Published in Hereditas on January 01, 1978
A new method for the analysis of cohort studies: implications of the multistage theory of carcinogenesis applied to occupational arsenic exposure. Environ Health Perspect (1983) 1.33
Enhancement of chromosomal damage by arsenic: implications for mechanism. Environ Health Perspect (1993) 0.87
Biomonitoring exposure to metal compounds with carcinogenic properties. Environ Health Perspect (1993) 0.82
Micronucleus frequency in peripheral blood lymphocytes and buccal mucosa cells of copper smelter workers, with special regard to arsenic exposure. Int Arch Occup Environ Health (2007) 0.82
Metallic elements in fossil fuel combustion products: amounts and form of emissions and evaluation of carcinogenicity and mutagenicity. Environ Health Perspect (1983) 0.78
Environmental toxicants in developing countries. Environ Health Perspect (1996) 0.78
Chemical interaction: enhancement and inhibition of clastogenicity. Environ Health Perspect (1993) 0.77
Evaluation of the genetic alterations in direct and indirect exposures of hexavalent chromium [Cr(VI)] in leather tanning industry workers North Arcot District, South India. Int Arch Occup Environ Health (2010) 0.76
Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language. Am J Hum Genet (2000) 4.72
Genes and languages in Europe: an analysis of mitochondrial lineages. Genome Res (1995) 2.93
Is p53 polymorphism maintained by natural selection? Hum Hered (1994) 1.92
Cancer risk in humans predicted by increased levels of chromosomal aberrations in lymphocytes: Nordic study group on the health risk of chromosome damage. Cancer Res (1994) 1.70
The deltaccr5 mutation conferring protection against HIV-1 in Caucasian populations has a single and recent origin in Northeastern Europe. Hum Mol Genet (1998) 1.67
Superoxide dismutase isozymes in different human tissues, their genetic control and intracellular localization. Hum Hered (1973) 1.45
Occupational and environmental risks in and around a smelter in northern Sweden. III. Frequencies of spontaneous abortion. Hereditas (1978) 1.30
p53 polymorphisms and haplotypes in breast cancer. Carcinogenesis (1996) 1.26
Occupational and environmental risks in and around a smelter in northern Sweden. V. Spontaneous abortion among female employees and decreased birth weight in their offspring. Hereditas (1979) 1.26
Chronic recurrent multifocal osteomyelitis and pustulosis palmoplantaris. J Pediatr (1978) 1.19
p53 polymorphisms and haplotypes in different ethnic groups. Hum Hered (1995) 1.18
Fragile X syndrome in mildly mentally retarded children in a northern Swedish county. A prevalence study. Clin Genet (1983) 1.16
Superoxide dismutase in Bacteroides fragilis and related Bacteroides species. J Clin Microbiol (1977) 1.15
Familial X-linked mental retardation and fragile X chromosomes in two Swedish families. Clin Genet (1981) 1.11
Geographical distribution of TTR met30 carriers in northern Sweden: discrepancy between carrier frequency and prevalence rate. J Med Genet (1994) 1.10
The gene for Best's macular dystrophy is located at 11q13 in a Swedish family. Clin Genet (1992) 1.08
The effect of superoxide dismutase and catalase on radiation-induced chromosome breaks. Hereditas (1976) 1.06
P53 polymorphisms and haplotypes in lung cancer. Carcinogenesis (1995) 1.06
p53 polymorphisms and haplotypes show distinct differences between major ethnic groups. Hum Hered (1996) 1.06
Homozygosity for the transthyretin-met30-gene in two Swedish sibs with familial amyloidotic polyneuropathy. Clin Genet (1988) 1.06
A comparison between the common type and a rare genetic variant of human cupro-zinc superoxide dismutase. Eur J Biochem (1976) 1.06
Placental alkaline phosphatase, relation between phenotype and enzyme activity. Hum Hered (1970) 1.05
Induction of the "pregnancy zone" protein by oral contraceptives. Acta Obstet Gynecol Scand (1971) 1.04
Interaction between haemochromatosis and transferrin receptor genes in different neoplastic disorders. Carcinogenesis (1999) 1.01
P53 germ line haplotypes associated with increased risk for colorectal cancer. Carcinogenesis (1995) 1.01
Individual differences with respect to the sneezing reflex: an inherited physiological trait in man? Hum Hered (1983) 1.01
Catalase Hybrid Enzymes in Maize. Science (1964) 1.01
Occupational and environmental risks in and around a smelter in northern Sweden. I. Variations in birth weight. Hereditas (1978) 1.00
Fine mapping of Best's macular dystrophy localizes the gene in close proximity to but distinct from the D11S480/ROM1 loci. Genomics (1994) 1.00
Is the PiF allele of alpha 1-antitrypsin associated with pulmonary disease? Clin Genet (1984) 0.97
Effect of superoxide dismutase and catalase on spontaneously occurring chromosome breaks in patients with Fanconi's anemia. Hereditas (1977) 0.97
Is the genotoxic effect of arsenic mediated by oxygen free radicals? Hum Hered (1991) 0.96
An inter-Nordic prospective study on cytogenetic endpoints and cancer risk. Nordic Study Group on the Health Risk of Chromosome Damage. Cancer Genet Cytogenet (1990) 0.96
Geographical, linguistic, and cultural influences on genetic diversity: Y-chromosomal distribution in Northern European populations. Mol Biol Evol (2001) 0.96
Occupational and environmental risks in and around a smelter in northern Sweden. IV. Chromosomal aberrations in workers exposed to lead. Hereditas (1978) 0.95
Fragile site X chromosomes and X-linked mental retardation in severely retarded boys in a northern Swedish county. A prevalence study. Clin Genet (1982) 0.94
Vascular complications in the Ehlers-Danlos syndrome. Acta Chir Scand (1983) 0.94
The "pregnancy zone" protein and abortion. Acta Obstet Gynecol Scand (1974) 0.94
Bf and C3 complement types in rheumatoid arthritis. Hum Hered (1985) 0.93
Purification and partial characterization of the I variant of placental alkaline phosphatase. Biochem Genet (1977) 0.92
Population studies in northern Sweden. XVII. Estimates of Finnish and Saamish influence. Hum Hered (1991) 0.92
Occupational and environmental risks in and around a smelter in northern Sweden. VI. Congenital malformations. Hereditas (1979) 0.92
Incidence of Down's syndrome in Sweden during the years 1968-1977. Hum Genet Suppl (1981) 0.91
Chromosome aberrations in workers exposed to arsenic. Environ Health Perspect (1977) 0.90
Occupational and environmental risks in and around a smelter in northern Sweden. IX. Fetal mortality among wives of smelter workers. Hereditas (1982) 0.90
Reproductive hazards among workers at high voltage substations. Bioelectromagnetics (1983) 0.89
Haemoglobin variants, beta-thalassaemia and G-6-PD types in Liberia. Hum Hered (1981) 0.89
Blood-groups and serum lipids and phosphatases. Lancet (1969) 0.89
HLA antigens in allergic contact dermatitis. Acta Derm Venereol Suppl (Stockh) (1978) 0.89
Influence of oscillatory mixing on the injectability of three acrylic and two calcium-phosphate bone cements for vertebroplasty. J Biomed Mater Res B Appl Biomater (2004) 0.88
Manganese-containing superoxide dismutase signal sequence polymorphism associated with sporadic motor neuron disease. Eur J Neurol (1999) 0.88
Dominantly inherited macular degeneration (Best's disease) in a homozygous father with 11 children. Clin Genet (1980) 0.88
Membrane lipid composition and cell size of Acholeplasma laidlawii strain A are strongly influenced by lipid acyl chain length. Eur J Biochem (1995) 0.87
Subtypes of transferrin C. Hum Hered (1979) 0.87
Isozyme variations in human cells grown in vitro. IV. Identity between alkaline phosphatases from HeLa cells and placenta? Hum Hered (1970) 0.87
Hereditary maculardegeneration (HMD) in 246 cases traced to one gene-source in central Sweden. Hereditas (1977) 0.87
p53 polymorphisms and haplotypes in nasopharyngeal cancer. Hum Hered (1996) 0.87
Transferrin phenotype and level of carbohydrate-deficient transferrin in healthy individuals. Alcohol Clin Exp Res (1988) 0.87
Cancer predictive value of cytogenetic markers used in occupational health surveillance programs: a report from an ongoing study by the European Study Group on Cytogenetic Biomarkers and Health. Mutat Res (1998) 0.87
Individual andorgan-specific variations of human acid phosphatase. Biochem Genet (1967) 0.86
Erythrocyte lactate dehydrogenase variants in the Icelandic and Swedish populations. Acta Genet Stat Med (1968) 0.86
Placental alkaline phosphatase phenotypes and pre-natal selection. Evidence from studies of spontaneous and induced abortions. Hum Hered (1972) 0.86
High frequency of the HIV-1 protective CCR5 delta32 deletion in native Estonians. Eur J Epidemiol (2000) 0.86
Fragility of the centromeric region of chromosome 1 associated with combined immunodeficiency in siblings. A recessively inherited entity? Acta Paediatr Scand (1990) 0.86
Transferrin C2, metal binding and Alzheimer's disease. Neuroreport (1998) 0.86
Prognostic impact of bone marrow karyotype in childhood acute lymphoblastic leukaemia: Swedish experiences 1986-91. Acta Paediatr (1997) 0.86
Characterization of two human ovarian carcinoma cell lines. Gynecol Oncol (1979) 0.86