild I A, Stefansson, Kari, Terracciano, Antonio, Tiemeier, Henning, Wagner, Gert G, Yang, Jian, Smith, George Davey, Hofman, Albert, Johannesson, Magnus, Laibson, David I, Meyer, Michelle N, Beauchamp, Jonathan P, Koellinger, Philipp D, Bartels, Meike, Cesarini, David

“… Daniel Benjamin, Meike Bartels, Philipp Koellinger and colleagues report a genome-wide association meta-analysis of subjective well-being, depressive symptoms …”
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Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease von Stitziel, Nathan O, Stirrups, Kathleen E, Masca, Nicholas G D, Erdmann, Jeanette, Ferrario, Paola G, König, Inke R, Weeke, Peter E, Webb, Thomas R, Auer, Paul L, Schick, Ursula M, Lu, Yingchang, Zhang, He, Dube, Marie-Pierre, Goel, Anuj, Farrall, Martin, Peloso, Gina M, Won, Hong-Hee, Do, Ron, van Iperen, Erik, Kanoni, Stavroula, Kruppa, Jochen, Mahajan, Anubha, Scott, Robert A, Willenberg, Christina, Braund, Peter S, van Capelleveen, Julian C, Doney, Alex S F, Donnelly, Louise A, Asselta, Rosanna, Merlini, Piera A, Duga, Stefano, Marziliano, Nicola, Denny, Josh C, Shaffer, Christian M, El-Mokhtari, Nour Eddine, Franke, Andre, Gottesman, Omri, Heilmann, Stefanie, Hengstenberg, Christian, Hoffman, Per, Holmen, Oddgeir L, Hveem, Kristian, Jansson, Jan-Håkan, Jöckel, Karl-Heinz, Kessler, Thorsten, Kriebel, Jennifer, Laugwitz, Karl L, Marouli, Eirini, Martinelli, Nicola, McCarthy, Mark I, Van Zuydam, Natalie R, Meisinger, Christa, Esko, Tõnu, Mihailov, Evelin, Escher, Stefan A, Alver, Maris, Moebus, Susanne, Morris, Andrew D, Müller-Nurasyid, Martina, Nikpay, Majid, Olivieri, Oliviero, Lemieux Perreault, Louis-Philippe, AlQarawi, Alaa, Robertson, Neil R, Akinsanya, Karen O, Reilly, Dermot F, Vogt, Thomas F, Yin, Wu, Asselbergs, Folkert W, Kooperberg, Charles, Jackson, Rebecca D, Stahl, Eli, Strauch, Konstantin, Varga, Tibor V, Waldenberger, Melanie, Zeng, Lingyao, Kraja, Aldi T, Liu, Chunyu, Ehret, George B, Newton-Cheh, Christopher, Chasman, Daniel I, Chowdhury, Rajiv, Ferrario, Marco, Ford, Ian, Jukema, J Wouter, Kee, Frank, Kuulasmaa, Kari, Nordestgaard, Børge G, Perola, Markus, Saleheen, Danish, Sattar, Naveed, Surendran, Praveen, Tregouet, David, Young, Robin, Howson, Joanna M M, Butterworth, Adam S, Danesh, John, Ardissino, Diego, Bottinger, Erwin P, Erbel, Raimund

“… Searching for genes in which loss-of-function mutations confer protection against disease is a strategy to identity drug targets. This study reports an …”
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Genomic analyses inform on migration events during the peopling of Eurasia von Pagani, Luca, Lawson, Daniel John, Jagoda, Evelyn, Mörseburg, Alexander, Eriksson, Anders, Mitt, Mario, Clemente, Florian, Hudjashov, Georgi, DeGiorgio, Michael, Saag, Lauri, Wall, Jeffrey D., Cardona, Alexia, Mägi, Reedik, Sayres, Melissa A. Wilson, Kaewert, Sarah, Inchley, Charlotte, Scheib, Christiana L., Järve, Mari, Karmin, Monika, Jacobs, Guy S., Antao, Tiago, Iliescu, Florin Mircea, Kushniarevich, Alena, Ayub, Qasim, Tyler-Smith, Chris, Xue, Yali, Yunusbayev, Bayazit, Tambets, Kristiina, Mallick, Chandana Basu, Saag, Lehti, Pocheshkhova, Elvira, Andriadze, George, Muller, Craig, Westaway, Michael C., Lambert, David M., Zoraqi, Grigor, Turdikulova, Shahlo, Dalimova, Dilbar, Sabitov, Zhaxylyk, Sultana, Gazi Nurun Nahar, Lachance, Joseph, Tishkoff, Sarah, Momynaliev, Kuvat, Isakova, Jainagul, Damba, Larisa D., Gubina, Marina, Nymadawa, Pagbajabyn, Evseeva, Irina, Atramentova, Lubov, Utevska, Olga, Ricaut, François-Xavier, Brucato, Nicolas, Sudoyo, Herawati, Letellier, Thierry, Cox, Murray P., Barashkov, Nikolay A., Škaro, Vedrana, Mulahasanovic´, Lejla, Primorac, Dragan, Sahakyan, Hovhannes, Mormina, Maru, Eichstaedt, Christina A., Lichman, Daria V., Abdullah, Syafiq, Chaubey, Gyaneshwer, Wee, Joseph T. S., Mihailov, Evelin, Karunas, Alexandra, Litvinov, Sergei, Khusainova, Rita, Ekomasova, Natalya, Akhmetova, Vita, Khidiyatova, Irina, Marjanović, Damir, Yepiskoposyan, Levon, Behar, Doron M., Balanovska, Elena, Metspalu, Andres, Derenko, Miroslava, Malyarchuk, Boris, Voevoda, Mikhail, Fedorova, Sardana A., Osipova, Ludmila P., Lahr, Marta Mirazón, Gerbault, Pascale, Leavesley, Matthew, Migliano, Andrea Bamberg, Petraglia, Michael, Balanovsky, Oleg, Khusnutdinova, Elza K., Metspalu, Ene, Thomas, Mark G., Manica, Andrea, Nielsen, Rasmus, Villems, Richard, Willerslev, Eske, Kivisild, Toomas, Metspalu, Mait

“… Whole-genome sequencing of individuals from 125 populations provides insight into patterns of genetic diversity, natural selection and human demographic …”
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Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank von Coleman, Jonathan R I, Peyrot, Wouter J, Purves, Kirstin L, Davis, Katrina A S, Rayner, Christopher, Choi, Shing Wan, Hübel, Christopher, Gaspar, Héléna A, Kan, Carol, Van der Auwera, Sandra, Adams, Mark James, Lyall, Donald M, Choi, Karmel W, Dunn, Erin C, Vassos, Evangelos, Danese, Andrea, Maughan, Barbara, Grabe, Hans J, Lewis, Cathryn M, O'Reilly, Paul F, McIntosh, Andrew M, Smith, Daniel J, Wray, Naomi R, Hotopf, Matthew, Eley, Thalia C, Breen, Gerome

“… Depression is more frequent among individuals exposed to traumatic events. Both trauma exposure and depression are heritable. However, the relationship between …”
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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine von Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S, Palta, Priit, Esko, Tonu, Pers, Tune H, Farh, Kai-How, Cuenca-Leon, Ester, Furlotte, Nicholas A, Kurth, Tobias, Ingason, Andres, McMahon, George, Ligthart, Lannie, Terwindt, Gisela M, Kallela, Mikko, Freilinger, Tobias M, Ran, Caroline, Gordon, Scott G, Stam, Anine H, Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H H, Lehtimäki, Terho, Sarin, Antti-Pekka, Wedenoja, Juho, Hinds, David A, Buring, Julie E, Schürks, Markus, Ridker, Paul M, Hrafnsdottir, Maria Gudlaug, Stefansson, Hreinn, Ring, Susan M, Hottenga, Jouke-Jan, Penninx, Brenda W J H, Färkkilä, Markus, Kaunisto, Mari, Vepsäläinen, Salli, Malik, Rainer, Heath, Andrew C, Madden, Pamela A F, Martin, Nicholas G, Kurki, Mitja I, Kals, Mart, Mägi, Reedik, Pärn, Kalle, Hämäläinen, Eija, Huang, Hailiang, Byrnes, Andrea E, Franke, Lude, Huang, Jie, Stergiakouli, Evie, Lee, Phil H, Sandor, Cynthia, Webber, Caleb, Cader, Zameel, Muller-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Eriksson, Johan G, Salomaa, Veikko, Heikkilä, Kauko, Loehrer, Elizabeth, Uitterlinden, Andre G, Hofman, Albert, van Duijn, Cornelia M, Cherkas, Lynn, Pedersen, Linda M, Stubhaug, Audun, Nielsen, Christopher S, Männikkö, Minna, Mihailov, Evelin, Milani, Lili, Göbel, Hartmut, Esserlind, Ann-Louise, Christensen, Anne Francke, Werge, Thomas, Kaprio, Jaakko, Aromaa, Arpo J, Raitakari, Olli, Ikram, M Arfan, Spector, Tim, Järvelin, Marjo-Riitta, Metspalu, Andres, Kubisch, Christian, Strachan, David P, Dichgans, Martin, Wessman, Maija, Zwart, John-Anker, Boomsma, Dorret I, Smith, George Davey, Stefansson, Kari, Eriksson, Nicholas, Daly, Mark J, Neale, Benjamin M, Olesen, Jes, Chasman, Daniel I, Nyholt, Dale R, Palotie, Aarno

“… Aarno Palotie and colleagues present results of a large genome-wide association study of migraine. They identified significant associations at 38 distinct loci …”
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Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection von Adlam, David, Olson, Timothy M, Combaret, Nicolas, Kovacic, Jason C, Iismaa, Siiri E, Al-Hussaini, Abtehale, O'Byrne, Megan M, Bouajila, Sara, Georges, Adrien, Mishra, Ketan, Braund, Peter S, d'Escamard, Valentina, Huang, Siying, Margaritis, Marios, Nelson, Christopher P, de Andrade, Mariza, Kadian-Dodov, Daniella, Welch, Catherine A, Mazurkiewicz, Stephani, Jeunemaitre, Xavier, Wong, Claire Mei Yi, Giannoulatou, Eleni, Sweeting, Michael, Muller, David, Wood, Alice, McGrath-Cadell, Lucy, Fatkin, Diane, Dunwoodie, Sally L, Harvey, Richard, Holloway, Cameron, Empana, Jean-Philippe, Jouven, Xavier, Olin, Jeffrey W, Gulati, Rajiv, Tweet, Marysia S, Hayes, Sharonne N, Samani, Nilesh J, Graham, Robert M, Motreff, Pascal, Bouatia-Naji, Nabila

“… Spontaneous coronary artery dissection (SCAD) is an increasingly recognized cause of acute coronary syndromes (ACS) afflicting predominantly younger to …”
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Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair von Thompson, Deborah J, Pervjakova, Natalia, Chasman, Daniel I, Esko, Tõnu, Elks, Cathy E, He, Chunyan, Altmaier, Elisabeth, Huffman, Jennifer E, Keller, Margaux F, McArdle, Patrick F, Nutile, Teresa, Porcu, Eleonora, Corre, Tanguy, Smith, Albert V, Antoniou, Antonis C, Barbieri, Caterina, Bielinski, Suzette J, Blomqvist, Carl, Boerwinkle, Eric, Bogdanova, Natalia V, Bojesen, Stig E, Borresen-Dale, Anne-Lise, Chapman, J Ross, Couch, Fergus J, Coviello, Andrea D, Cox, Angela, Czene, Kamila, Demerath, Ellen W, Devilee, Peter, Dörk, Thilo, dos-Santos-Silva, Isabel, Dunning, Alison M, Eicher, John D, Fasching, Peter A, Faul, Jessica D, Garcia, Melissa E, Girotto, Giorgia G, Goldberg, Mark S, Gudbjartsson, Daniel F, Haiman, Christopher A, Homuth, Georg, Hu, Frank B, Hunter, David J, Jakubowska, Anna, Kosma, Veli-Matti, Kriebel, Jennifer, Kristensen, Vessela, Langenberg, Claudia, Liu, Yongmei, Luan, Jian'an, Manz, Judith, Masciullo, Corrado, Milani, Lili, Milne, Roger L, Müller-Nurasyid, Martina, Neale, Benjamin M, Neven, Patrick, Newman, Anne B, Nordestgaard, Børge G, Padmanabhan, Sandosh, Peters, Ulrike, Peto, Julian, Pirie, Ailith, Pistis, Giorgio, Porteous, David, Psaty, Bruce M, Pylkäs, Katri, Radice, Paolo, Rivadeneira, Fernando, Rudan, Igor, Sawyer, Elinor J, Schlessinger, David, Schmidt, Marjanka K, Schmidt, Frank, Seynaeve, Caroline M, Simard, Jacques, Southey, Melissa C, Stöckl, Doris, Strauch, Konstantin, Toland, Amanda E, Tomlinson, Ian, Tryggvadottir, Laufey, Turner, Stephen T, Willemsen, Gonneke, Wright, Alan F, Zygmunt, Marek, Bergmann, Sven, Boomsma, Dorret I, Montgomery, Grant W, van Duijn, Cornelia M, Alizadeh, Behrooz Z, Crisponi, Laura, Easton, Douglas F, Harris, Tamara B, Kraft, Peter, McKnight, Barbara, Rotter, Jerome I, Ulivi, Sheila, Wareham, Nicholas J, Yerges-Armstrong, Laura M

“… John Perry and colleagues report the results of a large genome-wide association study meta-analysis to identify variants influencing age at natural menopause …”
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Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension von Surendran, Praveen, Drenos, Fotios, Witkowska, Kate, Tragante, Vinicius, Freitag, Daniel F, Tinker, Andrew, Harakalova, Magdalena, Rasheed, Asif, Bonnycastle, Lori L, Jackson, Anne U, Narisu, Narisu, Swift, Amy J, Ohlsson, Therese, Matchan, Angela, Stirrups, Kathleen E, Bork-Jensen, Jette, Gjesing, Anette P, Havulinna, Aki S, Zhang, He, Donnelly, Louise A, Neville, Matt J, Robertson, Neil R, Yiorkas, Andrianos M, Herzig, Karl-Heinz, Zhang, Weihua, Trabetti, Elisabetta, Evangelou, Evangelos, Moayyeri, Alireza, Nelson, Christopher P, de Craen, Anton J M, Trompet, Stella, Scott, Robert A, Marioni, Riccardo, Farmaki, Aliki-Eleni, Hallmans, Göran, Hassinen, Maija, Burgess, Stephen, Uria-Nickelsen, Maria, Reilly, Dermot F, Vogt, Thomas F, Traylor, Matthew, Justice, Anne E, Marouli, Eirini, Uusitupa, Matti, Polasek, Ozren, Rudan, Igor, Rolandsson, Olov, Dedoussis, George, Starr, John M, Brown, Morris J, Sattar, Naveed, Packard, Chris J, Mägi, Reedik, Metspalu, Andres, de Boer, Rudolf A, van der Meer, Peter, van der Harst, Pim, Lind, Lars, de Bakker, Paul I W, Korpi-Hyövälti, Eeva, Oksa, Heikki, Linneberg, Allan, Thuesen, Betina, Doney, Alex S F, Morris, Andrew D, Palmer, Colin N A, Holmen, Oddgeir Lingaas, Willer, Cristen J, Palotie, Aarno, Ripatti, Samuli, Majumder, Abdulla al Shafi, Chowdhury, Rajiv, Poulter, Neil, Sever, Peter, Amouyel, Philippe, Arveiler, Dominique, Blankenberg, Stefan, Ferrières, Jean, Müller-Nurasyid, Martina, Veronesi, Giovanni, Virtamo, Jarmo, Deloukas, Panos, Elliott, Paul, Melander, Olle, Kuusisto, Johanna, Laakso, Markku, Padmanabhan, Sandosh, Porteous, David J, Mohlke, Karen L, Pedersen, Oluf, Stringham, Heather M, Newton-Cheh, Christopher, Caulfield, Mark J, Morris, Andrew P, Tomaszewski, Maciej, Saleheen, Danish, Asselbergs, Folkert W, Wain, Louise V, Butterworth, Adam S, Howson, Joanna M M

“… Patricia Munroe, Joanna Howson and colleagues genotype ∼350,000 individuals and identify 30 new blood pressure– or hypertension-associated risk loci. Their …”
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A recent bottleneck of Y chromosome diversity coincides with a global change in culture von Karmin, Monika, Saag, Lauri, Vicente, Mário, Wilson Sayres, Melissa A, Järve, Mari, Talas, Ulvi Gerst, Rootsi, Siiri, Ilumäe, Anne-Mai, Mägi, Reedik, Mitt, Mario, Pagani, Luca, Puurand, Tarmo, Faltyskova, Zuzana, Clemente, Florian, Cardona, Alexia, Metspalu, Ene, Sahakyan, Hovhannes, Yunusbayev, Bayazit, Hudjashov, Georgi, DeGiorgio, Michael, Loogväli, Eva-Liis, Eichstaedt, Christina, Eelmets, Mikk, Chaubey, Gyaneshwer, Tambets, Kristiina, Litvinov, Sergei, Mormina, Maru, Xue, Yali, Ayub, Qasim, Zoraqi, Grigor, Korneliussen, Thorfinn Sand, Akhatova, Farida, Lachance, Joseph, Tishkoff, Sarah, Momynaliev, Kuvat, Ricaut, François-Xavier, Kusuma, Pradiptajati, Razafindrazaka, Harilanto, Pierron, Denis, Cox, Murray P, Sultana, Gazi Nurun Nahar, Willerslev, Rane, Muller, Craig, Westaway, Michael, Lambert, David, Skaro, Vedrana, Kovačevic, Lejla, Turdikulova, Shahlo, Dalimova, Dilbar, Khusainova, Rita, Trofimova, Natalya, Akhmetova, Vita, Khidiyatova, Irina, Lichman, Daria V, Isakova, Jainagul, Pocheshkhova, Elvira, Sabitov, Zhaxylyk, Barashkov, Nikolay A, Nymadawa, Pagbajabyn, Mihailov, Evelin, Seng, Joseph Wee Tien, Evseeva, Irina, Migliano, Andrea Bamberg, Abdullah, Syafiq, Andriadze, George, Primorac, Dragan, Atramentova, Lubov, Utevska, Olga, Yepiskoposyan, Levon, Marjanovic, Damir, Kushniarevich, Alena, Behar, Doron M, Gilissen, Christian, Vissers, Lisenka, Veltman, Joris A, Balanovska, Elena, Derenko, Miroslava, Malyarchuk, Boris, Metspalu, Andres, Fedorova, Sardana, Eriksson, Anders, Manica, Andrea, Mendez, Fernando L, Karafet, Tatiana M, Veeramah, Krishna R, Bradman, Neil, Hammer, Michael F, Osipova, Ludmila P, Balanovsky, Oleg, Khusnutdinova, Elza K, Johnsen, Knut, Remm, Maido, Thomas, Mark G, Tyler-Smith, Chris, Underhill, Peter A, Willerslev, Eske, Nielsen, Rasmus, Metspalu, Mait, Villems, Richard, Kivisild, Toomas

“… It is commonly thought that human genetic diversity in non-African populations was shaped primarily by an out-of-Africa dispersal 50-100 thousand yr ago (kya) …”
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Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci von Erzurumluoglu, A Mesut, Liu, Mengzhen, Jackson, Victoria E, Barnes, Daniel R, Datta, Gargi, Melbourne, Carl A, Young, Robin, Batini, Chiara, Surendran, Praveen, Jiang, Tao, Adnan, Sheikh Daud, Afaq, Saima, Agrawal, Arpana, Altmaier, Elisabeth, Antoniou, Antonis C, Asselbergs, Folkert W, Baumbach, Clemens, Bierut, Laura, Bertelsen, Sarah, Boehnke, Michael, Bots, Michiel L, Brazel, David M, Chambers, John C, Chang-Claude, Jenny, Chen, Chu, Corley, Janie, Chou, Yi-Ling, David, Sean P, de Boer, Rudolf A, de Leeuw, Christiaan A, Dennis, Joe G, Dominiczak, Anna F, Dunning, Alison M, Easton, Douglas F, Eaton, Charles, Elliott, Paul, Evangelou, Evangelos, Faul, Jessica D, Foroud, Tatiana, Goate, Alison, Gong, Jian, Grabe, Hans J, Haessler, Jeff, Haiman, Christopher, Hallmans, Göran, Hammerschlag, Anke R, Harris, Sarah E, Hattersley, Andrew, Heath, Andrew, Hsu, Chris, Iacono, William G, Kanoni, Stavroula, Kapoor, Manav, Kaprio, Jaakko, Kardia, Sharon L, Karpe, Fredrik, Kontto, Jukka, Kooner, Jaspal S, Kooperberg, Charles, Kuulasmaa, Kari, Laakso, Markku, Lai, Dongbing, Langenberg, Claudia, Le, Nhung, Lettre, Guillaume, Loukola, Anu, Luan, Jian'an, Madden, Pamela A F, Mangino, Massimo, Marioni, Riccardo E, Marouli, Eirini, Marten, Jonathan, Martin, Nicholas G, McGue, Matt, Michailidou, Kyriaki, Mihailov, Evelin, Moayyeri, Alireza, Moitry, Marie, Müller-Nurasyid, Martina, Naheed, Aliya, Nauck, Matthias, Neville, Matthew J, Nielsen, Sune Fallgaard, North, Kari, Perola, Markus, Pharoah, Paul D P, Pistis, Giorgio, Polderman, Tinca J, Posthuma, Danielle, Poulter, Neil, Qaiser, Beenish, Rasheed, Asif, Reiner, Alex, Renström, Frida, Rice, John, Rohde, Rebecca, Rolandsson, Olov, Samani, Nilesh J, Samuel, Maria, Schlessinger, David

“… Smoking is a major heritable and modifiable risk factor for many diseases, including cancer, common respiratory disorders and cardiovascular diseases. Fourteen …”
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