Kerstin Lindblad-Toh (Former)

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2024
Mark The HLA region in ANCA-associated vasculitis : characterisation of genetic associations in a Scandinavian patient population
Lundtoft, Christian ; Knight, Ann ; Meadows, Jennifer R S ; Karlsson, Åsa ; Rantapää-Dahlqvist, Solbritt ; Berglin, Ewa ; Palm, Øyvind ; Haukeland, Hilde ; Gunnarsson, Iva and Bruchfeld, Annette , et al. (2024) In RMD Open 10(2). p.1-10
- Contribution to journal › Article
Mark A burden of rare copy number variants in obsessive-compulsive disorder
Halvorsen, Matthew W. ; de Schipper, Elles ; Bäckman, Julia ; Strom, Nora I. ; Hagen, Kristen ; Zayats, Tetyana ; Eide, Thorstein Olsen ; Noh, Hyun Ji ; Morrill, Kathleen and Lichtenstein, Paul , et al. (2024) In Molecular Psychiatry
- Contribution to journal › Article
2023
Mark Stratified Genetic Analysis Reveals Sex Differences In MPO-ANCA-associated Vasculitis
Ekman, Diana ; Sennblad, Bengt ; Knight, Ann ; Karlsson, Åsa ; Rantapää-Dahlqvist, Solbritt ; Berglin, Ewa ; Stegmayr, Bernd ; Baslund, Bo ; Palm, Øyvind and Haukeland, Hilde , et al. (2023) In Rheumatology (Oxford, England) 62(9). p.3213-3218
- Contribution to journal › Article
2022
Mark Identification and Functional Characterization of a Novel Susceptibility Locus for Small Vessel Vasculitis with MPO-ANCA
Dahlqvist, Johanna ; Ekman, Diana ; Sennblad, Bengt ; Kozyrev, Sergey V ; Nordin, Jessika ; Karlsson, Åsa ; Meadows, Jennifer R S ; Hellbacher, Erik ; Rantapää-Dahlqvist, Solbritt and Berglin, Ewa , et al. (2022) In Rheumatology (Oxford, England) 61(8). p.3461-3470
- Contribution to journal › Article
Mark Complement C4 copy number variation is linked to SSA/Ro and SSB/La autoantibodies in systemic inflammatory autoimmune diseases
Lundtoft, Christian ; Pucholt, Pascal ; Martin, Myriam ^LU ; Bianchi, Matteo ; Lundström, Emeli ; Eloranta, Maija-Leena ; Sandling, Johanna K ; Sjöwall, Christopher ; Jönsen, Andreas ^LU and Gunnarsson, Iva , et al. (2022) In Arthritis & Rheumatology 74(8). p.1440-1450
- Contribution to journal › Article
Mark Mer-tyrosine kinase : a novel susceptibility gene for SLE related end-stage renal disease
Yavuz, Sule ; Pucholt, Pascal ; Sandling, Johanna K. ; Bianchi, Matteo ; Leonard, Dag ; Bolin, Karin ; Imgenberg-Kreuz, Juliana ; Eloranta, Maija Leena ; Kozyrev, Sergey V. and Lanata, Cristina M. , et al. (2022) In Lupus Science and Medicine 9(1).
- Contribution to journal › Article
2021
Mark Molecular pathways in patients with systemic lupus erythematosus revealed by gene-centred DNA sequencing
Sandling, Johanna K. ; Pucholt, Pascal ; Hultin Rosenberg, Lina ; Farias, Fabiana H.G. ; Kozyrev, Sergey V. ; Eloranta, Maija Leena ; Alexsson, Andrei ; Bianchi, Matteo ; Padyukov, Leonid and Bengtsson, Christine ^LU , et al. (2021) In Annals of the Rheumatic Diseases 80(1). p.109-117
- Contribution to journal › Article
Mark Toll-like receptors revisited; A possible role for TLR1 in lupus nephritis
Yavuz, Sule ; Bianchi, Matteo ; Kozyrev, Sergey ; Bolin, Karin ; Leonard, Dag ; Pucholt, Pascal ; Sandling, Johanna K. ; Bengtsson, Anders ^LU ; Jönsen, Andreas ^LU and Rantapää-Dahlqvist, Solbritt , et al. (2021) In Annals of the Rheumatic Diseases 80(3). p.404-406
- Contribution to journal › Letter
Mark The genetic consequences of dog breed formation - Accumulation of deleterious genetic variation and fixation of mutations associated with myxomatous mitral valve disease in cavalier King Charles spaniels
Axelsson, Erik ; Ljungvall, Ingrid ; Bhoumik, Priyasma ; Conn, Laura Bas ; Muren, Eva ; Ohlsson, Åsa ; Olsen, Lisbeth Høier ; Engdahl, Karolina ; Hagman, Ragnvi and Hanson, Jeanette , et al. (2021) In PLoS Genetics 17(9). p.1-34
- Contribution to journal › Article
2019
Mark A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts
Farias, Fabiana H.G. ; Dahlqvist, Johanna ; Kozyrev, Sergey V. ; Leonard, Dag ; Wilbe, Maria ; Abramov, Sergei N. ; Alexsson, Andrei ; Pielberg, Gerli R. ; Hansson-Hamlin, Helene and Andersson, Göran , et al. (2019) In European Journal of Human Genetics 27(3). p.432-441
- Contribution to journal › Article

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