Published in J Allergy Clin Immunol on August 01, 2004
Induction of the CTLA-4 gene in human lymphocytes is dependent on NFAT binding the proximal promoter. J Immunol (2007) 1.06
CTLA-4, position 49 A/G polymorphism associated with coronary artery lesions in Kawasaki disease. J Clin Immunol (2010) 0.96
Asthma from a pharmacogenomic point of view. Br J Pharmacol (2008) 0.89
Cytotoxic T-lymphocyte associated antigen 4 polymorphisms and asthma risk: a meta-analysis. PLoS One (2012) 0.88
Association of CTLA4 gene polymorphisms with susceptibility and pathology correlation to pulmonary tuberculosis in Southern Han Chinese. Int J Biol Sci (2012) 0.87
Surfactant protein D-mediated decrease of allergen-induced inflammation is dependent upon CTLA4. J Immunol (2010) 0.86
Maternal microchimerism protects against the development of asthma. J Allergy Clin Immunol (2013) 0.82
The CTLA-4 gene polymorphisms are associated with CTLA-4 protein expression levels in multiple sclerosis patients and with susceptibility to disease. Immunology (2009) 0.80
Combining genomewide association study and lung eQTL analysis provides evidence for novel genes associated with asthma. Allergy (2016) 0.76
CTLA4 polymorphism and primary Sjögren's syndrome. Arthritis Res Ther (2007) 0.76
Checkpoint Inhibitors: Applications for Autoimmunity. Curr Allergy Asthma Rep (2017) 0.75
Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease. Nature (2003) 13.00
A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci. PLoS Genet (2009) 6.93
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nat Genet (2013) 4.62
An official American Thoracic Society/European Respiratory Society statement: pulmonary function testing in preschool children. Am J Respir Crit Care Med (2007) 4.10
Air pollution from traffic and the development of respiratory infections and asthmatic and allergic symptoms in children. Am J Respir Crit Care Med (2002) 3.71
Racemic adrenaline and inhalation strategies in acute bronchiolitis. N Engl J Med (2013) 3.51
Maternal vitamin D intake during pregnancy and early childhood wheezing. Am J Clin Nutr (2007) 3.40
Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci. Nat Genet (2013) 2.87
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. Nat Genet (2010) 2.61
Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor. N Engl J Med (2007) 2.56
Maternal food consumption during pregnancy and the longitudinal development of childhood asthma. Am J Respir Crit Care Med (2008) 2.42
Early identification of atopy in the prediction of persistent asthma in children. Lancet (2008) 2.27
Paracetamol in early infancy: the risk of childhood allergy and asthma. Acta Paediatr (2011) 2.19
SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome. Am J Hum Genet (2008) 2.16
Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. Diabetes (2008) 2.15
The significance of early recurrent wheeze for asthma outcomes in late childhood. Eur Respir J (2012) 2.06
Remapping the insulin gene/IDDM2 locus in type 1 diabetes. Diabetes (2004) 2.02
Clinical, immunological, and genetic features of autoimmune primary adrenal insufficiency: observations from a Norwegian registry. J Clin Endocrinol Metab (2009) 2.01
Lung function and exercise capacity in young adults born prematurely. Am J Respir Crit Care Med (2006) 1.98
The prevention and incidence of asthma and mite allergy (PIAMA) birth cohort study: design and first results. Pediatr Allergy Immunol (2002) 1.88
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. PLoS Genet (2011) 1.80
Cholangiocarcinoma in primary sclerosing cholangitis is associated with NKG2D polymorphisms. Hepatology (2008) 1.79
Killer immunoglobulin-like receptor ligand HLA-Bw4 protects against multiple sclerosis. Ann Neurol (2009) 1.76
Off-label prescribing to children in primary care: retrospective observational study. Eur J Clin Pharmacol (2004) 1.71
Genome-wide association analysis in primary sclerosing cholangitis. Gastroenterology (2009) 1.69
Genetic polymorphisms associated with inflammatory bowel disease do not confer risk for primary sclerosing cholangitis. Am J Gastroenterol (2006) 1.68
HLA associated genetic predisposition to autoimmune diseases: Genes involved and possible mechanisms. Transpl Immunol (2005) 1.64
Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency. J Clin Endocrinol Metab (2008) 1.51
Electrostatic modifications of the human leukocyte antigen-DR P9 peptide-binding pocket and susceptibility to primary sclerosing cholangitis. Hepatology (2011) 1.51
Low maternal vitamin E intake during pregnancy is associated with asthma in 5-year-old children. Am J Respir Crit Care Med (2006) 1.51
Interrupter resistance and wheezing phenotypes at 4 years of age. Am J Respir Crit Care Med (2003) 1.49
Comparative high-resolution analysis of linkage disequilibrium and tag single nucleotide polymorphisms between populations in the vitamin D receptor gene. Hum Mol Genet (2004) 1.48
Nasal epithelial cells as surrogates for bronchial epithelial cells in airway inflammation studies. Am J Respir Cell Mol Biol (2008) 1.47
Analysis of MAdCAM-1 and ICAM-1 polymorphisms in 365 Scandinavian patients with primary sclerosing cholangitis. J Hepatol (2006) 1.42
Childhood lung function and the association with β2-adrenergic receptor haplotypes. Acta Paediatr (2013) 1.41
Does bronchial hyperresponsiveness in childhood predict active asthma in adolescence? Am J Respir Crit Care Med (2012) 1.41
Celiac disease genetics: current concepts and practical applications. Clin Gastroenterol Hepatol (2005) 1.37
LYP inhibits T-cell activation when dissociated from CSK. Nat Chem Biol (2012) 1.37
Reported versus measured body weight and height of 4-year-old children and the prevalence of overweight. Eur J Public Health (2006) 1.37
DNA methylation and gene expression changes in monozygotic twins discordant for psoriasis: identification of epigenetically dysregulated genes. PLoS Genet (2012) 1.35
CMIP and ATP2C2 modulate phonological short-term memory in language impairment. Am J Hum Genet (2009) 1.34
Association analysis of the interleukin 17A gene in Caucasian rheumatoid arthritis patients from Norway and New Zealand. Rheumatology (Oxford) (2009) 1.34
Off-label prescribing to children: attitudes and experience of general practitioners. Br J Clin Pharmacol (2005) 1.31
Does early indoor microbial exposure reduce the risk of asthma? The Prevention and Incidence of Asthma and Mite Allergy birth cohort study. J Allergy Clin Immunol (2006) 1.30
Placebo-controlled trial of house dust mite-impermeable mattress covers: effect on symptoms in early childhood. Am J Respir Crit Care Med (2002) 1.29
Allergen exposure in infancy and the development of sensitization, wheeze, and asthma at 4 years. J Allergy Clin Immunol (2005) 1.27
Antibiotic prescribing for children. Too much and too little? Retrospective observational study in primary care. Br J Clin Pharmacol (2003) 1.25
Traffic-related air pollution and otitis media. Environ Health Perspect (2006) 1.22
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08. Ann Neurol (2012) 1.19
The PTPN22 R263Q polymorphism is a risk factor for rheumatoid arthritis in Caucasian case-control samples. Arthritis Rheum (2011) 1.18
Polymorphisms in the cytotoxic T lymphocyte antigen-4 gene region confer susceptibility to Addison's disease. J Clin Endocrinol Metab (2004) 1.17
Gender-specific presentations for asthma, allergic rhinitis and eczema in primary care. Prim Care Respir J (2007) 1.11
Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease. Eur J Hum Genet (2008) 1.10
Limitations and possibilities of low cell number ChIP-seq. BMC Genomics (2012) 1.09
Comorbidities of obesity in school children: a cross-sectional study in the PIAMA birth cohort. BMC Public Health (2010) 1.09
Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes. Nat Genet (2005) 1.09
Attitudes and experiences of community pharmacists towards paediatric off-label prescribing: a prospective survey. Br J Clin Pharmacol (2007) 1.08
Mutational characterization of the bile acid receptor TGR5 in primary sclerosing cholangitis. PLoS One (2010) 1.07
Extensive variation and low heritability of DNA methylation identified in a twin study. Genome Res (2011) 1.07
Autoimmune adrenocortical failure in Norway autoantibodies and human leukocyte antigen class II associations related to clinical features. J Clin Endocrinol Metab (2002) 1.06
Paralytic rabies after a two week holiday in India. BMJ (2005) 1.06
A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with systemic sclerosis in a large European cohort. Ann Rheum Dis (2010) 1.05
A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis. Eur J Hum Genet (2009) 1.05
First trimester maternal tobacco smoking habits and fetal growth. Thorax (2010) 1.05
Changing trends in sex specific prevalence rates for childhood asthma, eczema, and hay fever. Pediatr Pulmonol (2007) 1.04
Respiratory symptoms in the first 7 years of life and birth weight at term: the PIAMA Birth Cohort. Am J Respir Crit Care Med (2007) 1.04
CTLA4 polymorphisms are associated with vitiligo, in patients with concomitant autoimmune diseases. Pigment Cell Res (2005) 1.02
Gender differences in respiratory symptoms in 19-year-old adults born preterm. Respir Res (2005) 1.02
Lack of association of the Ala(45)Thr polymorphism and other common variants of the NeuroD gene with type 1 diabetes. Diabetes (2004) 1.01
Burden of corticosteroids in children with asthma in primary care: retrospective observational study. BMJ (2002) 1.01
Haplotype structure, LD blocks, and uneven recombination within the LRP5 gene. Genome Res (2003) 1.01
A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis. Ann Rheum Dis (2009) 0.99
Breastfeeding, weight gain in infancy, and overweight at seven years of age: the prevention and incidence of asthma and mite allergy birth cohort study. Am J Epidemiol (2007) 0.99
Analysis of the vitamin D receptor gene sequence variants in type 1 diabetes. Diabetes (2004) 0.98
Particular genetic variants of ligands for natural killer cell receptors may contribute to the HLA associated risk of primary sclerosing cholangitis. J Hepatol (2007) 0.98
A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families: evidence for a major susceptibility locus on chromosome 2p. Eur J Hum Genet (2006) 0.98
Programmed death ligand 1 (PD-L1) gene variants contribute to autoimmune Addison's disease and Graves' disease susceptibility. J Clin Endocrinol Metab (2009) 0.97
The effect of prenatal exposure on total IgE at birth and sensitization at twelve months and four years of age: The PIAMA study. Pediatr Allergy Immunol (2005) 0.95
Multiple loci in the HLA complex are associated with Addison's disease. J Clin Endocrinol Metab (2011) 0.94
Mite and pet allergen levels in homes of children born to allergic and nonallergic parents: the PIAMA study. Environ Health Perspect (2002) 0.94
Understanding the complexity of IgE-related phenotypes from childhood to young adulthood: a Mechanisms of the Development of Allergy (MeDALL) seminar. J Allergy Clin Immunol (2012) 0.93
Early daycare is associated with an increase in airway symptoms in early childhood but is no protection against asthma or atopy at 8 years. Am J Respir Crit Care Med (2009) 0.93
Long-term muscular outcome and predisposing and prognostic factors in juvenile dermatomyositis: A case-control study. Arthritis Care Res (Hoboken) (2010) 0.93
Parental smoking and childhood asthma: clinical implications. Treat Respir Med (2005) 0.93
Proteasome immunosubunits protect against the development of CD8 T cell-mediated autoimmune diseases. J Immunol (2011) 0.93
Lack of association between the chemokine receptor 5 polymorphism CCR5delta32 in rheumatoid arthritis and juvenile idiopathic arthritis. BMC Med Genet (2007) 0.93
House dust mite allergen reduction and allergy at 4 yr: follow up of the PIAMA-study. Pediatr Allergy Immunol (2006) 0.92
Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. PLoS One (2013) 0.92
Paediatric homoeopathy in general practice: where, when and why? Br J Clin Pharmacol (2005) 0.92
Importance of human leukocyte antigen (HLA) class I and II alleles on the risk of multiple sclerosis. PLoS One (2012) 0.92
Can finger-prick sampling replace venous sampling to determine the pharmacokinetic profile of oral paracetamol? Br J Clin Pharmacol (2010) 0.92