Pages that link to "Q30418816"

The following pages link to Imputing amino acid polymorphisms in human leukocyte antigens (Q30418816):

Displayed 50 items.

• Autoimmune diseases - connecting risk alleles with molecular traits of the immune system (Q26767040) ‎ (← links)
• Identification and utilization of donor and recipient genetic variants to predict survival after HCT: are we ready for primetime? (Q28080914) ‎ (← links)
• A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy (Q28242687) ‎ (← links)
• Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma (Q28248768) ‎ (← links)
• Schizophrenia risk from complex variation of complement component 4 (Q28272545) ‎ (← links)
• 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 (Q28651183) ‎ (← links)
• Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci (Q29248527) ‎ (← links)
• A genome-wide association study of rheumatoid arthritis without antibodies against citrullinated peptides (Q29417125) ‎ (← links)
• Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases (Q30278872) ‎ (← links)
• Additive and interaction effects at three amino acid positions in HLA-DQ and HLA-DR molecules drive type 1 diabetes risk (Q30279028) ‎ (← links)
• HLA-DPB1*04:01 Protects Genetically Susceptible Children from Celiac Disease Autoimmunity in the TEDDY Study (Q30279299) ‎ (← links)
• Design and Implementation of the International Genetics and Translational Research in Transplantation Network (Q30366188) ‎ (← links)
• HLA-DPB1 and HLA class I confer risk of and protection from narcolepsy (Q30370632) ‎ (← links)
• HLA-DRB1*07:01 is associated with a higher risk of asparaginase allergies. (Q30371340) ‎ (← links)
• The impact of host genetic variation on infection with HIV-1. (Q30374810) ‎ (← links)
• Immune DNA signature of T-cell infiltration in breast tumor exomes. (Q30377226) ‎ (← links)
• Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritis (Q30407889) ‎ (← links)
• Predicting HLA alleles from high-resolution SNP data in three Southeast Asian populations (Q30793085) ‎ (← links)
• High-accuracy imputation for HLA class I and II genes based on high-resolution SNP data of population-specific references. (Q30898115) ‎ (← links)
• Imputation of KIR Types from SNP Variation Data (Q31000729) ‎ (← links)
• HLA imputation in an admixed population: An assessment of the 1000 Genomes data as a training set. (Q31025957) ‎ (← links)
• Evaluation of computational programs to predict HLA genotypes from genomic sequencing data. (Q31140417) ‎ (← links)
• Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only (Q31154691) ‎ (← links)
• A genome-wide association study of heparin-induced thrombocytopenia using an electronic medical record (Q33419319) ‎ (← links)
• The MHC locus and genetic susceptibility to autoimmune and infectious diseases (Q33608703) ‎ (← links)
• Genetics of rheumatoid arthritis susceptibility, severity, and treatment response. (Q33841329) ‎ (← links)
• HLA-check: evaluating HLA data from SNP information (Q33892400) ‎ (← links)
• Fine mapping major histocompatibility complex associations in psoriasis and its clinical subtypes (Q34030756) ‎ (← links)
• Genetics, genomics, and their relevance to pathology and therapy (Q34108958) ‎ (← links)
• Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles (Q34138234) ‎ (← links)
• Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region (Q34288685) ‎ (← links)
• Whole-genome sequence variation, population structure and demographic history of the Dutch population (Q34426935) ‎ (← links)
• Risk for ACPA-positive rheumatoid arthritis is driven by shared HLA amino acid polymorphisms in Asian and European populations (Q34575685) ‎ (← links)
• A novel Acute Retroviral Syndrome Severity Score predicts the key surrogate markers for HIV-1 disease progression (Q34662516) ‎ (← links)
• Association of host genome with intestinal microbial composition in a large healthy cohort (Q34679029) ‎ (← links)
• Refinement of the MHC risk map in a scandinavian primary sclerosing cholangitis population (Q34733835) ‎ (← links)
• A genome-wide association study of marginal zone lymphoma shows association to the HLA region (Q34881099) ‎ (← links)
• Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitis (Q34996471) ‎ (← links)
• Genome-wide association study identifies peanut allergy-specific loci and evidence of epigenetic mediation in US children (Q35120318) ‎ (← links)
• A large-scale genetic analysis reveals a strong contribution of the HLA class II region to giant cell arteritis susceptibility (Q35266391) ‎ (← links)
• Additive effects of HLA alleles and innate immune genes determine viral outcome in HCV infection (Q35350883) ‎ (← links)
• Construction and application of a Korean reference panel for imputing classical alleles and amino acids of human leukocyte antigen genes. (Q35421663) ‎ (← links)
• Association of valine and leucine at HLA-DRB1 position 11 with radiographic progression in rheumatoid arthritis, independent of the shared epitope alleles but not independent of anti-citrullinated protein antibodies. (Q35563220) ‎ (← links)
• Imputation of class I and II HLA loci using high-density SNPs from ImmunoChip and their associations with Kawasaki disease in family-based study (Q35602584) ‎ (← links)
• Major histocompatibility complex associations of ankylosing spondylitis are complex and involve further epistasis with ERAP1. (Q35645174) ‎ (← links)
• Fine mapping in the MHC region accounts for 18% additional genetic risk for celiac disease (Q35665929) ‎ (← links)
• Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci (Q35671405) ‎ (← links)
• Identification of new susceptibility loci for IgA nephropathy in Han Chinese. (Q35692714) ‎ (← links)
• Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study (Q35863499) ‎ (← links)
• A Genome Wide Study of Copy Number Variation Associated with Nasopharyngeal Carcinoma in Malaysian Chinese Identifies CNVs at 11q14.3 and 6p21.3 as Candidate Loci (Q35885173) ‎ (← links)