Published in Am J Hum Genet on November 01, 1977
Detection of genetic variation with radioactive ligands. I. Electrophoretic screening of plasma proteins with a selected panel of compounds. Am J Hum Genet (1977) 0.96
Heritability of quantitative variation at the group-specific component (Gc) locus. Am J Hum Genet (1984) 0.87
Quantitative studies of the interaction of cholecalciferol ((vitamin D3) and its metabolites with different genetic variants of the serum binding protein for these sterols. Biochem J (1979) 0.84
Immune-electrophoretic demonstration of qualitative differences in human sera and their relation to the haptoglobins. Acta Pathol Microbiol Scand (1959) 2.92
Skin-pigment regulation of vitamin-D biosynthesis in man. Science (1967) 2.22
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
25-Hydroxyvitamin D transport in human plasma. Isolation and partial characterization of calcifidiol-binding protein. J Biol Chem (1976) 1.39
The variants of the group-specific component. A review of their distribution in human populations. Isr J Med Sci (1974) 1.31
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The physiologic significance of plasma transport of vitamin D and metabolites. Am J Med (1974) 1.20
The purification and characterisation of the human-serum binding protein for the 25-hydroxycholecalciferol (transcalciferin). Identity with group-specific component. Eur J Biochem (1976) 1.13
Immunological and immunoassay studies of the binding protein for vitamin D and its metabolites in human serum. J Clin Invest (1977) 1.01
THE DISTRIBUTION OF THE GROUP SPECIFIC COMPONENT (GC) IN SELECTED POPULATIONS IN SOUTH EAST ASIA AND OCEANIA. Acta Genet Stat Med (1963) 1.01
Detection of genetic variation with radioactive ligands. I. Electrophoretic screening of plasma proteins with a selected panel of compounds. Am J Hum Genet (1977) 0.96
A NEW ALLELE IN THE GC-SYSTEM: GC. Vox Sang (1965) 0.91
A new variant in the Gc system. Acta Genet Stat Med (1965) 0.90
Variants of the group-specific component system as demonstrated by immunofixation electrophoresis. Report of a new variant, Gc Boston (Ge B). Am J Hum Genet (1975) 0.86
The distribution of several serological and biochemical traits in east Asia. 3. The distribution of gamma-globulin (Gm(1), Gm(2), Gm(5) and Inv(1) and Gc groups in Taiwan and Ryukyu. Hum Hered (1971) 0.86
Gc Norway (Ge1C): a second mother-child combination. Vox Sang (1969) 0.82
Immunoelectrophoretic study of group specific components (Gc system). Frequency of distribution of Gc system in Japanese population. Jinrui Idengaku Zasshi (1966) 0.82
A faster migrating Gc-variant: Gc Darmstadt. Humangenetik (1970) 0.82
A comparison of the fast migrating Gc-variant of Australian aborigines, New Guinean indigenes, South African Bantu, and black Americans. Hum Hered (1972) 0.82
A new rapid migrating variant in the Gc-system: Gc Wien. Humangenetik (1972) 0.80
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
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
Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8. Genomics (1991) 3.93
Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuria. Am J Hum Genet (1985) 3.77
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
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies. Hum Mutat (2001) 3.07
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
Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis. Nat Genet (2000) 2.85
Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria. Hum Genet (1987) 2.73
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
Cultural variation in Africa: role of mechanisms of transmission and adaptation. Proc Natl Acad Sci U S A (1995) 2.35
Apparent heterozygote deficiencies observed in DNA typing data and their implications in forensic applications. Ann Hum Genet (1992) 2.32
A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene. Am J Hum Genet (1998) 2.29
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
Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa. Nat Genet (1999) 2.13
A systematic approach for detecting high-frequency restriction fragment length polymorphisms using large genomic probes. Am J Hum Genet (1985) 2.12
Prevalence of AIPL1 mutations in inherited retinal degenerative disease. Mol Genet Metab (2000) 2.07
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
Cleft lip and palate: no evidence of linkage to transforming growth factor alpha. Am J Hum Genet (1991) 1.94
Cultural versus genetic adaptation. Proc Natl Acad Sci U S A (1983) 1.93
Localization of two genes for Usher syndrome type I to chromosome 11. Genomics (1992) 1.90
The great human expansion. Proc Natl Acad Sci U S A (2012) 1.86
Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation in codon 23 of rhodopsin. Arch Ophthalmol (1991) 1.81
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
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
Spinocerebellar ataxia: variable age of onset and linkage to human leukocyte antigen in a large kindred. Ann Neurol (1988) 1.54
X-linked dominant cone-rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP 15) to Xp22.13-p22.11. Am J Hum Genet (1995) 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
Sequences on the human Y chromosome homologous to the autosomal gene for argininosuccinate synthetase. Nature (1982) 1.46
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
Synthetic gene frequency maps of man and selective effects of climate. Proc Natl Acad Sci U S A (1981) 1.39
Two RFLPs for the human dihydrofolate reductase gene (DHFR). Nucleic Acids Res (1987) 1.39
Multilocus linkage analysis with the human argininosuccinate synthetase gene. Genomics (1989) 1.36
Localization of retina/pineal-expressed sequences: identification of novel candidate genes for inherited retinal disorders. Genomics (1999) 1.36
The human apolipoprotein B-100 gene: a highly polymorphic gene that maps to the short arm of chromosome 2. Biochem Biophys Res Commun (1985) 1.36
Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa. Hum Mol Genet (1999) 1.35
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
Evidence for a major gene (RP10) for autosomal dominant retinitis pigmentosa on chromosome 7q: linkage mapping in a second, unrelated family. Hum Genet (1995) 1.29
The evolution of surnames: an analysis of their distribution and extinction. Theor Popul Biol (1974) 1.28
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15. Am J Hum Genet (2000) 1.28
Polymorphisms at VNTR loci suggest homogeneity of the white population of Utah. Hum Biol (1991) 1.27
Exclusion of Usher syndrome gene from much of chromosome 4. Cytogenet Cell Genet (1989) 1.27
The effect of parental age on rates of mutation for hemophilia and evidence for differing mutation rates for hemophilia A and B. Am J Hum Genet (1968) 1.27
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
Nonsyndromic cleft lip and palate: no evidence of linkage to HLA or factor 13A. Am J Hum Genet (1993) 1.23
Cultural and biological evolutionary processes: gene-culture disequilibrium. Proc Natl Acad Sci U S A (1984) 1.21