Published in Hereditas on January 01, 1979
The hazard evaluation system and information service: a physician's resource in toxicology and occupational medicine. West J Med (1982) 2.11
Chronic arsenic exposure and risk of infant mortality in two areas of Chile. Environ Health Perspect (2000) 1.85
Chemical exposures at work in early pregnancy and congenital defect: a case-referent study. Br J Ind Med (1987) 1.37
Congenital malformations and maternal occupation in Finland: multivariate analysis. J Epidemiol Community Health (1981) 1.23
Spontaneous abortions in an industrialized community in Finland. Am J Public Health (1983) 1.19
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
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
Fragile X syndrome in mildly mentally retarded children in a northern Swedish county. A prevalence study. Clin Genet (1983) 1.16
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
Homozygosity for the transthyretin-met30-gene in two Swedish sibs with familial amyloidotic polyneuropathy. Clin Genet (1988) 1.06
p53 polymorphisms and haplotypes show distinct differences between major ethnic groups. Hum Hered (1996) 1.06
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
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
Individual differences with respect to the sneezing reflex: an inherited physiological trait in man? Hum Hered (1983) 1.01
P53 germ line haplotypes associated with increased risk for colorectal cancer. Carcinogenesis (1995) 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
Effect of superoxide dismutase and catalase on spontaneously occurring chromosome breaks in patients with Fanconi's anemia. Hereditas (1977) 0.97
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
Is the genotoxic effect of arsenic mediated by oxygen free radicals? Hum Hered (1991) 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
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. II. Chromosomal aberrations in workers exposed to arsenic. Hereditas (1978) 0.91
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
Blood-groups and serum lipids and phosphatases. Lancet (1969) 0.89
Haemoglobin variants, beta-thalassaemia and G-6-PD types in Liberia. Hum Hered (1981) 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
p53 polymorphisms and haplotypes in nasopharyngeal cancer. Hum Hered (1996) 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
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
Characterization of two human ovarian carcinoma cell lines. Gynecol Oncol (1979) 0.86
High frequency of the HIV-1 protective CCR5 delta32 deletion in native Estonians. Eur J Epidemiol (2000) 0.86
Transferrin C2, metal binding and Alzheimer's disease. Neuroreport (1998) 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
Placental alkaline phosphatase phenotypes and pre-natal selection. Evidence from studies of spontaneous and induced abortions. Hum Hered (1972) 0.86
Prognostic impact of bone marrow karyotype in childhood acute lymphoblastic leukaemia: Swedish experiences 1986-91. Acta Paediatr (1997) 0.86
Polymorphism in the interferon-alpha gene family. Am J Hum Genet (1996) 0.85
The codon 31 polymorphism of the p53-inducible gene p21 shows distinct differences between major ethnic groups. Hum Hered (1997) 0.85
Pregnancy enzymes and placental polymorphism. I. Alkaline phosphatse. Acta Genet Stat Med (1966) 0.85
Diagnosis of familial amyloidotic polyneuropathy in Sweden by RFLP analysis. Clin Genet (1988) 0.85
Chromosomal abnormality in dementia of Alzheimer type. Lancet (1980) 0.85
Thromboplastin-induced hypercoagulability and its prevention. Nature (1965) 0.85
Variations in human placental alkaline phosphatase. Acta Genet Stat Med (1967) 0.84
Acid phosphatase activity in the synovial fluid of patients with rheumatoid arthritis and other joint disorders. Acta Rheumatol Scand (1971) 0.84
Efficient modulation of glucolipid enzyme activities in membranes of Acholeplasma laidlawii by the type of lipids in the bilayer matrix. Biochemistry (1995) 0.84
Secondary aortoenteric fistulas--an analysis of 42 cases. Eur J Vasc Surg (1987) 0.83
Interferon-alpha and p53 alleles involved in nasopharyngeal carcinoma. Carcinogenesis (1997) 0.83
Cytogenetic abnormalities and leukemic transformation in hydroxyurea-treated patients with Philadelphia chromosome negative chronic myeloproliferative disease. Cancer Genet Cytogenet (1990) 0.83
Acute mechanical injury of the human intervertebral disc: link to degeneration and pain. Eur Cell Mater (2014) 0.83
Serum protein markers in systemic lupus erythematosus. Hum Hered (1988) 0.83
Transferrin types, iron-binding capacity and body iron stores. Hum Hered (1994) 0.83
Serum protein and red cell enzyme polymorphisms in affective disorders. Hum Hered (1978) 0.82
Serum-cholesterol and ABO and Lewis blood-groups. Lancet (1970) 0.82
Experimental investigations on the antithromboplastic and antifibrinolytic activity of Trasylol. Ann N Y Acad Sci (1968) 0.82
Interaction between haemochromatosis and transferrin receptor genes in hepatocellular carcinoma. Oncology (2000) 0.82
Ethnic differences in the HFE codon 282 (Cys/Tyr) polymorphism. Hum Hered (1997) 0.82
Multiple molecular forms of leucine aminopeptidase in man. Acta Genet Stat Med (1966) 0.81
Thoracolumbar epidural anaesthesia blocks the circulatory response to laryngoscopy and intubation. Acta Anaesthesiol Scand (1987) 0.81
Interaction between haemochromatosis and transferrin receptor genes in multiple myeloma. Lancet (1998) 0.81
Chromosome aberrations in psoriatic patients treated with arsenic. Hum Genet (1979) 0.81
Chromosomal aberrations and male infertility. J Urol (1982) 0.81
Chromosomal aberrations and cancer risk. Hum Hered (1984) 0.81
C3 and C6 complement types in schizophrenia. Hum Hered (1985) 0.81