Show
Sort by
-
Personalized genetic counseling for Stargardt disease : offspring risk estimates based on variant severity
-
- Journal Article
- A1
- open access
Autoantibodies against type I IFNs in patients with critical influenza pneumonia
-
- Journal Article
- A2
- open access
Association of vitamin D receptor gene polymorphisms with the occurrence of low bone density, osteopenia, and osteoporosis in patients with type 2 diabetes
-
Genomic analysis of inherited hearing loss in the Palestinian population
(2020) PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 117(33). p.20070-20076 -
- Journal Article
- A1
- open access
Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants
-
Immune-array analysis in sporadic inclusion body myositis reveals HLA-DRB1 amino acid heterogeneity across the myositis spectrum
-
High-density mapping of the MHC identifies a shared role for HLA-DRB1⋆01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis
-
Analysis of Malus S-RNase gene diversity based on a comparative study of old and modern apple cultivars and European wild apple
-
Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers
-
Haplotype 4 of the multiple sclerosis-associated interleukin-7 receptor alpha gene influences the frequency of recent thymic emigrants