BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

219 related articles for article (PubMed ID: 33574239)

  • 1. GWAS for autoimmune Addison's disease identifies multiple risk loci and highlights AIRE in disease susceptibility.
    Eriksson D; Røyrvik EC; Aranda-Guillén M; Berger AH; Landegren N; Artaza H; Hallgren Å; Grytaas MA; Ström S; Bratland E; Botusan IR; Oftedal BE; Breivik L; Vaudel M; Helgeland Ø; Falorni A; Jørgensen AP; Hulting AL; Svartberg J; Ekwall O; Fougner KJ; Wahlberg J; Nedrebø BG; Dahlqvist P; ; ; Knappskog PM; Wolff ASB; Bensing S; Johansson S; Kämpe O; Husebye ES
    Nat Commun; 2021 Feb; 12(1):959. PubMed ID: 33574239
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison's disease in Sweden.
    Eriksson D; Bianchi M; Landegren N; Dalin F; Skov J; Hultin-Rosenberg L; Mathioudaki A; Nordin J; Hallgren Å; Andersson G; Tandre K; Rantapää Dahlqvist S; Söderkvist P; Rönnblom L; Hulting AL; Wahlberg J; Dahlqvist P; Ekwall O; Meadows JRS; Lindblad-Toh K; Bensing S; Rosengren Pielberg G; Kämpe O
    Sci Rep; 2018 May; 8(1):8395. PubMed ID: 29849176
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association analysis of the cytotoxic T lymphocyte antigen-4 (CTLA-4) and autoimmune regulator-1 (AIRE-1) genes in sporadic autoimmune Addison's disease.
    Vaidya B; Imrie H; Geatch DR; Perros P; Ball SG; Baylis PH; Carr D; Hurel SJ; James RA; Kelly WF; Kemp EH; Young ET; Weetman AP; Kendall-Taylor P; Pearce SH
    J Clin Endocrinol Metab; 2000 Feb; 85(2):688-91. PubMed ID: 10690877
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    J Intern Med; 2016 Dec; 280(6):595-608. PubMed ID: 27807919
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Variant in the BACH2 Gene Is Associated With Susceptibility to Autoimmune Addison's Disease in Humans.
    Pazderska A; Oftedal BE; Napier CM; Ainsworth HF; Husebye ES; Cordell HJ; Pearce SH; Mitchell AL
    J Clin Endocrinol Metab; 2016 Nov; 101(11):3865-3869. PubMed ID: 27680876
    [TBL] [Abstract][Full Text] [Related]  

  • 6. From Genetic Predisposition to Molecular Mechanisms of Autoimmune Primary Adrenal Insufficiency.
    Falorni A; Brozzetti A; Perniola R
    Front Horm Res; 2016; 46():115-32. PubMed ID: 27211051
    [TBL] [Abstract][Full Text] [Related]  

  • 7. CTLA-4 as a genetic determinant in autoimmune Addison's disease.
    Wolff AS; Mitchell AL; Cordell HJ; Short A; Skinningsrud B; Ollier W; Badenhoop K; Meyer G; Falorni A; Kampe O; Undlien D; Pearce SH; Husebye ES
    Genes Immun; 2015 Sep; 16(6):430-6. PubMed ID: 26204230
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Replication of association at the LPP and UBASH3A loci in a UK autoimmune Addison's disease cohort.
    Howarth S; Sneddon G; Allinson KR; Razvi S; Mitchell AL; Pearce SHS
    Eur J Endocrinol; 2023 Jan; 188(1):. PubMed ID: 36651163
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cytotoxic T lymphocyte antigen-4 Ala17 polymorphism is a genetic marker of autoimmune adrenal insufficiency: Italian association study and meta-analysis of European studies.
    Brozzetti A; Marzotti S; Tortoioli C; Bini V; Giordano R; Dotta F; Betterle C; De Bellis A; Arnaldi G; Toscano V; Arvat E; Bellastella A; Mantero F; Falorni A;
    Eur J Endocrinol; 2010 Feb; 162(2):361-9. PubMed ID: 19884265
    [TBL] [Abstract][Full Text] [Related]  

  • 10. AIRE variations in Addison's disease and autoimmune polyendocrine syndromes (APS): partial gene deletions contribute to APS I.
    Bøe Wolff AS; Oftedal B; Johansson S; Bruland O; Løvås K; Meager A; Pedersen C; Husebye ES; Knappskog PM
    Genes Immun; 2008 Mar; 9(2):130-6. PubMed ID: 18200029
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rare copy number variation in autoimmune Addison's disease.
    Artaza H; Eriksson D; Lavrichenko K; Aranda-Guillén M; Bratland E; Vaudel M; Knappskog P; Husebye ES; Bensing S; Wolff ASB; Kämpe O; Røyrvik EC; Johansson S
    Front Immunol; 2024; 15():1374499. PubMed ID: 38562931
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Heritability of Addison's disease and prevalence of associated autoimmunity in a cohort of 112,100 Swedish twins.
    Skov J; Höijer J; Magnusson PKE; Ludvigsson JF; Kämpe O; Bensing S
    Endocrine; 2017 Dec; 58(3):521-527. PubMed ID: 29039147
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Linkage Analysis in Autoimmune Addison's Disease: NFATC1 as a Potential Novel Susceptibility Locus.
    Mitchell AL; Bøe Wolff A; MacArthur K; Weaver JU; Vaidya B; ; Erichsen MM; Darlay R; Husebye ES; Cordell HJ; Pearce SH
    PLoS One; 2015; 10(6):e0123550. PubMed ID: 26042420
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association of autoimmune Addison's disease with alleles of STAT4 and GATA3 in European cohorts.
    Mitchell AL; Macarthur KD; Gan EH; Baggott LE; Wolff AS; Skinningsrud B; Platt H; Short A; Lobell A; Kämpe O; Bensing S; Betterle C; Kasperlik-Zaluska A; Zurawek M; Fichna M; Kockum I; Nordling Eriksson G; Ekwall O; Wahlberg J; Dahlqvist P; Hulting AL; Penna-Martinez M; Meyer G; Kahles H; Badenhoop K; Hahner S; Quinkler M; Falorni A; Phipps-Green A; Merriman TR; Ollier W; Cordell HJ; Undlien D; Czarnocka B; Husebye E; Pearce SH
    PLoS One; 2014; 9(3):e88991. PubMed ID: 24614117
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism is associated with autoimmune Addison's disease in English patients.
    Kemp EH; Ajjan RA; Husebye ES; Peterson P; Uibo R; Imrie H; Pearce SH; Watson PF; Weetman AP
    Clin Endocrinol (Oxf); 1998 Nov; 49(5):609-13. PubMed ID: 10197076
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Screening for an AIRE-1 mutation in patients with Addison's disease, type 1 diabetes, Graves' disease and Hashimoto's thyroiditis as well as in APECED syndrome.
    Meyer G; Donner H; Herwig J; Böhles H; Usadel KH; Badenhoop K
    Clin Endocrinol (Oxf); 2001 Mar; 54(3):335-8. PubMed ID: 11298085
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sex-specific association of PTPN22 1858T with type 1 diabetes but not with Hashimoto's thyroiditis or Addison's disease in the German population.
    Kahles H; Ramos-Lopez E; Lange B; Zwermann O; Reincke M; Badenhoop K
    Eur J Endocrinol; 2005 Dec; 153(6):895-9. PubMed ID: 16322396
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Understanding the genetics of autoimmune disease: two loci that regulate late onset Addison's disease in Portuguese Water Dogs.
    Chase K; Sargan D; Miller K; Ostrander EA; Lark KG
    Int J Immunogenet; 2006 Jun; 33(3):179-84. PubMed ID: 16712648
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Polymorphisms in the cytotoxic T lymphocyte antigen-4 gene region confer susceptibility to Addison's disease.
    Blomhoff A; Lie BA; Myhre AG; Kemp EH; Weetman AP; Akselsen HE; Huseby ES; Undlien DE
    J Clin Endocrinol Metab; 2004 Jul; 89(7):3474-6. PubMed ID: 15240634
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CYP21A2 polymorphisms in patients with autoimmune Addison's disease, and linkage disequilibrium to HLA risk alleles.
    Brønstad I; Skinningsrud B; Bratland E; Løvås K; Undlien D; Sverre Husebye E; Wolff AS
    Eur J Endocrinol; 2014 Dec; 171(6):743-50. PubMed ID: 25249698
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.