Published in Am J Hum Genet on September 01, 1988
Comparative map for mice and humans. Mamm Genome (1991) 0.81
Strategies for multilocus linkage analysis in humans. Proc Natl Acad Sci U S A (1984) 48.41
Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies. Am J Hum Genet (1974) 23.66
Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculations. Ann Hum Genet (1987) 13.98
Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man. Proc Natl Acad Sci U S A (1985) 3.22
Nonuniform recombination within the human beta-globin gene cluster. Am J Hum Genet (1986) 2.78
High frequency of nonclassical steroid 21-hydroxylase deficiency. Am J Hum Genet (1985) 2.44
Alternative bioassays of kinship between loci. Am J Hum Genet (1988) 1.66
Genetic analysis of idiopathic hemochromatosis using both qualitative (disease status) and quantitative (serum iron) information. Am J Hum Genet (1985) 1.59
Frequent deletion and duplication of the steroid 21-hydroxylase genes. Am J Hum Genet (1986) 1.54
Report of the Committee on the Genetic Constitution of Chromosomes 5 and 6. Cytogenet Cell Genet (1985) 1.47
Combined analysis of genetic segregation and linkage under an oligogenic model. Comput Biomed Res (1984) 1.41
Recent advances in 21-hydroxylase deficiency. Annu Rev Med (1984) 1.39
Kinship mapping of multilocus systems. Hum Genet (1983) 1.09
Gene order and gene distances in the HLA region studied by the haplotype method. Ann Hum Genet (1983) 0.89
Genetic mapping: chromosomes 6-22. Am J Hum Genet (1982) 0.86
A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiency. Am J Hum Genet (1988) 0.85
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
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Endocr Rev (2000) 3.99
FMR1 and the fragile X syndrome: human genome epidemiology review. Genet Med (2001) 3.84
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
Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man. Proc Natl Acad Sci U S A (1985) 3.22
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
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
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
Population-based study of congenital heart defects in Down syndrome. Am J Med Genet (1998) 2.74
International system for human gene nomenclature (1979) ISGN (1979). Cytogenet Cell Genet (1979) 2.58
HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation. Proc Natl Acad Sci U S A (1984) 2.56
Mapping a disease locus by allelic association. Proc Natl Acad Sci U S A (1998) 2.51
High frequency of nonclassical steroid 21-hydroxylase deficiency. Am J Hum Genet (1985) 2.44
Structure of human steroid 21-hydroxylase genes. Proc Natl Acad Sci U S A (1986) 2.34
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
Report of the committee on the genetic constitution of chromosome 1. Cytogenet Cell Genet (1989) 2.18
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
Long term outcome in adult males with classic congenital adrenal hyperplasia. J Clin Endocrinol Metab (2001) 2.01
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
Cloning and expression of cDNA encoding a bovine adrenal cytochrome P-450 specific for steroid 21-hydroxylation. Proc Natl Acad Sci U S A (1984) 1.89
Genetic effects of cumulative x irradiation on the secondary sex ratio of the laboratory rat. Genetics (1968) 1.88
Genotyping steroid 21-hydroxylase deficiency: hormonal reference data. J Clin Endocrinol Metab (1983) 1.77
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
Cultural and biological determinants of lipoprotein concentrations. Ann Hum Genet (1979) 1.72
A new form of congenital adrenal hyperplasia. J Clin Endocrinol Metab (1967) 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
Microfilter paper method for 17 alpha-hydroxyprogesterone radioimmunoassay: its application for rapid screening for congenital adrenal hyperplasia. J Clin Endocrinol Metab (1977) 1.69
Analysis of family resemblance. V. Height and weight in northeastern Brazil. Am J Hum Genet (1975) 1.67
Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing. N Engl J Med (1977) 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
Effect of meiotic recombination on the production of aneuploid gametes in humans. Cytogenet Genome Res (2005) 1.61
Genetic analysis of idiopathic hemochromatosis using both qualitative (disease status) and quantitative (serum iron) information. Am J Hum Genet (1985) 1.59
Two steroid 21-hydroxylase genes are located in the murine S region. Nature (1985) 1.58
Distinct missense mutations of the FGFR3 lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotype. Am J Hum Genet (2000) 1.58
Effect of inbreeding on IQ and mental retardation. Proc Natl Acad Sci U S A (1978) 1.58
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
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
Frequent deletion and duplication of the steroid 21-hydroxylase genes. Am J Hum Genet (1986) 1.54
A map of the human genome in linkage disequilibrium units. Proc Natl Acad Sci U S A (2005) 1.54
Familial transmission of the FMR1 CGG repeat. Am J Hum Genet (1996) 1.53
Acrocentric chromosome associations in man. Am J Hum Genet (1976) 1.53
Congenital adrenal hyperplasia (21-hydroxylase deficiency) without demonstrable genetic mutations. J Clin Endocrinol Metab (1999) 1.52
Steroid 21-hydroxylase deficiency: genotype may not predict phenotype. J Clin Endocrinol Metab (1995) 1.51
Identification of non-amplifying CYP21 genes when using PCR-based diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH) affected pedigrees. Hum Mol Genet (1996) 1.51
Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency. Proc Natl Acad Sci U S A (1988) 1.50
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
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
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
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
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
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
Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency. J Clin Invest (1992) 1.40
Guidelines for human gene nomenclature. An international system for human gene nomenclature (ISGN, 1987). Cytogenet Cell Genet (1987) 1.40