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How much should we sequence? An analysis of the Swiss SARS-CoV-2 surveillance effort Wegner, Fanny; Cabrera-Gil, Blanca; Tanguy, Araud; Beckmann, Christiane; Beerenwinkel, Niko; Bertelli, Claire; Carrara, Matteo; Cerutti, Lorenzo; Chen, Chaoran; Cordey, Samuel; Dumoulin, Alexis; du Plessis, Louis; Friedli, Marc; Gerth, Yannick; Greub, Gilbert; Haerri, Adrian; Hirsch, Hans; Howald, Cedric; Huber, Michael; Imhof, Alexander; Kaiser, Laurent; Kufner, Verena; Leib, Stephen L.; Leuzinger, Karoline; Lleshi, Etleva; Martinetti, Gladys; Maeusezahl, Mirjam; Moraz, Milo; Neher, Richard; Nolte, Oliver; Ramette, Alban; Redondo, Maurice; Risch, Lorenz; Rohner, Lionel; Roloff, Tim; Schlaeepfer, Pascal; Schneider, Katrin; Singer, Franziska; Spina, Valeria; Stadler, Tanja; Studer, Erik; Topolsky, Ivan; Trkola, Alexandra; Walther, Daniel; Wohlwend, Nadia; Zehnder, Cinzia; Neves, Aitana; Egli, Adrian 分享 收藏
Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits 血液分子表型的遗传分析揭示了影响复杂性状的调控网络中的共同特性 Brown, Andrew A.; Fernandez-Tajes, Juan A.; Hong, Mun-gwan W.; Brorsson, Caroline A.; Koivula, Robert W.; Davtian, David; Dupuis, Theo; Sartori, Ambra M.; Michalettou, Theodora-Dafni; Forgie, Ian H.; Adam, Jonathan; Allin, Kristine; Caiazzo, Robert; Cederberg, Henna; De Masi, Federico N.; Elders, Petra J. M.; Giordano, Giuseppe; Haid, Mark; Hansen, Torben; Hansen, Tue H.; Hattersley, Andrew T.; Heggie, Alison G.; Howald, Cedric; Jones, Angus G.; Kokkola, Tarja; Laakso, Markku; Mahajan, Anubha; Mari, Andrea; McDonald, Timothy J.; McEvoy, Donna; Mourby, Miranda; Musholt, Petra B.; Nilsson, Birgitte; Pattou, Francois; Penet, Deborah; Raverdy, Violeta; Ridderstrale, Martin; Romano, Luciana; Rutters, Femke; Sharma, Sapna; Teare, Harriet D.; 't Hart, Leen; Tsirigos, Konstantinos D.; Vangipurapu, Jagadish; Vestergaard, Henrik; Brunak, Soren; Franks, Paul; Frost, Gary; Grallert, Harald I.; Jablonka, Bernd; McCarthy, Mark, I; Pavo, Imre; Pedersen, Oluf; Ruetten, Hartmut; Walker, Mark; Adamski, Jerzy; Schwenk, Jochen M.; Pearson, Ewan R.; Dermitzakis, Emmanouil T.; Vinuela, Ana; Adragni, Kofi; Allesoe, Rosa Lundbye L. A.; Artati, Anna; Arumugam, Manimozhiyan; Atabaki-Pasdar, Naeimeh; Baltauss, Tania; Banasik, Karina; Barnett, Anna L.; Baum, Patrick; Bell, Jimmy D.; Beulens, Joline B.; Bianzano, Susanna; Bizzotto, Roberto; Bonnefond, Amelie; Cabrelli, Louise; Dale, Matilda; Dawed, Adem Y.; de Preville, Nathalie; Dekkers, Koen F.; Deshmukh, Harshal A.; Dings, Christiane; Donnelly, Louise; Dutta, Avirup; Ehrhardt, Beate; Engelbrechtsen, Line; Eriksen, Rebeca; Fan, Yong; Ferrer, Jorge; Fitipaldi, Hugo; Forman, Annemette; Fritsche, Andreas; Froguel, Philippe; Gassenhuber, Johann; Gough, Stephen; Graefe-Mody, Ulrike; Grempler, Rolf; Groeneveld, Lenka; Groop, Leif; Gudmundsdottir, Valborg; Gupta, Ramneek; Hennige, Anita M. H.; Hill, Anita V.; Holl, Reinhard W.; Hudson, Michelle; Jacobsen, Ulrik Plesner; Jennison, Christopher; Johansen, Joachim; Jonsson, Anna; Karaderi, Tugce; Kaye, Jane; Kennedy, Gwen; Klintenberg, Maria; Kuulasmaa, Teemu; Lehr, Thorsten; Loftus, Heather; Lundgaard, Agnete Troen T.; Mazzoni, Gianluca; McRobert, Nicky; McVittie, Ian; Nice, Rachel; Nicolay, Claudia; Nijpels, Giel N.; Palmer, Colin K.; Pedersen, Helle H.; Perry, Mandy H.; Pomares-Millan, Hugo; Prehn, Cornelia P.; Ramisch, Anna; Rasmussen, Simon; Robertson, Neil; Rodriquez, Marianne; Sackett, Peter; Scherer, Nina; Shah, Nisha; Sihinevich, Iryna; Slieker, Roderick C.; Sondertoft, Nadja B.; Steckel-Hamann, Birgit; Thomas, Melissa K.; Thomas, Cecilia Engel E.; Thomas, Elizabeth Louise L.; Thorand, Barbara; Thorne, Claire E.; Tillner, Joachim; Tura, Andrea; Uhlen, Mathias; van Leeuwen, Nienke; van Oort, Sabine; Verkindt, Helene; Vogt, Josef; Wad Sackett, Peter W.; Wesolowska-Andersen, Agata; Whitcher, Brandon; White, Margaret W. 分享 收藏
Integrated multi-omics reveals anaplerotic rewiring in methylmalonyl-CoA mutase deficiency 整合的多组学揭示了甲基丙二酰辅酶a突变酶缺乏症的回补重布线 Forny, Patrick; Bonilla, Ximena; Lamparter, David; Shao, Wenguang; Plessl, Tanja; Frei, Caroline; Bingisser, Anna; Goetze, Sandra; van Drogen, Audrey; Harshman, Keith; Pedrioli, Patrick G. A.; Howald, Cedric; Poms, Martin; Traversi, Florian; Burer, Celine; Cherkaoui, Sarah; Morscher, Raphael J.; Simmons, Luke; Forny, Merima; Xenarios, Ioannis; Aebersold, Ruedi; Zamboni, Nicola; Ratsch, Gunnar; Dermitzakis, Emmanouil T.; Wollscheid, Bernd; Baumgartner, Matthias R.; Froese, D. Sean 分享 收藏
Genetic variant effects on gene expression in human pancreatic islets and their implications for T2D Vinuela, Ana; Varshney, Arushi; van de Bunt, Martijn; Prasad, Rashmi B.; Asplund, Olof; Bennett, Amanda; Boehnke, Michael; Brown, Andrew A.; Erdos, Michael R.; Fadista, Joao; Hansson, Ola; Hatem, Gad; Howald, Cedric; Iyengar, Apoorva K.; Johnson, Paul; Krus, Ulrika; MacDonald, Patrick E.; Mahajan, Anubha; Manning Fox, Jocelyn E.; Narisu, Narisu; Nylander, Vibe; Orchard, Peter; Oskolkov, Nikolay; Panousis, Nikolaos I.; Payne, Anthony; Stitzel, Michael L.; Vadlamudi, Swarooparani; Welch, Ryan; Collins, Francis S.; Mohlke, Karen L.; Gloyn, Anna L.; Scott, Laura J.; Dermitzakis, Emmanouil T.; Groop, Leif; Parker, Stephen C. J.; McCarthy, Mark I. 分享 收藏
Cellular circadian period length inversely correlates with HbA1c levels in individuals with type 2 diabetes Sinturel, Flore; Makhlouf, Anne-Marie; Meyer, Patrick; Tran, Christel; Pataky, Zoltan; Golay, Alain; Rey, Guillaume; Howald, Cedric; Dermitzakis, Emmanouil T.; Pichard, Claude; Philippe, Jacques; Brown, Steven A.; Dibner, Charna 分享 收藏
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Transcriptomic analyses reveal rhythmic and CLOCK-driven pathways in human skeletal muscle Perrin, Laurent; Loizides-Mangold, Ursula; Chanon, Stephanie; Gobet, Cedric; Hulo, Nicolas; Isenegger, Laura; Weger, Benjamin D.; Migliavacca, Eugenia; Charpagne, Aline; Betts, James A.; Walhin, Jean-Philippe; Templeman, Lain; Stokes, Keith; Thompson, Dylan; Tsintzas, Kostas; Robert, Maud; Howald, Cedric; Riezman, Howard; Feige, Jerome N.; Karagounis, Leonidas G.; Johnston, Jonathan D.; Dermitzakis, Emmanouil T.; Gachon, Frederic; Lefai, Etienne; Dibner, Charna 分享 收藏
The genomic landscape of human cellular circadian variation points to a novel role for the signalosome Gaspar, Ludmila; Howald, Cedric; Popadin, Konstantin; Maier, Bert; Mauvoisin, Daniel; Moriggi, Ermanno; Gutierrez-Arcelus, Maria; Falconnet, Emilie; Borel, Christelle; Kunz, Dieter; Kramer, Achim; Gachon, Frederic; Dermitzakis, Emmanouil T.; Antonarakis, Stylianos E.; Brown, Steven A. 分享 收藏
Extension of human lncRNA transcripts by RACE coupled with long-read high-throughput sequencing (RACE-Seq) Lagarde, Julien; Uszczynska-Ratajczak, Barbara; Santoyo-Lopez, Javier; Gonzalez, Jose Manuel; Tapanari, Electra; Mudge, Jonathan M.; Steward, Charles A.; Wilming, Laurens; Tanzer, Andrea; Howald, Cedric; Chrast, Jacqueline; Vela-Boza, Alicia; Rueda, Antonio; Lopez-Domingo, Francisco J.; Dopazo, Joaquin; Reymond, Alexandre; Guigo, Roderic; Harrow, Jennifer 分享 收藏
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Genome-wide analyses implicate 33 loci in heritable dog osteosarcoma, including regulatory variants near CDKN2A/B Karlsson, Elinor K.; Sigurdsson, Snaevar; Ivansson, Emma; Thomas, Rachael; Elvers, Ingegerd; Wright, Jason; Howald, Cedric; Tonomura, Noriko; Perloski, Michele; Swofford, Ross; Biagi, Tara; Fryc, Sarah; Anderson, Nathan; Courtay-Cahen, Celine; Youell, Lisa; Ricketts, Sally L.; Mandlebaum, Sarah; Rivera, Patricio; von Euler, Henrik; Kisseberth, William C.; London, Cheryl A.; Lander, Eric S.; Couto, Guillermo; Comstock, Kenine; Starkey, Mike P.; Modiano, Jaime F.; Breen, Matthew; Lindblad-Toh, Kerstin 分享 收藏
GENCODE: The reference human genome annotation for The ENCODE Project GENCODE: ENCODE项目的参考人类基因组注释 Harrow, Jennifer; Frankish, Adam; Gonzalez, Jose M.; Tapanari, Electra; Diekhans, Mark; Kokocinski, Felix; Aken, Bronwen L.; Barrell, Daniel; Zadissa, Amonida; Searle, Stephen; Barnes, If; Bignell, Alexandra; Boychenko, Veronika; Hunt, Toby; Kay, Mike; Mukherjee, Gaurab; Rajan, Jeena; Despacio-Reyes, Gloria; Saunders, Gary; Steward, Charles; Harte, Rachel; Lin, Michael; Howald, Cedric; Tanzer, Andrea; Derrien, Thomas; Chrast, Jacqueline; Walters, Nathalie; Balasubramanian, Suganthi; Pei, Baikang; Tress, Michael; Manuel Rodriguez, Jose; Ezkurdia, Iakes; van Baren, Jeltje; Brent, Michael; Haussler, David; Kellis, Manolis; Valencia, Alfonso; Reymond, Alexandre; Gerstein, Mark; Guigo, Roderic; Hubbard, Tim J. 分享 收藏
Combining RT-PCR-seq and RNA-seq to catalog all genic elements encoded in the human genome Howald, Cedric; Tanzer, Andrea; Chrast, Jacqueline; Kokocinski, Felix; Derrien, Thomas; Walters, Nathalie; Gonzalez, Jose M.; Frankish, Adam; Aken, Bronwen L.; Hourlier, Thibaut; Vogel, Jan-Hinnerk; White, Simon; Searle, Stephen; Harrow, Jennifer; Hubbard, Tim J.; Guigo, Roderic; Reymond, Alexandre 分享 收藏
The GENCODE pseudogene resource Pei, Baikang; Sisu, Cristina; Frankish, Adam; Howald, Cedric; Habegger, Lukas; Mu, Xinmeng Jasmine; Harte, Rachel; Balasubramanian, Suganthi; Tanzer, Andrea; Diekhans, Mark; Reymond, Alexandre; Hubbard, Tim J.; Harrow, Jennifer; Gerstein, Mark B. 分享 收藏
An atypical 7q11.23 deletion in a normal IQ Williams-Beuren syndrome patient Ferrero, Giovanni Battista; Howald, Cedric; Micale, Lucia; Biamino, Elisa; Augello, Bartolomeo; Fusco, Carmela; Turturo, Maria Giuseppina; Forzano, Serena; Reymond, Alexandre; Merla, Giuseppe 分享 收藏
Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11 Marshall, Christian R.; Young, Edwin J.; Pani, Ariel M.; Freckmann, Mary-Louise; Lacassie, Yves; Howald, Cedric; Fitzgerald, Kristi K.; Peippo, Maarit; Morris, Colleen A.; Shane, Kate; Priolo, Manuela; Morimoto, Masafumi; Kondo, Ikuko; Manguoglu, Esra; Berker-Karauzum, Sibel; Edery, Patrick; Hobart, Holly H.; Mervis, Carolyn B.; Zuffardi, Orsetta; Reymond, Alexandre; Kaplan, Paige; Tassabehji, May; Gregg, Ronald G.; Scherer, Stephen W.; Osborne, Lucy R. 分享 收藏
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Two high throughput technologies to detect segmental aneuploidies identify new Williams-Beuren syndrome patients with atypical deletions Howald, C; Merla, G; Digilio, MC; Amenta, S; Lyle, R; Deutsch, S; Choudhury, U; Bottani, A; Antonarakis, SE; Fryssira, H; Dallapiccola, B; Reymond, A 分享 收藏
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