Found: 7
Select item for more details and to access through your institution.
Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.
- Published in:
- Human Genetics, 2010, v. 127, n. 5, p. 525, doi. 10.1007/s00439-010-0789-4
- By:
- Publication type:
- Article
Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA–CLEC16A–SOCS1 gene complex.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 17, p. 3517, doi. 10.1093/hmg/ddr250
- By:
- Publication type:
- Article
Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12 566 individuals.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 21, p. 4286
- By:
- Publication type:
- Article
CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 11, p. 2331
- By:
- Publication type:
- Article
Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality.
- Published in:
- Genetic Epidemiology, 2011, v. 35, n. 8, p. 887, doi. 10.1002/gepi.20639
- By:
- Publication type:
- Article
High Density GWAS for LDL Cholesterol in African Americans Using Electronic Medical Records Reveals a Strong Protective Variant in APOE.
- Published in:
- CTS: Clinical & Translational Science, 2012, v. 5, n. 5, p. 394, doi. 10.1111/j.1752-8062.2012.00446.x
- By:
- Publication type:
- Article
Variation Within DNA Repair Pathway Genes and Risk of Multiple Sclerosis.
- Published in:
- American Journal of Epidemiology, 2010, v. 172, n. 2, p. 217, doi. 10.1093/aje/kwq086
- By:
- Publication type:
- Article