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A novel canine reference genome resolves genomic architecture and uncovers transcript complexity.
Wang C, Wallerman O, Arendt ML, Sundström E, Karlsson Å, Nordin J, Mäkeläinen S, Pielberg GR, Hanson J, Ohlsson Å, Saellström S, Rönnberg H, Ljungvall I, Häggström J, Bergström TF, Hedhammar Å, Meadows JRS, Lindblad-Toh K. Wang C, et al. Among authors: karlsson a. Commun Biol. 2021 Feb 10;4(1):185. doi: 10.1038/s42003-021-01698-x. Commun Biol. 2021. PMID: 33568770 Free PMC article.
Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease.
Eriksson D, Bianchi M, Landegren N, Nordin J, Dalin F, Mathioudaki A, Eriksson GN, Hultin-Rosenberg L, Dahlqvist J, Zetterqvist H, Karlsson Å, Hallgren Å, Farias FH, Murén E, Ahlgren KM, Lobell A, Andersson G, Tandre K, Dahlqvist SR, Söderkvist P, Rönnblom L, Hulting AL, Wahlberg J, Ekwall O, Dahlqvist P, Meadows JR, Bensing S, Lindblad-Toh K, Kämpe O, Pielberg GR. Eriksson D, et al. Among authors: karlsson a. J Intern Med. 2016 Dec;280(6):595-608. doi: 10.1111/joim.12569. Epub 2016 Nov 2. J Intern Med. 2016. PMID: 27807919 Free article.
Long-term follow-up in primary Sjögren's syndrome reveals differences in clinical presentation between female and male patients.
Ramírez Sepúlveda JI, Kvarnström M, Eriksson P, Mandl T, Norheim KB, Johnsen SJ, Hammenfors D, Jonsson MV, Skarstein K, Brun JG; DISSECT consortium; Rönnblom L, Forsblad-d'Elia H, Magnusson Bucher S, Baecklund E, Theander E, Omdal R, Jonsson R, Nordmark G, Wahren-Herlenius M. Ramírez Sepúlveda JI, et al. Biol Sex Differ. 2017 Aug 8;8(1):25. doi: 10.1186/s13293-017-0146-6. Biol Sex Differ. 2017. PMID: 28789696 Free PMC article.
Whole-genome genotyping and resequencing reveal the association of a deletion in the complex interferon alpha gene cluster with hypothyroidism in dogs.
Bianchi M, Rafati N, Karlsson Å, Murén E, Rubin CJ, Sundberg K, Andersson G, Kämpe O, Hedhammar Å, Lindblad-Toh K, Rosengren Pielberg G. Bianchi M, et al. Among authors: karlsson a. BMC Genomics. 2020 Apr 16;21(1):307. doi: 10.1186/s12864-020-6700-3. BMC Genomics. 2020. PMID: 32299354 Free PMC article.
Genetic and clinical basis for two distinct subtypes of primary Sjögren's syndrome.
Thorlacius GE, Hultin-Rosenberg L, Sandling JK, Bianchi M, Imgenberg-Kreuz J, Pucholt P, Theander E, Kvarnström M, Forsblad-d'Elia H, Bucher SM, Norheim KB, Johnsen SJA, Hammenfors D, Skarstein K, Jonsson MV, Baecklund E, Aqrawi LA, Jensen JL, Palm Ø, Morris AP; DISSECT consortium; the ImmunoArray consortium; Meadows JRS, Rantapää-Dahlqvist S, Mandl T, Eriksson P, Lind L, Omdal R, Jonsson R, Lindblad-Toh K, Rönnblom L, Wahren-Herlenius M, Nordmark G. Thorlacius GE, et al. Rheumatology (Oxford). 2021 Feb 1;60(2):837-848. doi: 10.1093/rheumatology/keaa367. Rheumatology (Oxford). 2021. PMID: 32889544 Free PMC article.
Contribution of Rare Genetic Variation to Disease Susceptibility in a Large Scandinavian Myositis Cohort.
Bianchi M, Kozyrev SV, Notarnicola A, Hultin Rosenberg L, Karlsson Å, Pucholt P, Rothwell S, Alexsson A, Sandling JK, Andersson H, Cooper RG, Padyukov L, Tjärnlund A, Dastmalchi M; ImmunoArray Development Consortium; DISSECT Consortium; Meadows JRS, Pyndt Diederichsen L, Molberg Ø, Chinoy H, Lamb JA, Rönnblom L, Lindblad-Toh K, Lundberg IE. Bianchi M, et al. Among authors: karlsson a. Arthritis Rheumatol. 2022 Feb;74(2):342-352. doi: 10.1002/art.41929. Epub 2021 Dec 23. Arthritis Rheumatol. 2022. PMID: 34279065
1,241 results