Population genetics and disease control.

Equilibrium frequencies in X-linked recessive disease. Am J Hum Genet (1973) 1.31

Effects of reproductive compensation and genetic drift on X-linked lethals. Am J Hum Genet (1978) 1.20

Inferences about the distribution of dominance drawn from yeast gene knockout data. Genetics (2010) 1.16

Effects of various medical and social pracitices on the frequency of genetic disorders. Am J Hum Genet (1975) 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

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

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

Analysis of family resemblance. IV. Operational characteristics of segregation analysis. Am J Hum Genet (1975) 2.97

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

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

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

Racial admixture in north-eastern Brazil. Ann Hum Genet (1965) 2.19

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

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

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

Pingelap and Mokil Atolls: migration. Am J Hum Genet (1971) 1.75

Cultural and biological determinants of lipoprotein concentrations. Ann Hum Genet (1979) 1.72

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

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

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

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

Allelic association between marker loci. Proc Natl Acad Sci U S A (1999) 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

A map of the human genome in linkage disequilibrium units. Proc Natl Acad Sci U S A (2005) 1.54

Acrocentric chromosome associations in man. Am J Hum Genet (1976) 1.53

Data and theory for a revised chiasma map of man. Hum Genet (1982) 1.49

A genetic study of cleft lip and palate in Hawaii. II. Complex segregation analysis and genetic risks. Am J Hum Genet (1974) 1.49

Malformations in northeastern Brazil. Acta Genet Stat Med (1965) 1.46

Multilocus recombination frequencies. Genet Res (1984) 1.46

Pingelap and mokil atolls: genealogy. Am J Hum Genet (1971) 1.45

Genetic counseling in sex linkage. Birth Defects Orig Artic Ser (1979) 1.43

Genetic structure of Switzerland. Am J Hum Genet (1973) 1.42

Analysis of crossingover in man. Cytogenet Cell Genet (1978) 1.42

Combined analysis of genetic segregation and linkage under an oligogenic model. Comput Biomed Res (1984) 1.41

Isolation by distance in Japan and Sweden compared with other countries. Hum Hered (1969) 1.41

Guidelines for human gene nomenclature. An international system for human gene nomenclature (ISGN, 1987). Cytogenet Cell Genet (1987) 1.40

Tests of hypotheses on recombination frequencies. Genet Res (1985) 1.39

Guidelines for human linkage maps: an international system for human linkage maps (ISLM, 1990). Genomics (1991) 1.37

Blood factor association. Vox Sang (1967) 1.37

Genetic epidemiology of early onset breast cancer. J Med Genet (1994) 1.37

The origin of 47,XXY and 47,XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination. Hum Mol Genet (1994) 1.36

Path analysis under generalized assortative mating. I. Theory. Genet Res (1979) 1.36

Origin of human trisomics and polyploids. Hum Hered (1977) 1.34

Genetic epidemiology of Lesch-Nyhan disease. Am J Hum Genet (1977) 1.33

Comparison of parametric and nonparametric methods to map oligogenes by linkage. Proc Natl Acad Sci U S A (1997) 1.31

Behavioral, social, and physiological determinants of lipoprotein concentrations. Soc Biol (1977) 1.31

Dominant genes for colorectal cancer are not rare. Ann Hum Genet (1992) 1.30

Estimation of myriad haplotype frequencies. Genet Epidemiol (1985) 1.29

Achromatopsia in Pingelap Islanders. Study of a genetic isolate. Am J Ophthalmol (1971) 1.29

Estimation of demographic parameters from isolation by distance. Hum Hered (1982) 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

Heterozygous expression of insulin-dependent diabetes mellitus (IDDM) determinants in the HLA system. Am J Hum Genet (1983) 1.25

Linkage studies in spinocerebellar ataxia (SCA). Am J Med Genet (1980) 1.25

Trials of the beta model for complex inheritance. Proc Natl Acad Sci U S A (1996) 1.24

Trisomy 18: studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunction. Am J Hum Genet (1995) 1.23

Determinants of blood pressure in Japanese-American Families. Hum Genet (1980) 1.23

Path analysis of qualitative data on pairs of relatives: application to schizophrenia. Hum Hered (1981) 1.23

A chiasma map of man. Hum Hered (1977) 1.22

Bioassay of kinship in a South American Indian population. Am J Hum Genet (1973) 1.22

The optimal measure of linkage disequilibrium reduces error in association mapping of affection status. Hum Mol Genet (2004) 1.21

Large deviations in the distribution of rare genes. Am J Hum Genet (1973) 1.19

The effect of structural aberrations of the chromosomes on reproductive fitness in man. II. Results. Clin Genet (1975) 1.16

Origin of teratomas and twins. Hum Genet (1986) 1.15

Quantitative hemagglutination in the ABO system. Am J Hum Genet (1969) 1.15

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

Allelic association under map error and recombinational heterogeneity: a tale of two sites. Proc Natl Acad Sci U S A (1998) 1.13

International Genetic Epidemiology Society: commentary on Darkness in El Dorado by Patrick Tierney. Genet Epidemiol (2001) 1.13

Path analysis of family resemblance in the presence of gene-environment interaction. Am J Hum Genet (1974) 1.10

Genetic epidemiology of ovarian cancer: segregation analysis. Ann Hum Genet (1991) 1.10

Integration of gene maps: chromosome 21. Proc Natl Acad Sci U S A (1993) 1.10