Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping von Vaysse, Amaury, Ratnakumar, Abhirami, Derrien, Thomas, Axelsson, Erik, Rosengren Pielberg, Gerli, Sigurdsson, Snaevar, Fall, Tove, Seppälä, Eija H, Hansen, Mark S T, Lawley, Cindy T, Karlsson, Elinor K, Bannasch, Danika, Vilà, Carles, Lohi, Hannes, Galibert, Francis, Fredholm, Merete, Häggström, Jens, Hedhammar, Ake, André, Catherine, Lindblad-Toh, Kerstin, Hitte, Christophe, Webster, Matthew T

Volltext

A novel canine reference genome resolves genomic architecture and uncovers transcript complexity von Wang, Chao, Wallerman, Ola, Arendt, Maja-Louise, Sundström, Elisabeth, Karlsson, Åsa, Nordin, Jessika, Mäkeläinen, Suvi, Pielberg, Gerli Rosengren, Hanson, Jeanette, Ohlsson, Åsa, Saellström, Sara, Rönnberg, Henrik, Ljungvall, Ingrid, Häggström, Jens, Bergström, Tomas F., Hedhammar, Åke, Meadows, Jennifer R. S., Lindblad-Toh, Kerstin

Volltext

A cis -acting regulatory mutation causes premature hair graying and susceptibility to melanoma in the horse von Strömberg, Sara, Sundström, Elisabeth, Lindblad-Toh, Kerstin, Baumung, Roswitha, Pontén, Fredrik, Rosengren Pielberg, Gerli, Vetterlein, Monika, Golovko, Anna, Lennartsson, Johan, Lindgren, Gabriella, Seltenhammer, Monika H, Binns, Matthew, Curik, Ino, Fitzsimmons, Carolyn, Sölkner, Johann, Grabherr, Manfred, Wade, Claire, Heldin, Carl-Henrik, Andersson, Leif, Druml, Thomas, Sandberg, Kaj

Volltext

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

Volltext

A novel unstable duplication upstream of HAS2 predisposes to a breed-defining skin phenotype and a periodic fever syndrome in Chinese Shar-Pei dogs von Olsson, Mia, Meadows, Jennifer R S, Truvé, Katarina, Rosengren Pielberg, Gerli, Puppo, Francesca, Mauceli, Evan, Quilez, Javier, Tonomura, Noriko, Zanna, Giordana, Docampo, Maria José, Bassols, Anna, Avery, Anne C, Karlsson, Elinor K, Thomas, Anne, Kastner, Daniel L, Bongcam-Rudloff, Erik, Webster, Matthew T, Sanchez, Armand, Hedhammar, Ake, Remmers, Elaine F, Andersson, Leif, Ferrer, Lluis, Tintle, Linda, Lindblad-Toh, Kerstin

Volltext

Relation between HLA and copy number variation of steroid 21-hydroxylase in a Swedish cohort of patients with autoimmune Addison's disease von Lundtoft, Christian, Eriksson, Daniel, Bianchi, Matteo, Aranda-Guillén, Maribel, Landegren, Nils, Rantapää-Dahlqvist, Solbritt, Söderkvist, Peter, Meadows, Jennifer R S, Bensing, Sophie, Pielberg, Gerli Rosengren, Lindblad-Toh, Kerstin, Rönnblom, Lars, Kämpe, Olle

Volltext

Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison’s disease in Sweden von Eriksson, Daniel, Bianchi, Matteo, Landegren, Nils, Dalin, Frida, Skov, Jakob, Hultin-Rosenberg, Lina, Mathioudaki, Argyri, Nordin, Jessika, Hallgren, Åsa, Andersson, Göran, Tandre, Karolina, Rantapää Dahlqvist, Solbritt, Söderkvist, Peter, Rönnblom, Lars, Hulting, Anna-Lena, Wahlberg, Jeanette, Dahlqvist, Per, Ekwall, Olov, Meadows, Jennifer R. S., Lindblad-Toh, Kerstin, Bensing, Sophie, Rosengren Pielberg, Gerli, Kämpe, Olle

Volltext

A simple repeat polymorphism in the MITF-M promoter is a key regulator of white spotting in dogs von Baranowska Körberg, Izabella, Sundström, Elisabeth, Meadows, Jennifer R S, Rosengren Pielberg, Gerli, Gustafson, Ulla, Hedhammar, Åke, Karlsson, Elinor K, Seddon, Jennifer, Söderberg, Arne, Vilà, Carles, Zhang, Xiaolan, Åkesson, Mikael, Lindblad-Toh, Kerstin, Andersson, Göran, Andersson, Leif

Volltext

Cytokine Autoantibody Screening in the Swedish Addison Registry Identifies Patients With Undiagnosed APS1 von Eriksson, Daniel, Dalin, Frida, Eriksson, Gabriel Nordling, Landegren, Nils, Bianchi, Matteo, Hallgren, Åsa, Dahlqvist, Per, Wahlberg, Jeanette, Ekwall, Olov, Winqvist, Ola, Catrina, Sergiu-Bogdan, Rönnelid, Johan, Hulting, Anna-Lena, Lindblad-Toh, Kerstin, Alimohammadi, Mohammad, Husebye, Eystein S, Knappskog, Per Morten, Rosengren Pielberg, Gerli, Bensing, Sophie, Kämpe, Olle, Olsson, Tommy, Kriström, Berit, Laudius, Maria, Isaksson, Magnus, Stenlid, Maria Halldin, Gustafsson, Jan, Gebre-Medhin, Gennet, Björnsdottir, Sigridur, Eriksson, Gabriel-Nordling, Janson, Annika, Åkerman, Anna-Karin, Bergthorsdottir, Ragnhildur, Johannsson, Gudmundur, Lindskog, Emma, Elfving, Maria, Waldenström, Erik, Svensson, Johan, Kalcheva, Zlatka, Eliasson, Mats, Hedman, Erik, Wahlin, Karin, Magnusson, Anders, Ekman, Bertil, Munoz, Karel Duchen

Volltext

A Multi-Breed Genome-Wide Association Analysis for Canine Hypothyroidism Identifies a Shared Major Risk Locus on CFA12 von Bianchi, Matteo, Dahlgren, Stina, Massey, Jonathan, Dietschi, Elisabeth, Kierczak, Marcin, Lund-Ziener, Martine, Sundberg, Katarina, Thoresen, Stein Istre, Kämpe, Olle, Andersson, Göran, Ollier, William E R, Hedhammar, Åke, Leeb, Tosso, Lindblad-Toh, Kerstin, Kennedy, Lorna J, Lingaas, Frode, Rosengren Pielberg, Gerli

Volltext

Complex inheritance of melanoma and pigmentation of coat and skin in Grey horses von Curik, Ino, Druml, Thomas, Seltenhammer, Monika, Sundström, Elisabeth, Pielberg, Gerli Rosengren, Andersson, Leif, Sölkner, Johann

Volltext

Efficient mapping of mendelian traits in dogs through genome-wide association von Karlsson, Elinor K, Andersson, Leif, Lindblad-Toh, Kerstin, Baranowska, Izabella, Wade, Claire M, Salmon Hillbertz, Nicolette H C, Zody, Michael C, Anderson, Nathan, Biagi, Tara M, Patterson, Nick, Pielberg, Gerli Rosengren, Kulbokas, Edward J, Comstock, Kenine E, Keller, Evan T, Mesirov, Jill P, von Euler, Henrik, Kämpe, Olle, Hedhammar, Åke, Lander, Eric S, Andersson, Göran

Volltext

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

Volltext

Duplication of FGF3 , FGF4 , FGF19 and ORAOV1 causes hair ridge and predisposition to dermoid sinus in Ridgeback dogs von Nilsson, Mats, Isaksson, Magnus, Hellmén, Eva, Andersson, Leif, Lindblad-Toh, Kerstin, Savolainen, Peter, Andersson, Göran, Wade, Claire M, Pielberg, Gerli Rosengren, Hedhammar, Åke, Karlsson, Elinor K, Gustafson, Ulla, von Euler, Henrik, Salmon Hillbertz, Nicolette H C

Volltext

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

Volltext

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

Volltext

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.

Volltext

Copy number expansion of the STX17 duplication in melanoma tissue from Grey horses von Sundström, Elisabeth, Imsland, Freyja, Mikko, Sofia, Wade, Claire, Sigurdsson, Snaevar, Pielberg, Gerli Rosengren, Golovko, Anna, Curik, Ino, Seltenhammer, Monika H, Sölkner, Johann, Lindblad-Toh, Kerstin, Andersson, Leif

Volltext

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, Alexsson, Andrei, Backlin, Carin, Rönnblom, Lars, Vasaitis, Lilian, Eloranta, Maija Leena, Syvänen, Ann Christine, Mathioudaki, Argyri, Farias, Fabiana H.G, Meadows, Jennifer, Nordin, Jessika, Lindblad-Toh, Kerstin, Björk, Albin, Lundberg, Ingrid E, Sepúlveda, Jorge I.Ramírez, Wahren-Herlenius, Marie, Eriksson, Daniel, Eriksson, Per, Sjöwall, Christopher, Mandl, Thomas, Rantapaä¨-Dahlqvist, Solbritt, Brokstad, Karl A, Jonsson, Roland, Appel, Silke, Brun, Johan G, Norheim, Katrine Brække, Omdal, Roald, Aqrawi, Lara Adnan, Pielberg, Gerli Rosengren, Murén, Eva, Karlsson, Åsa, Andersson, Göran, Ahlgren, Kerstin M, Lobell, Anna, Söderkvist, Peter, Kämpe, Olle, Landegren, Nils, Meadows, Jennifer R.S, Lind, Lars, Nordmark, Gunnel

Volltext

Cytokine autoantibody screening in the Swedish Addison Register identifies patients with undiagnosed APS1 von Eriksson, Daniel, Dalin, Frida, Eriksson, Gabriel Nordling, Landegren, Nils, Bianchi, Matteo, Hallgren, Åsa, Dahlqvist, Per, Wahlberg, Jeanette, Ekwall, Olov, Winqvist, Ola, Catrina, Sergiu-Bogdan, Rönnelid, Johan, Hulting, Anna-Lena, Lindblad-Toh, Kerstin, Alimohammadi, Mohammad, Husebye, Eystein S, Knappskog, Per Morten, Pielberg, Gerli Rosengren, Bensing, Sophie, Kämpe, Olle

Volltext