Exploring and visualizing large-scale genetic associations by using PheWeb von Gagliano Taliun, Sarah A., VandeHaar, Peter, Boughton, Andrew P., Welch, Ryan P., Taliun, Daniel, Schmidt, Ellen M., Zhou, Wei, Nielsen, Jonas B., Willer, Cristen J., Lee, Seunggeun, Fritsche, Lars G., Boehnke, Michael, Abecasis, Gonçalo R.

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Efficient haplotype block recognition of very long and dense genetic sequences von Taliun, Daniel, Gamper, Johann, Pattaro, Cristian

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GWAtoolbox: an R package for fast quality control and handling of genome-wide association studies meta-analysis data von Fuchsberger, Christian, Taliun, Daniel, Pramstaller, Peter P., Pattaro, Cristian

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Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association Studies von Wojcik, Genevieve L, Fuchsberger, Christian, Taliun, Daniel, Welch, Ryan, Martin, Alicia R, Shringarpure, Suyash, Carlson, Christopher S, Abecasis, Goncalo, Kang, Hyun Min, Boehnke, Michael, Bustamante, Carlos D, Gignoux, Christopher R, Kenny, Eimear E

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A cost-effective sequencing method for genetic studies combining high-depth whole exome and low-depth whole genome von Bhérer, Claude, Eveleigh, Robert, Trajanoska, Katerina, St-Cyr, Janick, Paccard, Antoine, Nadukkalam Ravindran, Praveen, Caron, Elizabeth, Bader Asbah, Nimara, McClelland, Peyton, Wei, Clare, Baumgartner, Iris, Schindewolf, Marc, Döring, Yvonne, Perley, Danielle, Lefebvre, François, Lepage, Pierre, Bourgey, Mathieu, Bourque, Guillaume, Ragoussis, Jiannis, Mooser, Vincent, Taliun, Daniel

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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 von 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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P710: Phenome-wide association study (PheWAS) for the Canadian HostSeq Biobank von Frangione, Erika, Xinyi, Xu, Chapdelaine, Vincent, Casalino, Selina, Aujla, Navneet, Mahajan, Radhika, Jayachandran, Lochana, Morgan, Gregory, Scott, Mackenzie, Young, Juliet, Dickson, Brendan, Arnoldo, Saranya, Bearss, Erin, Binnie, Alexandra, Borgundvaag, Bjug, Chertkow, Howard, Clausen, Marc, Dagher, Marc, Devine, Luke, Friedman, Steven, Gingras, Anne-Claude, Goneau, Lee, Kaushik, Deepanjali, Khan, Zeeshan, Lapadula, Elisa, MacDonald, Georgia, Mazzulli, Tony, McGeer, Allison, McLeod, Shelley, Mighton, Chloe, Pugh, Trevor, Richardson, David, Simpson, Jared, Stern, Seth, Strug, Lisa, Taher, Ahmed, Wong, Iris, Zarei, Natasha, Greenfeld, Elena, Bombard, Yvonne, Noor, Abdul, Faghfoury, Hanna, Taher, Jennifer, Taliun, Daniel, Lerner-Ellis, Jordan

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From target discovery to clinical drug development with human genetics von Trajanoska, Katerina, Bhérer, Claude, Taliun, Daniel, Zhou, Sirui, Richards, J. Brent, Mooser, Vincent

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LocusZoom.js: interactive and embeddable visualization of genetic association study results von Boughton, Andrew P., Welch, Ryan P., Flickinger, Matthew, VandeHaar, Peter, Taliun, Daniel, Abecasis, Goncalo R., Boehnke, Michael

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A global reference for human genetic variation von Auton, Adam, Brooks, Lisa D, Durbin, Richard M, Garrison, Erik P, Kang, Hyun Min, Korbel, Jan O, Marchini, Jonathan L, McCarthy, Shane, McVean, Gil A, Abecasis, Gonçalo R

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Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks von Fritsche, Lars G., Patil, Snehal, Beesley, Lauren J., VandeHaar, Peter, Salvatore, Maxwell, Ma, Ying, Peng, Robert B., Taliun, Daniel, Zhou, Xiang, Mukherjee, Bhramar

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Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article von Mahajan, Anubha, Wessel, Jennifer, Willems, Sara M, Zhao, Wei, Robertson, Neil R, Chu, Audrey Y., Kravic, Jasmina, Ahlqvist, Emma, Rosengren, Anders, Groop, Leif, V Varga, Tibor, Franks, Paul, Almgren, Peter, Melander, Olle, Orho-Melander, Marju, McCarthy, Mark I.

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Imputation Server PGS: an automated approach to calculate polygenic risk scores on imputation servers von Forer, Lukas, Taliun, Daniel, LeFaive, Jonathon, Smith, Albert V, Boughton, Andrew P, Coassin, Stefan, Lamina, Claudia, Kronenberg, Florian, Fuchsberger, Christian, Schönherr, Sebastian

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The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits von Massung, Jeffrey, Jang, Dongkeun, Gilbert, Clint, Hoang, Quy, Duby, Marc, Nguyen, Trang, Smadbeck, Patrick, Alexander, Benjamin R., Carmichael, Mary, Dornbos, Peter, Green, Todd, Ji, Yue, Kluge, Alexandria, McMahon, Aoife C., Mercader, Josep M., Sengupta, Sebanti, Spalding, Dylan, Abecasis, Gonçalo, Akolkar, Beena, Below, Jennifer E., Blangero, John, Boehnke, Michael, Bokvist, Krister, Bottinger, Erwin, Bowden, Donald, Burtt, Noël P., Cebola, Inês, Chambers, John, Ida Chen, Yii-Der, Chu, Audrey Y., Claussnitzer, Melina, Cox, Nancy J., Dong, Duc, Duggirala, Ravindranath, Ferrer, Jorge, Flannick, Jason, Flicek, Paul, Florez, Jose C., Frazer, Kelly A., Gilbert, Clint, Gloyn, Anna L., Hanis, Craig L., Hanson, Robert, Hoang, Quy, Im, Hae Kyung, Iqbal, Sidra, Jacobs, Suzanne B.R., Kamphaus, Tania, Keane, Thomas M., Kluge, Alexandria, Lange, Leslie A., Liu, Ching-Ti, Loos, Ruth J.F., Ma, Ronald Ching-wan, Massung, Jeffrey, Maurano, Matthew T., McCarthy, Mark I., McVean, Gil, Meigs, James B., Mitchell, Braxton, Narendra, Sharvari, Parker, Stephen C.J., Parrado, Antonio, Pearson, Ewan R., Redline, Susan, Ren, Bing, Rich, Stephen S., Rotter, Jerome I., Ruetten, Hartmut, Salem, Rany M., Sander, Maike, Sanghera, Dharambir, Scott, Laura J., Sengupta, Sebanti, Sladek, Robert, Small, Kerrin, Stringham, Heather M., Sun, Ying, ’t Hart, Leen M., Taliun, Daniel, Thomas, Melissa K., Todd, Jennifer A., Udler, Miriam S., von Grotthuss, Marcin, Wan, Andre, Wholley, David, Yuksel, Kaan, Zaghloul, Norann A., Thomas, Melissa K., Akolkar, Beena, Cherkas, Andriy, Chu, Audrey Y., Kamphaus, Tania Nayak, Parsa, Afshin, Ruetten, Hartmut, Wholley, David, Zaghloul, Norann A., Altshuler, David, Florez, Jose C., Boehnke, Michael

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emeraLD: rapid linkage disequilibrium estimation with massive datasets von Quick, Corbin, Fuchsberger, Christian, Taliun, Daniel, Abecasis, Gonçalo, Boehnke, Michael, Kang, Hyun Min

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Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes von Teumer, Alexander, Tin, Adrienne, Sorice, Rossella, Gorski, Mathias, Yeo, Nan Cher, Chu, Audrey Y, Li, Man, Li, Yong, Mijatovic, Vladan, Ko, Yi-An, Taliun, Daniel, Luciani, Alessandro, Chen, Ming-Huei, Yang, Qiong, Foster, Meredith C, Olden, Matthias, Hiraki, Linda T, Tayo, Bamidele O, Fuchsberger, Christian, Dieffenbach, Aida Karina, Shuldiner, Alan R, Smith, Albert V, Zappa, Allison M, Lupo, Antonio, Kollerits, Barbara, Ponte, Belen, Stengel, Bénédicte, Krämer, Bernhard K, Paulweber, Bernhard, Mitchell, Braxton D, Hayward, Caroline, Helmer, Catherine, Meisinger, Christa, Gieger, Christian, Shaffer, Christian M, Müller, Christian, Langenberg, Claudia, Ackermann, Daniel, Siscovick, David, Boerwinkle, Eric, Kronenberg, Florian, Ehret, Georg B, Homuth, Georg, Waeber, Gerard, Navis, Gerjan, Gambaro, Giovanni, Malerba, Giovanni, Eiriksdottir, Gudny, Li, Guo, Wichmann, H Erich, Grallert, Harald, Wallaschofski, Henri, Völzke, Henry, Brenner, Herrmann, Kramer, Holly, Mateo Leach, I, Rudan, Igor, Hillege, Hans L, Beckmann, Jacques S, Lambert, Jean Charles, Luan, Jian'an, Zhao, Jing Hua, Chalmers, John, Coresh, Josef, Denny, Joshua C, Butterbach, Katja, Launer, Lenore J, Ferrucci, Luigi, Kedenko, Lyudmyla, Haun, Margot, Metzger, Marie, Woodward, Mark, Hoffman, Matthew J, Nauck, Matthias, Waldenberger, Melanie, Pruijm, Menno, Bochud, Murielle, Rheinberger, Myriam, Verweij, Niek, Wareham, Nicholas J, Endlich, Nicole, Soranzo, Nicole, Polasek, Ozren, van der Harst, Pim, Pramstaller, Peter Paul, Vollenweider, Peter, Wild, Philipp S, Gansevoort, Ron T, Rettig, Rainer, Biffar, Reiner, Carroll, Robert J, Katz, Ronit, Loos, Ruth J F, Hwang, Shih-Jen, Coassin, Stefan, Bergmann, Sven, Rosas, Sylvia E, Stracke, Sylvia, Harris, Tamara B, Corre, Tanguy

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De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population von Kessler, Michael D., Loesch, Douglas P., Perry, James A., Heard-Costa, Nancy L., Taliun, Daniel, Cade, Brian E., Wang, Heming, Daya, Michelle, Ziniti, John, Datta, Soma, Celedón, Juan C., Soto-Quiros, Manuel E., Avila, Lydiana, Weiss, Scott T., Barnes, Kathleen, Redline, Susan S., Vasan, Ramachandran S., Johnson, Andrew D., Mathias, Rasika A., Hernandez, Ryan, Wilson, James G., Nickerson, Deborah A., Abecasis, Goncalo, Browning, Sharon R., Zöllne, Sebastian, O’Connell, Jeffrey R., Mitchell, Braxton D., O’Connor, Timothy D.

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LASER server: ancestry tracing with genotypes or sequence reads von Taliun, Daniel, Chothani, Sonia P, Schönherr, Sebastian, Forer, Lukas, Boehnke, Michael, Abecasis, Gonçalo R, Wang, Chaolong

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Fast Sampling-Based Whole-Genome Haplotype Block Recognition von Taliun, Daniel, Gamper, Johann, Leser, Ulf, Pattaro, Cristian

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FamAgg: an R package to evaluate familial aggregation of traits in large pedigrees von Rainer, Johannes, Taliun, Daniel, D'Elia, Yuri, Pattaro, Cristian, Domingues, Francisco S, Weichenberger, Christian X

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