Published in Metabolism on August 01, 2004
Evidence for association of the TCF7 locus with type I diabetes. Genes Immun (2009) 1.15
Association analysis of SNPs in the IL4R locus with type I diabetes. Genes Immun (2009) 0.87
The adenosine deaminase gene polymorphism is associated with chronic heart failure risk in Chinese. Int J Mol Sci (2014) 0.75
Haptoglobin genotype and natural fertility in humans. Fertil Steril (1999) 2.05
Favism: association with erythrocyte acid phosphatase phenotype. Science (1971) 1.61
Enzyme polymorphism and clinical variability of diseases: a study of diabetes mellitus. Hum Biol (1989) 1.42
Inflammatory bowel disease: Are there gender differences in the genetics of signal transduction? A preliminary study of cytosolic low molecular weight protein tyrosine phosphatase. Dis Markers (2000) 1.39
Association of single nucleotide polymorphisms in the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction. J Med Genet (2003) 1.12
ABO/Secretor genetic complex and susceptibility to asthma in childhood. Eur Respir J (2001) 1.08
A marker locus for fertility?-- Real or spurious? Fertil Steril (1999) 1.08
ABO system incompatibility: relationship between direct Coombs test positivity and neonatal jaundice. Pediatrics (1973) 1.04
In vitro effect of acetylphenylhydrazine on acid phosphatases of fetal red blood cells. Biol Neonate (1970) 1.03
A patient with nucleoside phosphorylase deficiency, selective t-cell deficiency, and autoimmune hemolytic anemia. J Pediatr (1978) 1.02
Impact of the CYP4F2 p.V433M polymorphism on coumarin dose requirement: systematic review and meta-analysis. Clin Pharmacol Ther (2012) 1.00
An asthma-associated genetic variant of STAT6 predicts low burden of ascaris worm infestation. Genes Immun (2004) 0.99
Interaction between placental alkaline phosphatase and ABO system polymorphisms. Effects on the clinical manifestations of feto-maternal ABO incompatibility. Vox Sang (1972) 0.99
Red cell acid phosphatase: another polymorphism correlated with Malaria? Am J Phys Anthropol (1975) 0.96
ACP1 genetic polymorphism and coronary artery disease: an association study. Cardiology (2009) 0.92
HLA Bw35 antigen and human reproduction. J Med Genet (1980) 0.90
Effect of oxidized glutathione on human red cell acid phosphatases. Biochem Biophys Res Commun (1964) 0.90
A study of nine polymorphic systems in the population of the Po Delta. Am J Phys Anthropol (1976) 0.89
A genetic basis for heterogeneity of asthma syndrome in pediatric ages: adenosine deaminase phenotypes. J Allergy Clin Immunol (1984) 0.88
Genetic differentiation among Sardinian villages. Am J Phys Anthropol (1975) 0.88
ACP1 and human adaptability. 1. Association with common diseases: a case-control study. Hum Genet (1995) 0.88
Genetic polymorphisms and intrauterine development. Evidence of decreased heterozygosity in light-for-dates human newborn babies. Experientia (1979) 0.88
Interaction of integrin alpha IIb beta 3 with multiple fibrinogen domains during platelet adhesion. J Biol Chem (1995) 0.88
Letter: Neonatal jaundice and erythrocyte-acid-phosphatase phenotype. Lancet (1976) 0.88
Further studies on acid phosphatase in obese subjects. Dis Markers (1992) 0.87
Erythrocyte acid phosphatase polymorphism and haemolysis. J Med Genet (1972) 0.87
3020insC mutation within the NOD2 gene in Crohn's disease: frequency and association with clinical pattern in an Italian population. Dig Liver Dis (2002) 0.86
Autism: evidence of association with adenosine deaminase genetic polymorphism. Neurogenetics (2001) 0.85
On the relation between malaria and G-6-PD deficiency. J Med Genet (1978) 0.85
Adenosine deaminase polymorphism in Sardinia. Humangenetik (1971) 0.85
Phosphotyrosine protein phosphatases and diabetic pregnancy: an association between low molecular weight acid phosphatase and degree of glycemic control. Experientia (1996) 0.85
Favism: current problems and investigations. J Med Genet (1973) 0.84
Differential effect of oxidized glutathione or acetylphenylhydrazine on individual electrophoretic components of red cell acid phosphatases. Experientia (1967) 0.84
Phosphotyrosine-protein-phosphatase and diabetic disorders. Further studies on the relationship between low molecular weight acid phosphatase genotype and degree of glycemic control. Dis Markers (1998) 0.84
Interleukin-23R Arg381Gln is associated with susceptibility to Crohn's disease but not with phenotype in an Italian population. Gastroenterology (2007) 0.84
[Acute renal failure caused by VIP-secreting tumor]. G Ital Nefrol (2003) 0.83
The genetic component of quantitative perinatal variables. An analysis of relations between erythrocyte acid phosphatase phenotype and birth weight, gestational age and serum bilirubin level in the first days of life. J Perinat Med (1980) 0.83
Is delayed childbearing changing gene frequencies in Western populations? Hum Biol (2005) 0.83
[New insights in atherosclerosis research: LOX-1, leading actor of cardiovascular diseases]. Clin Ter (2007) 0.83
Atherosclerosis and PTPN22: a study in coronary artery disease. Cardiology (2011) 0.83
ADA genetic polymorphism and the effect of smoking on neonatal bilirubinemia and developmental parameters. Early Hum Dev (2008) 0.82
Adenosine deaminase polymorphism. Associations at clinical level suggest a role in cell functions and immune reactions. J Med Genet (1981) 0.82
Blood groups and histocompatibility antigens in habitual abortion. Haematologia (Budap) (1980) 0.82
Convulsive disorder and genetic polymorphism. Association of idiopathic generalized epilepsy with haptoglobin polymorphism. Neurogenetics (2004) 0.82
Genetic polymorphisms in juvenile-onset diabetes. Hum Hered (1978) 0.82
[Research on the "toxic principle" of Vicia faba]. Minerva Pediatr (1967) 0.82
Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian population. Mol Cell Probes (2004) 0.82
Enzyme variability and neonatal jaundice. The role of adenosine deaminase and acid phosphatase. J Perinat Med (1989) 0.81
Stability of acid phosphatase of fetal red blood cells during incubation with acetylphenylhydrazine. Acta Paediatr Scand (1971) 0.81
Is there a relationship between sex of cystic fibrosis carriers and sex ratio of their offspring? Hum Genet (1980) 0.81
IL-4 receptor alpha chain genetic polymorphism and total IgE levels in the English population: two-locus haplotypes are more informative than individual SNPs. Clin Genet (2002) 0.81
Malaria as a possible evolutionary cause of allergy. Allergy (1999) 0.81
ACP1 and Th class of immunological disease: evidence of interaction with gender. Int Arch Allergy Immunol (2007) 0.81
Placental alkaline phosphatase polymorphism in some Italian populations. Humangenetik (1970) 0.81
Risk of type 1 diabetes in childhood and maternal age at delivery, interaction with ACP1 and sex. Diabetes Metab Res Rev (2005) 0.81
Adenosine deaminase and body mass index in non-insulin-dependent diabetes mellitus. Metabolism (1999) 0.81
Functional modulation of the isolated glycoprotein Ib binding domain of von Willebrand factor expressed in Escherichia coli. Biochemistry (1991) 0.81
The association of PTPN22 polymorphism with endometriosis: effect of genetic and clinical factors. Eur J Obstet Gynecol Reprod Biol (2013) 0.80
Genotypes of cytosolic low-molecular-weight protein-tyrosine-phosphatase correlate with age at onset of type 1 diabetes in a sex-specific manner. Metabolism (2002) 0.80
Acid phosphatases and hemoglobin in normal and G-6-PD deficient erythrocytes incubated with acetylphenylhydrazine under various conditions. Experientia (1965) 0.80
Coronary artery disease: evidence of interaction between PTPN22 and p53 genetic polymorphisms. Cardiology (2011) 0.80
The genetics of signal transduction and the effect of smoking on intrauterine growth. Int J Epidemiol (2001) 0.80