Influence of mechanical and plasma shockwaves on the structure and properties of superconductors von Mihailov, B P, Alibekov, S Ya, Krutskih, N A, Egorov, A V, Pavlov, A I, Lysyannikov, A V, Kaizer, Yu F, Kuznetsov, A V

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Identification of common genetic risk variants for autism spectrum disorder von Grove, Jakob, Ripke, Stephan, Als, Thomas D., Mattheisen, Manuel, Walters, Raymond K., Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A., Anney, Richard, Awashti, Swapnil, Belliveau, Rich, Bettella, Francesco, Buxbaum, Joseph D., Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Christensen, Jane H., Churchhouse, Claire, Dellenvall, Karin, Demontis, Ditte, De Rubeis, Silvia, Devlin, Bernie, Djurovic, Srdjan, Dumont, Ashley L., Goldstein, Jacqueline I., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Hope, Sigrun, Howrigan, Daniel P., Huang, Hailiang, Hultman, Christina M., Klei, Lambertus, Maller, Julian, Martin, Joanna, Martin, Alicia R., Moran, Jennifer L., Nyegaard, Mette, Nærland, Terje, Palmer, Duncan S., Palotie, Aarno, Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, dPoterba, Timothy, Poulsen, Jesper Buchhave, Pourcain, Beate St, Qvist, Per, Rehnström, Karola, Reichenberg, Abraham, Reichert, Jennifer, Robinson, Elise B., Roeder, Kathryn, Roussos, Panos, Saemundsen, Evald, Sandin, Sven, Satterstrom, F. Kyle, Davey Smith, George, Stefansson, Hreinn, Steinberg, Stacy, Stevens, Christine R., Sullivan, Patrick F., Turley, Patrick, Walters, G. Bragi, Xu, Xinyi, Stefansson, Kari, Geschwind, Daniel H., Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Neale, Benjamin M., Daly, Mark J., Børglum, Anders D.

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Depression during the COVID-19 pandemic. A retrospective study on depressive disorders among psychiatric patients admitted at “elisabeta doamna” hospital galati, romania von Mihailov, O., Rădulescu, I.D., Moraru, C., Nechita, P., Ciubară, A.B., Ciubară, A.

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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.

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Fiber bragg gratings made with a phase mask and 800-nm femtosecond radiation von Mihailov, Stephen J, Smelser, Christopher W, Lu, Ping, Walker, Robert B, Grobnic, Dan, Ding, Huimin, Henderson, George, Unruh, James

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Genetic variants linked to education predict longevity von Marioni, Riccardo E., Ritchie, Stuart J., Joshi, Peter K., Hagenaars, Saskia P., Okbay, Aysu, Fischer, Krista, Adams, Mark J., Hill, W. David, Davies, Gail, Nagy, Reka, Amador, Carmen, Läll, Kristi, Metspalu, Andres, Liewald, David C., Campbell, Archie, Wilson, James F., Hayward, Caroline, Esko, Tõnu, Porteous, David J., Gale, Catharine R., Deary, Ian J.

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Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection von Adlam, David, Al-Hussaini, Abtehale, Bouajila, Sara, d’Escamard, Valentina, Huang, Siying, Margaritis, Marios, Nelson, Christopher P., Welch, Catherine A., Jeunemaitre, Xavier, Barnay, Pierre, Rioufol, Gilles, Range, Grégoire, Harbaoui, Brahim, Cayla, Guillaume, Champin, Stanislas, Saint-Etienne, Christophe, Marliere, Stéphanie, Karrillon, Gaëtan, Gerbay, Antoine, Houpe, David, Wong, Claire Mei Yi, Giannoulatou, Eleni, Sweeting, Michael, McGrath-Cadell, Lucy, Dunwoodie, Sally L., Harvey, Richard, Holloway, Cameron, Nikpay, Majid, Goel, Anuj, Won, Hong-Hee, Willenborg, Christina, Kanoni, Stavroula, Kyriakou, Theodosios, Nelson, Christopher P., Webb, Thomas R., Alver, Maris, Auro, Kirsi, Bjonnes, Andrew, Chasman, Daniel I., Franceschini, Nora, Gieger, Christian, Hwang, Shih-Jen, Kleber, Marcus E., Morrison, Alanna, Rose, Lynda M., Scholz, Markus, Smith, Albert V., Uitterlinden, Andre, Beutner, Frank, Gauguier, Dominique, Goodall, Alison H., Gottesman, Omri, Han, Bok-Ghee, Kessler, Thorsten, König, Inke R., Lannfelt, Lars, Lind, Lars, Lindgren, Cecilia M., Mallick, Nadeem H., Meitinger, Thomas, Morris, Andrew P., Nieminen, Markku S., Pedersen, Nancy L., Rasheed, Asif, Sinisalo, Juha, Trompet, Stella, Wang, Laiyuan, Boerwinkle, Eric, Demuth, Ilja, Epstein, Stephen E., Esko, Tõnu, Franco, Oscar H., Franzosi, Maria Grazia, Granger, Christopher B., Harris, Tamara B., Hofman, Albert, Ingelsson, Erik, Iribarren, Carlos, Jukema, J Wouter, Karhunen, Pekka J., Kim, Bong-Jo, Kooner, Jaspal S., Kullo, Iftikhar J., Palmer, Colin N., Perola, Markus, Ridker, Paul M., Ripatti, Samuli, Salomaa, Veikko, Seedorf, Udo, Stewart, Alexandre F., Stott, David J., Thiery, Joachim, Zalloua, Pierre A., Reilly, Muredach P., Clarke, Robert, Watkins, Hugh, Samani, Nilesh J., Farrall, Martin, Hayes, Sharonne N., Samani, Nilesh J.

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Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease von Zanoni, Paolo, Khetarpal, Sumeet A., Larach, Daniel B., Hancock-Cerutti, William F., Millar, John S., Cuchel, Marina, DerOhannessian, Stephanie, Kontush, Anatol, Surendran, Praveen, Saleheen, Danish, Trompet, Stella, Jukema, J. Wouter, De Craen, Anton, Deloukas, Panos, Sattar, Naveed, Ford, Ian, Packard, Chris, Majumder, Abdullah al Shafi, Alam, Dewan S., Di Angelantonio, Emanuele, Abecasis, Goncalo, Chowdhury, Rajiv, Erdmann, Jeanette, Nordestgaard, Børge G., Nielsen, Sune F., Tybjærg-Hansen, Anne, Schmidt, Ruth Frikke, Kuulasmaa, Kari, Liu, Dajiang J., Perola, Markus, Blankenberg, Stefan, Salomaa, Veikko, Männistö, Satu, Amouyel, Philippe, Arveiler, Dominique, Ferrieres, Jean, Müller-Nurasyid, Martina, Ferrario, Marco, Kee, Frank, Willer, Cristen J., Samani, Nilesh, Schunkert, Heribert, Butterworth, Adam S., Howson, Joanna M. M., Peloso, Gina M., Stitziel, Nathan O., Danesh, John, Kathiresan, Sekar, Rader, Daniel J.

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The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study von Giannakopoulou, Olga, Lin, Kuang, Meng, Xiangrui, Su, Mei-Hsin, Kuo, Po-Hsiu, Peterson, Roseann E, Awasthi, Swapnil, Moscati, Arden, Coleman, Jonathan R. I, Bass, Nick, Millwood, Iona Y, Chen, Yiping, Chen, Zhengming, Chen, Hsi-Chung, Lu, Mong-Liang, Huang, Ming-Chyi, Chen, Chun-Hsin, Stahl, Eli A, Loos, Ruth J. F, Mullins, Niamh, Ursano, Robert J, Kessler, Ronald C, Stein, Murray B, Sen, Srijan, Scott, Laura J, Burmeister, Margit, Fang, Yu, Tyrrell, Jess, Jiang, Yunxuan, Tian, Chao, McIntosh, Andrew M, Ripke, Stephan, Dunn, Erin C, Kendler, Kenneth S, Walters, Robin G, Lewis, Cathryn M, Kuchenbaecker, Karoline

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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

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Genetic Association of Major Depression With Atypical Features and Obesity-Related Immunometabolic Dysregulations von Milaneschi, Yuri, Lamers, Femke, Peyrot, Wouter J, Baune, Bernhard T, Breen, Gerome, Dehghan, Abbas, Forstner, Andreas J, Grabe, Hans J, Homuth, Georg, Kan, Carol, Lewis, Cathryn, Mullins, Niamh, Nauck, Matthias, Pistis, Giorgio, Preisig, Martin, Rivera, Margarita, Rietschel, Marcella, Streit, Fabian, Strohmaier, Jana, Teumer, Alexander, Van der Auwera, Sandra, Wray, Naomi R, Boomsma, Dorret I, Penninx, Brenda W. J. H

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Fiber Bragg gratings with suppressed cladding modes made in SMF-28 with a femtosecond IR laser and a phase mask von Grobnic, D., Smelser, C.W., Mihailov, S.J., Walker, R.B., Lu, P.

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Identification of seven loci affecting mean telomere length and their association with disease von Codd, Veryan, Nelson, Christopher P, Albrecht, Eva, Mangino, Massimo, Deelen, Joris, Buxton, Jessica L, Hottenga, Jouke Jan, Fischer, Krista, Esko, Tõnu, Surakka, Ida, Broer, Linda, Nyholt, Dale R, Leach, Irene Mateo, Salo, Perttu, Hägg, Sara, Matthews, Mary K, Palmen, Jutta, Norata, Giuseppe D, O'Reilly, Paul F, Saleheen, Danish, Amin, Najaf, Balmforth, Anthony J, Beekman, Marian, de Boer, Rudolf A, Böhringer, Stefan, Braund, Peter S, Burton, Paul R, Craen, Anton J Mde, Denniff, Matthew, Dong, Yanbin, Douroudis, Konstantinos, Dubinina, Elena, Eriksson, Johan G, Garlaschelli, Katia, Guo, Dehuang, Hartikainen, Anna-Liisa, Henders, Anjali K, Houwing-Duistermaat, Jeanine J, Kananen, Laura, Karssen, Lennart C, Kettunen, Johannes, Klopp, Norman, Lagou, Vasiliki, van Leeuwen, Elisabeth M, Madden, Pamela A, Mägi, Reedik, Magnusson, Patrik K E, Männistö, Satu, McCarthy, Mark I, Medland, Sarah E, Mihailov, Evelin, Montgomery, Grant W, Oostra, Ben A, Palotie, Aarno, Peters, Annette, Pollard, Helen, Pouta, Anneli, Prokopenko, Inga, Ripatti, Samuli, Salomaa, Veikko, Suchiman, H Eka D, Valdes, Ana M, Verweij, Niek, Viñuela, Ana, Wang, Xiaoling, Wichmann, H-Erich, Widen, Elisabeth, Willemsen, Gonneke, Wright, Margaret J, Xia, Kai, Xiao, Xiangjun, van Veldhuisen, Dirk J, Catapano, Alberico L, Tobin, Martin D, Hall, Alistair S, Blakemore, Alexandra I F, van Gilst, Wiek H, Zhu, Haidong, Erdmann, Jeanette, Reilly, Muredach P, Kathiresan, Sekar, Schunkert, Heribert, Talmud, Philippa J, Pedersen, Nancy L, Perola, Markus, Ouwehand, Willem, Kaprio, Jaakko, Martin, Nicholas G, van Duijn, Cornelia M, Hovatta, Iiris, Gieger, Christian, Metspalu, Andres, Boomsma, Dorret I, Jarvelin, Marjo-Riitta, Slagboom, P Eline, Thompson, John R, Spector, Tim D, van der Harst, Pim, Samani, Nilesh J

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Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia von Verhoeven, Virginie J M, Hysi, Pirro G, Wojciechowski, Robert, Guggenheim, Jeremy A, Höhn, René, MacGregor, Stuart, Hewitt, Alex W, Nag, Abhishek, Cheng, Ching-Yu, Yonova-Doing, Ekaterina, Zhou, Xin, Ikram, M Kamran, McMahon, George, Kemp, John P, Pourcain, Beate St, Simpson, Claire L, Mäkelä, Kari-Matti, Lehtimäki, Terho, Kähönen, Mika, Paterson, Andrew D, Hosseini, S Mohsen, Wong, Hoi Suen, Xu, Liang, Wedenoja, Juho, Yip, Shea Ping, Ho, Daniel W H, Pang, Chi Pui, Chen, Li Jia, Burdon, Kathryn P, Craig, Jamie E, Klein, Barbara E K, Klein, Ronald, Haller, Toomas, Metspalu, Andres, Khor, Chiea-Chuen, Tai, E-Shyong, Aung, Tin, Vithana, Eranga, Tay, Wan-Ting, Barathi, Veluchamy A, Chen, Peng, Li, Ruoying, Liao, Jiemin, Zheng, Yingfeng, Ong, Rick T, Döring, Angela, Evans, David M, Timpson, Nicholas J, Verkerk, Annemieke J M H, Meitinger, Thomas, Raitakari, Olli, Hawthorne, Felicia, Spector, Tim D, Pirastu, Mario, Murgia, Federico, Ang, Wei, Mishra, Aniket, Montgomery, Grant W, Pennell, Craig E, Cumberland, Phillippa M, Cotlarciuc, Ioana, Mitchell, Paul, Wang, Jie Jin, Schache, Maria, Janmahasatian, Sarayut, Jr, Robert P Igo, Lass, Jonathan H, Chew, Emily, Iyengar, Sudha K, Gorgels, Theo G M F, Rudan, Igor, Hayward, Caroline, Wright, Alan F, Polasek, Ozren, Vatavuk, Zoran, Wilson, James F, Fleck, Brian, Zeller, Tanja, Mirshahi, Alireza, Müller, Christian, Uitterlinden, André G, Rivadeneira, Fernando, Vingerling, Johannes R, Hofman, Albert, Oostra, Ben A, Amin, Najaf, Bergen, Arthur A B, Teo, Yik-Ying, Rahi, Jugnoo S, Vitart, Veronique, Williams, Cathy, Baird, Paul N, Oexle, Konrad, Pfeiffer, Norbert, Mackey, David A, Young, Terri L, Saw, Seang-Mei, Stambolian, Dwight, Klaver, Caroline C, Hammond, Christopher J

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Association of Adiposity Genetic Variants With Menarche Timing in 92,105 Women of European Descent von FERNANDEZ-RHODES, Lindsay, DEMERATH, Ellen W, MCARDLE, Patrick F, YERGES-ARMSTRONG, Laura M, ELKS, Cathy E, STRACHAN, David P, KUTALIK, Zoltán, VOLLENWEIDER, Peter, FEENSTRA, Bjarke, BOYD, Heather A, METSPALU, Andres, MIHAILOV, Evelin, COUSMINER, Diana L, BROER, Linda, ZILLIKENS, M. Carola, OOSTRA, Ben, VAN DUIJN, Cornelia M, LUNETTA, Kathryn L, PERRY, John R. B, MURRAY, Anna, KOLLER, Daniel L, DONGBING LAI, CORRE, Tanguy, RAN TAO, TONIOLO, Daniela, ALBRECHT, Eva, STÖCKL, Doris, GRALLERT, Harald, GIEGER, Christian, HAYWARD, Caroline, POLASEK, Ozren, RUDAN, Igor, WILSON, James F, CHUNYAN HE, DREYFUS, Jill G, KRAFT, Peter, HU, Frank B, HUNTER, David J, HOTTENGA, Jouke-Jan, WILLEMSEN, Gonneke, BOOMSMA, Dorret I, BYRNE, Enda M, MARTIN, Nicholas G, MONTGOMERY, Grant W, WARRINGTON, Nicole M, ESKO, Tõnu, PENNELL, Craig E, STOLK, Lisette, VISSER, Jenny A, HOFMAN, Albert, UITTERLINDEN, André G, RIVADENEIRA, Fernando, PENG LIN, FISHER, Sherri L, BIERUT, Laura J, CRISPONI, Laura, SMITH, Albert V, GUDNASON, Vilmundur, HARRIS, Tamara B, LAUNER, Lenore

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Bragg grating inscription in various optical fibers with femtosecond infrared lasers and a phase mask von Mihailov, Stephen J., Grobnic, Dan, Smelser, Christopher W., Lu, Ping, Walker, Robert B., Ding, Huimin

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Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use von Jiang, Yu, Hughey, Jordan M., Zhan, Xiaowei, Gong, Jian, Batini, Chiara, Liu, MengZhen, Surendran, Praveen, Young, Robin, Nielsen, Sune Fallgaard, Kontto, Jukka, Perola, Markus, Caslake, Muriel, Reily, Dermot F., Vogt, Thomas, Sattar, Naveed, Ford, Ian, Alam, Dewan S., Majumder, Abdulla al Shafi, Di Angelantonio, Emanuele, Chowdhury, Rajiv, Arveiler, Dominique, Blankenberg, Stefan, Veronesi, Giovanni, EPIC-CVD Consortium, Frossard, Philippe, Nordestgaard, Børge Grønne, Saleheen, Danish, Danesh, John, Butterworth, Adam S., Warren, Helen R., Tragante, Vinicius, Altmaier, Elisabeth, Luan, Jian’an, Scott, Robert A., Stirrups, Kathleen, Marouli, Eirini, Karpe, Fredrik, Poulter, Neil, Rolandsson, Olov, Chambers, John C., Kooner, Jaspal S., Wareham, Nicholas J., Renström, Frida, Hallmans, Göran, Marioni, Riccardo E., Corley, Janie, Starr, John M., van der Meer, Peter, Yavas, Ersin, Vaartjes, Ilonca, Asselbergs, Folkert W., Grabe, Hans J., Nauck, Matthias, Pharoah, Paul D.P., Dunning, Alison M., Dennis, Joe G., Tyrrell, Jessica, Mihailov, Evelin, Metspalu, Andres, Palmer, Colin N.A., Hall, Ian P., Strachan, David P., Understanding Society Scientific Group, Munroe, Patricia B., Jansson, Jan-Håkan, Franks, Paul W., Deloukas, Panos, Chou, Yi-Ling, Faul, Jessica D., Hammerschlag, Anke R., Hsu, Chris, Lai, Dongbing, Le, Nhung, Loukola, Anu, Mangino, Massimo, Melbourne, Carl A., Pistis, Giorgio, Qaiser, Beenish, Stringham, Heather, Wetherill, Leah, Bierut, Laura, Chen, Chu, Eaton, Charles B., Iacono, William G., Polderman, Tinca J., Schlessinger, David, Scholte, H. Steven, Smith, Jennifer A., Boehnke, Michael, Cucca, Francesco, David, Sean P., Foroud, Tatiana, Kardia, Sharon L.R., Madden, Pamela, McGue, Matt, Posthuma, Danielle, Spector, Timothy, Stram, Daniel, Kaprio, Jaakko, Vrieze, Scott

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Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error von Ikram, M. Kamran, Barathi, Veluchamy A., Kemp, John P., Wang, Ya Xing, Wright, Alan F., Amin, Najaf, Tay, Wan-Ting, Hayward, Caroline, Polasek, Ozren, Vatavuk, Zoran, Pang, Chi Pui, Wegner, Aharon, Yip, Shea Ping, Murgia, Federico, Portas, Laura, Ang, Wei, Fan, Qiao, Zhou, Xin, Iyengar, Sudha K., Vital, Mark, Yoo, Sonia, Maguire, Leo, McCulley, James, Renucci, Ann, Oliva, Matt, Brown, Marlene, Reeves, Sherman, Hamilton, Stephen, Kelly, Kathleen, Shaughnessy, Michael, Steinemann, Thomas, Mifflin, Mark, Chodosh, James, Galentine, Paul G., Mannis, Mark, Varma, Rohit, Wedenoja, Juho, Mirshahi, Alireza, Brown, Matthew A., Corvin, Aiden, Duncanson, Audrey, Markus, Hugh S., Rautanen, Anna, Viswanathan, Ananth C., Giannoulatou, Eleni, Donnelly, Peter, Hammond, Naomi, McCann, Owen T., Ricketts, Michelle, Widaa, Sara, Yonova-Doing, Ekaterina, Klein, Ronald, Miller, D., Whitehouse, F., McLellan, M., Golden, E., Arrigg, P., Gauthier-Kelly, C., Lopes-Virella, M., Colwell, J., Farr, A., Elsing, S., Kaminski, L., Lorenzi, G., Johnsonbaugh, S., Liss, R., Gordon, J., Martin, C.L., Pop-Busui, R., Smith, A., Gothrup, J., Prosser, L., Schwartz, S., Maschak-Carey, B.J., Morrison, A., Meyer, D., Strowig, S., Gordon, A., Hokanson, J., Ginsberg, J., Van Ottingham, L., Harth, J., May, M., Adkins, T., White, N., Fradkin, J., Siebert, C., Danis, R., Dingledine, J., Chavers, B., Burzuk, B., Low, P., Wong, N., Fox, M., Clark, C., Zhang, L., Pang, Chi Pui, Inoko, Hidetoshi, Mitchell, Paul, Stambolian, Dwight

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Polygenic risk prediction: why and when out-of-sample prediction R2 can exceed SNP-based heritability von Wang, Xiaotong, Revez, Joana A., Ni, Guiyan, Adams, Mark J., McIntosh, Andrew M., Ripke, Stephan, Trzaskowski, Maciej, Byrne, Enda M., Adams, Mark J., Air, Tracy M., Andlauer, Till F.M., Bacanu, Silviu-Alin, Bryois, Julien, Bybjerg-Grauholm, Jonas, Castelao, Enrique, Clarke, Toni-Kim, Colodro-Conde, Lucía, Couvy-Duchesne, Baptiste, Craddock, Nick, Davies, Gail, Derks, Eske M., Direk, Nese, Dolan, Conor V., Kiadeh, Farnush Farhadi Hassan, Gaspar, Héléna A., Gill, Michael, Goes, Fernando S., Gordon, Scott D., Grove, Jakob, Hall, Lynsey S., Homuth, Georg, Horn, Carsten, Jones, Ian, Jones, Lisa A., Jorgenson, Eric, Kraft, Julia, Kretzschmar, Warren W., Li, Yihan, MacIntyre, Donald J., MacKinnon, Dean F., Maier, Wolfgang, Marchini, Jonathan, Mbarek, Hamdi, McGuffin, Peter, Medland, Sarah E., Mehta, Divya, Middeldorp, Christel M., Mihailov, Evelin, Mondimore, Francis M., Montgomery, Grant W., Mullins, Niamh, Ng, Bernard, Nivard, Michel G., Nyholt, Dale R., Oskarsson, Hogni, Owen, Michael J., Bøcker Pedersen, Carsten, Giørtz Pedersen, Marianne, Peterson, Roseann E., Pistis, Giorgio, Saeed Mirza, Saira, Schoevers, Robert, Schulte, Eva C., Shen, Ling, Shi, Jianxin, Shyn, Stanley I., Sinnamon, Grant C.B., Smit, Johannes H., Stefansson, Hreinn, Strohmaier, Jana, Trubetskoy, Vassily, Uitterlinden, André G., Van der Auwera, Sandra, van Hemert, Albert M., Visscher, Peter M., Wang, Yunpeng, Weinsheimer, Shantel Marie, Wellmann, Jürgen, Willemsen, Gonneke, Xi, Hualin S., Berger, Klaus, Kendler, Kenneth S., Lewis, Glyn, Li, Qingqin S., Madden, Pamela A.F., McIntosh, Andrew M., Metspalu, Andres, Mors, Ole, Nöthen, Markus M., O'Donovan, Michael C., Paciga, Sara A., Pedersen, Nancy L., Porteous, David J., Potash, James B., Rietschel, Marcella, Smoller, Jordan W., Stefansson, Kari, Tiemeier, Henning, Völzke, Henry, Weissman, Myrna M.

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Features of the Left Ventricular Functional Geometry in Patients with Myocardial Diseases with Varying Degrees of Systolic Dysfunction von Chumarnaya, T. V., Alueva, Yu. S., Kochmasheva, V. V., Mihailov, S. P., Revishvili, A. Sh, Tsyv’ian, P. B., Solov’eva, O. E.

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