Published in Genet Epidemiol Suppl on January 01, 1986
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Bioassay of kinship. Theor Popul Biol (1971) 6.09
A clinical trial of antioxidant vitamins to prevent colorectal adenoma. Polyp Prevention Study Group. N Engl J Med (1994) 5.98
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Calcium supplements for the prevention of colorectal adenomas. Calcium Polyp Prevention Study Group. N Engl J Med (1999) 4.11
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Further segregation analysis of the fragile X syndrome with special reference to transmitting males. Hum Genet (1985) 3.42
Skewness in commingled distributions. Biometrics (1976) 3.19
The marker (X) syndrome: a cytogenetic and genetic analysis. Ann Hum Genet (1984) 3.17
Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II. Nat Genet (1996) 3.13
Multipoint linkage analysis. Am J Hum Genet (1986) 3.12
Association of FMR1 repeat size with ovarian dysfunction. Hum Reprod (2004) 3.01
Complex segregation analysis. Am J Hum Genet (1971) 2.80
Association of prostate cancer risk with genetic polymorphisms in vitamin D receptor and androgen receptor. J Natl Cancer Inst (1997) 2.74
Population-based study of congenital heart defects in Down syndrome. Am J Med Genet (1998) 2.74
Glutathione transferase null genotype, broccoli, and lower prevalence of colorectal adenomas. Cancer Epidemiol Biomarkers Prev (1998) 2.62
Replication of linkage studies of complex traits: an examination of variation in location estimates. Am J Hum Genet (1999) 2.50
Relation between homozygous viability and average dominance in Drosophila melanogaster. Genetics (1968) 2.30
Resolution of cultural and biological inheritance by path analysis. Am J Hum Genet (1976) 2.25
Report of the committee on the genetic constitution of chromosome 1. Cytogenet Cell Genet (1989) 2.18
Variability of human linkage data. Am J Hum Genet (1978) 1.97
Aromatase and breast cancer susceptibility. Endocr Relat Cancer (1999) 1.89
Support for a possible schizophrenia vulnerability locus in region 5q22-31 in Irish families. Mol Psychiatry (1997) 1.87
Serum cholesterol and hemorrhagic stroke in the Honolulu Heart Program. Stroke (1989) 1.76
Association and linkage of the dopamine transporter gene and attention-deficit hyperactivity disorder in children: heterogeneity owing to diagnostic subtype and severity. Am J Hum Genet (1998) 1.75
Pingelap and Mokil Atolls: migration. Am J Hum Genet (1971) 1.75
The incidence and prognosis of unrecognized myocardial infarction in the Honolulu, Hawaii, Heart Program. Arch Intern Med (1989) 1.74
Cultural and biological determinants of lipoprotein concentrations. Ann Hum Genet (1979) 1.72
Hierarchical regression analysis applied to a study of multiple dietary exposures and breast cancer. Epidemiology (1994) 1.71
A meta-analysis of body mass index and risk of premenopausal breast cancer. Epidemiology (1995) 1.70
A genetic epidemiologic investigation of breast cancer in families with bilateral breast cancer. I. Segregation analysis. J Natl Cancer Inst (1987) 1.70
Estimation of the inbreeding coefficient from ABO blood-group gene frequencies. Am J Hum Genet (1970) 1.70
Analysis of family resemblance. V. Height and weight in northeastern Brazil. Am J Hum Genet (1975) 1.67
Distance and kinship in northeastern Brazil. Am J Hum Genet (1969) 1.67
Pulmonary function as a predictor of coronary heart disease. Am J Epidemiol (1989) 1.66
Segregation analysis of balanced pericentric inversions in pedigree data. Clin Genet (1986) 1.65
Strength of linkage disequilibrium between two vitamin D receptor markers in five ethnic groups: implications for association studies. Cancer Epidemiol Biomarkers Prev (1997) 1.64
Effect of meiotic recombination on the production of aneuploid gametes in humans. Cytogenet Genome Res (2005) 1.61
Structural and functional analysis of the interaction between the agonistic monoclonal antibody Apomab and the proapoptotic receptor DR5. Cell Death Differ (2008) 1.61
Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome. Am J Hum Genet (2000) 1.57
Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21. Hum Mol Genet (1997) 1.57
Genome-wide scans of three independent sets of 90 Irish multiplex schizophrenia families and follow-up of selected regions in all families provides evidence for multiple susceptibility genes. Mol Psychiatry (2002) 1.56
A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22). Am J Med Genet (1996) 1.55
Functional oral-motor skills: Do they change with age? Dysphagia (1998) 1.55
Familial transmission of the FMR1 CGG repeat. Am J Hum Genet (1996) 1.53
Evidence for a schizophrenia vulnerability locus on chromosome 8p in the Irish Study of High-Density Schizophrenia Families. Am J Psychiatry (1996) 1.53
Relation of vegetable, fruit, and grain consumption to colorectal adenomatous polyps. Am J Epidemiol (1996) 1.53
Relative impact of smoking and reduced pulmonary function on peptic ulcer risk. A prospective study of Japanese men in Hawaii. Gastroenterology (1989) 1.52
Data and theory for a revised chiasma map of man. Hum Genet (1982) 1.49
Report of the committee on linkage and gene order. Cytogenet Cell Genet (1990) 1.48
XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region. Am J Hum Genet (1991) 1.47
Multilocus recombination frequencies. Genet Res (1984) 1.46
Predictors of sudden cardiac death among Hawaiian-Japanese men. Am J Epidemiol (1989) 1.46
Pingelap and mokil atolls: genealogy. Am J Hum Genet (1971) 1.45
Examination of reproductive aging milestones among women who carry the FMR1 premutation. Hum Reprod (2007) 1.42
Genetic structure of Switzerland. Am J Hum Genet (1973) 1.42
Combined analysis of genetic segregation and linkage under an oligogenic model. Comput Biomed Res (1984) 1.41
Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population. Am J Hum Genet (1999) 1.41
Tests of hypotheses on recombination frequencies. Genet Res (1985) 1.39
Human genes containing polymorphic trinucleotide repeats. Nat Genet (1992) 1.37
Guidelines for human linkage maps: an international system for human linkage maps (ISLM, 1990). Genomics (1991) 1.37
Irish study on high-density schizophrenia families: field methods and power to detect linkage. Am J Med Genet (1996) 1.35
Possible heterogeneity in the segregation pattern of breast cancer in families with bilateral breast cancer. Genet Epidemiol (1988) 1.33
Co-occurring diagnoses among FMR1 premutation allele carriers. Clin Genet (2010) 1.33
Dietary patterns associated with a low-fat diet in the national health examination follow-up study: identification of potential confounders for epidemiologic analyses. Am J Epidemiol (1993) 1.32
Estimation of myriad haplotype frequencies. Genet Epidemiol (1985) 1.29
Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study. Am J Hum Genet (1996) 1.28
Non-disjunction in human sperm: evidence for an effect of increasing paternal age. Hum Mol Genet (1995) 1.26
HLA-linked and unlinked determinants of multiple sclerosis. Immunogenetics (1982) 1.25
Guidelines for human linkage maps. An International System for Human Linkage Maps (ISLM, 1990). Ann Hum Genet (1991) 1.25
Germline mutation of microRNA-125a is associated with breast cancer. J Med Genet (2009) 1.25
Women with a reduced ovarian complement may have an increased risk for a child with Down syndrome. Am J Hum Genet (2000) 1.25
Linkage studies in spinocerebellar ataxia (SCA). Am J Med Genet (1980) 1.25
Medical and dental findings in the Brandywine isolate. Ala J Med Sci (1966) 1.24
Trials of the beta model for complex inheritance. Proc Natl Acad Sci U S A (1996) 1.24
Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population. Am J Med Genet (1996) 1.23
A chiasma map of man. Hum Hered (1977) 1.22
Folate intake, alcohol consumption, cigarette smoking, and risk of colorectal adenomas. J Natl Cancer Inst (1998) 1.22
The expression of Myf5 in the developing mouse embryo is controlled by discrete and dispersed enhancers specific for particular populations of skeletal muscle precursors. Development (2000) 1.22
Obesity, weight gain, large weight changes, and adenomatous polyps of the left colon and rectum. Am J Epidemiol (1998) 1.21
Clinical features of schizophrenia and linkage to chromosomes 5q, 6p, 8p, and 10p in the Irish Study of High-Density Schizophrenia Families. Am J Psychiatry (2000) 1.21
A method for the study of incest. Ann Hum Genet (1973) 1.20
Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1. Hum Mol Genet (1998) 1.18
Vitamin D receptor genotype and breast cancer in Latinas (United States). Cancer Causes Control (2000) 1.18
Vitamin D receptor 3'-untranslated region polymorphisms: lack of effect on mRNA stability. Biochim Biophys Acta (1999) 1.18
Fanconi anemia: evidence for linkage heterogeneity on chromosome 20q. Genomics (1991) 1.18
Hierarchical modeling of gene-environment interactions: estimating NAT2 genotype-specific dietary effects on adenomatous polyps. Cancer Epidemiol Biomarkers Prev (1997) 1.17
Evaluation of a stereotactic frame for repositioning of the rat brain in serial positron emission tomography imaging studies. J Neurosci Methods (2001) 1.17
A revised map of chromosome 1. Ann Hum Genet (1984) 1.16