A comparative genomics multitool for scientific discovery and conservation von Genereux, Diane P., Serres, Aitor, Armstrong, Joel, Johnson, Jeremy, Marinescu, Voichita D., Muren, Eva, Juan, David, Bejerano, Gill, Casewell, Nicholas R., Chemnick, Leona G., Damas, Joana, Di Palma, Federica, Diekhans, Mark, Fiddes, Ian T., Garber, Manuel, Gladyshev, Vadim N., Goodman, Linda, Haerty, Wilfried, Houck, Marlys L., Hubley, Robert, Kivioja, Teemu, Koepfli, Klaus-Peter, Kuderna, Lukas F. K., Lander, Eric S., Meadows, Jennifer R. S., Murphy, William J., Nash, Will, Noh, Hyun Ji, Nweeia, Martin, Pfenning, Andreas R., Pollard, Katherine S., Ray, David A., Shapiro, Beth, Smit, Arian F. A., Springer, Mark S., Steiner, Cynthia C., Swofford, Ross, Taipale, Jussi, Teeling, Emma C., Turner-Maier, Jason, Alfoldi, Jessica, Birren, Bruce, Ryder, Oliver A., Lewin, Harris A., Paten, Benedict, Marques-Bonet, Tomas, Lindblad-Toh, Kerstin, Karlsson, Elinor K.

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Utilizing the Dog Genome in the Search for Novel Candidate Genes Involved in Glioma Development-Genome Wide Association Mapping followed by Targeted Massive Parallel Sequencing Ide... von Truvé, Katarina, Dickinson, Peter, Xiong, Anqi, York, Daniel, Jayashankar, Kartika, Pielberg, Gerli, Koltookian, Michele, Murén, Eva, Fuxelius, Hans-Henrik, Weishaupt, Holger, Swartling, Fredrik J, Andersson, Göran, Hedhammar, Åke, Bongcam-Rudloff, Erik, Forsberg-Nilsson, Karin, Bannasch, Danika, Lindblad-Toh, Kerstin

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The genetic consequences of dog breed formation-Accumulation of deleterious genetic variation and fixation of mutations associated with myxomatous mitral valve disease in cavalier... von Axelsson, Erik, Ljungvall, Ingrid, Bhoumik, Priyasma, Conn, Laura Bas, Muren, Eva, Ohlsson, Asa, Olsen, Lisbeth Hoier, Engdahl, Karolina, Hagman, Ragnvi, Hanson, Jeanette, Kryvokhyzha, Dmytro, Pettersson, Mats, Grenet, Olivier, Moggs, Jonathan, Del Rio-Espinola, Alberto, Epe, Christian, Taillon, Bruce, Tawari, Nilesh, Mane, Shrinivas, Hawkins, Troy, Hedhammar, Ake, Gruet, Philippe, Haggstrom, Jens, Lindblad-Toh, Kerstin

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Author Correction: Targeted sequencing reveals the somatic mutation landscape in a Swedish breast cancer cohort von Mathioudaki, Argyri, Ljungström, Viktor, Melin, Malin, Arendt, Maja Louise, Nordin, Jessika, Karlsson, Åsa, Murén, Eva, Saksena, Pushpa, Meadows, Jennifer R. S., Marinescu, Voichita D., Sjöblom, Tobias, Lindblad-Toh, Kerstin

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Whole-genome genotyping and resequencing reveal the association of a deletion in the complex interferon alpha gene cluster with hypothyroidism in dogs von Bianchi, Matteo, Rafati, Nima, Karlsson, Asa, Muren, Eva, Rubin, Carl-Johan, Sundberg, Katarina, Andersson, Goran, Kampe, Olle, Hedhammar, Ake, Lindblad-Toh, Kerstin, Rosengren Pielberg, Gerli

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Variants within the SP110 nuclear body protein modify risk of canine degenerative myelopathy von Ivansson, Emma L., Megquier, Kate, Kozyrev, Sergey V., Murén, Eva, Körberg, Izabella Baranowska, Swofford, Ross, Koltookian, Michele, Tonomura, Noriko, Zeng, Rong, Kolicheski, Ana L., Hansen, Liz, Katz, Martin L., Johnson, Gayle C., Johnson, Gary S., Coates, Joan R., Lindblad-Toh, Kerstin

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Genome-Wide Analysis Identifies Germ-Line Risk Factors Associated with Canine Mammary Tumours von Melin, Malin, Rivera, Patricio, Arendt, Maja, Elvers, Ingegerd, Murén, Eva, Gustafson, Ulla, Starkey, Mike, Borge, Kaja Sverdrup, Lingaas, Frode, Häggström, Jens, Saellström, Sara, Rönnberg, Henrik, Lindblad-Toh, Kerstin

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Identification and functional characterization of a novel susceptibility locus for small vessel vasculitis with MPO-ANCA von Dahlqvist, Johanna, Ekman, Diana, Sennblad, Bengt, Kozyrev, Sergey V, Nordin, Jessika, Karlsson, Åsa, Meadows, Jennifer R S, Hellbacher, Erik, Rantapää-Dahlqvist, Solbritt, Berglin, Ewa, Stegmayr, Bernd, Baslund, Bo, Palm, Øyvind, Haukeland, Hilde, Gunnarsson, Iva, Bruchfeld, Annette, Segelmark, Mårten, Ohlsson, Sophie, Mohammad, Aladdin J, Svärd, Anna, Pullerits, Rille, Herlitz, Hans, Söderbergh, Annika, Rosengren Pielberg, Gerli, Hultin Rosenberg, Lina, Bianchi, Matteo, Murén, Eva, Omdal, Roald, Jonsson, Roland, Eloranta, Maija-Leena, Rönnblom, Lars, Söderkvist, Peter, Knight, Ann, Eriksson, Per, Lindblad-Toh, Kerstin

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Association of Protective HLA-A With HLA-B∗27 Positive Ankylosing Spondylitis von Nordin, Jessika, Pettersson, Mats, Rosenberg, Lina Hultin, Mathioudaki, Argyri, Karlsson, Åsa, Murén, Eva, Tandre, Karolina, Rönnblom, Lars, Kastbom, Alf, Cedergren, Jan, Eriksson, Per, Söderkvist, Peter, Lindblad-Toh, Kerstin, Meadows, Jennifer R. S.

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Thorough investigation of a canine autoinflammatory disease (AID) confirms one main risk locus and suggests a modifier locus for amyloidosis von Olsson, Mia, Tintle, Linda, Kierczak, Marcin, Perloski, Michele, Tonomura, Noriko, Lundquist, Andrew, Murén, Eva, Fels, Max, Tengvall, Katarina, Pielberg, Gerli, Dufaure de Citres, Caroline, Dorso, Laetitia, Abadie, Jérôme, Hanson, Jeanette, Thomas, Anne, Leegwater, Peter, Hedhammar, Åke, Lindblad-Toh, Kerstin, Meadows, Jennifer R S

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Targeted sequencing reveals the somatic mutation landscape in a Swedish breast cancer cohort von Mathioudaki, Argyri, Ljungström, Viktor, Melin, Malin, Arendt, Maja Louise, Nordin, Jessika, Karlsson, Åsa, Murén, Eva, Saksena, Pushpa, Meadows, Jennifer R. S., Marinescu, Voichita D., Sjöblom, Tobias, Lindblad-Toh, Kerstin

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Combinatorial control of gene expression by the three yeast repressors Mig1, Mig2 and Mig3 von Westholm, Jakub Orzechowski, Nordberg, Niklas, Murén, Eva, Ameur, Adam, Komorowski, Jan, Ronne, Hans

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A Ham1p-dependent mechanism and modulation of the pyrimidine biosynthetic pathway can both confer resistance to 5-fluorouracil in yeast von Carlsson, Mattias, Gustavsson, Marie, Hu, Guo-Zhen, Murén, Eva, Ronne, Hans

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Rescue and Characterization of Episomally Replicating DNA from the Moss Physcomitrella von Murén, Eva, Nilsson, Anders, Ulfstedt, Mikael, Johansson, Monika, Ronne, Hans

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Association of Protective HLA-A With HLA-B27 Positive Ankylosing Spondylitis von Nordin, Jessika, Pettersson, Mats, Rosenberg, Lina Hultin, Mathioudaki, Argyri, Karlsson, Asa, Muren, Eva, Tandre, Karolina, Ronnblom, Lars, Kastbom, Alf, Cedergren, Jan, Eriksson, Per, Soderkvist, Peter, Lindblad-Toh, Kerstin, Meadows, Jennifer R. S.

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Complement C4 Copy Number Variation is Linked to SSA/Ro and SSB/La Autoantibodies in Systemic Inflammatory Autoimmune Diseases von Lundtoft, Christian, Martin, Myriam, Bianchi, Matteo, Lundström, Emeli, Eloranta, Maija‐Leena, Sjöwall, Christopher, Gunnarsson, Iva, Rantapää‐Dahlqvist, Solbritt, Leonard, Dag, Jonsson, Roland, Hammenfors, Daniel, Forsblad‐d'Elia, Helena, Mandl, Thomas, Magnusson Bucher, Sara, Norheim, Katrine B., Auglænd Johnsen, Svein Joar, Omdal, Roald, Kvarnström, Marika, Wahren‐Herlenius, Marie, Notarnicola, Antonella, Andersson, Helena, Molberg, Øyvind, Diederichsen, Louise Pyndt, Almlöf, Jonas, Syvänen, Ann‐Christine, Kozyrev, Sergey V., Lindblad‐Toh, Kerstin, Rönnblom, Lars, Nordmark, Gunnel, Sandling, Johanna K., Pucholt, Pascal, Kozyrev, Sergey V., Eloranta, Maija‐Leena, Alexsson, Andrei, Bianchi, Matteo, Jonsson, Roland, Omdal, Roald, Molberg, Øyvind, Syvänen, Ann‐Christine, Jönsen, Andreas, Gunnarsson, Iva, Svenungsson, Elisabet, Rantapää‐Dahlqvist, Solbritt, Bengtsson, Anders A., Sjöwall, Christopher, Lindblad‐Toh, Kerstin, Almlöf, Jonas Carlsson, Hagberg, Niklas, Meadows, Jennifer R. S., Nordin, Jessika, Wahren‐Herlenius, Marie, Tjärnlund, Anna, Hammenfors, Daniel, Theander, Elke, Baecklund, Eva, Thorlacius, Guðný Ella, Chinoy, Hector, Enocsson, Helena, Forsblad‐d'Elia, Helena, Lamb, Janine, Brun, Johan G., Wetterö, Jonas, Ramírez Sepúlveda, Jorge I., Imgenberg‐Kreuz, Juliana, Hjorton, Karin, Skarstein, Kathrine, Norheim, Katrine Brække, Vasaitis, Lilian, Diederichsen, Louise Pyndt, Jonsson, Malin V., Kvarnström, Marika, Eriksson, Per, Cooper, Robert G., Appel, Silke, Rothwell, Simon, Johnsen, Svein Joar, Mandl, Thomas, Jensen, Janicke Liaaen, Palm, Øyvind, Liden, Maria, Skogh, Thomas, Hanna, Balsam, Hallengren, Christina Ståhl, Hellström, Helena, Häggström, Åsa, Mohammad, Aladdin, Lindblad‐Toh, Kerstin, Pielberg, Gerli Rosengren, Lobell, Anna, Karlsson, Åsa, Murén, Eva, Andersson, Göran, Ahlgren, Kerstin M., Kämpe, Olle, Nilsson, Bo, Blom, Anna M., Lundberg, Ingrid E., Nordmark, Gunnel, Diaz‐Gallo, Lina Marcela, Svenungsson, Elisabet

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Correction: The genetic consequences of dog breed formation-Accumulation of deleterious genetic variation and fixation of mutations associated with myxomatous mitral valve disease... von Axelsson, Erik, Ljungvall, Ingrid, Bhoumik, Priyasma, Conn, Laura Bas, Muren, Eva, Ohlsson, Åsa, Olsen, Lisbeth Høier, Engdahl, Karolina, Hagman, Ragnvi, Hanson, Jeanette, Kryvokhyzha, Dmytro, Pettersson, Mats, Grenet, Olivier, Moggs, Jonathan, Rio-Espinola, Alberto Del, Epe, Christian, Taillon, Bruce, Tawari, Nilesh, Mane, Shrinivas, Hawkins, Troy, Hedhammar, Åke, Gruet, Philippe, Häggström, Jens, Lindblad-Toh, Kerstin

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Genetic and clinical basis for two distinct subtypes of primary Sjögren’s syndrome von Thorlacius, Guðný Ella, Hultin-Rosenberg, Lina, Sandling, Johanna K, Bianchi, Matteo, Imgenberg-Kreuz, Juliana, Pucholt, Pascal, Theander, Elke, Kvarnström, Marika, Forsblad-d’Elia, Helena, Bucher, Sara Magnusson, Norheim, Katrine B, Johnsen, Svein Joar Auglænd, Hammenfors, Daniel, Skarstein, Kathrine, Jonsson, Malin V, Baecklund, Eva, Aqrawi, Lara A, Jensen, Janicke Liaaen, Palm, Øyvind, Morris, Andrew P, Meadows, Jennifer R S, Rantapää-Dahlqvist, Solbritt, Mandl, Thomas, Eriksson, Per, Lind, Lars, Omdal, Roald, Jonsson, Roland, Lindblad-Toh, Kerstin, Rönnblom, Lars, Wahren-Herlenius, Marie, Nordmark, Gunnel

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Contribution of Rare Genetic Variation to Disease Susceptibility in a Large Scandinavian Myositis Cohort von Bianchi, Matteo, Kozyrev, Sergey V., Notarnicola, Antonella, Hultin Rosenberg, Lina, Karlsson, Åsa, Pucholt, Pascal, Rothwell, Simon, Alexsson, Andrei, Sandling, Johanna K., Andersson, Helena, Cooper, Robert G., Padyukov, Leonid, Tjärnlund, Anna, Dastmalchi, Maryam, Lindblad‐Toh, Kerstin, Pielberg, Gerli Rosengren, Lobell, Anna, Karlsson, Åsa, Murén, Eva, Ahlgren, Kerstin M., Rönnblom, Lars, Eloranta, Maija‐Leena, Andersson, Göran, Landegren, Nils, Kämpe, Olle, Söderkvist, Peter, Bianchi, Matteo, Kozyrev, Sergey V., Rosenberg, Lina Hultin, Pucholt, Pascal, Alexsson, Andrei, Sandling, Johanna K., Rönnblom, Lars, Eloranta, Maija‐Leena, Syvänen, Ann‐Christine, Leonard, Dag, Almlöf, Jonas Carlsson, Dahlqvist, Johanna, Hagberg, Niklas, Lidén, Maria, Mathioudaki, Argyri, Meadows, Jennifer R. S., Nordin, Jessika, Nordmark, Gunnel, Yavuz, Sule, Lundberg, Ingrid E., Padyukov, Leonid, Gunnarsson, Iva, Svenungsson, Elisabet, Eriksson, Daniel, Molberg, Øyvind, Lindblad‐Toh, Kerstin, Farias, Fabiana H. G., Bengtsson, Christine, Rantapää‐Dahlqvist, Solbritt, Jonsson, Roland, Omdal, Roald, Jönsen, Andreas, Bengtsson, Anders A., Sjöwall, Christopher, Skogh, Thomas, Wahren‐Herlenius, Marie, Jalal, Awat, Hanna, Balsam, Hellström, Helena, Husmark, Tomas, Häggström, Åsa, Svärd, Anna, Meadows, Jennifer R. S., Pyndt Diederichsen, Louise, Molberg, Øyvind, Chinoy, Hector, Lamb, Janine A., Rönnblom, Lars, Lindblad‐Toh, Kerstin, Lundberg, Ingrid E.

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Relation between HLA and copy number variation of steroid 21-hydroxylase in a Swedish cohort of patients with autoimmune Addisons disease von Lundtoft, Christian, Eriksson, Daniel, Bianchi, Matteo, Aranda-Guillen, Maribel, Landegren, Nils, Rantapaa-Dahlqvist, Solbritt, Söderkvist, Peter, Meadows, Jeniffer R. S., DISSECT Consortium, Immunoarray Consortium, Swedish Addison Registry Study Grp, Gerli Rosengren Pielberg, Bensing, Sophie, Pielberg, Gerli Rosengren, Lindblad-Toh, Kerstin, Ronnblom, Lars, Kampe, Olle

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