263 related articles for article (PubMed ID: 29903748)
1. Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome.
Debiec H; Dossier C; Letouzé E; Gillies CE; Vivarelli M; Putler RK; Ars E; Jacqz-Aigrain E; Elie V; Colucci M; Debette S; Amouyel P; Elalaoui SC; Sefiani A; Dubois V; Simon T; Kretzler M; Ballarin J; Emma F; Sampson MG; Deschênes G; Ronco P
J Am Soc Nephrol; 2018 Jul; 29(7):2000-2013. PubMed ID: 29903748
[No Abstract] [Full Text] [Related]
2. Strong Association of the
Jia X; Horinouchi T; Hitomi Y; Shono A; Khor SS; Omae Y; Kojima K; Kawai Y; Nagasaki M; Kaku Y; Okamoto T; Ohwada Y; Ohta K; Okuda Y; Fujimaru R; Hatae K; Kumagai N; Sawanobori E; Nakazato H; Ohtsuka Y; Nakanishi K; Shima Y; Tanaka R; Ashida A; Kamei K; Ishikura K; Nozu K; Tokunaga K; Iijima K;
J Am Soc Nephrol; 2018 Aug; 29(8):2189-2199. PubMed ID: 30012571
[No Abstract] [Full Text] [Related]
3. Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome.
Dufek S; Cheshire C; Levine AP; Trompeter RS; Issler N; Stubbs M; Mozere M; Gupta S; Klootwijk E; Patel V; Hothi D; Waters A; Webb H; Tullus K; Jenkins L; Godinho L; Levtchenko E; Wetzels J; Knoers N; Teeninga N; Nauta J; Shalaby M; Eldesoky S; Kari JA; Thalgahagoda S; Ranawaka R; Abeyagunawardena A; Adeyemo A; Kristiansen M; Gbadegesin R; Webb NJ; Gale DP; Stanescu HC; Kleta R; Bockenhauer D
J Am Soc Nephrol; 2019 Aug; 30(8):1375-1384. PubMed ID: 31263063
[TBL] [Abstract][Full Text] [Related]
4. Association of HLA-DR/DQ alleles and haplotypes with nephrotic syndrome.
Ramanathan AS; Senguttuvan P; Chinniah R; Vijayan M; Thirunavukkarasu M; Raju K; Mani D; Ravi PM; Rajendran P; Krishnan JI; Karuppiah B
Nephrology (Carlton); 2016 Sep; 21(9):745-52. PubMed ID: 26566811
[TBL] [Abstract][Full Text] [Related]
5. HLA-DQA1 and APOL1 as Risk Loci for Childhood-Onset Steroid-Sensitive and Steroid-Resistant Nephrotic Syndrome.
Adeyemo A; Esezobor C; Solarin A; Abeyagunawardena A; Kari JA; El Desoky S; Greenbaum LA; Kamel M; Kallash M; Silva C; Young A; Hunley TE; de Jesus-Gonzalez N; Srivastava T; Gbadegesin R
Am J Kidney Dis; 2018 Mar; 71(3):399-406. PubMed ID: 29277510
[TBL] [Abstract][Full Text] [Related]
6. HLA-DQB1 and DRB1 alleles in Egyptian children with steroid-sensitive nephrotic syndrome.
Bakr AM; El-Chenawy F
Pediatr Nephrol; 1998 Apr; 12(3):234-7. PubMed ID: 9630045
[TBL] [Abstract][Full Text] [Related]
7. HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome.
Gbadegesin RA; Adeyemo A; Webb NJ; Greenbaum LA; Abeyagunawardena A; Thalgahagoda S; Kale A; Gipson D; Srivastava T; Lin JJ; Chand D; Hunley TE; Brophy PD; Bagga A; Sinha A; Rheault MN; Ghali J; Nicholls K; Abraham E; Janjua HS; Omoloja A; Barletta GM; Cai Y; Milford DD; O'Brien C; Awan A; Belostotsky V; Smoyer WE; Homstad A; Hall G; Wu G; Nagaraj S; Wigfall D; Foreman J; Winn MP;
J Am Soc Nephrol; 2015 Jul; 26(7):1701-10. PubMed ID: 25349203
[TBL] [Abstract][Full Text] [Related]
8. Multiple sclerosis risk variant HLA-DRB1*1501 associates with high expression of DRB1 gene in different human populations.
Alcina A; Abad-Grau Mdel M; Fedetz M; Izquierdo G; Lucas M; Fernández O; Ndagire D; Catalá-Rabasa A; Ruiz A; Gayán J; Delgado C; Arnal C; Matesanz F
PLoS One; 2012; 7(1):e29819. PubMed ID: 22253788
[TBL] [Abstract][Full Text] [Related]
9. Association of Parkinson disease with structural and regulatory variants in the HLA region.
Wissemann WT; Hill-Burns EM; Zabetian CP; Factor SA; Patsopoulos N; Hoglund B; Holcomb C; Donahue RJ; Thomson G; Erlich H; Payami H
Am J Hum Genet; 2013 Nov; 93(5):984-93. PubMed ID: 24183452
[TBL] [Abstract][Full Text] [Related]
10. The rare HLA-DQA1*03-DQB1*02 haplotype confers susceptibility to type 1 diabetes in whites and is preferentially associated with early clinical disease onset in male subjects.
van Autreve JE; Weets I; Gulbis B; Vertongen F; Gorus FK; van der Auwera BJ;
Hum Immunol; 2004 Jul; 65(7):729-36. PubMed ID: 15301863
[TBL] [Abstract][Full Text] [Related]
11. Association of DQB1*0302 alloantigens in Japanese pediatric patients with steroid-sensitive nephrotic syndrome.
Abe KK; Michinaga I; Hiratsuka T; Ogahara S; Naito S; Arakawa K; Tsuru N; Tokieda K
Nephron; 1995; 70(1):28-34. PubMed ID: 7617114
[TBL] [Abstract][Full Text] [Related]
12. Type 1 Diabetes Risk in African-Ancestry Participants and Utility of an Ancestry-Specific Genetic Risk Score.
Onengut-Gumuscu S; Chen WM; Robertson CC; Bonnie JK; Farber E; Zhu Z; Oksenberg JR; Brant SR; Bridges SL; Edberg JC; Kimberly RP; Gregersen PK; Rewers MJ; Steck AK; Black MH; Dabelea D; Pihoker C; Atkinson MA; Wagenknecht LE; Divers J; Bell RA; ; ; Erlich HA; Concannon P; Rich SS
Diabetes Care; 2019 Mar; 42(3):406-415. PubMed ID: 30659077
[TBL] [Abstract][Full Text] [Related]
13. HLA-DRB1, DQA1 and DQB1 DNA polymorphisms in healthy Algerian and genetic relationships with other populations.
Djoulah S; Sanchez-Mazas A; Khalil I; Benhamamouch S; Degos L; Deschamps I; Hors J
Tissue Antigens; 1994 Feb; 43(2):102-9. PubMed ID: 8016836
[TBL] [Abstract][Full Text] [Related]
14. HLA class II associations with idiopathic nephrotic syndrome in children.
Konrad M; Mytilineos J; Bouissou F; Scherer S; Gulli MP; Meissner I; Cambon-Thomsen A; Opelz G; Schärer K
Tissue Antigens; 1994 May; 43(5):275-80. PubMed ID: 7940495
[TBL] [Abstract][Full Text] [Related]
15. Analysis of antibody markers, DRB1, DRB5, DQA1 and DQB1 genes and modeling of DR2 molecules in DR2-positive patients with insulin-dependent diabetes mellitus.
Sanjeevi CB; Lybrand TP; Landin-Olsson M; Kockum I; Dahlquist G; Hagopian WA; Palmer JP; Lernmark A
Tissue Antigens; 1994 Aug; 44(2):110-9. PubMed ID: 7817375
[TBL] [Abstract][Full Text] [Related]
16. Heterogeneity of HLA-DR2 haplotypes in Caucasoid Americans, African Americans, Chinese Americans, Native Americans and Xiamen Chinese.
Lee A; Huang R; Yan L; Shaw CK; Zeng S; Lin PY; Lee TD
Eur J Immunogenet; 1999 Aug; 26(4):275-80. PubMed ID: 10457891
[TBL] [Abstract][Full Text] [Related]
17. Complex interaction between HLA DR and DQ in conferring risk for childhood type 1 diabetes.
Kockum I; Sanjeevi CB; Eastman S; Landin-Olsson M; Dahlquist G; Lernmark A
Eur J Immunogenet; 1999 Oct; 26(5):361-72. PubMed ID: 10553503
[TBL] [Abstract][Full Text] [Related]
18. HLA-DR2 haplotypic diversity in populations of South-East Asia, northern China, Melanesia and Australian aborigines using PCR-RFLP for DRB1, DRB5, DQA1 and DQB1. A novel DRB1 allele: DRB1*16022.
Trejaut J; Bhatia K; Greville WD; Hu KR; Duraisamy G; Nuchprayoon C; Donald J; Aziz A; Dunckley H
Eur J Immunogenet; 1996 Dec; 23(6):437-49. PubMed ID: 8971541
[TBL] [Abstract][Full Text] [Related]
19. Interrelationship of major histocompatibility complex class II alleles and autoantibodies in four ethnic groups with various forms of myositis.
Arnett FC; Targoff IN; Mimori T; Goldstein R; Warner NB; Reveille JD
Arthritis Rheum; 1996 Sep; 39(9):1507-18. PubMed ID: 8814062
[TBL] [Abstract][Full Text] [Related]
20. Ethnicity-dependent association of HLA DRB1-DQA1-DQB1 alleles in Brazilian multiple sclerosis patients.
Alves-Leon SV; Papais-Alvarenga R; Magalhães M; Alvarenga M; Thuler LC; Fernández y Fernandez O
Acta Neurol Scand; 2007 May; 115(5):306-11. PubMed ID: 17489940
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
