The genetics of celiac disease: A comprehensive review of clinical implications

R Dieli-Crimi, MC Cénit, C Nunez - Journal of autoimmunity, 2015 - Elsevier
Celiac disease (CD) is a complex immune-related disease with a very strong genetic
component. Multiple genetic findings over the last decade have added to the already known …

[HTML][HTML] Host genetic factors affecting hepatitis B infection outcomes: Insights from genome-wide association studies

IM Akcay, S Katrinli, K Ozdil, GD Doganay… - World journal of …, 2018 - ncbi.nlm.nih.gov
The clinical outcome of hepatitis B virus (HBV) infection depends on the success or failure of
the immune responses to HBV, and varies widely among individuals, ranging from …

Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis

CJ Rhodes, K Batai, M Bleda, M Haimel… - The Lancet …, 2019 - thelancet.com
Background Rare genetic variants cause pulmonary arterial hypertension, but the
contribution of common genetic variation to disease risk and natural history is poorly …

Accurate prediction of HLA class II antigen presentation across all loci using tailored data acquisition and refined machine learning

JB Nilsson, S Kaabinejadian, H Yari, MGD Kester… - Science …, 2023 - science.org
Accurate prediction of antigen presentation by human leukocyte antigen (HLA) class II
molecules is crucial for rational development of immunotherapies and vaccines targeting …

[PDF][PDF] Identification of functional and expression polymorphisms associated with risk for antineutrophil cytoplasmic autoantibody–associated vasculitis

PA Merkel, G Xie, PA Monach, X Ji… - Arthritis & …, 2017 - Wiley Online Library
Objective To identify risk alleles relevant to the causal and biologic mechanisms of
antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis (AAV). Methods A …

A T-cell epitope encoded by a subset of HLA-DPB1 alleles determines nonpermissive mismatches for hematologic stem cell transplantation

E Zino, G Frumento, S Marktel, MP Sormani, F Ficara… - Blood, 2004 - ashpublications.org
The importance of HLA-DPB1 matching for the outcome of allogeneic hematologic stem cell
(HSC) transplantation is controversial. We have previously identified HLA-DPB1* 0901 as a …

New loci associated with chronic hepatitis B virus infection in Han Chinese

Z Hu, Y Liu, X Zhai, J Dai, G Jin, L Wang, L Zhu… - Nature …, 2013 - nature.com
Chronic hepatitis B virus (HBV) infection is a challenging global health problem. To identify
genetic loci involved in chronic HBV infection, we designed a three-phase genome-wide …

[PDF][PDF] Genetic variants in human leukocyte antigen/DP‐DQ influence both hepatitis B virus clearance and hepatocellular carcinoma development

L Hu, X Zhai, J Liu, M Chu, S Pan, J Jiang… - …, 2012 - Wiley Online Library
Recent genome‐wide association studies showed that four single‐nucleotide
polymorphisms (SNPs) in human leukocyte antigen (HLA)‐DP (rs3077and rs9277535) and …

In silico identification of supertypes for class II MHCs

IA Doytchinova, DR Flower - The Journal of Immunology, 2005 - journals.aai.org
The development of epitope-based vaccines, which have wide population coverage, is
greatly complicated by MHC polymorphism. The grouping of alleles into supertypes, on the …

[HTML][HTML] The impact of amino acid variability on alloreactivity defines a functional distance predictive of permissive HLA-DPB1 mismatches in hematopoietic stem cell …

P Crivello, L Zito, F Sizzano, E Zino, M Maiers… - Biology of Blood and …, 2015 - Elsevier
A major challenge in unrelated hematopoietic stem cell transplantation (HSCT) is the
prediction of permissive HLA mismatches, ie, those associated with lower clinical risks …