Human Genome Epidemiology Literature Finder
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Records 1 - 7 (of 7 Records) |
| Query Trace: Disease and IKZF4[original query] |
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| Genome-wide association study in alopecia areata implicates both innate and adaptive immunity.
Nature 2010 Jul 466 (7302): 113-7. Petukhova Lynn, Duvic Madeleine, Hordinsky Maria, Norris David, Price Vera, Shimomura Yutaka, Kim Hyunmi, Singh Pallavi, Lee Annette, Chen Wei V, Meyer Katja C, Paus Ralf, Jahoda Colin A B, Amos Christopher I, Gregersen Peter K, Christiano Angela |
| An allele of IKZF1 (Ikaros) conferring susceptibility to childhood acute lymphoblastic leukemia protects against type 1 diabetes. Diabetes 2011 Mar 60 (3): 1041-4. Swafford Austin D-E, Howson Joanna M M, Davison Lucy J, Wallace Chris, Smyth Deborah J, Schuilenburg Helen, Maisuria-Armer Meeta, Mistry Trupti, Lenardo Michael J, Todd John |
| Associations of polymorphisms in non-HLA loci with autoantibodies at the diagnosis of type 1 diabetes: INS and IKZF4 associate with insulin autoantibodies. Pediatric diabetes 2013 Nov 14 (7): 490-6. Lempainen J, Härkönen T, Laine Ap, Knip M, Ilonen J, |
| Non-HLA gene effects on the disease process of type 1 diabetes: From HLA susceptibility to overt disease. Journal of autoimmunity 2015 Jul 61 45-53. Lempainen Johanna, Laine Antti-Pekka, Hammais Anna, Toppari Jorma, Simell Olli, Veijola Riitta, Knip Mikael, Ilonen Jor |
| Genetic variation at ERBB3/IKZF4 and sexual dimorphism in epitope spreading in single autoantibody-positive relatives. Diabetologia 2021 8 64 (11): 2511-2516. Vandewalle Julie, Van der Auwera Bart J, Amin Henna, Quartier Erik, Desouter Aster K, Tenoutasse Sylvie, Gillard Pieter, De Block Christophe, Keymeulen Bart, Gorus Frans K, Van de Casteele Mark, |
| Colocalization analysis of polycystic ovary syndrome to identify potential disease-mediating genes and proteins. European journal of human genetics : EJHG 2021 Mar . Censin Jenny C, Bovijn Jonas, Holmes Michael V, Lindgren Cecilia |
| Associations between deduced first islet specific autoantibody with sex, age at diagnosis and genetic risk factors in young children with type 1 diabetes. Pediatric diabetes 2022 4 23 (6): 693-702. Ilonen Jorma, Laine Antti-Pekka, Kiviniemi Minna, Härkönen Taina, Lempainen Johanna, Knip Mikael, |
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