Published in Am J Hum Genet on May 01, 1968
A probable sex difference in some mutation rates. Am J Hum Genet (1977) 1.49
Genetic epidemiology of Lesch-Nyhan disease. Am J Hum Genet (1977) 1.33
Sex ratio of the mutation frequencies in haemophilia A: coagulation assays and RFLP analysis. J Med Genet (1991) 0.97
Studies on hemophilia A in Sardinia bearing on the problems of multiple allelism, carrier detection, and differential mutation rate in the two sexes. Am J Hum Genet (1984) 0.96
Christmas disease in one of a pair of monozygotic twin girls, possibly the effect of lyonization. J Med Genet (1972) 0.96
Segregation analysis of hemophilia A and B. Am J Hum Genet (1985) 0.90
Segregation analysis of hemophilia A and B. Am J Hum Genet (1979) 0.85
Genetic tests under incomplete ascertainment. Am J Hum Genet (1959) 11.24
Christmas disease: a condition previously mistaken for haemophilia. Br Med J (1952) 8.27
Formal genetics of muscular dystrophy. Am J Hum Genet (1959) 6.03
Plasma thromboplastin component (PTC) deficiency; a new disease resembling hemophilia. Proc Soc Exp Biol Med (1952) 5.06
Parental age and mutation. Lancet (1955) 4.58
ESTIMATION OF PREVALENCE UNDER INCOMPLETE SELECTION. Am J Hum Genet (1965) 3.95
The relationship between parental age, birth order and the secondary sex ratio in humans. Ann Hum Genet (1956) 2.08
Birth order, parental ages, and sex of off-spring. Am J Hum Genet (1958) 1.95
Sporadic cases of hemophilia and the question of a possible sex difference in mutation rates. Am J Hum Genet (1962) 1.67
[Influence of the age of parents on the masculinity of living births]. C R Hebd Seances Acad Sci (1957) 1.58
The dependence of the secondary sex ratio in humans on the age of the father. Science (1953) 1.52
A study of the carrier state for plasma thromboplastin component (PTC, Christmas factor) deficiency, utilizing a new assay procedure. J Lab Clin Med (1960) 1.37
Parental age in acondroplasia and mongolism. Am J Hum Genet (1957) 1.20
Anti-hemophilic globulin levels in carriers of hemophilia A. J Clin Invest (1960) 0.99
An estimation of the cumulative mutation rate for sex-linked lethals in man which produce fetal deaths. Am J Hum Genet (1966) 0.98
High resolution of human evolutionary trees with polymorphic microsatellites. Nature (1994) 28.48
Phylogenetic analysis. Models and estimation procedures. Am J Hum Genet (1967) 17.65
Multilocus genotypes, a tree of individuals, and human evolutionary history. Am J Hum Genet (1997) 14.46
Maternal inheritance of human mitochondrial DNA. Proc Natl Acad Sci U S A (1980) 9.48
Genetic absolute dating based on microsatellites and the origin of modern humans. Proc Natl Acad Sci U S A (1995) 9.25
An evaluation of genetic distances for use with microsatellite loci. Genetics (1995) 8.79
Population structure and human evolution. Proc R Soc Lond B Biol Sci (1966) 8.78
Y chromosome sequence variation and the history of human populations. Nat Genet (2000) 8.34
Drift, admixture, and selection in human evolution: a study with DNA polymorphisms. Proc Natl Acad Sci U S A (1991) 8.14
Radiation of human mitochondria DNA types analyzed by restriction endonuclease cleavage patterns. J Mol Evol (1983) 6.80
Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography. Genome Res (1997) 6.73
The genetic legacy of Paleolithic Homo sapiens sapiens in extant Europeans: a Y chromosome perspective. Science (2000) 6.57
Cultural transmission and evolution: a quantitative approach. Monogr Popul Biol (1981) 6.42
The phylogeography of Y chromosome binary haplotypes and the origins of modern human populations. Ann Hum Genet (2001) 6.24
The probability of consanguineous marriages. Genetics (1966) 5.85
Genetic evidence for a higher female migration rate in humans. Nat Genet (1998) 5.77
Nuclear DNA polymorphism in a Mandenka population from Senegal: comparison with eight other human populations. Ann Hum Genet (1995) 5.34
A genomic screen of autism: evidence for a multilocus etiology. Am J Hum Genet (1999) 4.96
A migration matrix model for the study of random genetic drift. Genetics (1968) 4.59
A pre-Columbian Y chromosome-specific transition and its implications for human evolutionary history. Proc Natl Acad Sci U S A (1996) 4.52
Comparison of 79 DNA polymorphisms tested in Australians, Japanese and Papua New Guineans with those of five other human populations. Gene Geogr (1994) 4.50
Theory and observation in cultural transmission. Science (1982) 4.05
Study of 47 DNA markers in five populations from four continents. Gene Geogr (1987) 4.04
Ethnic variation in Hpa 1 endonuclease cleavage patterns of human mitochondrial DNA. Proc Natl Acad Sci U S A (1981) 3.71
Demographic history of India and mtDNA-sequence diversity. Am J Hum Genet (1995) 3.47
Human mitochondrial DNA types in two Israeli populations--a comparative study at the DNA level. Am J Hum Genet (1986) 3.17
Detecting linkage for genetically heterogeneous diseases and detecting heterogeneity with linkage data. Am J Hum Genet (1986) 3.16
An apportionment of human DNA diversity. Proc Natl Acad Sci U S A (1997) 3.15
Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents. Proc Natl Acad Sci U S A (1990) 3.09
Multiple DNA fragment polymorphisms associated with immunoglobulin mu chain switch-like regions in man. Proc Natl Acad Sci U S A (1983) 3.07
Inference of human evolution through cladistic analysis of nuclear DNA restriction polymorphisms. Proc Natl Acad Sci U S A (1994) 3.07
Population genetic implications from sequence variation in four Y chromosome genes. Proc Natl Acad Sci U S A (2000) 2.62
Cultural versus biological inheritance: phenotypic transmission from parents to children. (A theory of the effect of parental phenotypes on children's phenotypes). Am J Hum Genet (1973) 2.61
Assortment of encounters and evolution of cooperativeness. Proc Natl Acad Sci U S A (1982) 2.60
Uralic genes in Europe. Am J Phys Anthropol (1990) 2.57
Construction of human Y-chromosomal haplotypes using a new polymorphic A to G transition. Hum Mol Genet (1994) 2.47
Fetal cells in the blood of pregnant women: detection and enrichment by fluorescence-activated cell sorting. Proc Natl Acad Sci U S A (1979) 2.45
Cultural variation in Africa: role of mechanisms of transmission and adaptation. Proc Natl Acad Sci U S A (1995) 2.35
Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretion. N Engl J Med (1982) 2.34
The Levant versus the Horn of Africa: evidence for bidirectional corridors of human migrations. Am J Hum Genet (2004) 2.20
Analysis of evolution: evolutionary rates, independence and treeness. Theor Popul Biol (1975) 2.15
Detection of genetic variation with radioactive ligands. III. genetic polymorphism of transcobalamin II in human plasma. Am J Hum Genet (1978) 2.13
Cultural and biological evolutionary processes, selection for a trait under complex transmission. Theor Popul Biol (1976) 2.13
A systematic approach for detecting high-frequency restriction fragment length polymorphisms using large genomic probes. Am J Hum Genet (1985) 2.12
Statistical properties of the variation at linked microsatellite loci: implications for the history of human Y chromosomes. Mol Biol Evol (1996) 2.07
Analytic review: some current problems of human population genetics. Am J Hum Genet (1973) 2.05
Study of an additional 58 DNA markers in five human populations from four continents. Gene Geogr (1991) 1.98
Evidence against linkage of schizophrenia to markers on chromosome 5 in a northern Swedish pedigree. Nature (1988) 1.96
Paradox of the evolution of communication and of social interactivity. Proc Natl Acad Sci U S A (1983) 1.95
Cultural versus genetic adaptation. Proc Natl Acad Sci U S A (1983) 1.93
The great human expansion. Proc Natl Acad Sci U S A (2012) 1.86
Studies on African Pygmies. I. A pilot investigation of Babinga Pygmies in the Central African Republic (with an analysis of genetic distances). Am J Hum Genet (1969) 1.81
Group-specific component (Gc) proteins bind vitamin D and 25-hydroxyvitamin D. Proc Natl Acad Sci U S A (1975) 1.77
Genetics and the origin of European languages. Proc Natl Acad Sci U S A (1995) 1.76
Darwinian selection and "altruism". Theor Popul Biol (1978) 1.75
Distribution of haplotypes from a chromosome 21 region distinguishes multiple prehistoric human migrations. Proc Natl Acad Sci U S A (1999) 1.68
Paleolithic and Neolithic lineages in the European mitochondrial gene pool. Am J Hum Genet (1997) 1.64
The Fifth Histocompatibility Workshop gene frequency data: a phylogenetic analysis. Tissue Antigens (1975) 1.64
Report of the Second International Workshop on Human Chromosome 6. Genomics (1994) 1.64
DNA markers and genetic variation in the human species. Cold Spring Harb Symp Quant Biol (1986) 1.59
Ethnic variation of genetic disease: roles of drift for recessive lethal genes. Am J Hum Genet (1978) 1.55
Insulin-like growth factors in pygmies. The role of puberty in determining final stature. N Engl J Med (1987) 1.55
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds. Am J Hum Genet (1991) 1.53
The genetics of psoriasis. Arch Dermatol (1972) 1.49
T-cell receptor V alpha and C alpha alleles associated with multiple and myasthenia gravis. Proc Natl Acad Sci U S A (1989) 1.47
A discordant sibship analysis between beta-NGF and neurofibromatosis. Am J Hum Genet (1985) 1.44
The probability of exclusion of ancestries based on genetic observations. Am J Hum Genet (1985) 1.43
Evolution of continuous variation: direct approach through joint distribution of genotypes and phenotypes. Proc Natl Acad Sci U S A (1976) 1.42
Autism and the X chromosome. Multipoint sib-pair analysis. Arch Gen Psychiatry (1996) 1.42
Subdivision and inbreeding. Am J Hum Genet (1971) 1.40
Two RFLPs for the human dihydrofolate reductase gene (DHFR). Nucleic Acids Res (1987) 1.39
Synthetic gene frequency maps of man and selective effects of climate. Proc Natl Acad Sci U S A (1981) 1.39
Polymorphic restriction endonuclease fragment segregates and correlates with the gene for HLA-B8. Proc Natl Acad Sci U S A (1983) 1.33
An analysis of the genetics of schizophrenia. Soc Biol (1973) 1.31
RFLP analysis on a sample from northern Italy. Gene Geogr (1994) 1.31
Peopling of three Mediterranean islands (Corsica, Sardinia, and Sicily) inferred by Y-chromosome biallelic variability. Am J Phys Anthropol (2003) 1.30
Population genetics in the province of Ferrara. I. Genetic distances and geographic distances. Am J Hum Genet (1977) 1.30
The evolution of surnames: an analysis of their distribution and extinction. Theor Popul Biol (1974) 1.28
Polymorphic markers of human T-cell receptor alpha and beta genes. Family studies and comparison of frequencies in healthy individuals and patients with multiple sclerosis and myasthenia gravis. Hum Immunol (1988) 1.27
Aspects of variance and covariance analysis with cultural inheritance. Theor Popul Biol (1979) 1.24
Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13. Am J Hum Genet (1987) 1.24
Genetic analysis of eight linked polymorphisms within the human immunoglobulin heavy-chain region. Am J Hum Genet (1985) 1.23
Cultural and biological evolutionary processes: gene-culture disequilibrium. Proc Natl Acad Sci U S A (1984) 1.21
Polymorphisms of a human variable heavy chain gene show linkage with constant heavy chain genes. Proc Natl Acad Sci U S A (1984) 1.20
Maori origins, Y-chromosome haplotypes and implications for human history in the Pacific. Hum Mutat (2001) 1.19
A genetic nomenclature for human blood coagulation. Thromb Diath Haemorrh (1973) 1.18
The human "interferon-beta 2/hepatocyte stimulating factor/interleukin-6" gene: DNA polymorphism studies and localization to chromosome 7p21. Genomics (1988) 1.17
Evolution of modern humans: evidence from nuclear DNA polymorphisms. Philos Trans R Soc Lond B Biol Sci (1992) 1.16
Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locus. Am J Hum Genet (1995) 1.15
Screening for beta-thalassaemia heterozygotes. Lancet (1980) 1.15
Genetic analysis of cystic fibrosis: linkage of DNA and classical markers in multiplex families. Am J Hum Genet (1986) 1.15
Hereditary hydrometrocolpos with polydactyly in infancy. Pediatrics (1971) 1.15
Reproductive compensation in families segregating for Cooley's anaemia in Ferrara. Ann Hum Genet (1978) 1.14
Microsatellite evolution in modern humans: a comparison of two data sets from the same populations. Ann Hum Genet (2000) 1.14
Metabolic and genetic studies of a family with ornithine transcarbamylase deficiency. Pediatr Res (1974) 1.14
Barriers to gene flow estimated by surname distribution in Italy. Ann Hum Genet (1993) 1.14
Detection and isolation of fetal cells from maternal blood using the flourescence-activated cell sorter (FACS). Prenat Diagn (1981) 1.12
Assessment of prospective genetic counseling in the Ferrara area. Am J Med Genet (1980) 1.12