NATO Advanced Research Workshop on Environmental and Biological Risks of Hybrid Organic-Silicon Nanodevices

por Magarshak, Yuri, Kozyrev, Sergey, Vaseashta, Ashok
Publicado 2009

Genetic associations in type I interferon related pathways with autoimmunity

por Delgado-Vega, Angélica M, Alarcón-Riquelme, Marta E, Kozyrev, Sergey V
Publicado 2010

Hierarchical Structure of Protein Sequence

por Nekrasov, Alexei N., Kozmin, Yuri P., Kozyrev, Sergey V., Ziganshin, Rustam H., de Brevern, Alexandre G., Anashkina, Anastasia A.
Publicado 2021

Using evolutionary constraint to define novel candidate driver genes in medulloblastoma

por Roy, Ananya, Sakthikumar, Sharadha, Kozyrev, Sergey V., Nordin, Jessika, Pensch, Raphaela, Mäkeläinen, Suvi, Pettersson, Mats, Karlsson, Elinor K., Lindblad-Toh, Kerstin, Forsberg-Nilsson, Karin
Publicado 2023

Whole Exome Sequencing of Patients from Multicase Families with Systemic Lupus Erythematosus Identifies Multiple Rare Variants

por Delgado-Vega, Angélica M., Martínez-Bueno, Manuel, Oparina, Nina Y., López Herráez, David, Kristjansdottir, Helga, Steinsson, Kristján, Kozyrev, Sergey V., Alarcón-Riquelme, Marta E.
Publicado 2018

Multiple regulatory variants located in cell type-specific enhancers within the PKP2 locus form major risk and protective haplotypes for canine atopic dermatitis in German shepherd...

por Tengvall, Katarina, Kozyrev, Sergey, Kierczak, Marcin, Bergvall, Kerstin, Farias, Fabiana H. G., Ardesjö-Lundgren, Brita, Olsson, Mia, Murén, Eva, Hagman, Ragnvi, Leeb, Tosso, Pielberg, Gerli, Hedhammar, Åke, Andersson, Göran, Lindblad-Toh, Kerstin
Publicado 2016

Toll-like receptors revisited; a possible role for TLR1 in lupus nephritis

por Yavuz, Sule, Bianchi, Matteo, Kozyrev, Sergey, Bolin, Karin, Leonard, Dag, Pucholt, Pascal, Sandling, Johanna K, Bengtsson, Anders, Jönsen, Andreas, Rantapää-Dahlqvist, Solbritt, Sjöwall, Christopher, Svenungsson, Elisabet, Gunnarsson, Iva, Lindblad-Toh, Kerstin, Rönnblom, Lars
Publicado 2021

Multiple Changes of Gene Expression and Function Reveal Genomic and Phenotypic Complexity in SLE-like Disease

por Wilbe, Maria, Kozyrev, Sergey V., Farias, Fabiana H. G., Bremer, Hanna D., Hedlund, Anna, Pielberg, Gerli R., Seppälä, Eija H., Gustafson, Ulla, Lohi, Hannes, Carlborg, Örjan, Andersson, Göran, Hansson-Hamlin, Helene, Lindblad-Toh, Kerstin
Publicado 2015

Mer-tyrosine kinase: a novel susceptibility gene for SLE related end-stage renal disease

por Yavuz, Sule, Pucholt, Pascal, Sandling, Johanna K, Bianchi, Matteo, Leonard, Dag, Bolin, Karin, Imgenberg-Kreuz, Juliana, Eloranta, Maija-Leena, Kozyrev, Sergey V, Lanata, Cristina M, Jönsen, Andreas, Bengtsson, Anders A, Sjöwall, Christopher, Svenungsson, Elisabet, Gunnarsson, Iva, Rantapää-Dahlqvist, Solbritt, Nititham, Joanne, Criswell, Lindsey A, Lindblad-Toh, Kerstin, Rönnblom, Lars
Publicado 2022

A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts

por Farias, Fabiana H. G., Dahlqvist, Johanna, Kozyrev, Sergey V., Leonard, Dag, Wilbe, Maria, Abramov, Sergei N., Alexsson, Andrei, Pielberg, Gerli R., Hansson-Hamlin, Helene, Andersson, Göran, Tandre, Karolina, Bengtsson, Anders A., Sjöwall, Christopher, Svenungsson, Elisabet, Gunnarsson, Iva, Rantapää-Dahlqvist, Solbritt, Syvänen, Ann-Christine, Sandling, Johanna K., Eloranta, Maija-Leena, Rönnblom, Lars, Lindblad-Toh, Kerstin
Publicado 2018

Fine mapping and conditional analysis identify a new mutation in the autoimmunity susceptibility gene BLK that leads to reduced half-life of the BLK protein

por Delgado-Vega, Angélica M, Dozmorov, Mikhail G, Quirós, Manuel Bernal, Wu, Ying-Yu, Martínez-García, Belén, Kozyrev, Sergey V, Frostegård, Johan, Truedsson, Lennart, de Ramón, Enrique, González-Escribano, María F, Ortego-Centeno, Norberto, Pons-Estel, Bernardo A, D'Alfonso, Sandra, Sebastiani, Gian Domenico, Witte, Torsten, Lauwerys, Bernard R, Endreffy, Emoke, Kovács, László, Vasconcelos, Carlos, da Silva, Berta Martins, Wren, Jonathan D, Martin, Javier, Castillejo-López, Casimiro, Alarcón-Riquelme, Marta E
Publicado 2012

Molecular pathways in patients with systemic lupus erythematosus revealed by gene-centred DNA sequencing

por Sandling, Johanna K, Pucholt, Pascal, Hultin Rosenberg, Lina, Farias, Fabiana H G, Kozyrev, Sergey V, Eloranta, Maija-Leena, Alexsson, Andrei, Bianchi, Matteo, Padyukov, Leonid, Bengtsson, Christine, Jonsson, Roland, Omdal, Roald, Lie, Benedicte A, Massarenti, Laura, Steffensen, Rudi, Jakobsen, Marianne A, Lillevang, Søren T, Lerang, Karoline, Molberg, Øyvind, Voss, Anne, Troldborg, Anne, Jacobsen, Søren, Syvänen, Ann-Christine, Jönsen, Andreas, Gunnarsson, Iva, Svenungsson, Elisabet, Rantapää-Dahlqvist, Solbritt, Bengtsson, Anders A, Sjöwall, Christopher, Leonard, Dag, Lindblad-Toh, Kerstin, Rönnblom, Lars
Publicado 2021

Identification and functional characterization of a novel susceptibility locus for small vessel vasculitis with MPO-ANCA

por 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
Publicado 2021

Strong Association of Combined Genetic Deficiencies in the Classical Complement Pathway With Risk of Systemic Lupus Erythematosus and Primary Sjögren's Syndrome

por Lundtoft, Christian, Sjöwall, Christopher, Rantapää‐Dahlqvist, Solbritt, Bengtsson, Anders A., Jönsen, Andreas, Pucholt, Pascal, Wu, Yee Ling, Lundström, Emeli, Eloranta, Maija‐Leena, Gunnarsson, Iva, Baecklund, Eva, Jonsson, Roland, Hammenfors, Daniel, Forsblad‐d'Elia, Helena, Eriksson, Per, Mandl, Thomas, Bucher, Sara, Norheim, Katrine B., Auglaend Johnsen, Svein Joar, Omdal, Roald, Kvarnström, Marika, Wahren‐Herlenius, Marie, Truedsson, Lennart, Nilsson, Bo, Kozyrev, Sergey V., Bianchi, Matteo, Lindblad‐Toh, Kerstin, Yu, Chack‐Yung, Nordmark, Gunnel, Sandling, Johanna K., Svenungsson, Elisabet, Leonard, Dag, Rönnblom, Lars
Publicado 2022

Complement C4 Copy Number Variation is Linked to SSA/Ro and SSB/La Autoantibodies in Systemic Inflammatory Autoimmune Diseases

por Lundtoft, Christian, Pucholt, Pascal, Martin, Myriam, Bianchi, Matteo, Lundström, Emeli, Eloranta, Maija‐Leena, Sandling, Johanna K., Sjöwall, Christopher, Jönsen, Andreas, Gunnarsson, Iva, Rantapää‐Dahlqvist, Solbritt, Bengtsson, Anders A., Leonard, Dag, Baecklund, Eva, Jonsson, Roland, Hammenfors, Daniel, Forsblad‐d'Elia, Helena, Eriksson, Per, 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, Nilsson, Bo, Blom, Anna M., Lundberg, Ingrid E., Nordmark, Gunnel, Diaz‐Gallo, Lina Marcela, Svenungsson, Elisabet, Rönnblom, Lars
Publicado 2022