Published in Hum Hered on January 01, 1977
Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. Am J Hum Genet (1985) 87.59
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
Multipoint linkage analysis. Am J Hum Genet (1986) 3.12
Trisomy 21: association between reduced recombination and nondisjunction. Am J Hum Genet (1991) 3.08
Characterization of human crossover interference. Am J Hum Genet (2000) 2.42
Variability of human linkage data. Am J Hum Genet (1978) 1.97
Error filtration, interference, and the human linkage map. Proc Natl Acad Sci U S A (1991) 1.91
Recombination within and between the human insulin and beta-globin gene loci. Proc Natl Acad Sci U S A (1983) 1.82
On genetic map functions. Genetics (1996) 1.64
A map of the human genome in linkage disequilibrium units. Proc Natl Acad Sci U S A (2005) 1.54
XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region. Am J Hum Genet (1991) 1.47
Models of multilocus recombination: nonrandomness in chiasma number and crossover positions. Am J Hum Genet (1988) 1.45
Nondisjunction of chromosome 15: origin and recombination. Am J Hum Genet (1993) 1.34
Multipoint gene mapping using seriation. II. Analysis of simulated and empirical data. Am J Hum Genet (1987) 1.21
Integration of gene maps: chromosome 1. Proc Natl Acad Sci U S A (1992) 1.14
The use of map functions in multipoint mapping. Am J Hum Genet (1987) 1.13
Integration of gene maps: chromosome 21. Proc Natl Acad Sci U S A (1993) 1.10
Tight linkage of the gene for spinocerebellar ataxia to D6S89 on the short arm of chromosome 6 in a kindred for which close linkage to both HLA and F13A1 is excluded. Am J Hum Genet (1991) 1.05
A sequence-based integrated map of chromosome 22. Genome Res (2001) 1.04
Statistical analysis of ordered tetrads. Genetics (1998) 0.93
A novel X-linked dominant condition: X-linked congenital isolated ptosis. Am J Hum Genet (2000) 0.92
Genetic mapping: chromosomes 6-22. Am J Hum Genet (1982) 0.86
DSLINK: a computer program for gene-centromere linkage analysis in families with a trisomic offspring. Am J Hum Genet (1987) 0.85
The human salivary protein complex (SPC): a large block of related genes. Am J Hum Genet (1985) 0.84
Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28. J Med Genet (1993) 0.82
Mapping functions. Genetica (2007) 0.78
Interpretation of RFLP linkage data. J Med Genet (1984) 0.75
Linkage studies of Friedreich ataxia by means of blood-group and protein markers. Am J Hum Genet (1987) 0.75
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
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
Chiasma distribution at diakinesis in the normal human male. Hereditas (1974) 3.25
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
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
Rapid and simple prenatal DNA diagnosis of Down's syndrome. Lancet (1998) 2.85
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
Genomic imprinting in an Angelman and Prader-Willi translocation family. Lancet (1991) 2.41
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
Lp(a) lipoprotein as a risk factor for myocardial infarction. JAMA (1986) 2.08
A genetic study of immunoglobulin E. Am J Hum Genet (1978) 2.07
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
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
A family study of genetic and environmental factors determining polymorphic hydroxylation of debrisoquin. Clin Pharmacol Ther (1985) 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
The 11q;22q translocation: a European collaborative analysis of 43 cases. Hum Genet (1980) 1.82
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
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
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