Development and evaluation of a notes pelvictrainer von Crouzet, Sebastien, Haber, Georges-Pascal, Kamoi, Kazumi, Bergen, Andre, Gatmaitan, Patrick, Gill, Inderbir

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The DNA-binding factor Ctcf critically controls gene expression in macrophages von Nikolic, Tatjana, Movita, Dowty, Lambers, Margaretha EH, de Almeida, Claudia Ribeiro, Biesta, Paula, Kreefft, Kim, de Bruijn, Marjolein JW, Bergen, Ingrid, Galjart, Niels, Boonstra, Andre, Hendriks, Rudi

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Budgeted Matching and Budgeted Matroid Intersection Via the Gasoline Puzzle von Berger, André, Bonifaci, Vincenzo, Grandoni, Fabrizio, Schäfer, Guido

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Comprehensive cellular-resolution atlas of the adult human brain von Ding, Song-Lin, Royall, Joshua J., Sunkin, Susan M., Ng, Lydia, Facer, Benjamin A.C., Lesnar, Phil, Guillozet-Bongaarts, Angie, McMurray, Bergen, Szafer, Aaron, Dolbeare, Tim A., Stevens, Allison, Tirrell, Lee, Benner, Thomas, Caldejon, Shiella, Dalley, Rachel A., Dee, Nick, Lau, Christopher, Nyhus, Julie, Reding, Melissa, Riley, Zackery L., Sandman, David, Shen, Elaine, van der Kouwe, Andre, Varjabedian, Ani, Write, Michelle, Zollei, Lilla, Dang, Chinh, Knowles, James A., Koch, Christof, Phillips, John W., Sestan, Nenad, Wohnoutka, Paul, Zielke, H. Ronald, Hohmann, John G., Jones, Allan R., Bernard, Amy, Hawrylycz, Michael J., Hof, Patrick R., Fischl, Bruce, Lein, Ed S.

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Dysbiotic gut microbiota causes transmissible Crohn's disease-like ileitis independent of failure in antimicrobial defence von Schaubeck, Monika, Clavel, Thomas, Calasan, Jelena, Lagkouvardos, Ilias, Haange, Sven Bastiaan, Jehmlich, Nico, Basic, Marijana, Dupont, Aline, Hornef, Mathias, Bergen, Martin von, Bleich, André, Haller, Dirk

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Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets von Zhao, Jing Hua, Stacey, David, Eriksson, Niclas, Macdonald-Dunlop, Erin, Hedman, Åsa K., Kalnapenkis, Anette, Enroth, Stefan, Cozzetto, Domenico, Digby-Bell, Jonathan, Marten, Jonathan, Folkersen, Lasse, Herder, Christian, Jonsson, Lina, Bergen, Sarah E., Gieger, Christian, Needham, Elise J., Surendran, Praveen, Paul, Dirk S., Polasek, Ozren, Thorand, Barbara, Grallert, Harald, Roden, Michael, Võsa, Urmo, Esko, Tonu, Hayward, Caroline, Johansson, Åsa, Gyllensten, Ulf, Powell, Nick, Hansson, Oskar, Mattsson-Carlgren, Niklas, Joshi, Peter K., Danesh, John, Padyukov, Leonid, Klareskog, Lars, Landén, Mikael, Wilson, James F., Siegbahn, Agneta, Wallentin, Lars, Mälarstig, Anders, Butterworth, Adam S., Peters, James E.

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A genome-wide association study of optic disc parameters von Ramdas, Wishal D, van Koolwijk, Leonieke M E, Ikram, M Kamran, Jansonius, Nomdo M, de Jong, Paulus T V M, Bergen, Arthur A B, Isaacs, Aaron, Amin, Najaf, Aulchenko, Yurii S, Wolfs, Roger C W, Hofman, Albert, Rivadeneira, Fernando, Oostra, Ben A, Uitterlinden, Andre G, Hysi, Pirro, Hammond, Christopher J, Lemij, Hans G, Vingerling, Johannes R, Klaver, Caroline C W, van Duijn, Cornelia M

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Complement Factor H Polymorphism, Complement Activators, and Risk of Age-Related Macular Degeneration von Despriet, Dominiek D. G, Klaver, Caroline C. W, Witteman, Jacqueline C. M, Bergen, Arthur A. B, Kardys, Isabella, de Maat, Moniek P. M, Boekhoorn, Sharmila S, Vingerling, Johannes R, Hofman, Albert, Oostra, Ben A, Uitterlinden, André G, Stijnen, Theo, van Duijn, Cornelia M, de Jong, Paulus T. V. M

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Complement Component C3 and Risk of Age-Related Macular Degeneration von Despriet, Dominiek D.G., MD, PhD, van Duijn, Cornelia M., PhD, Oostra, Ben A., PhD, Uitterlinden, Andre G., PhD, Hofman, Albert, MD, PhD, Wright, Alan F., PhD, ten Brink, Jacoline B., Ing, Bakker, Arne, de Jong, Paulus T.V.M., MD, PhD, Vingerling, Johannes R., MD, PhD, Bergen, Arthur A.B., PhD, Klaver, Caroline C.W., MD, PhD

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HumanMetagenomeDB: a public repository of curated and standardized metadata for human metagenomes von Kasmanas, Jonas Coelho, Bartholomäus, Alexander, Corrêa, Felipe Borim, Tal, Tamara, Jehmlich, Nico, Herberth, Gunda, von Bergen, Martin, Stadler, Peter F, Carvalho, André Carlos Ponce de Leon Ferreira de, Nunes da Rocha, Ulisses

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Common genetic variants associated with open-angle glaucoma von RAMDAS, Wishal D, VAN KOOLWIJK, Leonieke M. E, WOLFS, Roger C. W, BRAGI WALTERS, G, JONASSON, Fridbert, WEISSCHUH, Nicole, MARDIN, Christian Y, GIBSON, Jane, ZEGERS, Richard H. C, HOFMAN, Albert, DE JONG, Paulus T. V. M, UITTERLINDEN, Andre G, LEMIJ, Hans G, OOSTRA, Ben A, THORSTEINSDOTTIR, Unnur, GRAMER, Eugen, WELGEN-LÜBEN, Ulrich C, KIRWAN, James F, BERGEN, Arthur A. B, REIS, Andre, STEFANSSON, Kari, LOTERY, Andrew J, VINGERLING, Johannes R, PASUTTO, Francesca, JANSONIUS, Nomdo M, KLAVER, Caroline C. W, VAN DUIJN, Cornelia M, CREE, Angela J, THORLEIFSSON, Gudmar, JANSSEN, Sarah F, BRINK JACOLINE, Ten, AMIN, Najaf, RIVADENEIRA, Fernando

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Integrated genomic and molecular characterization of cervical cancer von Saller, Charles, Tarvin, Katherine, Yau, Christina, Robertson, A. Gordon, Mungall, Karen, Lim, Lynette, Mar, Richard, Clarke, Amanda, Tam, Angela, Dhalla, Noreen, Carlsen, Rebecca, Holt, Robert A, Jones, Steven J. M, Hadjipanayis, Angela, Seidman, Jonathan, Rabeno, Brenda, Huelsenbeck-Dill, Lori, Iacocca, Mary, Petrelli, Nicholas, Adebamowo, Sally N, Adebamowo, Clement, Shelton, Candace, Crain, Daniel, Mallery, David, Curley, Erin, Gardner, Johanna, Shelton, Troy, Wu, Ye, Birrer, Michael, Miller, Christopher A, Fulton, Robert S, Appelbaum, Elizabeth L, Rader, Janet S, Behmaram, Behnaz, Bradley, William, Wrangle, John, Schultz, Nikolaus, Ladanyi, Marc, Felau, Ina, Zenklusen, Jean C, Demchok, John A, Sheth, Margi, Ferguson, Martin L, Tarnuzzer, Roy, Zhang, Jiashan, Wang, Zhining, Olaniyan, Olayinka, Sofia, Heidi J, Chen, Zhong, Saleh, Anthony D, Cheng, Hui, Parfitt, Jeremy, Albert, Monique, Sekhon, Harman, Gilbert, Sebastien, Myers, Jerome, Tucker, Kelinda, Lester, Jenny, Wan, Yunhu, Miller, Judy, Cherniack, Andrew D, Meyerson, Matthew, Voet, Doug, Kim, Jaegil, Lawrence, Michael S, Gehlenborg, Nils, Lin, Pei, Gabriel, Stacey B, Schumacher, Steven E, Leraas, Kristen M, Gastier-Foster, Julie M, Danilova, Ludmila, Salvesen, Helga B, Ju, Zhenlin, Diao, Lixia, Zhao, Hao, Ryan, Michael C, Averett Byers, Lauren, Yuan, Yuan, Bristow, Christopher A, Shaw, Kenna R. Mills, Radenbaugh, Amie, Chalise, Prabhakar, Godwin, Andrew K, Auman, J. Todd, Perou, Charles M, Veluvolu, Umadevi, Rathmell, W. Kimryn, Simons, Janae V, Mose, Lisle E, Shi, Yan, Thorne, Leigh B, Walker, Joan, Moore, Kathleen, McMeekin, Scott, Nelson, Tina, Bhargava, Rohit, Bootwalla, Moiz S, Triche, Timothy, Jr, Agnew, Kathy J

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Author Correction: Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets von Zhao, Jing Hua, Stacey, David, Eriksson, Niclas, Macdonald-Dunlop, Erin, Hedman, Åsa K., Kalnapenkis, Anette, Enroth, Stefan, Cozzetto, Domenico, Digby-Bell, Jonathan, Marten, Jonathan, Folkersen, Lasse, Herder, Christian, Jonsson, Lina, Bergen, Sarah E., Gieger, Christian, Needham, Elise J., Surendran, Praveen, Paul, Dirk S., Polasek, Ozren, Thorand, Barbara, Grallert, Harald, Roden, Michael, Võsa, Urmo, Esko, Tonu, Hayward, Caroline, Johansson, Åsa, Gyllensten, Ulf, Powell, Nick, Hansson, Oskar, Mattsson-Carlgren, Niklas, Joshi, Peter K., Danesh, John, Padyukov, Leonid, Klareskog, Lars, Landén, Mikael, Wilson, James F., Siegbahn, Agneta, Wallentin, Lars, Mälarstig, Anders, Butterworth, Adam S., Peters, James E.

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Genomic sequencing highlights the diverse molecular causes of Perrault syndrome: a peroxisomal disorder (PEX6), metabolic disorders (CLPP, GGPS1), and mtDNA maintenance/translation... von Tucker, Elena J., Rius, Rocio, Jaillard, Sylvie, Bell, Katrina, Lamont, Phillipa J., Travessa, André, Dupont, Juliette, Sampaio, Lurdes, Dulon, Jérôme, Vuillaumier-Barrot, Sandrine, Whalen, Sandra, Isapof, Arnaud, Stojkovic, Tanya, Quijano-Roy, Susana, Robevska, Gorjana, van den Bergen, Jocelyn, Hanna, Chloe, Simpson, Andrea, Ayers, Katie, Thorburn, David R., Christodoulou, John, Touraine, Philippe, Sinclair, Andrew H.

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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.

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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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The ERCC6 gene and age-related macular degeneration von Baas, Dominique C, Despriet, Dominiek D, Gorgels, Theo G M F, Bergeron-Sawitzke, Julie, Uitterlinden, André G, Hofman, Albert, van Duijn, Cornelia M, Merriam, Joanna E, Smith, R Theodore, Barile, Gaetano R, ten Brink, Jacoline B, Vingerling, Johannes R, Klaver, Caroline C W, Allikmets, Rando, Dean, Michael, Bergen, Arthur A B

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DNGR1-mediated deletion of A20/Tnfaip3 in dendritic cells alters T and B-cell homeostasis and promotes autoimmune liver pathology von Das, Tridib, Bergen, Ingrid M., Koudstaal, Thomas, van Hulst, Jennifer A.C., van Loo, Geert, Boonstra, André, Vanwolleghem, Thomas, Leung, Patrick S.C., Gershwin, M. Eric, Hendriks, Rudi W., Kool, Mirjam

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A common polymorphism in the complement factor H gene is associated with increased risk of myocardial infarction: the Rotterdam Study von Kardys, Isabella, Klaver, Caroline C W, Despriet, Dominiek D G, Bergen, Arthur A B, Uitterlinden, André G, Hofman, Albert, Oostra, Ben A, Van Duijn, Cornelia M, de Jong, Paulus T V M, Witteman, Jacqueline C M

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Clonal hematopoiesis in patients with stem cell mobilization failure: a nested case-control study von Hazenberg, Carin L. E., de Graaf, Aniek O., Mulder, René, Bungener, Laura B., van Bergen, Maaike G. J. M., Mulder, André B., Choi, Goda, Schuringa, Jan Jacob, de Groot, Marco R., Vellenga, Edo, Jansen, Joop H., Huls, Gerwin, van Zeventer, Isabelle A.

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