Published in Am J Hum Genet on January 01, 1978
A unified model for complex segregation analysis. Am J Hum Genet (1983) 5.67
Maximum likelihood estimation by counting methods under polygenic and mixed models in human pedigrees. Am J Hum Genet (1979) 3.36
Major genes regulating total serum immunoglobulin E levels in families with asthma. Am J Hum Genet (2000) 1.63
Major locus analysis for quantitative traits. Am J Hum Genet (1979) 1.48
Confirmation of genetic linkage between atopic IgE responses and chromosome 11q13. J Med Genet (1992) 1.32
Errors of inference in the detection of major gene effects on psychological test scores. Am J Hum Genet (1983) 1.11
Immunoglobulin E revisited. Am J Hum Genet (1980) 1.01
Evidence for two unlinked loci regulating total serum IgE levels. Am J Hum Genet (1995) 0.99
Examining the association between childhood asthma and parent and grandparent asthma status: implications for practice. Clin Pediatr (Phila) (2010) 0.96
Trials of structural exploratory data analysis. Am J Hum Genet (1982) 0.96
Inheritance of total serum IgE (basal levels) in man. Am J Hum Genet (1987) 0.95
Commingling and segregation analysis of blood pressure in a French-Canadian population. Am J Hum Genet (1990) 0.95
Evidence for Mendelian inheritance of serum IgE levels in Hispanic and non-Hispanic white families. Am J Hum Genet (1994) 0.90
Allergen-specific IgG1 provides parsimonious heritability estimates for atopy-associated immune responses to allergens. Hum Immunol (2006) 0.88
Polymorphism in intron 1 of the interferon-gamma gene influences both serum immunoglobulin E levels and the risk for chronic hepatitis B virus infection in Polynesians. Immunogenetics (2007) 0.87
Functional polymorphisms in IL13 are protective against high Schistosoma mansoni infection intensity in a Brazilian population. PLoS One (2012) 0.84
Association of HLA antigens and total serum immunoglobulin E level with allergic response and failure to respond to ragweed allergen Ra3. Proc Natl Acad Sci U S A (1979) 0.80
A defense of path analysis in genetic epidemiology. Am J Hum Genet (1983) 0.79
Linkage/association study of a locus modulating total serum IgE on chromosome 14q13-24 in families with asthma. Thorax (2004) 0.77
Chronic sinopulmonary inflammatory diseases in adults with undetectable serum IgE in inner-city Chicago: a preliminary observation. Lung (2012) 0.77
Bronchiolitis and asthma: are they related? Thorax (1994) 0.76
Genetics of asthma. Arch Dis Child (1993) 0.75
Candidate gene loci in asthmatic and allergic inflammation. Thorax (1996) 0.75
Mouse Chromosome 4 Is Associated with the Baseline and Allergic IgE Phenotypes. G3 (Bethesda) (2017) 0.75
Analysis of family resemblance. 3. Complex segregation of quantitative traits. Am J Hum Genet (1974) 9.68
Raised levels of a new immunoglobulin class (IgND) in asthma. Lancet (1967) 3.63
Skewness in commingled distributions. Biometrics (1976) 3.19
The Behavior of Bronchial Asthma as an Inherited Character. Genetics (1920) 2.98
Physicochemical properties of reaginic antibody. V. Correlation of reaginic activity wth gamma-E-globulin antibody. J Immunol (1966) 2.92
Genetic control of basal serum immunoglobulin E level and its effect on specific reaginic sensitivity. Proc Natl Acad Sci U S A (1974) 1.98
IgE levels in normal infants and mothers and an inheritance hypothesis. J Immunol (1971) 1.61
Causes of variation in serum IgE levels in normal populations. J Allergy Clin Immunol (1975) 1.13
Serum IgE levels in parents and children. J Pediatr (1974) 1.07
Analysis of family resemblance. 3. Complex segregation of quantitative traits. Am J Hum Genet (1974) 9.68
Report of the Committee on the Genetic Constitution of Chromosomes 1 and 2. Cytogenet Cell Genet (1985) 7.70
A mapping function for man. Hum Hered (1977) 7.50
Resolution of linkage for irregular phenotype systems. Hum Hered (1981) 6.99
Analysis of family resemblance. II. A linear model for familial correlation. Am J Hum Genet (1974) 6.51
Bioassay of kinship. Theor Popul Biol (1971) 6.09
A unified model for complex segregation analysis. Am J Hum Genet (1983) 5.67
Report of the Committee on Methods of Linkage Analysis and Reporting. Cytogenet Cell Genet (1985) 5.61
Complex segregation analysis with pointers. Hum Hered (1981) 5.59
Analysis of family resemblance. I. Introduction. Am J Hum Genet (1974) 4.34
A maximum likelihood map of chromosome 1. Am J Hum Genet (1979) 4.34
A metric map of humans: 23,500 loci in 850 bands. Proc Natl Acad Sci U S A (1996) 4.30
Bioassay of population structure under isolation by distance. Am J Hum Genet (1968) 4.12
Natural selection on polymorphisms in northeastern Brazil. Am J Hum Genet (1966) 3.54
Further segregation analysis of the fragile X syndrome with special reference to transmitting males. Hum Genet (1985) 3.42
The transmission of schizophrenia under a multifactorial threshold model. Am J Hum Genet (1983) 3.24
NHLBI Family Heart Study: objectives and design. Am J Epidemiol (1996) 3.21
Skewness in commingled distributions. Biometrics (1976) 3.19
The marker (X) syndrome: a cytogenetic and genetic analysis. Ann Hum Genet (1984) 3.17
The detection of major genes under additive continuous variation. Am J Hum Genet (1967) 3.14
Multipoint linkage analysis. Am J Hum Genet (1986) 3.12
Melanocortin 4 receptor sequence variations are seldom a cause of human obesity: the Swedish Obese Subjects, the HERITAGE Family Study, and a Memphis cohort. J Clin Endocrinol Metab (2002) 3.04
Breast-feeding: second thoughts. Pediatrics (1974) 3.02
Race, visceral adipose tissue, plasma lipids, and lipoprotein lipase activity in men and women: the Health, Risk Factors, Exercise Training, and Genetics (HERITAGE) family study. Arterioscler Thromb Vasc Biol (2000) 3.01
Analysis of family resemblance. IV. Operational characteristics of segregation analysis. Am J Hum Genet (1975) 2.97
The effect of sex, age and race on estimating percentage body fat from body mass index: The Heritage Family Study. Int J Obes Relat Metab Disord (2002) 2.95
Familial aggregation of VO(2max) response to exercise training: results from the HERITAGE Family Study. J Appl Physiol (1985) (1999) 2.89
Genetic epidemiology of single-nucleotide polymorphisms. Proc Natl Acad Sci U S A (1999) 2.81
Complex segregation analysis. Am J Hum Genet (1971) 2.80
The first linkage disequilibrium (LD) maps: delineation of hot and cold blocks by diplotype analysis. Proc Natl Acad Sci U S A (2002) 2.80
Genome-wide linkage analysis of systolic and diastolic blood pressure: the Québec Family Study. Circulation (2000) 2.75
Effect of exercise training on plasma levels of C-reactive protein in healthy adults: the HERITAGE Family Study. Eur Heart J (2005) 2.69
Methods for handling multiple testing. Adv Genet (2008) 2.67
International system for human gene nomenclature (1979) ISGN (1979). Cytogenet Cell Genet (1979) 2.58
Mapping a disease locus by allelic association. Proc Natl Acad Sci U S A (1998) 2.51
Genomic predictors of the maximal O₂ uptake response to standardized exercise training programs. J Appl Physiol (1985) (2010) 2.43
Nocturnal enuresis: studies in bladder function in normal children and enuretics. Can Med Assoc J (1969) 2.37
Differences in left ventricular structure between black and white hypertensive adults: the Hypertension Genetic Epidemiology Network study. Hypertension (2004) 2.36
Multiple genes for essential-hypertension susceptibility on chromosome 1q. Am J Hum Genet (2006) 2.34
Relation between homozygous viability and average dominance in Drosophila melanogaster. Genetics (1968) 2.30
NHLBI family blood pressure program: methodology and recruitment in the HyperGEN network. Hypertension genetic epidemiology network. Ann Epidemiol (2000) 2.28
Resolution of cultural and biological inheritance by path analysis. Am J Hum Genet (1976) 2.25
Genomewide linkage analysis of quantitative spirometric phenotypes in severe early-onset chronic obstructive pulmonary disease. Am J Hum Genet (2002) 2.23
Racial admixture in north-eastern Brazil. Ann Hum Genet (1965) 2.19
Genomic scan for exercise blood pressure in the Health, Risk Factors, Exercise Training and Genetics (HERITAGE) Family Study. Hypertension (2001) 2.15
Cardiovascular risk factors in a French-Canadian population: resolution of genetic and familial environmental effects on blood pressure by using extensive information on environmental correlates. Am J Hum Genet (1989) 2.11
Familial resemblance for VO2max in the sedentary state: the HERITAGE family study. Med Sci Sports Exerc (1998) 2.11
Genetic studies on cystic fibrosis in Hawaii. Am J Hum Genet (1968) 2.10
Recurrent urinary infections in girls: relation to enuresis. Can Med Assoc J (1972) 2.09
Lp(a) lipoprotein as a risk factor for myocardial infarction. JAMA (1986) 2.08
Isolation by distance in artificial populations. Genetics (1970) 2.04
Variants in the CD36 gene associate with the metabolic syndrome and high-density lipoprotein cholesterol. Hum Mol Genet (2008) 1.98
Racial admixture and its impact on BMI and blood pressure in African and Mexican Americans. Hum Genet (2006) 1.98
Variability of human linkage data. Am J Hum Genet (1978) 1.97
Effects of exercise training on glucose homeostasis: the HERITAGE Family Study. Diabetes Care (2005) 1.96
The Collaborative Lipid Research Clinics Family Study: biological and cultural determinants of familial resemblance for plasma lipids and lipoproteins. Genet Epidemiol (1985) 1.95
X-linked mental retardation: a study of 7 families. Am J Med Genet (1980) 1.93
Error filtration, interference, and the human linkage map. Proc Natl Acad Sci U S A (1991) 1.91
Genetic epidemiology of breast cancer in Britain. Ann Hum Genet (1991) 1.89
Genetic effects of cumulative x irradiation on the secondary sex ratio of the laboratory rat. Genetics (1968) 1.88
Targeting the metabolic syndrome with exercise: evidence from the HERITAGE Family Study. Med Sci Sports Exerc (2003) 1.87
Adverse metabolic response to regular exercise: is it a rare or common occurrence? PLoS One (2012) 1.84
Race differences in the response of postheparin plasma lipoprotein lipase and hepatic lipase activities to endurance exercise training in men: results from the HERITAGE Family Study. Atherosclerosis (2001) 1.83
The HERITAGE family study. Aims, design, and measurement protocol. Med Sci Sports Exerc (1995) 1.83
Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study. Am J Nephrol (2009) 1.80
Immunoglobulin levels in smokers and non-smokers. Ann Allergy (1980) 1.76
Pingelap and Mokil Atolls: migration. Am J Hum Genet (1971) 1.75
Three ontologies to define phenotype measurement data. Front Genet (2012) 1.74
Cultural and biological determinants of lipoprotein concentrations. Ann Hum Genet (1979) 1.72
Familial resemblance of plasma lipids, lipoproteins and postheparin lipoprotein and hepatic lipases in the HERITAGE Family Study. Arterioscler Thromb Vasc Biol (1997) 1.71
The use of long PCR to confirm three common alleles at the CYP2A6 locus and the relationship between genotype and smoking habit. Ann Hum Genet (2000) 1.71
Estimation of the inbreeding coefficient from ABO blood-group gene frequencies. Am J Hum Genet (1970) 1.70
Effect of type 2 diabetes mellitus on left ventricular geometry and systolic function in hypertensive subjects: Hypertension Genetic Epidemiology Network (HyperGEN) study. Circulation (2001) 1.69
A genome-wide linkage scan for dietary energy and nutrient intakes: the Health, Risk Factors, Exercise Training, and Genetics (HERITAGE) Family Study. Am J Clin Nutr (2004) 1.68
Failure to thrive in the contented breast-fed baby. Can Med Assoc J (1984) 1.68
Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing. N Engl J Med (1977) 1.67
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
Milk allergy: clinical picture and familial incidence. Can Med Assoc J (1967) 1.66
Allelic association of gene markers on chromosomes 5q and 11q with atopy and bronchial hyperresponsiveness. Am J Respir Crit Care Med (1996) 1.65
Segregation analysis of balanced pericentric inversions in pedigree data. Clin Genet (1986) 1.65
The Cincinnati Lipid Research Clinic family study: cultural and biological determinants of lipids and lipoprotein concentrations. Am J Hum Genet (1982) 1.64
Genetic analysis of idiopathic hemochromatosis using both qualitative (disease status) and quantitative (serum iron) information. Am J Hum Genet (1985) 1.59
Effect of inbreeding on IQ and mental retardation. Proc Natl Acad Sci U S A (1978) 1.58
Increased nonspecific bronchial reactivity in cigarette smokers with normal lung function. Am Rev Respir Dis (1980) 1.57
Allelic association between marker loci. Proc Natl Acad Sci U S A (1999) 1.55
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. Am J Hum Genet (2013) 1.55
A summary of the effects of antihypertensive medications on measured blood pressure. Am J Hypertens (2005) 1.55
Oculoauriculovertebral anomaly: segregation analysis. Am J Med Genet (1992) 1.55
Reproductive and menstrual history of females with fragile X expansions. Eur J Hum Genet (2000) 1.55
Linkage map integration. Genomics (1996) 1.54