Published in Rev Environ Health on June 03, 2002
Risk factors for acute leukemia in children: a review. Environ Health Perspect (2007) 2.57
Roles of genetic polymorphisms in the folate pathway in childhood acute lymphoblastic leukemia evaluated by Bayesian relevance and effect size analysis. PLoS One (2013) 0.86
Maternal and offspring xenobiotic metabolism haplotypes and the risk of childhood acute lymphoblastic leukemia. Leuk Res (2013) 0.83
Association between NQO1 C609T polymorphism and acute lymphoblastic leukemia risk: evidence from an updated meta-analysis based on 17 case-control studies. J Cancer Res Clin Oncol (2014) 0.82
Gene variants of CYP1A1 and CYP2D6 and the risk of childhood acute lymphoblastic leukaemia; outcome of a case control study from Kashmir, India. Mol Biol Res Commun (2017) 0.75
Genome fingerprinting by simple sequence repeat (SSR)-anchored polymerase chain reaction amplification. Genomics (1994) 6.40
Pharmacogenomics and metabolite measurement for 6-mercaptopurine therapy in inflammatory bowel disease. Gastroenterology (2000) 2.99
Risk of childhood leukemia associated with exposure to pesticides and with gene polymorphisms. Epidemiology (1999) 2.85
Alu sequences in the coding regions of mRNA: a source of protein variability. Trends Genet (1994) 2.49
Standardized nomenclature for Alu repeats. J Mol Evol (1996) 2.00
Ethiopia: between Sub-Saharan Africa and western Eurasia. Ann Hum Genet (2005) 1.98
Relationship between 2'-hydroxyls and magnesium binding in the hammerhead RNA domain: a model for ribozyme catalysis. Biochemistry (1991) 1.75
Genetic structure of the ancestral population of modern humans. J Mol Evol (1998) 1.70
Linkage disequilibrium analysis in young populations: pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians. Am J Hum Genet (1996) 1.68
Reverse transcriptase activity from human embryonal carcinoma cells NTera2D1. EMBO J (1990) 1.68
Alu RNA secondary structure consists of two independent 7 SL RNA-like folding units. J Biol Chem (1991) 1.60
Phylogenetic and familial estimates of mitochondrial substitution rates: study of control region mutations in deep-rooting pedigrees. Am J Hum Genet (2001) 1.59
Splice-mediated insertion of an Alu sequence inactivates ornithine delta-aminotransferase: a role for Alu elements in human mutation. Proc Natl Acad Sci U S A (1991) 1.56
The gene for incontinentia pigmenti is assigned to Xq28. Genomics (1989) 1.52
CORE-SINEs: eukaryotic short interspersed retroposing elements with common sequence motifs. Proc Natl Acad Sci U S A (1999) 1.50
Susceptibility to childhood acute lymphoblastic leukemia: influence of CYP1A1, CYP2D6, GSTM1, and GSTT1 genetic polymorphisms. Blood (1999) 1.45
Prostate cancer susceptibility genes: lessons learned and challenges posed. Endocr Relat Cancer (2003) 1.44
Phylogenetic analysis of a reported complementary DNA sequence. Science (1994) 1.43
Is selection responsible for the low level of variation in the last intron of the ZFY locus? Mol Biol Evol (1999) 1.42
Alu RNA transcripts in human embryonal carcinoma cells. Model of post-transcriptional selection of master sequences. J Mol Biol (1992) 1.40
Mixed DNA/RNA polymers are cleaved by the hammerhead ribozyme. Biochemistry (1990) 1.35
The genetic clock and the age of the founder effect in growing populations: a lesson from French Canadians and Ashkenazim. Am J Hum Genet (1997) 1.32
Genetic characterisation of Toxoplasma gondii in wildlife from North America revealed widespread and high prevalence of the fourth clonal type. Int J Parasitol (2011) 1.30
Ubiquitous mammalian-wide interspersed repeats (MIRs) are molecular fossils from the mesozoic era. Nucleic Acids Res (1995) 1.29
FISH ordering of reference markers and of the gene for the alpha 5 subunit of the gamma-aminobutyric acid receptor (GABRA5) within the Angelman and Prader-Willi syndrome chromosomal regions. Hum Mol Genet (1993) 1.22
Nuclear DNA diversity in worldwide distributed human populations. Gene (1997) 1.22
Spatial and temporal distribution of the neutral polymorphisms in the last ZFX intron: analysis of the haplotype structure and genealogy. Genetics (1999) 1.21
Evolution of mouse B1 repeats: 7SL RNA folding pattern conserved. J Mol Evol (1991) 1.16
High intensity focused ultrasound--a surgical technique for the treatment of discrete liver tumours. Phys Med Biol (1989) 1.15
Alumorphs--human DNA polymorphisms detected by polymerase chain reaction using Alu-specific primers. Genomics (1990) 1.14
Risk of childhood leukemia associated with diagnostic irradiation and polymorphisms in DNA repair genes. Environ Health Perspect (2000) 1.13
Expression of glypican 3 (GPC3) in embryonal tumors. Int J Cancer (2000) 1.10
mtDNA and Y chromosome-specific polymorphisms in modern Ojibwa: implications about the origin of their gene pool. Am J Hum Genet (1997) 1.09
Use of gamma irradiation to eliminate DNA contamination for PCR. Nucleic Acids Res (1990) 1.09
Evolutionary inventions and continuity of CORE-SINEs in mammals. J Mol Biol (2000) 1.07
Genetic susceptibility to childhood acute lymphoblastic leukemia. Leuk Lymphoma (2000) 1.07
Antibiotic prophylaxis for post-operative wound infection in clean elective breast surgery. Eur J Surg Oncol (2000) 1.05
High resolution deletion mapping reveals frequent allelic losses at the DNA mismatch repair loci hMLH1 and hMSH3 in non-small cell lung cancer. Int J Cancer (1998) 1.03
Linkage study of chronic childhood-onset spinal muscular atrophy (SMA): confirmation of close linkage to D5S39 in French Canadian families. Genomics (1992) 1.01
The human gamma-aminobutyric acid receptor subunit beta 3 and alpha 5 gene cluster in chromosome 15q11-q13 is rich in highly polymorphic (CA)n repeats. Genomics (1994) 1.01
DNA methylation of retinoic acid receptor beta in breast cancer and possible therapeutic role of 5-aza-2'-deoxycytidine. Anticancer Drugs (1999) 1.01
A young Alu subfamily amplified independently in human and African great apes lineages. Nucleic Acids Res (1994) 1.01
Unique origin and specific ethnic distribution of the Friedreich ataxia GAA expansion. Neurology (2000) 1.01
Allelic loss in childhood acute lymphoblastic leukemia. Leuk Res (1997) 1.01
Monophyletic origin of Alu elements in primates. J Mol Evol (1998) 1.00
Dinucleotide repeat polymorphism at the GABAA receptor alpha 5 (GABRA5) locus at chromosome 15q11-q13. Hum Mol Genet (1992) 1.00
Demethylation by 5-aza-2'-deoxycytidine of specific 5-methylcytosine sites in the promoter region of the retinoic acid receptor beta gene in human colon carcinoma cells. Anticancer Drugs (1998) 1.00
Mutational and expression analysis of the chromosome 12p candidate tumor suppressor genes in pre-B acute lymphoblastic leukemia. Leukemia (2004) 1.00
Analysis of nucleotide diversity of NAT2 coding region reveals homogeneity across Native American populations and high intra-population diversity. Pharmacogenomics J (2006) 1.00
Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11. Hum Genet (1988) 0.99
Linkage mapping by simultaneous screening of multiple polymorphic loci using Alu oligonucleotide-directed PCR. Proc Natl Acad Sci U S A (1992) 0.99
Genetic susceptibility to breast cancer in French-Canadians: role of carcinogen-metabolizing enzymes and gene-environment interactions. Int J Cancer (2001) 0.99
Rapid detection of CYP1A1, CYP2D6, and NAT variants by multiplex polymerase chain reaction and allele-specific oligonucleotide assay. Anal Biochem (1999) 0.97
Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations. J Med Genet (2007) 0.96
Preconceptional paternal exposure to pesticides and increased risk of childhood leukaemia. Lancet (1999) 0.96
Mechanism of codon recognition by transfer RNA and codon-induced tRNA association. J Mol Biol (1984) 0.94
Colorectal breast metastases presenting with atypical imaging features. Br J Radiol (2008) 0.93
Deletions in the dystrophin gene: analysis of Duchenne and Becker muscular dystrophy patients in Quebec. Hum Genet (1992) 0.93
Phylogenetic affinities of tarsier in the context of primate Alu repeats. Mol Phylogenet Evol (1999) 0.92
Multistep mechanism of codon recognition by transfer ribonucleic acid. Biochemistry (1980) 0.92
Magnesium ion inner sphere complex in the anticodon loop of phenylalanine transfer ribonucleic acid. Biochemistry (1982) 0.91
The TP53 Arg72Pro and MDM2 309G>T polymorphisms are not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers. Br J Cancer (2009) 0.90
Parental smoking, CYP1A1 genetic polymorphisms and childhood leukemia (Québec, Canada). Cancer Causes Control (2000) 0.90
Codon-induced transfer RNA association. A property of transfer RNA involved in its adaptor function? J Mol Biol (1983) 0.90
Frequent loss of heterozygosity at the DNA mismatch-repair loci hMLH1 and hMSH3 in sporadic breast cancer. Br J Cancer (1999) 0.90
Expression of 2 variant forms of fibroblast growth factor receptor 1 in human breast. Int J Cancer (1995) 0.90
Human mitochondrial HMG CoA synthase: liver cDNA and partial genomic cloning, chromosome mapping to 1p12-p13, and possible role in vertebrate evolution. Genomics (1994) 0.89
Insulin modulation of newly synthesized apolipoproteins B-100 and B-48 in human fetal intestine: gene expression and mRNA editing are not involved. FEBS Lett (1996) 0.88
Mosaic evolution of rodent B1 elements. J Mol Evol (1996) 0.87
Single-strand conformational polymorphisms (SSCP): detection of useful polymorphisms at the dystrophin locus. Hum Genet (1992) 0.87
Genetic polymorphisms of N-acetyltransferases 1 and 2 and gene-gene interaction in the susceptibility to childhood acute lymphoblastic leukemia. Cancer Epidemiol Biomarkers Prev (2000) 0.87
Human gamma-aminobutyric acid-type A receptor alpha5 subunit gene (GABRA5): characterization and structural organization of the 5' flanking region. Genomics (1997) 0.87
Microsatellite instability in childhood T cell acute lymphoblastic leukemia. Leukemia (1997) 0.85
Methylation analysis of the glypican 3 gene in embryonal tumours. Br J Cancer (2004) 0.85
Small cytoplasmic Ro RNA pseudogene and an Alu repeat in the human alpha-1 globin gene. Nucleic Acids Res (1988) 0.84
Iron-ascorbic acid-induced oxidant stress and its quenching by paraoxonase 1 in HDL and the liver: comparison between humans and rats. J Cell Biochem (2005) 0.84
Detection of a mutator phenotype in cancer cells by inter-Alu polymerase chain reaction. Cancer Res (1996) 0.84
Are CpG sites mutation hot spots in the dystrophin gene? Hum Mol Genet (1994) 0.84
Association between genetic variants in the HNF4A gene and childhood-onset Crohn's disease. Genes Immun (2012) 0.83
A new atypical highly mouse virulent Toxoplasma gondii genotype isolated from a wild black bear in Alaska. J Parasitol (2010) 0.83
Mechanism of codon recognition by transfer RNA studied with oligonucleotides larger than triplets. Nucleic Acids Res (1985) 0.83
Frequent deletion of chromosome 12p12.3 in children with acute lymphoblastic leukaemia. Br J Haematol (1997) 0.83
Genomic loci susceptible to replication errors in cancer cells. Br J Cancer (1998) 0.82
The three conformations of the anticodon loop of yeast tRNA(Phe). J Biomol Struct Dyn (1989) 0.82
Comparative analysis of the ETV6 gene in vertebrate genomes from pufferfish to human. Oncogene (2001) 0.82